# terms

id: PBO:0091735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 snRNA-specific guide RNA","termid":"PBO:0091735"}


id: GO:0009701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of isoflavonoid phytoalexins, a group of water-soluble phenolic derivatives isomeric with flavonoids that possess antibiotic activity and are produced by plant tissues in response to infection.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoflavonoid biosynthetic process","termid":"GO:0009717"},{"relation_name":"is_a","term_name":"isoflavonoid phytoalexin metabolic process","termid":"GO:0046289"},{"relation_name":"is_a","term_name":"phytoalexin biosynthetic process","termid":"GO:0052315"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"isoflavonoid phytoalexin biosynthetic process","synonyms":[{"name":"isoflavonoid phytoalexin anabolism","type":"exact"},{"name":"isoflavonoid phytoalexin biosynthesis","type":"exact"},{"name":"isoflavonoid phytoalexin formation","type":"exact"},{"name":"isoflavonoid phytoalexin synthesis","type":"exact"}],"termid":"GO:0009701"}


id: PBO:0042408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle 20B","termid":"PBO:0042408"}


id: PBO:0080600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 35","termid":"PBO:0080600"}


id: MONDO:0001744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The sudden increase of intraocular pressure, resulting in pain and an abrupt decrease in visual acuity.","definition_xrefs":["NCIT:C34639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glaucoma","termid":"MONDO:0005041"}],"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":"angle-closure glaucoma","secondary_identifiers":["MESH:D015812","UMLS:C0017605","SCTID:392291006","DOID:13550","MEDGEN:6610"],"synonyms":[{"name":"ACG - angle-closure glaucoma","type":"exact"},{"name":"Narrow cleft glaucoma","type":"exact"},{"name":"angle closure glaucoma","type":"exact"},{"name":"primary open-angle glaucoma with narrow angles","type":"exact"}],"termid":"MONDO:0001744","xrefs":{"Monarch":{"xref_id":"0001744"}}}


id: PBO:0039464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 13A","termid":"PBO:0039464"}


id: GO:0042891
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of an antibiotic, a substance produced by or derived from certain fungi, bacteria, and other organisms, that can destroy or inhibit the growth of other microorganisms, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete antibiotic transport (obsolete GO:0042891)","termid":"GO:0042891"}


id: PBO:0066138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RB transcriptional corepressor 1","termid":"PBO:0066138"}


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


id: MONDO:0014652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any exudative vitreoretinopathy in which the cause of the disease is a mutation in the ZNF408 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exudative vitreoretinopathy","termid":"MONDO:0019516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005328"],"is_obsolete":false,"name":"exudative vitreoretinopathy 6","secondary_identifiers":["DOID:0111410","UMLS:C4225316","OMIM:616468","MEDGEN:902559","GARD:16118"],"synonyms":[{"name":"EVR6","type":"related"},{"name":"ZNF408 exudative vitreoretinopathy","type":"exact"},{"name":"exudative vitreoretinopathy 6","type":"exact"},{"name":"exudative vitreoretinopathy caused by mutation in ZNF408","type":"exact"},{"name":"exudative vitreoretinopathy type 6","type":"exact"}],"termid":"MONDO:0014652","xrefs":{"Monarch":{"xref_id":"0014652"}}}


id: MONDO:0008832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A visceral heterotaxy characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and may be associated with bilateral trilobed lungs, midline liver, asplenia and situs inversus affecting other organs that has material basis in homozygous mutation in the GDF1 gene on chromosome 19p12.","definition_xrefs":["PMID:14648004","PMID:20413652","DOID:0060856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"visceral heterotaxy","termid":"MONDO:0018677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"right atrial isomerism","secondary_identifiers":["GARD:6795","HP:0011536","Orphanet:97548","MedDRA:10068335","UMLS:C3178806","MEDGEN:465274","NORD:1305","OMIM:208530"],"synonyms":[{"name":"Ivemark Syndrome","type":"exact"},{"name":"Ivemark syndrome","type":"exact"},{"name":"Polyasplenia","type":"related"},{"name":"RAI","type":"related"},{"name":"Vah, autosomal recessive","type":"related"},{"name":"asplenia syndrome","type":"related"},{"name":"asplenia with cardiovascular anomalies","type":"exact"},{"name":"bilateral right-sidedness sequence","type":"related"},{"name":"heterotaxy, Visceroatrial, autosomal recessive","type":"related"},{"name":"polysplenia syndrome","type":"related"},{"name":"right atrial isomerism","type":"exact"},{"name":"right atrial isomerism (disease)","type":"exact"},{"name":"right atrial isomerism (ivemark)","type":"exact"},{"name":"right isomerism","type":"related"},{"name":"splenic agenesis syndrome","type":"related"}],"termid":"MONDO:0008832","xrefs":{"Monarch":{"xref_id":"0008832"}}}


id: PBO:0081156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein, FOG family member 1","termid":"PBO:0081156"}


id: PBO:0056178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAFA antisense RNA 1","termid":"PBO:0056178"}


id: GO:0062175
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of brexanolone.","definition_xrefs":["PMID:24390875"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid catabolic process","termid":"GO:0006706"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"brexanolone metabolic process","termid":"GO:0062173"}],"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:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"brexanolone catabolic process","synonyms":[{"name":"allopregnanolone breakdown","type":"exact"},{"name":"allopregnanolone catabolic process","type":"exact"},{"name":"allopregnanolone catabolism","type":"exact"},{"name":"allopregnanolone degradation","type":"exact"},{"name":"allotetrahydroprogesterone breakdown","type":"exact"},{"name":"allotetrahydroprogesterone catabolic process","type":"exact"},{"name":"allotetrahydroprogesterone catabolism","type":"exact"},{"name":"allotetrahydroprogesterone degradation","type":"exact"},{"name":"brexanolone breakdown","type":"exact"},{"name":"brexanolone catabolism","type":"exact"},{"name":"brexanolone degradation","type":"exact"}],"termid":"GO:0062175"}


id: PBO:0003531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tspO homolog/ peripheral benzodiazepine receptor homolog, involved in the transport cytoplas/mitochondrial of haem (predicted)","termid":"PBO:0003531"}


id: GO:0051139
data:
  {"annotated_genes":["SJAG_01541","SJAG_04698","SJAG_04616","SJAG_04028","SJAG_04096"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115061,90185,90686,97829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015369"},{"annotations":[90687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010486"},{"annotations":[88795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015386"},{"annotations":[96230,88796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015385"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: metal ion(in) + H+(out) = metal ion(out) + H+(in).","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton transmembrane transporter activity","termid":"GO:0015078"},{"relation_name":"is_a","term_name":"metal cation:monoatomic cation antiporter activity","termid":"GO:0140828"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01541":null,"SJAG_04028":null,"SJAG_04096":null,"SJAG_04616":null,"SJAG_04698":null},"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":"metal cation:proton antiporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-435171"],"synonyms":[{"name":"metal ion:hydrogen antiporter activity","type":"exact"},{"name":"metal ion:proton antiporter activity","type":"exact"}],"termid":"GO:0051139","terms_by_termid":{"GO:0010486":null,"GO:0015369":null,"GO:0015385":null,"GO:0015386":null}}


id: GO:0051769
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of a nitric-oxide synthase enzyme.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of nitric-oxide synthase biosynthetic process (obsolete GO:0051769)","synonyms":[{"name":"regulation of NO synthase biosynthesis","type":"exact"},{"name":"regulation of NO synthase biosynthetic process","type":"exact"},{"name":"regulation of NOS biosynthesis","type":"exact"},{"name":"regulation of NOS biosynthetic process","type":"exact"},{"name":"regulation of NOS2 synthase biosynthesis","type":"narrow"},{"name":"regulation of NOS2 synthase biosynthetic process","type":"narrow"},{"name":"regulation of nitric-oxide synthase (type 2) biosynthesis","type":"narrow"},{"name":"regulation of nitric-oxide synthase (type 2) biosynthetic process","type":"narrow"},{"name":"regulation of nitric-oxide synthase (type II) biosynthesis","type":"narrow"},{"name":"regulation of nitric-oxide synthase (type II) biosynthetic process","type":"narrow"},{"name":"regulation of nitric-oxide synthase 2 biosynthetic process","type":"narrow"}],"termid":"GO:0051769"}


id: PBO:0069311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 567, pseudogene","termid":"PBO:0069311"}


id: PBO:0054961
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 2375","termid":"PBO:0054961"}


id: MONDO:0023199
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":"frontonasal dysplasia phocomelic upper limbs","termid":"MONDO:0023199","xrefs":{"Monarch":{"xref_id":"0023199"}}}


id: PBO:0051052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 2-15","termid":"PBO:0051052"}


id: MONDO:0001884
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm involving a abducens nerve.","definition_xrefs":["MONDO:patterns/neoplasm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve neoplasm","termid":"MONDO:0002633"},{"relation_name":"is_a","term_name":"abducens nerve disorder","termid":"MONDO:0020594"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abducens nerve neoplasm","secondary_identifiers":["UMLS:C1263898","ICD9:239.7","DOID:14125","MEDGEN:224732","SCTID:126972009","NCIT:C5826"],"synonyms":[{"name":"VIth cranial nerve neoplasms","type":"exact"},{"name":"VIth cranial nerve tumors","type":"exact"},{"name":"VIth cranial nerve tumours","type":"exact"},{"name":"abducens nerve neoplasm (disease)","type":"exact"},{"name":"abducens nerve neoplasms","type":"exact"},{"name":"abducens nerve tumor","type":"exact"},{"name":"abducens nerve tumors","type":"exact"},{"name":"abducens nerve tumour","type":"exact"},{"name":"abducens nerve tumours","type":"exact"},{"name":"neoplasm of abducens nerve","type":"exact"},{"name":"neoplasm of sixth cranial nerve","type":"exact"},{"name":"neoplasm of the abducens nerve","type":"exact"},{"name":"neoplasm of the sixth cranial nerve","type":"exact"},{"name":"sixth cranial nerve neoplasm","type":"exact"},{"name":"sixth cranial nerve neoplasms","type":"exact"},{"name":"sixth cranial nerve tumor","type":"exact"},{"name":"sixth cranial nerve tumors","type":"exact"},{"name":"sixth cranial nerve tumour","type":"exact"},{"name":"sixth cranial nerve tumours","type":"exact"},{"name":"tumor of abducens nerve","type":"exact"},{"name":"tumor of sixth cranial nerve","type":"exact"},{"name":"tumor of the abducens nerve","type":"exact"},{"name":"tumor of the sixth cranial nerve","type":"exact"},{"name":"tumour of abducens nerve","type":"exact"},{"name":"tumour of sixth cranial nerve","type":"exact"},{"name":"tumour of the abducens nerve","type":"exact"},{"name":"tumour of the sixth cranial nerve","type":"exact"}],"termid":"MONDO:0001884","xrefs":{"Monarch":{"xref_id":"0001884"}}}


id: FYPO:0003684
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the amount of any macromolecular complex present in a cell differs from wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of macromolecular complex","termid":"FYPO:0007316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"altered level of macromolecular complex during vegetative growth","synonyms":[{"name":"abnormal level of macromolecular complex during vegetative growth","type":"exact"},{"name":"altered level of macromolecular complex during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003684"}


id: PBO:0074885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 63","termid":"PBO:0074885"}


id: GO:1902925
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(hydroxyalkanoate) from fatty acid.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie","PMID:21129764","GO_REF:0000092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid metabolic process","termid":"GO:0006631"},{"relation_name":"is_a","term_name":"poly(hydroxyalkanoate) biosynthetic process","termid":"GO:1901441"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"poly(hydroxyalkanoate) biosynthetic process from fatty acid","synonyms":[{"name":"poly(hydroxyalkanoate) anabolism from fatty acid","type":"exact"},{"name":"poly(hydroxyalkanoate) biosynthesis from fatty acid","type":"exact"},{"name":"poly(hydroxyalkanoate) formation from fatty acid","type":"exact"},{"name":"poly(hydroxyalkanoate) synthesis from fatty acid","type":"exact"}],"termid":"GO:1902925"}


id: PBO:0017861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexose transmembrane transporter Ght4","termid":"PBO:0017861"}


id: PBO:0076641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-box brain transcription factor 1","termid":"PBO:0076641"}


id: CHEBI:278547
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium azide","termid":"CHEBI:278547"}


id: MONDO:0014215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the CCDC65 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 27","secondary_identifiers":["MEDGEN:816031","GARD:15976","UMLS:C3809701","DOID:0110611","OMIM:615504"],"synonyms":[{"name":"CCDC65 primary ciliary dyskinesia","type":"exact"},{"name":"CILD27","type":"exact"},{"name":"ciliary dyskinesia, primary, 27","type":"related"},{"name":"ciliary dyskinesia, primary, 27, without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 27","type":"exact"},{"name":"primary ciliary dyskinesia 27 without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in CCDC65","type":"exact"},{"name":"primary ciliary dyskinesia type 27","type":"exact"}],"termid":"MONDO:0014215","xrefs":{"Monarch":{"xref_id":"0014215"}}}


id: PBO:0082612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cofilin, involved in pH-dependent actin filament depolarization; binds both actin monomers and filaments and severs filaments; involved in the selective sorting, export of the secretory cargo from the late golgi; genetically interacts with pmr1; thought to be regulated by phosphorylation at SER4; ubiquitous and essential in eukaryotes","termid":"PBO:0082612"}


id: GO:0000718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of the oligonucleotide that contains the DNA damage. The oligonucleotide is formed by dual incisions that flank the site of DNA damage.","definition_xrefs":["GOC:elh","PMID:10197977"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleotide-excision repair, DNA damage removal (obsolete GO:0000718)","termid":"GO:0000718"}


id: PBO:0036166
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-protein_interaction","termid":"PBO:0036166"}


id: PBO:0072468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 32","termid":"PBO:0072468"}


id: PBO:0083490
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 gene YBR301W; YBR300C is not an essential gene","termid":"PBO:0083490"}


id: PBO:0058116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4418","termid":"PBO:0058116"}


id: FYPO:0009095
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is increased relative to normal in a medium containing fructose as the carbon source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0002057","FYPO:0000003","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"increased cell population growth on fructose carbon source","synonyms":[{"name":"increased growth on fructose carbon source","type":"broad"},{"name":"increased vegetative cell growth on fructose carbon source","type":"exact"}],"termid":"FYPO:0009095"}


id: GO:1903609
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of inward rectifier potassium channel activity.","definition_xrefs":["GOC:BHF","GO_REF:0000059","PMID:18923542","GOC:rl","GOC:mtg_cardiac_conduct_nov11","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inward rectifier potassium channel activity","termid":"GO:1901979"},{"relation_name":"is_a","term_name":"negative regulation of voltage-gated potassium channel activity","termid":"GO:1903817"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of inward rectifier potassium channel activity","synonyms":[{"name":"down regulation of Kir channel activity","type":"exact"},{"name":"down regulation of inward rectifier potassium channel activity","type":"exact"},{"name":"down-regulation of Kir channel activity","type":"exact"},{"name":"down-regulation of inward rectifier potassium channel activity","type":"exact"},{"name":"downregulation of Kir channel activity","type":"exact"},{"name":"downregulation of inward rectifier potassium channel activity","type":"exact"},{"name":"inhibition of Kir channel activity","type":"narrow"},{"name":"inhibition of inward rectifier potassium channel activity","type":"narrow"},{"name":"negative regulation of Kir channel activity","type":"exact"}],"termid":"GO:1903609"}


id: GO:0008111
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2S)-2-methylacyl-CoA = (2R)-2-methylacyl-CoA.","definition_xrefs":["EC:5.1.99.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity","termid":"GO:0016854"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"alpha-methylacyl-CoA racemase activity","secondary_identifiers":["Reactome:R-HSA-193763","Reactome:R-HSA-193452","Reactome:R-HSA-192056","RHEA:12657","MetaCyc:5.1.99.4-RXN","Reactome:R-HSA-389897","Reactome:R-HSA-193736"],"synonyms":[{"name":"2-methylacyl-CoA 2-epimerase activity","type":"related"}],"termid":"GO:0008111"}


id: FYPO:0007244
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 kinetochore of a chromosome is decreased during metaphase of mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to centromere during mitotic metaphase","termid":"FYPO:0003002"},{"relation_name":"is_a","term_name":"decreased protein localization to kinetochore during mitotic M phase","termid":"FYPO:0005215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to kinetochore during mitotic metaphase","synonyms":[{"name":"decreased protein localisation to kinetochore during mitotic metaphase","type":"exact"},{"name":"decreased protein localization to kinetochore during metaphase during mitotic cell cycle","type":"exact"},{"name":"reduced protein localization to kinetochore during mitotic metaphase","type":"exact"}],"termid":"FYPO:0007244"}


id: GO:1904664
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of N-terminal peptidyl-methionine acetylation.","definition_xrefs":["GO_REF:0000058","PMID:20807799","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein acetylation","termid":"GO:1901984"},{"relation_name":"is_a","term_name":"negative regulation of protein maturation","termid":"GO:1903318"},{"relation_name":"is_a","term_name":"regulation of N-terminal peptidyl-methionine acetylation","termid":"GO:1904663"},{"relation_name":"negatively_regulates","term_name":"N-terminal peptidyl-methionine acetylation","termid":"GO:0017196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"negatively_regulates","termid":"GO:0051604"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0051604"],"is_obsolete":false,"name":"negative regulation of N-terminal peptidyl-methionine acetylation","termid":"GO:1904664"}


id: PBO:0071971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 kinase C1","termid":"PBO:0071971"}


id: MOD:00993
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenyl ester","synonyms":[{"name":"OPh","type":"exact"}],"termid":"MOD:00993"}


id: PBO:0052732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 24","termid":"PBO:0052732"}


id: RO:0002527
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x does not overlaps the sequence of x if and only if there is no z such that x has a subsequence z and z is a subsequence of y.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequentially_related_to","termid":"RO:0002514"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does_not_overlap_sequence_of","termid":"RO:0002527"}


id: GO:1900854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of terrequinone A biosynthetic process.","definition_xrefs":["PMID:24066102","GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"positively_regulates","term_name":"terrequinone A biosynthetic process","termid":"GO:1900796"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of terrequinone A biosynthetic process","secondary_identifiers":["GO:1900852"],"synonyms":[{"name":"regulation of terrequinone A biosynthetic process","type":"broad"},{"name":"up regulation of terrequinone A biosynthetic process","type":"exact"},{"name":"up-regulation of terrequinone A biosynthetic process","type":"exact"},{"name":"upregulation of terrequinone A biosynthetic process","type":"exact"}],"termid":"GO:1900854"}


id: GO:0120243
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-iminopropanoate + H2O = NH4(+) + pyruvate.","definition_xrefs":["RHEA:40671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-iminobutanoate/2-iminopropanoate deaminase","termid":"GO:0120241"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-iminopropanoate deaminase activity","secondary_identifiers":["KEGG_REACTION:R11099","MetaCyc:RXN-15127"],"synonyms":[{"name":"2-iminobutanoate/2-iminopropanoate deaminase","type":"broad"}],"termid":"GO:0120243"}


id: PBO:0083449
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 gene CDC9/YDL164C encoding DNA ligase","termid":"PBO:0083449"}


id: PBO:0042081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC148 antisense RNA 1","termid":"PBO:0042081"}


id: PR:Q9P7J2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- xlf1 gene.","definition_xrefs":["UniProtKB:Q9P7J2","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":"Xrcc4-like factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC24B10.14c","synonyms":[{"name":"Spom972h-xlf1","type":"exact"},{"name":"meiotically up-regulated gene 104 protein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"non-homologous end-joining protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7J2"}


id: PBO:0087119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RING-finger peroxin and E3 ubiquitin ligase; peroxisomal membrane protein with a C-terminal zinc-binding RING domain, forms translocation subcomplex with Pex10p and Pex12p which functions in peroxisomal matrix protein import","termid":"PBO:0087119"}


id: FYPO:0005055
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell has two and more than one septum, and the septa are grouped together between the two compartments, one or more of which may contain multiple nuclei.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binucleate multiseptate vegetative cell","termid":"FYPO:0001223"},{"relation_name":"is_a","term_name":"multinucleate multiseptate vegetative cell, septa grouped","termid":"FYPO:0001254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000631","FYPO:0001320","FYPO:0000032","FYPO:0000002"],"is_obsolete":false,"name":"binucleate multiseptate cell, septa grouped","synonyms":[{"name":"binucleate multiseptate cell, septa grouped during mitotic cell cycle","type":"related"},{"name":"binucleate multiseptate cell, septa grouped during vegetative growth","type":"exact"}],"termid":"FYPO:0005055"}


id: PR:O94411
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug55 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94411"],"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":"meiotic fizzy-related protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.04c","synonyms":[{"name":"Spom972h-mug55","type":"exact"},{"name":"meiotically up-regulated gene 55 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94411"}


id: PBO:0083143
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; almost completely overlaps 5' end of ORF YMR317W","termid":"PBO:0083143"}


id: MONDO:0024685
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukemia","termid":"MONDO:0004643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"Philadelphia-positive myelogenous leukemia","secondary_identifiers":["NCIT:C3177","UMLS:C0023476","MEDGEN:9731"],"synonyms":[{"name":"Ph1-positive granulocytic leukaemia","type":"exact"},{"name":"Ph1-positive granulocytic leukemia","type":"exact"},{"name":"Ph1-positive myelocytic leukaemia","type":"exact"},{"name":"Ph1-positive myelocytic leukemia","type":"exact"},{"name":"Ph1-positive myelogenous leukaemia","type":"exact"},{"name":"Ph1-positive myelogenous leukemia","type":"exact"},{"name":"Ph1-positive myeloid leukaemia","type":"exact"},{"name":"Ph1-positive myeloid leukemia","type":"exact"},{"name":"Philadelphia-positive granulocytic leukaemia","type":"exact"},{"name":"Philadelphia-positive granulocytic leukemia","type":"exact"},{"name":"Philadelphia-positive myelocytic leukaemia","type":"exact"},{"name":"Philadelphia-positive myelocytic leukemia","type":"exact"},{"name":"Philadelphia-positive myelogenous leukemia","type":"exact"},{"name":"Philadelphia-positive myeloid leukaemia","type":"exact"},{"name":"Philadelphia-positive myeloid leukemia","type":"exact"}],"termid":"MONDO:0024685","xrefs":{"Monarch":{"xref_id":"0024685"}}}


id: GO:0006860
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed extracellular movement of amino acids.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular transport","termid":"GO:0006858"},{"relation_name":"is_a","term_name":"amino acid transport","termid":"GO:0006865"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"extracellular amino acid transport","termid":"GO:0006860"}


id: GO:0034429
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Generation of a long process of a CNS neuron, that carries efferent (outgoing) action potentials from the cell body in the optic tectum towards target cells in the premotor reticulospinal system in the hindbrain.","definition_xrefs":["PMID:8038988","PMID:17507550","PMID:15065115","GOC:dsf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system projection neuron axonogenesis","termid":"GO:0021952"}],"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":"tectobulbar tract morphogenesis","termid":"GO:0034429"}


id: PR:Q10408
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sro7 gene.","definition_xrefs":["UniProtKB:Q10408","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 C1F3.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F3.03","synonyms":[{"name":"Spom972h-sro7","type":"exact"}],"termid":"PR:Q10408"}


id: PBO:0063472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein disulfide isomerase family A member 2","termid":"PBO:0063472"}


id: PBO:0087705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; component of the Middle domain of mediator; required for regulation of RNA polymerase II activity; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0087705"}


id: PBO:0000259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAD-dependent oxidoreductase (predicted)","termid":"PBO:0000259"}


id: MONDO:0037847
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that involves the intervertebral joint.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"arthropathy","termid":"MONDO:0006816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertebral joint disorder","secondary_identifiers":["MEDGEN:1853166","SCTID:372109003","EFO:0009477","UMLS:C0541407"],"synonyms":[{"name":"disease of intervertebral joint","type":"exact"},{"name":"disease or disorder of intervertebral joint","type":"exact"},{"name":"disorder of intervertebral joint","type":"exact"},{"name":"disorder of joint of spine","type":"exact"},{"name":"intervertebral joint disease","type":"exact"},{"name":"intervertebral joint disease or disorder","type":"exact"},{"name":"spondyloarthropathy","type":"related"}],"termid":"MONDO:0037847","xrefs":{"Monarch":{"xref_id":"0037847"}}}


id: MONDO:0007163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Episodic ataxia type 2 (EA2) is the most frequent form of Hereditary episodic ataxia (EA) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.","definition_xrefs":["Orphanet:97"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary episodic ataxia","termid":"MONDO:0016227"},{"relation_name":"is_a","term_name":"CACNA1A-related complex neurodevelopmental disorder","termid":"MONDO:0100254"}],"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":"episodic ataxia type 2","secondary_identifiers":["OMIM:108500","UMLS:C1720416","GARD:9602","MESH:C535506","DOID:0050990","SCTID:420932006","MEDGEN:314039"],"synonyms":[{"name":"APCA","type":"related"},{"name":"Acetazolamide-responsive episodic ataxia syndrome","type":"related"},{"name":"Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia","type":"related"},{"name":"Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia","type":"related"},{"name":"CACNA1A hereditary episodic ataxia","type":"exact"},{"name":"CAPA","type":"related"},{"name":"Cerebellopathy, hereditary paroxysmal","type":"related"},{"name":"EA2","type":"related"},{"name":"Nystagmus-associated episodic ataxia","type":"related"},{"name":"ataxia, episodic, with Nystagmus","type":"related"},{"name":"ataxia, familial paroxysmal","type":"related"},{"name":"ataxia, familial, paroxysmal","type":"related"},{"name":"cerebellar ataxia, paroxysmal, Acetazolamide-responsive","type":"related"},{"name":"episodic ataxia type 2","type":"exact"},{"name":"episodic ataxia with nystagmus","type":"related"},{"name":"episodic ataxia, Nystagmus-associated","type":"related"},{"name":"episodic ataxia, type 2","type":"related"},{"name":"familial paroxysmal ataxia","type":"related"},{"name":"hereditary episodic ataxia caused by mutation in CACNA1A","type":"exact"}],"termid":"MONDO:0007163","xrefs":{"Monarch":{"xref_id":"0007163"}}}


id: GO:0019694
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving alkanesulfonates, the anion of alkanesulfonic acids, sulfonic acid derivatives containing an aliphatic hydrocarbon group.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic acid metabolic process","termid":"GO:0006082"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"alkanesulfonate metabolic process","secondary_identifiers":["MetaCyc:ALKANEMONOX-PWY"],"synonyms":[{"name":"alkanesulfonate metabolism","type":"exact"},{"name":"alkanesulphonate metabolic process","type":"exact"},{"name":"alkanesulphonate metabolism","type":"exact"}],"termid":"GO:0019694"}


