# terms

id: PBO:0030357
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-stubby_cell_during_cellular_hyperosmotic_response","termid":"PBO:0030357"}


id: FYPO:0005847
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of H3-K9 specific histone methyltransferase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone methyltransferase activity","termid":"FYPO:0004784"},{"relation_name":"is_a","term_name":"abnormal histone methyltransferase activity (H3-K9 specific) activity","termid":"FYPO:0005846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0005447","FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000002","FYPO:0000654"],"is_obsolete":false,"name":"decreased histone methyltransferase activity (H3-K9 specific) activity","synonyms":[{"name":"decreased H3-K9 specific histone methyltransferase activity","type":"exact"},{"name":"reduced histone methyltransferase activity (H3-K9 specific) activity","type":"exact"}],"termid":"FYPO:0005847"}


id: PBO:0090074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding splicing factor Ntr1","termid":"PBO:0090074"}


id: PBO:0065824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB5C, member RAS oncogene family pseudogene 2","termid":"PBO:0065824"}


id: PBO:0054501
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 1901","termid":"PBO:0054501"}


id: PBO:0065133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein activator of interferon induced protein kinase EIF2AK2","termid":"PBO:0065133"}


id: PBO:0061728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear RNA export factor 2","termid":"PBO:0061728"}


id: PBO:0056019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSM family member 14B","termid":"PBO:0056019"}


id: GO:0035366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of thymine, 5-methyluracil, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:sl","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound transport","termid":"GO:0032240"},{"relation_name":"is_a","term_name":"regulation of thymine transport","termid":"GO:0035365"},{"relation_name":"negatively_regulates","term_name":"thymine transport","termid":"GO:0035364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of thymine transport","synonyms":[{"name":"negative regulation of 5-methyluracil transport","type":"exact"}],"termid":"GO:0035366"}


id: PBO:0116305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation termination factor eRF3; has a role in mRNA deadenylation and decay; altered protein conformation creates the [PSI(+)] prion, self-perpetuating amyloid fibrils that modify cellular fitness, alter translational fidelity by affecting reading frame selection, and result in a nonsense suppressor phenotype; forms reversible liquid condensates in response to both acidic and osmotic stress to promote survival; many stress-response genes are repressed in the presence of [PSI(+)]","termid":"PBO:0116305"}


id: PBO:0045794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelial differentiation related factor 1","termid":"PBO:0045794"}


id: MONDO:0010084
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":"sucrosuria, hiatus hernia and intellectual disability","secondary_identifiers":["OMIM:272000","MEDGEN:338583","UMLS:C1848963","MESH:C564792"],"synonyms":[{"name":"sucrosuria, hiatus hernia and intellectual disability","type":"exact"},{"name":"sucrosuria, hiatus hernia and mental retardation","type":"exact"}],"termid":"MONDO:0010084","xrefs":{"Monarch":{"xref_id":"0010084"}}}


id: PBO:0013818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABC1 kinase family protein, implicted in mitochondrial ergosterol and phospholipd homeostasis","termid":"PBO:0013818"}


id: PBO:0051855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly 1 pseudogene 1","termid":"PBO:0051855"}


id: GO:0072185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of the metanephric cap from an initial condition to its mature state. The metanephric cap is formed by the condensation of metanephric mesenchymal cells surrounding the ureteric bud tip.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metanephric mesenchyme development","termid":"GO:0072075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric cap development","termid":"GO:0072185"}


id: PR:Q9C0X8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rrp12 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0X8"],"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":"ribosomal RNA-processing protein 12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB8E5.07c","synonyms":[{"name":"Spom972h-rrp12","type":"exact"}],"termid":"PR:Q9C0X8"}


id: MONDO:0004122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive, small cell, poorly differentiated thymic neuroendocrine carcinoma, characterized by the presence of a high mitotic rate and numerous apoptotic bodies.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"thymic neuroendocrine carcinoma","termid":"MONDO:0020516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"thymus small cell carcinoma","secondary_identifiers":["NCIT:C6460","UMLS:C1335980","DOID:7142","MEDGEN:234784","EFO:1000578"],"synonyms":[{"name":"Thymus small cell carcinoma","type":"exact"},{"name":"small cell carcinoma of Thymus","type":"exact"},{"name":"small cell carcinoma of the Thymus","type":"exact"},{"name":"small cell carcinoma of thymus","type":"exact"},{"name":"thymic small cell carcinoma","type":"exact"},{"name":"thymic small cell carcinoma neuroendocrine type","type":"exact"},{"name":"thymus small cell carcinoma","type":"exact"}],"termid":"MONDO:0004122","xrefs":{"Monarch":{"xref_id":"0004122"}}}


id: PBO:0053345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 226","termid":"PBO:0053345"}


id: GO:0019250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cobalamin (vitamin B12) in the presence of oxygen.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cobalamin biosynthetic process","termid":"GO:0009236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0033013","GO:0006766","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"aerobic cobalamin biosynthetic process","secondary_identifiers":["MetaCyc:P381-PWY"],"synonyms":[{"name":"aerobic cobalamin anabolism","type":"exact"},{"name":"aerobic cobalamin biosynthesis","type":"exact"},{"name":"aerobic cobalamin formation","type":"exact"},{"name":"aerobic cobalamin synthesis","type":"exact"},{"name":"aerobic vitamin B12 biosynthesis","type":"exact"},{"name":"aerobic vitamin B12 biosynthetic process","type":"exact"},{"name":"cobalamin biosynthesis, aerobic","type":"exact"},{"name":"cobalamin biosynthetic process, aerobic","type":"exact"},{"name":"vitamin B12 biosynthesis, aerobic","type":"exact"},{"name":"vitamin B12 biosynthetic process, aerobic","type":"exact"}],"termid":"GO:0019250"}


id: GO:0044470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant stopping, prevention or reduction in the frequency, rate or extent of blood coagulation in the bitten organism.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of blood coagulation in another organism","termid":"GO:0044468"},{"relation_name":"is_a","term_name":"envenomation resulting in impairment of hemostasis in another organism","termid":"GO:0044483"}],"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":"envenomation resulting in negative regulation of blood coagulation in another organism","synonyms":[{"name":"envenomation resulting in negative regulation of blood coagulation in other organism","type":"exact"}],"termid":"GO:0044470"}


id: PBO:0069405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 665, pseudogene","termid":"PBO:0069405"}


id: PBO:0070465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5","termid":"PBO:0070465"}


id: PBO:0039814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor 4 pseudogene 5","termid":"PBO:0039814"}


id: FYPO:0007425
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A DNA recombination phenotype observed in the vegetative growth phase of the life cycle in which gene conversion is normal (i.e. indistinguishably from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal metabolic process during vegetative growth","termid":"FYPO:0000859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal gene conversion","synonyms":[{"name":"normal gene conversion during mitotic cell cycle","type":"related"},{"name":"normal gene conversion during vegetative growth","type":"exact"}],"termid":"FYPO:0007425"}


id: PBO:0113516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin; becomes conjugated to proteins, marking them for selective degradation via ubiquitin-26S proteasome system; essential for cellular stress response; encoded as polyubiquitin precursor comprised of 5 head-to-tail repeats; number of repeats is evolutionarily unstable within and between yeast species; protein abundance increases in response to DNA replication stress; implicated as modulator of replicative lifespan and meiotic recombination","termid":"PBO:0113516"}


id: MONDO:0009021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Toriello Carey syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysmorphic features, cerebral anomalies, swallowing difficulties, cardiac defects and hypotonia.","definition_xrefs":["Orphanet:3338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Toriello-Carey syndrome","secondary_identifiers":["icd11.foundation:147297969","MEDGEN:163225","GARD:5225","MESH:C563127","OMIM:217980","SCTID:722477003","UMLS:C0796184"],"synonyms":[{"name":"Toriello-Carey syndrome","type":"exact"},{"name":"agenesis of corpus callosum with facial anomalies and Robin sequence","type":"related"},{"name":"corpus callosum agenesis facial anomalies Robin sequence","type":"related"},{"name":"corpus callosum agenesis-blepharophimosis-Robin sequence syndrome","type":"exact"},{"name":"corpus callosum, agenesis of, with facial anomalies and ROBIN sequence","type":"related"}],"termid":"MONDO:0009021","xrefs":{"Monarch":{"xref_id":"0009021"}}}


id: PBO:0060528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase 1","termid":"PBO:0060528"}


id: MONDO:0017736
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease","termid":"MONDO:0002561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"disorder of sialic acid metabolism","secondary_identifiers":["MEDGEN:575253","Orphanet:309319","UMLS:C0342851","ICD9:277.89","SCTID:238050009","GARD:21332","icd11.foundation:1709765980"],"termid":"MONDO:0017736","xrefs":{"Monarch":{"xref_id":"0017736"}}}


id: GO:0071269
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-homocysteine, the L-enantiomer of 2-amino-4-sulfanylbutanoic acid.","definition_xrefs":["GOC:ecd","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine family amino acid biosynthetic process","termid":"GO:0009070"},{"relation_name":"is_a","term_name":"homocysteine biosynthetic process","termid":"GO:0071268"},{"relation_name":"is_a","term_name":"L-amino acid biosynthetic process","termid":"GO:0170034"}],"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:0006520"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520","GO:0006790"],"is_obsolete":false,"name":"L-homocysteine biosynthetic process","synonyms":[{"name":"L-homocysteine anabolism","type":"exact"},{"name":"L-homocysteine biosynthesis","type":"exact"},{"name":"L-homocysteine formation","type":"exact"},{"name":"L-homocysteine synthesis","type":"exact"}],"termid":"GO:0071269"}


id: GO:0009296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The assembly of a flagellum. In bacteria, this is a whiplike motility appendage present on the surface of some species; in eukaryotes, flagella are threadlike protoplasmic extensions used to propel flagellates and sperm. Flagella are composed of flagellin and have the same basic structure as cilia but are longer in proportion to the cell and present in much smaller numbers.","definition_xrefs":["ISBN:0815316194","GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete flagellum assembly (obsolete GO:0009296)","synonyms":[{"name":"flagella assembly","type":"exact"},{"name":"flagella biogenesis","type":"related"},{"name":"flagellum assembly","type":"exact"},{"name":"flagellum biogenesis","type":"related"}],"termid":"GO:0009296"}


id: MOD:01574
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"},{"relation_name":"is_a","term_name":"iTRAQ8plex-119 reporter+balance reagent acylated residue","termid":"MOD:01570"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent N-acylated residue","termid":"MOD:01710"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-119 reporter+balance reagent N'-acylated histidine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"}],"termid":"MOD:01574"}


id: PBO:0038810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 17","termid":"PBO:0038810"}


id: MONDO:0007495
data:
  {"annotated_genes":["SJAG_03275"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84815],"is_not":false,"summary":null,"term":"MONDO:0007495"}]},"cv_name":"mondo","definition":"An autosomal dominant dopa-responsive dystonia in which the cause of the disease is a variation in the GCH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTP cyclohydrolase I deficiency","termid":"MONDO:0100184"},{"relation_name":"is_a","term_name":"autosomal dominant dopa-responsive dystonia","termid":"MONDO:0971063"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0003441"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736","MONDO:0003441"],"is_obsolete":false,"name":"dystonia 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:1200516","SCTID:715768000","NORD:1702","MEDGEN:342121","GARD:9817","OMIM:128230","UMLS:C1851920","DOID:0090043"],"synonyms":[{"name":"DRD","type":"related"},{"name":"DYT-GCH1","type":"exact"},{"name":"Dopa-responsive dystonia, autosomal dominant","type":"exact"},{"name":"Dopa-responsive dystonia; Segawa syndrome AD","type":"related"},{"name":"GTP cyclohydrolase 1-deficient dopa-responsive dystonia","type":"exact"},{"name":"Segawa Syndrome","type":"exact"},{"name":"Segawa syndrome, autosomal dominant","type":"exact"},{"name":"dystonia 5","type":"exact"},{"name":"dystonia type 5","type":"exact"},{"name":"dystonia, DOPA-responsive","type":"related"},{"name":"dystonia, DOPA-responsive, with or without hyperphenylalaninemia","type":"exact"},{"name":"dystonia, Dopa-responsive, autosomal dominant","type":"exact"},{"name":"dystonia, progressive, with diurnal variation","type":"exact"},{"name":"dystonia-Parkinsonism with diurnal fluctuation","type":"exact"}],"termid":"MONDO:0007495","terms_by_termid":{"MONDO:0007495":null},"xrefs":{"Monarch":{"xref_id":"0007495"}}}


id: FYPO:0001052
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype in which a cell enters mitosis when smaller than wild type, and then septates to give rise to a cut phenotype. In a cut phenotype, a cell undergoes septation despite abnormal mitosis such that the septum physically divides the nucleus into two parts.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable small vegetative cell","termid":"FYPO:0000951"},{"relation_name":"has_part","term_name":"cut with abnormal chromosome segregation","termid":"FYPO:0003165"},{"relation_name":"is_a","term_name":"inviable small vegetative cell","termid":"FYPO:0000951"},{"relation_name":"is_a","term_name":"cut with abnormal chromosome segregation","termid":"FYPO:0003165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000337","FYPO:0001320","FYPO:0001985","FYPO:0000005","FYPO:0000641","FYPO:0000004","FYPO:0000032","FYPO:0005447","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"cut, small cell","synonyms":[{"name":"cut following advanced onset of mitosis","type":"exact"},{"name":"cut, small cell during mitotic cell cycle","type":"related"},{"name":"cut, small cell during vegetative growth","type":"exact"},{"name":"mitotic catastrophe with cut, small cell","type":"related"},{"name":"septation following abnormal nuclear division, small cell","type":"exact"},{"name":"small cut cell","type":"exact"}],"termid":"FYPO:0001052"}


id: PBO:0053057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LARS2 antisense RNA 1","termid":"PBO:0053057"}


id: PBO:0027605
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_mitotic_spindle_assembly","termid":"PBO:0027605"}


id: MONDO:0017754
data:
  {"annotated_genes":["SJAG_02896","SJAG_01841","SJAG_02876","SJAG_05194","SJAG_03785","SJAG_03011","SJAG_03961","SJAG_04944","SJAG_04109","SJAG_00938","SJAG_01344","SJAG_05283","SJAG_03363","SJAG_05213","SJAG_01372"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[86288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[86543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011559"},{"annotations":[86727,86728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030810"},{"annotations":[85632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031040"},{"annotations":[85216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[85059,85058,85060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009380"},{"annotations":[85472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[85170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[85624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"},{"annotations":[85217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013000"},{"annotations":[86666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011156"},{"annotations":[85298],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011214"},{"annotations":[84908],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008319"},{"annotations":[85491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008297"},{"annotations":[86137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"},{"annotations":[86475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010420"},{"annotations":[86473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020721"}]},"cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"porphyrin metabolism disease","termid":"MONDO:0037821"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_01344":null,"SJAG_01372":null,"SJAG_01841":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03011":null,"SJAG_03363":null,"SJAG_03785":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04944":null,"SJAG_05194":null,"SJAG_05213":null,"SJAG_05283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"inborn disorder of porphyrin metabolism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:E80.4","GARD:21346","SCTID:403832004","Orphanet:309813"],"synonyms":[{"name":"disorder of porphyrin and haem metabolism","type":"broad"},{"name":"inborn disorder of porphyrin and haem metabolism","type":"exact"},{"name":"inborn error of porphyrin-containing compound metabolic process","type":"exact"},{"name":"inborn porphyrin-containing compound metabolic process disorder","type":"exact"},{"name":"inherited disorder of porphyrin metabolism","type":"exact"},{"name":"rare inborn error of porphyrin-containing compound metabolic process","type":"exact"}],"termid":"MONDO:0017754","terms_by_termid":{"MONDO:0007369":null,"MONDO:0008294":null,"MONDO:0008296":null,"MONDO:0008297":null,"MONDO:0008319":null,"MONDO:0008822":null,"MONDO:0009380":null,"MONDO:0009902":null,"MONDO:0010420":null,"MONDO:0011156":null,"MONDO:0011214":null,"MONDO:0011559":null,"MONDO:0013000":null,"MONDO:0020721":null,"MONDO:0030048":null,"MONDO:0030810":null,"MONDO:0031040":null,"MONDO:0957577":null},"xrefs":{"Monarch":{"xref_id":"0017754"}}}


id: GO:1990849
data:
  {"annotated_genes":["SJAG_01116","SJAG_04221"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106826,115012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990854"}]},"cv_name":"biological_process","definition":"Any process in which the vacuole is transported to, and/or maintained in, a specific location within the cell.","definition_xrefs":["PMID:26283797"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle localization","termid":"GO:0051640"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01116":null,"SJAG_04221":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"vacuolar localization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"maintenance of vacuolar localization","type":"exact"},{"name":"maintenance of vacuolar location","type":"narrow"},{"name":"maintenance of vacuole localization","type":"exact"},{"name":"maintenance of vacuole location","type":"exact"}],"termid":"GO:1990849","terms_by_termid":{"GO:1990854":null}}


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


id: PBO:0026974
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_level_of_substance_in_mitochondrion","termid":"PBO:0026974"}


id: MONDO:0800180
data:
  {"annotated_genes":["SJAG_04944"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[85624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"}]},"cv_name":"mondo","definition":"Any inherited porphyria in which the cause of the disease is monoallelic or biallelic variants in the CPOX gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited porphyria","termid":"MONDO:0019142"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04944":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0019142"}],"interesting_parent_ids":["MONDO:0019142","MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"CPOX-related hereditary coproporphyria","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0800180","terms_by_termid":{"MONDO:0007369":null,"MONDO:0030048":null},"xrefs":{"Monarch":{"xref_id":"0800180"}}}


id: PBO:0031207
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-monopolar_actin_cortical_patch_localization","termid":"PBO:0031207"}


id: PBO:0071377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL30 antisense RNA 1","termid":"PBO:0071377"}


id: FYPO:0000311
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a normal germ tube, but does not septate or go on to form a viable dividing cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, with normal germ tube morphology","termid":"FYPO:0000310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination with normal, unseptated germ tube morphology","synonyms":[{"name":"inviable following spore germination with normal, unseptated germ tube morphology","type":"exact"},{"name":"inviable germinated spore with normal, unseptated germ tube morphology","type":"exact"},{"name":"lethal after spore germination with normal, unseptated germ tube morphology","type":"exact"}],"termid":"FYPO:0000311"}


id: GO:1902507
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of thiazole synthase activity.","definition_xrefs":["GOC:bhm","GOC:TermGenie","PMID:12650933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfurtransferase complex","termid":"GO:1990228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005829","GO:0005737"],"is_obsolete":false,"name":"thiazole synthase complex","termid":"GO:1902507"}


id: FYPO:0001647
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the import of L-glutamate into the cell is abnormal when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glutamate import","termid":"FYPO:0001646"},{"relation_name":"is_a","term_name":"abnormal amino acid import during nitrogen starvation","termid":"FYPO:0001648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abnormal glutamate import during nitrogen starvation","synonyms":[{"name":"abnormal L-glutamate import across plasma membrane during nitrogen starvation","type":"exact"},{"name":"abnormal L-glutamate import during nitrogen starvation","type":"exact"},{"name":"abnormal glutamate import during nitrogen depletion","type":"exact"},{"name":"abnormal glutamate import during nitrogen deprivation","type":"exact"},{"name":"abnormal glutamate import into cell during nitrogen starvation","type":"exact"},{"name":"abnormal glutamate uptake during nitrogen starvation","type":"exact"}],"termid":"FYPO:0001647"}


id: GO:0021703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the locus ceruleus over time, from its formation to the mature structure. The locus ceruleus is a dense cluster of neurons within the dorsorostral pons. This nucleus is the major location of neurons that release norepinephrine throughout the brain, and is responsible for physiological responses to stress and panic.","definition_xrefs":["GOC:cls","GOC:dph","GOC:jid","GO_REF:0000021","GOC:dgh","ISBN:0838580343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"pons development","termid":"GO:0021548"}],"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":"locus ceruleus development","synonyms":[{"name":"locus caeruleus development","type":"exact"},{"name":"locus coeruleus development","type":"exact"}],"termid":"GO:0021703"}


id: PBO:0063610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PFDN1 pseudogene 1","termid":"PBO:0063610"}


id: PBO:0044031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate proteoglycan family member 4B, pseudogene","termid":"PBO:0044031"}


id: SO:0002071
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A CDS that is supported by proteomics data.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CDS_supported_by_sequence_similarity_data","termid":"SO:1001251"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDS_supported_by_peptide_spectrum_match","termid":"SO:0002071"}


id: PBO:0083154
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 ORF SSZ1/YHR064C","termid":"PBO:0083154"}


id: GO:0004022
data:
  {"annotated_genes":["SJAG_00240","SJAG_03822","SJAG_01457","SJAG_01414","SJAG_03196","SJAG_01869","SJAG_03370","SJAG_00237"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70821,77892],"is_not":false,"summary":null,"term":"GO:0004022"},{"annotations":[114423,114422,98514,98515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120542"},{"annotations":[91573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047018"},{"annotations":[72362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003939"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an alcohol + NAD+ = an aldehyde or ketone + NADH + H+.","definition_xrefs":["EC:1.1.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol dehydrogenase [NAD(P)+] activity","termid":"GO:0018455"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00237":null,"SJAG_00240":null,"SJAG_01414":null,"SJAG_01457":null,"SJAG_01869":null,"SJAG_03196":null,"SJAG_03370":null,"SJAG_03822":null},"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"alcohol dehydrogenase (NAD+) activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-71707","Reactome:R-HSA-2162078"],"synonyms":[{"name":"ADH","type":"related"},{"name":"NAD-dependent alcohol dehydrogenase","type":"related"},{"name":"NAD-specific aromatic alcohol dehydrogenase","type":"related"},{"name":"NADH-alcohol dehydrogenase","type":"related"},{"name":"NADH-aldehyde dehydrogenase","type":"related"},{"name":"alcohol dehydrogenase activity","type":"broad"},{"name":"alcohol:NAD+ oxidoreductase","type":"related"},{"name":"aldehyde dehydrogenase (NAD) activity","type":"narrow"},{"name":"aldo-keto reductase (NAD) activity","type":"exact"},{"name":"aliphatic alcohol dehydrogenase","type":"narrow"},{"name":"ethanol dehydrogenase","type":"narrow"},{"name":"primary alcohol dehydrogenase","type":"broad"},{"name":"yeast alcohol dehydrogenase","type":"narrow"}],"termid":"GO:0004022","terms_by_termid":{"GO:0003939":null,"GO:0004022":null,"GO:0047018":null,"GO:0120542":null}}


id: GO:0048675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Long distance growth of a single axon process involved in cellular development.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:rl","GOC:dph","GOC:lm","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection extension","termid":"GO:1990138"},{"relation_name":"part_of","term_name":"axonogenesis","termid":"GO:0007409"}],"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":"axon extension","secondary_identifiers":["GO:0048676"],"synonyms":[{"name":"axon extension involved in development","type":"exact"}],"termid":"GO:0048675"}


id: PR:O74434
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug174 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 174 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1682.03c","synonyms":[{"name":"Spom972h-mug174","type":"exact"}],"termid":"PR:O74434"}


id: GO:1905090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of type 2 mitophagy.","definition_xrefs":["PMID:26942284","GOC:vw","PMID:25009776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mitophagy","termid":"GO:1901525"},{"relation_name":"is_a","term_name":"regulation of type 2 mitophagy","termid":"GO:1905089"},{"relation_name":"negatively_regulates","term_name":"type 2 mitophagy","termid":"GO:0061734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006914"},{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"negative regulation of type 2 mitophagy","synonyms":[{"name":"negative regulation of PRKN-mediated stimulation of mitophagy in response to mitochondrial depolarization","type":"exact"},{"name":"negative regulation of Park2-mediated stimulation of mitophagy in response to mitochondrial depolarization","type":"exact"},{"name":"negative regulation of parkin-mediated stimulation of mitophagy in response to mitochondrial depolarization","type":"exact"}],"termid":"GO:1905090"}


id: GO:0097091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in grouping synaptic vesicles in presynaptic structures.","definition_xrefs":["PMID:19900895","GOC:pr","PMID:7568108","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptic vesicle localization","termid":"GO:0097479"},{"relation_name":"part_of","term_name":"synaptic vesicle cycle","termid":"GO:0099504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"synaptic vesicle clustering","termid":"GO:0097091"}


id: GO:0004520
data:
  {"annotated_genes":["SJAG_02031","SJAG_03675","SJAG_04752","SJAG_01832","SJAG_01262","SJAG_01173","SJAG_01648","SJAG_04183","SJAG_02708","SJAG_01948","SJAG_03994","SJAG_00623","SJAG_02556","SJAG_05237","SJAG_05373","SJAG_01044","SJAG_02828"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[118578],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990599"},{"annotations":[74044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048257"},{"annotations":[105744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990043"},{"annotations":[103948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990601"},{"annotations":[74247,75438,70990,78160,72335,65923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017108"},{"annotations":[59422,74039,78923,94496,100962,78288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008821"},{"annotations":[100964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106332"},{"annotations":[71467,79034,110622,109835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000014"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within deoxyribonucleic acid by creating internal breaks.","definition_xrefs":["GOC:mah","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endonuclease activity","termid":"GO:0004519"},{"relation_name":"is_a","term_name":"DNA nuclease activity","termid":"GO:0004536"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00623":null,"SJAG_01044":null,"SJAG_01173":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_01832":null,"SJAG_01948":null,"SJAG_02031":null,"SJAG_02556":null,"SJAG_02708":null,"SJAG_02828":null,"SJAG_03675":null,"SJAG_03994":null,"SJAG_04183":null,"SJAG_04752":null,"SJAG_05237":null,"SJAG_05373":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016788","GO:0140097","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"DNA endonuclease activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5690988","Reactome:R-HSA-5693584","Reactome:R-HSA-5687464","Reactome:R-HSA-110359","Reactome:R-HSA-6782204","Reactome:R-HSA-9023941","Reactome:R-HSA-5686657","Reactome:R-HSA-6782224","Reactome:R-HSA-5686440","Reactome:R-HSA-5693608"],"synonyms":[{"name":"DNA nicking activity","type":"related"},{"name":"endodeoxyribonuclease activity","type":"exact"},{"name":"endonuclease G activity","type":"related"}],"termid":"GO:0004520","terms_by_termid":{"GO:0000014":null,"GO:0008821":null,"GO:0017108":null,"GO:0048257":null,"GO:0106332":null,"GO:1990043":null,"GO:1990599":null,"GO:1990601":null}}


id: FYPO:0005881
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 ophthalmic acid measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"}],"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:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"ophthalmic acid absent from cell","synonyms":[{"name":"ophthalmic acid absent from cell during mitotic cell cycle","type":"related"},{"name":"ophthalmic acid absent from cell during vegetative growth","type":"exact"}],"termid":"FYPO:0005881"}


id: MONDO:0012964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal monosomy 15q is a rare chromosomal anomaly syndrome characterized by pre- and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, hand and foot anomalies (e.g. brachy-/clinodactyly, talipes equinovarus, nail hypoplasia, proximally placed digits) and mild craniofacial dysmorphism (incl. microcephaly, triangular face, broad nasal bridge, micrognathia). Neonatal lymphedema, heart malformations, aplasia cutis congenita, aortic root dilatation, and autistic spectrum disorder have also been reported.","definition_xrefs":["Orphanet:1596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 15","termid":"MONDO:0016913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 15q26-qter deletion syndrome","secondary_identifiers":["SCTID:766050000","UMLS:C2675463","OMIM:612626","MEDGEN:390804","GARD:16572","DOID:0060397","MESH:C567232"],"synonyms":[{"name":"15q26 deletion syndrome","type":"exact"},{"name":"Drayer syndrome","type":"exact"},{"name":"chromosome 15q26-qter deletion syndrome","type":"exact"},{"name":"chromosome 15q26-qter deletion syndrome, isolated cases","type":"exact"},{"name":"distal 15q deletion syndrome","type":"exact"},{"name":"distal monosomy 15q","type":"exact"},{"name":"distal monosomy type 15q","type":"exact"},{"name":"monosomy 15q26","type":"exact"},{"name":"telomeric 15q deletion syndrome","type":"exact"}],"termid":"MONDO:0012964","xrefs":{"Monarch":{"xref_id":"0012964"}}}


id: PBO:0048304
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 14","termid":"PBO:0048304"}


