# terms

id: MOD:00667
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with a decanoyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"},{"relation_name":"is_a","term_name":"lipoconjugated residue","termid":"MOD:01155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"decanoylated residue","synonyms":[{"name":"DecRes","type":"exact"}],"termid":"MOD:00667"}


id: PR:Q9HDZ9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC589.05c gene.","definition_xrefs":["UniProtKB:Q9HDZ9","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":"UPF0553 protein C589.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC589.05c","synonyms":[{"name":"Spom972h-SPAC589.05c","type":"exact"}],"termid":"PR:Q9HDZ9"}


id: GO:0086010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which membrane potential changes in the depolarizing direction from the negative resting potential towards the positive membrane potential that will be the peak of the action potential.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane depolarization","termid":"GO:0051899"},{"relation_name":"part_of","term_name":"action potential","termid":"GO:0001508"}],"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":"membrane depolarization during action potential","termid":"GO:0086010"}


id: MONDO:0020118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dense granule disease (obsolete MONDO:0020118)","secondary_identifiers":["icd11.foundation:1930060978","Orphanet:98456"],"synonyms":[{"name":"Delta granule disease","type":"exact"}],"termid":"MONDO:0020118","xrefs":{"Monarch":{"xref_id":"0020118"}}}


id: PBO:0059530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded termination associated sequence","termid":"PBO:0059530"}


id: FYPO:0001062
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of glutamine into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glutamine import","termid":"FYPO:0001061"},{"relation_name":"is_a","term_name":"decreased amino acid import during vegetative growth","termid":"FYPO:0001360"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased glutamine import","synonyms":[{"name":"decreased L-glutamine import","type":"narrow"},{"name":"decreased glutamine import across plasma membrane","type":"exact"},{"name":"decreased glutamine import during mitotic cell cycle","type":"related"},{"name":"decreased glutamine import during vegetative growth","type":"exact"},{"name":"decreased glutamine import into cell","type":"exact"},{"name":"decreased glutamine uptake","type":"exact"},{"name":"reduced glutamine import","type":"exact"}],"termid":"FYPO:0001062"}


id: PATO:0000292
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000292 mobility value (obsolete PATO:0000292)","termid":"PATO:0000292"}


id: GO:0062083
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a MHC class Ib molecule of the HLA-G subclass to mediate signaling that inhibits activation of a lymphocyte.","definition_xrefs":["DOI:10.1002/9780470015902.a0024246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inhibitory MHC class Ib receptor activity","termid":"GO:0062080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"HLA-G specific inhibitory MHC class Ib receptor activity","termid":"GO:0062083"}


id: PBO:0030883
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_cytoskeleton_organization_during_vegetative_growth","termid":"PBO:0030883"}


id: MONDO:0700071
data:
  {"annotated_genes":["SJAG_04053","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86421,86420],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[86414,86415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013154"},{"annotations":[86417,86418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"}]},"cv_name":"mondo","definition":"Any myopathy in which the cause of the disease is a variation in the POMT2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan","termid":"MONDO:0016155"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04053":null,"SJAG_04316":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0024322","MONDO:0005066","MONDO:0005336"],"is_obsolete":false,"name":"myopathy caused by variation in POMT2","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"POMT2 myopathy","type":"exact"},{"name":"POMT2-related myopathy","type":"exact"},{"name":"myopathy caused by mutation in POMT2","type":"exact"}],"termid":"MONDO:0700071","terms_by_termid":{"MONDO:0013154":null,"MONDO:0013160":null,"MONDO:0013162":null},"xrefs":{"Monarch":{"xref_id":"0700071"}}}


id: PBO:0082624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of both the SWI/SNF and RSC chromatin remodeling complexes; actin-related protein involved in transcriptional regulation","termid":"PBO:0082624"}


id: PR:Q92462
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pub1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q92462"],"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 pub1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11G7.02","synonyms":[{"name":"Spom972h-pub1","type":"exact"}],"termid":"PR:Q92462"}


id: PBO:0000388
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.3.48","termid":"PBO:0000388"}


id: GO:0033829
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a beta-D-GlcNAc residue from UDP-D-GlcNAc to the fucose residue of a fucosylated protein acceptor.","definition_xrefs":["EC:2.4.1.222"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase activity","secondary_identifiers":["Reactome:R-HSA-1912355","MetaCyc:2.4.1.222-RXN","Reactome:R-HSA-5096538"],"synonyms":[{"name":"O-fucosylpeptide beta-1,3-N-acetylglucosaminyltransferase activity","type":"related"},{"name":"UDP-D-GlcNAc:O-L-fucosylpeptide 3-beta-N-acetyl-D-glucosaminyltransferase activity","type":"related"}],"termid":"GO:0033829"}


id: PBO:0086921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative Zn(II)2Cys6 motif containing transcription factor; non-essential gene identified in a screen for mutants with increased levels of rDNA transcription; similar to S. kluyveri Urc2p involved in uracil catabolism","termid":"PBO:0086921"}


id: PR:Q9UTM7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone acetyltransferase type B catalytic subunit that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00406","PANTHER:PTHR12046:SF0","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":"histone acetyltransferase type B catalytic subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC139.06","secondary_identifiers":["UniProtKB:Q9UTM7"],"synonyms":[{"name":"Spom972h-HAT1","type":"exact"}],"termid":"PR:Q9UTM7"}


id: PBO:0113204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondria-associated F-box protein; tether that anchors higher-functioning mitochondria at the mother cell distal tip throughout the cell cycle and at the bud tip prior to cytokinesis; role in maintenance of normal mitochondrial morphology and quality control; interacts with Skp1p through the F-box motif; asymmetrically localized to the mother cell through the cell cycle with some bud tip localization just before cytokinesis; function regulated by the bud site selection machinery","termid":"PBO:0113204"}


id: PBO:0033809
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_DNA_recombination_at_telomere_following_meiotic_cell_cycle","termid":"PBO:0033809"}


id: GO:0021687
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the cerebellar molecular layer is generated and organized. The molecular layer is the outermost layer of the cerebellar cortex. It contains the parallel fibers of the granule cells, interneurons such as stellate and basket cells, and the dendrites of the underlying Purkinje cells.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:dph","ISBN:0838580343","GOC:cls","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"cerebellar molecular layer development","termid":"GO:0021679"},{"relation_name":"part_of","term_name":"cerebellar cortex morphogenesis","termid":"GO:0021696"}],"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":"cerebellar molecular layer morphogenesis","termid":"GO:0021687"}


id: _global:gene_product_of
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","definition":"definition \\\"x has gene product of y if and only if y is a gene (SO:0000704) that participates in some gene expression process (GO:0010467) where the output of that process is either y or something that is ribosomally translated from x\\\"","direct_ancestors":[{"relation_name":"is_a","term_name":"genomically_related_to","termid":"_global:genomically_related_to"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_product_of","secondary_identifiers":["GOREL:0001028","RO:0002204"],"termid":"_global:gene_product_of"}


id: GO:0009809
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lignins, a class of polymers formed by the dehydrogenetive radical polymerization of various phenylpropanoid monomers.","definition_xrefs":["ISBN:0198547684","GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylpropanoid biosynthetic process","termid":"GO:0009699"},{"relation_name":"is_a","term_name":"lignin metabolic process","termid":"GO:0009808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"lignin biosynthetic process","secondary_identifiers":["MetaCyc:PWY-361"],"synonyms":[{"name":"lignin anabolism","type":"exact"},{"name":"lignin biosynthesis","type":"exact"},{"name":"lignin formation","type":"exact"},{"name":"lignin synthesis","type":"exact"}],"termid":"GO:0009809"}


id: GO:0140808
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-tyrosyl-[protein] + NAD+ = H+ + nicotinamide + O-(ADP-D-ribosyl)-L-tyrosyl-[protein].","definition_xrefs":["PMID:29954836","RHEA:58236","PMID:30257210"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD+-protein mono-ADP-ribosyltransferase activity","termid":"GO:1990404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0140096","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"NAD+-protein-tyrosine ADP-ribosyltransferase activity","termid":"GO:0140808"}


id: PBO:0026949
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_chromatin_binding_at_centromere_central_core","termid":"PBO:0026949"}


id: PBO:0047690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fms related receptor tyrosine kinase 3","termid":"PBO:0047690"}


id: GO:0005579
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex produced by sequentially activated components of the complement cascade inserted into a target cell membrane and forming a pore leading to cell lysis via ion and water flow.","definition_xrefs":["GOC:add","ISBN:0781735149","ISBN:068340007X","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pore complex","termid":"GO:0046930"},{"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:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"membrane attack complex","secondary_identifiers":["Wikipedia:Complement_membrane_attack_complex"],"synonyms":[{"name":"MAC","type":"exact"},{"name":"TCC","type":"exact"},{"name":"membrane attack complex protein alphaM chain","type":"narrow"},{"name":"membrane attack complex protein beta2 chain","type":"narrow"},{"name":"terminal complement complex","type":"exact"}],"termid":"GO:0005579"}