id: MONDO:0015459
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising from the nasopharyngeal epithelium. It includes the following types: keratinizing squamous cell carcinoma, nonkeratinizing carcinoma (differentiated and undifferentiated), basaloid squamous cell carcinoma, and papillary adenocarcinoma.","definition_xrefs":["NCIT:C3871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"head and neck carcinoma","termid":"MONDO:0002038"},{"relation_name":"is_a","term_name":"Epstein-Barr virus-associated carcinoma","termid":"MONDO:0017344"},{"relation_name":"is_a","term_name":"malignant tumor of nasopharynx","termid":"MONDO:0021315"},{"relation_name":"is_a","term_name":"carcinoma of pharynx","termid":"MONDO:0021345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"nasopharyngeal carcinoma","secondary_identifiers":["SCTID:363398003","ICD9:147.9","Orphanet:150","ICD9:147.3","UMLS:C2931822","MESH:C538339","DOID:9261","MESH:D00007727","ICD9:147.1","MedDRA:10028793","icd11.foundation:1883313543","ICD9:147","MESH:D000077274","GARD:7163","ICD9:147.2","ICD9:147.0","MEDGEN:419909","ONCOTREE:NPC"],"synonyms":[{"name":"NPC","type":"exact"},{"name":"cancer of nasopharynx","type":"broad"},{"name":"cancer of the nasopharynx","type":"broad"},{"name":"carcinoma of nasopharynx","type":"exact"},{"name":"carcinoma of the nasopharynx","type":"exact"},{"name":"malignant nasopharyngeal tumor","type":"broad"},{"name":"malignant nasopharyngeal tumour","type":"broad"},{"name":"malignant neoplasm of anterior wall of nasopharynx","type":"broad"},{"name":"malignant neoplasm of lateral wall of nasopharynx","type":"broad"},{"name":"malignant neoplasm of nasopharyngeal wall","type":"broad"},{"name":"malignant neoplasm of nasopharynx","type":"broad"},{"name":"malignant neoplasm of nasopharynx (disorder) [ambiguous]","type":"broad"},{"name":"malignant neoplasm of other specified sites of nasopharynx","type":"broad"},{"name":"malignant neoplasm of posterior wall of nasopharynx","type":"broad"},{"name":"malignant neoplasm of roof of nasopharynx","type":"broad"},{"name":"malignant neoplasm of superior wall of nasopharynx","type":"broad"},{"name":"malignant tumor of anterior wall of nasopharynx","type":"broad"},{"name":"malignant tumor of lateral wall of nasopharynx","type":"broad"},{"name":"malignant tumor of posterior wall of nasopharynx","type":"broad"},{"name":"malignant tumour of anterior wall of nasopharynx","type":"broad"},{"name":"malignant tumour of lateral wall of nasopharynx","type":"broad"},{"name":"malignant tumour of posterior wall of nasopharynx","type":"broad"},{"name":"nasopharyngeal cancer","type":"broad"},{"name":"nasopharyngeal carcinoma","type":"exact"},{"name":"nasopharyngeal throat cancer","type":"broad"},{"name":"nasopharynx carcinoma","type":"exact"},{"name":"primary malignant neoplasm of anterior wall of nasopharynx","type":"broad"},{"name":"squamous cell carcinoma of the nasopharynx","type":"exact"}],"termid":"MONDO:0015459","xrefs":{"Monarch":{"xref_id":"0015459"}}}


id: GO:0042441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving eye pigments, any general or particular coloring matter in living organisms, found or utilized in the eye.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pigment metabolic process involved in developmental pigmentation","termid":"GO:0043324"},{"relation_name":"part_of","term_name":"eye pigmentation","termid":"GO:0048069"}],"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":"eye pigment metabolic process","synonyms":[{"name":"eye pigment metabolism","type":"exact"}],"termid":"GO:0042441"}


id: PBO:0048881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A6 family member G, pseudogene","termid":"PBO:0048881"}


id: FYPO:0000351
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the fungal-type cell wall is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell wall during vegetative growth","termid":"FYPO:0000027"},{"relation_name":"is_a","term_name":"abnormal cell wall morphology","termid":"FYPO:0002947"}],"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"},{"rel_name":"is_a","termid":"FYPO:0002946"}],"interesting_parent_ids":["FYPO:0002946","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal cell wall morphology during vegetative growth","synonyms":[{"name":"abnormal cell wall morphology during mitotic cell cycle","type":"related"},{"name":"cell wall morphology: abnormal during vegetative growth","type":"related"}],"termid":"FYPO:0000351"}


id: MONDO:0014783
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any preimplantation embryonic lethality in which the cause of the disease is a mutation in the TLE6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"gene_count":0,"genotype_count":0,"name":"obsolete preimplantation embryonic lethality 1 (obsolete MONDO:0014783)","secondary_identifiers":["OMIM:616814"],"synonyms":[{"name":"PREMBL1","type":"exact"},{"name":"Prembl","type":"related"},{"name":"TLE6 preimplantation embryonic lethality","type":"exact"},{"name":"preimplantation embryonic lethality","type":"broad"},{"name":"preimplantation embryonic lethality 1","type":"exact"},{"name":"preimplantation embryonic lethality 1; PREMBL1","type":"exact"},{"name":"preimplantation embryonic lethality caused by mutation in TLE6","type":"exact"},{"name":"preimplantation embryonic lethality type 1","type":"exact"}],"termid":"MONDO:0014783","xrefs":{"Monarch":{"xref_id":"0014783"}}}


id: GO:0140475
data:
  {"annotated_genes":["SJAG_04558","SJAG_03116","SJAG_02246","SJAG_04455","SJAG_02795","SJAG_05196","SJAG_07018","SJAG_03200"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97779,99357,100488,102551,109663],"is_not":false,"summary":null,"term":"GO:0140475"},{"annotations":[112337,89611,102322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106166"}]},"cv_name":"molecular_function","definition":"The binding activity of a protein that brings together the spindle pole body and one or more other molecules, permitting them to function in a coordinated way.","definition_xrefs":["PMID:19942852"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeletal anchor activity","termid":"GO:0008093"}],"gene_count":8,"genes_by_uniquename":{"SJAG_02246":null,"SJAG_02795":null,"SJAG_03116":null,"SJAG_03200":null,"SJAG_04455":null,"SJAG_04558":null,"SJAG_05196":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008093"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0060090","GO:0008093","GO:0030674","GO:0003674"],"is_obsolete":false,"name":"spindle pole body anchor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140475","terms_by_termid":{"GO:0106166":null,"GO:0140475":null}}


id: PBO:0055682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipase family member K","termid":"PBO:0055682"}


id: MONDO:1011830
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":"audiogenic seizure, non-human animal","secondary_identifiers":["OMIA:000093"],"termid":"MONDO:1011830","xrefs":{"Monarch":{"xref_id":"1011830"}}}


id: MONDO:0014265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Alzheimer disease in which the cause of the disease is a mutation in the ADAM10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alzheimer disease","termid":"MONDO:0004975"},{"relation_name":"is_a","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"Alzheimer disease 18","secondary_identifiers":["DOID:0110050","OMIM:615590","UMLS:C3810041","MEDGEN:816371"],"synonyms":[{"name":"AD18","type":"exact"},{"name":"ADAM10 Alzheimer disease","type":"exact"},{"name":"Alzheimer disease 18","type":"exact"},{"name":"Alzheimer disease 18, late-onset","type":"related"},{"name":"Alzheimer disease 18, susceptibility to","type":"related"},{"name":"Alzheimer disease caused by mutation in ADAM10","type":"exact"},{"name":"Alzheimer disease type 18","type":"exact"},{"name":"Alzheimer's disease 18","type":"exact"},{"name":"Alzheimer's disease type 18","type":"exact"}],"termid":"MONDO:0014265","xrefs":{"Monarch":{"xref_id":"0014265"}}}


id: PBO:0050089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group AT-hook 2","termid":"PBO:0050089"}


id: MONDO:0800342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cap myopathy 2 (obsolete MONDO:0800342)","termid":"MONDO:0800342","xrefs":{"Monarch":{"xref_id":"0800342"}}}


id: MONDO:0014148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Estrogen resistance syndrome is a rare, genetic endocrine disease characterized by estrogen-receptor insensitivity to estrogens and the presence of elevated estrogen and gonadotropin serum levels. Clinical manifestations include absent breast development and primary amenorrhea in association with multicystic ovaries and/or hypoplastic uterus in female patients, normal or abnormal gonadal development in male patients and markedly delayed bone maturation, persistence of open epiphyses, reduced bone mineral density, and variable tall stature in both sexes. Glucose intolerance, hyperinsulinemia and lipid abnormalities may also be present.","definition_xrefs":["Orphanet:785"],"direct_ancestors":[{"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":"reproductive system disorder","termid":"MONDO:0005039"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"estrogen resistance syndrome","secondary_identifiers":["icd11.foundation:1267163286","UMLS:C3809250","GARD:16548","MEDGEN:815580","OMIM:615363","SCTID:724555000"],"synonyms":[{"name":"ESTRR","type":"related"},{"name":"estrogen insensitivity","type":"related"},{"name":"estrogen resistance","type":"related"},{"name":"oestrogen insensitivity","type":"related"},{"name":"oestrogen resistance","type":"related"}],"termid":"MONDO:0014148","xrefs":{"Monarch":{"xref_id":"0014148"}}}


id: PBO:0012305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteiasome complex subunit alpha 7, Pre10 (predicted)","termid":"PBO:0012305"}


id: GO:0033130
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an acetylcholine receptor.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"acetylcholine receptor binding","termid":"GO:0033130"}


id: MOD:01189
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label -","definition_xrefs":["Unimod:212#C","PubMed:12766232"],"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 C","synonyms":[{"name":"N-ethyl iodoacetamide-d5","type":"related"},{"name":"NEIAA:2H(5)","type":"related"}],"termid":"MOD:01189"}


id: MONDO:0000640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroectodermal tumor that involves the central nervous system.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"primitive neuroectodermal tumor","termid":"MONDO:0005462"}],"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":"central nervous system primitive neuroectodermal neoplasm","secondary_identifiers":["NANDO:2200100","NCIT:C5398","DOID:0060103","UMLS:C3887678","MEDGEN:854517","NANDO:2200099"],"synonyms":[{"name":"CNS PNET","type":"exact"},{"name":"CNS primitive neuroectodermal neoplasm","type":"exact"},{"name":"CNS primitive neuroectodermal tumor","type":"exact"},{"name":"CNS primitive neuroectodermal tumour","type":"exact"},{"name":"central nervous system PNET","type":"exact"},{"name":"central nervous system neuroectodermal tumor","type":"exact"},{"name":"central nervous system neuroectodermal tumour","type":"exact"},{"name":"central nervous system primitive neuroectodermal neoplasm","type":"exact"},{"name":"central nervous system primitive neuroectodermal tumor","type":"exact"},{"name":"central nervous system primitive neuroectodermal tumor (WHO grade IV)","type":"exact"},{"name":"central nervous system primitive neuroectodermal tumour","type":"exact"},{"name":"central nervous system primitive neuroectodermal tumour (WHO grade IV)","type":"exact"},{"name":"central primitive neuroectodermal neoplasm","type":"exact"},{"name":"central primitive neuroectodermal tumor","type":"exact"},{"name":"central primitive neuroectodermal tumour","type":"exact"},{"name":"primitive neuroectodermal tumor of central nervous system","type":"exact"},{"name":"primitive neuroectodermal tumour of central nervous system","type":"exact"}],"termid":"MONDO:0000640","xrefs":{"Monarch":{"xref_id":"0000640"}}}


id: PBO:0080722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WT1 transcription factor","termid":"PBO:0080722"}


id: GO:1905283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of epidermal growth factor receptor signaling pathway involved in heart process.","definition_xrefs":["GOC:bc","GOC:BHF","PMID:23069713","GO_REF:0000058","GOC:BHF_miRNA","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epidermal growth factor receptor signaling pathway","termid":"GO:0042059"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of epidermal growth factor receptor signaling pathway involved in heart process","termid":"GO:1905282"},{"relation_name":"negatively_regulates","term_name":"epidermal growth factor receptor signaling pathway involved in heart process","termid":"GO:1905251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of epidermal growth factor receptor signaling pathway involved in heart process","synonyms":[{"name":"down regulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"down regulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"down regulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"down regulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"down regulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"down regulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"down regulation of ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"down regulation of ERBB1 signaling pathway involved in heart process","type":"exact"},{"name":"down regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"down regulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"down regulation of epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"down regulation of epidermal growth factor receptor signalling pathway involved in heart process","type":"exact"},{"name":"down regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"down regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"exact"},{"name":"down-regulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"down-regulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"down-regulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"down-regulation of ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of ERBB1 signaling pathway involved in heart process","type":"exact"},{"name":"down-regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"down-regulation of epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of epidermal growth factor receptor signalling pathway involved in heart process","type":"exact"},{"name":"down-regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"down-regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"exact"},{"name":"downregulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"downregulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"downregulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"downregulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"downregulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"downregulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"downregulation of ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"downregulation of ERBB1 signaling pathway involved in heart process","type":"exact"},{"name":"downregulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"downregulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"downregulation of epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"downregulation of epidermal growth factor receptor signalling pathway involved in heart process","type":"exact"},{"name":"downregulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"downregulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"exact"},{"name":"inhibition of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"inhibition of EGF receptor signaling pathway involved in heart process","type":"narrow"},{"name":"inhibition of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"inhibition of EGF receptor signalling pathway involved in heart process","type":"narrow"},{"name":"inhibition of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"inhibition of EGFR signaling pathway involved in heart process","type":"narrow"},{"name":"inhibition of ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"inhibition of ERBB1 signaling pathway involved in heart process","type":"narrow"},{"name":"inhibition of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"inhibition of epidermal growth factor receptor signaling pathway involved in heart process","type":"narrow"},{"name":"inhibition of epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"inhibition of epidermal growth factor receptor signalling pathway involved in heart process","type":"narrow"},{"name":"inhibition of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"inhibition of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"narrow"},{"name":"negative regulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"negative regulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"negative regulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"negative regulation of ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of ERBB1 signaling pathway involved in heart process","type":"exact"},{"name":"negative regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of epidermal growth factor receptor signalling pathway involved in heart process","type":"exact"},{"name":"negative regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"negative regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"exact"}],"termid":"GO:1905283"}


id: PBO:0005304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome component beta 3, Pup3 (predicted)","termid":"PBO:0005304"}


id: GO:0039670
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A turret-like appendage formed at the vertices of an icosahedral capsid.","definition_xrefs":["GOC:jh2","PMID:20592081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral capsid, decoration","termid":"GO:0098021"},{"relation_name":"part_of","term_name":"icosahedral viral capsid","termid":"GO:0019030"}],"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":"viral capsid, turret","termid":"GO:0039670"}


id: MONDO:0043294
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of localized scleroderma characterized by a long strip of indurated skin, which is typically found unilaterally on an arm or leg, and sometimes on the forehead or trunk. This disorder often affects the tissues beneath the skin, causing damage to bones, muscle or other organs. It can limit movement, alter growth, and disfigure the affected area.","definition_xrefs":["NCIT:C116780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localized scleroderma","termid":"MONDO:0019562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"linear scleroderma","secondary_identifiers":["MEDGEN:75518","GARD:9513","UMLS:C0263409","SCTID:22784002"],"synonyms":[{"name":"Scleroderma, linear","type":"related"},{"name":"en coup de saber","type":"related"},{"name":"en coup de sabre","type":"related"},{"name":"linear Scleroderma","type":"exact"},{"name":"linear morphea","type":"related"},{"name":"linear scleroderma","type":"exact"}],"termid":"MONDO:0043294","xrefs":{"Monarch":{"xref_id":"0043294"}}}


id: GO:0042626
data:
  {"annotated_genes":["SJAG_03358","SJAG_01879","SJAG_00516","SJAG_01344","SJAG_00212","SJAG_01129","SJAG_05294","SJAG_01447","SJAG_02399","SJAG_00136","SJAG_04277","SJAG_01435","SJAG_03406","SJAG_03415","SJAG_01397","SJAG_03363","SJAG_02023","SJAG_04258","SJAG_04015","SJAG_03497","SJAG_02457","SJAG_01913","SJAG_02077","SJAG_01669","SJAG_03560","SJAG_01471","SJAG_01817","SJAG_04955","SJAG_04757","SJAG_03866","SJAG_02602","SJAG_04167","SJAG_03502","SJAG_01400","SJAG_03785","SJAG_03515","SJAG_01597","SJAG_05213","SJAG_02782","SJAG_03850","SJAG_00373"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[117707],"is_not":false,"summary":null,"term":"GO:0042626"},{"annotations":[88752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140481"},{"annotations":[108156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015410"},{"annotations":[106677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015421"},{"annotations":[96543,117704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044604"},{"annotations":[101091,100377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140359"},{"annotations":[117453,95559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008559"},{"annotations":[100518,94943,114585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019829"},{"annotations":[101132,108160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005388"},{"annotations":[107345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043682"},{"annotations":[100520,114586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015662"},{"annotations":[107346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140581"},{"annotations":[111839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008556"},{"annotations":[111840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"},{"annotations":[87178,87179,113269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008553"},{"annotations":[111841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008554"},{"annotations":[94944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140358"},{"annotations":[107060,107081,99045,102786,104682,96375,111292,90379,99817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015450"},{"annotations":[102175,118227,99513,96106,98420,91538,95141,101138,87514,89642,99443,89325,103413,109368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046961"}]},"cv_name":"molecular_function","definition":"Primary active transporter of a solute across a membrane, via the reaction: ATP + H2O = ADP + phosphate, to directly drive the transport of a substance across a membrane. The transport protein may be transiently phosphorylated (P-type transporters), or not (ABC-type transporters and other families of transporters). Primary active transport occurs up the solute's concentration gradient and is driven by a primary energy source.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary active transmembrane transporter activity","termid":"GO:0015399"},{"relation_name":"is_a","term_name":"ATP-dependent activity","termid":"GO:0140657"}],"gene_count":41,"genes_by_uniquename":{"SJAG_00136":null,"SJAG_00212":null,"SJAG_00373":null,"SJAG_00516":null,"SJAG_01129":null,"SJAG_01344":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01435":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01597":null,"SJAG_01669":null,"SJAG_01817":null,"SJAG_01879":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02077":null,"SJAG_02399":null,"SJAG_02457":null,"SJAG_02602":null,"SJAG_02782":null,"SJAG_03358":null,"SJAG_03363":null,"SJAG_03406":null,"SJAG_03415":null,"SJAG_03497":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03560":null,"SJAG_03785":null,"SJAG_03850":null,"SJAG_03866":null,"SJAG_04015":null,"SJAG_04167":null,"SJAG_04258":null,"SJAG_04277":null,"SJAG_04757":null,"SJAG_04955":null,"SJAG_05213":null,"SJAG_05294":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"ATPase-coupled transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9753284","GO:0015405","Reactome:R-HSA-390393","Reactome:R-HSA-9794572","Reactome:R-HSA-2161538","EC:7.2.2.-","Reactome:R-HSA-2161506","Reactome:R-HSA-9750546","GO:0043492","Reactome:R-HSA-1467457","Reactome:R-HSA-9753278","Reactome:R-HSA-9033505","Reactome:R-HSA-9659680","Reactome:R-HSA-9794120","Reactome:R-HSA-9753283","Reactome:R-HSA-9759454","Reactome:R-HSA-9033499","GO:0016820","Reactome:R-HSA-9750617","Reactome:R-HSA-9759461"],"synonyms":[{"name":"ATP-coupled transmembrane transporter activity","type":"exact"},{"name":"ATP-dependent transmembrane transporter activity","type":"exact"},{"name":"ATPase activity, coupled to movement of substances","type":"broad"},{"name":"ATPase activity, coupled to transmembrane movement of substances","type":"exact"},{"name":"P-P-bond-hydrolysis-driven transmembrane transporter activity","type":"broad"},{"name":"P-P-bond-hydrolysis-driven transporter","type":"broad"},{"name":"hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances","type":"narrow"}],"termid":"GO:0042626","terms_by_termid":{"GO:0005388":null,"GO:0008553":null,"GO:0008554":null,"GO:0008556":null,"GO:0008559":null,"GO:0008900":null,"GO:0015410":null,"GO:0015421":null,"GO:0015450":null,"GO:0015662":null,"GO:0019829":null,"GO:0042626":null,"GO:0043682":null,"GO:0044604":null,"GO:0046961":null,"GO:0140358":null,"GO:0140359":null,"GO:0140481":null,"GO:0140581":null}}


id: PBO:0088200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc metalloendopeptidase; found in the cytoplasm and intermembrane space of mitochondria; with Cym1p, involved in degradation of mitochondrial proteins and of presequence peptides cleaved from imported proteins; protein abundance increases in response to DNA replication stress","termid":"PBO:0088200"}


id: PBO:0090986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIID complex subunit Taf3","termid":"PBO:0090986"}


id: PBO:0082199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Allantoin permease; expression sensitive to nitrogen catabolite repression and induced by allophanate, an intermediate in allantoin degradation","termid":"PBO:0082199"}


id: PBO:0085441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polypeptide release factor (eRF1) in translation termination; mutant form acts as a recessive omnipotent suppressor; methylated by Mtq2p-Trm112p in ternary complex eRF1-eRF3-GTP; mutation of methylation site confers resistance to zymocin; has a role in cytokinesis through interaction with Mlc1p","termid":"PBO:0085441"}


id: GO:0106299
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An active host response phase of acute inflammation driven by specialized pro-resolving mediators (SPMs) and signaling pathways, enabling timely tissue regeneration and return of function.","definition_xrefs":["PMID:28087575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute inflammatory response","termid":"GO:0002526"}],"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":"resolution phase response","termid":"GO:0106299"}


id: GO:0070426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of a nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway (NLR) pathway.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of pattern recognition receptor signaling pathway","termid":"GO:0062208"},{"relation_name":"is_a","term_name":"regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","termid":"GO:0070424"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","termid":"GO:0035872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","synonyms":[{"name":"positive regulation of NOD signaling pathway","type":"narrow"},{"name":"positive regulation of nucleotide-binding oligomerization domain containing signaling pathway","type":"narrow"},{"name":"positive regulation of nucleotide-binding oligomerization domain containing signalling pathway","type":"narrow"}],"termid":"GO:0070426"}


id: MOD:00318
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-cysteine residue and an L-tryptophan residue by a thioether bond to form 4'-(S-L-cysteinyl)-L-tryptophyl quinone.","definition_xrefs":["RESID:AA0313","PubMed:11717396","PubMed:11555656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thioether crosslinked residues","termid":"MOD:00687"},{"relation_name":"is_a","term_name":"crosslinked L-tryptophan residue","termid":"MOD:02057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"4'-(S-L-cysteinyl)-L-tryptophyl quinone","synonyms":[{"name":"(2R)-2-amino-3-[(3-[(2S)-2-amino-2-carboxyethyl]-6,7-dioxo-6,7-dihydro-1H-indol-4-yl)sulfanyl]propanoic acid","type":"exact"},{"name":"3-(2-amino-2-carboxyethyl)-4-[2-amino-2-carboxyethyl]sulfanyl-6,7-indolinedione","type":"exact"},{"name":"4'-(L-cystein-S-yl)-L-tryptophyl quinone","type":"exact"},{"name":"4-(S-cysteinyl)tryptophan-6,7-dione","type":"exact"},{"name":"CROSSLNK 4'-cysteinyl-tryptophylquinone (Cys-Trp)","type":"exact"},{"name":"CTQ","type":"exact"},{"name":"cysteine tryptophylquinone","type":"exact"}],"termid":"MOD:00318"}


id: PBO:0005056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexose transporter Ght1","termid":"PBO:0005056"}


id: MONDO:0019160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary progressive freezing gait is a rare, heterogeneous, progressively incapacitating neurodegenerative disease characterized by freezing of gait (usually during the first 3 years), later associating postural instability, eventually resulting in a wheelchair-bound state. Other features may include mild bradykinesia, rigidity, postural tremor, hyperreflexia, speech disorder and dementia. The disease is unresponsive to dopaminergic treatments.","definition_xrefs":["Orphanet:75567"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"},{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"primary progressive freezing gait","secondary_identifiers":["GARD:18930","MEDGEN:894846","icd11.foundation:431694225","SCTID:715627004","UMLS:C4275078"],"synonyms":[{"name":"PPFG","type":"exact"}],"termid":"MONDO:0019160","xrefs":{"Monarch":{"xref_id":"0019160"}}}


id: MONDO:0859531
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures","secondary_identifiers":["OMIM:620292","UMLS:C5830365","MEDGEN:1841001"],"termid":"MONDO:0859531","xrefs":{"Monarch":{"xref_id":"0859531"}}}


id: FYPO:0003695
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain fewer free small ribosomal subunits in the cytosol than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of macromolecular complex during vegetative growth","termid":"FYPO:0003684"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased cytosolic small ribosomal subunit level","synonyms":[{"name":"cytosolic small ribosomal subunit present at decreased level","type":"exact"},{"name":"decreased 40S ribosomal subunit level","type":"exact"},{"name":"decreased cytosolic small ribosomal subunit level during mitotic cell cycle","type":"related"},{"name":"decreased cytosolic small ribosomal subunit level during vegetative growth","type":"exact"},{"name":"decreased level of cytosolic small ribosomal subunits","type":"related"},{"name":"decreased small ribosomal subunit level","type":"broad"},{"name":"reduced cytosolic small ribosomal subunit level","type":"exact"}],"termid":"FYPO:0003695"}


id: PBO:0043933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cartilage acidic protein 1","termid":"PBO:0043933"}


id: PBO:0045197
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 B8","termid":"PBO:0045197"}


id: GO:0052716
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4 hydroquinone + O2 = 4 benzosemiquinone + 4 H2O.","definition_xrefs":["EC:1.10.3.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor","termid":"GO:0016682"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"hydroquinone:oxygen oxidoreductase activity","secondary_identifiers":["KEGG_REACTION:R00083","MetaCyc:LACCASE-RXN","RHEA:11276"],"synonyms":[{"name":"benzenediol:oxygen oxidoreductase activity","type":"broad"},{"name":"laccase reaction","type":"broad"},{"name":"p-diphenol:oxygen oxidoreductase activity","type":"exact"}],"termid":"GO:0052716"}


id: PBO:0002323
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.1.1.10","termid":"PBO:0002323"}


id: PBO:0002384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"seven transmembrane receptor protein (predicted)","termid":"PBO:0002384"}


id: MONDO:0001708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sarcoidosis affecting the lung parenchyma. It is characterized by the presence of non-necrotizing granulomas in the lung tissues. It is manifested with dyspnea, cough, fever, night sweats, fatigue, and weight loss.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease specific to adulthood","termid":"MONDO:0017026"},{"relation_name":"is_a","term_name":"sarcoidosis","termid":"MONDO:0019338"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary sarcoidosis","secondary_identifiers":["ICD9:517.8","NCIT:C34997","MESH:D017565","UMLS:C0036205","MEDGEN:19873","SCTID:24369008","DOID:13406"],"synonyms":[{"name":"lung sarcoidosis","type":"exact"},{"name":"sarcoidosis of lung","type":"exact"}],"termid":"MONDO:0001708","xrefs":{"Monarch":{"xref_id":"0001708"}}}