id: FYPO:0007717
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 potassium chloride. Cells stop growing (and may die) at a concentration of potassium nitrate 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:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0005447","FYPO:0002683","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to potassium nitrate","synonyms":[{"name":"hypersensitive to potassium nitrate","type":"exact"},{"name":"sensitive to KNO3","type":"exact"},{"name":"sensitive to potassium nitrate during mitotic cell cycle","type":"related"},{"name":"sensitive to potassium nitrate during vegetative growth","type":"exact"}],"termid":"FYPO:0007717"}


id: MOD:01804
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a glycosylphosphate through a phosphodiester bond.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoconjugated residue","termid":"MOD:00764"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"}],"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":"glycosylphosphorylated residue","termid":"MOD:01804"}


id: PR:P50514
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An argininosuccinate lyase 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":"argininosuccinate lyase ArgX (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1539.03c","secondary_identifiers":["UniProtKB:P50514"],"synonyms":[{"name":"ASAL (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"Arginosuccinase (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"SPBC1539.03c","type":"related"},{"name":"Spom972h-ASL","type":"exact"}],"termid":"PR:P50514"}


id: MONDO:0003715
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urachal cancer is a type of bladder cancer, making up less than 1% of all bladder cancers. The urachus is a structure normally only present during development in the womb that connects the bellybutton and the bladder. This connection normally disappears before birth, but in some people remains. Urachalcancers are usually diagnosed in adults in their 50's and 60's and may develop at the dome or anterior wall of the bladder, along the midline of the body (including the belly button), and between the pubis symphasis and the bladder.Most urachal cancersare adenocarcinomas (cancers that develop from gland cells).Others may besarcomas (which develop from connective tissue -such as leiomyosarcoma, rhabdomyosarcoma, and malignant fibrous histiocytoma), small cell carcinomas, transitional cell cancer, and mixed neoplasias. Most individuals with urachal cancer have symptoms of with hematuria (blood in urine). Other symptoms may include abdominal pain, a palpable abdominal mass, mucinuria, and bacteriuria. Treatment usually involved surgery to remove the cancer.","definition_xrefs":["GARD:0007836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder carcinoma","termid":"MONDO:0004986"}],"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":"bladder urachal carcinoma","secondary_identifiers":["DOID:5958","MESH:C536475","UMLS:C2931202","MEDGEN:419015","ONCOTREE:URCA","NCIT:C39842"],"synonyms":[{"name":"bladder urachal cancer","type":"exact"},{"name":"bladder urachal carcinoma","type":"exact"},{"name":"urachal carcinoma","type":"related"}],"termid":"MONDO:0003715","xrefs":{"Monarch":{"xref_id":"0003715"}}}


id: MONDO:0000520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ependymal tumor affecting the parietal lobe of the brain.","definition_xrefs":["NCIT:C131575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parietal lobe cancer","termid":"MONDO:0001952"},{"relation_name":"is_a","term_name":"ependymal tumor of brain","termid":"MONDO:0004245"}],"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":"parietal lobe ependymal tumor","secondary_identifiers":["DOID:0050903","UMLS:C4330935","MEDGEN:1392382"],"synonyms":[{"name":"ependymal tumor of parietal lobe","type":"exact"},{"name":"ependymal tumour of parietal lobe","type":"exact"},{"name":"parietal lobe ependymal tumor","type":"exact"},{"name":"parietal lobe ependymoma","type":"related"}],"termid":"MONDO:0000520","xrefs":{"Monarch":{"xref_id":"0000520"}}}


id: GO:0021852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a pyramidal neuron precursor from the ventricular zone to the correct layer of the cerebral cortex.","definition_xrefs":["PMID:22192824","GOC:cls","GOC:dgh","GOC:dph","GOC:jid","GO_REF:0000021","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cortex radial glia-guided migration","termid":"GO:0021801"},{"relation_name":"is_a","term_name":"radial glia-guided pyramidal neuron migration","termid":"GO:0140650"},{"relation_name":"part_of","term_name":"pyramidal neuron development","termid":"GO:0021860"}],"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":"pyramidal neuron migration to cerebral cortex","synonyms":[{"name":"projection neuron migration","type":"related"},{"name":"pyramidal neuron migration","type":"broad"}],"termid":"GO:0021852"}


id: PBO:0061889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OPCML intronic transcript 2","termid":"PBO:0061889"}


id: MONDO:0016964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal duplication","termid":"MONDO:0000762"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of the long arm of chromosome 14","secondary_identifiers":["Orphanet:262941","GARD:20884","MEDGEN:1826036","UMLS:C5679704"],"synonyms":[{"name":"14q duplication","type":"related"},{"name":"14q trisomy","type":"related"},{"name":"Duplication 14q","type":"related"},{"name":"chromosome 14q duplication","type":"related"},{"name":"partial duplication of chromosome 14q","type":"exact"},{"name":"partial duplication of the long arm of chromosome type 14","type":"exact"},{"name":"partial trisomy 14q","type":"related"},{"name":"partial trisomy of chromosome 14q","type":"exact"},{"name":"partial trisomy of the long arm of chromosome 14","type":"exact"},{"name":"trisomy 14q","type":"related"}],"termid":"MONDO:0016964","xrefs":{"Monarch":{"xref_id":"0016964"}}}


id: MONDO:0009794
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oral-facial-digital syndrome, type 4 is characterized by lingual hamartoma, postaxial polysyndactyly of hands and feet, and mesomelic shortening of the legs with supinate equinovarus feet.","definition_xrefs":["Orphanet:2753"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"orofaciodigital syndrome","termid":"MONDO:0015375"},{"relation_name":"is_a","term_name":"thoracic malformation","termid":"MONDO:0015929"},{"relation_name":"is_a","term_name":"short rib dysplasia","termid":"MONDO:0019691"}],"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":"orofaciodigital syndrome IV","secondary_identifiers":["MEDGEN:98358","DOID:0060374","MESH:C537133","SCTID:239031000","GARD:816","OMIM:258860","UMLS:C0406727"],"synonyms":[{"name":"Baraitser-Burn syndrome","type":"exact"},{"name":"Mohr-Majewski syndrome","type":"exact"},{"name":"OFD syndrome 4","type":"related"},{"name":"OFD4","type":"exact"},{"name":"Ofd syndrome with tibial defects","type":"related"},{"name":"Ofd syndrome, Baraitser-Burn type","type":"related"},{"name":"Ofds 4","type":"related"},{"name":"oral facial digital syndrome 4","type":"related"},{"name":"oral facial digital syndrome type 4","type":"related"},{"name":"oral-Facial-digital syndrome, type 4","type":"related"},{"name":"oral-facial-digital syndrome type 4","type":"exact"},{"name":"orofaciodigital syndrome 4","type":"related"},{"name":"orofaciodigital syndrome IV","type":"exact"},{"name":"orofaciodigital syndrome type 4","type":"exact"},{"name":"orofaciodigital syndrome type IV","type":"exact"},{"name":"orofaciodigital syndrome with tibial dysplasia","type":"related"}],"termid":"MONDO:0009794","xrefs":{"Monarch":{"xref_id":"0009794"}}}


id: PBO:0001222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab subfamily","termid":"PBO:0001222"}


id: MONDO:1011950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteochondroma causing progressive posterior paresis, non-human animal","secondary_identifiers":["OMIA:000749"],"termid":"MONDO:1011950","xrefs":{"Monarch":{"xref_id":"1011950"}}}


id: GO:0072559
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An inflammasome complex that consists of three components, NLRP3 (NALP3), PYCARD and caspase-1. It is activated upon exposure to whole pathogens, as well as a number of structurally diverse pathogen- and danger-associated molecular patterns (PAMPs and DAMPs) and environmental irritants. Whole pathogens demonstrated to activate the NLRP3 inflammasome complex include the fungi Candida albicans and Saccharomyces cerevisiae, bacteria that produce pore-forming toxins, including Listeria monocytogenes and Staphylococcus aureus, and viruses such as Sendai virus, adenovirus, and influenza virus.","definition_xrefs":["PMID:20303873","GOC:BHF","GOC:vp","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canonical inflammasome complex","termid":"GO:0061702"}],"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:0005829"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991","GO:0005829"],"is_obsolete":false,"name":"NLRP3 inflammasome complex","synonyms":[{"name":"NALP3 inflammasome complex","type":"exact"}],"termid":"GO:0072559"}


id: PBO:0086626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and the nucleus; overexpression causes a cell cycle delay or arrest; YML053C is not an essential gene","termid":"PBO:0086626"}


id: GO:0097232
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a lamellar body. A lamellar body is a membrane-bounded organelle, specialized for the storage and secretion of various substances (surfactant phospholipids, glycoproteins and acid phosphates) which are arranged in the form of tightly packed, concentric, membrane sheets or lamellae. Has some similar properties to, but is distinct from, a lysosome.","definition_xrefs":["PMID:11940594","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule membrane","termid":"GO:0030667"},{"relation_name":"part_of","term_name":"lamellar body","termid":"GO:0042599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"lamellar body membrane","termid":"GO:0097232"}


id: MONDO:0015440
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 6 syndrome is a rare chromosomal anomaly syndrome with highly variable phenotype principally characterized by prenatal/postnatal growth failure, intellectual disability, developmental delay, craniofacial dysmorphism (incl. microcephaly, microphthalmia, epicanthus, low-set and malformed ears, broad and flat nasal bridge, full lips, micrognathia), central nervous system anomalies (e.g. hydrocephalus, cortical atrophy, ventriculomegaly), short neck, and delayed bone age. Cardiac defects, limb anomalies, hip joint malformations, and seizures have also been reported.","definition_xrefs":["Orphanet:1448"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 6 disorder","termid":"MONDO:0700013"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 6","secondary_identifiers":["MESH:C537763","NCIT:C121985","GARD:6095","SCTID:765488003","UMLS:C0795814","NORD:958","MEDGEN:167069"],"synonyms":[{"name":"Chromosome 6 Ring","type":"exact"},{"name":"R6","type":"related"},{"name":"Ring 6","type":"related"},{"name":"Ring chromosome 6 syndrome","type":"related"},{"name":"Ring chromosome type 6","type":"exact"},{"name":"chromosome 6 ring","type":"related"},{"name":"rose cluster 6","type":"exact"}],"termid":"MONDO:0015440","xrefs":{"Monarch":{"xref_id":"0015440"}}}


id: PBO:0085764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase of unknown cellular role; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; null mutant is sensitive to expression of the top1-T722A allele; not an essential gene; relocalizes from nucleus to cytoplasm upon DNA replication stress","termid":"PBO:0085764"}


id: GO:1903033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of microtubule plus-end binding.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:16148041","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of microtubule binding","termid":"GO:1904528"}],"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 microtubule plus-end binding","synonyms":[{"name":"activation of microtubule plus-end binding","type":"narrow"},{"name":"up regulation of microtubule plus-end binding","type":"exact"},{"name":"up-regulation of microtubule plus-end binding","type":"exact"},{"name":"upregulation of microtubule plus-end binding","type":"exact"}],"termid":"GO:1903033"}


id: FYPO:0000104
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 cycloheximide. Cells stop growing (and may die) at a concentration of cycloheximide 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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002683","FYPO:0001985","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to cycloheximide","synonyms":[{"name":"hypersensitive to cycloheximide","type":"exact"},{"name":"sensitive to cycloheximide during mitotic cell cycle","type":"related"},{"name":"sensitive to cycloheximide during vegetative growth","type":"exact"}],"termid":"FYPO:0000104"}


id: MONDO:0013306
data:
  {"annotated_genes":["SJAG_00308"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86994],"is_not":false,"summary":null,"term":"MONDO:0013306"}]},"cv_name":"mondo","definition":"Combined oxidative phosphorylation defect type 7 is a rare mitochondrial disease due to a defect in mitochondrial protein synthesis characterized by a variable phenotype that includes onset in infancy or early childhood of failure to thrive and psychomotor regression (after initial normal development), as well as ocular manifestations (such as ptosis, nystagmus, optic atrophy, ophthalmoplegia and reduced vision). Additional manifestations include bulbar paresis with facial weakness, hypotonia, difficulty chewing, dysphagia, mild dysarthria, ataxia, global muscle atrophy, and areflexia. It has a relatively slow disease progression with patients often living into the third decade of life.","definition_xrefs":["Orphanet:254930"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00308":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 7","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:462151","UMLS:C3150801","OMIM:613559","DOID:0111487","GARD:17234","SCTID:763204003"],"synonyms":[{"name":"C12ORF65 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"C12orf65 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"COXPD7","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 7","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in C12ORF65","type":"exact"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in C12orf65","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 7","type":"exact"},{"name":"severe C12ORF65-related COXPD","type":"exact"},{"name":"severe C12ORF65-related combined oxidative phosphorylation defect","type":"exact"}],"termid":"MONDO:0013306","terms_by_termid":{"MONDO:0013306":null},"xrefs":{"Monarch":{"xref_id":"0013306"}}}


id: MONDO:0023152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrocartilaginous embolism (FCE) is a rare type of embolism (sudden blocking of an artery) that occurs in the spinal cord. FCE occurs when materials that are usually found within the vertebral disk of the spine enter into the nearby vascular system (veins and arteries) and block one of the spinal cord vessels. The signs and symptoms of FCE often develop after a minor or even unnoticed btriggering eventb such as lifting, straining, or falling. Symptoms of FCE may include neck and/or back pain, progressive muscle weakness, and paralysis.The exact underlying cause of FCE is poorly understood. Most cases occur sporadically in people with no family history of the disease. Diagnosis is based on imaging of the spinal cord and ruling out other causes of a blockage of the vascular system within the spinal cord. Treatment is generally focused on preventing possible complications and improving quality of life with medications and physical therapy.","definition_xrefs":["GARD:0009718"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrocartilaginous embolism","secondary_identifiers":["MESH:C537927","UMLS:C2931666","MEDGEN:419466"],"synonyms":[{"name":"embolism, fibrocartilaginous","type":"related"}],"termid":"MONDO:0023152","xrefs":{"Monarch":{"xref_id":"0023152"}}}


id: PBO:0002946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex subunit Spt20","termid":"PBO:0002946"}


id: PBO:0061501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative regulator of reactive oxygen species","termid":"PBO:0061501"}


id: PBO:0029971
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_cycle_regulation_during_cellular_response_to_ionizing_radiation","termid":"PBO:0029971"}


id: PR:Q9UUB7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swi5 gene.","definition_xrefs":["UniProtKB:Q9UUB7","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":"mating-type switching protein swi5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC409.03","synonyms":[{"name":"DNA repair protein swi5 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-swi5","type":"exact"}],"termid":"PR:Q9UUB7"}


id: GO:0102427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: allocryptopine + NADPH + O2 + H+ = 6-hydroxy-allocryptopine + NADP + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete allocryptopine 6-hydroxylase activity (obsolete GO:0102427)","termid":"GO:0102427"}


id: GO:0060768
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of epithelial cell proliferation that contributes to the progression of the prostate gland over time.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"regulates","term_name":"epithelial cell proliferation involved in prostate gland development","termid":"GO:0060767"}],"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 epithelial cell proliferation involved in prostate gland development","termid":"GO:0060768"}


id: PBO:0052526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 41","termid":"PBO:0052526"}


id: FYPO:0005289
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 maintenance of the mitotic actomyosin contractile ring in the correct location is abnormal.","definition_xrefs":["PMID:26132084","PomBase:mah","GO:0032189"],"direct_ancestors":[{"relation_name":"has_output","term_name":"actomyosin contractile ring displaced from midpoint","termid":"FYPO:0002026"},{"relation_name":"is_a","term_name":"abnormal cytokinesis","termid":"FYPO:0000032"},{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0000631","FYPO:0000032","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"actomyosin contractile ring sliding","synonyms":[{"name":"abnormal cytokinetic ring anchoring involved in mitotic cell cycle","type":"related"},{"name":"abnormal maintenance of mitotic actomyosin contractile ring localization","type":"exact"},{"name":"actomyosin contractile ring sliding during mitotic cell cycle","type":"related"},{"name":"actomyosin contractile ring sliding during vegetative growth","type":"exact"}],"termid":"FYPO:0005289"}


id: PBO:0113218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Moonlighting protein component of both the ERMES and SAM complex; subunit of the ERMES complex that acts as a molecular tether between the mitochondria and the ER, necessary for both efficient phospholipid exchange between organelles and for mitophagy; SAM/TOB complex subunit that functions in the assembly of outer membrane beta-barrel proteins; involved in mitochondrial inheritance and morphology; ERMES complex often co-localizes with peroxisomes adjacent to mitochondria-ER junctions","termid":"PBO:0113218"}


id: FYPO:0006507
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which duplication of DNA sequences in the subtelomeric region occur more frequently than in wild type cells during G0 phase.","definition_xrefs":["PMID:29167439","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased gross chromosomal rearrangement","termid":"FYPO:0001740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000641","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased subtelomeric DNA amplification during G0","synonyms":[{"name":"increased occurrence of subtelomeric DNA amplification during G0","type":"exact"},{"name":"increased subtelomeric DNA amplification during cell quiescence","type":"exact"},{"name":"increased subtelomeric DNA amplification during quiescence","type":"exact"},{"name":"increased subtelomeric DNA sequence duplication during G0","type":"exact"},{"name":"increased subtelomeric amplification during G0","type":"exact"}],"termid":"FYPO:0006507"}


id: FYPO:0002489
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype in which a spore lyses, i.e. the plasma membrane ruptures and cytoplasm is lost. Note that in fission yeast cell lysis, the integrity of the cell wall is also compromised.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable spore","termid":"FYPO:0002151"},{"relation_name":"is_a","term_name":"inviable spore","termid":"FYPO:0002151"},{"relation_name":"is_a","term_name":"cell lysis","termid":"FYPO:0002488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"spore lysis","synonyms":[{"name":"inviable, lysed spore","type":"exact"},{"name":"spore cytolysis","type":"exact"}],"termid":"FYPO:0002489"}


id: PBO:0039606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanyl aminopeptidase, membrane","termid":"PBO:0039606"}


id: PBO:0083063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydroorotase; catalyzes the third enzymatic step in the de novo biosynthesis of pyrimidines, converting carbamoyl-L-aspartate into dihydroorotate","termid":"PBO:0083063"}


id: PBO:0081874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 816","termid":"PBO:0081874"}


id: PBO:0116644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARF like GTPase 2","termid":"PBO:0116644"}


id: MONDO:0018272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A small cell carcinoma that involves the ovary.","definition_xrefs":["MONDO:patterns/location"],"gene_count":0,"genotype_count":0,"name":"obsolete small cell carcinoma of the ovary (obsolete MONDO:0018272)","termid":"MONDO:0018272","xrefs":{"Monarch":{"xref_id":"0018272"}}}


id: PR:O94684
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pmh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94684"],"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":"RNA polymerase II transcription factor B subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC776.18c","synonyms":[{"name":"CDK-activating kinase assembly factor MAT1 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RING finger protein pmh1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase II transcription factor B 38 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase II transcription factor B p38 subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pmh1","type":"exact"}],"termid":"PR:O94684"}


id: GO:0008983
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + protein L-glutamate = S-adenosyl-L-homocysteine + protein L-glutamate 5-methyl ester; this reaction is the methylation of peptidyl-L-glutamate to form peptidyl-L-glutamate 5-methyl ester.","definition_xrefs":["EC:2.1.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"},{"relation_name":"is_a","term_name":"protein carboxyl O-methyltransferase activity","termid":"GO:0051998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016741","GO:0003674","GO:0008276","GO:0140096","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"protein-glutamate O-methyltransferase activity","secondary_identifiers":["RESID:AA0072","RHEA:24452","MetaCyc:CHER-RXN"],"synonyms":[{"name":"MCP methyltransferase I","type":"related"},{"name":"MCP methyltransferase II","type":"related"},{"name":"S-adenosyl-L-methionine:protein-L-glutamate O-methyltransferase activity","type":"related"},{"name":"S-adenosylmethionine-glutamyl methyltransferase activity","type":"related"},{"name":"S-adenosylmethionine:protein-carboxyl O-methyltransferase activity","type":"related"},{"name":"methyl-accepting chemotaxis protein O-methyltransferase activity","type":"narrow"},{"name":"methyl-accepting chemotaxis protein methyltransferase II","type":"related"},{"name":"protein O-methyltransferase activity","type":"related"},{"name":"protein carboxyl-O-methyltransferase activity","type":"related"},{"name":"protein carboxyl-methylase activity","type":"related"},{"name":"protein carboxylmethyltransferase II","type":"related"},{"name":"protein carboxymethylase activity","type":"related"},{"name":"protein carboxymethyltransferase activity","type":"related"},{"name":"protein glutamate O-methylase activity","type":"exact"},{"name":"protein glutamate O-methyltransferase activity","type":"exact"},{"name":"protein methylase II","type":"related"},{"name":"protein(aspartate)methyltransferase activity","type":"related"},{"name":"protein(carboxyl)methyltransferase activity","type":"related"}],"termid":"GO:0008983"}


id: GO:0034475
data:
  {"annotated_genes":["SJAG_00854","SJAG_03179","SJAG_04321","SJAG_04818","SJAG_02156","SJAG_01176","SJAG_04824","SJAG_04527","SJAG_04084","SJAG_04153","SJAG_01521"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70901,71268,72078,72890,73396,74141,74793,75897,76429,77265,88125],"is_not":false,"summary":null,"term":"GO:0034475"}]},"cv_name":"biological_process","definition":"Any process involved in forming the mature 3' end of a U4 snRNA molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA 3'-end processing","termid":"GO:0034472"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00854":null,"SJAG_01176":null,"SJAG_01521":null,"SJAG_02156":null,"SJAG_03179":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04321":null,"SJAG_04527":null,"SJAG_04818":null,"SJAG_04824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016073"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016073"],"is_obsolete":false,"name":"U4 snRNA 3'-end processing","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"U4 snRNA 3' end processing","type":"exact"}],"termid":"GO:0034475","terms_by_termid":{"GO:0034475":null}}


id: GO:0008682
data:
  {"annotated_genes":["SJAG_00459"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73817],"is_not":false,"summary":null,"term":"GO:0008682"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 6-methoxy-3-methyl-2-all-trans-polyprenyl-1,4-benzoquinol + donor-H2 + O2 = acceptor + a 3-demethylubiquinol + H2O.","definition_xrefs":["RHEA:50908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"3-demethoxyubiquinol 3-hydroxylase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:1.14.99.60","MetaCyc:RXN-18458"],"synonyms":[{"name":"2-octoprenyl-3-methyl-6-methoxy-1,4-benzoquinone hydroxylase activity","type":"narrow"},{"name":"demethoxy-ubiquinone hydroxylase","type":"related"},{"name":"demethoxyubiquinone monooxygenase","type":"related"}],"termid":"GO:0008682","terms_by_termid":{"GO:0008682":null}}


id: GO:0035410
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 5alpha-dihydrotestosterone + NAD+ = 5alpha-androstane-3,17-dione + NADH.","definition_xrefs":["GOC:ecd","PMID:4152755"],"gene_count":0,"genotype_count":0,"name":"obsolete dihydrotestosterone 17-beta-dehydrogenase activity (obsolete GO:0035410)","termid":"GO:0035410"}


id: PBO:0060662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal calcium sensor 1","termid":"PBO:0060662"}


id: MONDO:0015726
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 14","termid":"MONDO:0016964"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 14q","secondary_identifiers":["GARD:18739","MESH:C538034","MEDGEN:444122","Orphanet:1705","UMLS:C2931702"],"synonyms":[{"name":"distal duplication 14q","type":"exact"},{"name":"distal trisomy type 14q","type":"exact"},{"name":"telomeric duplication 14q","type":"exact"},{"name":"trisomy 14qter","type":"exact"}],"termid":"MONDO:0015726","xrefs":{"Monarch":{"xref_id":"0015726"}}}


id: FYPO:0007913
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 organelle localization is normal.","direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000138","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal organelle localization","termid":"FYPO:0007913"}


id: PBO:0045301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 3","termid":"PBO:0045301"}


id: MONDO:0015142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ataxia syndrome (obsolete MONDO:0015142)","termid":"MONDO:0015142","xrefs":{"Monarch":{"xref_id":"0015142"}}}


id: SO:0002187
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An insertion of sequence from the HERV family of mobile elements with respect to a reference.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"Endogenous_Retrovirus_LTR_retrotransposon","termid":"SO:0002268"},{"relation_name":"is_a","term_name":"mobile_element_insertion","termid":"SO:0001837"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERV_insertion","synonyms":[{"name":"HERV insertion","type":"exact"}],"termid":"SO:0002187"}


id: PBO:0091019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multispanning membrane protein, CTNS/PQ domain protein","termid":"PBO:0091019"}


id: PBO:0047227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 229 member A","termid":"PBO:0047227"}


id: MONDO:0041751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lepromatous form of leprosy that is characterized by numerous infiltrated skin lesions displaying high bacillary loads, impaired peripheral nerves, possible involvement of internal organs, and a Th2-mediated immune response.","definition_xrefs":["PMID:27219008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leprosy","termid":"MONDO:0005124"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multibacillary leprosy","secondary_identifiers":["MESH:D056006","icd11.foundation:1123804548","SCTID:416257001","UMLS:C1562585","MEDGEN:288329"],"synonyms":[{"name":"lepromatous leprosy","type":"related"},{"name":"multibacillary leprosy","type":"exact"}],"termid":"MONDO:0041751","xrefs":{"Monarch":{"xref_id":"0041751"}}}


id: GO:1905251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any epidermal growth factor receptor signaling pathway that is involved in heart process.","definition_xrefs":["GOC:bc","GOC:BHF","PMID:23069713","GO_REF:0000060","GOC:TermGenie","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal growth factor receptor signaling pathway","termid":"GO:0007173"},{"relation_name":"part_of","term_name":"heart process","termid":"GO:0003015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"epidermal growth factor receptor signaling pathway involved in heart process","synonyms":[{"name":"EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"EGFR signaling pathway involved in heart process","type":"exact"},{"name":"ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"ERBB1 signaling pathway involved in heart process","type":"exact"},{"name":"epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"epidermal growth factor receptor signalling pathway involved in heart process","type":"exact"},{"name":"receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"exact"}],"termid":"GO:1905251"}


id: MONDO:0100122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive mucolipidosis disorder caused by bi-allelic variants in the GNPTAB gene. Symptoms of this condition occur across a clinical spectrum including mucolipidosis type II (ML II) and mucolipidosis type III alpha/beta (ML IIIα/β), and phenotypes intermediate between ML II and ML IIIα/β.","definition_xrefs":["PMID:32651481","PMID:20301728"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucolipidosis","termid":"MONDO:0019248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"GNPTAB-mucolipidosis","synonyms":[{"name":"GNPTAB-related disorder","type":"exact"},{"name":"UDP-N-acetylglucosamine-1-phosphotransferase subunit alpha/beta deficiency","type":"exact"}],"termid":"MONDO:0100122","xrefs":{"Monarch":{"xref_id":"0100122"}}}


id: GO:0045109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Control of the spatial distribution of intermediate filaments; includes organizing filaments into meshworks, bundles, or other structures, as by cross-linking.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament cytoskeleton organization","termid":"GO:0045104"},{"relation_name":"is_a","term_name":"supramolecular fiber organization","termid":"GO:0097435"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007010","GO:0008150"],"is_obsolete":false,"name":"intermediate filament organization","synonyms":[{"name":"intermediate filament organisation","type":"exact"}],"termid":"GO:0045109"}


id: GO:0017177
data:
  {"annotated_genes":["SJAG_03280","SJAG_03535"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76501,78171],"is_not":false,"summary":null,"term":"GO:0017177"}]},"cv_name":"cellular_component","definition":"A heterodimeric complex that catalyzes the trimming of glucose residues from N-linked core glycans on newly synthesized glycoproteins.","definition_xrefs":["PMID:10464333","PMID:8910335"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"},{"relation_name":"is_a","term_name":"glucosidase complex","termid":"GO:1902687"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03280":null,"SJAG_03535":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"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575","GO:0005783"],"is_obsolete":false,"name":"glucosidase II complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"alpha-glucosidase II complex","type":"related"}],"termid":"GO:0017177","terms_by_termid":{"GO:0017177":null}}


id: PBO:0017633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inorganic pyrophosphatase Ipp1 (predicted)","termid":"PBO:0017633"}