id: GO:0050173
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-phenylalanine + ATP = N-adenylyl-L-phenylalanine + diphosphate + 2 H+.","definition_xrefs":["EC:2.7.7.54"],"gene_count":0,"genotype_count":0,"name":"obsolete phenylalanine adenylyltransferase activity (obsolete GO:0050173)","synonyms":[{"name":"ATP:L-phenylalanine adenylyltransferase activity","type":"related"},{"name":"ATP:phenylalanine adenylyltransferase activity","type":"exact"},{"name":"L-phenylalanine adenylyltransferase activity","type":"related"}],"termid":"GO:0050173"}


id: PBO:0048354
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 65","termid":"PBO:0048354"}


id: PBO:0041129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTBD9 antisense RNA 1","termid":"PBO:0041129"}


id: PBO:0071138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 1","termid":"PBO:0071138"}


id: PBO:0084029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi matrix protein; involved in the structural organization of the cis-Golgi; interacts genetically with COG3 and USO1","termid":"PBO:0084029"}


id: GO:0046286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of flavonoid phytoalexins, a group of water-soluble phenolic derivatives containing a flavan skeleton, which possess antibiotic activity and are produced by plant tissues in response to infection.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavonoid catabolic process","termid":"GO:0046275"},{"relation_name":"is_a","term_name":"flavonoid phytoalexin metabolic process","termid":"GO:0046285"},{"relation_name":"is_a","term_name":"phytoalexin catabolic process","termid":"GO:0052316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0008150","GO:0044248","GO:0019748","GO:0098754"],"is_obsolete":false,"name":"flavonoid phytoalexin catabolic process","synonyms":[{"name":"flavonoid phytoalexin breakdown","type":"exact"},{"name":"flavonoid phytoalexin catabolism","type":"exact"},{"name":"flavonoid phytoalexin degradation","type":"exact"}],"termid":"GO:0046286"}


id: GO:0031306
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the mitochondrial outer 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":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of mitochondrial outer membrane (obsolete GO:0031306)","synonyms":[{"name":"intrinsic to mitochondrial outer membrane","type":"narrow"}],"termid":"GO:0031306"}


id: PBO:0045144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal heavy chain 1","termid":"PBO:0045144"}


id: PBO:0042679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEBPA divergent transcript","termid":"PBO:0042679"}


id: SO:0001756
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL11 RNA leader sequence to the 5' end of an mRNA. SL11 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":"SL11_acceptor_site","synonyms":[{"name":"SL11 acceptor site","type":"exact"}],"termid":"SO:0001756"}


id: PomGeneEx:0000005
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneEx","definition":"A gene expression qualifier that indicates that an RNA or protein is present under a given set of conditions or at an indicated time.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression qualifier","termid":"PomGeneEx:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"present","synonyms":[{"name":"gene expression present","type":"exact"},{"name":"gene product present","type":"exact"}],"termid":"PomGeneEx:0000005"}


id: GO:0015398
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of ammonium from one side of a membrane to the other, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by a chemiosmotic source of energy. Secondary active transporters include symporters and antiporters. In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations.","definition_xrefs":["GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete high-affinity secondary active ammonium transmembrane transporter activity (obsolete GO:0015398)","synonyms":[{"name":"high affinity secondary active ammonium transmembrane transporter activity","type":"exact"}],"termid":"GO:0015398"}


id: GO:1903904
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of establishment of T cell polarity.","definition_xrefs":["GOC:TermGenie","GOC:als","PMID:23575248","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell activation","termid":"GO:0050868"},{"relation_name":"is_a","term_name":"regulation of establishment of T cell polarity","termid":"GO:1903903"},{"relation_name":"negatively_regulates","term_name":"establishment of T cell polarity","termid":"GO:0001768"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007163"},{"rel_name":"negatively_regulates","termid":"GO:0007163"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155","GO:0007163"],"is_obsolete":false,"name":"negative regulation of establishment of T cell polarity","synonyms":[{"name":"down regulation of T cell polarization","type":"exact"},{"name":"down regulation of T lymphocyte polarization","type":"exact"},{"name":"down regulation of T-cell polarization","type":"exact"},{"name":"down regulation of establishment of T cell polarity","type":"exact"},{"name":"down regulation of establishment of T lymphocyte polarity","type":"exact"},{"name":"down regulation of establishment of T-cell polarity","type":"exact"},{"name":"down regulation of establishment of T-lymphocyte polarity","type":"exact"},{"name":"down-regulation of T cell polarization","type":"exact"},{"name":"down-regulation of T lymphocyte polarization","type":"exact"},{"name":"down-regulation of T-cell polarization","type":"exact"},{"name":"down-regulation of establishment of T cell polarity","type":"exact"},{"name":"down-regulation of establishment of T lymphocyte polarity","type":"exact"},{"name":"down-regulation of establishment of T-cell polarity","type":"exact"},{"name":"down-regulation of establishment of T-lymphocyte polarity","type":"exact"},{"name":"downregulation of T cell polarization","type":"exact"},{"name":"downregulation of T lymphocyte polarization","type":"exact"},{"name":"downregulation of T-cell polarization","type":"exact"},{"name":"downregulation of establishment of T cell polarity","type":"exact"},{"name":"downregulation of establishment of T lymphocyte polarity","type":"exact"},{"name":"downregulation of establishment of T-cell polarity","type":"exact"},{"name":"downregulation of establishment of T-lymphocyte polarity","type":"exact"},{"name":"inhibition of T cell polarization","type":"narrow"},{"name":"inhibition of T lymphocyte polarization","type":"narrow"},{"name":"inhibition of T-cell polarization","type":"narrow"},{"name":"inhibition of establishment of T cell polarity","type":"narrow"},{"name":"inhibition of establishment of T lymphocyte polarity","type":"narrow"},{"name":"inhibition of establishment of T-cell polarity","type":"narrow"},{"name":"inhibition of establishment of T-lymphocyte polarity","type":"narrow"},{"name":"negative regulation of T cell polarization","type":"exact"},{"name":"negative regulation of T lymphocyte polarization","type":"exact"},{"name":"negative regulation of T-cell polarization","type":"exact"},{"name":"negative regulation of establishment of T lymphocyte polarity","type":"exact"},{"name":"negative regulation of establishment of T-cell polarity","type":"exact"},{"name":"negative regulation of establishment of T-lymphocyte polarity","type":"exact"}],"termid":"GO:1903904"}


id: GO:0006353
data:
  {"annotated_genes":["SJAG_03689","SJAG_03923","SJAG_02037","SJAG_03179","SJAG_02922","SJAG_04106","SJAG_01713","SJAG_03761","SJAG_04855","SJAG_04527","SJAG_03126","SJAG_02242","SJAG_04006","SJAG_00637","SJAG_02156","SJAG_04942","SJAG_03624"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111761],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904595"},{"annotations":[102069,115797,114018,96147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006363"},{"annotations":[73888,73958,107496,73399,79182,115798,92586,97916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006369"},{"annotations":[97025,101961,107263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030847"},{"annotations":[92782,115799,99673,97930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006386"}]},"cv_name":"biological_process","definition":"The completion of transcription: the RNA polymerase pauses, the RNA-DNA hybrid dissociates, followed by the release of the RNA polymerase from its DNA template.","definition_xrefs":["GOC:txnOH","PMID:15020047","PMID:30978344","PMID:18280161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA biosynthetic process","termid":"GO:0032774"},{"relation_name":"part_of","term_name":"DNA-templated transcription","termid":"GO:0006351"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00637":null,"SJAG_01713":null,"SJAG_02037":null,"SJAG_02156":null,"SJAG_02242":null,"SJAG_02922":null,"SJAG_03126":null,"SJAG_03179":null,"SJAG_03624":null,"SJAG_03689":null,"SJAG_03761":null,"SJAG_03923":null,"SJAG_04006":null,"SJAG_04106":null,"SJAG_04527":null,"SJAG_04855":null,"SJAG_04942":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150"],"is_obsolete":false,"name":"DNA-templated transcription termination","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0001125"],"synonyms":[{"name":"DNA-dependent transcription, termination","type":"exact"},{"name":"DNA-templated transcription, termination","type":"exact"},{"name":"termination of DNA-dependent transcription","type":"exact"},{"name":"termination of transcription, DNA-dependent","type":"exact"},{"name":"transcription termination factor activity","type":"related"},{"name":"transcription termination from bacterial-type RNA polymerase promoter","type":"narrow"},{"name":"transcription termination, DNA-dependent","type":"related"},{"name":"transcriptional complex disassembly","type":"broad"}],"termid":"GO:0006353","terms_by_termid":{"GO:0006363":null,"GO:0006369":null,"GO:0006386":null,"GO:0030847":null,"GO:1904595":null}}


id: FYPO:0005001
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein having high molecular mass due to polyubiquitin conjugation is lower than normal.","definition_xrefs":["PomBase:mah","PMID:10082519"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular HMW ubiquitin conjugate level","synonyms":[{"name":"decreased cellular HMW ubiquitin conjugate level during mitotic cell cycle","type":"related"},{"name":"decreased cellular HMW ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"decreased cellular high molecular mass ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"decreased cellular high molecular weight ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"reduced cellular HMW ubiquitin conjugate level","type":"exact"}],"termid":"FYPO:0005001"}