id: PBO:0068574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 25, pseudogene","termid":"PBO:0068574"}


id: MONDO:0021209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the heart.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"neoplasm of thorax","termid":"MONDO:0021350"},{"relation_name":"is_a","term_name":"cardiovascular neoplasm","termid":"MONDO:0024757"}],"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":"heart neoplasm","secondary_identifiers":["NANDO:2200236","NANDO:2100061","NCIT:C3081","UMLS:C0018809","EFO:1001339","MEDGEN:9172"],"synonyms":[{"name":"Cardiac neoplasm","type":"exact"},{"name":"Cardiac neoplasms","type":"exact"},{"name":"Cardiac tumor","type":"exact"},{"name":"Cardiac tumour","type":"exact"},{"name":"Intracavitary tumors","type":"related"},{"name":"Intracavitary tumours","type":"related"},{"name":"heart neoplasm (disease)","type":"exact"},{"name":"heart tumor","type":"exact"},{"name":"heart tumour","type":"exact"},{"name":"myocardial tumors (rhabdomyomas and fibromas)","type":"related"},{"name":"myocardial tumours (rhabdomyomas and fibromas)","type":"related"},{"name":"neoplasm of heart","type":"exact"},{"name":"neoplasm of the heart","type":"exact"},{"name":"primary cardiac tumors, childhood","type":"related"},{"name":"tumor of heart","type":"exact"},{"name":"tumor of the heart","type":"exact"},{"name":"tumour of heart","type":"exact"},{"name":"tumour of the heart","type":"exact"}],"termid":"MONDO:0021209","xrefs":{"Monarch":{"xref_id":"0021209"}}}


id: PBO:0056307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase 3","termid":"PBO:0056307"}


id: GO:0047000
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-dehydro-3-deoxy-D-gluconate + NADP+ = (4S,5S)-4,5-dihydroxy-2,6-dioxohexanoate + H+ + NADPH.","definition_xrefs":["RHEA:15109","EC:1.1.1.126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"2-dehydro-3-deoxy-D-gluconate 6-dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R01543","MetaCyc:RXN-13040"],"synonyms":[{"name":"2-dehydro-3-deoxy-D-gluconate:NADP+ 6-oxidoreductase activity","type":"related"},{"name":"2-keto-3-deoxy-D-gluconate dehydrogenase activity","type":"related"}],"termid":"GO:0047000"}


id: PBO:0071870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 8","termid":"PBO:0071870"}


id: PBO:0081272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 37A","termid":"PBO:0081272"}


id: GO:0052448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of the levels of ethylene in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of ethylene levels in symbiont (obsolete GO:0052448)","synonyms":[{"name":"modulation by organism of ethylene levels in symbiont","type":"exact"}],"termid":"GO:0052448"}


id: GO:0033864
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the activity of the enzyme NAD(P)H oxidase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of NAD(P)H oxidase activity","termid":"GO:0033860"},{"relation_name":"is_a","term_name":"positive regulation of oxidoreductase activity","termid":"GO:0051353"}],"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 NAD(P)H oxidase activity","synonyms":[{"name":"activation of NAD(P)H oxidase activity","type":"narrow"},{"name":"stimulation of NAD(P)H oxidase activity","type":"narrow"},{"name":"up regulation of NAD(P)H oxidase activity","type":"exact"},{"name":"up-regulation of NAD(P)H oxidase activity","type":"exact"},{"name":"upregulation of NAD(P)H oxidase activity","type":"exact"}],"termid":"GO:0033864"}


id: PBO:0039446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and IBR domain containing 1","termid":"PBO:0039446"}


id: MONDO:0003425
data:
  {"annotated_genes":["SJAG_04183","SJAG_00885","SJAG_02658","SJAG_04816","SJAG_04665","SJAG_06022","SJAG_02050"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014062"},{"annotations":[86020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024528"},{"annotations":[84651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012238"},{"annotations":[85022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013117"},{"annotations":[85835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009783"},{"annotations":[84613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014656"},{"annotations":[85906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020845"},{"annotations":[85548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957993"}]},"cv_name":"mondo","definition":"Weakness or paralysis of at least one of the muscles controlling the movement of the eye. It results from degeneration of the muscles or the neural pathways involved in the eye movement. Representative disorders causing ophthalmoplegia include ocular myopathies and multiple sclerosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ocular motility disease","termid":"MONDO:0001584"},{"relation_name":"is_a","term_name":"palsy","termid":"MONDO:0006496"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00885":null,"SJAG_02050":null,"SJAG_02658":null,"SJAG_04183":null,"SJAG_04665":null,"SJAG_04816":null,"SJAG_06022":null},"genotype_count":0,"is_obsolete":false,"name":"ophthalmoplegia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1848588735","UMLS:C0029089","MEDGEN:45205","MESH:D009886","ICD9:378.56","SCTID:78097002","DOID:539"],"synonyms":[{"name":"oculomotor paralysis","type":"related"},{"name":"total ophthalmoplegia","type":"exact"}],"termid":"MONDO:0003425","terms_by_termid":{"MONDO:0009783":null,"MONDO:0012238":null,"MONDO:0013117":null,"MONDO:0014062":null,"MONDO:0014656":null,"MONDO:0020845":null,"MONDO:0024528":null,"MONDO:0957993":null},"xrefs":{"Monarch":{"xref_id":"0003425"}}}


id: MONDO:0025356
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":"azoospermia, obstructive, with nephrolithiasis","secondary_identifiers":["UMLS:C5542351","MEDGEN:1779119","OMIM:301060"],"synonyms":[{"name":"OAZON","type":"exact"},{"name":"azoospermia, obstructive, with nephrolithiasis, X-linked recessive","type":"exact"}],"termid":"MONDO:0025356","xrefs":{"Monarch":{"xref_id":"0025356"}}}


id: GO:0042421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of norepinephrine, a hormone secreted by the adrenal medulla, and a neurotransmitter in the sympathetic peripheral nervous system and in some tracts in the central nervous system. It is also the demethylated biosynthetic precursor of epinephrine.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"norepinephrine metabolic process","termid":"GO:0042415"},{"relation_name":"is_a","term_name":"catecholamine biosynthetic process","termid":"GO:0042423"}],"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":"norepinephrine biosynthetic process","synonyms":[{"name":"levarterenol biosynthesis","type":"exact"},{"name":"levarterenol biosynthetic process","type":"exact"},{"name":"noradrenaline biosynthesis","type":"exact"},{"name":"noradrenaline biosynthetic process","type":"exact"},{"name":"norepinephrine anabolism","type":"exact"},{"name":"norepinephrine biosynthesis","type":"exact"},{"name":"norepinephrine formation","type":"exact"},{"name":"norepinephrine synthesis","type":"exact"}],"termid":"GO:0042421"}


id: PBO:0047721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibromodulin","termid":"PBO:0047721"}


id: SO:0001690
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The restriction enzyme cleavage junction on the 3' strand of the nucleotide sequence.","direct_ancestors":[{"relation_name":"is_a","term_name":"single_strand_restriction_enzyme_cleavage_site","termid":"SO:0001694"},{"relation_name":"part_of","term_name":"sticky_end_restriction_enzyme_cleavage_site","termid":"SO:0001692"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_restriction_enzyme_junction","synonyms":[{"name":"3' restriction enzyme junction","type":"exact"}],"termid":"SO:0001690"}


id: PBO:0039988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 6 interacting protein 1 pseudogene 2","termid":"PBO:0039988"}


id: GO:0007425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell fate determination process in which a cell becomes capable of differentiating autonomously into an epithelial cell within an open tracheal system regardless of its environment; upon determination, the cell fate cannot be reversed. Tracheal cells are set aside as 10 clusters of approximately 80 cells on each side of the embryo (termed tracheal placodes). An example of this is found in Drosophila melanogaster.","definition_xrefs":["PMID:11063940","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate determination","termid":"GO:0001709"},{"relation_name":"part_of","term_name":"open tracheal system development","termid":"GO:0007424"}],"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":"epithelial cell fate determination, open tracheal system","secondary_identifiers":["GO:0046846"],"synonyms":[{"name":"tracheal cell fate determination","type":"broad"},{"name":"tracheal epithelial cell fate determination","type":"exact"},{"name":"tracheal placode cell fate determination","type":"related"}],"termid":"GO:0007425"}


id: GO:0000453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of methyl groups to the 2'-oxygen atom of nucleotide residues in an rRNA molecule during ribosome biogenesis where the methylase specifies the site that becomes methylated without using a guide RNA.","definition_xrefs":["ISBN:1555811337","GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme-directed rRNA 2'-O-methylation (obsolete GO:0000453)","termid":"GO:0000453"}


id: GO:0010644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that mediates signaling interactions between one cell and another cell by transfer of current between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:tb","GOC:kmv","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell communication","termid":"GO:0007154"}],"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":"cell communication by electrical coupling","termid":"GO:0010644"}


id: GO:0030215
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a semaphorin receptor.","definition_xrefs":["GOC:ceb","PMID:12001990"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"semaphorin receptor binding","synonyms":[{"name":"plexin binding","type":"narrow"},{"name":"plexin ligand","type":"narrow"},{"name":"semaphorin receptor ligand","type":"narrow"}],"termid":"GO:0030215"}


id: GO:0048911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an efferent axon in the anterior lateral line nerve over time from its formation to the mature structure. This process includes axonogenesis and pathfinding of the efferent axons in the anterior lateral line nerve.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"efferent axon development in a lateral line nerve","termid":"GO:0048894"},{"relation_name":"part_of","term_name":"anterior lateral line nerve development","termid":"GO:0048909"}],"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":"efferent axon development in anterior lateral line nerve","termid":"GO:0048911"}


id: GO:0035131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after embryonic development, by which the anatomical structures of the pelvic fin are generated and organized. The pelvic fins are bilaterally paired fins mounted in a ventral-lateral position on most fish. These fins are used primarily for lateral mobility and propulsion.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic appendage morphogenesis","termid":"GO:0035120"},{"relation_name":"is_a","term_name":"pelvic fin morphogenesis","termid":"GO:0035139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"post-embryonic pelvic fin morphogenesis","termid":"GO:0035131"}


id: PBO:0075854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family member 3","termid":"PBO:0075854"}


id: PBO:0027530
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-septation_following_abnormal_chromosome_segregation,_with_binucleate_and_anucleate_compartment_formation_during_cellular_response_to_hydroxyurea","termid":"PBO:0027530"}


id: PBO:0083326
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 ORFs PTC2/YER089C and YER088W-B","termid":"PBO:0083326"}


id: PBO:0061479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear respiratory factor 1","termid":"PBO:0061479"}


id: PBO:0082614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coiled-coil 12S polarisome subunit; required for polarity establishment, apical bud growth, shmoo formation, filamentous differentiation; involved in Bni1p localization at sites of polarized growth, controlling polarized assembly of actin cables; role in apical growth affects diploid-specific bipolar bud site selection; retains Slt2p at bud tip to regulate ER inheritance; role in Ca2+ influx, cell fusion; S288C allele encoding Leu409 rather than Met linked with non-invasion","termid":"PBO:0082614"}


id: GO:0061989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chromosome organization process in which meiotic chromosomes in the spem nucleus cluster together to form a compact spherical structure called the karyosome.","definition_xrefs":["PMID:19696886"],"direct_ancestors":[{"relation_name":"is_a","term_name":"karyosome formation","termid":"GO:0061988"},{"relation_name":"part_of","term_name":"spermatogenesis","termid":"GO:0007283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"sperm karyosome formation","termid":"GO:0061989"}


id: PBO:0016560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"di-trans,poly-cis-decaprenylcistransferase Nus1","termid":"PBO:0016560"}


id: PBO:0082157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adaptor protein that links actin to clathrin and endocytosis; involved in membrane cytoskeleton assembly and cell polarization; present in the actin cortical patch of the emerging bud tip; dimer in vivo","termid":"PBO:0082157"}


id: GO:0160047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + muramyl dipeptide = ADP + H+ + 6-O-phospho-muramyl dipeptide.","definition_xrefs":["PMID:36002575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016301"],"is_obsolete":false,"name":"muramyl dipeptide kinase activity","secondary_identifiers":["RHEA:75935"],"termid":"GO:0160047"}


id: PBO:0090313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA biosynthesis protein Cmr2","termid":"PBO:0090313"}


id: GO:1902885
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of proteasome-activating ATPase activity.","definition_xrefs":["GO_REF:0000059","GOC:di","PMID:23995839","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of proteasome-activating ATPase activity (obsolete GO:1902885)","synonyms":[{"name":"regulation of ATPase involved in positive regulation of proteasomal protein catabolic process","type":"exact"},{"name":"regulation of proteasomal ATPase activity","type":"exact"},{"name":"regulation of proteasome channel gating activity","type":"narrow"},{"name":"regulation of proteasome channel opening activity","type":"narrow"}],"termid":"GO:1902885"}


id: MONDO:0011290
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":"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability","secondary_identifiers":["MESH:C566408","UMLS:C1864183","OMIM:603133","MEDGEN:350359"],"synonyms":[{"name":"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability","type":"exact"},{"name":"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation","type":"exact"}],"termid":"MONDO:0011290","xrefs":{"Monarch":{"xref_id":"0011290"}}}


id: FYPO:0006450
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the substrate specificity of a gene product that executes histone H3 acetyltransferase activity is altered. For example, preference for modified (e.g. methylated) H3 molecules may be enhanced or diminished.","definition_xrefs":["PomBase:mah","PMID:26401015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered substrate specificity","termid":"FYPO:0003347"},{"relation_name":"is_a","term_name":"abnormal histone acetyltransferase activity","termid":"FYPO:0006453"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000002","FYPO:0000661","FYPO:0005447","FYPO:0000654","FYPO:0000641","FYPO:0000652"],"is_obsolete":false,"name":"altered histone H3 acetyltransferase substrate specificity","synonyms":[{"name":"altered H3 histone acetyltransferase substrate specificity","type":"exact"}],"termid":"FYPO:0006450"}


id: GO:0000315
data:
  {"annotated_genes":["SJAG_00315","SJAG_01829","SJAG_05573","SJAG_01727","SJAG_02071","SJAG_00799","SJAG_00844","SJAG_03636","SJAG_04244","SJAG_01413","SJAG_05270","SJAG_03649","SJAG_01045","SJAG_03192","SJAG_05221","SJAG_04493","SJAG_04216","SJAG_06253","SJAG_01719","SJAG_03284","SJAG_05218","SJAG_01303","SJAG_03297","SJAG_04207","SJAG_04893","SJAG_02762","SJAG_04689","SJAG_00086","SJAG_01591","SJAG_03176","SJAG_07009","SJAG_04490","SJAG_03459","SJAG_06110","SJAG_05244","SJAG_01630","SJAG_03040","SJAG_00497","SJAG_01463","SJAG_04889","SJAG_04019","SJAG_01473","SJAG_03402","SJAG_02836","SJAG_01478"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88499,101432,105344,107665,111949,97453,112387,117418,95748,114088,116493,114913,114866,105196,97474,95711,100591,107712,96385,98598,113804,114732,115760,88952,112212,102939,103186,106242,116608,107566,114206,115651,102117,98150,112942,111714,109334,110589,110264,96083,104355,87826,102832,103865,90949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005762"}]},"cv_name":"cellular_component","definition":"The larger of the two subunits of an organellar ribosome. Two sites on the ribosomal large subunit are involved in translation: the aminoacyl site (A site) and peptidyl site (P site).","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"large ribosomal subunit","termid":"GO:0015934"},{"relation_name":"part_of","term_name":"organellar ribosome","termid":"GO:0000313"}],"gene_count":45,"genes_by_uniquename":{"SJAG_00086":null,"SJAG_00315":null,"SJAG_00497":null,"SJAG_00799":null,"SJAG_00844":null,"SJAG_01045":null,"SJAG_01303":null,"SJAG_01413":null,"SJAG_01463":null,"SJAG_01473":null,"SJAG_01478":null,"SJAG_01591":null,"SJAG_01630":null,"SJAG_01719":null,"SJAG_01727":null,"SJAG_01829":null,"SJAG_02071":null,"SJAG_02762":null,"SJAG_02836":null,"SJAG_03040":null,"SJAG_03176":null,"SJAG_03192":null,"SJAG_03284":null,"SJAG_03297":null,"SJAG_03402":null,"SJAG_03459":null,"SJAG_03636":null,"SJAG_03649":null,"SJAG_04019":null,"SJAG_04207":null,"SJAG_04216":null,"SJAG_04244":null,"SJAG_04490":null,"SJAG_04493":null,"SJAG_04689":null,"SJAG_04889":null,"SJAG_04893":null,"SJAG_05218":null,"SJAG_05221":null,"SJAG_05244":null,"SJAG_05270":null,"SJAG_05573":null,"SJAG_06110":null,"SJAG_06253":null,"SJAG_07009":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"organellar large ribosomal subunit","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000315","terms_by_termid":{"GO:0005762":null}}


id: MONDO:0001305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Narrowing of the laryngeal airway.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngeal disorder","termid":"MONDO:0004382"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laryngostenosis","secondary_identifiers":["ICD9:478.74","DOID:11527","UMLS:C0023075","MEDGEN:7274","SCTID:75547007","ICD10CM:J38.6","MESH:D007829","HP:0001602"],"synonyms":[{"name":"stenosis of larynx","type":"exact"}],"termid":"MONDO:0001305","xrefs":{"Monarch":{"xref_id":"0001305"}}}


id: GO:0071076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The enzymatic addition of a sequence of uridylyl residues at the 3' end of an RNA molecule.","definition_xrefs":["GOC:vw","PMID:19430462"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA 3'-end processing","termid":"GO:0031123"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"RNA 3' uridylation","termid":"GO:0071076"}


id: MONDO:0015694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma (disease) that involves the mucosa.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant melanoma of the mucosa","secondary_identifiers":["UMLS:C5191057","MEDGEN:1676191","GARD:20110","Orphanet:168999"],"synonyms":[{"name":"melanoma (disease) of mucosa","type":"exact"},{"name":"mucosa melanoma","type":"exact"},{"name":"mucosa melanoma (disease)","type":"exact"}],"termid":"MONDO:0015694","xrefs":{"Monarch":{"xref_id":"0015694"}}}


id: GO:0035832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving berbamunine, an isoquinoline alkaloid.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzyl isoquinoline alkaloid metabolic process","termid":"GO:0046445"}],"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":"berbamunine metabolic process","synonyms":[{"name":"berbamunine metabolism","type":"exact"}],"termid":"GO:0035832"}


id: MONDO:0011619
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":"crumpled helices and small mouth","secondary_identifiers":["OMIM:605945","UMLS:C1853826","MEDGEN:342976","MESH:C536217"],"synonyms":[{"name":"crumpled helices and small mouth","type":"exact"},{"name":"sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay","type":"related"}],"termid":"MONDO:0011619","xrefs":{"Monarch":{"xref_id":"0011619"}}}


id: PBO:0046147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EIPR1 intronic transcript 1","termid":"PBO:0046147"}


id: GO:0033290
data:
  {"annotated_genes":["SJAG_03629","SJAG_04891","SJAG_00662","SJAG_02376","SJAG_02390","SJAG_03472","SJAG_03147","SJAG_04900","SJAG_02164","SJAG_02628","SJAG_03732","SJAG_04981","SJAG_04744"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89415,94270,95353,96339,96719,97219,97277,97880,99597,104809,105096,110184,110826],"is_not":false,"summary":null,"term":"GO:0033290"}]},"cv_name":"cellular_component","definition":"The protein-ribosome-tRNA complex that has just recognized the start codon of a capped mRNA. It is composed of the small ribosomal subunit, eukaryote initiation factors (eIF) eIF3 complex, eIF1, eIF1A, eIF2-GDP, eIF4 complex and initiatior-methionine-tRNA. Recognition of the start codon triggers downstream steps in the pathway, including eIF1 dissociation; Pi release from eIF2; and conversion to the closed, scanning-arrested conformation of the PIC.","definition_xrefs":["PMID:29735639","GOC:hjd","PMID:24319994","PMID:24499181","PMID:16510876"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation preinitiation complex","termid":"GO:0070993"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00662":null,"SJAG_02164":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02628":null,"SJAG_03147":null,"SJAG_03472":null,"SJAG_03629":null,"SJAG_03732":null,"SJAG_04744":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"eukaryotic 48S preinitiation complex","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0016283"],"synonyms":[{"name":"eukaryotic 48S initiation complex","type":"related"},{"name":"eukaryotic 48S pre-initiation complex","type":"exact"}],"termid":"GO:0033290","terms_by_termid":{"GO:0033290":null}}


id: PBO:0044141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 7","termid":"PBO:0044141"}


id: PBO:0064633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPARG coactivator 1 beta","termid":"PBO:0064633"}


id: PBO:0054196
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 1571","termid":"PBO:0054196"}


id: PBO:0002400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoxia induced family protein","termid":"PBO:0002400"}


id: SO:0000609
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The string of non-encoded U's at the 3' end of a guide RNA (SO:0000602).","direct_ancestors":[{"relation_name":"adjacent_to","term_name":"guide_RNA","termid":"SO:0000602"},{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligo_U_tail","synonyms":[{"name":"oligo U tail","type":"exact"}],"termid":"SO:0000609"}


id: PBO:0074289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIT and NTRK like family member 4","termid":"PBO:0074289"}


id: PATO:0000626
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being moved or displaced to one side so as to make lateral.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lateralized","termid":"PATO:0000626"}


id: PBO:0054212
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 1592","termid":"PBO:0054212"}


id: PBO:0050641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock transcription factor Y-linked 6, pseudogene","termid":"PBO:0050641"}


id: PBO:0067279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 359, pseudogene","termid":"PBO:0067279"}


id: PBO:0047399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 38","termid":"PBO:0047399"}


id: MONDO:0018463
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mild phosphoribosylpyrophosphate (PRPP) synthetase superactivity is the mild and late-onset form of PRPP synthetase superactivity, an X-linked disorder of purine metabolism associated with hyperuricemia and hyperuricosuria, leading to urolithiasis and gout. This form is not associated with any neuropathy or central nervous system (CNS) disorders.","definition_xrefs":["Orphanet:411536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoribosylpyrophosphate synthetase superactivity","termid":"MONDO:0010395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019254"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0005066"],"is_obsolete":false,"name":"mild phosphoribosylpyrophosphate synthetase superactivity","secondary_identifiers":["MEDGEN:1843112","UMLS:C5680016","GARD:17681"],"synonyms":[{"name":"mild PRPP synthetase superactivity","type":"exact"},{"name":"mild PRPS1 superactivity","type":"exact"}],"termid":"MONDO:0018463","xrefs":{"Monarch":{"xref_id":"0018463"}}}


id: PBO:0039681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloid beta precursor protein binding family A member 2","termid":"PBO:0039681"}


id: MONDO:0005214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm that arises from the vulva. Representative examples include childhood botryoid-type embryonal rhabdomyosarcoma, alveolar soft part sarcoma, and leiomyosarcoma.","definition_xrefs":["NCIT:C40317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vulva cancer","termid":"MONDO:0001528"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"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":"vulva sarcoma","secondary_identifiers":["MEDGEN:65972","DOID:2096","UMLS:C0238525","SCTID:254897006"],"synonyms":[{"name":"mammalian vulva sarcoma","type":"exact"},{"name":"sarcoma of mammalian vulva","type":"exact"},{"name":"sarcoma of vulva","type":"exact"},{"name":"vulvar sarcoma","type":"exact"}],"termid":"MONDO:0005214","xrefs":{"Monarch":{"xref_id":"0005214"}}}


id: PBO:0006227
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA level","termid":"PBO:0006227"}


id: PBO:0081461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 330","termid":"PBO:0081461"}


id: GO:0045453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which specialized cells known as osteoclasts degrade the organic and inorganic portions of bone, and endocytose and transport the degradation products.","definition_xrefs":["GOC:mah","PMID:10968780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue homeostasis","termid":"GO:0001894"},{"relation_name":"part_of","term_name":"bone remodeling","termid":"GO:0046849"}],"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":"bone resorption","secondary_identifiers":["Wikipedia:Bone_resorption"],"termid":"GO:0045453"}


id: PBO:0081214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger matrin-type 4","termid":"PBO:0081214"}


id: PBO:0047409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 47","termid":"PBO:0047409"}


id: PBO:0060240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin binding protein C3","termid":"PBO:0060240"}


id: GO:0036024
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex that contains protein C inhibitor (SERPINA5) and transmembrane protease serine 7 (TMPRSS7); formation of the complex inhibits the serine protease activity of transmembrane protease serine 7.","definition_xrefs":["PMID:15853774","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine protease inhibitor complex","termid":"GO:0097180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"protein C inhibitor-TMPRSS7 complex","synonyms":[{"name":"PCI-TMPRSS7 complex","type":"exact"},{"name":"SERPINA5-TMPRSS7 complex","type":"exact"},{"name":"plasma serine protease inhibitor-TMPRSS7 complex","type":"exact"},{"name":"protein C inhibitor-matriptase-3 complex","type":"exact"},{"name":"protein C inhibitor-transmembrane protease serine 7 complex","type":"exact"},{"name":"serpin A5-TMPRSS7 complex","type":"exact"}],"termid":"GO:0036024"}


id: PBO:0077532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 245","termid":"PBO:0077532"}


id: PR:Q9URV0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tho4 gene.","definition_xrefs":["UniProtKB:Q9URV0","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 RNA-binding protein C106.12c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC106.12c","synonyms":[{"name":"Spom972h-tho4","type":"exact"}],"termid":"PR:Q9URV0"}


id: PBO:0045334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dedicator of cytokinesis 9","termid":"PBO:0045334"}


id: MONDO:0010825
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrioventricular defect-blepharophimosis-radial and anal defect syndrome is a rare, genetic multiple congenital anomaly syndrome characterized by atrioventricular septal defects and blepharophimosis, in addition to radial (e.g. aplastic radius, shortened ulna, fifth finger clinodactyly, absent first metacarpal and thumb) and anal (e.g. imperforate or anteriorly place anus, rectovaginal fistula) defects.","definition_xrefs":["Orphanet:1352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"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":"atrioventricular defect-blepharophimosis-radial and anal defect syndrome","secondary_identifiers":["GARD:2742","MEDGEN:374010","MESH:C563994","UMLS:C1838606","OMIM:600123"],"synonyms":[{"name":"Houlston-Ironton-Temple syndrome","type":"exact"},{"name":"atrioventricular septal defect with blepharophimosis and anal and radial defects","type":"related"}],"termid":"MONDO:0010825","xrefs":{"Monarch":{"xref_id":"0010825"}}}