id: GO:0047822
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + hypotaurine + NADPH + O2 = H2O + NADP+ + taurine.","definition_xrefs":["RHEA:69819"],"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: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":"hypotaurine monooxygenase activity","secondary_identifiers":["MetaCyc:HYPOTAURINE-DEHYDROGENASE-RXN","Reactome:R-HSA-1655453"],"synonyms":[{"name":"hypotaurine dehydrogenase activity","type":"exact"}],"termid":"GO:0047822"}


id: SO:0001337
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Methylwyosine is a modified guanosine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_guanosine","termid":"SO:0001276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylwyosine","secondary_identifiers":["RNAMOD:042"],"synonyms":[{"name":"mimG","type":"exact"}],"termid":"SO:0001337"}


id: PBO:0029846
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_rDNA","termid":"PBO:0029846"}


id: MONDO:0013065
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ovarian failure in which the cause of the disease is a mutation in the NR5A1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"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":"premature ovarian failure 7","secondary_identifiers":["UMLS:C2751825","DOID:0080864","MEDGEN:414115","MESH:C567838","OMIM:612964"],"synonyms":[{"name":"NR5A1 primary ovarian failure","type":"exact"},{"name":"Pof7","type":"related"},{"name":"adrenal insufficiency, Nr5A1-related","type":"related"},{"name":"adrenocortical insufficiency","type":"broad"},{"name":"premature ovarian failure 7","type":"exact"},{"name":"premature ovarian failure type 7","type":"exact"},{"name":"primary ovarian failure caused by mutation in NR5A1","type":"exact"}],"termid":"MONDO:0013065","xrefs":{"Monarch":{"xref_id":"0013065"}}}


id: GO:0004130
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 ferrocytochrome c + hydrogen peroxide = 2 ferricytochrome c + 2 H2O.","definition_xrefs":["EC:1.11.1.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxidase activity","termid":"GO:0004601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"cytochrome-c peroxidase activity","secondary_identifiers":["RHEA:16581","MetaCyc:CYTOCHROME-C-PEROXIDASE-RXN"],"synonyms":[{"name":"apocytochrome c peroxidase activity","type":"related"},{"name":"cytochrome c peroxidase activity","type":"related"},{"name":"cytochrome c-551 peroxidase activity","type":"related"},{"name":"cytochrome c-H2O oxidoreductase activity","type":"related"},{"name":"cytochrome peroxidase activity","type":"related"},{"name":"ferrocytochrome-c:hydrogen-peroxide oxidoreductase activity","type":"related"},{"name":"mesocytochrome c peroxidase azide","type":"related"},{"name":"mesocytochrome c peroxidase cyanate","type":"related"},{"name":"mesocytochrome c peroxidase cyanide","type":"related"}],"termid":"GO:0004130"}


id: GO:1905586
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of outer hair cell apoptotic process.","definition_xrefs":["GOC:TermGenie","PMID:24472721","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of neuron apoptotic process","termid":"GO:0043524"},{"relation_name":"is_a","term_name":"regulation of outer hair cell apoptotic process","termid":"GO:1905585"},{"relation_name":"negatively_regulates","term_name":"outer hair cell apoptotic process","termid":"GO:1905584"}],"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 outer hair cell apoptotic process","synonyms":[{"name":"down regulation of cochlear outer hair cell apoptosis","type":"narrow"},{"name":"down regulation of cochlear outer hair cell apoptotic process","type":"exact"},{"name":"down regulation of outer hair cell apoptosis","type":"narrow"},{"name":"down regulation of outer hair cell apoptotic process","type":"exact"},{"name":"down-regulation of cochlear outer hair cell apoptosis","type":"narrow"},{"name":"down-regulation of cochlear outer hair cell apoptotic process","type":"exact"},{"name":"down-regulation of outer hair cell apoptosis","type":"narrow"},{"name":"down-regulation of outer hair cell apoptotic process","type":"exact"},{"name":"downregulation of cochlear outer hair cell apoptosis","type":"narrow"},{"name":"downregulation of cochlear outer hair cell apoptotic process","type":"exact"},{"name":"downregulation of outer hair cell apoptosis","type":"narrow"},{"name":"downregulation of outer hair cell apoptotic process","type":"exact"},{"name":"inhibition of cochlear outer hair cell apoptosis","type":"narrow"},{"name":"inhibition of cochlear outer hair cell apoptotic process","type":"narrow"},{"name":"inhibition of outer hair cell apoptosis","type":"narrow"},{"name":"inhibition of outer hair cell apoptotic process","type":"narrow"},{"name":"negative regulation of cochlear outer hair cell apoptosis","type":"narrow"},{"name":"negative regulation of cochlear outer hair cell apoptotic process","type":"exact"},{"name":"negative regulation of outer hair cell apoptosis","type":"narrow"}],"termid":"GO:1905586"}


id: MONDO:0020406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complete atrioventricular canal","termid":"MONDO:0015273"}],"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":"complete atrioventricular canal-left heart obstruction syndrome","secondary_identifiers":["Orphanet:99066"],"synonyms":[{"name":"CAVC type A","type":"exact"},{"name":"CAVC-left heart obstruction syndrome","type":"exact"},{"name":"complete atrioventricular canal type A","type":"exact"}],"termid":"MONDO:0020406","xrefs":{"Monarch":{"xref_id":"0020406"}}}


id: PBO:0031049
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_modification","termid":"PBO:0031049"}


id: FYPO:0004149
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of pyridoxal kinase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257","FYPO:0000654"],"is_obsolete":false,"name":"normal pyridoxal kinase activity","termid":"FYPO:0004149"}


id: PBO:0045427
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 7","termid":"PBO:0045427"}


id: GO:0140560
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalyzes the reaction: UDP-alpha-D-xylose + [protein with EGF-like domain]-3-O-(alpha-D-xylosyl-(1->3)-beta-D-glucosyl)-L-serine = UDP + [protein with EGF-like domain]-3-O-(alpha-D-xylosyl-(1->3)-alpha-D-xylosyl-(1->3)-beta-D-glucosyl)-L-serine. The enzyme, found in animals and insects, is involved in the biosynthesis of the alpha-D-xylosyl-(1->3)-alpha-D-xylosyl-(1->3)- beta-D-glucosyl trisaccharide on epidermal growth factor-like (EGF- like) domains.","definition_xrefs":["PMID:8982869","RHEA:22820","PMID:22117070"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-xylosyltransferase activity","termid":"GO:0035252"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"xylosyl alpha-1,3-xylosyltransferase activity","secondary_identifiers":["EC:2.4.2.62"],"termid":"GO:0140560"}


id: MONDO:0014737
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dehydrated hereditary stomatocytosis in which the cause of the disease is a mutation in the KCNN4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hemolytic anemia","termid":"MONDO:0003689"},{"relation_name":"is_a","term_name":"dehydrated hereditary stomatocytosis","termid":"MONDO:0017910"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"dehydrated hereditary stomatocytosis 2","secondary_identifiers":["UMLS:C4225242","GARD:16152","DOID:0111577","OMIM:616689","MEDGEN:908701"],"synonyms":[{"name":"DHS2","type":"exact"},{"name":"Dehydrated hereditary stomatocytosis 2","type":"exact"},{"name":"Dehydrated hereditary stomatocytosis type 2","type":"exact"},{"name":"Desiccytosis Gardos","type":"related"},{"name":"KCNN4 dehydrated hereditary stomatocytosis","type":"exact"},{"name":"dehydrated hereditary stomatocytosis 2; DHS2","type":"exact"},{"name":"dehydrated hereditary stomatocytosis caused by mutation in KCNN4","type":"exact"},{"name":"xerocytosis Gardos","type":"related"}],"termid":"MONDO:0014737","xrefs":{"Monarch":{"xref_id":"0014737"}}}


id: GO:0016323
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of the plasma membrane that includes the basal end and sides of the cell. Often used in reference to animal polarized epithelial membranes, where the basal membrane is the part attached to the extracellular matrix, or in plant cells, where the basal membrane is defined with respect to the zygotic axis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"},{"relation_name":"part_of","term_name":"basal plasma membrane","termid":"GO:0009925"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"basolateral plasma membrane","termid":"GO:0016323"}


id: PBO:0062911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purinergic receptor P2X 4","termid":"PBO:0062911"}


id: FYPO:0000905
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 ubiquitination of one or more specific proteins, or of specific protein sites, is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification during vegetative growth","termid":"FYPO:0000329"},{"relation_name":"is_a","term_name":"abnormal protein ubiquitination","termid":"FYPO:0006977"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0000002","FYPO:0002494","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal protein ubiquitination during vegetative growth","synonyms":[{"name":"abnormal protein ubiquitination during mitotic cell cycle","type":"related"},{"name":"abnormal protein ubiquitinylation during vegetative growth","type":"related"},{"name":"abnormal protein ubiquitylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000905"}


id: PBO:0059678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 44","termid":"PBO:0059678"}


id: GO:0019835
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The rupture of cell membranes and the loss of cytoplasm.","definition_xrefs":["UniProtKB-KW:KW-0204"],"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":"cytolysis","secondary_identifiers":["Wikipedia:Cytolysis"],"synonyms":[{"name":"autolysin activity","type":"related"},{"name":"bacteriocin activity","type":"related"},{"name":"bacteriolytic toxin activity","type":"related"},{"name":"holin","type":"related"},{"name":"lysin activity","type":"related"},{"name":"lysis","type":"broad"},{"name":"necrosis","type":"related"}],"termid":"GO:0019835"}


id: GO:0072229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric proximal convoluted tubule over time, from its formation to the mature structure. The metanephric proximal convoluted tubule is the most proximal portion of the metanephric proximal tubule and extends from the metanephric glomerular capsule to the metanephric proximal straight tubule.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proximal convoluted tubule development","termid":"GO:0072019"},{"relation_name":"is_a","term_name":"metanephric nephron tubule development","termid":"GO:0072234"},{"relation_name":"part_of","term_name":"metanephric proximal tubule development","termid":"GO:0072237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric proximal convoluted tubule development","termid":"GO:0072229"}


id: MONDO:0010282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mycobacterium tuberculosis, susceptibility","termid":"MONDO:0000070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mycobacterium tuberculosis, susceptibility to, X-linked","secondary_identifiers":["MEDGEN:357096","OMIM:300259","UMLS:C1866629"],"synonyms":[{"name":"MTBSX","type":"related"},{"name":"Mycobacterium tuberculosis, susceptibility, X-linked","type":"exact"}],"termid":"MONDO:0010282","xrefs":{"Monarch":{"xref_id":"0010282"}}}


id: GO:0140884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts a type II interferon-mediated signaling in the host organism. Type II interferon is also known as interferon-gamma.","definition_xrefs":["PMID:28901902"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host interferon-mediated signaling pathway","termid":"GO:0140886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host type II interferon-mediated signaling pathway","synonyms":[{"name":"negative regulation by virus of host type II interferon-mediated signaling pathway","type":"exact"},{"name":"suppression by virus of host type II IFN-mediated signaling pathway","type":"exact"},{"name":"suppression by virus of host type II interferon-mediated signaling pathway","type":"narrow"},{"name":"suppression by virus of host type II interferon-mediated signalling pathway","type":"exact"}],"termid":"GO:0140884"}


id: MONDO:0850470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma that is categorized as MCD with high probability by the LymphGen algorithm. This is based on a combination of genetic features and MCD DLBCLs often, but do not always, have the most common hot spot mutation in MYD88 (L265P) and/or activating mutations in CD79B. This subgroup also commonly has mutations due to aberrant somatic hypermutation affecting PIM1 and/or ETV6, which can be coding or non-coding.","definition_xrefs":["DOID:0081066"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"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:0005570","MONDO:0005046"],"is_obsolete":false,"name":"MCD diffuse large B-cell lymphoma","secondary_identifiers":["MEDGEN:1669702","UMLS:C4725002"],"termid":"MONDO:0850470","xrefs":{"Monarch":{"xref_id":"0850470"}}}


id: GO:0004019
data:
  {"annotated_genes":["SJAG_00044"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78618],"is_not":false,"summary":null,"term":"GO:0004019"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate + GTP + IMP = N(6)-(1,2-dicarboxyethyl)-AMP + GDP + 3 H+ + phosphate.","definition_xrefs":["RHEA:15753","EC:6.3.4.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00044":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"adenylosuccinate synthase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:ADENYLOSUCCINATE-SYNTHASE-RXN","KEGG_REACTION:R01135","Reactome:R-HSA-111524"],"synonyms":[{"name":"IMP--aspartate ligase activity","type":"related"},{"name":"IMP:L-aspartate ligase (GDP-forming)","type":"related"},{"name":"adenylosuccinate synthetase activity","type":"related"},{"name":"succino-AMP synthetase activity","type":"related"},{"name":"succinoadenylic kinosynthetase activity","type":"related"}],"termid":"GO:0004019","terms_by_termid":{"GO:0004019":null}}


id: MONDO:0014274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"hematologic disorder","termid":"MONDO:0005570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"L-ferritin deficiency","secondary_identifiers":["MEDGEN:816420","Orphanet:440731","GARD:17748","UMLS:C3810090","OMIM:615604"],"synonyms":[{"name":"L-ferritin deficiency","type":"exact"},{"name":"L-ferritin deficiency, dominant and recessive","type":"exact"},{"name":"LFTD","type":"related"}],"termid":"MONDO:0014274","xrefs":{"Monarch":{"xref_id":"0014274"}}}


id: GO:0050978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive an electrical stimulus relating to a magnetic field, convert it to a molecular signal, and recognize and characterize the signal. Movement in a magnetic field results in an induced electric field, which can be perceived by organisms such as elasmobranch fish.","definition_xrefs":["PMID:15886990","GOC:ai","Wikipedia:Magnetoception"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception of electrical stimulus","termid":"GO:0050952"},{"relation_name":"is_a","term_name":"magnetoreception","termid":"GO:0050958"}],"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":"magnetoreception by sensory perception of electrical stimulus","synonyms":[{"name":"magnetoreception by electrical stimulus","type":"exact"},{"name":"magnetoreception through electrical stimulus","type":"exact"},{"name":"magnetoreception, sensory perception of electrical stimulus","type":"exact"},{"name":"magnetoreception, using electrical stimulus","type":"exact"}],"termid":"GO:0050978"}


id: PBO:0025446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein, CENP-P ortholog Fta2","termid":"PBO:0025446"}


id: PBO:0065720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prader Willi/Angelman region RNA 6","termid":"PBO:0065720"}


id: MONDO:0012299
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nanophthalmia in which the cause of the disease is a mutation in the MFRP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nanophthalmia","termid":"MONDO:0005514"}],"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":"nanophthalmos 2","secondary_identifiers":["GARD:18626","MESH:C563700","OMIM:609549","UMLS:C1836006","MEDGEN:372177"],"synonyms":[{"name":"MFRP nanophthalmia","type":"exact"},{"name":"NNO2","type":"related"},{"name":"Nanophthalmia 2","type":"related"},{"name":"nanophthalmia caused by mutation in MFRP","type":"exact"},{"name":"nanophthalmos 2","type":"exact"},{"name":"nanophthalmos type 2","type":"exact"},{"name":"nanophthalmos, autosomal recessive","type":"related"}],"termid":"MONDO:0012299","xrefs":{"Monarch":{"xref_id":"0012299"}}}


id: PBO:0077406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 140","termid":"PBO:0077406"}


id: GO:0023053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a mechanical signal causes activation of a receptor.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal initiation by mechanical effect (obsolete GO:0023053)","synonyms":[{"name":"signal initiation by mechanical effect","type":"exact"}],"termid":"GO:0023053"}


id: PBO:0085037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-catalytic subunit of the NatC N-terminal acetyltransferase; required for replication of dsRNA virus; expression is glucose-repressible; human NatC ortholog, Naa35, requires co-expression of the human catalytic subunit, Naa30, to functionally complement the null allele","termid":"PBO:0085037"}


id: GO:0060122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a stereocilium. A stereocilium is an actin-based protrusion from the apical surface of inner ear receptor cells.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection development","termid":"GO:0031175"},{"relation_name":"part_of","term_name":"inner ear receptor cell development","termid":"GO:0060119"}],"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":"inner ear receptor cell stereocilium organization","synonyms":[{"name":"inner ear hair cell receptor stereocilium organization","type":"exact"},{"name":"inner ear receptor stereocilium organisation","type":"exact"},{"name":"inner ear receptor stereocilium organization and biogenesis","type":"related"}],"termid":"GO:0060122"}


id: PBO:0089072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GID complex WD repeat subunit Gid7","termid":"PBO:0089072"}


id: GO:0030246
data:
  {"annotated_genes":["SJAG_01858","SJAG_02131","SJAG_02951","SJAG_01991","SJAG_00667","SJAG_03824","SJAG_03535","SJAG_00839","SJAG_03280","SJAG_00981","SJAG_04571","SJAG_03818","SJAG_02839","SJAG_00530","SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57724,57880,60010,64985,67770,67824,93308],"is_not":false,"summary":null,"term":"GO:0030246"},{"annotations":[60368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030248"},{"annotations":[57174,64287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005536"},{"annotations":[113569,118327,110545,79043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005537"},{"annotations":[118330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001065"},{"annotations":[69779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048029"},{"annotations":[99940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030247"}]},"cv_name":"molecular_function","definition":"Binding to a carbohydrate, which includes monosaccharides, oligosaccharides and polysaccharides as well as substances derived from monosaccharides by reduction of the carbonyl group (alditols), by oxidation of one or more hydroxy groups to afford the corresponding aldehydes, ketones, or carboxylic acids, or by replacement of one or more hydroxy group(s) by a hydrogen atom. Cyclitols are generally not regarded as carbohydrates.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00530":null,"SJAG_00667":null,"SJAG_00839":null,"SJAG_00981":null,"SJAG_01858":null,"SJAG_01991":null,"SJAG_02131":null,"SJAG_02839":null,"SJAG_02951":null,"SJAG_03280":null,"SJAG_03535":null,"SJAG_03818":null,"SJAG_03824":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_04571":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"carbohydrate binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0005529"],"synonyms":[{"name":"selectin","type":"related"},{"name":"sugar binding","type":"exact"}],"termid":"GO:0030246","terms_by_termid":{"GO:0005536":null,"GO:0005537":null,"GO:0030246":null,"GO:0030247":null,"GO:0030248":null,"GO:0048029":null,"GO:2001065":null}}


id: GO:0045832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of light-activated channel activity.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of light-activated channel activity (obsolete GO:0045832)","synonyms":[{"name":"activation of light-activated channel activity","type":"narrow"},{"name":"stimulation of light-activated channel activity","type":"narrow"},{"name":"up regulation of light-activated channel activity","type":"exact"},{"name":"up-regulation of light-activated channel activity","type":"exact"},{"name":"upregulation of light-activated channel activity","type":"exact"}],"termid":"GO:0045832"}


id: MONDO:0003812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant epithelial tumor of the ovary characterized by the presence of glands and/or cysts lined by neoplastic cells that resemble endometrial cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrioid tumor","termid":"MONDO:0002480"},{"relation_name":"is_a","term_name":"malignant epithelial tumor of ovary","termid":"MONDO:0018364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian endometrial cancer","secondary_identifiers":["DOID:6212","NCIT:C40051","MEDGEN:276545","UMLS:C1518231"],"synonyms":[{"name":"endometrioid neoplasm of ovary","type":"exact"},{"name":"endometrioid tumor of ovary","type":"exact"},{"name":"endometrioid tumour of ovary","type":"exact"},{"name":"malignant ovarian endometrioid tumor","type":"exact"},{"name":"malignant ovarian endometrioid tumour","type":"exact"},{"name":"ovarian endometrioid neoplasm","type":"exact"},{"name":"ovary endometrioid tumor","type":"exact"},{"name":"ovary endometrioid tumour","type":"exact"},{"name":"ovary female reproductive endometrioid cancer","type":"exact"}],"termid":"MONDO:0003812","xrefs":{"Monarch":{"xref_id":"0003812"}}}


id: GO:0097292
data:
  {"annotated_genes":["SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving XMP, xanthosine monophosphate.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate metabolic process","termid":"GO:0009167"}],"gene_count":1,"genes_by_uniquename":{"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"XMP metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"XMP metabolism","type":"exact"}],"termid":"GO:0097292","terms_by_termid":{"GO:0032265":null}}


id: PBO:0072735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingosine-1-phosphate receptor 5","termid":"PBO:0072735"}


id: GO:0051714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the cytolysis by an organism of cells in another organism.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cytolysis in another organism (obsolete GO:0051714)","synonyms":[{"name":"activation of cytolysis of cells of another organism","type":"narrow"},{"name":"positive regulation of cytolysis in other organism","type":"exact"},{"name":"positive regulation of cytolysis of cells of another organism","type":"exact"},{"name":"stimulation of cytolysis of cells of another organism","type":"narrow"},{"name":"up regulation of cytolysis of cells of another organism","type":"exact"},{"name":"up-regulation of cytolysis of cells of another organism","type":"exact"},{"name":"upregulation of cytolysis of cells of another organism","type":"exact"}],"termid":"GO:0051714"}


id: PBO:0049089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 143 pseudogene","termid":"PBO:0049089"}


id: GO:2000489
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hepatic stellate cell activation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell activation","termid":"GO:0050865"},{"relation_name":"regulates","term_name":"hepatic stellate cell activation","termid":"GO:0035733"}],"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 hepatic stellate cell activation","termid":"GO:2000489"}


id: MONDO:0009874
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rabson-Mendenhall syndrome belongs to the group of extreme insulin-resistance syndromes (which also includes leprechaunism, the lipodystrophies, and the type A and B insulin resistance syndromes).","definition_xrefs":["Orphanet:769"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"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":"hypertrichosis","termid":"MONDO:0019280"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rabson-Mendenhall syndrome","secondary_identifiers":["OMIM:262190","GARD:226","ICD9:259.8","NORD:1645","UMLS:C0271695","NCIT:C131000","SCTID:33559001","MEDGEN:78783","icd11.foundation:1018973126","MESH:D056731"],"synonyms":[{"name":"Mendenhall syndrome","type":"related"},{"name":"Rabson-Mendenhall syndrome","type":"exact"},{"name":"pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities","type":"related"}],"termid":"MONDO:0009874","xrefs":{"Monarch":{"xref_id":"0009874"}}}


id: MONDO:0006869
data:
  {"annotated_genes":["SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007681"}]},"cv_name":"mondo","definition":"Goiter characterized by discrete tissue mass(es) that may or may not produce thyroid hormones.","definition_xrefs":["NCIT:C131437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"goiter","termid":"MONDO:0005397"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":0,"is_obsolete":false,"name":"nodular goiter","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:419153005","DOID:13197","HP:0005994","EFO:1001062","MEDGEN:42271","UMLS:C0018023","MedDRA:10018495","MESH:D006044"],"synonyms":[{"name":"goiter, nodular","type":"exact"},{"name":"nodular goiter","type":"exact"},{"name":"nodular goiter (disease)","type":"exact"},{"name":"nodular goitre (disease)","type":"exact"},{"name":"nodular goitre NOS","type":"related"}],"termid":"MONDO:0006869","terms_by_termid":{"MONDO:0007681":null},"xrefs":{"Monarch":{"xref_id":"0006869"}}}


id: MONDO:0003803
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the aortic valve.","direct_ancestors":[{"relation_name":"is_a","term_name":"heart valve disorder","termid":"MONDO:0002869"},{"relation_name":"is_a","term_name":"aortic disorder","termid":"MONDO:0005561"},{"relation_name":"is_a","term_name":"cardiac ventricle disorder","termid":"MONDO:0045001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"aortic valve disorder","secondary_identifiers":["ICD9:424.1","MEDGEN:226776","UMLS:C1260873","DOID:62","NCIT:C78650","EFO:0009531","ICD9:395"],"synonyms":[{"name":"aortic valve disease","type":"exact"},{"name":"aortic valve disease or disorder","type":"exact"},{"name":"aortic valve disorder","type":"exact"},{"name":"disease of aortic valve","type":"exact"},{"name":"disease or disorder of aortic valve","type":"exact"},{"name":"disorder of aortic valve","type":"exact"}],"termid":"MONDO:0003803","xrefs":{"Monarch":{"xref_id":"0003803"}}}


id: GO:0033869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a nucleoside bisphosphate, a compound consisting of a nucleobase linked to a deoxyribose or ribose sugar esterified with one phosphate group attached to each of two different hydroxyl groups on the sugar.","definition_xrefs":["GOC:mah","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside bisphosphate metabolic process","termid":"GO:0033865"},{"relation_name":"is_a","term_name":"nucleoside phosphate catabolic process","termid":"GO:1901292"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"nucleoside bisphosphate catabolic process","synonyms":[{"name":"nucleoside bisphosphate breakdown","type":"exact"},{"name":"nucleoside bisphosphate catabolism","type":"exact"},{"name":"nucleoside bisphosphate degradation","type":"exact"}],"termid":"GO:0033869"}


id: GO:0005482
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete vesicle targeting (obsolete GO:0005482)","synonyms":[{"name":"vesicle targeting","type":"exact"}],"termid":"GO:0005482"}


id: MONDO:0021503
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the gall bladder.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign digestive system neoplasm","termid":"MONDO:0000385"},{"relation_name":"is_a","term_name":"gallbladder neoplasm","termid":"MONDO:0021253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"benign neoplasm of gallbladder","secondary_identifiers":["SCTID:92117002","UMLS:C0345912","icd11.foundation:1439916526","NCIT:C4440","DOID:0080640","MEDGEN:87524"],"synonyms":[{"name":"benign gallbladder neoplasm","type":"exact"},{"name":"benign gallbladder tumor","type":"exact"},{"name":"benign gallbladder tumour","type":"exact"},{"name":"benign neoplasm of the gallbladder","type":"exact"},{"name":"benign tumor of gallbladder","type":"exact"},{"name":"benign tumor of the gallbladder","type":"exact"},{"name":"benign tumour of gallbladder","type":"exact"},{"name":"benign tumour of the gallbladder","type":"exact"},{"name":"gall bladder benign neoplasm","type":"exact"},{"name":"gallbladder benign neoplasm","type":"exact"},{"name":"gallbladder benign tumor","type":"exact"},{"name":"gallbladder benign tumour","type":"exact"}],"termid":"MONDO:0021503","xrefs":{"Monarch":{"xref_id":"0021503"}}}


id: GO:0033813
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + deacetylcephalosporin C = cephalosporin C + CoA.","definition_xrefs":["RHEA:23860","EC:2.3.1.175"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-acyltransferase activity","termid":"GO:0016408"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"deacetylcephalosporin-C acetyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.175-RXN","KEGG_REACTION:R03064"],"synonyms":[{"name":"CPC acetylhydrolase activity","type":"related"},{"name":"DAC acetyltransferase activity","type":"related"},{"name":"DAC-AT","type":"related"},{"name":"acetyl coenzyme A:DAC acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:DAC O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:DAC acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:deacetylcephalosporin-C O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:deacetylcephalosporin-C acetyltransferase activity","type":"related"},{"name":"cefG","type":"related"},{"name":"deacetylcephalosporin C acetyltransferase activity","type":"related"}],"termid":"GO:0033813"}


id: GO:1990259
data:
  {"annotated_genes":["SJAG_00943","SJAG_02350"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73040,109999],"is_not":false,"summary":null,"term":"GO:1990259"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + (histone H2A)-glutamine (position 104) = S-adenosyl-L-homocysteine + (histone H2A)-N5-methyl-glutamine (position 104). Note that this corresponds to Q105 in yeast.","definition_xrefs":["PMID:24352239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-glutamine N-methyltransferase activity","termid":"GO:0036009"},{"relation_name":"is_a","term_name":"histone H2A methyltransferase activity","termid":"GO:0140940"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00943":null,"SJAG_02350":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0008276","GO:0003674","GO:0016740","GO:0016741","GO:0140096"],"is_obsolete":false,"name":"histone H2AQ104 methyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"histone glutamine N-methyltransferase activity","type":"broad"},{"name":"histone glutamine methylase activity","type":"exact"},{"name":"histone glutamine methyltransferase activity","type":"exact"},{"name":"histone-glutamine N-methyltransferase activity","type":"exact"},{"name":"histone-glutamine methyltransferase activity","type":"exact"}],"termid":"GO:1990259","terms_by_termid":{"GO:1990259":null}}