id: MONDO:0030868
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"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":"spermatogenic failure 49","secondary_identifiers":["OMIM:619144","UMLS:C5436887","DOID:0112271","MEDGEN:1742668"],"synonyms":[{"name":"SPGF49","type":"exact"},{"name":"spermatogenic failure 49","type":"exact"}],"termid":"MONDO:0030868","xrefs":{"Monarch":{"xref_id":"0030868"}}}


id: FYPO:0002843
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a protein that is not normally found in the nucleoplasm is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to nucleus during vegetative growth","termid":"FYPO:0000784"},{"relation_name":"output_of","term_name":"abnormal protein localization to nucleoplasm","termid":"FYPO:0002529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"protein mislocalized to nucleoplasm","synonyms":[{"name":"ectopic protein localization to nucleoplasm","type":"exact"},{"name":"protein mislocalised to nucleoplasm","type":"exact"},{"name":"protein mislocalised to nucleoplasm during vegetative growth","type":"exact"},{"name":"protein mislocalized to nucleoplasm during mitotic cell cycle","type":"related"},{"name":"protein mislocalized to nucleoplasm during vegetative growth","type":"exact"}],"termid":"FYPO:0002843"}


id: PBO:0079909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1","termid":"PBO:0079909"}


id: MONDO:0011759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hurler-Scheie syndrome is the intermediate form of mucopolysaccharidosis type 1 (MPS1) between the two extremes Hurler syndrome and Scheie syndrome ; it is a rare lysosomal storage disease, characterized by skeletal deformities and a delay in motor development.","definition_xrefs":["Orphanet:93476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis type 1","termid":"MONDO:0001586"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0002561","MONDO:0005328"],"is_obsolete":false,"name":"Hurler-Scheie syndrome","secondary_identifiers":["DOID:0111389","NANDO:1200096","GARD:12560","SCTID:26745009","NCIT:C122782","MedDRA:10056916","MEDGEN:88566","NANDO:2201170","OMIM:607015","UMLS:C0086431"],"synonyms":[{"name":"Hurler-Scheie syndrome","type":"exact"},{"name":"Hurler–Scheie syndrome","type":"related"},{"name":"MPS I H-S","type":"exact"},{"name":"MPS1-HS","type":"related"},{"name":"MPS1H/S","type":"exact"},{"name":"MPSIH/S","type":"exact"},{"name":"Scheie disease mps type 1s","type":"related"},{"name":"Scheie's syndrome","type":"related"},{"name":"l-iduronidase deficiency, Scheie type","type":"related"},{"name":"mucopolysaccharidosis IH/S","type":"related"},{"name":"mucopolysaccharidosis type 1H/S","type":"exact"},{"name":"mucopolysaccharidosis type I mild form","type":"related"},{"name":"mucopolysaccharidosis type I-S","type":"related"},{"name":"mucopolysaccharidosis type IH/S","type":"exact"},{"name":"mucopolysaccharidosis type Ih/S","type":"related"},{"name":"mucopolysaccharidosis, mps-I-s","type":"exact"}],"termid":"MONDO:0011759","xrefs":{"Monarch":{"xref_id":"0011759"}}}


id: SO:0002014
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that causes the extension of 5' UTR, with regard to the reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5_prime_UTR_variant","termid":"SO:0001623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_prime_UTR_elongation","synonyms":[{"name":"5 prime UTR elongation","type":"exact"}],"termid":"SO:0002014"}


id: PBO:0078476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyrotropin releasing hormone receptor","termid":"PBO:0078476"}


id: PBO:0075094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 143","termid":"PBO:0075094"}


id: GO:0000727
data:
  {"annotated_genes":["SJAG_00857","SJAG_01762","SJAG_00327","SJAG_00696","SJAG_01044","SJAG_05180","SJAG_01354","SJAG_02348","SJAG_04995","SJAG_04210","SJAG_00884","SJAG_03160","SJAG_01624"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69588,70586,71744,72972,73169,74042,74327,77135,77932,79748,80057,99068,111830],"is_not":false,"summary":null,"term":"GO:0000727"}]},"cv_name":"biological_process","definition":"The error-free repair of a double-strand break in DNA in which the centromere-proximal end of a broken chromosome searches for a homologous region in an intact chromosome. DNA synthesis initiates from the 3' end of the invading DNA strand, using the intact chromosome as the template, and progresses to the end of the chromosome.","definition_xrefs":["GOC:elh","PMID:10357855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"double-strand break repair via homologous recombination","termid":"GO:0000724"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00327":null,"SJAG_00696":null,"SJAG_00857":null,"SJAG_00884":null,"SJAG_01044":null,"SJAG_01354":null,"SJAG_01624":null,"SJAG_01762":null,"SJAG_02348":null,"SJAG_03160":null,"SJAG_04210":null,"SJAG_04995":null,"SJAG_05180":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006310","GO:0006281"],"is_obsolete":false,"name":"double-strand break repair via break-induced replication","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0000727","terms_by_termid":{"GO:0000727":null}}


id: PBO:0049908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexosaminidase subunit alpha","termid":"PBO:0049908"}


id: MONDO:0016620
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetically and clinically heterogeneous inherited disorder characterized by digital clubbing and osteoarthropathy, with variable features of pachydermia, delayed closure of the fontanels, and congenital heart disease. There are two types of PHO: pachydermoperiostosis and cranio-osteoarthropathy.","definition_xrefs":["Orphanet:248095"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"excluded_subClassOf","term_name":"dermis disorder","termid":"MONDO:0021154"},{"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":"primary hypertrophic osteoarthropathy","secondary_identifiers":["NANDO:1200642","UMLS:C0029411","GARD:20667","icd11.foundation:792225761","NANDO:2100288","MESH:D010004","NANDO:2201004","DOID:14283","OMIMPS:259100","MEDGEN:18210","Orphanet:2796","MedDRA:10051686","SCTID:88220006","NCIT:C85023"],"synonyms":[{"name":"PDP","type":"exact"},{"name":"PHO","type":"exact"},{"name":"PHOAR1","type":"related"},{"name":"Touraine Solente Gole syndrome","type":"exact"},{"name":"Touraine-Solente-Gole syndrome","type":"exact"},{"name":"hypertrophic osteoarthropathy, primary","type":"exact"},{"name":"hypertrophic osteoarthropathy, primary, autosomal recessive, 1","type":"related"},{"name":"hypertrophic osteoarthropathy, primary, autosomal recessive, type 1","type":"exact"},{"name":"hypertropic osteoarthropathy, primary","type":"exact"},{"name":"idiopathic hypertrophic osteoarthropathy","type":"exact"},{"name":"pachydermoperiostosis","type":"exact"},{"name":"pachydermoperiostosis of nail","type":"exact"},{"name":"pachydermoperiostosis of nail [ambiguous]","type":"exact"},{"name":"pachydermoperiostosis syndrome","type":"exact"}],"termid":"MONDO:0016620","xrefs":{"Monarch":{"xref_id":"0016620"}}}


id: PBO:0049782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 17","termid":"PBO:0049782"}


id: PBO:0079850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unc-80 homolog, NALCN channel complex subunit","termid":"PBO:0079850"}


id: PBO:0025430
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Survival Motor Neuron","termid":"PBO:0025430"}


id: GO:0046068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cyclic GMP, guanosine 3',5'-phosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"cyclic purine nucleotide metabolic process","termid":"GO:0052652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"cGMP metabolic process","synonyms":[{"name":"cGMP metabolism","type":"exact"}],"termid":"GO:0046068"}


id: MONDO:0017447
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Congenital absence/hypoplasia of thumb is a rare developmental defect during embryogenesis characterized by underdevelopment of the thumb, ranging from a slight decrease in thumb size to complete absence of the thumb. The malformation may occur isolated, combined to other defects of the hand or upper limb, or as part of a multiple congenital anomaly syndrome.","definition_xrefs":["Orphanet:294988"],"gene_count":0,"genotype_count":0,"name":"obsolete congenital absence/hypoplasia of thumb (obsolete MONDO:0017447)","synonyms":[{"name":"thumb hypodactyly","type":"exact"},{"name":"thumb oligodactyly","type":"exact"}],"termid":"MONDO:0017447","xrefs":{"Monarch":{"xref_id":"0017447"}}}


id: MONDO:0016390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects.","definition_xrefs":["Orphanet:2238"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete metabolic disease with cataract (obsolete MONDO:0020280)","termid":"MONDO:0020280"},{"relation_name":"is_a","term_name":"hereditary hypoparathyroidism","termid":"MONDO:0016165"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"familial hypoparathyroidism","secondary_identifiers":["GARD:2910","MEDGEN:322005","OMIMPS:146200","icd11.foundation:1907423603","MESH:C537156","SCTID:725036000","NORD:1128","UMLS:C1832648","DOID:0111387"],"synonyms":[{"name":"FIH","type":"exact"},{"name":"Familial Isolated Hypoparathyroidism","type":"exact"},{"name":"familial isolated hypoparathyroidism","type":"exact"},{"name":"hypoparathyroidism familial isolated","type":"exact"},{"name":"hypoparathyroidism, familial","type":"exact"},{"name":"hypoparathyroidism, familial isolated","type":"exact"}],"termid":"MONDO:0016390","xrefs":{"Monarch":{"xref_id":"0016390"}}}