id: GO:0050992
data:
  {"annotated_genes":["SJAG_04307"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101377],"is_not":false,"summary":null,"term":"GO:0050992"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dimethylallyl diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid biosynthetic process","termid":"GO:0008654"},{"relation_name":"is_a","term_name":"dimethylallyl diphosphate metabolic process","termid":"GO:0050993"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04307":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"dimethylallyl diphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DPP biosynthesis","type":"exact"},{"name":"DPP biosynthetic process","type":"exact"},{"name":"dimethylallyl diphosphate anabolism","type":"exact"},{"name":"dimethylallyl diphosphate biosynthesis","type":"exact"},{"name":"dimethylallyl diphosphate formation","type":"exact"},{"name":"dimethylallyl diphosphate synthesis","type":"exact"},{"name":"dimethylallyl pyrophosphate biosynthesis","type":"exact"},{"name":"dimethylallyl pyrophosphate biosynthetic process","type":"exact"}],"termid":"GO:0050992","terms_by_termid":{"GO:0050992":null}}


id: PBO:0040971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 42","termid":"PBO:0040971"}


id: PBO:0056408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane associated ring-CH-type finger 6","termid":"PBO:0056408"}


id: MONDO:0011943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"systemic lupus erythematosus with nephritis, susceptibility to, 2","secondary_identifiers":["UMLS:C1842756","OMIM:607966","MEDGEN:375006"],"synonyms":[{"name":"SLEN2","type":"exact"},{"name":"systemic lupus erythematosus with nephritis, susceptibility to, 2","type":"exact"}],"termid":"MONDO:0011943","xrefs":{"Monarch":{"xref_id":"0011943"}}}


id: GO:0003070
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulation of blood pressure mediated by a neurotransmitter. A neurotransmitter is any of a group of substances that are released on excitation from the axon terminal of a presynaptic neuron of the central or peripheral nervous system and travel across the synaptic cleft to either excite or inhibit the target cell.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system process involved in regulation of systemic arterial blood pressure","termid":"GO:0001976"},{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure mediated by a chemical signal","termid":"GO:0003044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of systemic arterial blood pressure by neurotransmitter","termid":"GO:0003070"}


id: PBO:0045415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental pluripotency associated 5","termid":"PBO:0045415"}


id: MONDO:0043197
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":"ruvalcaba churesigaew myhre syndrome","secondary_identifiers":["MESH:C537190","UMLS:C2931437","MEDGEN:419412"],"synonyms":[{"name":"onset of senility in the early teens, atrophic skin, hypogonadism, retinal and vascular sclerosis","type":"related"}],"termid":"MONDO:0043197","xrefs":{"Monarch":{"xref_id":"0043197"}}}


id: PBO:0029762
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_curved_vacuolated_vegetative_cell","termid":"PBO:0029762"}


id: MONDO:1011084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, cattle","secondary_identifiers":["OMIA:001033-9913"],"termid":"MONDO:1011084","xrefs":{"Monarch":{"xref_id":"1011084"}}}


id: MONDO:0009954
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformation syndrome with odontal and/or periodontal component (obsolete MONDO:0015336)","termid":"MONDO:0015336"},{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ramon syndrome","secondary_identifiers":["OMIM:266270","Orphanet:3019","GARD:7523","icd11.foundation:122538435","UMLS:C0796133","MESH:C535285","MEDGEN:208669"],"synonyms":[{"name":"Ramon syndrome","type":"exact"},{"name":"cherubism, gingival fibromatosis, epilepsy, mental deficiency, hypertrichosis, and stunted Growth","type":"related"},{"name":"cherubism-gingival fibromatosis-intellectual disability syndrome","type":"exact"},{"name":"gingival fibromatosis combined with cherubism","type":"related"}],"termid":"MONDO:0009954","xrefs":{"Monarch":{"xref_id":"0009954"}}}


id: MONDO:0003063
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hydranencephaly (obsolete MONDO:0003063)","termid":"MONDO:0003063","xrefs":{"Monarch":{"xref_id":"0003063"}}}


id: GO:0002410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a plasmacytoid dendritic cell in response to an external stimulus.","definition_xrefs":["GOC:add","PMID:15159375","PMID:15814331"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendritic cell chemotaxis","termid":"GO:0002407"}],"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":"plasmacytoid dendritic cell chemotaxis","termid":"GO:0002410"}


id: PBO:0076796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane epididymal protein 3, pseudogene","termid":"PBO:0076796"}


id: PBO:0053032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysosomal protein transmembrane 5","termid":"PBO:0053032"}


id: MONDO:0020299
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spinocerebellar ataxia type 15/16 (obsolete MONDO:0020299)","termid":"MONDO:0020299","xrefs":{"Monarch":{"xref_id":"0020299"}}}


id: PBO:0018152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA endoribonuclease involved in mRNP quality control Swt1 (predicted)","termid":"PBO:0018152"}


id: PBO:0078407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon CCC) 2-1","termid":"PBO:0078407"}


id: PBO:0061316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore complex interacting protein family member A1","termid":"PBO:0061316"}


id: MONDO:0800187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing viral infections.","definition_xrefs":["MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encephalitis, acute, infection-induced, susceptibility to","termid":"MONDO:0800174"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunodeficiency 83, susceptibility to viral infections","secondary_identifiers":["UMLS:C2751803","OMIM:613002","MEDGEN:416638"],"synonyms":[{"name":"IMD83","type":"exact"}],"termid":"MONDO:0800187","xrefs":{"Monarch":{"xref_id":"0800187"}}}


id: PBO:0089337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi to ER retrograde transport protein","termid":"PBO:0089337"}


id: PBO:0038674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA synthetase medium chain family member 1","termid":"PBO:0038674"}


id: PBO:0027871
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_methylated_histone_binding","termid":"PBO:0027871"}


id: PBO:0013017
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCm Binding protein","termid":"PBO:0013017"}


id: GO:0031566
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular process in which the contractile ring cytokinetic ring attains its fully functional state.","definition_xrefs":["PMID:25451933","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component maintenance","termid":"GO:0043954"},{"relation_name":"is_a","term_name":"actomyosin contractile ring organization","termid":"GO:0044837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0007010","GO:0030036"],"is_obsolete":false,"name":"actomyosin contractile ring maturation","synonyms":[{"name":"actomyosin contractile ring maintenance","type":"related"},{"name":"cytokinesis, contractile ring maintenance","type":"related"}],"termid":"GO:0031566"}


id: PBO:0078926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon ACG) 2-2","termid":"PBO:0078926"}


id: GO:0043877
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-galactosamine 6-phosphate + H2O = D-tagatose 6-phosphate + NH3.","definition_xrefs":["PMID:10931310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"galactosamine-6-phosphate isomerase activity","synonyms":[{"name":"AgaI","type":"related"},{"name":"galactosamine-6-phosphate deaminase activity","type":"exact"}],"termid":"GO:0043877"}


id: MONDO:0015512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of hypertension that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete genetic hypertension (obsolete MONDO:0015512)","secondary_identifiers":["Orphanet:156629"],"synonyms":[{"name":"genetic hypertension","type":"exact"},{"name":"genetic hypertensive disorder","type":"exact"}],"termid":"MONDO:0015512","xrefs":{"Monarch":{"xref_id":"0015512"}}}


id: GO:0097684
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The anterior most point of a dinoflagellate hypocone.","definition_xrefs":["GOC:at","Wikipedia:Dinoflagellate#Morphology"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"dinoflagellate hypocone","termid":"GO:0097614"}],"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 antapex","synonyms":[{"name":"antapex","type":"broad"}],"termid":"GO:0097684"}


id: MONDO:0017208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete intermediate uveitis (obsolete MONDO:0017208)","termid":"MONDO:0017208","xrefs":{"Monarch":{"xref_id":"0017208"}}}


id: GO:2000019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of male gonad development.","definition_xrefs":["GOC:obol","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of gonad development","termid":"GO:1905940"},{"relation_name":"is_a","term_name":"regulation of male gonad development","termid":"GO:2000018"},{"relation_name":"negatively_regulates","term_name":"male gonad development","termid":"GO:0008584"}],"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 male gonad development","synonyms":[{"name":"negative regulation of testicular development","type":"exact"},{"name":"negative regulation of testis development","type":"exact"}],"termid":"GO:2000019"}


id: GO:0047520
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 11-cis-retinyl palmitate + H2O = 11-cis-retinol + H+ + palmitate.","definition_xrefs":["RHEA:19697","EC:3.1.1.63"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"11-cis-retinyl-palmitate hydrolase activity","secondary_identifiers":["KEGG_REACTION:R03049","MetaCyc:11-CIS-RETINYL-PALMITATE-HYDROLASE-RXN","Reactome:R-HSA-2465941"],"synonyms":[{"name":"11-cis-retinol palmitate esterase activity","type":"related"},{"name":"11-cis-retinyl-palmitate acylhydrolase activity","type":"related"},{"name":"RPH","type":"related"}],"termid":"GO:0047520"}


id: PBO:0076509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 9","termid":"PBO:0076509"}


id: MONDO:0957270
data:
  {"annotated_genes":["SJAG_03715"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86054],"is_not":false,"summary":null,"term":"MONDO:0957270"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03715":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005336"],"is_obsolete":false,"name":"muscular dystrophy, limb-girdle, autosomal recessive 28","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620375","MEDGEN:1841154","Orphanet:653725","UMLS:C5830518"],"termid":"MONDO:0957270","terms_by_termid":{"MONDO:0957270":null},"xrefs":{"Monarch":{"xref_id":"0957270"}}}


id: PBO:0028229
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_trehalose_level_during_cellular_response_to_salt_stress","termid":"PBO:0028229"}


id: GO:1903768
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of taste receptor activity.","definition_xrefs":["GOC:TermGenie","GOC:rl","GOC:BHF","PMID:16720576","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor complex","termid":"GO:0043235"}],"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":"taste receptor complex","termid":"GO:1903768"}


id: GO:0000149
data:
  {"annotated_genes":["SJAG_05345","SJAG_01925","SJAG_00072","SJAG_03499","SJAG_01748","SJAG_03536","SJAG_01697","SJAG_02349","SJAG_03963","SJAG_04023","SJAG_03403","SJAG_05344","SJAG_03848","SJAG_04978","SJAG_02241","SJAG_01309","SJAG_00826","SJAG_04909","SJAG_02811"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70927,71534,73176,74223,74655,75000,75510,75674,75896,76023,77244,77884],"is_not":false,"summary":null,"term":"GO:0000149"},{"annotations":[78973,76057,69249,69341,77514,75945,74753],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019905"}]},"cv_name":"molecular_function","definition":"Binding to a SNARE (soluble N-ethylmaleimide-sensitive factor attached protein receptor) protein.","definition_xrefs":["PMID:12642621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_00826":null,"SJAG_01309":null,"SJAG_01697":null,"SJAG_01748":null,"SJAG_01925":null,"SJAG_02241":null,"SJAG_02349":null,"SJAG_02811":null,"SJAG_03403":null,"SJAG_03499":null,"SJAG_03536":null,"SJAG_03848":null,"SJAG_03963":null,"SJAG_04023":null,"SJAG_04909":null,"SJAG_04978":null,"SJAG_05344":null,"SJAG_05345":null},"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:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"SNARE binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-372505","Reactome:R-HSA-372529","Reactome:R-HSA-376357","Reactome:R-HSA-376369","Reactome:R-HSA-376364","Reactome:R-HSA-380869","Reactome:R-HSA-210430","Reactome:R-HSA-265166","Reactome:R-HSA-380905","Reactome:R-HSA-380574","Reactome:R-HSA-374922","Reactome:R-HSA-380901","Reactome:R-HSA-210426","Reactome:R-HSA-374899","Reactome:R-HSA-888589","Reactome:R-HSA-9023173","Reactome:R-HSA-917744"],"synonyms":[{"name":"SNAP receptor binding","type":"exact"}],"termid":"GO:0000149","terms_by_termid":{"GO:0000149":null,"GO:0019905":null}}


id: GO:0051187
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of a cofactor, a substance that is required for the activity of an enzyme or other protein.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cofactor catabolic process (obsolete GO:0051187)","synonyms":[{"name":"cofactor breakdown","type":"exact"},{"name":"cofactor catabolism","type":"exact"},{"name":"cofactor degradation","type":"exact"}],"termid":"GO:0051187"}


id: PR:Q1MTN7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpm1 gene.","definition_xrefs":["UniProtKB:Q1MTN7","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":"exoribonuclease II, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1322.01","synonyms":[{"name":"RNase II (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rpm1","type":"exact"},{"name":"processome-associated RNase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ribonuclease II (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q1MTN7"}


id: GO:0031612
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The subcomplex of the proteasome regulatory particle that directly associates with the proteasome core complex located in the cytosol of the cell.","definition_xrefs":["GOC:mtg_sensu","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome regulatory particle, base subcomplex","termid":"GO:0008540"},{"relation_name":"part_of","term_name":"cytosolic proteasome regulatory particle","termid":"GO:0031600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005737","GO:0005829","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cytosolic proteasome regulatory particle, base subcomplex","termid":"GO:0031612"}


id: PBO:0086133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for maturation of mitochondrial [4Fe-4S] proteins; functions in a complex with Isa1p and possibly Iba57p; localizes to the mitochondrial intermembrane space, overexpression of ISA2 suppresses grx5 mutations","termid":"PBO:0086133"}


id: PBO:0044905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desumoylating isopeptidase 2","termid":"PBO:0044905"}


id: GO:1905456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lymphoid progenitor cell differentiation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:27010503"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hematopoietic progenitor cell differentiation","termid":"GO:1901532"},{"relation_name":"regulates","term_name":"lymphoid progenitor cell differentiation","termid":"GO:0002320"}],"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 lymphoid progenitor cell differentiation","termid":"GO:1905456"}


id: GO:0033220
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + H2O + amide(out) = ADP + phosphate + amide(in).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete ATPase-coupled amide-transporter activity (obsolete GO:0033220)","synonyms":[{"name":"ATP-dependent amide-transporter activity","type":"exact"},{"name":"amide-transporting ATPase activity","type":"exact"}],"termid":"GO:0033220"}


id: PBO:0072513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 42","termid":"PBO:0072513"}


id: PBO:0076220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPT3 homolog, SAGA and STAGA complex component","termid":"PBO:0076220"}


id: MOD:01354
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an N4 hydrogen atom of an asparagine residue with a carbohydrate-like group composed of Hex1HexNAc1NeuAc1 linked through a glycosidic bond.","definition_xrefs":["Unimod:149#N","PubMed:11698400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"},{"relation_name":"is_a","term_name":"Hex1HexNAc1NeuAc1 glycosylated residue","termid":"MOD:00517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"Hex1HexNAc1NeuAc1 N4-glycosylated asparagine","synonyms":[{"name":"Hex(1)HexNAc(1)NeuAc(1)","type":"related"},{"name":"Hex1HexNAc1NeuAc1","type":"related"}],"termid":"MOD:01354"}


id: PBO:0056884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MICOS10 pseudogene 4","termid":"PBO:0056884"}


id: PBO:0043601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collectin subfamily member 10","termid":"PBO:0043601"}


id: GO:0086077
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A wide pore channel activity that enables a direct cytoplasmic connection from an AV node cell to a bundle of His cell. The gap junction passes electrical signals between the cells contributing to cardiac conduction.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gap junction channel activity involved in cardiac conduction electrical coupling","termid":"GO:0086075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling","synonyms":[{"name":"gap junction channel activity involved in atrioventricular node cell-bundle of His cell electrical coupling","type":"exact"}],"termid":"GO:0086077"}


id: PBO:0060905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal differentiation 6","termid":"PBO:0060905"}


id: MONDO:0014931
data:
  {"annotated_genes":["SJAG_04274"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86633],"is_not":false,"summary":null,"term":"MONDO:0014931"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04274":null},"genotype_count":0,"is_obsolete":false,"name":"Alazami-Yuan syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4310702","MEDGEN:934669","OMIM:617126"],"synonyms":[{"name":"ALYUS","type":"exact"},{"name":"Alazami-Yuan syndrome","type":"exact"},{"name":"Alazami-Yuan syndrome; ALYUS","type":"exact"}],"termid":"MONDO:0014931","terms_by_termid":{"MONDO:0014931":null},"xrefs":{"Monarch":{"xref_id":"0014931"}}}


id: PBO:0087500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of GID complex; involved in proteasome-dependent catabolite inactivation of gluconeogenic enzymes FBPase, PEPCK, and c-MDH; forms dimer with Rmd5p that is then recruited to GID Complex by Gid8p; contains a degenerate RING finger motif needed for GID complex ubiquitin ligase activity in vivo, as well as CTLH and CRA domains; plays role in anti-apoptosis; required for survival upon exposure to K1 killer toxin","termid":"PBO:0087500"}


id: GO:0019712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The methyl esterification of peptidyl-glutamic acid.","definition_xrefs":["RESID:AA0072"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-L-glutamic acid 5-methyl ester biosynthetic process from glutamic acid (obsolete GO:0019712)","synonyms":[{"name":"peptidyl-L-glutamic acid 5-methyl ester anabolism from glutamic acid","type":"exact"},{"name":"peptidyl-L-glutamic acid 5-methyl ester formation from glutamic acid","type":"exact"},{"name":"peptidyl-L-glutamic acid 5-methyl ester synthesis from glutamic acid","type":"exact"}],"termid":"GO:0019712"}


id: GO:0004345
data:
  {"annotated_genes":["SJAG_02696","SJAG_02297","SJAG_02148"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96383,96472,117946],"is_not":false,"summary":null,"term":"GO:0004345"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucose 6-phosphate + NADP+ = D-glucono-1,5-lactone 6-phosphate + NADPH + H+.","definition_xrefs":["EC:1.1.1.49"],"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":3,"genes_by_uniquename":{"SJAG_02148":null,"SJAG_02297":null,"SJAG_02696":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"glucose-6-phosphate dehydrogenase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-70377","RHEA:15841","MetaCyc:GLU6PDEHYDROG-RXN"],"synonyms":[{"name":"6-phosphoglucose dehydrogenas","type":"related"},{"name":"6-phosphoglucose dehydrogenase activity","type":"exact"},{"name":"D-glucose 6-phosphate dehydrogenase activity","type":"exact"},{"name":"D-glucose-6-phosphate:NADP+ 1-oxidoreductase activity","type":"related"},{"name":"Entner-doudoroff enzyme","type":"related"},{"name":"G6PD activity","type":"related"},{"name":"G6PDH","type":"exact"},{"name":"GDH","type":"related"},{"name":"NADP-dependent glucose 6-phosphate dehydrogenase activity","type":"exact"},{"name":"NADP-glucose-6-phosphate dehydrogenase activity","type":"exact"},{"name":"Zwischenferment","type":"related"},{"name":"glucose 6-phosphate dehydrogenase (NADP) activity","type":"exact"},{"name":"glucose-6-phosphate 1-dehydrogenase activity","type":"exact"}],"termid":"GO:0004345","terms_by_termid":{"GO:0004345":null}}


id: MONDO:1011068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in Silvery lutung.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, Silvery lutung","secondary_identifiers":["OMIA:001033-122765"],"termid":"MONDO:1011068","xrefs":{"Monarch":{"xref_id":"1011068"}}}


id: PATO:0001944
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of yellow and orange hue.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orange","termid":"PATO:0000953"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yellow orange","termid":"PATO:0001944"}


id: FYPO:0006758
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 protein measured in a cell is too low to detect during G1 phase of the mitotic cell cycle. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein absent from cell during vegetative growth","termid":"FYPO:0001984"}],"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:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0006551"],"is_obsolete":false,"name":"protein absent from cell during mitotic G1 phase","synonyms":[{"name":"protein absent from cell during G1 phase during vegetative growth","type":"exact"},{"name":"protein absent from cell during G1 phase of mitotic cell cycle","type":"exact"},{"name":"undetectable cellular protein level during mitotic G1 phase","type":"exact"}],"termid":"FYPO:0006758"}


id: FYPO:0003853
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to fluconazole. Cells stop growing (and may die) at a concentration of fluconazole that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002683","FYPO:0000139","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to fluconazole","synonyms":[{"name":"hypersensitive to fluconazole","type":"exact"},{"name":"sensitive to fluconazole during mitotic cell cycle","type":"related"},{"name":"sensitive to fluconazole during vegetative growth","type":"exact"}],"termid":"FYPO:0003853"}


id: MONDO:1010753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertrichosis that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis, non-human animal","termid":"MONDO:1010130"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrichosis, cattle","secondary_identifiers":["OMIA:000513-9913"],"termid":"MONDO:1010753","xrefs":{"Monarch":{"xref_id":"1010753"}}}


id: PBO:0088222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RhoGAP for Cdc42, Rga6","termid":"PBO:0088222"}


id: PBO:0084520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of Hsp110 subclass of the heat shock protein 70 (HSP70) family; serves as nucleotide exchange factor to load ATP onto the SSA class of cytosolic Hsp70s; may be involved in protein folding; localized to the cytoplasm; SSE2 has a paralog, SSE1, that arose from the whole genome duplication","termid":"PBO:0084520"}


id: GO:0016297
data:
  {"annotated_genes":["SJAG_04107"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100245],"is_not":false,"summary":null,"term":"GO:0016297"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a fatty acyl-[ACP] + H2O = a fatty acid + H+ + holo-[acyl-carrier protein].","definition_xrefs":["RHEA:44596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiolester hydrolase activity","termid":"GO:0016790"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04107":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"fatty acyl-[ACP] hydrolase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0010281","GO:0016294","MetaCyc:RXN-7902","Reactome:R-HSA-5655955"],"synonyms":[{"name":"acyl-ACP hydrolase activity","type":"exact"},{"name":"acyl-ACP thioesterase activity","type":"exact"},{"name":"acyl-ACP-hydrolase activity","type":"related"},{"name":"acyl-[acyl-carrier protein] hydrolase activity","type":"exact"},{"name":"acyl-[acyl-carrier-protein] hydrolase activity","type":"exact"},{"name":"acyl-acyl carrier protein hydrolase activity","type":"related"},{"name":"acyl-acyl-carrier-protein hydrolase activity","type":"related"}],"termid":"GO:0016297","terms_by_termid":{"GO:0016297":null}}


id: MONDO:0019468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line.","definition_xrefs":["NCIT:C70649"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mature T-cell and NK-cell non-Hodgkin lymphoma","termid":"MONDO:0000430"},{"relation_name":"is_a","term_name":"prolymphocytic leukemia","termid":"MONDO:0001023"},{"relation_name":"is_a","term_name":"precursor T-lymphoblastic lymphoma/leukemia","termid":"MONDO:0003537"},{"relation_name":"is_a","term_name":"T-cell acute lymphoblastic leukemia","termid":"MONDO:0004963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"T-cell prolymphocytic leukemia","secondary_identifiers":["UMLS:C2363142","MEDGEN:391707","DOID:0081042","GARD:13731","MedDRA:10042985","ONCOTREE:TPLL","NCIT:C4752","SCTID:277567002","icd11.foundation:352523899","MESH:D015461","Orphanet:86871","EFO:1000560","SCTID:277545003","ICDO:9834/3"],"synonyms":[{"name":"CLL, T-cell","type":"exact"},{"name":"T cell CLL","type":"exact"},{"name":"T cell chronic lymphocytic leukaemia","type":"exact"},{"name":"T cell chronic lymphocytic leukemia","type":"exact"},{"name":"T cell prolymphocytic leukaemia","type":"exact"},{"name":"T cell prolymphocytic leukemia","type":"exact"},{"name":"T prolymphocytic leukaemia","type":"exact"},{"name":"T prolymphocytic leukemia","type":"exact"},{"name":"T-PLL","type":"exact"},{"name":"T-cell CLL","type":"exact"},{"name":"T-cell chronic lymphocytic leukaemia","type":"exact"},{"name":"T-cell chronic lymphocytic leukemia","type":"exact"},{"name":"T-cell prolymphocytic leukemia","type":"exact"},{"name":"TPLL","type":"related"},{"name":"chronic T-cell leukaemia","type":"narrow"},{"name":"chronic T-cell leukemia","type":"narrow"},{"name":"chronic T-cell lymphocytic leukaemia","type":"narrow"},{"name":"chronic T-cell lymphocytic leukemia","type":"narrow"},{"name":"leukemia, T-cell, chronic","type":"related"}],"termid":"MONDO:0019468","xrefs":{"Monarch":{"xref_id":"0019468"}}}


id: PBO:0046173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELK1 pseudogene 1","termid":"PBO:0046173"}


id: MONDO:0010854
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86626],"is_not":false,"summary":null,"term":"MONDO:0010854"}]},"cv_name":"mondo","definition":"Oculo-ectodermal syndrome (OES) is characterized by the association of epibulbar dermoids and aplasia cutis congenital.","definition_xrefs":["Orphanet:3339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Toriello-Lacassie-Droste syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:723554006","MESH:C563969","GARD:10366","MEDGEN:333068","OMIM:600268","DOID:0111705","UMLS:C1838329","icd11.foundation:1983176633"],"synonyms":[{"name":"Toriello Lacassie Droste syndrome","type":"related"},{"name":"aplasia cutis congenita with epibulbar dermoids","type":"related"},{"name":"aplasia cutis congenita-epibulbar dermoids syndrome","type":"exact"},{"name":"oculo-ectodermal syndrome","type":"related"},{"name":"oculoectodermal syndrome","type":"exact"},{"name":"oculoectodermal syndrome, somatic","type":"exact"},{"name":"oes","type":"related"}],"termid":"MONDO:0010854","terms_by_termid":{"MONDO:0010854":null},"xrefs":{"Monarch":{"xref_id":"0010854"}}}


id: GO:0050591
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + NADPH + O2 + quinine = 3-hydroxyquinine + H2O + NADP+.","definition_xrefs":["RHEA:20149","EC:1.14.14.55"],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"quinine 3-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R05727","MetaCyc:1.14.13.67-RXN"],"synonyms":[{"name":"nifedipine oxidase activity","type":"related"},{"name":"quinine 3-hydroxylase activity","type":"exact"},{"name":"quinine,NADPH:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0050591"}


id: RO:0002489
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x starts ends with y if and only if the time point at which x starts is equivalent to the time point at which y starts. Formally: x existence starts with y iff α(x) = α(y).","direct_ancestors":[{"relation_name":"is_a","term_name":"existence_starts_during","termid":"RO:0002488"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"existence_starts_with","termid":"RO:0002489"}


id: GO:0047408
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + 1-(1-alkenyl)-sn-glycero-3-phosphocholine = L-1-glycero-3-phosphocholine + an aldehyde.","definition_xrefs":["EC:3.3.2.2","MetaCyc:3.3.2.2-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ether hydrolase activity","termid":"GO:0016803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"alkenylglycerophosphocholine hydrolase activity","secondary_identifiers":["RHEA:22544"],"synonyms":[{"name":"1-(1-alkenyl)-sn-glycero-3-phosphocholine aldehydohydrolase activity","type":"related"},{"name":"lysoplasmalogenase activity","type":"related"}],"termid":"GO:0047408"}