id: GO:0098876
data:
  {"annotated_genes":["SJAG_00430","SJAG_00379","SJAG_01114","SJAG_01809","SJAG_01516","SJAG_01945","SJAG_00330","SJAG_01335","SJAG_03838","SJAG_00826","SJAG_03864","SJAG_03915","SJAG_04044","SJAG_02811","SJAG_00916","SJAG_02240","SJAG_01382","SJAG_04846","SJAG_02320","SJAG_03754","SJAG_02753","SJAG_02231","SJAG_04509","SJAG_03250","SJAG_02282","SJAG_03938","SJAG_00314","SJAG_00144","SJAG_04609","SJAG_03970","SJAG_00669","SJAG_00858","SJAG_04565","SJAG_04358","SJAG_01135"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79239,72770,72722,79228,79712,115453,115532,74388,80062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032456"},{"annotations":[91047,100917,118695,94654,112806,112585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099638"},{"annotations":[94907,106949,108599,69717,109382,106843,106211,112808,77187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043001"},{"annotations":[107186,99549,72306,77124,106093,57276,92030,100637,71623,75653,70430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006893"},{"annotations":[87835],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0042997"},{"annotations":[87644],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2001135"}]},"cv_name":"biological_process","definition":"The directed movement of substances to the plasma membrane in transport vesicles that fuse with the plasma membrane by exocytosis.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle-mediated transport","termid":"GO:0016192"},{"relation_name":"is_a","term_name":"localization within membrane","termid":"GO:0051668"}],"gene_count":35,"genes_by_uniquename":{"SJAG_00144":null,"SJAG_00314":null,"SJAG_00330":null,"SJAG_00379":null,"SJAG_00430":null,"SJAG_00669":null,"SJAG_00826":null,"SJAG_00858":null,"SJAG_00916":null,"SJAG_01114":null,"SJAG_01135":null,"SJAG_01335":null,"SJAG_01382":null,"SJAG_01516":null,"SJAG_01809":null,"SJAG_01945":null,"SJAG_02231":null,"SJAG_02240":null,"SJAG_02282":null,"SJAG_02320":null,"SJAG_02753":null,"SJAG_02811":null,"SJAG_03250":null,"SJAG_03754":null,"SJAG_03838":null,"SJAG_03864":null,"SJAG_03915":null,"SJAG_03938":null,"SJAG_03970":null,"SJAG_04044":null,"SJAG_04358":null,"SJAG_04509":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04846":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"vesicle-mediated transport to the plasma membrane","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0098876","terms_by_termid":{"GO:0006893":null,"GO:0032456":null,"GO:0042997":null,"GO:0043001":null,"GO:0099638":null,"GO:2001135":null}}


id: GO:0051311
data:
  {"annotated_genes":["SJAG_01837","SJAG_07002","SJAG_03926","SJAG_01224","SJAG_00418","SJAG_04076","SJAG_05295","SJAG_05266","SJAG_05220","SJAG_00794","SJAG_03683","SJAG_05319","SJAG_03698","SJAG_04259","SJAG_03989","SJAG_03327","SJAG_01805","SJAG_01278","SJAG_00918","SJAG_02731","SJAG_03220","SJAG_01211","SJAG_00678","SJAG_01775","SJAG_03437","SJAG_05019","SJAG_02346","SJAG_01371","SJAG_04508","SJAG_02814","SJAG_03217"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93588,87614],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"},{"annotations":[116869,93552,98405,107621,101121,115344,113585,87557,90036],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031619"},{"annotations":[116490],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904967"},{"annotations":[105278,100309,108946,110115,93569,115735,95320,113902,116726,97682,110158,101125,102226,98413,88890,107625,95072,90738,107306,89495,113035,109695,108689],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"A chromosome localization process whereby chromosomes are positioned in a specific order and orientation at the metaphase plate (spindle equator), during meiotic chromosome segregation. This alignment ensures that each daughter cell will receive the correct number of chromosomes during cell division.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metaphase chromosome alignment","termid":"GO:0051310"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"meiotic chromosome segregation","termid":"GO:0045132"}],"gene_count":31,"genes_by_uniquename":{"SJAG_00418":null,"SJAG_00678":null,"SJAG_00794":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01278":null,"SJAG_01371":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02346":null,"SJAG_02731":null,"SJAG_02814":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03327":null,"SJAG_03437":null,"SJAG_03683":null,"SJAG_03698":null,"SJAG_03926":null,"SJAG_03989":null,"SJAG_04076":null,"SJAG_04259":null,"SJAG_04508":null,"SJAG_05019":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05295":null,"SJAG_05319":null,"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0140013","GO:0051179","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"meiotic metaphase chromosome alignment","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"metaphase plate congression during meiosis","type":"exact"}],"termid":"GO:0051311","terms_by_termid":{"GO:0031619":null,"GO:0051455":null,"GO:0051456":null,"GO:1904967":null}}


id: PBO:0084944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multidrug transporter of the major facilitator superfamily; member of the 12-spanner drug:H(+) antiporter DHA1 family; involved in spore wall assembly; sequence similarity to DTR1 and QDR3, and the triple mutant dtr1 qdr1 qdr3 exhibits reduced dityrosine fluorescence relative to the single mutants; required for resistance to quinidine, ketoconazole, fluconazole, and barban; QDR1 has a paralog, AQR1, that arose from the whole genome duplication","termid":"PBO:0084944"}


id: PBO:0058609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6741","termid":"PBO:0058609"}


id: PR:O13858
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sle1 gene.","definition_xrefs":["UniProtKB:O13858","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":"eisosome protein sle1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1A6.07","synonyms":[{"name":"SEG1-like eisosome protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-sle1","type":"exact"}],"termid":"PR:O13858"}


id: PBO:0078658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon CTT) 11-1","termid":"PBO:0078658"}


id: PBO:0046761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome component 3","termid":"PBO:0046761"}


id: PBO:0064447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"podocan","termid":"PBO:0064447"}


id: MONDO:0003160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An adenocarcinoma with sebaceous differentiation. It presents as a painless mass and it may be multifocal. It grows in the ocular adnexae and in the skin of head and neck, trunk, genitals, and extremities. It is characterized by the presence of malignant cells with multivesicular and clear cytoplasm. It may recur and metastasize.","definition_xrefs":["NCIT:C40310"],"gene_count":0,"genotype_count":0,"name":"obsolete sebaceous carcinoma (obsolete MONDO:0003160)","termid":"MONDO:0003160","xrefs":{"Monarch":{"xref_id":"0003160"}}}


id: GO:1990910
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 stimulus indicating lowered oxygen tension combined with low atmospheric pressure. Hypoxia is defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95% and hypobaric is defined as atmospheric pressure below 0.74 atm (greater than 2,500 m above sea level).","definition_xrefs":["PMID:24590457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hypoxia","termid":"GO:0001666"}],"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 hypobaric hypoxia","termid":"GO:1990910"}


id: PBO:0067896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 198","termid":"PBO:0067896"}


id: PBO:0039728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein B receptor","termid":"PBO:0039728"}


id: PATO:0000947
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spheroid quality inhering in a bearer by virtue of the bearer's being oval with two axes of symmetry, as produced by a conical section.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"superelliptic","termid":"PATO:0002318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elliptic","synonyms":[{"name":"ellipse-shaped","type":"exact"},{"name":"ellipsoid","type":"exact"},{"name":"elliptical","type":"exact"},{"name":"oval","type":"related"},{"name":"ovoid","type":"related"}],"termid":"PATO:0000947"}


id: PBO:0047030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 95 member A","termid":"PBO:0047030"}


id: MONDO:0009267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1.","definition_xrefs":["Orphanet:77261"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lysosomal storage disease","termid":"MONDO:0002561"},{"relation_name":"excluded_subClassOf","term_name":"familial restrictive cardiomyopathy","termid":"MONDO:0016340"},{"relation_name":"excluded_subClassOf","term_name":"interstitial lung disease specific to childhood","termid":"MONDO:0017014"},{"relation_name":"excluded_subClassOf","term_name":"secondary avascular necrosis","termid":"MONDO:0018374"},{"relation_name":"excluded_subClassOf","term_name":"obsolete avascular necrosis of genetic origin (obsolete MONDO:0018384)","termid":"MONDO:0018384"},{"relation_name":"excluded_subClassOf","term_name":"sphingolipidosis","termid":"MONDO:0019255"},{"relation_name":"excluded_subClassOf","term_name":"cerebral lipidosis with dementia","termid":"MONDO:0020143"},{"relation_name":"is_a","term_name":"Gaucher disease","termid":"MONDO:0018150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005328","MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"Gaucher disease type III","secondary_identifiers":["UMLS:C0268251","GARD:2443","NANDO:2201212","DOID:0110959","SCTID:5963005","OMIM:231000","MEDGEN:78653","NANDO:1200059"],"synonyms":[{"name":"GD III","type":"exact"},{"name":"Gaucher disease type 3","type":"related"},{"name":"Gaucher disease type III","type":"exact"},{"name":"Gaucher disease, Norrbottnian type","type":"related"},{"name":"Gaucher disease, Subacute neuronopathic type","type":"exact"},{"name":"Gaucher disease, chronic neuronopathic type","type":"exact"},{"name":"Gaucher disease, juvenile and adult, cerebral","type":"exact"},{"name":"Gaucher disease, subacute neuronopathic type","type":"exact"},{"name":"Gaucher disease, type 3","type":"related"},{"name":"Gaucher disease, type 3A","type":"related"},{"name":"Gaucher disease, type 3B","type":"related"},{"name":"Gaucher disease, type III","type":"related"},{"name":"Gaucher's disease type III","type":"exact"},{"name":"Gd 3","type":"related"},{"name":"cerebral juvenile and adult form of Gaucher disease","type":"exact"},{"name":"chronic neuronopathic Gaucher disease","type":"exact"}],"termid":"MONDO:0009267","xrefs":{"Monarch":{"xref_id":"0009267"}}}


id: PBO:0053774
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 1019","termid":"PBO:0053774"}


id: MONDO:0013712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary pulmonary alveolar proteinosis in which the cause of the disease is a mutation in the CSF2RB gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfactant metabolism dysfunction, pulmonary, 5","secondary_identifiers":["GARD:15793","OMIM:614370","MEDGEN:482204","UMLS:C3280574"],"synonyms":[{"name":"CSF2RB hereditary pulmonary alveolar proteinosis","type":"exact"},{"name":"Csf2Rb deficiency","type":"related"},{"name":"Pap due to Csf2Rb deficiency","type":"related"},{"name":"SMDP5","type":"related"},{"name":"hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB","type":"exact"},{"name":"pulmonary alveolar proteinosis 5","type":"related"},{"name":"surfactant metabolism dysfunction, pulmonary, 5","type":"exact"},{"name":"surfactant metabolism dysfunction, pulmonary, type 5","type":"exact"}],"termid":"MONDO:0013712","xrefs":{"Monarch":{"xref_id":"0013712"}}}


id: PBO:0029567
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_septum_site_selection","termid":"PBO:0029567"}


id: PBO:0018044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TREX complex subunit Tho1 (predicted)","termid":"PBO:0018044"}


id: GO:0019910
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A mitochondrial complex of a regulatory and catalytic subunit that catalyzes the dephosphorylation and concomitant reactivation of the alpha subunit of the E1 component of the pyruvate dehydrogenase complex. An example of this component is found in Mus musculus.","definition_xrefs":["PMID:9395502","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase (lipoamide) phosphatase complex","termid":"GO:0045253"},{"relation_name":"is_a","term_name":"mitochondrial protein-containing complex","termid":"GO:0098798"},{"relation_name":"part_of","term_name":"mitochondrial matrix","termid":"GO:0005759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005737","GO:0005739"],"is_obsolete":false,"name":"mitochondrial pyruvate dehydrogenase (lipoamide) phosphatase complex","termid":"GO:0019910"}


id: FYPO:0000685
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular response phenotype in which pheromone-responsive positive regulation of transcription from an RNA polymerase II promoter occurs at a lower level of pheromone than normal.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete transcriptional response to pheromone at decreased pheromone level (obsolete FYPO:0000685)","synonyms":[{"name":"increased sensitivity of positive regulation of transcription from RNA polymerase II promoter by pheromones to pheromone","type":"related"},{"name":"increased transcriptional response to pheromone","type":"related"},{"name":"positive regulation of transcription from RNA polymerase II promoter by pheromones at decreased pheromone level","type":"exact"},{"name":"sensitive to pheromone","type":"related"}],"termid":"FYPO:0000685"}


id: FYPO:0004964
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 actin cortical patches than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cortical patch","termid":"FYPO:0003987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0004803","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"actin cortical patches present in decreased numbers","synonyms":[{"name":"F-actin patches present in decreased numbers","type":"exact"},{"name":"actin cortical patches present in decreased numbers during mitotic cell cycle","type":"related"},{"name":"actin cortical patches present in decreased numbers during vegetative growth","type":"exact"},{"name":"actin cortical patches present in reduced numbers","type":"exact"},{"name":"actin patches present in decreased numbers","type":"exact"},{"name":"decreased actin cortical patch formation during vegetative growth","type":"related"},{"name":"decreased number of actin cortical patches during vegetative growth","type":"exact"},{"name":"fewer actin cortical patches present during vegetative growth","type":"exact"}],"termid":"FYPO:0004964"}


id: PBO:0039163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate kinase 6 pseudogene 2","termid":"PBO:0039163"}


id: MONDO:0019482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dendritic cell sarcoma not otherwise specified (obsolete MONDO:0019482)","termid":"MONDO:0019482","xrefs":{"Monarch":{"xref_id":"0019482"}}}


id: PBO:0000767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO conjugating enzyme Hus5","termid":"PBO:0000767"}


id: MONDO:0018421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"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":"autosomal recessive spastic paraplegia type 69","secondary_identifiers":["MEDGEN:1679277","Orphanet:401830","UMLS:C5190577","GARD:21699"],"synonyms":[{"name":"SPG69","type":"exact"}],"termid":"MONDO:0018421","xrefs":{"Monarch":{"xref_id":"0018421"}}}


id: PBO:0082104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAA-peroxin; heterodimerizes with AAA-peroxin Pex1p and participates in the recycling of peroxisomal signal receptor Pex5p from the peroxisomal membrane to the cystosol; mutations in human PEX6 can lead to severe peroxisomal disorders and early death","termid":"PBO:0082104"}


id: MONDO:0018537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Squamous cell carcinoma of the gallbladder and extrahepatic biliary tract is a rare hepatic and biliary tract tumor, arising either in the gallbladder itself or in the epithelium lining the extrahepatic biliary tree, the cystic duct and peribiliary glands. It is characterized by a substantial keratinization with abundant keratohyalin pearls and central deposition of dense keratin material within infiltrative nests and locally aggressive nature. In the early stages of the disease symptoms are vague and nonspecific (abdominal pain, jaundice and vomiting). In the advanced stages it may present with a bulky tumor and symptoms of adjacent organ involvement.","definition_xrefs":["Orphanet:424996"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrahepatic bile duct squamous cell carcinoma","termid":"MONDO:0006203"},{"relation_name":"is_a","term_name":"carcinoma of gallbladder and extrahepatic biliary tract","termid":"MONDO:0018918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"squamous cell carcinoma of gallbladder and extrahepatic biliary tract","secondary_identifiers":["UMLS:C4707898","GARD:21792","MEDGEN:1635098","SCTID:766978002"],"synonyms":[{"name":"squamous cell carcinoma of gallblader and EBT","type":"exact"}],"termid":"MONDO:0018537","xrefs":{"Monarch":{"xref_id":"0018537"}}}


id: SO:0000480
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A clone which is part of a tiling path. A tiling path is a set of sequencing substrates, typically clones, which have been selected in order to efficiently cover a region of the genome in preparation for sequencing and assembly.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clone","termid":"SO:0000151"},{"relation_name":"is_a","term_name":"tiling_path_fragment","termid":"SO:0000474"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tiling_path_clone","synonyms":[{"name":"tiling path clone","type":"exact"}],"termid":"SO:0000480"}


id: PBO:0072240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 15","termid":"PBO:0072240"}


id: _global:produced_by
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"a produced_by b iff some process that occurs_in b has_output a.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"produced_by","secondary_identifiers":["RO:0003001"],"termid":"_global:produced_by"}


id: MONDO:0016546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary orthostatic tremor (POT), or ``shaky legs syndrome'', is a rare movement disorder characterized by fast, task-specific tremor, affecting the legs and trunk while standing.","definition_xrefs":["Orphanet:238606"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary orthostatic tremor","secondary_identifiers":["MESH:C536418","GARD:8563","SCTID:715902009","UMLS:C0878578","MEDGEN:164206","NORD:1612"],"synonyms":[{"name":"OT","type":"related"},{"name":"POT","type":"exact"},{"name":"orthostatic tremor, primary","type":"related"},{"name":"pot","type":"exact"},{"name":"shaky leg syndrome","type":"related"}],"termid":"MONDO:0016546","xrefs":{"Monarch":{"xref_id":"0016546"}}}


id: FYPO:0005930
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the occurrence of chromatin binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type) at the centromere outer repeat region.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin binding","termid":"FYPO:0003086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000257","FYPO:0000652"],"is_obsolete":false,"name":"normal chromatin binding at centromere outer repeat","synonyms":[{"name":"normal chromatin binding at centromere otr","type":"exact"},{"name":"normal chromatin binding at centromere outer repeat region","type":"exact"},{"name":"normal chromatin binding at centromeric outer repeat region","type":"exact"},{"name":"normal chromatin binding at pericentric region","type":"related"},{"name":"normal chromatin binding at pericentromeric region","type":"related"}],"termid":"FYPO:0005930"}


id: MONDO:0020683
data:
  {"annotated_genes":["SJAG_02896","SJAG_03905","SJAG_03081","SJAG_00358","SJAG_04622","SJAG_03786","SJAG_03453","SJAG_01013","SJAG_01059","SJAG_01748","SJAG_05979","SJAG_02763","SJAG_01349","SJAG_02520","SJAG_00640"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013111"},{"annotations":[85644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014744"},{"annotations":[85070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[86962,87114,86960,86961,87115,86959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[84943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012454"},{"annotations":[87018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011953"},{"annotations":[85286,85285,85287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013108"},{"annotations":[85879],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032716"},{"annotations":[86805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009992"}]},"cv_name":"mondo","definition":"Disease having a short and relatively severe course.","definition_xrefs":["MESH:D000208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00358":null,"SJAG_00640":null,"SJAG_01013":null,"SJAG_01059":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_02520":null,"SJAG_02763":null,"SJAG_02896":null,"SJAG_03081":null,"SJAG_03453":null,"SJAG_03786":null,"SJAG_03905":null,"SJAG_04622":null,"SJAG_05979":null},"genotype_count":0,"is_obsolete":false,"name":"acute disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:799.89","UMLS:C0001314","MEDGEN:1738","SCTID:2704003"],"synonyms":[{"name":"acute disease","type":"exact"},{"name":"acute diseases","type":"exact"},{"name":"disease, acute","type":"exact"}],"termid":"MONDO:0020683","terms_by_termid":{"MONDO:0008294":null,"MONDO:0009992":null,"MONDO:0011953":null,"MONDO:0012454":null,"MONDO:0013108":null,"MONDO:0013111":null,"MONDO:0014744":null,"MONDO:0018874":null,"MONDO:0032716":null},"xrefs":{"Monarch":{"xref_id":"0020683"}}}


id: PBO:0046101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4B pseudogene 4","termid":"PBO:0046101"}


id: MONDO:1012537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypopigmentation and deafness, non-human animal","termid":"MONDO:1011900"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypopigmentation and deafness, pig","secondary_identifiers":["OMIA:002287-9823"],"termid":"MONDO:1012537","xrefs":{"Monarch":{"xref_id":"1012537"}}}


id: PBO:0053535
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 537","termid":"PBO:0053535"}


id: GO:0035866
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphav-beta3 integrin complex bound to protein kinase C alpha.","definition_xrefs":["GOC:BHF","PMID:16014375","GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"alphav-beta3 integrin-PKCalpha complex","synonyms":[{"name":"alphav-beta3 integrin-PKCa complex","type":"exact"},{"name":"alphav-beta3 integrin-protein kinase C alpha complex","type":"exact"}],"termid":"GO:0035866"}


id: PBO:0087604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the CCR4-NOT transcriptional regulatory complex; CCR4-NOT complex is evolutionarily-conserved and involved in controlling mRNA initiation, elongation, and degradation","termid":"PBO:0087604"}


id: FYPO:0002891
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which any process of chromatin organization is normal (i.e. indistinguishable from wild type) in the vegetative growth phase of the life cycle. Chromatin organization results in the specification, formation or maintenance of the physical structure of eukaryotic chromatin.","definition_xrefs":["GO:0006325","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin organization","termid":"FYPO:0007940"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal chromatin organization during vegetative growth","synonyms":[{"name":"normal chromatin organisation during vegetative growth","type":"exact"},{"name":"normal chromatin organization during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002891"}


id: MONDO:0016125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infectious, fungal or parasitic myopathy (obsolete MONDO:0016125)","secondary_identifiers":["Orphanet:206988"],"termid":"MONDO:0016125","xrefs":{"Monarch":{"xref_id":"0016125"}}}


id: PBO:0064743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 79","termid":"PBO:0064743"}


id: PBO:0061296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptides B and W receptor 1","termid":"PBO:0061296"}


id: GO:0060191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of lipase activity, the hydrolysis of a lipid or phospholipid.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of lipase activity (obsolete GO:0060191)","termid":"GO:0060191"}


id: GO:0032602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of a chemokine due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels. All chemokines possess a number of conserved cysteine residues involved in intramolecular disulfide bond formation. Some chemokines are considered pro-inflammatory and can be induced during an immune response to recruit cells of the immune system to a site of infection, while others are considered homeostatic and are involved in controlling the migration of cells during normal processes of tissue maintenance or development. Chemokines are found in all vertebrates, some viruses and some bacteria.","definition_xrefs":["PMID:12183377","GOC:rl","ISBN:0198506732","GOC:BHF","Wikipedia:Chemokine"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"chemokine production","secondary_identifiers":["GO:0050755","GO:0042033","GO:0090195"],"synonyms":[{"name":"chemokine anabolism","type":"exact"},{"name":"chemokine biosynthesis","type":"exact"},{"name":"chemokine biosynthetic process","type":"narrow"},{"name":"chemokine formation","type":"exact"},{"name":"chemokine metabolic process","type":"narrow"},{"name":"chemokine secretion","type":"narrow"},{"name":"chemokine synthesis","type":"exact"}],"termid":"GO:0032602"}


id: PBO:0080305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 69 pseudogene","termid":"PBO:0080305"}


id: PR:O42978
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U6 snRNA-associated Sm-like protein LSm5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR20971:SF0","OMA:SCHPO03650"],"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":"U6 snRNA-associated Sm-like protein LSm5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC20F10.09","secondary_identifiers":["UniProtKB:O42978"],"synonyms":[{"name":"Spom972h-LSM5","type":"exact"}],"termid":"PR:O42978"}


id: GO:0005267
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the energy-independent facilitated diffusion of a potassium ion through a transmembrane aqueous pore or channel.","definition_xrefs":["GOC:mtg_transport","GOC:pr","GOC:BHF","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic cation channel activity","termid":"GO:0005261"},{"relation_name":"is_a","term_name":"potassium ion transmembrane transporter activity","termid":"GO:0015079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"potassium channel activity","secondary_identifiers":["Reactome:R-HSA-1299304","Reactome:R-HSA-1296024","Reactome:R-HSA-1299338","Reactome:R-HSA-1299359","Reactome:R-HSA-5578910","Reactome:R-HSA-1296037","Reactome:R-HSA-1299318","Reactome:R-HSA-1296039","Reactome:R-HSA-2534365","Reactome:R-HSA-1296035","Reactome:R-HSA-1296348","Reactome:R-HSA-1299297"],"termid":"GO:0005267"}


id: MONDO:0800047
data:
  {"annotated_genes":["SJAG_04003"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86391],"is_not":false,"summary":null,"term":"MONDO:0800047"}]},"cv_name":"mondo","definition":"Any autosomal dominant macrothrombocytopenia in which the cause of the disease is a mutation in the TUBB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant macrothrombocytopenia","termid":"MONDO:0015372"},{"relation_name":"is_a","term_name":"macrothrombocytopenia, isolated","termid":"MONDO:0031447"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04003":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"macrothrombocytopenia, isolated, 1, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0090102","GARD:18271","MESH:C567747","UMLS:C5676892","OMIM:613112","MEDGEN:1811721"],"synonyms":[{"name":"MACTHC1","type":"exact"},{"name":"TUBB1 autosomal dominant macrothrombocytopenia","type":"exact"},{"name":"autosomal dominant macrothrombocytopenia TUBB1-related","type":"related"},{"name":"autosomal dominant macrothrombocytopenia caused by mutation in TUBB1","type":"exact"},{"name":"macrothrombocytopenia, autosomal dominant, TUBB1-related","type":"exact"}],"termid":"MONDO:0800047","terms_by_termid":{"MONDO:0800047":null},"xrefs":{"Monarch":{"xref_id":"0800047"}}}


id: PBO:0027315
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_localization_to_cytoplasmic_stress_granule","termid":"PBO:0027315"}


id: MONDO:0023137
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":"feigenbaum Bergeron syndrome","termid":"MONDO:0023137","xrefs":{"Monarch":{"xref_id":"0023137"}}}


id: PBO:0057825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3144","termid":"PBO:0057825"}


id: GO:0050352
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + trimethylamine N-oxide = dimethylamine + formaldehyde.","definition_xrefs":["EC:4.1.2.32","RHEA:20217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"trimethylamine-oxide aldolase activity","secondary_identifiers":["KEGG_REACTION:R02512","UM-BBD_reactionID:r1409","MetaCyc:TRIMETHYLAMINE-OXIDE-ALDOLASE-RXN"],"synonyms":[{"name":"trimethylamine N-oxide aldolase activity","type":"related"},{"name":"trimethylamine N-oxide demethylase activity","type":"related"},{"name":"trimethylamine N-oxide formaldehyde-lyase activity","type":"related"},{"name":"trimethylamine-N-oxide formaldehyde-lyase (dimethylamine-forming)","type":"related"},{"name":"trimethylamine-N-oxide formaldehyde-lyase activity","type":"related"}],"termid":"GO:0050352"}


id: PBO:0016518
data:
  {"annotation_feature_type":"gene","cv_name":"pathway","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mkh1-Pek1-Pmk1 MAP kinase","termid":"PBO:0016518"}


id: GO:0072399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of cytokinesis checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cell cycle checkpoint signaling","termid":"GO:0072396"}],"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 cytokinesis checkpoint signaling","secondary_identifiers":["GO:0072420"],"synonyms":[{"name":"cytokinesis checkpoint effector process","type":"exact"},{"name":"response to signal involved in cytokinesis checkpoint","type":"exact"}],"termid":"GO:0072399"}


id: PBO:0084216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homo-isocitrate dehydrogenase; an NAD-linked mitochondrial enzyme required for the fourth step in the biosynthesis of lysine, in which homo-isocitrate is oxidatively decarboxylated to alpha-ketoadipate","termid":"PBO:0084216"}


id: GO:1900384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of flavonol biosynthetic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of flavonoid biosynthetic process","termid":"GO:0009962"},{"relation_name":"regulates","term_name":"flavonol biosynthetic process","termid":"GO:0051555"}],"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 flavonol biosynthetic process","termid":"GO:1900384"}


id: MONDO:0009076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive disorder caused by mutations in the GJB2 gene, encoding gap junction beta-2 protein. The condition is characterized by profound sensorineural hearing loss and may be associated with vestibular dysfunction.","definition_xrefs":["NCIT:C129022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 1A","secondary_identifiers":["UMLS:C2673759","MESH:C567134","OMIM:220290","DOID:0110475","GARD:1697","MEDGEN:388720"],"synonyms":[{"name":"DFNB1","type":"narrow"},{"name":"DFNB1A","type":"narrow"},{"name":"GJB2-related deafness","type":"narrow"},{"name":"autosomal recessive deafness 1A","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 1A","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 1A","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 1A","type":"exact"},{"name":"connexin 26 deafness","type":"narrow"},{"name":"deafness nonsyndromic, connexin 26 linked","type":"narrow"},{"name":"deafness, autosomal recessive 1A","type":"narrow"},{"name":"deafness, autosomal recessive 1a, autosomal recessive, digenic dominant","type":"narrow"},{"name":"deafness, autosomal recessive type 1A","type":"narrow"},{"name":"deafness, digenic GJB2/GJB6, Autosomal recessive, Digenic dominant","type":"exact"},{"name":"deafness, digenic, GJB2/GJB3","type":"narrow"},{"name":"deafness, digenic, GJB2/GJB3, Autosomal recessive, Digenic dominant","type":"exact"},{"name":"deafness, digenic, GJB2/GJB6","type":"narrow"}],"termid":"MONDO:0009076","xrefs":{"Monarch":{"xref_id":"0009076"}}}