id: GO:0048170
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that increases long-term neuronal synaptic plasticity, the ability of neuronal synapses to change long-term as circumstances require. Long-term neuronal synaptic plasticity generally involves increase or decrease in actual synapse numbers.","definition_xrefs":["GOC:jid","PMID:11891290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of long-term neuronal synaptic plasticity","termid":"GO:0048169"},{"relation_name":"is_a","term_name":"positive regulation of neurogenesis","termid":"GO:0050769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of long-term neuronal synaptic plasticity","synonyms":[{"name":"activation of long-term neuronal synaptic plasticity","type":"narrow"},{"name":"stimulation of long-term neuronal synaptic plasticity","type":"narrow"},{"name":"up regulation of long-term neuronal synaptic plasticity","type":"exact"},{"name":"up-regulation of long-term neuronal synaptic plasticity","type":"exact"},{"name":"upregulation of long-term neuronal synaptic plasticity","type":"exact"}],"termid":"GO:0048170"}


id: PBO:0071998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S7","termid":"PBO:0071998"}


id: PBO:0052188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNMA1 antisense RNA 1","termid":"PBO:0052188"}


id: PATO:0002350
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being located toward the stalk of an organism relative to another entity.","definition_xrefs":["merriam-webster:http://www.merriam-webster.com/dictionary/cauline"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cauline to","termid":"PATO:0002350"}


id: GO:0050215
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: propane-1,2-diol = H2O + propanal.","definition_xrefs":["EC:4.2.1.28","RHEA:14569"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"propanediol dehydratase activity","secondary_identifiers":["KEGG_REACTION:R02376","MetaCyc:PROPANEDIOL-DEHYDRATASE-RXN"],"synonyms":[{"name":"1,2-propanediol dehydratase activity","type":"related"},{"name":"DL-1,2-propanediol hydro-lyase activity","type":"related"},{"name":"adenosylcobalamin-dependent diol dehydratase activity","type":"related"},{"name":"coenzyme B12-dependent diol dehydrase activity","type":"related"},{"name":"diol dehydrase activity","type":"related"},{"name":"diol dehydratase activity","type":"related"},{"name":"dioldehydratase activity","type":"related"},{"name":"meso-2,3-butanediol dehydrase activity","type":"related"},{"name":"propane-1,2-diol hydro-lyase (propanal-forming)","type":"related"},{"name":"propane-1,2-diol hydro-lyase activity","type":"related"},{"name":"propanediol dehydrase activity","type":"related"}],"termid":"GO:0050215"}


id: SO:0000665
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that is monocistronic.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"monocistronic","termid":"SO:0000878"},{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monocistronic_transcript","synonyms":[{"name":"monocistronic transcript","type":"exact"}],"termid":"SO:0000665"}


id: PBO:0072563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRAS2 pseudogene 1","termid":"PBO:0072563"}


id: MONDO:0032726
data:
  {"annotated_genes":["SJAG_04862"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85891],"is_not":false,"summary":null,"term":"MONDO:0032726"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04862":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 deficiency 39","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618397","DOID:0111475","GARD:17999","Orphanet:565624","MEDGEN:1683958","UMLS:C5193075"],"synonyms":[{"name":"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 39","type":"related"},{"name":"COXPD39","type":"related"}],"termid":"MONDO:0032726","terms_by_termid":{"MONDO:0032726":null},"xrefs":{"Monarch":{"xref_id":"0032726"}}}


id: PBO:0057931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3658","termid":"PBO:0057931"}


id: PBO:0029375
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_site_of_double-strand_break","termid":"PBO:0029375"}


id: MONDO:0013770
data:
  {"annotated_genes":["SJAG_02730"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86410],"is_not":false,"summary":null,"term":"MONDO:0013770"}]},"cv_name":"mondo","definition":"Any atrial heart septal defect in which the cause of the disease is a mutation in the GATA6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septal defect","termid":"MONDO:0006664"},{"relation_name":"is_a","term_name":"GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes","termid":"MONDO:0100540"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02730":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial septal defect 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:482573","DOID:0110114","OMIM:614475","UMLS:C3280943"],"synonyms":[{"name":"ASD9","type":"exact"},{"name":"GATA6 atrial heart septal defect","type":"exact"},{"name":"atrial heart septal defect caused by mutation in GATA6","type":"exact"},{"name":"atrial heart septal defect type 9","type":"exact"},{"name":"atrial septal defect 9","type":"exact"},{"name":"atrial septal defect type 9","type":"exact"}],"termid":"MONDO:0013770","terms_by_termid":{"MONDO:0013770":null},"xrefs":{"Monarch":{"xref_id":"0013770"}}}


id: MONDO:0011346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Type II xanthinuria, a type of classical xanthinuria, is a rare autosomal recessive disorder of purine metabolism characterized by the deficiency of both xanthine dehydrogenase and aldehyde oxidase, leading to the formation of urinary xanthine urolithiasis and leading, in some patients, to kidney failure. Other less common manifestations include arthropathy, myopathy and duodenal ulcer, while some patients remain asymptomatic.","definition_xrefs":["Orphanet:93602"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary xanthinuria","termid":"MONDO:0018106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0005066"],"is_obsolete":false,"name":"xanthinuria type II","secondary_identifiers":["UMLS:C1863688","MEDGEN:350953","OMIM:603592","GARD:5620","MESH:C566358","DOID:0070453"],"synonyms":[{"name":"XAN2","type":"exact"},{"name":"XDH and AOX dual deficiency","type":"exact"},{"name":"type 2 xanthinuria","type":"related"},{"name":"type II xanthinuria","type":"related"},{"name":"xanthine dehydrogenase and aldehyde oxidase combined deficiency of","type":"related"},{"name":"xanthine dehydrogenase and aldehyde oxidase, combined deficiency of","type":"exact"},{"name":"xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency","type":"exact"},{"name":"xanthinuria type 2","type":"related"},{"name":"xanthinuria, type 2","type":"related"},{"name":"xanthinuria, type II","type":"related"}],"termid":"MONDO:0011346","xrefs":{"Monarch":{"xref_id":"0011346"}}}


id: PBO:0043802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexin 2","termid":"PBO:0043802"}


id: MONDO:0007038
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":"Achoo syndrome","secondary_identifiers":["OMIM:100820","UMLS:C1863416","MEDGEN:400287","MESH:C535300"],"synonyms":[{"name":"Achoo syndrome","type":"exact"},{"name":"Peroutka sneeze","type":"related"},{"name":"autosomal dominant compelling Helioophthalmic outburst syndrome","type":"related"},{"name":"autosomal dominant compelling helio ophthalmic outburst syndrome","type":"related"},{"name":"photic sneeze reflex","type":"related"},{"name":"sneezing from Light exposure","type":"related"}],"termid":"MONDO:0007038","xrefs":{"Monarch":{"xref_id":"0007038"}}}


id: PBO:0040135
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 1","termid":"PBO:0040135"}


id: PBO:0078651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon CTT) 4-1","termid":"PBO:0078651"}


id: PBO:0058216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4508","termid":"PBO:0058216"}


id: GO:0000051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving any of the intermediate compounds involved in the urea cycle, a cyclic metabolic pathway that converts waste nitrogen in the form of ammonium to urea.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete urea cycle intermediate metabolic process (obsolete GO:0000051)","synonyms":[{"name":"urea cycle intermediate metabolic process","type":"exact"},{"name":"urea cycle intermediate metabolism","type":"exact"}],"termid":"GO:0000051"}


id: PBO:0109629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin heavy chain 16 (pseudogene)","termid":"PBO:0109629"}


id: GO:0100049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that negatively regulates phosphatidylcholine biosynthetic process.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of phosphatidylcholine biosynthetic process by transcription from RNA polymerase II promoter (obsolete GO:0100049)","termid":"GO:0100049"}


id: PR:Q9UTG1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A purine nucleoside phosphorylase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01175","PANTHER:PTHR11904:SF9"],"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":"purine nucleoside phosphorylase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1805.16c","secondary_identifiers":["UniProtKB:Q9UTG1"],"synonyms":[{"name":"PNP (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PNP","type":"exact"},{"name":"inosine phosphorylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"inosine-guanosine phosphorylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTG1"}


id: MONDO:0011619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crumpled helices and small mouth","secondary_identifiers":["OMIM:605945","MESH:C536217","UMLS:C1853826","MEDGEN:342976"],"synonyms":[{"name":"crumpled helices and small mouth","type":"exact"},{"name":"sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay","type":"related"}],"termid":"MONDO:0011619","xrefs":{"Monarch":{"xref_id":"0011619"}}}


id: PBO:0075185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide F pseudogene 2","termid":"PBO:0075185"}


id: GO:1990562
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An exosome complex that is assembled in the multivesicular body (MVB) membrane and chaperoned to the exosome by the ESCRT-III machinery.","definition_xrefs":["GOC:bhm","PMID:22660413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular exosome complex","termid":"GO:1990563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0005576","GO:0032991"],"is_obsolete":false,"name":"syndecan-syntenin-ALIX complex","synonyms":[{"name":"exosome complex","type":"broad"}],"termid":"GO:1990562"}


id: PBO:0061429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor subfamily 1 group H member 2","termid":"PBO:0061429"}