id: GO:0007088
data:
  {"annotated_genes":["SJAG_02380","SJAG_01805","SJAG_02058","SJAG_01330","SJAG_01837","SJAG_02451","SJAG_03126","SJAG_03681","SJAG_01679","SJAG_02498","SJAG_02169","SJAG_04968","SJAG_00883","SJAG_04573","SJAG_02336","SJAG_03353","SJAG_03048","SJAG_01082","SJAG_04999","SJAG_01297","SJAG_04259","SJAG_04884","SJAG_00666","SJAG_04699","SJAG_04126"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110416],"is_not":false,"summary":null,"term":"GO:0007088"},{"annotations":[90204,106723,103394,107739,111451,113763,115397,113275,99089],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[109403,113996,105809,90206,101296,98933,113279,115052,116167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[115053,105810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045841"},{"annotations":[93685],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[116171],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[114265,110866,97188,99635,113764,101610,111454,93287,101883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045842"},{"annotations":[93686],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0090266"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mitosis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle","termid":"GO:0007346"},{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of nuclear division","termid":"GO:0051783"},{"relation_name":"regulates","term_name":"mitotic nuclear division","termid":"GO:0140014"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00666":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02058":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02380":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04573":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04968":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of mitotic nuclear division","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of mitosis","type":"exact"}],"termid":"GO:0007088","terms_by_termid":{"GO:0007088":null,"GO:0007094":null,"GO:0045841":null,"GO:0045842":null,"GO:0090266":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null}}


id: PBO:0078796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (GTT) 16-3","termid":"PBO:0078796"}


id: GO:0075131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont activates, maintains or increases the frequency, rate or extent of protein kinase-mediated signal transduction in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by symbiont of host protein kinase-mediated signal transduction (obsolete GO:0075131)","termid":"GO:0075131"}


id: PBO:0089616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial hydrogen/potassium transport system protein","termid":"PBO:0089616"}


id: GO:0098574
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the lysosomal membrane that faces the cytoplasm.","definition_xrefs":["GOC:dos","GOC:ab"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic side of membrane","termid":"GO:0098562"},{"relation_name":"part_of","term_name":"lysosomal membrane","termid":"GO:0005765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005773"],"is_obsolete":false,"name":"cytoplasmic side of lysosomal membrane","synonyms":[{"name":"external leaflet of lysosomal membrane","type":"exact"},{"name":"external side of lysosomal membrane","type":"exact"}],"termid":"GO:0098574"}


id: GO:0003271
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of activation of the transmembrane protein Smoothened contributing to the modulation of the frequency, rate or extent of cardioblast proliferation in the secondary heart field. A cardioblast is a cardiac precursor cell. It is a cell that has been committed to a cardiac fate, but will undergo more cell division rather than terminally differentiating.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smoothened signaling pathway","termid":"GO:0007224"},{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway involved in heart development","termid":"GO:0061311"},{"relation_name":"part_of","term_name":"regulation of secondary heart field cardioblast proliferation","termid":"GO:0003266"}],"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":"smoothened signaling pathway involved in regulation of secondary heart field cardioblast proliferation","synonyms":[{"name":"hedgehog signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"hh signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signaling pathway involved in regulation of secondary heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signalling pathway involved in regulation of secondary heart field cardioblast proliferation","type":"exact"}],"termid":"GO:0003271"}


id: PBO:0091229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dienelactone hydrolase family, implicated in cellular detoxification","termid":"PBO:0091229"}


id: MONDO:0020722
data:
  {"annotated_genes":["SJAG_02463","SJAG_01941"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85983,85984],"is_not":false,"summary":null,"term":"MONDO:0020722"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"},{"relation_name":"is_a","term_name":"nephrolithiasis, calcium oxalate","termid":"MONDO:0957318"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01941":null,"SJAG_02463":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephrolithiasis susceptibility caused by SLC26A1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1830325","OMIM:167030","UMLS:C5779632","DOID:0080652"],"synonyms":[{"name":"CAON","type":"related"},{"name":"nephrolithiasis, calcium oxalate","type":"related"},{"name":"urolithiasis, calcium oxalate","type":"related"}],"termid":"MONDO:0020722","terms_by_termid":{"MONDO:0020722":null},"xrefs":{"Monarch":{"xref_id":"0020722"}}}


id: GO:0002151
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a G-quadruplex RNA structure, in which groups of four guanines adopt a flat, cyclic hydrogen-bonding arrangement known as a guanine tetrad.","definition_xrefs":["PMID:18568163","PMID:19330720","PMID:18294969"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"G-quadruplex RNA binding","secondary_identifiers":["Reactome:R-HSA-9836998"],"synonyms":[{"name":"G quadruplex binding","type":"exact"},{"name":"G quartet RNA binding","type":"exact"},{"name":"G quartet binding","type":"broad"},{"name":"G-quartet binding","type":"broad"}],"termid":"GO:0002151"}


id: GO:0090464
data:
  {"annotated_genes":["SJAG_01471"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96101],"is_not":false,"summary":null,"term":"GO:0090464"}]},"cv_name":"biological_process","definition":"A homeostatic process involved in the maintenance of a steady state level of histidine within a cell.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular amino acid homeostasis","termid":"GO:0080144"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01471":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"intracellular histidine homeostasis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cellular histidine homeostasis","type":"exact"},{"name":"histidine homeostasis","type":"exact"}],"termid":"GO:0090464","terms_by_termid":{"GO:0090464":null}}


id: PBO:0078357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 3-1","termid":"PBO:0078357"}


id: FYPO:0004910
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that is localized normally (i.e. indistinguishably from wild type) to discrete regions in the nucleus, visible as foci or dots by microscopy.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to nucleus during vegetative growth","termid":"FYPO:0000838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000138","FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal punctate nuclear protein localization","synonyms":[{"name":"normal punctate nuclear protein localisation","type":"exact"},{"name":"normal punctate nuclear protein localization during mitotic cell cycle","type":"related"},{"name":"normal punctate nuclear protein localization during vegetative growth","type":"exact"}],"termid":"FYPO:0004910"}


id: MONDO:0008426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Shprintzen-Goldberg syndrome (SGS) is a very rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability.","definition_xrefs":["Orphanet:2462"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"},{"relation_name":"is_a","term_name":"Marfan and Marfan-related disorder","termid":"MONDO:0017310"}],"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":"Shprintzen-Goldberg syndrome","secondary_identifiers":["SCTID:719069008","MEDGEN:231160","UMLS:C1321551","GARD:4861","NORD:1908","NCIT:C124840","OMIM:182212"],"synonyms":[{"name":"Marfanoid craniosynostosis syndrome","type":"exact"},{"name":"Marfanoid disorder with craniosynostosis type 1","type":"related"},{"name":"Marfanoid disorder with craniosynostosis, type 1","type":"related"},{"name":"Marfanoid-craniosynostosis syndrome","type":"related"},{"name":"SGS","type":"exact"},{"name":"Shprintzen Goldberg Syndrome","type":"exact"},{"name":"Shprintzen-Goldberg craniosynostosis syndrome","type":"related"},{"name":"Shprintzen-Goldberg marfanoid syndrome","type":"related"},{"name":"Shprintzen-Goldberg syndrome","type":"exact"},{"name":"craniosynostosis with arachnodactyly and abdominal hernias","type":"related"}],"termid":"MONDO:0008426","xrefs":{"Monarch":{"xref_id":"0008426"}}}


id: GO:0060352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of a cell adhesion molecule due to biosynthesis or secretion.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"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":"cell adhesion molecule production","termid":"GO:0060352"}


id: PBO:0067301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 386, pseudogene","termid":"PBO:0067301"}


id: SO:0000426
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The long terminal repeat found at the three-prime end of the sequence to be inserted into the host genome.","direct_ancestors":[{"relation_name":"is_a","term_name":"long_terminal_repeat","termid":"SO:0000286"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_LTR","synonyms":[{"name":"3' LTR","type":"exact"},{"name":"3' long terminal repeat","type":"exact"},{"name":"three prime LTR","type":"exact"}],"termid":"SO:0000426"}


id: PATO:0001973
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being tapering gradually into a rigid point.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tapered","termid":"PATO:0001500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cuspidate","termid":"PATO:0001973"}


id: MONDO:0030925
data:
  {"annotated_genes":["SJAG_07002"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85083],"is_not":false,"summary":null,"term":"MONDO:0030925"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":1,"genes_by_uniquename":{"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte maturation defect 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1766720","GARD:18500","OMIM:619176","UMLS:C5436938"],"synonyms":[{"name":"OOMD10","type":"exact"},{"name":"oocyte maturation defect 10","type":"exact"}],"termid":"MONDO:0030925","terms_by_termid":{"MONDO:0030925":null},"xrefs":{"Monarch":{"xref_id":"0030925"}}}


id: PBO:0048817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 5B","termid":"PBO:0048817"}


id: PBO:0041378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C5","termid":"PBO:0041378"}


id: FYPO:0000598
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of vacuolar transport is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased intracellular transport","termid":"FYPO:0000464"},{"relation_name":"is_a","term_name":"abnormal vacuolar transport during vegetative growth","termid":"FYPO:0000597"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased vacuolar transport","synonyms":[{"name":"decreased vacuolar protein transport","type":"narrow"},{"name":"decreased vacuolar transport during mitotic cell cycle","type":"related"},{"name":"decreased vacuolar transport during vegetative growth","type":"exact"},{"name":"reduced vacuolar transport","type":"exact"},{"name":"vacuolar transport: decreased","type":"related"}],"termid":"FYPO:0000598"}


id: PBO:0089448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose dehydrogenase Gcd1","termid":"PBO:0089448"}


id: GO:0090272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of the appearance of a fibroblast growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of fibroblast growth factor production","termid":"GO:0090270"},{"relation_name":"negatively_regulates","term_name":"fibroblast growth factor production","termid":"GO:0090269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of fibroblast growth factor production","termid":"GO:0090272"}


id: MONDO:0014939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SLC5A7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome","termid":"MONDO:0018940"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital myasthenic syndrome 20","secondary_identifiers":["DOID:0110661","GARD:16202","UMLS:C4310694","OMIM:617143","MEDGEN:934661"],"synonyms":[{"name":"CMS20","type":"exact"},{"name":"SLC5A7 congenital myasthenic syndrome","type":"exact"},{"name":"congenital myasthenic syndrome 20 presynaptic","type":"exact"},{"name":"congenital myasthenic syndrome caused by mutation in SLC5A7","type":"exact"},{"name":"congenital myasthenic syndrome type 20","type":"exact"},{"name":"myasthenic syndrome, congenital, 20, presynaptic","type":"exact"}],"termid":"MONDO:0014939","xrefs":{"Monarch":{"xref_id":"0014939"}}}


id: PBO:0031542
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-unequal_homologous_chromosome_segregation","termid":"PBO:0031542"}


id: GO:0034306
data:
  {"annotated_genes":["SJAG_04140","SJAG_04853","SJAG_02169","SJAG_00993"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[101792],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[90209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[91673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of spore formation from the products of meiosis. An example of this is found in Saccharomyces cerevisiae.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sporulation","termid":"GO:0043937"},{"relation_name":"is_a","term_name":"regulation of meiotic cell cycle","termid":"GO:0051445"},{"relation_name":"regulates","term_name":"sexual sporulation","termid":"GO:0034293"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00993":null,"SJAG_02169":null,"SJAG_04140":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of sexual sporulation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"MAPKKK cascade during sporulation","type":"related"},{"name":"regulation of meiotic spore formation","type":"exact"},{"name":"regulation of meiotic sporulation","type":"exact"},{"name":"regulation of sexual spore formation","type":"exact"}],"termid":"GO:0034306","terms_by_termid":{"GO:0034307":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: PR:O36015
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ribosomal RNA methyltransferase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02006","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":"tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F10.03c","secondary_identifiers":["UniProtKB:O36015"],"synonyms":[{"name":"2'-O-ribose RNA methyltransferase TRM7 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FTSJ1","type":"exact"}],"termid":"PR:O36015"}


id: MONDO:0019411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Genochondromatosis is characterized by chondromatosis, typically involving the clavicles, upper end of the humerus, and lower end of the femur. Lesions are bilateral and symmetrical. It has been described four patients from the same family and is transmitted as an autosomal dominant trait. Another disorder, genochondromatosis II, shows strong similarities to genochondromatosis but is characterized by the involvement of the short tubular bones and by normal clavicles. It has been described in one unrelated family. Genochondromatosis II may also be inherited as an autosomal dominant trait. Genochondromatosis has a benign clinical course.","definition_xrefs":["Orphanet:85197"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"genochondromatosis","termid":"MONDO:0007653"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genochondromatosis type 1","secondary_identifiers":["GARD:16741","icd11.foundation:521879469","MEDGEN:1761731","UMLS:C5438970"],"termid":"MONDO:0019411","xrefs":{"Monarch":{"xref_id":"0019411"}}}


id: GO:0051896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of phosphatidylinositol 3-kinase/protein kinase B signal transduction.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"phosphatidylinositol 3-kinase/protein kinase B signal transduction","termid":"GO:0043491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction","secondary_identifiers":["Reactome:R-HSA-6811558"],"synonyms":[{"name":"regulation of AKT signaling cascade","type":"related"},{"name":"regulation of AKT signalling cascade","type":"related"},{"name":"regulation of PI3K-PKB/Akt pathway","type":"exact"},{"name":"regulation of PI3K/Akt signal transduction","type":"exact"},{"name":"regulation of PI3K/PKB signal transduction","type":"exact"},{"name":"regulation of PKB signaling cascade","type":"related"},{"name":"regulation of PKB signalling cascade","type":"related"},{"name":"regulation of phosphatidylinositol 3-kinase signaling/protein kinase B signal transduction","type":"exact"},{"name":"regulation of protein kinase B signaling","type":"related"},{"name":"regulation of protein kinase B signaling cascade","type":"related"},{"name":"regulation of protein kinase B signalling cascade","type":"related"}],"termid":"GO:0051896"}


id: PATO:0001389
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An aneuploidy quality inhering in a bearer by virtue of the bearer's containing three, instead of two, chromosomes of a particular numbered type in an organism.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Trisomy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aneuploid","termid":"PATO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy","termid":"PATO:0001389"}


id: MONDO:0014668
data:
  {"annotated_genes":["SJAG_02229"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84576],"is_not":false,"summary":null,"term":"MONDO:0014668"}]},"cv_name":"mondo","definition":"Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatal infantile encephalocardiomyopathy","termid":"MONDO:0015487"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02229":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0004069","MONDO:0005267","MONDO:0005066"],"is_obsolete":false,"name":"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080360","MEDGEN:905398","UMLS:C4225304","OMIM:616501","GARD:18573"],"synonyms":[{"name":"CEMCOX4","type":"related"},{"name":"COA6 fatal infantile encephalocardiomyopathy","type":"exact"},{"name":"cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 4","type":"exact"},{"name":"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4","type":"exact"},{"name":"fatal infantile encephalocardiomyopathy caused by mutation in COA6","type":"exact"},{"name":"mitochondrial complex IV deficiency, nuclear type 13","type":"exact"}],"termid":"MONDO:0014668","terms_by_termid":{"MONDO:0014668":null},"xrefs":{"Monarch":{"xref_id":"0014668"}}}


id: SO:0000209
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding a ribosomal RNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nc_primary_transcript","termid":"SO:0000483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA_primary_transcript","synonyms":[{"name":"rRNA primary transcript","type":"exact"},{"name":"ribosomal RNA primary transcript","type":"exact"}],"termid":"SO:0000209"}


id: PBO:0004010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folliculin ortholog Bhd1","termid":"PBO:0004010"}


id: MONDO:0971172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language","secondary_identifiers":["OMIM:620851"],"termid":"MONDO:0971172","xrefs":{"Monarch":{"xref_id":"0971172"}}}


id: PBO:0071413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 19","termid":"PBO:0071413"}


id: PBO:0063815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHLDA1 antisense RNA 1","termid":"PBO:0063815"}


id: GO:0000462
data:
  {"annotated_genes":["SJAG_04069","SJAG_01623","SJAG_02702","SJAG_01604","SJAG_03077","SJAG_05018","SJAG_03952","SJAG_04916","SJAG_04908","SJAG_01551","SJAG_03796","SJAG_04582","SJAG_05187","SJAG_03846","SJAG_00945","SJAG_00879","SJAG_04524","SJAG_02547","SJAG_02020","SJAG_01347","SJAG_03422","SJAG_00572","SJAG_01609","SJAG_02250","SJAG_00344","SJAG_00562","SJAG_00897","SJAG_00955","SJAG_02499","SJAG_03341","SJAG_01907","SJAG_04029","SJAG_04339","SJAG_03569","SJAG_04979","SJAG_02553","SJAG_06613","SJAG_03234","SJAG_00294","SJAG_04224","SJAG_04174","SJAG_02644","SJAG_02358","SJAG_04033","SJAG_00965","SJAG_00772","SJAG_03425","SJAG_02821"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87297,87793,88714,90714,92118,93813,95161,95162,96526,97836,97837,98660,98661,98698,99705,100256,100906,101070,105175,105176,105470,105708,106455,106595,108191,108583,109215,109882,111268,114218,115247,116241],"is_not":false,"summary":null,"term":"GO:0000462"},{"annotations":[114692,99317,107108],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000480"},{"annotations":[95984,105055,107109,105152,99318,114804,114892,102626,92895,108491,98992,104052,112983,96278,104269,105151,118089,107438,94194],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000447"},{"annotations":[105056],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000461"},{"annotations":[99319,107110,108492,114693],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000472"}]},"cv_name":"biological_process","definition":"Any process involved in the maturation of a precursor Small SubUnit (SSU) ribosomal RNA (rRNA) molecule into a mature SSU-rRNA molecule from the pre-rRNA molecule originally produced as a tricistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, 5.8S rRNA, and the Large Subunit (LSU) in that order from 5' to 3' along the primary transcript.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturation of SSU-rRNA","termid":"GO:0030490"}],"gene_count":48,"genes_by_uniquename":{"SJAG_00294":null,"SJAG_00344":null,"SJAG_00562":null,"SJAG_00572":null,"SJAG_00772":null,"SJAG_00879":null,"SJAG_00897":null,"SJAG_00945":null,"SJAG_00955":null,"SJAG_00965":null,"SJAG_01347":null,"SJAG_01551":null,"SJAG_01604":null,"SJAG_01609":null,"SJAG_01623":null,"SJAG_01907":null,"SJAG_02020":null,"SJAG_02250":null,"SJAG_02358":null,"SJAG_02499":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_02644":null,"SJAG_02702":null,"SJAG_02821":null,"SJAG_03077":null,"SJAG_03234":null,"SJAG_03341":null,"SJAG_03422":null,"SJAG_03425":null,"SJAG_03569":null,"SJAG_03796":null,"SJAG_03846":null,"SJAG_03952":null,"SJAG_04029":null,"SJAG_04033":null,"SJAG_04069":null,"SJAG_04174":null,"SJAG_04224":null,"SJAG_04339":null,"SJAG_04524":null,"SJAG_04582":null,"SJAG_04908":null,"SJAG_04916":null,"SJAG_04979":null,"SJAG_05018":null,"SJAG_05187":null,"SJAG_06613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0042254"}],"interesting_parent_ids":["GO:0044085","GO:0010467","GO:0042254","GO:0008150"],"is_obsolete":false,"name":"maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1990041"],"synonyms":[{"name":"maturation of 18S rRNA","type":"narrow"}],"termid":"GO:0000462","terms_by_termid":{"GO:0000447":null,"GO:0000461":null,"GO:0000462":null,"GO:0000472":null,"GO:0000480":null}}


id: PBO:0064956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 8","termid":"PBO:0064956"}


id: PBO:0071563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 29","termid":"PBO:0071563"}


id: GO:0010669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A tissue homeostatic process required for the maintenance of epithelial structure.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue homeostasis","termid":"GO:0001894"}],"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":"epithelial structure maintenance","termid":"GO:0010669"}


id: MONDO:0006588
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete nonepidermolytic palmoplantar keratoderma (obsolete MONDO:0006588)","termid":"MONDO:0006588","xrefs":{"Monarch":{"xref_id":"0006588"}}}


id: PR:O74823
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- red5 gene.","definition_xrefs":["UniProtKB:O74823","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCCH domain-containing protein C337.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC337.12","synonyms":[{"name":"Spom972h-red5","type":"exact"}],"termid":"PR:O74823"}


id: PBO:0001820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 snRNP-associated RNA-binding protein Sap49","termid":"PBO:0001820"}


id: PBO:0017938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxyacyl-CoA dehydratase involved in very long-chain fatty acid elongation Phs1 (predicted)","termid":"PBO:0017938"}


id: PBO:0026918
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_rRNA_modification","termid":"PBO:0026918"}


id: GO:0061502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances, in membrane-bounded vesicles, from the early sorting endosomes to the recycling endosomes.","definition_xrefs":["GOC:kmv","GOC:dph","PMID:21474295"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle-mediated transport between endosomal compartments","termid":"GO:0098927"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"early endosome to recycling endosome transport","termid":"GO:0061502"}


id: PBO:0089298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal cell surface protein, Kre9/Knh1 family, Adg2","termid":"PBO:0089298"}


id: PBO:0048587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-glutamyltransferase light chain 1","termid":"PBO:0048587"}


id: PBO:0089747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E4 Ufd2","termid":"PBO:0089747"}


id: GO:0070857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of bile acids.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone metabolic process","termid":"GO:0010565"},{"relation_name":"is_a","term_name":"regulation of steroid biosynthetic process","termid":"GO:0050810"},{"relation_name":"is_a","term_name":"regulation of bile acid metabolic process","termid":"GO:1904251"},{"relation_name":"regulates","term_name":"bile acid biosynthetic process","termid":"GO:0006699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"regulation of bile acid biosynthetic process","synonyms":[{"name":"regulation of bile acid anabolism","type":"exact"},{"name":"regulation of bile acid biosynthesis","type":"exact"},{"name":"regulation of bile acid formation","type":"exact"},{"name":"regulation of bile acid synthesis","type":"exact"}],"termid":"GO:0070857"}


id: MOD:00617
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a residue containing common isotopes to a 3x(2)H labeled residue methyl ester.","definition_xrefs":["Unimod:298","OMSSA:21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3x(2)H residue methyl ester","synonyms":[{"name":"Methyl:2H(3)","type":"related"},{"name":"ctermpeptrideuteromethyl","type":"exact"},{"name":"deuterated methyl ester","type":"related"}],"termid":"MOD:00617"}


id: GO:0031414
data:
  {"annotated_genes":["SJAG_02726","SJAG_04631","SJAG_04179","SJAG_01826","SJAG_03215","SJAG_04131","SJAG_02920","SJAG_03045","SJAG_06449"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88870,116287,117485,109909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031415"},{"annotations":[114841,102064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031416"},{"annotations":[104978,103078,112281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031417"}]},"cv_name":"cellular_component","definition":"A complex that catalyzes the transfer of an acetyl group to the N-terminal residue of a protein acceptor molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein acetyltransferase complex","termid":"GO:0031248"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":9,"genes_by_uniquename":{"SJAG_01826":null,"SJAG_02726":null,"SJAG_02920":null,"SJAG_03045":null,"SJAG_03215":null,"SJAG_04131":null,"SJAG_04179":null,"SJAG_04631":null,"SJAG_06449":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"N-terminal protein acetyltransferase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"NAT complex","type":"exact"}],"termid":"GO:0031414","terms_by_termid":{"GO:0031415":null,"GO:0031416":null,"GO:0031417":null}}


id: GO:0097135
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin E2 and cyclin-dependent kinase 2 (CDK2). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["GOC:so","PMID:15935619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cyclin E2-CDK2 complex","termid":"GO:0097135"}


id: PR:O74962
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pantothenate kinase 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03694"],"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":"pantothenate kinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4B4.01c","secondary_identifiers":["UniProtKB:O74962"],"synonyms":[{"name":"Spom972h-PANK3","type":"exact"},{"name":"pantothenic acid kinase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74962"}


id: PBO:0031734
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormally_arrested_meiosis","termid":"PBO:0031734"}


id: PBO:0068865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 105, pseudogene","termid":"PBO:0068865"}


id: PBO:0072936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 16","termid":"PBO:0072936"}


id: FYPO:0004860
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 beta-D-glucan measured in the cell wall is greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased beta-glucan level","termid":"FYPO:0001194"},{"relation_name":"is_a","term_name":"increased cell wall polysaccharide level","termid":"FYPO:0004859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002946"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0002946"],"is_obsolete":false,"name":"increased cell wall beta-glucan level","synonyms":[{"name":"increased cell wall beta-D-glucan level","type":"exact"},{"name":"increased cell wall beta-glucan accumulation","type":"related"},{"name":"increased cell wall beta-glucan level during mitotic cell cycle","type":"related"},{"name":"increased cell wall beta-glucan level during vegetative growth","type":"exact"}],"termid":"FYPO:0004860"}


id: PBO:0073261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 7 pseudogene 5","termid":"PBO:0073261"}


id: GO:0043917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-ribose 1,5-bisphosphate = D-ribulose 1,5-bisphosphate.","definition_xrefs":["RHEA:32243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"ribose 1,5-bisphosphate isomerase activity","secondary_identifiers":["EC:5.3.1.29","MetaCyc:RXN-8801"],"synonyms":[{"name":"ribose-1,5-bisphosphate isomerase activity","type":"exact"}],"termid":"GO:0043917"}


id: PBO:0044842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 130A","termid":"PBO:0044842"}


id: GO:0010087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of phloem and/or xylem over time, from formation to the mature structure. An example of this process is found in Arabidopsis thaliana.","definition_xrefs":["GOC:mtg_sensu","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"phloem or xylem histogenesis","synonyms":[{"name":"vascular tissue development","type":"broad"},{"name":"vascular tissue histogenesis","type":"exact"}],"termid":"GO:0010087"}