id: MONDO:0002621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma arising from the soft tissue.","definition_xrefs":["NCIT:C8810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteosarcoma","termid":"MONDO:0009807"},{"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":"extraosseous osteosarcoma","secondary_identifiers":["ICD9:170.9","DOID:3357","SCTID:404077005","MEDGEN:163186","UMLS:C0855052"],"synonyms":[{"name":"extraosseous osteosarcoma","type":"exact"},{"name":"extraskeletal osteogenic sarcoma","type":"exact"},{"name":"extraskeletal osteosarcoma","type":"exact"},{"name":"osteosarcoma, extraskeletal, malignant","type":"exact"},{"name":"soft tissue osteosarcoma","type":"exact"}],"termid":"MONDO:0002621","xrefs":{"Monarch":{"xref_id":"0002621"}}}


id: PBO:0087444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit III of cytochrome c oxidase (Complex IV); Complex IV is the terminal member of the mitochondrial inner membrane electron transport chain; one of three mitochondrially-encoded subunits","termid":"PBO:0087444"}


id: MONDO:0003525
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually malignant gastrin-producing neuroendocrine tumor arising from the pancreas. It may or may not be associated with inappropriate secretion of gastrin and an associated clinical syndrome.","definition_xrefs":["NCIT:C9069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastrin-producing neuroendocrine tumor","termid":"MONDO:0003523"},{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"}],"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 gastrin-producing neuroendocrine tumor","secondary_identifiers":["MESH:D015408","MEDGEN:235080","UMLS:C1368066","DOID:5580"],"synonyms":[{"name":"gastrin-producing neuroendocrine tumor of pancreas","type":"exact"},{"name":"gastrin-producing neuroendocrine tumour of pancreas","type":"exact"},{"name":"islet cell tumor, ulcerogenic","type":"related"},{"name":"pancreas gastrin-producing neuroendocrine tumor","type":"exact"},{"name":"pancreas gastrin-producing neuroendocrine tumour","type":"exact"},{"name":"pancreatic G-cell tumor","type":"exact"},{"name":"pancreatic G-cell tumour","type":"exact"},{"name":"pancreatic gastrin producing NET","type":"exact"},{"name":"pancreatic gastrin producing tumor","type":"exact"},{"name":"pancreatic gastrin producing tumour","type":"exact"},{"name":"pancreatic gastrin-producing neuroendocrine tumor","type":"exact"}],"termid":"MONDO:0003525","xrefs":{"Monarch":{"xref_id":"0003525"}}}


id: PBO:0049960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIG1 hypoxia inducible domain family member 1A pseudogene 6","termid":"PBO:0049960"}


id: GO:0048457
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the floral whorl are generated and organized.","definition_xrefs":["GOC:PO_curators","GOC:go_curators","PO:0025023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"post-embryonic plant morphogenesis","termid":"GO:0090698"},{"relation_name":"part_of","term_name":"floral whorl development","termid":"GO:0048438"},{"relation_name":"part_of","term_name":"flower morphogenesis","termid":"GO:0048439"}],"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":"floral whorl morphogenesis","secondary_identifiers":["GO:0048414"],"termid":"GO:0048457"}


id: PBO:0061867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligodendrocyte myelin glycoprotein","termid":"PBO:0061867"}


id: PBO:0003691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclophilin family peptidyl-prolyl cis-trans isomerase Cyp2","termid":"PBO:0003691"}


id: GO:0102081
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: homotaurine + 2-oxoglutarate(2-) = 3-sulfopropanal + L-glutamate(1-).","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete homotaurine:2-oxoglutarate aminotransferase activity (obsolete GO:0102081)","termid":"GO:0102081"}


id: PBO:0092006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Serine (gcu), mitochondrial","termid":"PBO:0092006"}


id: SO:0001748
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL3 RNA leader sequence to the 5' end of an mRNA. SL3 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL3_acceptor_site","synonyms":[{"name":"SL3 acceptor site","type":"exact"}],"termid":"SO:0001748"}


id: FYPO:0005855
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that undergoes a single round of cell division to produce daughter cells that have two or more septa apiece, which then die.","definition_xrefs":["PomBase:mah","PomBase:jh","PMID:12764130","PomBase:vw"],"direct_ancestors":[{"relation_name":"has_part","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"inviable after spore germination, single cell division","termid":"FYPO:0002280"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000032","FYPO:0000002","FYPO:0000004","FYPO:0000631","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"inviable after spore germination, single cell division, multiseptate cell","synonyms":[{"name":"inviable following spore germination, single cell division, multiseptate cell","type":"exact"},{"name":"inviable germinated spore, single cell division, multiseptate cell","type":"exact"},{"name":"lethal after spore germination, single cell division, multiseptate cell","type":"exact"}],"termid":"FYPO:0005855"}


id: MONDO:0006756
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete extracutaneous mastocytoma (obsolete MONDO:0006756)","termid":"MONDO:0006756","xrefs":{"Monarch":{"xref_id":"0006756"}}}


id: GO:0006373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete 3'-splice site cleavage, exon ligation (obsolete GO:0006373)","synonyms":[{"name":"3'-splice site cleavage, exon ligation","type":"exact"}],"termid":"GO:0006373"}


id: PBO:0065448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 5","termid":"PBO:0065448"}


id: PBO:0053138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactate dehydrogenase A","termid":"PBO:0053138"}


id: MONDO:0010193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Weaver syndrome (WVS) is a rare, multisystem disorder characterized by tall stature, a typical facial appearance (hypertelorism, retrognathia) and variable intellectual disability. Additional features may include camptodactyly, soft doughy skin, umbilical hernia, and a low hoarse cry.","definition_xrefs":["Orphanet:3447"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Weaver syndrome","secondary_identifiers":["NANDO:2200957","GTR:AN0102079","NCIT:C125599","GARD:7878","SCTID:63119004","DOID:14731","UMLS:C0265210","MESH:C536687","MEDGEN:120511","GTR:AN0102080","NANDO:1200659","NORD:1839","OMIM:277590","icd11.foundation:2042913723","ICD9:759.89"],"synonyms":[{"name":"EZH2 related overgrowth","type":"related"},{"name":"WEAVER syndrome","type":"related"},{"name":"WEAVER-like syndrome","type":"exact"},{"name":"WVS","type":"related"},{"name":"Weaver Smith syndrome","type":"related"},{"name":"Weaver Williams syndrome","type":"related"},{"name":"Weaver like syndrome","type":"related"},{"name":"Weaver syndrome","type":"exact"},{"name":"Weaver-Smith syndrome","type":"related"},{"name":"Weaver-like syndrome","type":"related"},{"name":"camptodactyly - overgrowth - unusual facies","type":"related"},{"name":"camptodactyly-overgrowth-unusual facies syndrome","type":"exact"},{"name":"intellectual disability, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate","type":"related"},{"name":"mental retardation, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate","type":"related"},{"name":"overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly","type":"related"}],"termid":"MONDO:0010193","xrefs":{"Monarch":{"xref_id":"0010193"}}}


id: PBO:0039224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo-keto reductase family 7 member A3","termid":"PBO:0039224"}


id: PBO:0116277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-dependent ATPase that stimulates strand exchange; modifies the topology of double-stranded DNA; drives ATP-hydrolysis-dependent sequence alignment during homologous recombination; involved in repair of dsDNA breaks during both mitosis and meiosis; promotes strand invasion, catalyzes nucleosome remodeling, and removes Rad51p from dsDNA; member of the SWI/SNF family of DNA translocases; forms nuclear foci upon DNA replication stress","termid":"PBO:0116277"}


id: GO:0051986
data:
  {"annotated_genes":["SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902424"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the attachment of spindle microtubules to the kinetochore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of chromosome segregation","termid":"GO:0051985"},{"relation_name":"is_a","term_name":"regulation of attachment of spindle microtubules to kinetochore","termid":"GO:0051988"},{"relation_name":"negatively_regulates","term_name":"attachment of spindle microtubules to kinetochore","termid":"GO:0008608"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of attachment of spindle microtubules to kinetochore","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of attachment of spindle microtubules to kinetochore","type":"exact"},{"name":"down-regulation of attachment of spindle microtubules to kinetochore","type":"exact"},{"name":"downregulation of attachment of spindle microtubules to kinetochore","type":"exact"},{"name":"inhibition of attachment of spindle microtubules to kinetochore","type":"narrow"}],"termid":"GO:0051986","terms_by_termid":{"GO:1902424":null}}


id: PBO:0066791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 90","termid":"PBO:0066791"}


id: PBO:0068093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 400","termid":"PBO:0068093"}


id: MONDO:0016864
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Duane-radial ray syndrome","termid":"MONDO:0011812"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0000426"],"is_obsolete":false,"name":"Okihiro syndrome due to a point mutation","secondary_identifiers":["Orphanet:261647","GARD:20788","UMLS:C5679683","MEDGEN:1842838"],"synonyms":[{"name":"Duane-radial ray syndrome due to a point mutation","type":"exact"}],"termid":"MONDO:0016864","xrefs":{"Monarch":{"xref_id":"0016864"}}}


id: PBO:0063977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 11","termid":"PBO:0063977"}


id: GO:0032384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of cholesterol within cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cholesterol transport","termid":"GO:0032375"},{"relation_name":"is_a","term_name":"negative regulation of intracellular sterol transport","termid":"GO:0032381"},{"relation_name":"is_a","term_name":"regulation of intracellular cholesterol transport","termid":"GO:0032383"},{"relation_name":"negatively_regulates","term_name":"intracellular cholesterol transport","termid":"GO:0032367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of intracellular cholesterol transport","synonyms":[{"name":"down regulation of intracellular cholesterol transport","type":"exact"},{"name":"down-regulation of intracellular cholesterol transport","type":"exact"},{"name":"downregulation of intracellular cholesterol transport","type":"exact"},{"name":"inhibition of intracellular cholesterol transport","type":"narrow"}],"termid":"GO:0032384"}


id: GO:0016512
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the formation of endothelin 1 by cleavage of the Trp21-Val22 bond in the precursor.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete endothelin-converting enzyme 1 activity (obsolete GO:0016512)","synonyms":[{"name":"ECE-1 activity","type":"related"},{"name":"endothelin-converting enzyme 1 activity","type":"exact"}],"termid":"GO:0016512"}


id: PBO:0058632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6764","termid":"PBO:0058632"}


id: MONDO:0020225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A cataract (disease) that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"gene_count":0,"genotype_count":0,"name":"obsolete syndromic cataract (obsolete MONDO:0020225)","secondary_identifiers":["Orphanet:98641"],"synonyms":[{"name":"syndrome associated with cataract (disease)","type":"exact"},{"name":"syndromic cataract (disease)","type":"exact"}],"termid":"MONDO:0020225","xrefs":{"Monarch":{"xref_id":"0020225"}}}


id: GO:0032988
data:
  {"annotated_genes":["SJAG_00206","SJAG_02560","SJAG_05025","SJAG_03301","SJAG_00597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87523,78285,104307,57137,74523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000390"}]},"cv_name":"biological_process","definition":"The disaggregation of a protein-RNA complex into its constituent components.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"is_a","term_name":"protein-RNA complex organization","termid":"GO:0071826"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00206":null,"SJAG_00597":null,"SJAG_02560":null,"SJAG_03301":null,"SJAG_05025":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein-RNA complex disassembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"RNA-protein complex disassembly","type":"exact"},{"name":"RNP complex disassembly","type":"exact"},{"name":"ribonucleoprotein complex disassembly","type":"exact"}],"termid":"GO:0032988","terms_by_termid":{"GO:0000390":null}}


id: GO:0120284
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 2-amino-3-(1H-indol-3-yl)propanoic acid.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"tryptophan binding","synonyms":[{"name":"Trp binding","type":"exact"}],"termid":"GO:0120284"}


id: MONDO:0100536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth agenesis","termid":"MONDO:0005486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth agenesis, selective, with orofacial cleft","secondary_identifiers":["UMLS:C1970117","MEDGEN:409991"],"termid":"MONDO:0100536","xrefs":{"Monarch":{"xref_id":"0100536"}}}


id: MONDO:0020417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anatomic abnormality that occurs during embryonic development, in which the aortic arch is right-sided.","definition_xrefs":["NCIT:C103917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aortic arch defects","termid":"MONDO:0015236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"right aortic arch","secondary_identifiers":["MEDGEN:48474","icd11.foundation:769265824","Orphanet:99081","MedDRA:10067407","SCTID:111321007","HP:0012020","UMLS:C0035615","GARD:19640"],"synonyms":[{"name":"right aortic arch","type":"exact"},{"name":"right aortic arch (disease)","type":"exact"}],"termid":"MONDO:0020417","xrefs":{"Monarch":{"xref_id":"0020417"}}}


id: PBO:0073619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sialic acid binding Ig like lectin 5","termid":"PBO:0073619"}


id: PBO:0029811
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population_including_divided_and_undivided_germinated_spores_(obsolete_FYPO:0002426)","termid":"PBO:0029811"}


id: PBO:0076819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminal nucleotidyltransferase 2","termid":"PBO:0076819"}


id: GO:0072120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for the pronephros to attain its fully functional state. In mammals, the pronephros is the first of the three embryonic kidneys to be established and exists only transiently. In lower vertebrates such as fish and amphibia, the pronephros is the fully functional embryonic kidney and is indispensable for larval life.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ maturation","termid":"GO:0048799"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"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":"pronephros maturation","synonyms":[{"name":"pronephric kidney maturation","type":"exact"}],"termid":"GO:0072120"}


id: MONDO:0016600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute neonatal citrullinemia type I is a severe form of citrullinemia type 1 characterized biologically by hyperammonemia and clinically by progressive lethargy, poor feeding and vomiting, seizures and possible loss of consciousness, within one to a few days of birth, with variable signs of increased intracranial pressure. The condition can lead to significant neurologic deficits.","definition_xrefs":["Orphanet:247546"],"direct_ancestors":[{"relation_name":"is_a","term_name":"citrullinemia type I","termid":"MONDO:0008988"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"acute neonatal citrullinemia type I","secondary_identifiers":["MEDGEN:1843387","UMLS:C5679618","GARD:20659","NANDO:2201094"],"synonyms":[{"name":"acute neonatal citrullinemia type 1","type":"exact"},{"name":"classic citrullinemia type 1","type":"exact"},{"name":"classic citrullinemia type I","type":"exact"}],"termid":"MONDO:0016600","xrefs":{"Monarch":{"xref_id":"0016600"}}}


id: PBO:0090510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, CBF1/Su(H)/LAG-1 family Cbf11","termid":"PBO:0090510"}


id: PBO:0048558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDNF family receptor alpha 3","termid":"PBO:0048558"}


id: PBO:0091462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.3 H4 heterotetramer chaperone Rtt106","termid":"PBO:0091462"}


id: MONDO:0001538
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A ischemic disease that involves the retina.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ischemic disease","termid":"MONDO:0005053"},{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"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":"retinal ischemia","secondary_identifiers":["MEDGEN:102372","ICD10CM:H35.82","DOID:12510","ICD9:362.84","SCTID:26468004","UMLS:C0162291"],"synonyms":[{"name":"ischaemic disease of retina","type":"exact"},{"name":"ischemic disease of retina","type":"exact"},{"name":"retina ischaemic disease","type":"exact"},{"name":"retina ischemic disease","type":"exact"}],"termid":"MONDO:0001538","xrefs":{"Monarch":{"xref_id":"0001538"}}}


id: GO:0072238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a metanephric long nephron over time, from its formation to the mature structure. Long nephrons are associated with juxtamedullary glomeruli and extend into the inner medulla in the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long nephron development","termid":"GO:0072029"},{"relation_name":"is_a","term_name":"metanephric nephron development","termid":"GO:0072210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric long nephron development","synonyms":[{"name":"metanephric juxtamedullary nephron development","type":"related"}],"termid":"GO:0072238"}


id: MONDO:0005565
data:
  {"annotated_genes":["SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011014"}]},"cv_name":"mondo","definition":"A malignant neoplasm composed of undifferentiated cells.","definition_xrefs":["NCIT:C8997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"embryonal neoplasm","termid":"MONDO:0005564"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"blastoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:4766","MEDGEN:181704","ICDO:8981/3","UMLS:C0936282","DOID:0070003","EFO:0005785"],"synonyms":[{"name":"blastoma","type":"exact"},{"name":"embryoma","type":"exact"}],"termid":"MONDO:0005565","terms_by_termid":{"MONDO:0011014":null},"xrefs":{"Monarch":{"xref_id":"0005565"}}}


id: PBO:0052831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 224, pseudogene","termid":"PBO:0052831"}


id: GO:0090256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the multiplication or reproduction of cells, resulting in the expansion of a cell population that contributes to imaginal disc-derived wing morphogenesis.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"is_a","term_name":"regulation of post-embryonic development","termid":"GO:0048580"},{"relation_name":"part_of","term_name":"imaginal disc-derived wing morphogenesis","termid":"GO:0007476"},{"relation_name":"regulates","term_name":"cell proliferation involved in imaginal disc-derived wing morphogenesis","termid":"GO:0090255"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell proliferation involved in imaginal disc-derived wing morphogenesis","termid":"GO:0090256"}


id: GO:0050451
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 CoA + NADP+ = CoA-disulfide + NADPH + H+.","definition_xrefs":["RHEA:14705"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disulfide oxidoreductase activity","termid":"GO:0015036"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0015036"},{"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:0015036","GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"CoA-disulfide reductase (NADPH) activity","secondary_identifiers":["MetaCyc:COA-DISULFIDE-REDUCTASE-NADH-RXN","EC:1.8.1.14"],"synonyms":[{"name":"CoA-disulfide reductase (NADH) activity","type":"related"},{"name":"CoA-disulfide reductase (NADP) activity","type":"exact"},{"name":"CoA-disulfide reductase activity","type":"broad"},{"name":"CoA-disulphide reductase activity","type":"broad"},{"name":"CoADR activity","type":"related"},{"name":"NADH:CoA-disulfide oxidoreductase activity","type":"related"},{"name":"coenzyme A disulfide reductase activity","type":"related"}],"termid":"GO:0050451"}


id: GO:0061000
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of dendritic spine development, the process whose specific outcome is the progression of the dendritic spine over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of dendritic spine development","termid":"GO:0060998"},{"relation_name":"negatively_regulates","term_name":"dendritic spine development","termid":"GO:0060996"}],"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 dendritic spine development","termid":"GO:0061000"}


id: PBO:0003206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rheb GTPase Rhb1","termid":"PBO:0003206"}


id: GO:0045884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of survival gene product expression; survival gene products are those that antagonize the apoptotic program. Regulation can be at the transcriptional, translational, or posttranslational level.","definition_xrefs":["GOC:mtg_apoptosis","GOC:tb","GOC:dph","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of survival gene product expression (obsolete GO:0045884)","synonyms":[{"name":"regulation of survival gene product activity","type":"broad"},{"name":"regulation of survival gene product expression","type":"exact"},{"name":"regulation of survival gene products","type":"broad"}],"termid":"GO:0045884"}


id: PBO:0072741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100 calcium binding protein A6","termid":"PBO:0072741"}


id: PBO:0039558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain containing 50","termid":"PBO:0039558"}


id: PR:Q9C0W2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- abo2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0W2"],"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 AAA domain-containing protein P22H7.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP22H7.05c","synonyms":[{"name":"Spom972h-abo2","type":"exact"}],"termid":"PR:Q9C0W2"}


id: PBO:0061664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 42","termid":"PBO:0061664"}


id: GO:0050452
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CoA + glutathione + NADP+ = CoA-glutathione + NADPH + H+.","definition_xrefs":["RHEA:14617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"CoA-glutathione reductase (NADPH) activity","secondary_identifiers":["EC:1.8.1.10","MetaCyc:COA-GLUTATHIONE-REDUCTASE-NADPH-RXN"],"synonyms":[{"name":"CoA-glutathione reductase (NADP) activity","type":"exact"},{"name":"CoA-glutathione reductase activity","type":"broad"},{"name":"NADPH-dependent coenzyme A-SS-glutathione reductase activity","type":"exact"},{"name":"NADPH:CoA-glutathione oxidoreductase activity","type":"exact"},{"name":"coenzyme A disulfide-glutathione reductase activity","type":"broad"},{"name":"coenzyme A glutathione disulfide reductase activity","type":"broad"},{"name":"glutathione:NADP+ oxidoreductase (CoA-acylating)","type":"exact"}],"termid":"GO:0050452"}


id: SO:0001527
data:
  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id: PBO:0048182
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRB2 associated binding protein 3","termid":"PBO:0048182"}


id: GO:0050539
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + maleimide = H+ + maleamate.","definition_xrefs":["RHEA:24476","EC:3.5.2.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides","termid":"GO:0016812"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016810"],"is_obsolete":false,"name":"maleimide hydrolase activity","secondary_identifiers":["KEGG_REACTION:R05781","MetaCyc:3.5.2.16-RXN"],"synonyms":[{"name":"cyclic imide hydrolase activity","type":"related"},{"name":"cyclic-imide amidohydrolase (decyclicizing)","type":"related"},{"name":"cyclic-imide amidohydrolase (decyclizing)","type":"related"},{"name":"imidase activity","type":"broad"}],"termid":"GO:0050539"}


id: PBO:0002452
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAK-related kinase Ppk11","termid":"PBO:0002452"}


id: MONDO:0005543
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune hepatitis characterized by the presence of antinuclear antibody (ANA) and antismooth-muscle antibody (ASMA).","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune hepatitis","termid":"MONDO:0016264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"autoimmune hepatitis type 1","secondary_identifiers":["icd11.foundation:260422751","GARD:22251","ICD9:571.49","Orphanet:563576","UMLS:C4303164","SCTID:721711009","SCTID:197284004","MEDGEN:928833"],"synonyms":[{"name":"autoimmune hepatitis type 1","type":"exact"},{"name":"type 1 AIH","type":"exact"}],"termid":"MONDO:0005543","xrefs":{"Monarch":{"xref_id":"0005543"}}}


id: PBO:0076621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBCC domain containing 1","termid":"PBO:0076621"}


id: GO:0050195
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 5-phosphate + ATP = D-ribose 1,5-diphosphate + ADP + 2 H+.","definition_xrefs":["RHEA:21216","EC:2.7.1.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"phosphoribokinase activity","secondary_identifiers":["MetaCyc:PHOSPHORIBOKINASE-RXN","KEGG_REACTION:R01050"],"synonyms":[{"name":"ATP:D-ribose-5-phosphate 1-phosphotransferase activity","type":"related"},{"name":"phosphoribokinase (phosphorylating)","type":"related"}],"termid":"GO:0050195"}


id: PBO:0090473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP I, II, and III complex subunit Trs23","termid":"PBO:0090473"}


id: PBO:0110061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nifs homolog, possible cysteine desulfurase, implicated in iron-sulfur cluster assembly","termid":"PBO:0110061"}


id: PR:O14206
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A suppressor of SWI4 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01002","PRO:DNx","PANTHER:PTHR12661:SF3"],"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":"brix domain-containing protein C1B9.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B9.03c","secondary_identifiers":["UniProtKB:O14206"],"synonyms":[{"name":"Spom972h-PPAN","type":"exact"}],"termid":"PR:O14206"}


id: MONDO:0035776
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"combined deficiency of factor VII and factor X","secondary_identifiers":["MEDGEN:1843297","GARD:22418","Orphanet:600691","UMLS:C5681529"],"termid":"MONDO:0035776","xrefs":{"Monarch":{"xref_id":"0035776"}}}


id: MONDO:0018385
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of osteochondrosis that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete osteochondrosis of genetic origin (obsolete MONDO:0018385)","secondary_identifiers":["Orphanet:399391"],"synonyms":[{"name":"genetic osteochondrosis","type":"exact"}],"termid":"MONDO:0018385","xrefs":{"Monarch":{"xref_id":"0018385"}}}


id: PBO:0053689
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 882","termid":"PBO:0053689"}


id: GO:0048296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of isotype switching to IgA isotypes.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of isotype switching","termid":"GO:0045191"},{"relation_name":"regulates","term_name":"isotype switching to IgA isotypes","termid":"GO:0048290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0010467","GO:0006310"],"is_obsolete":false,"name":"regulation of isotype switching to IgA isotypes","synonyms":[{"name":"regulation of class switch recombination to IgA isotypes","type":"exact"},{"name":"regulation of class switching to IgA isotypes","type":"exact"},{"name":"regulation of isotype switch recombination to IgA isotypes","type":"exact"}],"termid":"GO:0048296"}


id: PBO:0087643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the glycosylphosphatidylinositol transamidase complex; involved in attachment of glycosylphosphatidylinositol (GPI) anchors to proteins; may have a role in recognition of the attachment signal or the lipid portion of GPI; ortholog of human PIGU; partially complements a class U CHO cell line with a mutation in the PIGU ortholog","termid":"PBO:0087643"}


id: GO:0033786
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-beta-D-heptose-1-phosphate + ATP = ADP-D-glycero-D-manno-heptose.","definition_xrefs":["MetaCyc:RXN0-4342"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016779"],"is_obsolete":false,"name":"heptose-1-phosphate adenylyltransferase activity","secondary_identifiers":["RHEA:27465"],"synonyms":[{"name":"D-beta-D-heptose 1-phosphate adenylyltransferase activity","type":"exact"},{"name":"heptose 1-phosphate adenyltransferase activity","type":"exact"}],"termid":"GO:0033786"}


id: PBO:0040133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and SOCS box containing 17","termid":"PBO:0040133"}


id: MONDO:0010040
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":"ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability","secondary_identifiers":["OMIM:270500","MEDGEN:462969","UMLS:C3151619"],"synonyms":[{"name":"ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability","type":"exact"},{"name":"ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation","type":"exact"}],"termid":"MONDO:0010040","xrefs":{"Monarch":{"xref_id":"0010040"}}}


id: GO:0032992
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A macromolecular complex containing separate protein and carbohydrate molecules. Separate in this context means not covalently bound to each other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"protein-carbohydrate complex","termid":"GO:0032992"}


id: GO:0010610
data:
  {"annotated_genes":["SJAG_02573","SJAG_03886","SJAG_05014"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89548,89945,91281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000815"}]},"cv_name":"biological_process","definition":"Any process that modulates the propensity of mRNA molecules to degradation that is part of a change in state or activity of a cell as a result of an exogenous disturbance.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mRNA stability","termid":"GO:0043488"},{"relation_name":"part_of","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02573":null,"SJAG_03886":null,"SJAG_05014":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of mRNA stability involved in response to stress","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010610","terms_by_termid":{"GO:2000815":null}}


id: PR:O94275
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An E3 ubiquitin-protein ligase HECTD2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03811"],"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":"E3 ubiquitin-protein ligase mug30 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP8B7.27","secondary_identifiers":["UniProtKB:O94275"],"synonyms":[{"name":"Spom972h-HECTD2","type":"exact"},{"name":"meiotically up-regulated gene 30 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94275"}


id: GO:0034239
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of macrophage fusion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of syncytium formation by plasma membrane fusion","termid":"GO:0060142"},{"relation_name":"regulates","term_name":"macrophage fusion","termid":"GO:0034238"}],"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 macrophage fusion","termid":"GO:0034239"}


id: PBO:0088246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIIA","termid":"PBO:0088246"}


id: PBO:0030309
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_nucleus_localization","termid":"PBO:0030309"}


id: SO:0001484
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An X element combinatorial repeat is a repeat region located between the X element and the telomere or adjacent Y' element.","direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_region","termid":"SO:0000657"},{"relation_name":"part_of","term_name":"telomere","termid":"SO:0000624"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X_element_combinatorial_repeat","synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:x_element_combinatorial_repeat","type":"exact"},{"name":"X element combinatorial repeat","type":"exact"}],"termid":"SO:0001484"}


id: PBO:0083934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G1 cyclin involved in regulation of the cell cycle; activates Cdc28p kinase to promote the G1 to S phase transition; late G1 specific expression depends on transcription factor complexes, MBF (Swi6p-Mbp1p) and SBF (Swi6p-Swi4p); CLN2 has a paralog, CLN1, that arose from the whole genome duplication; cell cycle arrest phenotype of the cln1 cln2 cln3 triple null mutant is complemented by any of human cyclins CCNA2, CCNB1, CCNC, CCND1, or CCNE1","termid":"PBO:0083934"}