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


id: PBO:0062262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily D member 18","termid":"PBO:0062262"}


id: GO:0180004
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: RNA polymerase II large subunit CTD heptapeptide repeat--phospho-L-tyrosine (consensus YSPTSPS)(position 1) + H2O = RNA polymerase II large subunit + phosphate.","definition_xrefs":["PMID:22622228"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II CTD heptapeptide repeat phosphatase activity","termid":"GO:0008420"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0004721"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016788","GO:0140096","GO:0003674","GO:0004721"],"is_obsolete":false,"name":"RNA polymerase II CTD heptapeptide repeat Y1 phosphatase activity","synonyms":[{"name":"RNA polymerase II C-terminal domain Y1 phosphatase activity","type":"exact"}],"termid":"GO:0180004"}


id: PBO:0055459
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 2891","termid":"PBO:0055459"}


id: MONDO:1011071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in American mink.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, American mink","secondary_identifiers":["OMIA:001033-452646"],"termid":"MONDO:1011071","xrefs":{"Monarch":{"xref_id":"1011071"}}}


id: GO:0004793
data:
  {"annotated_genes":["SJAG_02450"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008732"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-threonine = glycine + acetaldehyde.","definition_xrefs":["EC:4.1.2.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02450":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"threonine aldolase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:19625","MetaCyc:THREONINE-ALDOLASE-RXN"],"synonyms":[{"name":"L-threonine acetaldehyde-lyase (glycine-forming)","type":"related"},{"name":"L-threonine acetaldehyde-lyase activity","type":"related"},{"name":"L-threonine aldolase activity","type":"exact"}],"termid":"GO:0004793","terms_by_termid":{"GO:0008732":null}}


id: GO:0008903
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-hydroxypyruvate = 2-hydroxy-3-oxopropanoate.","definition_xrefs":["RHEA:11952","EC:5.3.1.22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"hydroxypyruvate isomerase activity","secondary_identifiers":["KEGG_REACTION:R01394","MetaCyc:RXN0-305"],"synonyms":[{"name":"hydroxypyruvate aldose-ketose-isomerase activity","type":"related"},{"name":"hydroxypyruvate ketol-isomerase activity","type":"related"}],"termid":"GO:0008903"}


id: SO:1001273
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non-canonical start codon of sequence CTG.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_canonical_start_codon","termid":"SO:0000680"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTG_start_codon","synonyms":[{"name":"CTG start codon","type":"exact"}],"termid":"SO:1001273"}


id: GO:0032469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maintenance of an internal steady state of calcium ions within the endoplasmic reticulum of a cell or between the endoplasmic reticulum and its surroundings.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular calcium ion homeostasis","termid":"GO:0006874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098771","GO:0008150"],"is_obsolete":false,"name":"endoplasmic reticulum calcium ion homeostasis","synonyms":[{"name":"ER calcium ion concentration regulation","type":"exact"},{"name":"ER calcium ion homeostasis","type":"exact"},{"name":"calcium ion homeostasis in ER","type":"exact"},{"name":"calcium ion homeostasis in endoplasmic reticulum","type":"exact"},{"name":"endoplasmic reticulum calcium ion concentration regulation","type":"exact"},{"name":"regulation of ER calcium ion concentration","type":"exact"},{"name":"regulation of calcium ion concentration in ER","type":"exact"},{"name":"regulation of calcium ion concentration in endoplasmic reticulum","type":"exact"},{"name":"regulation of endoplasmic reticulum calcium ion concentration","type":"exact"}],"termid":"GO:0032469"}


id: GO:1905913
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of calcium ion export across the plasma membrane.","definition_xrefs":["GOC:BHF","GOC:rph","GOC:TermGenie","GO_REF:0000058","PMID:22362515","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of calcium ion transmembrane transport","termid":"GO:1903170"},{"relation_name":"is_a","term_name":"regulation of calcium ion export across plasma membrane","termid":"GO:1905912"},{"relation_name":"negatively_regulates","term_name":"calcium ion export across plasma membrane","termid":"GO:1990034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"negative regulation of calcium ion export across plasma membrane","synonyms":[{"name":"down regulation of calcium ion efflux from cell","type":"exact"},{"name":"down regulation of calcium ion export from cell","type":"exact"},{"name":"down-regulation of calcium ion efflux from cell","type":"exact"},{"name":"down-regulation of calcium ion export from cell","type":"exact"},{"name":"downregulation of calcium ion efflux from cell","type":"exact"},{"name":"downregulation of calcium ion export from cell","type":"exact"},{"name":"inhibition of calcium ion efflux from cell","type":"narrow"},{"name":"inhibition of calcium ion export from cell","type":"narrow"},{"name":"negative regulation of calcium ion efflux from cell","type":"exact"},{"name":"negative regulation of calcium ion export from cell","type":"exact"}],"termid":"GO:1905913"}


id: FYPO:0000173
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the DNA replication checkpoint in a mitotic cell cycle is abnormal. The DNA replication checkpoint normally prevents the initiation of mitosis until DNA replication is complete. In a mutant, the checkpoint may fail to arrest or delay cell cycle progression under appropriate conditions, or the incidence or duration of arrest or delay may differ from wild type under any specified set of conditions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of G2/M transition of mitotic cell cycle","termid":"FYPO:0000166"},{"relation_name":"is_a","term_name":"abnormal mitotic DNA integrity checkpoint","termid":"FYPO:0000643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000298","FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitotic cell cycle DNA replication checkpoint","secondary_identifiers":["FYPO:0000823"],"synonyms":[{"name":"abnormal DNA replication checkpoint","type":"broad"},{"name":"abnormal mitotic cell cycle DNA replication checkpoint activation","type":"exact"}],"termid":"FYPO:0000173"}


id: PBO:0059255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L21","termid":"PBO:0059255"}


id: PBO:0076585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 8B","termid":"PBO:0076585"}


id: RO:0003307
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between an entity (e.g. a genotype, genetic variation, chemical, or environmental exposure) and a condition (a phenotype or disease), where the presence of the entity reduces or eliminates some or all aspects of the condition.","direct_ancestors":[{"relation_name":"is_a","term_name":"contributes_to_severity_of_condition","termid":"RO:0003305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ameliorates_condition","termid":"RO:0003307"}


id: GO:1903886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chemokine (C-C motif) ligand 20 production.","definition_xrefs":["GOC:krc","GOC:TermGenie","PMID:20054338","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of chemokine production","termid":"GO:0032722"},{"relation_name":"is_a","term_name":"regulation of chemokine (C-C motif) ligand 20 production","termid":"GO:1903884"},{"relation_name":"positively_regulates","term_name":"chemokine (C-C motif) ligand 20 production","termid":"GO:0036392"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of chemokine (C-C motif) ligand 20 production","synonyms":[{"name":"activation of C-C motif chemokine 20 production","type":"narrow"},{"name":"activation of CCL-20 production","type":"narrow"},{"name":"activation of CCL20 production","type":"narrow"},{"name":"activation of chemokine (C-C motif) ligand 20 production","type":"narrow"},{"name":"positive regulation of C-C motif chemokine 20 production","type":"exact"},{"name":"positive regulation of CCL-20 production","type":"exact"},{"name":"positive regulation of CCL20 production","type":"exact"},{"name":"up regulation of C-C motif chemokine 20 production","type":"exact"},{"name":"up regulation of CCL-20 production","type":"exact"},{"name":"up regulation of CCL20 production","type":"exact"},{"name":"up regulation of chemokine (C-C motif) ligand 20 production","type":"exact"},{"name":"up-regulation of C-C motif chemokine 20 production","type":"exact"},{"name":"up-regulation of CCL-20 production","type":"exact"},{"name":"up-regulation of CCL20 production","type":"exact"},{"name":"up-regulation of chemokine (C-C motif) ligand 20 production","type":"exact"},{"name":"upregulation of C-C motif chemokine 20 production","type":"exact"},{"name":"upregulation of CCL-20 production","type":"exact"},{"name":"upregulation of CCL20 production","type":"exact"},{"name":"upregulation of chemokine (C-C motif) ligand 20 production","type":"exact"}],"termid":"GO:1903886"}


id: MONDO:0002499
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete astrocytoma (obsolete MONDO:0002499)","termid":"MONDO:0002499","xrefs":{"Monarch":{"xref_id":"0002499"}}}


id: MONDO:0013005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"SeSAME syndrome is characterized by seizures, sensorineural deafness, ataxia, intellectual deficit, and electrolyte imbalance (hypokalemia, metabolic alkalosis, and hypomagnesemia).","definition_xrefs":["Orphanet:199343"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"inherited renal tubular disease","termid":"MONDO:0015962"},{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"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":"EAST syndrome","secondary_identifiers":["SCTID:721207002","MESH:C557674","GARD:10514","MEDGEN:411243","OMIM:612780","UMLS:C2748572","DOID:0060484"],"synonyms":[{"name":"EAST syndrome","type":"exact"},{"name":"SESAMES","type":"related"},{"name":"epilepsy, ataxia, sensorineural deafness and tubulopathy","type":"exact"},{"name":"epilepsy, ataxia, sensorineural deafness, and tubulopathy","type":"related"},{"name":"seizures - sensorineural deafness - ataxia - intellectual disability - electrolyte imbalance","type":"related"},{"name":"seizures, sensorineural deafness, ataxia, intellectual disability and electrolyte imbalance","type":"exact"},{"name":"seizures, sensorineural deafness, ataxia, intellectual disability, and electrolyte imbalance","type":"related"},{"name":"seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance","type":"exact"},{"name":"seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance","type":"related"},{"name":"seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome","type":"exact"},{"name":"sesame syndrome","type":"exact"}],"termid":"MONDO:0013005","xrefs":{"Monarch":{"xref_id":"0013005"}}}