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


id: PBO:0054503
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 1903","termid":"PBO:0054503"}


id: PBO:0079376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin alpha pseudogene 11","termid":"PBO:0079376"}


id: PBO:0061492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative regulator of interferon response","termid":"PBO:0061492"}


id: PBO:0084458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannosyltransferase, involved in N-linked glycosylation; catalyzes the transfer of both the seventh mannose residue on B-arm and ninth mannose residue on the C-arm from Dol-P-Man to lipid-linked oligosaccharides; human homolog ALG9 can complement yeast null mutant; mutation of human homolog causes type 1 congenital disorders of glycosylation","termid":"PBO:0084458"}


id: SO:0002207
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A hexameric RNA motif consisting of nucleotides UNAAAC (where N can be any nucleotide) that targets the RNA for degradation.","definition_xrefs":["PMID:22645662","PMID:28765164","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA_stability_element","termid":"SO:0001979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UNAAAC_motif","synonyms":[{"name":"UNAAAC motif","type":"exact"}],"termid":"SO:0002207"}


id: MONDO:0033980
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ependymal tumor","termid":"MONDO:0003266"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RELA fusion-positive ependymoma","secondary_identifiers":["Orphanet:530792","DOID:0080892","GARD:22210","UMLS:C4289581","MEDGEN:927113"],"termid":"MONDO:0033980","xrefs":{"Monarch":{"xref_id":"0033980"}}}


id: PBO:0068462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 39, pseudogene","termid":"PBO:0068462"}


id: PBO:0082571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chitin deacetylase; together with Cda1p involved in the biosynthesis ascospore wall component, chitosan; required for proper rigidity of the ascospore wall","termid":"PBO:0082571"}


id: MONDO:0014523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome","secondary_identifiers":["MEDGEN:863873","GARD:17768","OMIM:616192","Orphanet:445062","UMLS:C4015436"],"synonyms":[{"name":"ACPHD","type":"related"},{"name":"ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus","type":"related"},{"name":"combined cerebellar and peripheral ataxia-hearing loss-diabetes mellitus syndrome","type":"exact"}],"termid":"MONDO:0014523","xrefs":{"Monarch":{"xref_id":"0014523"}}}


id: MONDO:0016799
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial oxidative phosphorylation disorder with no known mechanism (obsolete MONDO:0016799)","secondary_identifiers":["Orphanet:254822"],"synonyms":[{"name":"OXPHOS disease with no known mechanism","type":"exact"}],"termid":"MONDO:0016799","xrefs":{"Monarch":{"xref_id":"0016799"}}}


id: GO:0071741
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of two identical immunoglobulin heavy chains of the IgD isotype and two identical immunoglobulin light chains, held together by disulfide bonds, and bound via a GPI-anchor to the plasma membrane of B cells.","definition_xrefs":["ISBN:0781765196","GOC:add","PMID:11282392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"IgD immunoglobulin complex","termid":"GO:0071738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"IgD immunoglobulin complex, GPI-anchored","synonyms":[{"name":"GPI-anchored IgD","type":"exact"}],"termid":"GO:0071741"}


id: GO:1902604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of N-(4-aminobenzoyl)-L-glutamate across a membrane.","definition_xrefs":["GOC:pr","GO_REF:0000069","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"p-aminobenzoyl-glutamate transport","termid":"GO:0015814"},{"relation_name":"is_a","term_name":"dipeptide transmembrane transport","termid":"GO:0035442"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"p-aminobenzoyl-glutamate transmembrane transport","synonyms":[{"name":"N-(4-aminobenzoyl)-L-glutamate transmembrane transport","type":"exact"}],"termid":"GO:1902604"}


id: PATO:0002163
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's bodily structure that has protruded through an abnormal opening in the wall that contains it into the surface or boundary of another entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protruding into","termid":"PATO:0001645"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"herniated into","termid":"PATO:0002163"}


id: PBO:0070200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 125 pseudogene","termid":"PBO:0070200"}


id: PBO:0061413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide VF precursor","termid":"PBO:0061413"}


id: FYPO:0003547
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 DNA damage measured in a cell is greater than normal. The number, extent, or both of damage sites may be increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased DNA damage","termid":"FYPO:0003546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased DNA damage during vegetative growth","synonyms":[{"name":"increased DNA damage during mitotic cell cycle","type":"related"},{"name":"increased number of DNA lesions during vegetative growth","type":"related"},{"name":"increased spontaneous DNA lesions during vegetative growth","type":"related"}],"termid":"FYPO:0003547"}


id: GO:0140024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of an endosome towards the plus end of a microtubule, mediated by motor proteins. This process begins with the attachment of an endosome to a microtubule, and ends when the endosome reaches its final destination.","definition_xrefs":["PMID:25706234","PMID:24803650"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plus-end-directed vesicle transport along microtubule","termid":"GO:0072383"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"plus-end-directed endosome transport along mitotic spindle midzone microtubule","termid":"GO:0140024"}


id: GO:1905130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of carcinine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GO_REF:0000075","GOC:TermGenie","GOC:dph","PMID:26653853","PMID:26713872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"},{"relation_name":"is_a","term_name":"azole transmembrane transport","termid":"GO:0045117"},{"relation_name":"is_a","term_name":"modified amino acid transport","termid":"GO:0072337"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"carcinine import across plasma membrane","termid":"GO:1905130"}


id: PR:O14026
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- set2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14026"],"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":"histone-lysine N-methyltransferase, H3 lysine-36 specific (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29B12.02c","synonyms":[{"name":"SET domain-containing protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-set2","type":"exact"},{"name":"lysine N-methyltransferase 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14026"}


id: PBO:0075734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP14 pseudogene 2","termid":"PBO:0075734"}


id: MONDO:0000338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"smallpox","termid":"MONDO:0004651"},{"relation_name":"is_a","term_name":"exanthem","termid":"MONDO:0006547"},{"relation_name":"is_a","term_name":"skin disorder caused by infection","termid":"MONDO:0024294"}],"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":"variola major infectious disease","secondary_identifiers":["DOID:0050508","ICD9:050.0","MEDGEN:740750","SCTID:47452006","UMLS:C1812609"],"synonyms":[{"name":"variola major","type":"broad"}],"termid":"MONDO:0000338","xrefs":{"Monarch":{"xref_id":"0000338"}}}


id: GO:1905894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cellular response to tunicamycin.","definition_xrefs":["GOC:bc","GO_REF:0000058","GOC:aruk","GOC:TermGenie","PMID:21803450"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular response to tunicamycin (obsolete GO:1905894)","termid":"GO:1905894"}


id: GO:0007202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The initiation of the activity of the inactive enzyme phospolipase C as the result of The series of molecular signals generated as a consequence of a G protein-coupled receptor binding to its physiological ligand.","definition_xrefs":["GOC:mah","PMID:8280098","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of phospholipase C activity (obsolete GO:0007202)","synonyms":[{"name":"phospholipase C activation","type":"exact"}],"termid":"GO:0007202"}


id: PBO:0082550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Central component of the peroxisomal importomer complex; peroxisomal protein import machinery docking complex component; interacts with both PTS1 (Pex5p) and PTS2 (Pex7p) peroxisomal matrix protein signal recognition factors and membrane receptor Pex13p","termid":"PBO:0082550"}


id: GO:0103002
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 16-hydroxypalmitate + NADP = H+ + 16-oxo-palmitate + NADPH.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"16-hydroxypalmitate dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-9802"],"termid":"GO:0103002"}


id: GO:0001930
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or extent of exocyst assembly.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of exocyst assembly","termid":"GO:0001928"},{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"positively_regulates","term_name":"exocyst assembly","termid":"GO:0001927"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0140056"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150","GO:0140056"],"is_obsolete":false,"name":"positive regulation of exocyst assembly","synonyms":[{"name":"activation of exocyst assembly","type":"narrow"},{"name":"stimulation of exocyst assembly","type":"narrow"},{"name":"up regulation of exocyst assembly","type":"exact"},{"name":"up-regulation of exocyst assembly","type":"exact"},{"name":"upregulation of exocyst assembly","type":"exact"}],"termid":"GO:0001930"}


id: PBO:0076405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 3","termid":"PBO:0076405"}


id: PBO:0034404
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_development_of","termid":"PBO:0034404"}


id: MONDO:0017902
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic variant of Mendelian susceptibility to mycobacterial diseases characterized by a partial deficiency in IFN-gammaR2, leading to a residual response to IFN-gamma and consequently to recurrent, moderately severe infections with bacillus Calmette-Guerin (BCG) and other environmental mycobacteria (EM).","definition_xrefs":["Orphanet:319574"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"immunodeficiency 28","termid":"MONDO:0013953"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency","secondary_identifiers":["MEDGEN:1387677","UMLS:C4511098"],"synonyms":[{"name":"IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency","type":"exact"},{"name":"autosomal recessive MSMD due to partial IFNgammaR2 deficiency","type":"exact"},{"name":"autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency","type":"exact"},{"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR2","type":"exact"},{"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency","type":"exact"}],"termid":"MONDO:0017902","xrefs":{"Monarch":{"xref_id":"0017902"}}}


id: MONDO:0016821
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":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shoulder and girdle defects-familial intellectual disability syndrome","secondary_identifiers":["Orphanet:2580"],"synonyms":[{"name":"shoulder girdle defect intellectual disability familial","type":"related"},{"name":"shoulder girdle defect mental retardation familial","type":"related"}],"termid":"MONDO:0016821","xrefs":{"Monarch":{"xref_id":"0016821"}}}


id: PBO:0000772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA recombination protein Rad22","termid":"PBO:0000772"}


id: PBO:0045424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"divergent-paired related homeobox pseudogene 4","termid":"PBO:0045424"}


id: MONDO:0009433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypoplastic left heart syndrome in which the cause of the disease is a mutation in the GJA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypoplastic left heart syndrome","termid":"MONDO:0004933"}],"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":"hypoplastic left heart syndrome 1","secondary_identifiers":["MEDGEN:1646779","OMIM:241550","UMLS:C4551854"],"synonyms":[{"name":"GJA1 hypoplastic left heart syndrome","type":"exact"},{"name":"HLHS","type":"broad"},{"name":"HLHS1","type":"related"},{"name":"hypoplastic left heart syndrome 1","type":"exact"},{"name":"hypoplastic left heart syndrome caused by mutation in GJA1","type":"exact"},{"name":"hypoplastic left heart syndrome type 1","type":"exact"}],"termid":"MONDO:0009433","xrefs":{"Monarch":{"xref_id":"0009433"}}}


id: PBO:0072069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S11 pseudogene 7","termid":"PBO:0072069"}


id: GO:0032847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of a process that reduces the internal pH of a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"is_a","term_name":"regulation of intracellular pH","termid":"GO:0051453"},{"relation_name":"regulates","term_name":"intracellular pH reduction","termid":"GO:0051452"}],"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 cellular pH reduction","synonyms":[{"name":"regulation of cell pH reduction","type":"exact"},{"name":"regulation of cellular acidification","type":"exact"},{"name":"regulation of intracellular acidification","type":"related"},{"name":"regulation of intracellular pH reduction","type":"exact"},{"name":"regulation of reduction of cellular pH","type":"exact"},{"name":"regulation of reduction of pH in cell","type":"exact"}],"termid":"GO:0032847"}


id: MONDO:0018136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Type 1 minimal pigment oculocutaneous albinism (OCA1-MP) is an extremely rare form of OCA1 with minimal pigment present, characterized by blond hair, variable iris transillumination, visual acuity ranging from 20/80-20/200 and white skin, with or without skin nevi.","definition_xrefs":["Orphanet:352734"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism type 1","termid":"MONDO:0018135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"minimal pigment oculocutaneous albinism type 1","secondary_identifiers":["MEDGEN:1842241","GARD:21529","SCTID:237919007","ICD9:270.2","UMLS:C5679923"],"synonyms":[{"name":"MP OCA type 1","type":"exact"},{"name":"OCA1-MP","type":"exact"}],"termid":"MONDO:0018136","xrefs":{"Monarch":{"xref_id":"0018136"}}}


id: PBO:0048270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GALNT7 divergent transcript","termid":"PBO:0048270"}


id: GO:0102311
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (6E)-8-hydroxygeraniol + 2 NADP = (6E)-8-oxogeranial + 2 NADPH + 2 H+.","definition_xrefs":["EC:1.1.1.324","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"8-hydroxygeraniol dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-12961","RHEA:32659"],"termid":"GO:0102311"}


id: PR:000050476
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein kinase wis1 (Schizosaccharomyces pombe) that has not been phosphorylated on residues equivalent to Ser-469 and Thr-473 of the amino acid sequence represented by UniProtKB:P33886. Example: UniProtKB:P33886, Ser-469/Thr-473, PR:000026291.","definition_xrefs":["PRO:DAN","PMID:12181336","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase wis1 (Schizosaccharomyces pombe)","termid":"PR:000050474"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wis1/UnPhos:(S469,T473)","pombase_gene_id":"SPBC409.07c","synonyms":[{"name":"PomBase_original_PRO_term_name: protein kinase wis1 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-wis1/UnPhos:1","type":"exact"},{"name":"UniProtKB:P33886, Ser-469/Thr-473, PR:000026291","type":"narrow"},{"name":"wis1/UnPhos:(S469,T473)","type":"exact"}],"termid":"PR:000050476"}


id: GO:0071304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a vitamin B6 stimulus. Vitamin B6 encompasses pyridoxal, pyridoxamine and pyridoxine and the active form, pyridoxal phosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to vitamin B6","termid":"GO:0034516"},{"relation_name":"is_a","term_name":"cellular response to vitamin","termid":"GO:0071295"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to vitamin B6","termid":"GO:0071304"}


id: PBO:0072104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S13 pseudogene 2","termid":"PBO:0072104"}


id: GO:1904828
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hydrogen sulfide biosynthetic process.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:rph","GOC:TermGenie","GO_REF:0000058","PMID:22034194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of biosynthetic process","termid":"GO:0009891"},{"relation_name":"is_a","term_name":"positive regulation of sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"regulation of hydrogen sulfide biosynthetic process","termid":"GO:1904826"},{"relation_name":"positively_regulates","term_name":"hydrogen sulfide biosynthetic process","termid":"GO:0070814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"positive regulation of hydrogen sulfide biosynthetic process","synonyms":[{"name":"activation of hydrogen sulfide anabolism","type":"narrow"},{"name":"activation of hydrogen sulfide biosynthesis","type":"narrow"},{"name":"activation of hydrogen sulfide biosynthetic process","type":"narrow"},{"name":"activation of hydrogen sulfide formation","type":"narrow"},{"name":"activation of hydrogen sulfide synthesis","type":"narrow"},{"name":"activation of hydrogen sulphide biosynthesis","type":"narrow"},{"name":"activation of hydrogen sulphide biosynthetic process","type":"narrow"},{"name":"positive regulation of hydrogen sulfide anabolism","type":"exact"},{"name":"positive regulation of hydrogen sulfide biosynthesis","type":"exact"},{"name":"positive regulation of hydrogen sulfide formation","type":"exact"},{"name":"positive regulation of hydrogen sulfide synthesis","type":"exact"},{"name":"positive regulation of hydrogen sulphide biosynthesis","type":"exact"},{"name":"positive regulation of hydrogen sulphide biosynthetic process","type":"exact"},{"name":"up regulation of hydrogen sulfide anabolism","type":"exact"},{"name":"up regulation of hydrogen sulfide biosynthesis","type":"exact"},{"name":"up regulation of hydrogen sulfide biosynthetic process","type":"exact"},{"name":"up regulation of hydrogen sulfide formation","type":"exact"},{"name":"up regulation of hydrogen sulfide synthesis","type":"exact"},{"name":"up regulation of hydrogen sulphide biosynthesis","type":"exact"},{"name":"up regulation of hydrogen sulphide biosynthetic process","type":"exact"},{"name":"up-regulation of hydrogen sulfide anabolism","type":"exact"},{"name":"up-regulation of hydrogen sulfide biosynthesis","type":"exact"},{"name":"up-regulation of hydrogen sulfide biosynthetic process","type":"exact"},{"name":"up-regulation of hydrogen sulfide formation","type":"exact"},{"name":"up-regulation of hydrogen sulfide synthesis","type":"exact"},{"name":"up-regulation of hydrogen sulphide biosynthesis","type":"exact"},{"name":"up-regulation of hydrogen sulphide biosynthetic process","type":"exact"},{"name":"upregulation of hydrogen sulfide anabolism","type":"exact"},{"name":"upregulation of hydrogen sulfide biosynthesis","type":"exact"},{"name":"upregulation of hydrogen sulfide biosynthetic process","type":"exact"},{"name":"upregulation of hydrogen sulfide formation","type":"exact"},{"name":"upregulation of hydrogen sulfide synthesis","type":"exact"},{"name":"upregulation of hydrogen sulphide biosynthesis","type":"exact"},{"name":"upregulation of hydrogen sulphide biosynthetic process","type":"exact"}],"termid":"GO:1904828"}


id: GO:0047753
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: choline sulfate + H2O = choline + H+ + sulfate.","definition_xrefs":["EC:3.1.6.6","RHEA:20820"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfuric ester hydrolase activity","termid":"GO:0008484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"choline-sulfatase activity","secondary_identifiers":["MetaCyc:CHOLINE-SULFATASE-RXN","KEGG_REACTION:R01028"],"synonyms":[{"name":"choline-sulfate sulfohydrolase activity","type":"related"},{"name":"choline-sulphatase activity","type":"exact"}],"termid":"GO:0047753"}


id: GO:0002351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis or release of serotonin following a stimulus as part of an inflammatory response, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["PMID:16730260","ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator involved in inflammatory response","termid":"GO:0002532"}],"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":"serotonin production involved in inflammatory response","synonyms":[{"name":"serotonin production involved in acute inflammatory response","type":"broad"}],"termid":"GO:0002351"}


id: GO:0005865
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Filaments formed of actin and associated proteins; attached to Z discs at either end of sarcomeres in myofibrils.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myofilament","termid":"GO:0036379"},{"relation_name":"part_of","term_name":"actin cytoskeleton","termid":"GO:0015629"},{"relation_name":"part_of","term_name":"sarcomere","termid":"GO:0030017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0015629"}],"interesting_parent_ids":["GO:0005575","GO:0015629","GO:0005737"],"is_obsolete":false,"name":"striated muscle thin filament","termid":"GO:0005865"}


id: PBO:0060331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin IIIA","termid":"PBO:0060331"}


id: GO:1990575
data:
  {"annotated_genes":["SJAG_00543"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107396],"is_not":false,"summary":null,"term":"GO:1990575"}]},"cv_name":"biological_process","definition":"The process in which L-ornithine is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:9237680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-ornithine transmembrane transport","termid":"GO:1903352"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00543":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"mitochondrial L-ornithine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000066"],"synonyms":[{"name":"mitochondrial ornithine transmembrane transport","type":"broad"},{"name":"mitochondrial ornithine transport","type":"related"}],"termid":"GO:1990575","terms_by_termid":{"GO:1990575":null}}


id: PBO:0088713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"circularly permuted 1,3-beta-glucanase","termid":"PBO:0088713"}


id: PBO:0031572
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-vegetative_cell_lysis","termid":"PBO:0031572"}


id: PBO:0047664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase like","termid":"PBO:0047664"}


id: PBO:0030891
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_response_to_stress_during_vegetative_growth","termid":"PBO:0030891"}


id: MONDO:1010419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Narcolepsy that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"narcolepsy, non-human animal","termid":"MONDO:1010003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcolepsy, domestic cat","secondary_identifiers":["OMIA:000703-9685"],"termid":"MONDO:1010419","xrefs":{"Monarch":{"xref_id":"1010419"}}}


id: GO:0001967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Specific behavior of a newborn or infant mammal that results in the derivation of nourishment from the breast.","definition_xrefs":["GOC:pr","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feeding behavior","termid":"GO:0007631"}],"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":"suckling behavior","synonyms":[{"name":"nursing behavior","type":"exact"}],"termid":"GO:0001967"}


id: GO:0021991
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of apical-basal elongation of individual ectodermal cells during the formation of the neural placode.","definition_xrefs":["GOC:jid","PMID:15806586","GO_REF:0000021","GOC:dgh","GOC:dph","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelial sheet","termid":"GO:0002011"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"neural plate morphogenesis","termid":"GO:0001839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural plate thickening","termid":"GO:0021991"}


id: GO:0032042
data:
  {"annotated_genes":["SJAG_03068","SJAG_03906","SJAG_02658","SJAG_02528","SJAG_00611","SJAG_01807","SJAG_01648","SJAG_03957","SJAG_00198","SJAG_04752","SJAG_01948","SJAG_03724","SJAG_01262","SJAG_03780","SJAG_00153","SJAG_05280"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92042,94220,96614,111076],"is_not":false,"summary":null,"term":"GO:0032042"},{"annotations":[89857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032043"},{"annotations":[112006,95629,98808,102380,102400,88070,105431,108041,113395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043504"},{"annotations":[115854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006264"},{"annotations":[95233],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090297"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving mitochondrial DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"part_of","term_name":"mitochondrial genome maintenance","termid":"GO:0000002"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00153":null,"SJAG_00198":null,"SJAG_00611":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_01807":null,"SJAG_01948":null,"SJAG_02528":null,"SJAG_02658":null,"SJAG_03068":null,"SJAG_03724":null,"SJAG_03780":null,"SJAG_03906":null,"SJAG_03957":null,"SJAG_04752":null,"SJAG_05280":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007005"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0007005"],"is_obsolete":false,"name":"mitochondrial DNA metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial DNA metabolism","type":"exact"},{"name":"mtDNA metabolic process","type":"exact"},{"name":"mtDNA metabolism","type":"exact"}],"termid":"GO:0032042","terms_by_termid":{"GO:0006264":null,"GO:0032042":null,"GO:0032043":null,"GO:0043504":null,"GO:0090297":null}}


id: PBO:0057344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 532","termid":"PBO:0057344"}


id: PBO:0086189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein similar to GDP/GTP exchange factors; without detectable GEF activity; required for asymmetric localization of Bfa1p at daughter-directed spindle pole bodies and for mitotic exit at low temperatures","termid":"PBO:0086189"}


id: PBO:0082389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta-adaptin subunit of the clathrin-associated protein (AP-1) complex; binds clathrin; involved in clathrin-dependent Golgi protein sorting; protein abundance increases in response to DNA replication stress","termid":"PBO:0082389"}


id: PBO:0041761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain 1","termid":"PBO:0041761"}


id: GO:0010129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of cyclohexane-1-carboxylate, a alicyclic acid, in the absence of oxygen.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"}],"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":"anaerobic cyclohexane-1-carboxylate catabolic process","secondary_identifiers":["MetaCyc:PWY-301"],"synonyms":[{"name":"anaerobic cyclohexane-1-carboxylate breakdown","type":"exact"},{"name":"anaerobic cyclohexane-1-carboxylate catabolism","type":"exact"},{"name":"anaerobic cyclohexane-1-carboxylate degradation","type":"exact"}],"termid":"GO:0010129"}


id: PBO:0086637
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; YMR196W is not an essential gene","termid":"PBO:0086637"}


id: PBO:0056481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrilin 3","termid":"PBO:0056481"}


id: PBO:0049145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione peroxidase 2","termid":"PBO:0049145"}


id: MONDO:0005905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Excessive periodic leg movements during sleep that cause micro-arousals and interfere with the maintenance of sleep. This condition induces a state of relative sleep deprivation which manifests as excessive daytime hypersomnolence. The movements are characterized by repetitive contractions of the tibialis anterior muscle, extension of the toe, and intermittent flexion of the hip, knee and ankle. (Adams et al., Principles of Neurology, 6th ed, p387)","definition_xrefs":["MESH:D020189"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mental disorder","termid":"MONDO:0005084"},{"relation_name":"is_a","term_name":"sleep-wake disorder","termid":"MONDO:0003406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periodic limb movement disorder","secondary_identifiers":["ICD9:327.51","ICD10CM:G47.61","MEDGEN:199731","SCTID:418763003","UMLS:C0751774","DOID:9207","EFO:0007428","icd11.foundation:1846518306"],"synonyms":[{"name":"nocturnal myoclonus","type":"exact"}],"termid":"MONDO:0005905","xrefs":{"Monarch":{"xref_id":"0005905"}}}


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


id: PBO:0082794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the U4/U6.U5 snRNP complex; involved in mRNA splicing via spliceosome","termid":"PBO:0082794"}


id: PBO:0041917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonyl reductase 1","termid":"PBO:0041917"}


id: GO:0098581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which an external biotic stimulus is detected and converted into a molecular signal. An external biotic stimulus is defined as one caused or produced by a living organism other than the one being stimulated.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of biotic stimulus","termid":"GO:0009595"},{"relation_name":"is_a","term_name":"response to external biotic stimulus","termid":"GO:0043207"}],"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 external biotic stimulus","synonyms":[{"name":"detection of exogenous biotic stimulus","type":"exact"}],"termid":"GO:0098581"}


id: PBO:0048343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 54","termid":"PBO:0048343"}


id: PBO:0062517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily K member 3 (gene/pseudogene)","termid":"PBO:0062517"}


id: PBO:0029400
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_localization_to_nucleoplasm","termid":"PBO:0029400"}


id: PBO:0089068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L57","termid":"PBO:0089068"}


id: PBO:0029843
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_acetylation","termid":"PBO:0029843"}


id: FYPO:0007348
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which trimethylation of lysine at position 36 of histone H3 is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K36 methylation during vegetative growth","termid":"FYPO:0002918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased histone H3-K36 trimethylation during vegetative growth","synonyms":[{"name":"decreased histone H3 K36 trimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3-K36 trimethylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K36me3 during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K36 trimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K36 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0007348"}


id: PBO:0012863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome subunit Csl4","termid":"PBO:0012863"}


id: PBO:0067887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 189","termid":"PBO:0067887"}