id: PBO:0088089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP-glucose pyrophosphorylase (UGPase); catalyses the reversible formation of UDP-Glc from glucose 1-phosphate and UTP, involved in a wide variety of metabolic pathways, expression modulated by Pho85p through Pho4p; involved in PKA-mediated oxidative stress resistance and long-term survival in stationary phase; UGP1 has a paralog, YHL012W, that arose from the whole genome duplication","termid":"PBO:0088089"}


id: GO:1902083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of peptidyl-cysteine S-nitrosylation.","definition_xrefs":["GOC:TermGenie","PMID:19198614","GOC:rl","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein modification process","termid":"GO:0031400"},{"relation_name":"is_a","term_name":"regulation of peptidyl-cysteine S-nitrosylation","termid":"GO:2000169"},{"relation_name":"negatively_regulates","term_name":"peptidyl-cysteine S-nitrosylation","termid":"GO:0018119"}],"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 peptidyl-cysteine S-nitrosylation","synonyms":[{"name":"down regulation of S-nitrosylation","type":"exact"},{"name":"down regulation of peptidyl-cysteine S-nitrosylation","type":"exact"},{"name":"down regulation of protein S-nitrosylation","type":"exact"},{"name":"down-regulation of S-nitrosylation","type":"exact"},{"name":"down-regulation of peptidyl-cysteine S-nitrosylation","type":"exact"},{"name":"down-regulation of protein S-nitrosylation","type":"exact"},{"name":"downregulation of S-nitrosylation","type":"exact"},{"name":"downregulation of peptidyl-cysteine S-nitrosylation","type":"exact"},{"name":"downregulation of protein S-nitrosylation","type":"exact"},{"name":"inhibition of S-nitrosylation","type":"exact"},{"name":"inhibition of peptidyl-cysteine S-nitrosylation","type":"narrow"},{"name":"inhibition of protein S-nitrosylation","type":"exact"},{"name":"negative regulation of S-nitrosylation","type":"exact"},{"name":"negative regulation of protein S-nitrosylation","type":"exact"}],"termid":"GO:1902083"}


id: GO:0021639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the trochlear nerve is generated and organized. The trochlear nerve is a motor nerve and is the only cranial nerve to exit the brain dorsally. The trochlear nerve innervates the superior oblique muscle.","definition_xrefs":["ISBN:0838580343","GO_REF:0000021","GOC:dgh","GOC:cls","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve morphogenesis","termid":"GO:0021602"},{"relation_name":"part_of","term_name":"trochlear nerve development","termid":"GO:0021558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"trochlear nerve morphogenesis","synonyms":[{"name":"CH IV morphogenesis","type":"related"}],"termid":"GO:0021639"}


id: SO:0002017
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant located in a conserved intergenic region, between genes.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intergenic_variant","termid":"SO:0001628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved_intergenic_variant","secondary_identifiers":["http://snpeff.sourceforge.net/SnpEff_manual.html"],"synonyms":[{"name":"Jannovar:conserved_intergenic_variant","type":"exact"},{"name":"conserved intergenic variant","type":"exact"},{"name":"snpEff:INTERGENIC_CONSERVED","type":"exact"}],"termid":"SO:0002017"}


id: GO:0015746
data:
  {"annotated_genes":["SJAG_01872","SJAG_00275"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71331,72198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006843"}]},"cv_name":"biological_process","definition":"The directed movement of citrate, 2-hydroxy-1,2,3-propanetricarboyxlate, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tricarboxylic acid transport","termid":"GO:0006842"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00275":null,"SJAG_01872":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"citrate transport","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0015746","terms_by_termid":{"GO:0006843":null}}


id: PBO:0089504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane-associated serine-rich cell wall sensor Wsc1","termid":"PBO:0089504"}


id: GO:0097336
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 risperidone stimulus.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"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 risperidone","termid":"GO:0097336"}


id: PBO:0088532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP1 regulatory subunit Reg1","termid":"PBO:0088532"}


id: PBO:0114432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PFKFB3 antisense RNA 1","termid":"PBO:0114432"}


id: PBO:0052590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin subunit alpha 1","termid":"PBO:0052590"}


id: PBO:0074736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 94","termid":"PBO:0074736"}


id: GO:0044853
data:
  {"annotated_genes":["SJAG_04714","SJAG_04001","SJAG_03536","SJAG_04620"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88190,89080,103042,118337],"is_not":false,"summary":null,"term":"GO:0044853"}]},"cv_name":"cellular_component","definition":"A membrane raft that is part of the plasma membrane.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane raft","termid":"GO:0045121"},{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"}],"gene_count":4,"genes_by_uniquename":{"SJAG_03536":null,"SJAG_04001":null,"SJAG_04620":null,"SJAG_04714":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"plasma membrane raft","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0044853","terms_by_termid":{"GO:0044853":null}}


id: GO:0004777
data:
  {"annotated_genes":["SJAG_00674","SJAG_03293"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75786,77330],"is_not":false,"summary":null,"term":"GO:0004777"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: succinate semialdehyde + NAD+ + H2O = succinate + NADH + H+.","definition_xrefs":["RHEA:13217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinate-semialdehyde dehydrogenase [NAD(P)+] activity","termid":"GO:0009013"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00674":null,"SJAG_03293":null},"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":"succinate-semialdehyde dehydrogenase (NAD+) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:1.2.1.24","MetaCyc:SUCCINATE-SEMIALDEHYDE-DEHYDROGENASE-RXN","GO:0008952","Reactome:R-HSA-888548"],"synonyms":[{"name":"succinate semialdehyde dehydrogenase activity","type":"broad"},{"name":"succinate semialdehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"succinate-semialdehyde dehydrogenase activity","type":"broad"},{"name":"succinate-semialdehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"succinic semialdehyde dehydrogenase activity","type":"broad"},{"name":"succinyl semialdehyde dehydrogenase activity","type":"related"}],"termid":"GO:0004777","terms_by_termid":{"GO:0004777":null}}


id: PBO:0085032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-canonical poly(A) polymerase; involved in nuclear RNA degradation as a component of the TRAMP complex; catalyzes polyadenylation of hypomodified tRNAs, and snoRNA and rRNA precursors; overlapping but non-redundant functions with Pap2p","termid":"PBO:0085032"}


id: PBO:0079107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSC22 domain family member 2","termid":"PBO:0079107"}


id: PBO:0077677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF superfamily member 8","termid":"PBO:0077677"}


id: PR:Q10214
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC4H3.06 gene.","definition_xrefs":["UniProtKB:Q10214","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 C4H3.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.06","synonyms":[{"name":"Spom972h-SPAC4H3.06","type":"exact"}],"termid":"PR:Q10214"}


id: PBO:0055693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIX1 and RIOK2 antisense RNA 1","termid":"PBO:0055693"}


id: MONDO:0035775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome","secondary_identifiers":["GARD:22417","MEDGEN:1842919","Orphanet:600668","UMLS:C5681527"],"termid":"MONDO:0035775","xrefs":{"Monarch":{"xref_id":"0035775"}}}


id: PATO:0002132
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A disposition inhering in a tumour by virtue of the bearer's disposition not to invade surrounding tissues.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplastic","termid":"PATO:0002011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplastic, non-invasive","termid":"PATO:0002132"}


id: _global:acts_upstream_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"c acts upstream of p if and only if c enables some f that is involved in p' and p' occurs chronologically before p, is not part of p, and affects the execution of p. c is a material entity and f, p, p' are processes.","direct_ancestors":[{"relation_name":"is_a","term_name":"acts_upstream_of_or_within","termid":"_global:acts_upstream_of_or_within"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acts_upstream_of","secondary_identifiers":["RO:0002263"],"termid":"_global:acts_upstream_of"}


id: GO:0046632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of an alpha-beta T cell. An alpha-beta T cell is a T cell that expresses an alpha-beta T cell receptor complex.","definition_xrefs":["CL:0000789","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell differentiation","termid":"GO:0030217"},{"relation_name":"is_a","term_name":"alpha-beta T cell activation","termid":"GO:0046631"}],"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":"alpha-beta T cell differentiation","synonyms":[{"name":"alpha-beta T cell development","type":"related"},{"name":"alpha-beta T lymphocyte differentiation","type":"exact"},{"name":"alpha-beta T-cell differentiation","type":"exact"},{"name":"alpha-beta T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0046632"}


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:dph","GOC:tb","GOC:mah","PMID:8280098"],"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: GO:0046829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the movement of RNA from the cytoplasm into the nucleus.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound transport","termid":"GO:0032240"},{"relation_name":"is_a","term_name":"negative regulation of nucleocytoplasmic transport","termid":"GO:0046823"},{"relation_name":"is_a","term_name":"regulation of RNA import into nucleus","termid":"GO:0046828"},{"relation_name":"negatively_regulates","term_name":"RNA import into nucleus","termid":"GO:0006404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006913"},{"rel_name":"regulates","termid":"GO:0006913"}],"interesting_parent_ids":["GO:0008150","GO:0006913","GO:0006810"],"is_obsolete":false,"name":"negative regulation of RNA import into nucleus","synonyms":[{"name":"down regulation of RNA import into nucleus","type":"exact"},{"name":"down-regulation of RNA import into nucleus","type":"exact"},{"name":"downregulation of RNA import into nucleus","type":"exact"},{"name":"inhibition of RNA import into nucleus","type":"narrow"},{"name":"negative regulation of RNA import into cell nucleus","type":"exact"},{"name":"negative regulation of RNA transport from cytoplasm to nucleus","type":"exact"},{"name":"negative regulation of RNA-nucleus import","type":"exact"}],"termid":"GO:0046829"}


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


id: PBO:0029332
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H2A_phosphorylation","termid":"PBO:0029332"}


id: PR:Q9P3U4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dbl4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P3U4"],"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":"E3 ubiquitin-protein ligase dbl4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC328.02","synonyms":[{"name":"DNA-break-localizing protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-dbl4","type":"exact"},{"name":"histone E3 ligase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P3U4"}


id: FYPO:0004009
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 of ribosomal DNA into ribosomal RNA occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"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:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0000294","FYPO:0005447"],"is_obsolete":false,"name":"decreased rRNA transcription","synonyms":[{"name":"decreased rDNA transcription","type":"exact"},{"name":"decreased rRNA transcription during mitotic cell cycle","type":"related"},{"name":"decreased rRNA transcription during vegetative growth","type":"exact"},{"name":"decreased ribosomal RNA transcription","type":"exact"},{"name":"reduced rRNA transcription","type":"exact"}],"termid":"FYPO:0004009"}


id: PBO:0064911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 4 regulatory subunit 2","termid":"PBO:0064911"}


id: FYPO:0004756
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which regulation of the initiation of DNA-dependent DNA replication is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype","termid":"FYPO:0000145"},{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal regulation of DNA replication initiation","synonyms":[{"name":"abnormal regulation of DNA replication initiation during mitotic cell cycle","type":"related"},{"name":"abnormal regulation of DNA-dependent DNA replication initiation","type":"exact"}],"termid":"FYPO:0004756"}


id: PBO:0080096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UST antisense RNA 2","termid":"PBO:0080096"}


id: PBO:0052115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily C member 3","termid":"PBO:0052115"}


id: PBO:0003946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate carboxylase Pyr1","termid":"PBO:0003946"}


id: PBO:0073348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family B member 9","termid":"PBO:0073348"}


id: MONDO:0033967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immune dysregulation with inflammatory bowel disease (obsolete MONDO:0033967)","secondary_identifiers":["Orphanet:529974"],"termid":"MONDO:0033967","xrefs":{"Monarch":{"xref_id":"0033967"}}}


id: FYPO:0000641
data:
  {"alleles_by_uniquename":{"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119260,119258,119259],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"FYPO:0000671"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which any process of chromosome organization is abnormal. Chromosome organization results in the assembly, arrangement of constituent parts, or disassembly of chromosomes.","definition_xrefs":["PomBase:mah","GO:0051276"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component organization","termid":"FYPO:0000335"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03449":null},"genotype_count":3,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]}},"in_subsets":["fypo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal chromosome organization","references_by_uniquename":{"PMID:24184107":null},"single_locus_annotated_genes":["SJAG_03449"],"single_locus_genotype_uniquenames":["man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","man1delta"],"synonyms":[{"name":"abnormal chromosome organisation","type":"exact"}],"termid":"FYPO:0000641","terms_by_termid":{"FYPO:0000671":null}}


id: PBO:0069988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1283, pseudogene","termid":"PBO:0069988"}


id: GO:0015217
data:
  {"annotated_genes":["SJAG_02050"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005471"}]},"cv_name":"molecular_function","definition":"Enables the transfer of ADP, adenosine diphosphate, from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transmembrane transporter activity","termid":"GO:0000295"},{"relation_name":"is_a","term_name":"purine ribonucleotide transmembrane transporter activity","termid":"GO:0005346"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02050":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":"ADP transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0015217","terms_by_termid":{"GO:0005471":null}}


id: PBO:0051981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JADE1 adjacent regulatory RNA","termid":"PBO:0051981"}


id: GO:0060743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process, independent of morphogenetic (shape) change, that is required for an epithelial cell of the prostate gland to attain its fully functional state. An epithelial cell is a cell usually found in a two-dimensional sheet with a free surface.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell maturation","termid":"GO:0002070"},{"relation_name":"part_of","term_name":"epithelial cell differentiation involved in prostate gland development","termid":"GO:0060742"}],"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 maturation involved in prostate gland development","synonyms":[{"name":"prostate gland epithelial cell development","type":"exact"}],"termid":"GO:0060743"}


id: GO:0000256
data:
  {"annotated_genes":["SJAG_00035","SJAG_05287"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62012,74986],"is_not":false,"summary":null,"term":"GO:0000256"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of allantoin, (2,5-dioxo-4-imidazolidinyl)urea.","definition_xrefs":["ISBN:0198547684","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"allantoin metabolic process","termid":"GO:0000255"},{"relation_name":"is_a","term_name":"amide catabolic process","termid":"GO:0043605"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00035":null,"SJAG_05287":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"allantoin catabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"allantoin breakdown","type":"exact"},{"name":"allantoin catabolism","type":"exact"},{"name":"allantoin degradation","type":"exact"}],"termid":"GO:0000256","terms_by_termid":{"GO:0000256":null}}


id: PBO:0048520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerophosphodiester phosphodiesterase domain containing 3","termid":"PBO:0048520"}


id: MONDO:0013332
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":"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability","secondary_identifiers":["UMLS:C3150890","OMIM:613627","MEDGEN:462240","SCTID:719162001"],"synonyms":[{"name":"Tsukahara syndrome","type":"related"},{"name":"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability","type":"exact"},{"name":"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation","type":"exact"}],"termid":"MONDO:0013332","xrefs":{"Monarch":{"xref_id":"0013332"}}}


id: PBO:0036355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-body assembly protein","termid":"PBO:0036355"}


id: PBO:0045816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 6","termid":"PBO:0045816"}


id: MONDO:0004589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary retinal dystrophy (obsolete MONDO:0004589)","termid":"MONDO:0004589","xrefs":{"Monarch":{"xref_id":"0004589"}}}


id: MONDO:0021759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acquired fructose intolerance is a condition in which the body can not properly absorb the sugar, fructose. As a result, affected people may experience gastrointestinal symptoms, such as gas, abdominal pain, bloating and/or diarrhea, depending on the quantity of fructose consumed and the presence of other sugars ingested with it. Gastrointestinal symptoms related to acquired fructose intolerance appear to be more common in people who have an underlying functional bowel disorder such as irritable bowel syndrome. The underlying cause of the condition is poorly understood. It is distinct from the rare, genetic form of fructose intolerance (called hereditary fructose intolerance), which usually develops earlier in life and often affects more than one family member. Acquired fructose intolerance is generally managed with dietary modifications.","definition_xrefs":["GARD:0002399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of fructose metabolism","termid":"MONDO:0017689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"acquired fructose intolerance","secondary_identifiers":["MEDGEN:288539","UMLS:C1531694","SCTID:413427002"],"synonyms":[{"name":"acquired fructose intolerance","type":"exact"},{"name":"dietary fructose intolerance","type":"related"},{"name":"fructose malabsorption","type":"related"},{"name":"intestinal fructose intolerance","type":"related"}],"termid":"MONDO:0021759","xrefs":{"Monarch":{"xref_id":"0021759"}}}


id: GO:0140327
data:
  {"annotated_genes":["SJAG_01945","SJAG_00669","SJAG_01731","SJAG_05209","SJAG_02897"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97707,94186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140351"},{"annotations":[99265],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180013"},{"annotations":[97709,94188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140345"},{"annotations":[112296,99267,97711,99984,94190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090555"},{"annotations":[112298,99268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140346"}]},"cv_name":"molecular_function","definition":"Catalysis of the movement of lipids from the exoplasmic to the cytosolic leaflet of a membrane, using energy from the hydrolysis of ATP.","definition_xrefs":["PMID:25284293","Wikipedia:Flippase","PMID:20043909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase-coupled intramembrane lipid transporter activity","termid":"GO:0140326"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00669":null,"SJAG_01731":null,"SJAG_01945":null,"SJAG_02897":null,"SJAG_05209":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0140303","GO:0003674"],"is_obsolete":false,"name":"flippase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"flippase activity (exoplasmic to cytosolic leaflet)","type":"exact"}],"termid":"GO:0140327","terms_by_termid":{"GO:0090555":null,"GO:0140345":null,"GO:0140346":null,"GO:0140351":null,"GO:0180013":null}}


id: PBO:0068788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 25, pseudogene","termid":"PBO:0068788"}


id: GO:0035715
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to chemokine (C-C motif) ligand 2.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-C chemokine binding","termid":"GO:0019957"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 2 binding","synonyms":[{"name":"CCL2 binding","type":"exact"}],"termid":"GO:0035715"}


id: PBO:0031096
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_population_growth_following_spore_germination","termid":"PBO:0031096"}


id: MONDO:0850282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An asthma that is characterized by the development of persistent airway inflammation and recurrent attacks of breathlessness and wheezing, which vary in severity and frequency.","definition_xrefs":["DOID:0080809"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asthma","termid":"MONDO:0004979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic asthma","secondary_identifiers":["UMLS:C0877430","MEDGEN:1843404"],"synonyms":[{"name":"adult-onset severe asthma","type":"narrow"},{"name":"persistent mild asthma","type":"narrow"},{"name":"persistent moderate asthma","type":"narrow"},{"name":"persistent severe asthma","type":"narrow"}],"termid":"MONDO:0850282","xrefs":{"Monarch":{"xref_id":"0850282"}}}


id: PBO:0005896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal small subunit (predicted)","termid":"PBO:0005896"}


id: GO:0016980
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: creatine + H2O = sarcosine + urea.","definition_xrefs":["RHEA:22456","EC:3.5.3.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"creatinase activity","secondary_identifiers":["MetaCyc:CREATINASE-RXN","KEGG_REACTION:R01566"],"synonyms":[{"name":"creatine amidinohydrolase activity","type":"related"}],"termid":"GO:0016980"}


id: PBO:0058403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4773-2","termid":"PBO:0058403"}


id: GO:0047816
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinose + NAD+ = D-arabinono-1,4-lactone + NADH.","definition_xrefs":["RHEA:20457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-arabinose 1-dehydrogenase [NAD(P)+] activity","termid":"GO:0045290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"D-arabinose 1-dehydrogenase (NAD+) activity","secondary_identifiers":["MetaCyc:D-ARABINOSE-1-DEHYDROGENASE-RXN","EC:1.1.1.116"],"synonyms":[{"name":"D-arabinose:NAD+ 1-oxidoreductase activity","type":"related"},{"name":"NAD-pentose-dehydrogenase activity","type":"related"},{"name":"arabinose(fucose)dehydrogenase activity","type":"related"}],"termid":"GO:0047816"}


id: GO:0014742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of muscle hypertrophy.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle hypertrophy","termid":"GO:0014743"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"muscle hypertrophy","termid":"GO:0014896"}],"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 muscle hypertrophy","termid":"GO:0014742"}


id: FYPO:0004500
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the rate or occurrence of DNA polymerase processivity factor activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA polymerase processivity factor activity","termid":"FYPO:0004499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased DNA polymerase processivity factor activity","synonyms":[{"name":"reduced DNA polymerase processivity factor activity","type":"exact"}],"termid":"FYPO:0004500"}


id: GO:0045778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ossification, the formation of bone or of a bony substance or the conversion of fibrous tissue or of cartilage into bone or a bony substance.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ossification","termid":"GO:0030278"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"ossification","termid":"GO:0001503"}],"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 ossification","synonyms":[{"name":"activation of ossification","type":"narrow"},{"name":"positive regulation of bone biosynthesis","type":"exact"},{"name":"positive regulation of bone formation","type":"exact"},{"name":"stimulation of ossification","type":"narrow"},{"name":"up regulation of ossification","type":"exact"},{"name":"up-regulation of ossification","type":"exact"},{"name":"upregulation of ossification","type":"exact"}],"termid":"GO:0045778"}


id: MONDO:0006411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, highly aggressive carcinoma that arises from the sinonasal tract. It is characterized by the presence of small to medium size malignant cells. The prognosis is poor.","definition_xrefs":["NCIT:C54294"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undifferentiated carcinoma","termid":"MONDO:0005617"}],"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":"sinonasal undifferentiated carcinoma","secondary_identifiers":["ONCOTREE:SNUC","SCTID:697993003","UMLS:C1710096","MEDGEN:313704","MESH:C537344","EFO:1000527","DOID:0080799"],"synonyms":[{"name":"SNUC","type":"related"},{"name":"Sinonasal anaplastic carcinoma","type":"exact"},{"name":"highly aggressive undifferentiated carcinoma of the nasal cavity and paranasal sinuses","type":"related"},{"name":"sinonasal undifferentiated carcinoma","type":"exact"},{"name":"undifferentiated Sinonasal cancer","type":"exact"}],"termid":"MONDO:0006411","xrefs":{"Monarch":{"xref_id":"0006411"}}}


id: PBO:0089969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activating signal cointegrator 1 complex subunit, human ASCC1 ortholog","termid":"PBO:0089969"}


id: MONDO:0007188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary basilar impression (PBI) is a very rare skeletal developmental defect characterized by congenital upward translocation of the upper cervical spine and clivus into the foramen magnum. PBI can be asymptomatic or associated with severe neurological dysfunction.","definition_xrefs":["Orphanet:2285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary basilar invagination","secondary_identifiers":["MEDGEN:400018","UMLS:C1862299","MESH:C566226","GARD:1037","OMIM:109500"],"synonyms":[{"name":"Bull-Nixon syndrome","type":"exact"},{"name":"basilar impression, primary","type":"related"},{"name":"primary basilar impression","type":"related"}],"termid":"MONDO:0007188","xrefs":{"Monarch":{"xref_id":"0007188"}}}


id: MONDO:0013127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22.","definition_xrefs":["DOID:0110087","PMID:19442771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"asphyxiating thoracic dystrophy 3","secondary_identifiers":["MESH:C537602","MEDGEN:19860","NCIT:C163755","Orphanet:93270","SCTID:254051008","ICD9:759.89","OMIM:613091","SCTID:27330009","UMLS:C0036069","GARD:15613","Orphanet:93271","DOID:0050549"],"synonyms":[{"name":"ATD3","type":"exact"},{"name":"SRPS type 1","type":"exact"},{"name":"SRPS type 3","type":"exact"},{"name":"SRPS1","type":"exact"},{"name":"SRPS2B","type":"exact"},{"name":"SRPS3","type":"exact"},{"name":"SRTD3","type":"exact"},{"name":"Saldino-Noonan syndrome","type":"exact"},{"name":"Verma-Naumoff syndrome","type":"exact"},{"name":"asphyxiating thoracic dystrophy 3","type":"exact"},{"name":"asphyxiating thoracic dystrophy type 3","type":"exact"},{"name":"polydactyly with neonatal chondrodystrophy type 1","type":"exact"},{"name":"polydactyly with neonatal chondrodystrophy type III","type":"exact"},{"name":"polydactyly with neonatal chondrodystrophy, type 3","type":"exact"},{"name":"polydactyly with neonatal chondrodystrophy, type I","type":"exact"},{"name":"short rib polydactyly syndrome Verma Naumoff type","type":"exact"},{"name":"short rib-polydactyly syndrome Saldino-Noonan type","type":"exact"},{"name":"short rib-polydactyly syndrome type 1","type":"exact"},{"name":"short rib-polydactyly syndrome type 3","type":"exact"},{"name":"short rib-polydactyly syndrome type III","type":"exact"},{"name":"short rib-polydactyly syndrome, type 2B","type":"exact"},{"name":"short rib-polydactyly syndrome, type IIB","type":"exact"},{"name":"short-rib thoracic dysplasia 3 with or without polydactyly","type":"exact"},{"name":"type I short rib polydactyly syndrome","type":"exact"}],"termid":"MONDO:0013127","xrefs":{"Monarch":{"xref_id":"0013127"}}}


id: GO:0030226
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an apolipoprotein to initiate a change in cell activity.","definition_xrefs":["ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cargo receptor activity","termid":"GO:0038024"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038024"}],"interesting_parent_ids":["GO:0003674","GO:0038024"],"is_obsolete":false,"name":"apolipoprotein receptor activity","termid":"GO:0030226"}


id: GO:0021523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroepithelial cells in the neural tube acquire specialized structural and/or functional features of somatic motor neurons. Somatic motor neurons innervate skeletal muscle targets and are responsible for transmission of motor impulses from the brain to the periphery. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:jid","GOC:cls","GOC:dgh","GOC:dph","GO_REF:0000021","PMID:11262869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal cord motor neuron differentiation","termid":"GO:0021522"}],"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":"somatic motor neuron differentiation","termid":"GO:0021523"}


id: PBO:0084538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the p24 family involved in ER to Golgi transport; role in misfolded protein quality control; forms a heterotrimeric complex with Erp1, Erp2p, and Emp24,","termid":"PBO:0084538"}


id: PBO:0113308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in magnesium homeostasis; required for Mg2+ sequestration in vacuole; required for normal mitochondrial morphology; has similarity to hemolysins","termid":"PBO:0113308"}


id: GO:1900082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of arginine catabolic process.","definition_xrefs":["GOC:TermGenie","GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amine catabolic process","termid":"GO:0033242"},{"relation_name":"is_a","term_name":"negative regulation of amino acid metabolic process","termid":"GO:0045763"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of arginine catabolic process","termid":"GO:1900081"},{"relation_name":"negatively_regulates","term_name":"arginine catabolic process","termid":"GO:0006527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044248"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"negatively_regulates","termid":"GO:0044248"},{"rel_name":"negatively_regulates","termid":"GO:0006520"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520","GO:0044248"],"is_obsolete":false,"name":"negative regulation of arginine catabolic process","synonyms":[{"name":"down regulation of arginine breakdown","type":"exact"},{"name":"down regulation of arginine catabolic process","type":"exact"},{"name":"down regulation of arginine catabolism","type":"exact"},{"name":"down regulation of arginine degradation","type":"exact"},{"name":"down-regulation of arginine breakdown","type":"exact"},{"name":"down-regulation of arginine catabolic process","type":"exact"},{"name":"down-regulation of arginine catabolism","type":"exact"},{"name":"down-regulation of arginine degradation","type":"exact"},{"name":"downregulation of arginine breakdown","type":"exact"},{"name":"downregulation of arginine catabolic process","type":"exact"},{"name":"downregulation of arginine catabolism","type":"exact"},{"name":"downregulation of arginine degradation","type":"exact"},{"name":"inhibition of arginine breakdown","type":"narrow"},{"name":"inhibition of arginine catabolic process","type":"narrow"},{"name":"inhibition of arginine catabolism","type":"narrow"},{"name":"inhibition of arginine degradation","type":"narrow"},{"name":"negative regulation of arginine breakdown","type":"exact"},{"name":"negative regulation of arginine catabolism","type":"exact"},{"name":"negative regulation of arginine degradation","type":"exact"}],"termid":"GO:1900082"}


id: PBO:0049214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate receptor interacting protein 1","termid":"PBO:0049214"}