id: PR:O13910
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U3 small nucleolar ribonucleoprotein protein MPP10 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00881","PANTHER:PTHR17039:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 small nucleolar ribonucleoprotein protein mpp10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23C11.03","secondary_identifiers":["UniProtKB:O13910"],"synonyms":[{"name":"Spom972h-MPHOSPH10","type":"exact"}],"termid":"PR:O13910"}


id: MONDO:0021444
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the large intestine.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal benign neoplasm","termid":"MONDO:0003062"},{"relation_name":"is_a","term_name":"large intestine disorder","termid":"MONDO:0024634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"benign neoplasm of large intestine","secondary_identifiers":["SCTID:92170008","UMLS:C0347272","NCIT:C4610","MEDGEN:91125"],"synonyms":[{"name":"benign colorectal neoplasm","type":"exact"},{"name":"benign colorectal neoplasms","type":"exact"},{"name":"benign colorectal tumor","type":"exact"},{"name":"benign colorectal tumors","type":"exact"},{"name":"benign colorectal tumour","type":"exact"},{"name":"benign colorectal tumours","type":"exact"},{"name":"benign large bowel neoplasm","type":"exact"},{"name":"benign large bowel tumor","type":"exact"},{"name":"benign large bowel tumour","type":"exact"},{"name":"benign large intestine neoplasm","type":"exact"},{"name":"benign large intestine tumor","type":"exact"},{"name":"benign large intestine tumour","type":"exact"},{"name":"benign neoplasm of large bowel","type":"exact"},{"name":"benign neoplasm of the large bowel","type":"exact"},{"name":"benign neoplasm of the large intestine","type":"exact"},{"name":"benign tumor of large bowel","type":"exact"},{"name":"benign tumor of large intestine","type":"exact"},{"name":"benign tumor of the large bowel","type":"exact"},{"name":"benign tumor of the large intestine","type":"exact"},{"name":"benign tumour of large bowel","type":"exact"},{"name":"benign tumour of large intestine","type":"exact"},{"name":"benign tumour of the large bowel","type":"exact"},{"name":"benign tumour of the large intestine","type":"exact"},{"name":"colorectal neoplasms, benign","type":"exact"},{"name":"colorectal tumors, benign","type":"exact"},{"name":"large intestine benign neoplasm","type":"exact"},{"name":"neoplasms, colorectal, benign","type":"exact"},{"name":"tumors, colorectal, benign","type":"exact"}],"termid":"MONDO:0021444","xrefs":{"Monarch":{"xref_id":"0021444"}}}


id: PBO:0110267
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSF-Responsive amino acid Transporter","termid":"PBO:0110267"}


id: FYPO:0001592
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of arginine into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased amino acid import during vegetative growth","termid":"FYPO:0001360"},{"relation_name":"is_a","term_name":"abnormal arginine import","termid":"FYPO:0001654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased arginine import","synonyms":[{"name":"decreased L-arginine import","type":"exact"},{"name":"decreased L-arginine import across plasma membrane","type":"exact"},{"name":"decreased arginine import during mitotic cell cycle","type":"related"},{"name":"decreased arginine import during vegetative growth","type":"exact"},{"name":"decreased arginine import into cell","type":"exact"},{"name":"decreased arginine uptake","type":"exact"},{"name":"reduced arginine import","type":"exact"}],"termid":"FYPO:0001592"}


id: PBO:0058579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6516","termid":"PBO:0058579"}


id: GO:0120511
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: methyl (2E,6E)-farnesoate + O2 + reduced [NADPH--hemoprotein reductase] = H+ + H2O + juvenile hormone III + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["PMID:38741075","RHEA:43728","PMID:23586995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"methyl farnesoate epoxidase activity","secondary_identifiers":["EC:1.14.14.127","MetaCyc:RXN-11621"],"synonyms":[{"name":"CYP15A1 activity","type":"related"}],"termid":"GO:0120511"}


id: GO:1990347
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the removal of adenine misinserted into nascent strand opposite 8-oxoG in the template by adenine DNA glycosylase activity. The reaction leaves an apyrimidinic (AP) site.","definition_xrefs":["PMID:24559510"],"gene_count":0,"genotype_count":0,"name":"obsolete G*/A mismatch-specific adenine-DNA glycosylase activity (obsolete GO:1990347)","synonyms":[{"name":"G*/A mismatch-specific adenine-DNA glycosylase activity","type":"exact"}],"termid":"GO:1990347"}


id: GO:0046128
data:
  {"annotated_genes":["SJAG_01859","SJAG_00044","SJAG_02582","SJAG_01070","SJAG_03096","SJAG_03881","SJAG_02959","SJAG_02580","SJAG_06634","SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046086"},{"annotations":[87330,87329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"},{"annotations":[90299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046085"},{"annotations":[116646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"},{"annotations":[69550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006190"},{"annotations":[93515,61545,66242,73201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006166"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving any ribonucleoside, a nucleoside in which purine base is linked to a ribose (beta-D-ribofuranose) molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoside metabolic process","termid":"GO:0009119"},{"relation_name":"is_a","term_name":"purine nucleoside metabolic process","termid":"GO:0042278"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00134":null,"SJAG_01070":null,"SJAG_01859":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02959":null,"SJAG_03096":null,"SJAG_03881":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"purine ribonucleoside metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"purine ribonucleoside metabolism","type":"exact"}],"termid":"GO:0046128","terms_by_termid":{"GO:0006154":null,"GO:0006166":null,"GO:0006169":null,"GO:0006190":null,"GO:0046085":null,"GO:0046086":null}}


id: PBO:0004049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactosylxylosylprotein 3-beta-galactosyltransferase Pvg1 (predicted)","termid":"PBO:0004049"}


id: PBO:0089550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eisosome assembly protein Fhn1","termid":"PBO:0089550"}


id: MONDO:0014632
data:
  {"annotated_genes":["SJAG_00120"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84992],"is_not":false,"summary":null,"term":"MONDO:0014632"}]},"cv_name":"mondo","definition":"Any leukodystrophy in which the cause of the disease is a mutation in the PYCR2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00120":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hypomyelinating leukodystrophy 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4225332","OMIM:616420","DOID:0060788","MEDGEN:904191"],"synonyms":[{"name":"HLD10","type":"exact"},{"name":"PYCR2 leukodystrophy","type":"exact"},{"name":"hypomyelinating leukodystrophy type 10","type":"exact"},{"name":"leukodystrophy caused by mutation in PYCR2","type":"exact"},{"name":"leukodystrophy, hypomyelinating, 10","type":"related"},{"name":"leukodystrophy, hypomyelinating, type 10","type":"exact"}],"termid":"MONDO:0014632","terms_by_termid":{"MONDO:0014632":null},"xrefs":{"Monarch":{"xref_id":"0014632"}}}


id: GO:0004254
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: acylaminoacyl-peptide + H2O = acylamino acid + peptide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete acylaminoacyl-peptidase activity (obsolete GO:0004254)","synonyms":[{"name":"N-acylpeptide hydrolase activity","type":"related"},{"name":"N-formylmethionine (fMet) aminopeptidase activity","type":"related"},{"name":"acylamino-acid-releasing enzyme activity","type":"related"},{"name":"acylaminoacyl-peptidase activity","type":"exact"}],"termid":"GO:0004254"}


id: PBO:0075151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 7","termid":"PBO:0075151"}


id: MONDO:0003588
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant adipose tissue neoplasm of the larynx. It predominantly affects males. Clinical presentation includes dysphonia, dysphagia and respiratory symptoms. The supraglottis is the most common site of involvement.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngeal sarcoma","termid":"MONDO:0002448"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"larynx liposarcoma","secondary_identifiers":["DOID:5696","MEDGEN:235252","UMLS:C1334372","NCIT:C6021"],"synonyms":[{"name":"laryngeal liposarcoma","type":"exact"},{"name":"larynx liposarcoma","type":"exact"},{"name":"lip larynx sarcoma","type":"exact"},{"name":"liposarcoma of larynx","type":"exact"},{"name":"liposarcoma of the larynx","type":"exact"}],"termid":"MONDO:0003588","xrefs":{"Monarch":{"xref_id":"0003588"}}}


id: GO:0070096
data:
  {"annotated_genes":["SJAG_03416","SJAG_02361"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58692,69612],"is_not":false,"summary":null,"term":"GO:0070096"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a mitochondrial outer membrane translocase complex.","definition_xrefs":["GOC:BHF","GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"outer mitochondrial membrane organization","termid":"GO:0007008"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02361":null,"SJAG_03416":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0061024","GO:0065003","GO:0007005","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"mitochondrial outer membrane translocase complex assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"TOM complex assembly","type":"exact"},{"name":"mitochondrion outer membrane translocase complex assembly","type":"exact"}],"termid":"GO:0070096","terms_by_termid":{"GO:0070096":null}}