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":["ONCOTREE:SNSC","ICDO:8121/3","UMLS:C0334270","DOID:4003","MEDGEN:83119"],"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:0007284
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cataract (disease) in which the cause of the disease is a mutation in the CRYGS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"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":"cataract 20 multiple types","secondary_identifiers":["DOID:0110240","OMIM:116100","UMLS:C0524524","MEDGEN:101117"],"synonyms":[{"name":"CRYGS cataract (disease)","type":"exact"},{"name":"CTRCT20","type":"exact"},{"name":"cataract (disease) caused by mutation in CRYGS","type":"exact"},{"name":"cataract 20, multiple types","type":"related"}],"termid":"MONDO:0007284","xrefs":{"Monarch":{"xref_id":"0007284"}}}


id: PBO:0018122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complementation functionally complemented by S. cerevisiae VAM7","termid":"PBO:0018122"}


id: PBO:0016082
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae SNR128","termid":"PBO:0016082"}


id: GO:0045737
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of CDK activity.","definition_xrefs":["GOC:pr","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cyclin-dependent protein serine/threonine kinase activity","termid":"GO:0000079"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle","termid":"GO:0045787"},{"relation_name":"is_a","term_name":"positive regulation of protein serine/threonine kinase activity","termid":"GO:0071902"},{"relation_name":"is_a","term_name":"positive regulation of cyclin-dependent protein kinase activity","termid":"GO:1904031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"positive regulation of cyclin-dependent protein serine/threonine kinase activity","synonyms":[{"name":"activation of cyclin-dependent protein kinase activity","type":"broad"},{"name":"positive regulation of CDK activity","type":"broad"},{"name":"positive regulation of cyclin-dependent protein kinase activity","type":"broad"},{"name":"stimulation of cyclin-dependent protein kinase activity","type":"broad"},{"name":"up regulation of cyclin-dependent protein kinase activity","type":"broad"},{"name":"up-regulation of cyclin-dependent protein kinase activity","type":"broad"},{"name":"upregulation of cyclin-dependent protein kinase activity","type":"broad"}],"termid":"GO:0045737"}


id: RO:HOM0000028
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Biological homology that is characterized by changes, over evolutionary time, in the rate or timing of developmental events of homologous structures.","definition_xrefs":["ISBN:978-0674639416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in_biological_homology_relationship_with","termid":"RO:HOM0000008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_heterochronous_homology_relationship_with","synonyms":[{"name":"heterochronous homologous to","type":"exact"},{"name":"heterochrony","type":"exact"}],"termid":"RO:HOM0000028"}


id: PATO:0000611
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000611 absolute orientation value (obsolete PATO:0000611)","termid":"PATO:0000611"}


id: PBO:0070059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 16, pseudogene","termid":"PBO:0070059"}


id: PBO:0035907
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-C-shaped_vegetative_cell","termid":"PBO:0035907"}


id: GO:0033590
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cobalamin (vitamin B12) stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to vitamin","termid":"GO:0033273"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cobalamin","synonyms":[{"name":"response to vitamin B12","type":"exact"}],"termid":"GO:0033590"}


id: GO:0141133
data:
  {"annotated_genes":["SJAG_02467"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[116956],"is_not":false,"summary":null,"term":"GO:0141133"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-[(3S)-amino-3-carboxypropyl]-L-histidyl-[translation elongation factor 2] + 4 S-adenosyl-L-methionine = diphthine methyl ester-[translation elongation factor 2] + 3 H+ + 4 S-adenosyl-L-homocysteine.","definition_xrefs":["PMID:24739148","RHEA:42652"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein methyltransferase activity","termid":"GO:0008276"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008276","GO:0003674","GO:0140096","GO:0016741","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"diphthine methyl ester synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5358484","EC:2.1.1.314","MetaCyc:RXN-15775"],"termid":"GO:0141133","terms_by_termid":{"GO:0141133":null}}


id: PR:O74995
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A general transcription factor IIH subunit 2 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":"TFIIH basal transcription factor complex p47 subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1682.07","secondary_identifiers":["UniProtKB:O74995"],"synonyms":[{"name":"SPCC1682.07","type":"related"},{"name":"SSL1 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GTF2H2","type":"exact"},{"name":"ssl1","type":"related"},{"name":"suppressor of stem-loop protein 1 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74995"}


id: MONDO:0003470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ependymoma which shows conspicuous cellularity without a significant increase in mitotic rate. (Adapted from WHO)","definition_xrefs":["NCIT:C4713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ependymoma","termid":"MONDO:0016698"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular ependymoma","secondary_identifiers":["UMLS:C1384403","DOID:5500","MEDGEN:235137","NCIT:C4714"],"termid":"MONDO:0003470","xrefs":{"Monarch":{"xref_id":"0003470"}}}


id: GO:0009304
data:
  {"annotated_genes":["SJAG_04261","SJAG_02101","SJAG_04408","SJAG_01765"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93394,115167,91521,113296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042797"}]},"cv_name":"biological_process","definition":"The synthesis of transfer RNA (tRNA) from a DNA template.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription","termid":"GO:0006351"},{"relation_name":"is_a","term_name":"tRNA metabolic process","termid":"GO:0006399"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01765":null,"SJAG_02101":null,"SJAG_04261":null,"SJAG_04408":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0006399","GO:0006351","GO:0010467"],"is_obsolete":false,"name":"tRNA transcription","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"tRNA biosynthesis","type":"broad"},{"name":"tRNA biosynthetic process","type":"broad"},{"name":"tRNA synthesis","type":"broad"}],"termid":"GO:0009304","terms_by_termid":{"GO:0042797":null}}


id: MONDO:0020467
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"monosomy X","termid":"MONDO:0020466"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"mosaic monosomy X","secondary_identifiers":["GARD:19677","UMLS:C4040907","MEDGEN:873772","SCTID:710010005","Orphanet:99228"],"synonyms":[{"name":"Mosaic Turner syndrome","type":"exact"},{"name":"Mosaic monosomy type X","type":"exact"},{"name":"XX/XO","type":"exact"}],"termid":"MONDO:0020467","xrefs":{"Monarch":{"xref_id":"0020467"}}}


id: GO:0048760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a parenchymal cell. Parenchymal cells are the most abundant and versatile cells in plants. They have very few distinguishing characteristics and botanists classify them as any cell type that cannot be assigned to any other structural or functional class. They can redifferentiate and dedifferentiate and are involved in storage, basic metabolism and other processes. The cells are polyhedral, typically with thin, non-lignified cellulose cell walls and nucleate living protoplasm. They vary in size, form, and wall structure.","definition_xrefs":["ISBN:069716957X","GOC:jid","CL:0000668","PO:0005421"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"plant parenchymal cell differentiation","synonyms":[{"name":"parenchymal cell differentiation","type":"exact"}],"termid":"GO:0048760"}


id: PBO:0003620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal ubiquitin-protein ligase E3 (predicted)","termid":"PBO:0003620"}


id: GO:0046417
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving chorismate, the anion of (3R-trans)-3-((1-carboxyethenyl)oxy)-4-hydroxy-1,5-cyclohexadiene-1-carboxylic acid.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid metabolic process","termid":"GO:0043648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"chorismate metabolic process","synonyms":[{"name":"chorismate metabolism","type":"exact"}],"termid":"GO:0046417"}


id: PBO:0061154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide nucleotide adenylyltransferase 2","termid":"PBO:0061154"}


id: PBO:0056667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 28 pseudogene 5","termid":"PBO:0056667"}


id: PBO:0113433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Small gene in chromosome III recombination enhancer; activated during mating-type switching; bound by condensin complex, deletion drastically changes chromosome III structure, alters donor preference; promoter functions as locus control region (LCR) that regulates both transcription and long-range chromatin interactions","termid":"PBO:0113433"}


id: PBO:0039879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 36","termid":"PBO:0039879"}


id: PBO:0000661
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.1.1.-","termid":"PBO:0000661"}


id: PBO:0048459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucagon","termid":"PBO:0048459"}


id: PBO:0065544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin D2 receptor","termid":"PBO:0065544"}


id: PATO:0000591
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A thickness which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"increased size","termid":"PATO:0000586"},{"relation_name":"is_a","term_name":"thickness","termid":"PATO:0000915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased thickness","synonyms":[{"name":"high thickness","type":"exact"},{"name":"stout","type":"exact"},{"name":"thick","type":"related"},{"name":"thickened","type":"exact"}],"termid":"PATO:0000591"}


id: GO:0031763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a galanin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide receptor binding","termid":"GO:0071855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"galanin receptor binding","synonyms":[{"name":"galanin receptor ligand","type":"narrow"}],"termid":"GO:0031763"}


id: PATO:0001795
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A coiling which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"coiled","termid":"PATO:0000404"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased coiling","synonyms":[{"name":"high coiling","type":"exact"}],"termid":"PATO:0001795"}


id: PBO:0067850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 152","termid":"PBO:0067850"}


id: GO:0140691
data:
  {"annotated_genes":["SJAG_00886","SJAG_03070","SJAG_00195","SJAG_03460","SJAG_02469","SJAG_04266","SJAG_01819"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97985,106760,108031,112384,113320,114435,115370],"is_not":false,"summary":null,"term":"GO:0140691"}]},"cv_name":"molecular_function","definition":"Binding to an RNA or an RNA-containing complex to assist the folding process.","definition_xrefs":["PMID:31165735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00886":null,"SJAG_01819":null,"SJAG_02469":null,"SJAG_03070":null,"SJAG_03460":null,"SJAG_04266":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"RNA folding chaperone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140691","terms_by_termid":{"GO:0140691":null}}


id: PR:Q96VG0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC16G5.19 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q96VG0"],"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 C16G5.19 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16G5.19","synonyms":[{"name":"Spom972h-SPBC16G5.19","type":"exact"}],"termid":"PR:Q96VG0"}


id: FYPO:0002255
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the nucleus is larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear morphology","termid":"FYPO:0002256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002403","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"enlarged nucleus","synonyms":[{"name":"enlarged nuclei","type":"exact"}],"termid":"FYPO:0002255"}


id: SO:0000886
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Recoded mRNA where a block of nucleotides is not translated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recoded","termid":"SO:0000881"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recoded_by_translational_bypass","synonyms":[{"name":"recoded by translational bypass","type":"exact"}],"termid":"SO:0000886"}


id: MONDO:0010721
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":"reticuloendotheliosis, X-linked","secondary_identifiers":["UMLS:C0035288","OMIM:312500","MESH:C538362","MEDGEN:19757"],"synonyms":[{"name":"reticuloendotheliosis","type":"related"},{"name":"reticuloendotheliosis, X-linked","type":"exact"}],"termid":"MONDO:0010721","xrefs":{"Monarch":{"xref_id":"0010721"}}}


id: PBO:0058617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6749","termid":"PBO:0058617"}


id: PBO:0001032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk4/ sensor for unfolded proteins in the ER (predicted)","termid":"PBO:0001032"}


id: FYPO:0002203
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells in which the cell diameter is larger than normal and the cell length is shorter than normal. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:vw","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, stubby cells (obsolete FYPO:0002203)","synonyms":[{"name":"inviable microcolony, stubby vegetative cells","type":"exact"}],"termid":"FYPO:0002203"}


id: GO:0160217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of transcription initiation-coupled chromatin remodeling.","definition_xrefs":["PMID:33980486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"},{"relation_name":"is_a","term_name":"negative regulation of chromatin organization","termid":"GO:1905268"},{"relation_name":"negatively_regulates","term_name":"transcription initiation-coupled chromatin remodeling","termid":"GO:0045815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0006325"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0006325","GO:0010467"],"is_obsolete":false,"name":"negative regulation of transcription initiation-coupled chromatin remodeling","termid":"GO:0160217"}


id: GO:0051056
data:
  {"annotated_genes":["SJAG_04462","SJAG_00883","SJAG_02514","SJAG_06270","SJAG_02379","SJAG_03488","SJAG_03353","SJAG_04943","SJAG_03631","SJAG_01464","SJAG_03592","SJAG_03936","SJAG_04329","SJAG_00082","SJAG_04455","SJAG_00329","SJAG_03681","SJAG_04776","SJAG_03048","SJAG_01386","SJAG_01790","SJAG_00526","SJAG_02169","SJAG_01805","SJAG_00078","SJAG_00600","SJAG_03508","SJAG_00229"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046580"},{"annotations":[104836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035024"},{"annotations":[99091,104530,100773,106725,92940,107030,91216,92323,90208,99169,95126,109662,115400,106586,92407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[90645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046579"},{"annotations":[87014,101888,110015,89478,93290],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031031"},{"annotations":[115997,69573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032483"},{"annotations":[112859,89440,104003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031029"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of small GTPase mediated signal transduction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"small GTPase-mediated signal transduction","termid":"GO:0007264"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00078":null,"SJAG_00082":null,"SJAG_00229":null,"SJAG_00329":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00883":null,"SJAG_01386":null,"SJAG_01464":null,"SJAG_01790":null,"SJAG_01805":null,"SJAG_02169":null,"SJAG_02379":null,"SJAG_02514":null,"SJAG_03048":null,"SJAG_03353":null,"SJAG_03488":null,"SJAG_03508":null,"SJAG_03592":null,"SJAG_03631":null,"SJAG_03681":null,"SJAG_03936":null,"SJAG_04329":null,"SJAG_04455":null,"SJAG_04462":null,"SJAG_04776":null,"SJAG_04943":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of small GTPase mediated signal transduction","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9012999"],"synonyms":[{"name":"regulation of small GTPase-mediated signal transduction","type":"exact"}],"termid":"GO:0051056","terms_by_termid":{"GO:0031029":null,"GO:0031030":null,"GO:0031031":null,"GO:0032483":null,"GO:0035024":null,"GO:0046579":null,"GO:0046580":null}}


id: GO:0047587
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5alpha-ergosta-7,22-diene-3beta,5-diol = ergosterol + H2O.","definition_xrefs":["RHEA:22064","EC:4.2.1.62"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"5-alpha-hydroxysteroid dehydratase activity","secondary_identifiers":["KEGG_REACTION:R03675","MetaCyc:5-ALPHA-HYDROXYSTEROID-DEHYDRATASE-RXN"],"synonyms":[{"name":"5alpha-ergosta-7,22-diene-3beta,5-diol 5,6-hydro-lyase (ergosterol-forming)","type":"related"},{"name":"5alpha-ergosta-7,22-diene-3beta,5-diol 5,6-hydro-lyase activity","type":"related"},{"name":"5alpha-hydroxysteroid dehydratase activity","type":"related"}],"termid":"GO:0047587"}


id: PBO:0069436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 701, pseudogene","termid":"PBO:0069436"}


id: FYPO:0005172
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 import of uracil into the cell occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal uracil import","termid":"FYPO:0005170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased uracil import","synonyms":[{"name":"increased uracil import across plasma membrane","type":"exact"},{"name":"increased uracil import during mitotic cell cycle","type":"related"},{"name":"increased uracil import during vegetative growth","type":"exact"},{"name":"increased uracil import into cell","type":"exact"},{"name":"increased uracil uptake","type":"exact"}],"termid":"FYPO:0005172"}


id: GO:0044530
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Multicomponent complex of RNA and proteins that is composed of four active spliceosomes, termed native spliceosomes, connected to each other by the pre-mRNA. The supraspliceosome is the nuclear machine where the pre-mRNA processing takes place, like the 5'-end capping, 3'-end cleavage, splicing and editing.","definition_xrefs":["GOC:ans","GOC:jl","PMID:19282290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal complex","termid":"GO:0005681"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"supraspliceosomal complex","synonyms":[{"name":"supraspliceosome complex","type":"exact"}],"termid":"GO:0044530"}


id: GO:0008263
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the removal of mismatched pyrimidine bases in DNA. Enzymes with this activity recognize and remove pyrimidines present in mismatches by cleaving the N-C1' glycosidic bond between the target damaged DNA base and the deoxyribose sugar. The reaction releases a free base and leaves an apyrimidinic (AP) site.","definition_xrefs":["PMID:9224623","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mismatch base pair DNA N-glycosylase activity","termid":"GO:0000700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016798","GO:0003674","GO:0003824","GO:0016787","GO:0140097"],"is_obsolete":false,"name":"pyrimidine-specific mismatch base pair DNA N-glycosylase activity","synonyms":[{"name":"G/T-mismatch-specific thymine-DNA glycosylase activity","type":"exact"}],"termid":"GO:0008263"}


id: PBO:0026652
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_RNA_level_during_cellular_response_to_zinc_ion","termid":"PBO:0026652"}


id: PR:Q09894
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC24B11.07c gene.","definition_xrefs":["UniProtKB:Q09894","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C24B11.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.07c","synonyms":[{"name":"Spom972h-SPAC24B11.07c","type":"exact"}],"termid":"PR:Q09894"}


id: PBO:0074168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 35 member G5","termid":"PBO:0074168"}


id: MONDO:1011022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lissencephaly and cerebellar hypoplasia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly and cerebellar hypoplasia, non-human animal","termid":"MONDO:1010247"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lissencephaly and cerebellar hypoplasia, dog","secondary_identifiers":["OMIA:001867-9615"],"termid":"MONDO:1011022","xrefs":{"Monarch":{"xref_id":"1011022"}}}


id: GO:0046739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The transport of a virus between cells in a multicellular organism. The cells can be adjacent or spatially separated (e.g. in different tissues or organs).","definition_xrefs":["ISBN:0781718325","GOC:bf","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"migration in host","termid":"GO:0044001"},{"relation_name":"is_a","term_name":"transport of virus","termid":"GO:0046794"}],"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":"transport of virus in multicellular host","synonyms":[{"name":"spread of virus in multicellular host","type":"related"},{"name":"spread of virus within multicellular host","type":"exact"},{"name":"viral spread within multicellular host","type":"exact"}],"termid":"GO:0046739"}


id: MOD:00756
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-valine residue to 4-hydroxy-D-valine.","definition_xrefs":["PubMed:15853325","RESID:AA0388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monohydroxylated residue","termid":"MOD:00425"},{"relation_name":"is_a","term_name":"stereoisomerized residue","termid":"MOD:00664"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-hydroxy-D-valine","synonyms":[{"name":"(2R,3Xi)-2-amino-4-hydroxy-3-methylbutanoic acid","type":"exact"},{"name":"4-hydroxy-D-valine","type":"exact"},{"name":"D-4HyVal","type":"exact"},{"name":"D-gamma-hydroxyvaline","type":"exact"},{"name":"MOD_RES D-4-hydroxyvaline","type":"exact"}],"termid":"MOD:00756"}


id: PBO:0067573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 728, pseudogene","termid":"PBO:0067573"}


id: PR:O36030
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nup37 gene.","definition_xrefs":["UniProtKB:O36030","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 WD repeat-containing protein C4F10.18 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F10.18","synonyms":[{"name":"Spom972h-nup37","type":"exact"}],"termid":"PR:O36030"}


id: PBO:0067763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 63","termid":"PBO:0067763"}


id: GO:0034209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of an acetyl group to a sterol molecule. An acetyl group is CH3CO-, derived from acetic [ethanoic] acid.","definition_xrefs":["PMID:18034159","GOC:rb"],"gene_count":0,"genotype_count":0,"name":"obsolete sterol acetylation (obsolete GO:0034209)","termid":"GO:0034209"}


id: PBO:0080696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wnt family member 3","termid":"PBO:0080696"}


id: PBO:0029708
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_population_growth_at_low_pH","termid":"PBO:0029708"}


id: PBO:0068870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 110, pseudogene","termid":"PBO:0068870"}


id: GO:0034834
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-mercaptobenzothiazole + O2 + 2 H+ + 2 e- = 2-mercaptobenzothiazole-cis-6,7-dihydrodiol.","definition_xrefs":["UM-BBD_reactionID:r1177"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-mercaptobenzothiazole dioxygenase activity (obsolete GO:0034834)","termid":"GO:0034834"}


id: GO:0032427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a GTPase protein binding domain (GDB) domain. The GBD is a short motif, including a minimum region of 16 amino acids, identified in proteins that bind to small GTPases such as Cdc42 and Rac.","definition_xrefs":["GOC:mah","GOC:pg","PMID:9119069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"GBD domain binding","synonyms":[{"name":"CRIB motif binding","type":"exact"},{"name":"Cdc42/Rac interactive binding motif binding","type":"exact"},{"name":"P21-Rho-binding domain binding","type":"exact"},{"name":"PMD binding","type":"exact"}],"termid":"GO:0032427"}


id: GO:0050773
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dendrite development.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neuron projection development","termid":"GO:0010975"},{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"dendrite development","termid":"GO:0016358"}],"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 dendrite development","termid":"GO:0050773"}


id: PBO:0087136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein, subunit of Nrd1 complex (Nrd1p-Nab3p-Sen1p); complex interacts with exosome to mediate 3'-end formation of some mRNAs, snRNAs, snoRNAs, and CUTs; required for termination of non-poly(A) transcripts and efficient splicing; Nrd1-Nab3 pathway appears to have a role in rapid suppression of some genes when cells are shifted to poor growth conditions, indicating role for Nrd1-Nab3 in regulating cellular response to nutrient availability","termid":"PBO:0087136"}


id: GO:0140041
data:
  {"annotated_genes":["SJAG_02960"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104537],"is_not":false,"summary":null,"term":"GO:0140041"}]},"cv_name":"biological_process","definition":"Any process carried out at the cellular level that reduces or removes the toxicity of methylglyoxal. These may include chemical modification or transport of methylglyoxal away from sensitive areas and to compartments or complexes whose purpose is sequestration of the toxic substance.","definition_xrefs":["PMID:15042280"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular detoxification of aldehyde","termid":"GO:0110095"},{"relation_name":"part_of","term_name":"cellular response to methylglyoxal","termid":"GO:0097238"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"cellular detoxification of methylglyoxal","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140041","terms_by_termid":{"GO:0140041":null}}


id: PBO:0030157
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell,_abnormal_cell_shape,_normal_cell_size","termid":"PBO:0030157"}


id: GO:0050761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving depsipeptides, a linear or cyclic compound composed of both amino acids and hydroxy acids in peptide and ester bonds respectively.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"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":"depsipeptide metabolic process","synonyms":[{"name":"depsipeptide metabolism","type":"exact"}],"termid":"GO:0050761"}


id: PBO:0002015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1748 family protein","termid":"PBO:0002015"}


id: PBO:0041173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B and T lymphocyte associated","termid":"PBO:0041173"}


id: PBO:0045709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double zinc ribbon and ankyrin repeat domains 1","termid":"PBO:0045709"}


id: PBO:0047120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 166 member C","termid":"PBO:0047120"}


id: MONDO:1011190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinal stenosis that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal stenosis, non-human animal","termid":"MONDO:1010303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal stenosis, cattle","secondary_identifiers":["OMIA:000947-9913"],"termid":"MONDO:1011190","xrefs":{"Monarch":{"xref_id":"1011190"}}}


id: PBO:0061667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUP50 divergent transcript","termid":"PBO:0061667"}


id: MONDO:0100465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A complex neurodevelopmental disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy), in addition to one or more structural or functional anomaly(ies) that develops prenatally.","direct_ancestors":[{"relation_name":"is_a","term_name":"complex neurodevelopmental disorder","termid":"MONDO:0100038"}],"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":"complex neurodevelopmental disorder with or without congenital anomalies","termid":"MONDO:0100465","xrefs":{"Monarch":{"xref_id":"0100465"}}}


id: GO:1900577
data:
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id: PBO:0048789
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id: PBO:0075211
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id: PBO:0056003
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id: PBO:0029123
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id: PBO:0079165
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id: MONDO:1011463
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id: MONDO:1011725
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id: PBO:0090392
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id: MONDO:0005336
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id: MONDO:0017568
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id: PR:Q2L4W6
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id: PATO:0001594
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id: PBO:0039457
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id: GO:0046502
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id: GO:0051581
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id: GO:0016064
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id: PBO:0050341
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id: PBO:0112790
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id: GO:0051881
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id: PBO:0052509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 23","termid":"PBO:0052509"}


id: PBO:0049404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate cyclase activator 1C","termid":"PBO:0049404"}


id: PBO:0073520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain binding protein 2","termid":"PBO:0073520"}


id: GO:0031879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 2 somatostatin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatostatin receptor binding","termid":"GO:0031877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"type 2 somatostatin receptor binding","synonyms":[{"name":"type 2 somatostatin receptor ligand","type":"narrow"}],"termid":"GO:0031879"}


id: MONDO:0000204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete skin creases, congenital symmetric circumferential (obsolete MONDO:0000204)","secondary_identifiers":["OMIMPS:156610"],"termid":"MONDO:0000204","xrefs":{"Monarch":{"xref_id":"0000204"}}}


id: PBO:0026776
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_spatio-temporal_regulation_of_replication_fork_localization","termid":"PBO:0026776"}


id: MONDO:0000017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete deafness, autosomal recessive (obsolete MONDO:0000017)","termid":"MONDO:0000017","xrefs":{"Monarch":{"xref_id":"0000017"}}}


id: PBO:0076072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STE20 related adaptor alpha","termid":"PBO:0076072"}


id: PBO:0042428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle 34, ubiqiutin conjugating enzyme","termid":"PBO:0042428"}


id: PBO:0047640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 1A pseudogene 3","termid":"PBO:0047640"}


id: PBO:0086583
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; detected in highly purified mitochondria in high-throughput studies; proposed to be involved in resistance to mechlorethamine and streptozotocin; null mutant sensitive to expression of top1-T722A allele","termid":"PBO:0086583"}


id: MONDO:0043166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"duodenal obstruction","termid":"MONDO:0002688"},{"relation_name":"is_a","term_name":"lipomatosis","termid":"MONDO:0006574"},{"relation_name":"is_a","term_name":"benign duodenal neoplasm","termid":"MONDO:0006734"},{"relation_name":"is_a","term_name":"benign neoplasm of pancreas","termid":"MONDO:0021470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic lipomatosis duodenal stenosis","secondary_identifiers":["MEDGEN:419702","MESH:C535839","UMLS:C2931040"],"synonyms":[{"name":"pancreatic lipomatosis and duodenal atresia","type":"related"}],"termid":"MONDO:0043166","xrefs":{"Monarch":{"xref_id":"0043166"}}}


id: PBO:0030423
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-excess_endoplasmic_reticulum_membrane_present","termid":"PBO:0030423"}


id: GO:0106219
data:
  {"annotated_genes":["SJAG_02853"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102938],"is_not":false,"summary":null,"term":"GO:0106219"}]},"cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of zinc.","definition_xrefs":["GOC:vw","PMID:31239353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal ion sensor activity","termid":"GO:0140784"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0003674","GO:0140299","GO:0098772"],"is_obsolete":false,"name":"zinc ion sensor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106219","terms_by_termid":{"GO:0106219":null}}


id: GO:0001994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that results in a decrease in the diameter of an artery during the norepinephrine-epinephrine response to decreased blood pressure.","definition_xrefs":["GOC:mtg_cardio","ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasoconstriction","termid":"GO:0042310"},{"relation_name":"part_of","term_name":"positive regulation of blood pressure by epinephrine-norepinephrine","termid":"GO:0003321"}],"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":"norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure","synonyms":[{"name":"noradrenaline-adrenaline vasoconstriction involved in regulation of blood pressure","type":"exact"},{"name":"norepinephrine-epinephrine vasoconstriction during blood pressure control","type":"related"},{"name":"norepinephrine-epinephrine vasoconstriction during blood pressure regulation","type":"exact"},{"name":"norepinephrine-epinephrine vasoconstriction during control of blood pressure","type":"related"}],"termid":"GO:0001994"}


id: GO:0120188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the controlled release of bile acid from a cell or a tissue.","definition_xrefs":["PMID:22767443","GOC:BHF_miRNA","GOC:rph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organic acid transport","termid":"GO:0032890"},{"relation_name":"is_a","term_name":"regulation of secretion","termid":"GO:0051046"},{"relation_name":"regulates","term_name":"bile acid secretion","termid":"GO:0032782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of bile acid secretion","termid":"GO:0120188"}


id: PBO:0065504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paraspeckle component 1 pseudogene 1","termid":"PBO:0065504"}


id: MONDO:0010518
data:
  {"annotated_genes":["SJAG_01732"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85408],"is_not":false,"summary":null,"term":"MONDO:0010518"}]},"cv_name":"mondo","definition":"Wiskott-Aldrich syndrome (WAS) is a primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies.","definition_xrefs":["Orphanet:906"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01732":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Wiskott-Aldrich syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:301000","UMLS:C0043194","GARD:7895","ICD9:279.12","MESH:D014923","SCTID:36070007","ICD10CM:D82.0","icd11.foundation:168952525","MedDRA:10047992","MEDGEN:21921","NCIT:C3448","NANDO:1200330","NANDO:2200704","DOID:9169"],"synonyms":[{"name":"Aldrich syndrome","type":"related"},{"name":"Imd 2","type":"related"},{"name":"WAS","type":"exact"},{"name":"Wiskott Aldrich syndrome","type":"exact"},{"name":"Wiskott syndrome","type":"exact"},{"name":"Wiskott-Aldrich syndrome","type":"exact"},{"name":"Wiskott-Aldrich syndrome 1","type":"exact"},{"name":"Wiskott-Aldrich syndrome, X-linked recessive","type":"exact"},{"name":"eczema thrombocytopenia immunodeficiency syndrome","type":"related"},{"name":"eczema-thrombocytopenia-immunodeficiency syndrome","type":"exact"},{"name":"immunodeficiency 2","type":"exact"}],"termid":"MONDO:0010518","terms_by_termid":{"MONDO:0010518":null},"xrefs":{"Monarch":{"xref_id":"0010518"}}}