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: MONDO:0030997
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 37","secondary_identifiers":["GARD:16440","MEDGEN:1783339","UMLS:C5543281","OMIM:619272"],"synonyms":[{"name":"MC1DN37","type":"exact"},{"name":"mitochondrial complex 1 deficiency, nuclear type 37","type":"exact"},{"name":"mitochondrial complex I deficiency, nuclear type 37","type":"exact"}],"termid":"MONDO:0030997","xrefs":{"Monarch":{"xref_id":"0030997"}}}


id: PBO:0065339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prune exopolyphosphatase 1","termid":"PBO:0065339"}


id: GO:0009902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which chloroplasts in photosynthetic cells migrate toward illuminated sites to optimize photosynthesis and move away from excessively illuminated areas to protect the photosynthetic machinery.","definition_xrefs":["PMID:11309623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloroplast organization","termid":"GO:0009658"},{"relation_name":"is_a","term_name":"chloroplast localization","termid":"GO:0019750"},{"relation_name":"is_a","term_name":"establishment of plastid localization","termid":"GO:0051667"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"chloroplast relocation","synonyms":[{"name":"chloroplast movement","type":"exact"}],"termid":"GO:0009902"}


id: PBO:0089364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isoamyl acetate hydrolytic enzyme Iah1","termid":"PBO:0089364"}


id: FYPO:0005032
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 mutations occur at a normal (i.e. indistinguishable from wild type) frequency.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"},{"relation_name":"is_a","term_name":"vegetative cell phenotype","termid":"FYPO:0001320"}],"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:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal mutation rate","synonyms":[{"name":"normal mutation rate during mitotic cell cycle","type":"related"},{"name":"normal mutation rate during vegetative growth","type":"exact"}],"termid":"FYPO:0005032"}


id: MONDO:0018433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute myeloid leukemia with t(6;9)(p23;q34) is a rare subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by clonal proliferation of poorly differentiated myeloid blasts in the bone marrow, blood, or other tissues in patients who present the t(6;9)(p23;q34) translocation. Frequently associated with multilineage bone marrow dysplasia, it usually presents with anemia, thrombocytopenia (often pancytopenia), and other nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). Basophilia, as well as poor response to chemotherapy, has been reported.","definition_xrefs":["Orphanet:402014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"acute myeloid leukemia with t(6;9)(p23;q34)","secondary_identifiers":["GARD:21710","MEDGEN:1376401","UMLS:C4518837"],"synonyms":[{"name":"AML with t(6;9)(p23;q34)","type":"exact"}],"termid":"MONDO:0018433","xrefs":{"Monarch":{"xref_id":"0018433"}}}


id: PBO:0062065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 3 subfamily A member 3","termid":"PBO:0062065"}


id: GO:0022036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a rhombomere cell.","definition_xrefs":["GOC:dph","GOC:jid","GOC:cls","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"rhombomere development","termid":"GO:0021546"}],"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":"rhombomere cell differentiation","termid":"GO:0022036"}


id: GO:1903007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of Lys63-specific deubiquitinase activity.","definition_xrefs":["GO_REF:0000059","GOC:bf","GOC:PARL","GOC:TermGenie","PMID:22970133"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peptidase activity","termid":"GO:0010952"},{"relation_name":"is_a","term_name":"positive regulation of protein K63-linked deubiquitination","termid":"GO:1903006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0070647"},{"rel_name":"regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"positive regulation of Lys63-specific deubiquitinase activity","synonyms":[{"name":"activation of Lys63-specific deubiquitinase activity","type":"narrow"},{"name":"up regulation of Lys63-specific deubiquitinase activity","type":"exact"},{"name":"up-regulation of Lys63-specific deubiquitinase activity","type":"exact"},{"name":"upregulation of Lys63-specific deubiquitinase activity","type":"exact"}],"termid":"GO:1903007"}


id: MONDO:0968986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare dysraphic spinal cord lipoma characterized by the lipomatous mass extending ventrally to the dorsal root entry zone, indicating a more severe malformation of the spinal cord. The diagnosis can be suggested on imaging but usually confirmed during surgery.","definition_xrefs":["Orphanet:645285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conus spinal cord lipoma","termid":"MONDO:0958350"}],"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":"chaotic conus spinal cord lipoma","secondary_identifiers":["UMLS:C5816729","MEDGEN:1853143"],"termid":"MONDO:0968986","xrefs":{"Monarch":{"xref_id":"0968986"}}}


id: PBO:0076914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-2 beta","termid":"PBO:0076914"}


id: GO:0140938
data:
  {"annotated_genes":["SJAG_02873","SJAG_03487","SJAG_00769","SJAG_01193","SJAG_04574"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140954"},{"annotations":[78344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046975"},{"annotations":[63956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140955"},{"annotations":[57748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062122"},{"annotations":[78343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042800"},{"annotations":[58414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140999"},{"annotations":[110291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140948"},{"annotations":[62695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140949"},{"annotations":[110293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140947"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + a histone H3 = S-adenosyl-L-homocysteine + a methylated histone H3. Histone methylation generally occurs on either an arginine or a lysine residue.","definition_xrefs":["PMID:28450737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone methyltransferase activity","termid":"GO:0042054"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00769":null,"SJAG_01193":null,"SJAG_02873":null,"SJAG_03487":null,"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008276"}],"interesting_parent_ids":["GO:0008276","GO:0016741","GO:0140096","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"histone H3 methyltransferase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5638332","Reactome:R-HSA-5634750","Reactome:R-HSA-5244692","Reactome:R-HSA-3788748","Reactome:R-HSA-4827382","Reactome:R-HSA-5159245","Reactome:R-HSA-5634802","Reactome:R-HSA-5649801","Reactome:R-HSA-9842833","Reactome:R-HSA-4827383","Reactome:R-HSA-8936608","Reactome:R-HSA-8937113","Reactome:R-HSA-5638157","Reactome:R-HSA-5638141","Reactome:R-HSA-5634729","Reactome:R-HSA-5638333","Reactome:R-HSA-8936584","Reactome:R-HSA-5649802","Reactome:R-HSA-9844006","Reactome:R-HSA-5649799","Reactome:R-HSA-8937022","Reactome:R-HSA-9844057","Reactome:R-HSA-5205799","Reactome:R-HSA-3788745","Reactome:R-HSA-5637686","Reactome:R-HSA-5649764","Reactome:R-HSA-5649800","Reactome:R-HSA-5661117"],"synonyms":[{"name":"histone H3 methylase activity","type":"exact"},{"name":"histone H3 methylation","type":"related"}],"termid":"GO:0140938","terms_by_termid":{"GO:0042800":null,"GO:0046975":null,"GO:0062122":null,"GO:0140947":null,"GO:0140948":null,"GO:0140949":null,"GO:0140954":null,"GO:0140955":null,"GO:0140999":null}}


id: GO:0120528
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: a 2-(omega-methylsulfanyl)alkylmalate = a 2-(omega-methylsulfanyl)alkylmaleate + H2O and a 3-(omega-methylsulfanyl)alkylmalate = a 2-(omega-methylsulfanyl)alkylmaleate + H2O.","definition_xrefs":["EC:4.2.1.170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"2-(omega-methylthio)alkylmalate dehydratase activity","termid":"GO:0120528"}


id: PBO:0061107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family CARD domain containing 5","termid":"PBO:0061107"}


id: GO:1905092
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 diosgenin stimulus.","definition_xrefs":["GO_REF:0000071","GOC:BHF","GOC:TermGenie","GOC:bc","PMID:25765596","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to sterol","termid":"GO:0036314"},{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"},{"relation_name":"is_a","term_name":"response to triterpenoid","termid":"GO:1905836"}],"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 diosgenin","termid":"GO:1905092"}


id: GO:0001746
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The morphogenetic process in which the anatomical structures of the larval eye in Drosophila are generated and organized. The larval eye in Drosophila is a relatively simple sensory system composed of Bolwig's organs: two clusters, each composed of 12 photoreceptor cells from which axons extend in a single fascicle to the brain.","definition_xrefs":["PMID:6185380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye morphogenesis","termid":"GO:0048592"},{"relation_name":"part_of","term_name":"Bolwig's organ development","termid":"GO:0055034"}],"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":"Bolwig's organ morphogenesis","termid":"GO:0001746"}


id: GO:0016764
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transfer of a glycosyl group, other than hexosyl or pentosyl, from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete transferase activity, transferring other glycosyl groups (obsolete GO:0016764)","synonyms":[{"name":"transferase activity, transferring other glycosyl groups","type":"exact"}],"termid":"GO:0016764"}


id: GO:0014725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of extraocular skeletal muscle development. Extraocular skeletal muscle development is the process whose specific outcome is the progression of the extraocular skeletal muscle over time, from its formation to the mature structure. The extraocular muscle is derived from cranial mesoderm and controls eye movements. The muscle begins its development with the differentiation of the muscle cells and ends with the mature muscle.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle tissue development","termid":"GO:0048641"},{"relation_name":"regulates","term_name":"extraocular skeletal muscle development","termid":"GO:0002074"}],"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 extraocular skeletal muscle development","termid":"GO:0014725"}


id: GO:0072387
data:
  {"annotated_genes":["SJAG_01937"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006747"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving flavin adenine dinucleotide, which acts as a coenzyme or prosthetic group of various flavoprotein oxidoreductase enzymes.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide metabolic process","termid":"GO:0009117"},{"relation_name":"is_a","term_name":"flavin-containing compound metabolic process","termid":"GO:0042726"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01937":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"flavin adenine dinucleotide metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"FAD or FADH2 metabolic process","type":"exact"},{"name":"flavin adenine dinucleotide metabolism","type":"exact"},{"name":"flavin-adenine dinucleotide metabolic process","type":"exact"}],"termid":"GO:0072387","terms_by_termid":{"GO:0006747":null}}


id: FYPO:0005807
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the movement of one or more proteins within the plasma membrane is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:25837586","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process","termid":"FYPO:0000627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein movement within plasma membrane","termid":"FYPO:0005807"}


id: GO:0038162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by erythropoietin (EPO) binding to the erythropoietin receptor (EPO-R) on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:nhn","PMID:12489509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to erythropoietin","termid":"GO:0036018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"erythropoietin-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-9006335"],"synonyms":[{"name":"EPO-R signaling pathway","type":"exact"},{"name":"erythropoietin receptor signaling pathway","type":"exact"}],"termid":"GO:0038162"}


id: PBO:0065583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine kinase 7 (inactive)","termid":"PBO:0065583"}


id: GO:0070555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-1 stimulus.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"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 interleukin-1","synonyms":[{"name":"response to IL-1","type":"exact"}],"termid":"GO:0070555"}


id: GO:0018426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of O3-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine. The polypeptide backbones of glycoproteins and mucin-like proteoglycans are extensively modified with a complex array of phosphoglycan chains that are linked to Ser/Thr-rich domains via a common Man-alpha1-phosphate-Ser linkage.","definition_xrefs":["RESID:AA0297"],"gene_count":0,"genotype_count":0,"name":"obsolete O3-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine biosynthetic process (obsolete GO:0018426)","synonyms":[{"name":"O3-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine anabolism","type":"exact"},{"name":"O3-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine biosynthesis","type":"exact"},{"name":"O3-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine formation","type":"exact"},{"name":"O3-(phosphoglycosyl-D-mannose-1-phosphoryl)-L-serine synthesis","type":"exact"}],"termid":"GO:0018426"}


id: PBO:0083418
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 ribosomal gene RPL7B","termid":"PBO:0083418"}


id: PBO:0000660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA methyltransferase Spb1 (predicted)","termid":"PBO:0000660"}


id: PBO:0088214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger C2H2-type","termid":"PBO:0088214"}


id: GO:0009466
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete class I cytochrome c (obsolete GO:0009466)","synonyms":[{"name":"class I cytochrome c","type":"exact"}],"termid":"GO:0009466"}


id: PATO:0000717
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000717 viability value (obsolete PATO:0000717)","termid":"PATO:0000717"}


id: PBO:0055793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LOXL2 antisense RNA 1","termid":"PBO:0055793"}


id: MONDO:0003521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete VIPoma (obsolete MONDO:0003521)","termid":"MONDO:0003521","xrefs":{"Monarch":{"xref_id":"0003521"}}}


id: GO:1905952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lipid localization.","definition_xrefs":["GO_REF:0000058","PMID:17564681","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"lipid localization","termid":"GO:0010876"}],"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 lipid localization","synonyms":[{"name":"regulation of lipid localisation","type":"exact"}],"termid":"GO:1905952"}


id: PBO:0001173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBA/TPR/DNAJ domain protein Ucp7","termid":"PBO:0001173"}


id: MONDO:0017925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"T-cell immunodeficiency with epidermodysplasia verruciformis is a rare primary immunodeficiency characterized by increased susceptibility to infection by human papillomavirus, presenting in childhood with disseminated flat wart-like cutaneous lesions. Burkitt lymphoma has also been reported. Whilst total T-cell counts are normal, there is impaired TCR signaling, profound peripheral naive T-cell lymphopenia with memory T-cells displaying an exhaustion phenotype.","definition_xrefs":["Orphanet:324294"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"}],"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":"T-cell immunodeficiency with epidermodysplasia verruciformis","secondary_identifiers":["UMLS:C4749500","GARD:17483","MEDGEN:1648416"],"synonyms":[{"name":"T-cell immunodeficiency due to RHOH deficiency","type":"exact"}],"termid":"MONDO:0017925","xrefs":{"Monarch":{"xref_id":"0017925"}}}


id: GO:0002309
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a T cell population by cell division as part of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell activation involved in immune response","termid":"GO:0002286"},{"relation_name":"is_a","term_name":"T cell proliferation","termid":"GO:0042098"}],"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":"T cell proliferation involved in immune response","synonyms":[{"name":"T cell proliferation during immune response","type":"related"},{"name":"T lymphocyte proliferation during immune response","type":"related"},{"name":"T-cell proliferation during immune response","type":"related"},{"name":"T-lymphocyte proliferation during immune response","type":"related"}],"termid":"GO:0002309"}


id: GO:0015786
data:
  {"annotated_genes":["SJAG_04162","SJAG_04406"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74864],"is_not":false,"summary":null,"term":"GO:0015786"},{"annotations":[112171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120112"}]},"cv_name":"biological_process","definition":"The process in which UDP-glucose is transported across a membrane.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"pyrimidine nucleotide-sugar transmembrane transport","termid":"GO:0090481"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04162":null,"SJAG_04406":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"UDP-glucose transmembrane transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015786","terms_by_termid":{"GO:0015786":null,"GO:0120112":null}}


id: PBO:0091101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-W ortholog","termid":"PBO:0091101"}


id: GO:1902640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of propan-2-ol.","definition_xrefs":["PMID:16346237","GOC:mengo_curators","GOC:TermGenie","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"propan-2-ol metabolic process","termid":"GO:1902639"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"},{"relation_name":"is_a","term_name":"fatty alcohol biosynthetic process","termid":"GO:1903175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"propan-2-ol biosynthetic process","synonyms":[{"name":"Isopropanol biosynthetic process","type":"exact"},{"name":"Isopropyl alcohol biosynthetic process","type":"exact"},{"name":"propan-2-ol anabolism","type":"exact"},{"name":"propan-2-ol biosynthesis","type":"exact"},{"name":"propan-2-ol formation","type":"exact"},{"name":"propan-2-ol synthesis","type":"exact"}],"termid":"GO:1902640"}


id: PBO:0089086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane copper transporter complex subunit Ctr5","termid":"PBO:0089086"}


id: PBO:0004350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U6 snRNP-associated protein Lsm4 (predicted)","termid":"PBO:0004350"}


id: MONDO:0850007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"syndromic lacrimal system disorder","secondary_identifiers":["UMLS:C5681383","GARD:22083","MEDGEN:1842875","Orphanet:519274"],"termid":"MONDO:0850007","xrefs":{"Monarch":{"xref_id":"0850007"}}}


id: MONDO:0020109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete constitutional megaloblastic anemia due to vitamin B12 metabolism disorder (obsolete MONDO:0020109)","secondary_identifiers":["Orphanet:98396"],"termid":"MONDO:0020109","xrefs":{"Monarch":{"xref_id":"0020109"}}}


id: GO:0018341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-lysine to form peptidyl-N6-pyruvic acid 2-iminyl-L-lysine.","definition_xrefs":["PSI-MOD:00292"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lysine modification to peptidyl-N6-pyruvic acid 2-iminyl-L-lysine (obsolete GO:0018341)","synonyms":[{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine anabolism","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine biosynthesis","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine biosynthetic process","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine formation","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine synthesis","type":"exact"}],"termid":"GO:0018341"}


id: GO:0062072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H3 trimethylated at lysine 9.","definition_xrefs":["PMID:30110338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 reader activity","termid":"GO:0140006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0140566","GO:0030674","GO:0060090"],"is_obsolete":false,"name":"histone H3K9me3 reader activity","synonyms":[{"name":"H3K9me3 modified histone binding","type":"narrow"}],"termid":"GO:0062072"}


id: PBO:0046330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ecto-NOX disulfide-thiol exchanger 1","termid":"PBO:0046330"}


id: PBO:0038433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetoacetyl-CoA synthetase pseudogene 1","termid":"PBO:0038433"}


id: GO:0050674
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of urothelial cells, resulting in the expansion of a cell population. Urothelial cells make up a layer of transitional epithelium in the wall of the bladder, ureter, and renal pelvis, external to the lamina propria.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell proliferation","termid":"GO:0050673"}],"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":"urothelial cell proliferation","termid":"GO:0050674"}


id: PBO:0063721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progesterone receptor","termid":"PBO:0063721"}


id: PBO:0043721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6C","termid":"PBO:0043721"}


id: PBO:0087641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the GET complex; involved in insertion of proteins into the ER membrane; required for the retrieval of HDEL proteins from the Golgi to the ER in an ERD2 dependent fashion and for normal mitochondrial morphology and inheritance","termid":"PBO:0087641"}


id: GO:1901317
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of flagellated sperm motility.","definition_xrefs":["GOC:TermGenie","GOC:krc","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cilium movement involved in cell motility","termid":"GO:0060295"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"flagellated sperm motility","termid":"GO:0030317"}],"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 flagellated sperm motility","synonyms":[{"name":"regulation of sperm motility","type":"broad"},{"name":"regulation of sperm movement","type":"broad"}],"termid":"GO:1901317"}


id: PBO:0084735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial intermediate peptidase; cleaves destabilizing N-terminal residues of a subset of proteins upon import, after their cleavage by mitochondrial processing peptidase (Mas1p-Mas2p); may contribute to mitochondrial iron homeostasis","termid":"PBO:0084735"}


id: GO:0008777
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N2-acetyl-L-ornithine + H2O = acetate + L-ornithine.","definition_xrefs":["EC:3.5.1.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0019213","GO:0016810","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"acetylornithine deacetylase activity","secondary_identifiers":["RHEA:15941","MetaCyc:ACETYLORNDEACET-RXN"],"synonyms":[{"name":"2-N-acetyl-L-ornithine amidohydrolase activity","type":"related"},{"name":"N-acetylornithinase activity","type":"broad"},{"name":"N2-acetyl-L-ornithine amidohydrolase activity","type":"related"},{"name":"acetylornithinase activity","type":"broad"}],"termid":"GO:0008777"}


id: PBO:0086392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative component of the protein phosphatase type 2A complex","termid":"PBO:0086392"}


id: MONDO:1011471
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Amyloidosis that occurs in goat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amyloidosis, non-human animal","termid":"MONDO:1011415"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloidosis, goat","secondary_identifiers":["OMIA:000037-9925"],"termid":"MONDO:1011471","xrefs":{"Monarch":{"xref_id":"1011471"}}}


id: MONDO:0016188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative defects of myofibrillar proteins","termid":"MONDO:0016186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of alphaB-cristallin","secondary_identifiers":["GARD:20427","UMLS:C5680838","MEDGEN:1843314","Orphanet:209044"],"termid":"MONDO:0016188","xrefs":{"Monarch":{"xref_id":"0016188"}}}


id: PBO:0052828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 128, pseudogene","termid":"PBO:0052828"}


id: GO:0090387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a phagosome, a vesicle formed by phagocytosis, fuses with a lysosome as a part of apoptotic cell clearance.","definition_xrefs":["GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phagolysosome assembly","termid":"GO:0001845"},{"relation_name":"part_of","term_name":"phagosome maturation involved in apoptotic cell clearance","termid":"GO:0090386"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0044085","GO:0016192"],"is_obsolete":false,"name":"phagolysosome assembly involved in apoptotic cell clearance","termid":"GO:0090387"}


id: GO:0060799
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals generated as a consequence of a transforming growth factor beta receptor binding to one of its physiological ligands and ultimately resulting in the commitment of an unspecified fate to adopt an endoderm fate.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor signaling pathway involved in endodermal cell fate specification (obsolete GO:0060799)","synonyms":[{"name":"transforming growth factor beta receptor signalling pathway involved in endodermal cell fate specification","type":"exact"}],"termid":"GO:0060799"}


id: PBO:0062905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxidative stress responsive kinase 1","termid":"PBO:0062905"}


id: MONDO:1011005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukodystrophy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy, non-human animal","termid":"MONDO:1010238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukodystrophy, dog","secondary_identifiers":["OMIA:001130-9615"],"termid":"MONDO:1011005","xrefs":{"Monarch":{"xref_id":"1011005"}}}


id: GO:0004243
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of an N-terminal octapeptide as second stage of processing of some proteins imported in the mitochondrion.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial intermediate peptidase activity (obsolete GO:0004243)","synonyms":[{"name":"MIP","type":"broad"},{"name":"mitochondrial intermediate peptidase activity","type":"exact"},{"name":"mitochondrial intermediate precursor-processing proteinase activity","type":"related"}],"termid":"GO:0004243"}


id: MONDO:0006249
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyp found mainly in the stomach and colon. Microscopically, it is characterized by elongated, serrated crypts lined by proliferative epithelium. Hyperplastic polyps are traditionally considered non-neoplastic, but ras mutation is common, clonality has been demonstrated and biochemical abnormalities and epidemiological associations that occur in colorectal adenomas and carcinomas have been found (WHO Tumors of the Digestive System, 2000).","definition_xrefs":["NCIT:C4083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperplastic polyp","secondary_identifiers":["UMLS:C0333983","EFO:1000299","MEDGEN:87189"],"synonyms":[{"name":"HP","type":"exact"},{"name":"MP","type":"exact"},{"name":"metaplastic polyp","type":"exact"}],"termid":"MONDO:0006249","xrefs":{"Monarch":{"xref_id":"0006249"}}}


id: MONDO:0013896
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the TCTN3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 18","secondary_identifiers":["UMLS:C3553758","MEDGEN:766672","GARD:15843","DOID:0110987","OMIM:614815"],"synonyms":[{"name":"JBTS18","type":"exact"},{"name":"Joubert syndrome 18","type":"exact"},{"name":"Joubert syndrome caused by mutation in TCTN3","type":"exact"},{"name":"Joubert syndrome type 18","type":"exact"},{"name":"TCTN3 Joubert syndrome","type":"exact"}],"termid":"MONDO:0013896","xrefs":{"Monarch":{"xref_id":"0013896"}}}


id: PBO:0069681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 958, pseudogene","termid":"PBO:0069681"}


id: MONDO:0006961
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A fatal disease of the nervous system in sheep and goats, characterized by pruritus, debility, and locomotor incoordination. It is caused by proteinaceous infectious particles called prions.","definition_xrefs":["MESH:D012608"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prion disease","termid":"MONDO:0005429"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scrapie","secondary_identifiers":["UMLS:C0036457","DOID:5434","EFO:1001168","MEDGEN:19903"],"termid":"MONDO:0006961","xrefs":{"Monarch":{"xref_id":"0006961"}}}


id: GO:0036447
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 the accumulation of sugar-phosphate.","definition_xrefs":["GOC:am","PMID:17383224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to chemical stress","termid":"GO:0062197"}],"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 sugar-phosphate stress","synonyms":[{"name":"cellular response to presence of non-metabolizable sugars","type":"related"}],"termid":"GO:0036447"}


id: PBO:0086357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative 2-methylcitrate dehydratase; mitochondrial protein that participates in respiration; induced by diauxic shift; homologous to E. coli PrpD, may take part in the conversion of 2-methylcitrate to 2-methylisocitrate","termid":"PBO:0086357"}


id: PBO:0075334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SORBS2 antisense RNA 1","termid":"PBO:0075334"}


id: GO:0044637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the negative regulation of complement activation via the classical pathway of the bitten/stung organism.","definition_xrefs":["PMID:20837040","GOC:fj","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in negative regulation of complement activation, classical pathway in another organism (obsolete GO:0044637)","synonyms":[{"name":"envenomation resulting in negative regulation of complement activation, classical pathway in other organism","type":"exact"}],"termid":"GO:0044637"}


id: PBO:0001716
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by mammalian rab5","termid":"PBO:0001716"}


id: GO:1990146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a rhabdomere.","definition_xrefs":["GOC:sart","PMID:8335687"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to rhabdomere","termid":"GO:1990146"}


id: GO:1903058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of melanosome organization.","definition_xrefs":["GOC:TermGenie","GOC:rl","GOC:BHF","PMID:24769727","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"regulation of melanosome organization","termid":"GO:1903056"},{"relation_name":"positively_regulates","term_name":"melanosome organization","termid":"GO:0032438"}],"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 melanosome organization","synonyms":[{"name":"activation of melanosome organisation","type":"narrow"},{"name":"activation of melanosome organization","type":"narrow"},{"name":"activation of melanosome organization and biogenesis","type":"related"},{"name":"positive regulation of melanosome organisation","type":"exact"},{"name":"positive regulation of melanosome organization and biogenesis","type":"related"},{"name":"up regulation of melanosome organisation","type":"exact"},{"name":"up regulation of melanosome organization","type":"exact"},{"name":"up regulation of melanosome organization and biogenesis","type":"related"},{"name":"up-regulation of melanosome organisation","type":"exact"},{"name":"up-regulation of melanosome organization","type":"exact"},{"name":"up-regulation of melanosome organization and biogenesis","type":"related"},{"name":"upregulation of melanosome organisation","type":"exact"},{"name":"upregulation of melanosome organization","type":"exact"},{"name":"upregulation of melanosome organization and biogenesis","type":"related"}],"termid":"GO:1903058"}


id: GO:0075137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of the symbiont organism or its cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of detecting the redox environment in host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to host","termid":"GO:0075136"}],"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 host redox environment","synonyms":[{"name":"response of symbiont to host redox environment","type":"exact"}],"termid":"GO:0075137"}


id: SO:0002157
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene cassette array containing H+ mating type specific information.","definition_xrefs":["PMID:18354497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"silent_mating_type_cassette_array","termid":"SO:0001984"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mat2P","termid":"SO:0002157"}


id: GO:0047218
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-coumarate + UDP-D-glucose = 4-O-beta-D-glucosyl-4-hydroxycinnamate + UDP. Also acts on ferulate, caffeate and sinapate, forming a mixture of 4-glucosides and glucose esters.","definition_xrefs":["EC:2.4.1.126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"hydroxycinnamate 4-beta-glucosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.126-RXN","RHEA:21636"],"synonyms":[{"name":"UDP-glucose-hydroxycinnamate glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:trans-4-hydroxycinnamate 4-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:trans-4-hydroxycinnamate 4-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"hydroxycinnamoyl glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-hydroxycinnamate glucosyltransferase activity","type":"related"}],"termid":"GO:0047218"}


id: PATO:0005017
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's being compressed from the side facing the lips to the side facing the tongue.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flattened","termid":"PATO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"labiolingually compressed","termid":"PATO:0005017"}


id: GO:0034413
data:
  {"annotated_genes":["SJAG_04771","SJAG_03587","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94222],"is_not":false,"summary":null,"term":"GO:0034413"},{"annotations":[87264,92179],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140748"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (1->3)-beta-D-glucans, compounds composed of glucose residues linked by (1->3)-beta-D-glucosidic bonds, found in the walls of ascospores.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ascospore wall (1->3)-beta-D-glucan metabolic process","termid":"GO:0034409"},{"relation_name":"is_a","term_name":"ascospore wall beta-glucan biosynthetic process","termid":"GO:0034412"},{"relation_name":"is_a","term_name":"fungal-type cell wall (1->3)-beta-D-glucan biosynthetic process","termid":"GO:0071970"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03587":null,"SJAG_04666":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"part_of","termid":"GO:0030437"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0030437","GO:0071554","GO:0005975","GO:0044085"],"is_obsolete":false,"name":"ascospore wall (1->3)-beta-D-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ascospore wall 1,3-beta-D-glucan biosynthetic process","type":"broad"},{"name":"ascospore wall 1,3-beta-glucan anabolism","type":"exact"},{"name":"ascospore wall 1,3-beta-glucan biosynthesis","type":"exact"},{"name":"ascospore wall 1,3-beta-glucan biosynthetic process","type":"broad"},{"name":"ascospore wall 1,3-beta-glucan formation","type":"exact"},{"name":"ascospore wall 1,3-beta-glucan synthesis","type":"exact"},{"name":"ascospore wall beta-1,3-glucan anabolism","type":"exact"},{"name":"ascospore wall beta-1,3-glucan biosynthesis","type":"exact"},{"name":"ascospore wall beta-1,3-glucan biosynthetic process","type":"exact"},{"name":"ascospore wall beta-1,3-glucan formation","type":"exact"},{"name":"ascospore wall beta-1,3-glucan synthesis","type":"exact"}],"termid":"GO:0034413","terms_by_termid":{"GO:0034413":null,"GO:0140748":null}}