id: PR:O13656
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial import receptor subunit TOM40 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02828","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial import receptor subunit tom40 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC27B12.13","secondary_identifiers":["UniProtKB:O13656"],"synonyms":[{"name":"Spom972h-TOMM40","type":"exact"},{"name":"translocase of outer membrane 40 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13656"}


id: GO:1904489
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A negative regulation of transcription from RNA polymerase II promoter that results in regulation of reactive oxygen species metabolic process.","definition_xrefs":["GO_REF:0000063","PMID:25961505","GOC:TermGenie","GOC:kmv"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of reactive oxygen species metabolic process by negative regulation of transcription from RNA polymerase II promoter (obsolete GO:1904489)","synonyms":[{"name":"regulation of ROS metabolic process by down regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of ROS metabolic process by down regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of ROS metabolic process by down-regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of ROS metabolic process by down-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of ROS metabolic process by downregulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of ROS metabolic process by downregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of ROS metabolic process by inhibition of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of ROS metabolic process by inhibition of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of ROS metabolic process by negative regulation of gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of ROS metabolic process by negative regulation of global transcription from Pol II promoter","type":"related"},{"name":"regulation of ROS metabolic process by negative regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of ROS metabolic process by negative regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of ROS metabolic process by negative regulation of transcription from RNA polymerase II promoter, global","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by down regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by down regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolic process by down-regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by down-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolic process by downregulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by downregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolic process by inhibition of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by inhibition of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolic process by negative regulation of gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by negative regulation of global transcription from Pol II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolic process by negative regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolic process by negative regulation of transcription from RNA polymerase II promoter, global","type":"related"},{"name":"regulation of reactive oxygen species metabolism by down regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolism by down regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolism by down-regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolism by down-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolism by downregulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolism by downregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolism by inhibition of global transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolism by inhibition of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolism by negative regulation of gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolism by negative regulation of global transcription from Pol II promoter","type":"related"},{"name":"regulation of reactive oxygen species metabolism by negative regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolism by negative regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of reactive oxygen species metabolism by negative regulation of transcription from RNA polymerase II promoter, global","type":"related"}],"termid":"GO:1904489"}


id: GO:0102941
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3,5-dihydroxyanisole + S-adenosyl-L-methionine = H+ + 3,5-dimethoxyphenol + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3,5-dihydroxyanisole O-methyltransferase activity (obsolete GO:0102941)","termid":"GO:0102941"}


id: PBO:0063087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAQR5 divergent transcript","termid":"PBO:0063087"}


id: MONDO:0000671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An agnosia characterized by an inability to distinguish, name, or recognize the fingers","definition_xrefs":["Wikipedia:Finger_agnosia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"agnosia","termid":"MONDO:0005638"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"finger agnosia","secondary_identifiers":["DOID:0060141","HP:0010525","MEDGEN:115960","UMLS:C0234509"],"synonyms":[{"name":"finger agnosia","type":"exact"},{"name":"finger agnosia (disease)","type":"exact"},{"name":"manual digit agnosia","type":"exact"}],"termid":"MONDO:0000671","xrefs":{"Monarch":{"xref_id":"0000671"}}}


id: PBO:0090632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiolipin synthase/ hydrolase fusion protein Crd1","termid":"PBO:0090632"}


id: MONDO:0011032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 11","secondary_identifiers":["GARD:18104","MESH:C563353","OMIM:601317","UMLS:C1832475","MEDGEN:331297","DOID:0110543"],"synonyms":[{"name":"DFNA11","type":"narrow"},{"name":"MYO7A autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 11","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 11","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in MYO7A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 11","type":"narrow"},{"name":"deafness, autosomal dominant 11","type":"narrow"},{"name":"deafness, autosomal dominant type 11","type":"narrow"}],"termid":"MONDO:0011032","xrefs":{"Monarch":{"xref_id":"0011032"}}}


id: GO:0071297
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 cobalamin (vitamin B12) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cobalamin","termid":"GO:0033590"},{"relation_name":"is_a","term_name":"cellular response to vitamin","termid":"GO:0071295"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to cobalamin","synonyms":[{"name":"cellular response to vitamin B12","type":"exact"}],"termid":"GO:0071297"}


id: PBO:0005856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexed with Cdc5 protein Cwf18","termid":"PBO:0005856"}


id: MONDO:0007026
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-alcoholic fatty liver (obsolete MONDO:0007026)","termid":"MONDO:0007026","xrefs":{"Monarch":{"xref_id":"0007026"}}}


id: MONDO:1010299
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteochondrosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"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":"osteochondrosis, non-human animal","secondary_identifiers":["OMIA:000750"],"termid":"MONDO:1010299","xrefs":{"Monarch":{"xref_id":"1010299"}}}


id: PBO:0070349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 22","termid":"PBO:0070349"}


id: PBO:0049112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 174","termid":"PBO:0049112"}


id: PBO:0003432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin type I","termid":"PBO:0003432"}


id: PBO:0063792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD finger protein 20 like 1","termid":"PBO:0063792"}


id: GO:0004009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete ATP-binding cassette (ABC) transporter activity (obsolete GO:0004009)","synonyms":[{"name":"ATP-binding cassette (ABC) transporter activity","type":"exact"}],"termid":"GO:0004009"}


id: GO:0106160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of small RNA loading onto RISC.","definition_xrefs":["GOC:ha","PMID:29775584"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of small RNA loading onto RISC (obsolete GO:0106160)","termid":"GO:0106160"}


id: PBO:0065113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase C eta","termid":"PBO:0065113"}


id: PBO:0000357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglucosamine-phosphate mutase (predicted)","termid":"PBO:0000357"}


id: PBO:0030538
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cAMP_level_during_glucose_starvation","termid":"PBO:0030538"}


id: GO:0044527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a peptidyl-cystine residue in a protein by the direct addition of H2S, followed by the removal of 2 protons to form peptidyl-cysteine persulfide.","definition_xrefs":["GOC:jsg","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete formation of peptidyl-cystine persulfide by sulphur transfer from H2S (obsolete GO:0044527)","termid":"GO:0044527"}


id: PBO:0086446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative mannosidase; GPI-anchored membrane protein required for cell wall biosynthesis in bud formation;homologous to Dfg5p","termid":"PBO:0086446"}


id: GO:0007250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The stimulation of the activity of NF-kappaB-inducing kinase through phosphorylation at specific residues.","definition_xrefs":["GOC:jl","PMID:12773372"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activation of protein kinase activity","termid":"GO:0032147"},{"relation_name":"part_of","term_name":"non-canonical NF-kappaB signal transduction","termid":"GO:0038061"}],"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":"activation of NF-kappaB-inducing kinase activity","synonyms":[{"name":"activation of NIK activity","type":"exact"},{"name":"positive regulation of NF-kappaB-inducing kinase activity","type":"broad"}],"termid":"GO:0007250"}


id: PBO:0027219
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cytosolic_monomeric_ribosome_level","termid":"PBO:0027219"}


id: GO:1900830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of D-tyrosine.","definition_xrefs":["PMID:10766779","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete D-tyrosine biosynthetic process (obsolete GO:1900830)","synonyms":[{"name":"D-tyrosine anabolism","type":"exact"},{"name":"D-tyrosine biosynthesis","type":"exact"},{"name":"D-tyrosine formation","type":"exact"},{"name":"D-tyrosine synthesis","type":"exact"}],"termid":"GO:1900830"}


id: PBO:0067414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 525, pseudogene","termid":"PBO:0067414"}


id: PBO:0040041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aryl hydrocarbon receptor nuclear translocator","termid":"PBO:0040041"}


id: PR:C6Y4C3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ecl3 gene.","definition_xrefs":["UniProtKB:C6Y4C3","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":"extender of the chronological lifespan protein ecl3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8E4.12c","synonyms":[{"name":"Spom972h-ecl3","type":"exact"}],"termid":"PR:C6Y4C3"}


id: PBO:0111744
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-fungal Zn(2)-Cys(6) binuclear cluster domain","termid":"PBO:0111744"}


id: PBO:0065524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patched 1","termid":"PBO:0065524"}


id: PBO:0061689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 188","termid":"PBO:0061689"}


id: GO:0044387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The stopping, prevention, or reduction in frequency, rate or extent of protein kinase activity as a result of regulating the phosphorylation status of that protein kinase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein kinase activity","termid":"GO:0006469"}],"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 protein kinase activity by regulation of protein phosphorylation","termid":"GO:0044387"}


id: PBO:0069490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 757, pseudogene","termid":"PBO:0069490"}


id: PBO:0030030
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_shmoo_formation","termid":"PBO:0030030"}


id: PBO:0046979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 86 member C2, pseudogene","termid":"PBO:0046979"}


id: PBO:0043018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHL1 antisense RNA 2","termid":"PBO:0043018"}


id: PBO:0063114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase 1 pseudogene 1","termid":"PBO:0063114"}


id: PBO:0028552
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_nucleus_during_mitosis","termid":"PBO:0028552"}


id: PBO:0002449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA 2'-phosphotransferase Tpt1 (predicted)","termid":"PBO:0002449"}


id: PBO:0062568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily AG member 1","termid":"PBO:0062568"}