id: GO:0060629
data:
  {"annotated_genes":["SJAG_02104","SJAG_03048","SJAG_04457"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109678,93368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090006"},{"annotations":[101894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062123"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of homologous chromosome segregation, the cell cycle process in which replicated homologous chromosomes are organized and then physically separated and apportioned to two sets during the first division of the meiotic cell cycle. Each replicated chromosome, composed of two sister chromatids, aligns at the cell equator, paired with its homologous partner; this pairing off, referred to as synapsis, permits genetic recombination. One homolog (both sister chromatids) of each morphologic type goes into each of the resulting chromosome sets.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome segregation","termid":"GO:0051983"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"homologous chromosome segregation","termid":"GO:0045143"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02104":null,"SJAG_03048":null,"SJAG_04457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of homologous chromosome segregation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0060629","terms_by_termid":{"GO:0062123":null,"GO:0090006":null}}


id: MONDO:0060593
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete actn3 deficiency (obsolete MONDO:0060593)","secondary_identifiers":["OMIM:617749"],"synonyms":[{"name":"ACTN3 deficiency","type":"exact"},{"name":"alpha-actinin-3 deficiency","type":"exact"},{"name":"sprinting performance","type":"exact"}],"termid":"MONDO:0060593","xrefs":{"Monarch":{"xref_id":"0060593"}}}


id: FYPO:0002882
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which transcription occurs to is normal (i.e. indistinguishable from wild type) in extent, timing, start or termination site, etc. All genes, or a specific subset of genes, may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription phenotype","termid":"FYPO:0004847"},{"relation_name":"is_a","term_name":"normal RNA metabolic process","termid":"FYPO:0004850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal transcription","synonyms":[{"name":"normal transcription, DNA-dependent","type":"exact"}],"termid":"FYPO:0002882"}


id: PBO:0039933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho guanine nucleotide exchange factor 38","termid":"PBO:0039933"}


id: GO:0008653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving lipopolysaccharides, a group of related, structurally complex components of the outer membrane of Gram-negative bacteria. Lipopolysaccharides consist three covalently linked regions, lipid A, core oligosaccharide, and an O side chain. Lipid A is responsible for the toxicity of the lipopolysaccharide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule metabolic process","termid":"GO:0043170"},{"relation_name":"is_a","term_name":"liposaccharide metabolic process","termid":"GO:1903509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"lipopolysaccharide metabolic process","synonyms":[{"name":"LPS metabolic process","type":"exact"},{"name":"lipopolysaccharide metabolism","type":"exact"}],"termid":"GO:0008653"}


id: PBO:0070310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY1 pseudogene 16","termid":"PBO:0070310"}


id: MONDO:0800210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile open angle glaucoma","termid":"MONDO:0020367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"glaucoma 1, open angle, l","synonyms":[{"name":"GLC1L","type":"exact"}],"termid":"MONDO:0800210","xrefs":{"Monarch":{"xref_id":"0800210"}}}


id: FYPO:0004262
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, does not occur during G2 phase of the mitotic cell cycle and during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation during cellular response to ionizing radiation","termid":"FYPO:0002471"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein phosphorylation during mitotic G2 phase during cellular response to ionizing radiation","synonyms":[{"name":"abolished protein phosphorylation during cellular response to ionizing radiation during G2 phase of mitotic cell cycle","type":"exact"},{"name":"abolished protein phosphorylation during cellular response to ionizing radiation during mitotic G2 phase","type":"exact"},{"name":"abolished protein phosphorylation during mitotic G2 phase during cellular response to IR","type":"exact"},{"name":"abolished protein phosphorylation during mitotic G2 phase during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"protein phosphorylation abolished during mitotic G2 phase during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0004262"}


id: MONDO:0002309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Conjunctivitis that is characterized by the formation of papillae on the palpebral conjunctiva.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conjunctivitis","termid":"MONDO:0003799"}],"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":"papillary conjunctivitis","secondary_identifiers":["ICD9:372.39","SCTID:416878008","UMLS:C0854165","NCIT:C35616","MEDGEN:167698","DOID:2458","icd11.foundation:392841027"],"termid":"MONDO:0002309","xrefs":{"Monarch":{"xref_id":"0002309"}}}


id: PBO:0053303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lin-28 homolog A","termid":"PBO:0053303"}


id: GO:0042335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a cuticle, the outer layer of some animals and plants, which acts to prevent water loss.","definition_xrefs":["ISBN:0192800825"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cuticle development","synonyms":[{"name":"cuticle anabolism","type":"exact"},{"name":"cuticle biosynthesis","type":"exact"},{"name":"cuticle biosynthetic process","type":"exact"},{"name":"cuticle formation","type":"exact"},{"name":"cuticle synthesis","type":"exact"}],"termid":"GO:0042335"}


id: GO:0090163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification and formation of the polarity of an epithelial cell along the plane of the epithelial tissue.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of epithelial cell polarity","termid":"GO:0090162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"establishment of epithelial cell planar polarity","termid":"GO:0090163"}


id: GO:0075259
data:
  {"annotated_genes":["SJAG_03501"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117728],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0075319"}]},"cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a spore-bearing structure over time, from its formation to the mature structure. A spore-bearing structure is an anatomical structure that produces new spores.","definition_xrefs":["GOC:pamgo_curators","GOC:di","GOC:mah","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03501":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"spore-bearing structure development","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"fruiting structure development","type":"exact"},{"name":"sporangium development","type":"broad"},{"name":"spore-bearing organ development","type":"related"},{"name":"sporophore development","type":"exact"}],"termid":"GO:0075259","terms_by_termid":{"GO:0075319":null}}


id: PBO:0012570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome complex subunit Ecm29","termid":"PBO:0012570"}


id: GO:2000210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of anoikis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of apoptotic process","termid":"GO:0043065"},{"relation_name":"is_a","term_name":"regulation of anoikis","termid":"GO:2000209"},{"relation_name":"positively_regulates","term_name":"anoikis","termid":"GO:0043276"}],"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 anoikis","synonyms":[{"name":"positive regulation of detachment induced cell death","type":"exact"},{"name":"positive regulation of suspension induced apoptosis","type":"exact"}],"termid":"GO:2000210"}


id: PBO:0065476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, non-ATPase 13","termid":"PBO:0065476"}


id: GO:0120507
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that catalyzes the base-exchange of a guanine residue with queuine at the wobble position of the anticodon of tRNAs. The eukaryotic tRNA-guanine transglycosylase exists as a heterodimer of a catalytic subunit (QTRT1 in humans) and an accessory subunit (QTRT2 in humans), whereas the bacterial enzyme is homodimeric.","definition_xrefs":["GOC:sjm","PMID:20354154","PMID:38181786"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"tRNA-guanine transglycosylase complex","synonyms":[{"name":"TGT","type":"exact"},{"name":"queuine tRNA-ribosyltransferase complex","type":"exact"}],"termid":"GO:0120507"}


id: PR:O14085
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC2F3.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocation protein sec72 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F3.02","synonyms":[{"name":"Spom972h-SPAC2F3.02","type":"exact"}],"termid":"PR:O14085"}


id: PBO:0034432
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_duration_of_mitosis","termid":"PBO:0034432"}


id: PBO:0073903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 15 member 1","termid":"PBO:0073903"}


id: GO:0003082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which angiotensin directly increases the rate of natriuresis and diuresis in the kidney.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mtg_cardio"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of renal output by angiotensin (obsolete GO:0003082)","synonyms":[{"name":"angiotensin mediated positive regulation of renal output","type":"exact"},{"name":"angiotensin-mediated positive regulation of renal output","type":"exact"},{"name":"positive regulation of renal output by angiotensin","type":"exact"}],"termid":"GO:0003082"}


id: PBO:0001316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fructose-2,6-bisphosphate 2-phosphatase activity (predicted)","termid":"PBO:0001316"}


id: MONDO:0030999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism","secondary_identifiers":["GARD:18542","UMLS:C5543228","OMIM:619244","MEDGEN:1786662"],"synonyms":[{"name":"NEDCAFD","type":"exact"}],"termid":"MONDO:0030999","xrefs":{"Monarch":{"xref_id":"0030999"}}}


id: GO:1904459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of substance P secretion.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:11278900"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of peptide hormone secretion","termid":"GO:0090278"},{"relation_name":"is_a","term_name":"regulation of substance P secretion","termid":"GO:1904458"},{"relation_name":"negatively_regulates","term_name":"substance P secretion","termid":"GO:1990772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of substance P secretion","synonyms":[{"name":"down regulation of substance P secretion","type":"exact"},{"name":"down-regulation of substance P secretion","type":"exact"},{"name":"downregulation of substance P secretion","type":"exact"},{"name":"inhibition of substance P secretion","type":"narrow"}],"termid":"GO:1904459"}


id: GO:2000191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of fatty acid transport.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipid transport","termid":"GO:0032368"},{"relation_name":"is_a","term_name":"regulation of organic acid transport","termid":"GO:0032890"},{"relation_name":"regulates","term_name":"fatty acid transport","termid":"GO:0015908"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of fatty acid transport","termid":"GO:2000191"}


id: FYPO:0001830
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 gluconate as the carbon source.","definition_xrefs":["PomBase:mah"],"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:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0002058","FYPO:0002060","FYPO:0000003"],"is_obsolete":false,"name":"decreased cell population growth on gluconate carbon source","synonyms":[{"name":"decreased growth on gluconate carbon source","type":"broad"},{"name":"decreased vegetative cell growth on gluconate carbon source","type":"exact"},{"name":"reduced cell growth on gluconate carbon source","type":"exact"},{"name":"slow cell growth on gluconate carbon source","type":"narrow"}],"termid":"FYPO:0001830"}


id: PBO:0091361
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complented by human NRAS","termid":"PBO:0091361"}


id: FYPO:0006189
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 actin cables is normal (i.e. indistinguishable from wild type). Actin cables are parallel actin filament bundles nucleated by formin, and are the most common form of actin filament bundles found in yeasts.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to actin cytoskeleton during vegetative growth","termid":"FYPO:0003441"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000138","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to actin cable","synonyms":[{"name":"normal protein localisation to actin cable","type":"exact"},{"name":"normal protein localization to actin cable during mitotic cell cycle","type":"related"},{"name":"normal protein localization to actin cable during vegetative growth","type":"exact"},{"name":"normal protein localization to formin-nucleated actin cable","type":"exact"}],"termid":"FYPO:0006189"}


id: PBO:0012041
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lives if zapped","termid":"PBO:0012041"}


id: PBO:0088552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gpl1-Gih35-Wdr83 complex WD repeat subunit Wdr83","termid":"PBO:0088552"}


id: MONDO:0017929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital achiasma is a rare, genetic, non-syndromic cranial nerve and nuclear aplasia malformation characterized by the congenital absence of the optic chiasm, resulting from the failure of the optic nerve fibers to cross over and decussate to the contralateral hemisphere, leading to decreased vision, strabismus and congenital nystagmus in infancy.","definition_xrefs":["Orphanet:324353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"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":"congenital achiasma","secondary_identifiers":["MEDGEN:1392790","UMLS:C4518345","GARD:21438","ICD10CM:H47.4","SCTID:734031008"],"termid":"MONDO:0017929","xrefs":{"Monarch":{"xref_id":"0017929"}}}


id: PBO:0066096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAS protein activator like 1","termid":"PBO:0066096"}


id: GO:0038164
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the glycoprotein thrombopoietin and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:bf","PMID:19630807","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"thrombopoietin receptor activity","termid":"GO:0038164"}


id: MONDO:0015928
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease (obsolete MONDO:0015928)","secondary_identifiers":["Orphanet:182104"],"synonyms":[{"name":"CTD-ILD","type":"exact"},{"name":"secondary ILD in childhood and adulthood associated with a connective tissue disease","type":"exact"}],"termid":"MONDO:0015928","xrefs":{"Monarch":{"xref_id":"0015928"}}}


id: MONDO:0004901
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndromes which feature dyskinesias as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions.","definition_xrefs":["MESH:D009069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lingual-facial-buccal dyskinesia","secondary_identifiers":["DOID:9854","SCTID:49386006","ICD9:333.82","UMLS:C0152115","MEDGEN:57747"],"synonyms":[{"name":"oro-facial dyskinesia","type":"exact"}],"termid":"MONDO:0004901","xrefs":{"Monarch":{"xref_id":"0004901"}}}


id: PBO:0051597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 22 receptor subunit alpha 1","termid":"PBO:0051597"}


id: MONDO:0011040
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":"spinal dysplasia, Anhalt type","secondary_identifiers":["UMLS:C1832464","MEDGEN:318632","MESH:C563348","OMIM:601344"],"synonyms":[{"name":"spinal dysplasia, Anhalt type","type":"exact"}],"termid":"MONDO:0011040","xrefs":{"Monarch":{"xref_id":"0011040"}}}


id: PBO:0073809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 6 member 14","termid":"PBO:0073809"}


id: MONDO:0024636
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory disease involving a pathogenic inflammatory response in the heart layer.","definition_xrefs":["MONDO:patterns/inflammatory_disease_by_site"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"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":"inflammation of heart layer","secondary_identifiers":["SCTID:399617002","UMLS:C0869523","MEDGEN:163689","ICD9:429.89"],"synonyms":[{"name":"carditis","type":"exact"},{"name":"heart layer inflammation","type":"exact"}],"termid":"MONDO:0024636","xrefs":{"Monarch":{"xref_id":"0024636"}}}


id: PBO:0051600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 23 receptor","termid":"PBO:0051600"}


id: PBO:0028278
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-merotelic_kinetochore_attachment_during_mitosis","termid":"PBO:0028278"}


id: PBO:0030526
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_localization_to_chromatin","termid":"PBO:0030526"}


id: SO:0001374
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"5_carboxymethyluridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_carboxymethyluridine","secondary_identifiers":["RNAMOD:087"],"synonyms":[{"name":"5-carboxymethyluridine","type":"exact"},{"name":"cm5U","type":"exact"},{"name":"five carboxymethyluridine","type":"exact"}],"termid":"SO:0001374"}


id: MONDO:0002943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal cell carcinoma that arises from the skin of the external ear.","definition_xrefs":["NCIT:C6082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external ear squamous cell carcinoma","termid":"MONDO:0003501"},{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"external ear basal cell carcinoma","secondary_identifiers":["DOID:4287","MEDGEN:234239","UMLS:C1333491"],"synonyms":[{"name":"basal cell carcinoma of external Ear","type":"exact"},{"name":"basal cell carcinoma of external ear","type":"related"},{"name":"basal cell carcinoma of the external Ear","type":"exact"},{"name":"basal cell carcinoma of the external ear","type":"exact"},{"name":"basal cell external ear carcinoma","type":"exact"},{"name":"external Ear basal cell carcinoma","type":"exact"},{"name":"external ear skin basal cell carcinoma","type":"exact"},{"name":"skin basal cell carcinoma of external ear","type":"exact"}],"termid":"MONDO:0002943","xrefs":{"Monarch":{"xref_id":"0002943"}}}


id: GO:1904098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein O-linked glycosylation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24509081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein glycosylation","termid":"GO:0060049"},{"relation_name":"regulates","term_name":"protein O-linked glycosylation","termid":"GO:0006493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006486"}],"interesting_parent_ids":["GO:0008150","GO:0006486"],"is_obsolete":false,"name":"regulation of protein O-linked glycosylation","synonyms":[{"name":"regulation of protein amino acid O-linked glycosylation","type":"exact"}],"termid":"GO:1904098"}


id: GO:0009522
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A photosystem that contains an iron-sulfur reaction center associated with accessory pigments and electron carriers. In cyanobacteria and chloroplasts, photosystem I functions as a light-dependent plastocyanin-ferredoxin oxidoreductase, transferring electrons from plastocyanin to ferredoxin; in photosynthetic bacteria that have only a single type I photosystem, such as the green sulfur bacteria, electrons can go either to ferredoxin (Fd) -> NAD+ or to menaquinone (MK) -> Cytb/FeS -> Cytc555 -> photosystem I (cyclic photophosphorylation).","definition_xrefs":["GOC:mah","PMID:9821949","GOC:ds","ISBN:0140514031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photosystem","termid":"GO:0009521"}],"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:0005575","GO:0032991"],"is_obsolete":false,"name":"photosystem I","termid":"GO:0009522"}


id: FYPO:0003652
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription initiation from an RNA polymerase III promoter is abnormal.","definition_xrefs":["PomBase:mah","GO:0006384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transcription during vegetative growth","termid":"FYPO:0004064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000294","FYPO:0006551","FYPO:0001985"],"is_obsolete":false,"name":"abnormal transcription initiation from RNA polymerase III promoter","synonyms":[{"name":"abnormal transcription initiation from RNA polymerase III promoter during mitotic cell cycle","type":"related"},{"name":"abnormal transcription initiation from RNA polymerase III promoter during vegetative growth","type":"exact"}],"termid":"FYPO:0003652"}


id: PBO:0059575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 2 pseudogene 1","termid":"PBO:0059575"}


id: MONDO:0859571
data:
  {"annotated_genes":["SJAG_03786"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85213],"is_not":false,"summary":null,"term":"MONDO:0859571"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital diaphragmatic hernia","termid":"MONDO:0005711"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03786":null},"genotype_count":0,"is_obsolete":false,"name":"diaphragmatic hernia 4, with cardiovascular defects","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5774210","OMIM:620025","MEDGEN:1823983"],"termid":"MONDO:0859571","terms_by_termid":{"MONDO:0859571":null},"xrefs":{"Monarch":{"xref_id":"0859571"}}}


id: MONDO:0003589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant adipose tissue neoplasm of the ovary.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian sarcoma","termid":"MONDO:0002225"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"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":"liposarcoma of the ovary","secondary_identifiers":["NCIT:C6419","UMLS:C1335165","DOID:5697","MEDGEN:233808"],"synonyms":[{"name":"liposarcoma of ovary","type":"exact"},{"name":"ovarian liposarcoma","type":"exact"},{"name":"ovary liposarcoma","type":"exact"}],"termid":"MONDO:0003589","xrefs":{"Monarch":{"xref_id":"0003589"}}}


id: GO:0061184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of the progression of the dermatome over time, from its initial formation to the mature structure. The dermatome is the portion of a somite that will form skin.","definition_xrefs":["GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of embryonic development","termid":"GO:0040019"},{"relation_name":"is_a","term_name":"regulation of dermatome development","termid":"GO:0061183"},{"relation_name":"positively_regulates","term_name":"dermatome development","termid":"GO:0061054"}],"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 dermatome development","termid":"GO:0061184"}


id: PR:Q09815
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pom2 gene.","definition_xrefs":["UniProtKB:Q09815","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":"serine/threonine-protein kinase ppk5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16C9.07","synonyms":[{"name":"Spom972h-pom2","type":"exact"},{"name":"meiotically up-regulated gene 189 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09815"}


id: PBO:0078591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 60 pseudogene 4, Y-linked","termid":"PBO:0078591"}


id: GO:0061780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The protein localization to chromatin by which a cohesin ring complex is topologically linked to DNA as part of the mitotic cell cycle.","definition_xrefs":["GOC:dph","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete mitotic cohesin loading (obsolete GO:0061780)","termid":"GO:0061780"}


id: MONDO:0003802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the cornea.","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular cancer","termid":"MONDO:0002236"},{"relation_name":"is_a","term_name":"cornea neoplasm","termid":"MONDO:0021238"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"cornea cancer","secondary_identifiers":["NCIT:C3565","MEDGEN:102282","UMLS:C0153629","DOID:6199","SCTID:363464006","ICD9:190.4"],"synonyms":[{"name":"cancer of cornea","type":"exact"},{"name":"cornea cancer","type":"exact"},{"name":"corneal tumor","type":"broad"},{"name":"corneal tumour","type":"broad"},{"name":"malignant cornea neoplasm","type":"exact"},{"name":"malignant cornea tumor","type":"exact"},{"name":"malignant cornea tumour","type":"exact"},{"name":"malignant corneal neoplasm","type":"exact"},{"name":"malignant corneal tumor","type":"exact"},{"name":"malignant corneal tumour","type":"exact"},{"name":"malignant neoplasm of cornea","type":"exact"},{"name":"malignant neoplasm of cornea (primary)","type":"exact"},{"name":"malignant neoplasm of the cornea","type":"exact"},{"name":"malignant tumor of cornea","type":"exact"},{"name":"malignant tumor of the cornea","type":"exact"},{"name":"malignant tumour of cornea","type":"exact"},{"name":"malignant tumour of the cornea","type":"exact"}],"termid":"MONDO:0003802","xrefs":{"Monarch":{"xref_id":"0003802"}}}


id: GO:0052159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts the induced systemic resistance in the host organism; induced systemic resistance is a response that confers broad spectrum systemic resistance to disease and that does not depend upon salicylic acid signaling. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host immune response","termid":"GO:0052553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host induced systemic resistance","secondary_identifiers":["GO:0052298"],"synonyms":[{"name":"modulation by organism of induced systemic resistance in other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of induced systemic resistance in host","type":"exact"},{"name":"perturbation of host induced systemic resistance","type":"exact"}],"termid":"GO:0052159"}


id: GO:0005907
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete HA1 clathrin adaptor (obsolete GO:0005907)","synonyms":[{"name":"AP1","type":"related"},{"name":"HA1 clathrin adaptor","type":"exact"}],"termid":"GO:0005907"}


id: MONDO:0007639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fundus albipunctatus is a rare, genetic retinal dystrophy characterized by the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age.","definition_xrefs":["Orphanet:227796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial flecked retinopathy","termid":"MONDO:0016420"},{"relation_name":"is_a","term_name":"RDH5-related retinopathy","termid":"MONDO:0100443"},{"relation_name":"is_a","term_name":"RLBP1-related retinopathy","termid":"MONDO:0100444"},{"relation_name":"is_a","term_name":"PRPH2-related retinopathy","termid":"MONDO:1040055"}],"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":"fundus albipunctatus","secondary_identifiers":["MESH:C562733","SCTID:68222009","ICD9:362.76","UMLS:C0311338","DOID:11105","ICD10CM:H35.5","icd11.foundation:1981512475","ICD9:362.74","OMIM:136880","MEDGEN:86317","GARD:13809"],"synonyms":[{"name":"fundus albipunctatus","type":"exact"},{"name":"pigmentary retinal dystrophy","type":"exact"},{"name":"retinitis punctata albescens","type":"broad"}],"termid":"MONDO:0007639","xrefs":{"Monarch":{"xref_id":"0007639"}}}


id: GO:1903645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of chaperone-mediated protein folding.","definition_xrefs":["GOC:TermGenie","PMID:24375412","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein folding","termid":"GO:1903333"},{"relation_name":"is_a","term_name":"regulation of chaperone-mediated protein folding","termid":"GO:1903644"},{"relation_name":"negatively_regulates","term_name":"chaperone-mediated protein folding","termid":"GO:0061077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006457"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006457"}],"interesting_parent_ids":["GO:0006457","GO:0008150"],"is_obsolete":false,"name":"negative regulation of chaperone-mediated protein folding","synonyms":[{"name":"down regulation of chaperone-mediated protein folding","type":"exact"},{"name":"down-regulation of chaperone-mediated protein folding","type":"exact"},{"name":"downregulation of chaperone-mediated protein folding","type":"exact"},{"name":"inhibition of chaperone-mediated protein folding","type":"narrow"}],"termid":"GO:1903645"}


id: PR:O94533
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An elongator complex protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13729:SF2","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":"elongator complex protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC895.06","secondary_identifiers":["UniProtKB:O94533"],"synonyms":[{"name":"SPCC895.06","type":"related"},{"name":"Spom972h-ELP2","type":"exact"}],"termid":"PR:O94533"}


id: PBO:0060706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 3","termid":"PBO:0060706"}


id: GO:0035137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the hindlimb are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"limb morphogenesis","termid":"GO:0035108"}],"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":"hindlimb morphogenesis","termid":"GO:0035137"}


id: PBO:0066927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 229","termid":"PBO:0066927"}


id: PBO:0064276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology, MyTH4 and FERM domain containing H2","termid":"PBO:0064276"}


id: PBO:0084023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycosyltransferase involved in protein glycosylation; transfers GDP-mannose to methyl-alpha-mannoside in vitro; member of the KRE2/MNT1 mannosyltransferase family of type II membrane proteins with a short cytoplasmic N-terminus, a membrane-spanning region and a highly conserved catalytic lumenal domain","termid":"PBO:0084023"}


id: PR:G2TRU0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ost5 gene.","definition_xrefs":["UniProtKB:G2TRU0","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":"dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit ost5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.19c","synonyms":[{"name":"Spom972h-ost5","type":"exact"},{"name":"oligosaccharyl transferase subunit ost5 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"oligosaccharyl transferase subunit zeta (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:G2TRU0"}


id: MONDO:0017149
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Drug- or toxin-induced pulmonary arterial hypertension (PAH) is a form of pulmonary arterial hypertension (PAH) secondary to the exposition to drugs. Drug- or toxin-induced PAH is characterized by elevated pulmonary arterial resistance leading to right heart failure. Drug or toxin induced PAH is progressive and potentially fatal.","definition_xrefs":["Orphanet:275786"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary arterial hypertension","termid":"MONDO:0015924"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"drug- or toxin-induced pulmonary arterial hypertension","secondary_identifiers":["UMLS:C0340544","EFO:0009192","GARD:21026","MEDGEN:573792"],"synonyms":[{"name":"drug- or toxin-induced PAH","type":"exact"}],"termid":"MONDO:0017149","xrefs":{"Monarch":{"xref_id":"0017149"}}}


id: FYPO:0004390
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more arginine catabolism RNAs measured in a cell is higher than normal (i.e. higher than observed in wild-type cells). Arginine catabolism RNAs are transcribed from genes whose products are involved in arginine catabolism.","definition_xrefs":["PMID:23695302","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of amino acid catabolism gene mRNA during vegetative growth","termid":"FYPO:0004389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased level of arginine catabolism gene mRNA during vegetative growth","synonyms":[{"name":"increased arginine catabolism gene mRNA accumulation during vegetative growth","type":"related"},{"name":"increased level of arginine catabolism gene RNA during vegetative growth","type":"exact"},{"name":"increased level of arginine catabolism gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of arginine catabolism gene transcripts during vegetative growth","type":"exact"}],"termid":"FYPO:0004390"}


id: PBO:0043534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"component of oligomeric golgi complex 2","termid":"PBO:0043534"}


id: _global:assayed_protein
data:
  {"annotation_feature_type":"gene","cv_name":"fypo_extension_relations","definition":"Relation between a phenotype and a protein gene product with which the phenotype was assayed.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"assayed_using","termid":"_global:assayed_using"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assayed_protein","termid":"_global:assayed_protein"}


id: MONDO:0016128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"},{"relation_name":"is_a","term_name":"infectious myositis","termid":"MONDO:0023483"}],"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":"parasitic myositis","secondary_identifiers":["GARD:20379","SCTID:60970005","UMLS:C0263997","MEDGEN:538249","icd11.foundation:110646208","ICD9:728.2","Orphanet:206997"],"termid":"MONDO:0016128","xrefs":{"Monarch":{"xref_id":"0016128"}}}