id: GO:0140455
data:
  {"annotated_genes":["SJAG_03794","SJAG_02419","SJAG_00173","SJAG_02341","SJAG_00552","SJAG_00436","SJAG_01556"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104793,118389],"is_not":false,"summary":null,"term":"GO:0140455"},{"annotations":[109544,110131,109440,107803,113425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071629"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of misfolded proteins in the cytoplasm, which are either targeted to cytoplasmic proteasomes for degradation or protected by chaperones to shield thermosensitive proteins from degradation until conditions allow disaggregation and refolding.","definition_xrefs":["PMID:32075773"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein quality control for misfolded or incompletely synthesized proteins","termid":"GO:0006515"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00173":null,"SJAG_00436":null,"SJAG_00552":null,"SJAG_01556":null,"SJAG_02341":null,"SJAG_02419":null,"SJAG_03794":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"cytoplasm protein quality control","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140455","terms_by_termid":{"GO:0071629":null,"GO:0140455":null}}


id: GO:1900494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of butyryl-CoA biosynthetic process from acetyl-CoA.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of fatty acid biosynthetic process","termid":"GO:0042304"},{"relation_name":"is_a","term_name":"regulation of acyl-CoA biosynthetic process","termid":"GO:0050812"},{"relation_name":"regulates","term_name":"butyryl-CoA biosynthetic process from acetyl-CoA","termid":"GO:0044579"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0006790","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"regulation of butyryl-CoA biosynthetic process from acetyl-CoA","synonyms":[{"name":"regulation of butyryl-CoA biosynthesis from acetyl-CoA","type":"exact"}],"termid":"GO:1900494"}


id: PBO:0071852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 47","termid":"PBO:0071852"}


id: PBO:0041318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 69 pseudogene 4","termid":"PBO:0041318"}


id: PBO:0112873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lincRNA regulator of IL2RA","termid":"PBO:0112873"}


id: MONDO:0004397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A schwannoma that arises from the posterior mediastinum. It is characterized by the presence of psammoma bodies.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mediastinal schwannoma","termid":"MONDO:0004398"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign mediastinal psammomatous neurilemmoma","secondary_identifiers":["DOID:7921","MEDGEN:231937","UMLS:C1332513","NCIT:C6636"],"synonyms":[{"name":"benign mediastinal psammomatous schwannoma","type":"exact"},{"name":"benign psammomatous neurilemmoma of mediastinum","type":"exact"},{"name":"benign psammomatous neurilemmoma of the mediastinum","type":"exact"},{"name":"benign psammomatous schwannoma of mediastinum","type":"exact"},{"name":"benign psammomatous schwannoma of the mediastinum","type":"exact"}],"termid":"MONDO:0004397","xrefs":{"Monarch":{"xref_id":"0004397"}}}


id: GO:0140280
data:
  {"annotated_genes":["SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905757"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mitotic division septum formation. Division septum formation is the assembly and arrangement of a septum that spans the plasma membrane interface between progeny cells following cytokinesis.","definition_xrefs":["PMID:22786806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of division septum assembly","termid":"GO:0010974"},{"relation_name":"is_a","term_name":"regulation of mitotic division septum assembly","termid":"GO:0140279"},{"relation_name":"is_a","term_name":"negative regulation of mitotic cytokinetic process","termid":"GO:1903437"},{"relation_name":"negatively_regulates","term_name":"mitotic division septum assembly","termid":"GO:0140278"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000281"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0000281"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0000281","GO:0007049","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic division septum assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of division septum formation involved in mitotic cell cycle","type":"exact"},{"name":"down regulation of formation of division septum involved in mitotic cell cycle","type":"exact"},{"name":"down regulation of mitotic division septum assembly","type":"exact"},{"name":"down regulation of septin assembly and septum biosynthesis involved in mitotic cell cycle","type":"exact"},{"name":"down regulation of septin assembly and septum formation involved in mitotic cell cycle","type":"exact"},{"name":"down-regulation of division septum formation involved in mitotic cell cycle","type":"exact"},{"name":"down-regulation of formation of division septum involved in mitotic cell cycle","type":"exact"},{"name":"down-regulation of mitotic division septum assembly","type":"exact"},{"name":"down-regulation of septin assembly and septum biosynthesis involved in mitotic cell cycle","type":"exact"},{"name":"down-regulation of septin assembly and septum formation involved in mitotic cell cycle","type":"exact"},{"name":"downregulation of division septum formation involved in mitotic cell cycle","type":"exact"},{"name":"downregulation of formation of division septum involved in mitotic cell cycle","type":"exact"},{"name":"downregulation of mitotic division septum assembly","type":"exact"},{"name":"downregulation of septin assembly and septum biosynthesis involved in mitotic cell cycle","type":"exact"},{"name":"downregulation of septin assembly and septum formation involved in mitotic cell cycle","type":"exact"},{"name":"inhibition of division septum formation involved in mitotic cell cycle","type":"narrow"},{"name":"inhibition of formation of division septum involved in mitotic cell cycle","type":"narrow"},{"name":"inhibition of mitotic division septum assembly","type":"narrow"},{"name":"inhibition of septin assembly and septum biosynthesis involved in mitotic cell cycle","type":"exact"},{"name":"inhibition of septin assembly and septum formation involved in mitotic cell cycle","type":"exact"},{"name":"negative regulation of division septum formation involved in mitotic cell cycle","type":"exact"},{"name":"negative regulation of formation of division septum involved in mitotic cell cycle","type":"exact"},{"name":"negative regulation of septin assembly and septum biosynthesis involved in mitotic cell cycle","type":"exact"},{"name":"negative regulation of septin assembly and septum formation involved in mitotic cell cycle","type":"exact"}],"termid":"GO:0140280","terms_by_termid":{"GO:1905757":null}}


id: GO:0150036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of trans-synaptic signaling by endocannabinoid, modulating synaptic transmission.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:27296803"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of chemical synaptic transmission","termid":"GO:0050804"},{"relation_name":"regulates","term_name":"trans-synaptic signaling by endocannabinoid, modulating synaptic transmission","termid":"GO:0099553"}],"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 trans-synaptic signaling by endocannabinoid, modulating synaptic transmission","termid":"GO:0150036"}


id: GO:0043615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of an astrocyte, a class of large neuroglial (macroglial) cells in the central nervous system, the largest and most numerous neuroglial cells in the brain and spinal cord.","definition_xrefs":["GOC:go_curators","CL:0000127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell migration","termid":"GO:0008347"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"astrocyte cell migration","synonyms":[{"name":"astrocyte migration","type":"exact"},{"name":"astrocytic glial cell migration","type":"exact"}],"termid":"GO:0043615"}


id: GO:1990693
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the Golgi cis cisterna membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["PMID:24119662","GOC:bhm","PMID:16038056"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of Golgi cis cisterna membrane (obsolete GO:1990693)","synonyms":[{"name":"intrinsic component of cis-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990693"}


id: PBO:0085823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; expression is regulated by phosphate levels; green fluorescent protein (GFP)-fusion protein localizes to the cell periphery and vacuole; protein abundance increases in response to DNA replication stress","termid":"PBO:0085823"}


id: MONDO:0019389
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome (obsolete MONDO:0019389)","secondary_identifiers":["Orphanet:83648"],"termid":"MONDO:0019389","xrefs":{"Monarch":{"xref_id":"0019389"}}}


id: PBO:0044947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrofolate reductase pseudogene 2","termid":"PBO:0044947"}


id: PBO:0003934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidinol dehydrogenase His2 (predicted)","termid":"PBO:0003934"}


id: PBO:0088907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane borate efflux transmembrane transporter Bor1","termid":"PBO:0088907"}


id: PBO:0036079
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transport_along_microtubule_during_vegetative_growth","termid":"PBO:0036079"}


id: FYPO:0001071
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 transport is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"transport phenotype during vegetative growth","termid":"FYPO:0001336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal transport","synonyms":[{"name":"normal transport during mitotic cell cycle","type":"related"},{"name":"normal transport during vegetative growth","type":"exact"}],"termid":"FYPO:0001071"}


id: PBO:0078234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 16","termid":"PBO:0078234"}


id: GO:0098037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The encapsulation of the viral DNA genome within the capsid, which proceeds via cleavage of the viral DNA at specific sites to produce 5' protruding ends.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA genome packaging via site-specific sequence recognition","termid":"GO:0098035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"viral DNA genome packaging, 5' extended cos packaging","termid":"GO:0098037"}


id: GO:0101016
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to the FMN-binding domain of a protein.","definition_xrefs":["PMID:15752726"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"FMN-binding domain binding","termid":"GO:0101016"}


id: FYPO:0004972
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 more actin cortical patches than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cortical patch","termid":"FYPO:0003987"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0004803","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"actin cortical patches present in increased numbers","synonyms":[{"name":"F-actin patches present in increased numbers","type":"exact"},{"name":"actin cortical patches present in greater numbers","type":"exact"},{"name":"actin cortical patches present in increased numbers during mitotic cell cycle","type":"related"},{"name":"actin cortical patches present in increased numbers during vegetative growth","type":"exact"},{"name":"actin patches present in increased numbers","type":"exact"},{"name":"increased actin cortical patch formation during vegetative growth","type":"related"},{"name":"more actin cortical patches present during vegetative growth","type":"exact"}],"termid":"FYPO:0004972"}


id: MONDO:0032733
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":"global developmental delay, progressive ataxia, and elevated glutamine","secondary_identifiers":["UMLS:C5193080","OMIM:618412","MEDGEN:1680160"],"synonyms":[{"name":"GDPAG","type":"related"},{"name":"GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE ATAXIA, AND ELEVATED GLUTAMINE","type":"related"},{"name":"Glutaminase Deficiency With Impaired Intellectual Development and Progressive Ataxia","type":"related"}],"termid":"MONDO:0032733","xrefs":{"Monarch":{"xref_id":"0032733"}}}


id: PBO:0087582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Anaphase-Promoting Complex/Cyclosome (APC/C); APC/C is a ubiquitin-protein ligase required for degradation of anaphase inhibitors, including mitotic cyclins, during the metaphase/anaphase transition; component of the platform domain of the APC/C, based on structural analysis; relative distribution to nuclear foci decreases upon DNA replication stress","termid":"PBO:0087582"}


id: MONDO:0002579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm that arises from the orbit. It is characterized by the presence of skeletal muscle tissue exhibiting embryonic features.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orbit rhabdomyosarcoma","termid":"MONDO:0002580"},{"relation_name":"is_a","term_name":"embryonal rhabdomyosarcoma","termid":"MONDO:0009993"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"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":"orbit embryonal rhabdomyosarcoma","secondary_identifiers":["DOID:3258","MEDGEN:233267","UMLS:C1335127","NCIT:C6246"],"synonyms":[{"name":"embryonal rhabdomyosarcoma of orbit","type":"exact"},{"name":"embryonal rhabdomyosarcoma of the orbit","type":"exact"}],"termid":"MONDO:0002579","xrefs":{"Monarch":{"xref_id":"0002579"}}}


id: PBO:0113285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Poly (A)+ RNA-binding protein; abundant mRNP-component protein that binds cell wall mRNAs; required for stability of many mRNAs; component of glucose deprivation induced stress granules, involved in P-body-dependent granule assembly; implicated in regulation of translation; carries Q/N-rich domain at C- terminus, identified as candidate prion; ribosome-bound Pub1p modulates stop codon decoding during translation termination","termid":"PBO:0113285"}


id: PBO:0057299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 513c","termid":"PBO:0057299"}


id: PR:O74762
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 26S proteasome non-ATPase regulatory subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10943:SF2","OMA:SCHPO03658","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":"26S proteasome regulatory subunit rpn2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17D11.07c","secondary_identifiers":["UniProtKB:O74762"],"synonyms":[{"name":"Spom972h-PSMD1","type":"exact"}],"termid":"PR:O74762"}


id: PBO:0029006
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-intron-specific_abnormal_mRNA_splicing,_via_spliceosome","termid":"PBO:0029006"}


id: GO:0003931
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: GTP + H2O = GDP + phosphate. Any member of the Rho subfamily of the RAS superfamily of monomeric GTPases. Proteins in the Rho subfamily are involved in relaying signals from cell-surface receptors to the actin cytoskeleton.","definition_xrefs":["GOC:mah","ISBN:0198547684","EC:3.6.1.47"],"gene_count":0,"genotype_count":0,"name":"obsolete Rho small monomeric GTPase activity (obsolete GO:0003931)","synonyms":[{"name":"Rho small monomeric GTPase activity","type":"exact"}],"termid":"GO:0003931"}


id: PBO:0064135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase M1/2 pseudogene 2","termid":"PBO:0064135"}


id: GO:0008972
data:
  {"annotated_genes":["SJAG_04282","SJAG_02421","SJAG_02420"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69663,73610,73715],"is_not":false,"summary":null,"term":"GO:0008972"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + 4-amino-2-methyl-5-phosphomethylpyrimidine = ADP + 4-amino-2-methyl-5-diphosphomethylpyrimidine.","definition_xrefs":["EC:2.7.4.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02420":null,"SJAG_02421":null,"SJAG_04282":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"phosphomethylpyrimidine kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:19893","MetaCyc:PYRIMSYN3-RXN"],"synonyms":[{"name":"ATP:4-amino-2-methyl-5-phosphomethylpyrimidine phosphotransferase activity","type":"related"},{"name":"hydroxymethylpyrimidine phosphokinase activity","type":"related"}],"termid":"GO:0008972","terms_by_termid":{"GO:0008972":null}}


id: MONDO:0009191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lowry-Wood syndrome is characterized by the association of epiphyseal dysplasia, short stature, microcephaly and, in the first reported cases, congenital nystagmus. So far, less than 10 cases have been described in the literature. Variable degrees of intellectual deficit have also been reported. Other occasional features include retinitis pigmentosa and coxa vara. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:1824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNU4ATAC spectrum disorder","termid":"MONDO:0100558"},{"relation_name":"is_a","term_name":"primordial dwarfism and slender bone disorder","termid":"MONDO:0800063"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lowry-Wood syndrome","secondary_identifiers":["SCTID:721975004","UMLS:C0796021","MEDGEN:162899","OMIM:226960","MESH:C537038","GARD:264","MedDRA:10062600","icd11.foundation:1713071905"],"synonyms":[{"name":"LWS","type":"exact"},{"name":"Lowry Wood syndrome","type":"exact"},{"name":"Lowry-Wood syndrome","type":"exact"},{"name":"epiphyseal dysplasia, microcephaly and nystagmus","type":"related"},{"name":"epiphyseal dysplasia, multiple, with microcephaly and retinal dystrophy","type":"exact"},{"name":"epiphyseal dysplasia-microcephaly-nystagmus syndrome","type":"exact"}],"termid":"MONDO:0009191","xrefs":{"Monarch":{"xref_id":"0009191"}}}


id: GO:0008190
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to eukaryotic initiation factor 4E, a polypeptide factor involved in the initiation of ribosome-mediated translation.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation initiation factor binding","termid":"GO:0031369"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"eukaryotic initiation factor 4E binding","synonyms":[{"name":"eIF4E binding","type":"exact"}],"termid":"GO:0008190"}


id: internal:broad
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"broad","termid":"internal:broad"}


id: GO:0060836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a venous blood vessel endothelial cell acquires specialized features of a lymphatic vessel endothelial cell, a thin flattened cell that lines the inside surfaces of lymph vessels.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell differentiation","termid":"GO:0045446"},{"relation_name":"part_of","term_name":"lymph vessel development","termid":"GO:0001945"}],"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":"lymphatic endothelial cell differentiation","termid":"GO:0060836"}


id: GO:2001280
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of unsaturated fatty acid biosynthetic process.","definition_xrefs":["GO:0006636"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of fatty acid biosynthetic process","termid":"GO:0045723"},{"relation_name":"is_a","term_name":"regulation of unsaturated fatty acid biosynthetic process","termid":"GO:2001279"},{"relation_name":"positively_regulates","term_name":"unsaturated fatty acid biosynthetic process","termid":"GO:0006636"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006629"],"is_obsolete":false,"name":"positive regulation of unsaturated fatty acid biosynthetic process","synonyms":[{"name":"positive regulation of fatty acid desaturation","type":"related"},{"name":"positive regulation of polyunsaturated fatty acid biosynthesis","type":"related"},{"name":"positive regulation of unsaturated fatty acid anabolism","type":"exact"},{"name":"positive regulation of unsaturated fatty acid biosynthesis","type":"exact"},{"name":"positive regulation of unsaturated fatty acid formation","type":"exact"},{"name":"positive regulation of unsaturated fatty acid synthesis","type":"exact"}],"termid":"GO:2001280"}


id: PBO:0018004
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ssb1 stimulates helicase activity at low ATP concentration (0.2 mM)","termid":"PBO:0018004"}


id: PBO:0005047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically upregulated gene Mug46","termid":"PBO:0005047"}


id: GO:0021509
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a single row of glia at the dorsal midline of the developing neural tube. This region provides inductive signals for the specification of neuronal cell types and of the specification of neural crest cells. The cells comprising the roof plate are the precursors to radial glial cells.","definition_xrefs":["GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","GOC:dgh","PMID:15936325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"neural tube formation","termid":"GO:0001841"}],"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":"roof plate formation","termid":"GO:0021509"}


id: MONDO:0100070
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that affects the neuroendocrine gland, any of the organized aggregations of cells that function as secretory or excretory organs and that release hormones in response to neural stimuli.","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroendocrine disorder","secondary_identifiers":["MEDGEN:1843486","UMLS:C0541403"],"synonyms":[{"name":"neuroendocrine system disease","type":"exact"}],"termid":"MONDO:0100070","xrefs":{"Monarch":{"xref_id":"0100070"}}}


id: PBO:0079041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon CAC) 1-3","termid":"PBO:0079041"}


id: MONDO:0004803
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"collagenopathy","termid":"MONDO:0004603"},{"relation_name":"is_a","term_name":"hypereosinophilic syndrome","termid":"MONDO:0015691"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"disseminated eosinophilic collagen disease","secondary_identifiers":["SCTID:423486005","MEDGEN:538043","ICD9:710.8","UMLS:C0263662","DOID:9499"],"termid":"MONDO:0004803","xrefs":{"Monarch":{"xref_id":"0004803"}}}


id: PBO:0081752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 681","termid":"PBO:0081752"}


id: GO:1902046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of Fas signaling pathway.","definition_xrefs":["GOC:TermGenie","PMID:17245429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of Fas signaling pathway","termid":"GO:1902044"},{"relation_name":"positively_regulates","term_name":"Fas signaling pathway","termid":"GO:0036337"}],"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 Fas signaling pathway","synonyms":[{"name":"activation of Apo-1 signaling pathway","type":"narrow"},{"name":"activation of CD95 signaling pathway","type":"narrow"},{"name":"activation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"activation of Fas receptor signaling pathway","type":"narrow"},{"name":"activation of Fas signaling pathway","type":"narrow"},{"name":"activation of Fas-FasL signaling pathway","type":"narrow"},{"name":"activation of FasL signaling pathway","type":"related"},{"name":"activation of FasR signaling pathway","type":"narrow"},{"name":"positive regulation of Apo-1 signaling pathway","type":"exact"},{"name":"positive regulation of CD95 signaling pathway","type":"exact"},{"name":"positive regulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"positive regulation of Fas receptor signaling pathway","type":"exact"},{"name":"positive regulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"positive regulation of FasL signaling pathway","type":"related"},{"name":"positive regulation of FasR signaling pathway","type":"exact"},{"name":"up regulation of Apo-1 signaling pathway","type":"exact"},{"name":"up regulation of CD95 signaling pathway","type":"exact"},{"name":"up regulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"up regulation of Fas receptor signaling pathway","type":"exact"},{"name":"up regulation of Fas signaling pathway","type":"exact"},{"name":"up regulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"up regulation of FasL signaling pathway","type":"related"},{"name":"up regulation of FasR signaling pathway","type":"exact"},{"name":"up-regulation of Apo-1 signaling pathway","type":"exact"},{"name":"up-regulation of CD95 signaling pathway","type":"exact"},{"name":"up-regulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"up-regulation of Fas receptor signaling pathway","type":"exact"},{"name":"up-regulation of Fas signaling pathway","type":"exact"},{"name":"up-regulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"up-regulation of FasL signaling pathway","type":"related"},{"name":"up-regulation of FasR signaling pathway","type":"exact"},{"name":"upregulation of Apo-1 signaling pathway","type":"exact"},{"name":"upregulation of CD95 signaling pathway","type":"exact"},{"name":"upregulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"upregulation of Fas receptor signaling pathway","type":"exact"},{"name":"upregulation of Fas signaling pathway","type":"exact"},{"name":"upregulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"upregulation of FasL signaling pathway","type":"related"},{"name":"upregulation of FasR signaling pathway","type":"exact"}],"termid":"GO:1902046"}


id: PBO:0078185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 2","termid":"PBO:0078185"}


id: PBO:0064790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPM1J divergent transcript","termid":"PBO:0064790"}


id: PBO:0002576
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human moe1","termid":"PBO:0002576"}


id: GO:0032526
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 retinoic acid stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"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 retinoic acid","synonyms":[{"name":"response to vitamin A acid","type":"exact"}],"termid":"GO:0032526"}


id: MOD:01251
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-[3-(carboxamidomethylthio)propanoyl]lysine.","definition_xrefs":["PubMed:15121203","Unimod:293#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3-(carboxamidomethylthio)propanoylated residue","termid":"MOD:00612"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"N6-[3-(carboxamidomethylthio)propanoyl]lysine","synonyms":[{"name":"3-(carbamidomethylthio)propanoyl","type":"related"},{"name":"CAMthiopropanoyl","type":"related"}],"termid":"MOD:01251"}


id: PBO:0057704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1291","termid":"PBO:0057704"}


id: GO:0071201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A voltage-gated potassium channel complex that contains the peptidase-related protein DPP6 associated with the channel via interaction with the Kv alpha subunit 4.3.","definition_xrefs":["PMID:12575952","PMID:15911355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"Kv4.3-DPP6 channel complex","secondary_identifiers":["CORUM:599"],"synonyms":[{"name":"Kv4.3-DPPX channel complex","type":"exact"}],"termid":"GO:0071201"}


id: PR:O94292
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 50S ribosomal protein L14 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03758"],"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":"54S ribosomal protein L38, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC887.07","secondary_identifiers":["UniProtKB:O94292"],"synonyms":[{"name":"Spom972h-rplN","type":"exact"}],"termid":"PR:O94292"}


id: PBO:0063210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCBP3 antisense RNA 1","termid":"PBO:0063210"}


id: PBO:0028005
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete_mitotic_sister_chromatid_segregation,_with_phi-shaped_DNA_mass","termid":"PBO:0028005"}


id: GO:0001993
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the secretion of norepinephrine or epinephrine into the bloodstream modulates the force with which blood passes through the circulatory system.","definition_xrefs":["ISBN:0721643949"],"direct_ancestors":[{"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 norepinephrine-epinephrine","synonyms":[{"name":"noradrenaline-adrenaline regulation of blood pressure","type":"related"},{"name":"norepinephrine-epinephrine blood pressure control","type":"related"},{"name":"norepinephrine-epinephrine blood pressure regulation","type":"exact"}],"termid":"GO:0001993"}


id: PBO:0051968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isovaleryl-CoA dehydrogenase","termid":"PBO:0051968"}


id: GO:0141087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of an inflammasome-mediated signaling pathway.","definition_xrefs":["PMID:33467177"],"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 inflammasome-mediated signaling pathway","termid":"GO:0141085"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"inflammasome-mediated signaling pathway","termid":"GO:0141084"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of inflammasome-mediated signaling pathway","synonyms":[{"name":"positive regulation of inflammasome-mediated signal transduction","type":"exact"}],"termid":"GO:0141087"}


id: GO:0019619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 3,4-dihydroxybenzoate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound catabolic process","termid":"GO:0019614"},{"relation_name":"is_a","term_name":"3,4-dihydroxybenzoate metabolic process","termid":"GO:0046278"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044248","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"3,4-dihydroxybenzoate catabolic process","synonyms":[{"name":"protocatechuate breakdown","type":"exact"},{"name":"protocatechuate catabolic process","type":"exact"},{"name":"protocatechuate catabolism","type":"exact"},{"name":"protocatechuate degradation","type":"exact"}],"termid":"GO:0019619"}


id: GO:0021883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which the cell cycle is halted during one of the normal phases (G1, S, G2, M) in a cell that has been committed to become a neuron that will reside in the forebrain.","definition_xrefs":["PMID:16226447","GOC:cls","GOC:dph","GO_REF:0000021","GOC:dgh","GOC:tb","GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete cell cycle arrest of committed forebrain neuronal progenitor cell (obsolete GO:0021883)","termid":"GO:0021883"}


id: PBO:0054302
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 1694","termid":"PBO:0054302"}


id: PBO:0063571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"period circadian regulator 1","termid":"PBO:0063571"}


id: MONDO:1010575
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes mellitus that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes mellitus, non-human animal","termid":"MONDO:1010052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes mellitus, domestic cat","secondary_identifiers":["OMIA:000279-9685"],"termid":"MONDO:1010575","xrefs":{"Monarch":{"xref_id":"1010575"}}}


id: PBO:0081033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZC3H12A divergent transcript","termid":"PBO:0081033"}


id: PBO:0052984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L antigen family member 3","termid":"PBO:0052984"}


id: GO:0010471
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-beta-L-galactose + alpha-D-mannose 1-phosphate = GDP-alpha-D-mannose + beta-L-galactose-1-phosphate.","definition_xrefs":["PMID:17485667","RHEA:65708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanylyltransferase activity","termid":"GO:0070568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016779"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016779"],"is_obsolete":false,"name":"GDP-galactose:mannose-1-phosphate guanylyltransferase activity","secondary_identifiers":["MetaCyc:RXN4FS-12"],"synonyms":[{"name":"GDP-L-galactose phosphorylase activity","type":"broad"},{"name":"GDP-L-galactose:mannose-1-phosphate guanylyltransferase activity","type":"exact"}],"termid":"GO:0010471"}


id: GO:0035714
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 nitrogen dioxide (NO2) stimulus.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen dioxide","termid":"GO:0035713"},{"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 nitrogen dioxide","synonyms":[{"name":"cellular response to NO2","type":"exact"}],"termid":"GO:0035714"}


id: MONDO:0005114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the species streptococcus pneumoniae.","definition_xrefs":["MESH:D011008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"streptococcal infection","termid":"MONDO:0021680"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumococcal infection","secondary_identifiers":["MEDGEN:18528","SCTID:16814004","ICD9:041.2","UMLS:C0032269","EFO:0000772"],"synonyms":[{"name":"Streptococcus pneumoniae caused disease or disorder","type":"exact"},{"name":"Streptococcus pneumoniae disease or disorder","type":"exact"},{"name":"Streptococcus pneumoniae infection","type":"related"},{"name":"Streptococcus pneumoniae infections","type":"related"},{"name":"Streptococcus pneumoniae infectious disease","type":"exact"},{"name":"infection, Streptococcus pneumoniae","type":"related"},{"name":"infection, pneumococcal","type":"related"},{"name":"infections, Streptococcus pneumoniae","type":"related"},{"name":"infections, pneumococcal","type":"related"},{"name":"pneumococcal infection","type":"exact"},{"name":"pneumoniae infection, Streptococcus","type":"related"},{"name":"pneumoniae infections, Streptococcus","type":"related"}],"termid":"MONDO:0005114","xrefs":{"Monarch":{"xref_id":"0005114"}}}