id: MONDO:0001890
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tooth erosion, non-bacterial that involves the dental pulp.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tooth erosion, non-bacterial","termid":"MONDO:0002325"},{"relation_name":"is_a","term_name":"dental pulp disorder","termid":"MONDO:0003394"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulp erosion","secondary_identifiers":["ICD9:521.33","MEDGEN:1843466","DOID:14140","UMLS:C1456163"],"synonyms":[{"name":"dental pulp tooth erosion, non-bacterial","type":"exact"},{"name":"tooth erosion, non-bacterial of dental pulp","type":"exact"}],"termid":"MONDO:0001890","xrefs":{"Monarch":{"xref_id":"0001890"}}}


id: GO:0050069
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysine + NAD+ = 1,2-didehydropiperidine-2-carboxylate + NH3 + NADH.","definition_xrefs":["EC:1.4.1.15","MetaCyc:LYSINE-DEHYDROGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor","termid":"GO:0016639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"lysine dehydrogenase activity","secondary_identifiers":["RHEA:18505"],"synonyms":[{"name":"L-lysine:NAD+ oxidoreductase (deaminating, cyclizing)","type":"related"}],"termid":"GO:0050069"}


id: PBO:0067559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 712, pseudogene","termid":"PBO:0067559"}


id: GO:0070564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of vitamin D receptor signaling pathway activity.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vitamin D receptor signaling pathway","termid":"GO:0070562"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"vitamin D receptor signaling pathway","termid":"GO:0070561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of vitamin D receptor signaling pathway","synonyms":[{"name":"activation of vitamin D receptor signaling pathway","type":"narrow"},{"name":"positive regulation of VDR signaling pathway","type":"exact"},{"name":"positive regulation of vitamin D receptor signalling pathway","type":"exact"},{"name":"stimulation of vitamin D receptor signaling pathway","type":"narrow"},{"name":"up regulation of vitamin D receptor signaling pathway","type":"exact"},{"name":"up-regulation of vitamin D receptor signaling pathway","type":"exact"},{"name":"upregulation of vitamin D receptor signaling pathway","type":"exact"}],"termid":"GO:0070564"}


id: PBO:0085748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase; implicated in activation of the plasma membrane H(+)-ATPase Pma1p in response to glucose metabolism; plays a role in ion homeostasis; protein abundance increases in response to DNA replication stress","termid":"PBO:0085748"}


id: PBO:0085861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the vacuole; YDL211C has a paralog, TDA7, that arose from the whole genome duplication","termid":"PBO:0085861"}


id: PBO:0062960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein cytoplasmic 1 pseudogene 3","termid":"PBO:0062960"}


id: MONDO:0025514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Livedoid vasculopathy is a blood vessel disorder that causes painful ulcers and scarring (atrophie blanche) on the feet and lower legs. These symptoms can persist for months to years and the ulcers often recur.Livedoid vasculopathy lesions appear as painful red or purple marks and spots that may progress to small, tender, irregular ulcers. Symptoms tend to worsen in the winter and summer months, and affect women more often then men. Livedoid vasculopathy may occur alone or in combination with another condition, such as lupus or thrombophilia.","definition_xrefs":["GARD:0012784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"is_a","term_name":"vasculitis","termid":"MONDO:0018882"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"livedoid vasculopathy","secondary_identifiers":["Orphanet:542643","SCTID:238762002","MESH:D000090122","GARD:12784","UMLS:C0343081","ICD9CM:709.1","icd11.foundation:1237292304","DOID:0040099","ICD10CM:L95.0","ICD9:709.1","MEDGEN:575376"],"synonyms":[{"name":"idiopathic atrophic blanche","type":"related"},{"name":"livedo reticularis with summer ulcerations","type":"related"},{"name":"livedo reticularis with winter ulcerations","type":"related"},{"name":"livedo vasculitis","type":"related"},{"name":"livedoid vasculitis","type":"exact"},{"name":"livedoid vasculopathy","type":"exact"},{"name":"segmental hyalinizing vasculopathy","type":"related"},{"name":"white atrophy","type":"related"}],"termid":"MONDO:0025514","xrefs":{"Monarch":{"xref_id":"0025514"}}}


id: FYPO:0002692
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 paraquat. Cells stop growing (and may die) at a concentration of paraquat 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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0001985","FYPO:0000139","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to paraquat","synonyms":[{"name":"hypersensitive to paraquat","type":"exact"},{"name":"sensitive to paraquat during mitotic cell cycle","type":"related"},{"name":"sensitive to paraquat during vegetative growth","type":"exact"}],"termid":"FYPO:0002692"}


id: FYPO:0003109
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the telomere of a chromosome does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to chromosome during vegetative growth","termid":"FYPO:0002841"},{"relation_name":"is_a","term_name":"abnormal protein localization to telomere during vegetative growth","termid":"FYPO:0003108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to telomere during vegetative growth","synonyms":[{"name":"abolished protein localisation to chromosome, telomeric region, during vegetative growth","type":"exact"},{"name":"abolished protein localisation to telomere during vegetative growth","type":"exact"},{"name":"abolished protein localization to chromosome, telomeric region, during vegetative growth","type":"exact"},{"name":"abolished protein localization to telomere during mitotic cell cycle","type":"related"},{"name":"protein absent from telomere during vegetative growth","type":"related"},{"name":"protein localization to telomere abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0003109"}


id: MONDO:0003303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing encapsulated neoplasm arising from nerves in the gallbladder. Morphologically, it is characterized by the presence of fibroblasts and Schwann cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallbladder cancer","termid":"MONDO:0005411"},{"relation_name":"is_a","term_name":"neurofibroma","termid":"MONDO:0016755"},{"relation_name":"is_a","term_name":"peripheral nervous system cancer","termid":"MONDO:0021089"},{"relation_name":"is_a","term_name":"malignant glioma","termid":"MONDO:0100342"}],"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:0002515","MONDO:0004335"],"is_obsolete":false,"name":"neurofibroma of gallbladder","secondary_identifiers":["NCIT:C5746","UMLS:C1333751","DOID:5150","MEDGEN:232540"],"synonyms":[{"name":"gall bladder neurofibroma","type":"exact"},{"name":"gallbladder neurofibroma","type":"exact"},{"name":"neurofibroma of gall bladder","type":"exact"},{"name":"neurofibroma of gallbladder","type":"exact"},{"name":"neurofibroma of the gallbladder","type":"exact"}],"termid":"MONDO:0003303","xrefs":{"Monarch":{"xref_id":"0003303"}}}


id: MONDO:0014806
data:
  {"annotated_genes":["SJAG_02096"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85564],"is_not":false,"summary":null,"term":"MONDO:0014806"}]},"cv_name":"mondo","definition":"Any prenatal-onset spinal muscular atrophy with congenital bone fractures in which the cause of the disease is a mutation in the TRIP4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenatal-onset spinal muscular atrophy with congenital bone fractures","termid":"MONDO:0000209"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02096":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005559"],"is_obsolete":false,"name":"spinal muscular atrophy with congenital bone fractures 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:271225","MESH:C564805","GARD:4947","OMIM:616866","UMLS:C4225177","MEDGEN:896011"],"synonyms":[{"name":"SMA1 with congenital bone fractures","type":"related"},{"name":"SMABF1","type":"exact"},{"name":"TRIP4 prenatal-onset spinal muscular atrophy with congenital bone fractures","type":"exact"},{"name":"prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in TRIP4","type":"exact"},{"name":"spinal muscular atrophy type 1 with congenital bone fractures","type":"related"},{"name":"spinal muscular atrophy with congenital bone fractures 1","type":"exact"},{"name":"spinal muscular atrophy with congenital bone fractures type 1","type":"exact"},{"name":"spinal muscular atrophy, type I, with congenital bone fractures","type":"exact"}],"termid":"MONDO:0014806","terms_by_termid":{"MONDO:0014806":null},"xrefs":{"Monarch":{"xref_id":"0014806"}}}


id: MONDO:0000564
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cerebellar ataxia, mental retardation and dysequlibrium syndrome (obsolete MONDO:0000564)","termid":"MONDO:0000564","xrefs":{"Monarch":{"xref_id":"0000564"}}}


id: PBO:0072135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 12","termid":"PBO:0072135"}


id: GO:0051248
data:
  {"annotated_genes":["SJAG_00786","SJAG_03501","SJAG_00052","SJAG_02638","SJAG_02026","SJAG_00169","SJAG_02244","SJAG_03869","SJAG_00423","SJAG_01528","SJAG_00690","SJAG_03048","SJAG_01942","SJAG_04291","SJAG_02592","SJAG_05000","SJAG_00475"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[99228,114659,95350,118039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000766"},{"annotations":[91064,111952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904689"},{"annotations":[69580,94126,99122,115423,109473,74920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[77307,77808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904293"},{"annotations":[76984,106749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"},{"annotations":[74973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001125"},{"annotations":[99236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141014"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of chemical reactions and pathways involving a protein.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macromolecule metabolic process","termid":"GO:0010605"},{"relation_name":"is_a","term_name":"regulation of protein metabolic process","termid":"GO:0051246"},{"relation_name":"negatively_regulates","term_name":"protein metabolic process","termid":"GO:0019538"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00169":null,"SJAG_00423":null,"SJAG_00475":null,"SJAG_00690":null,"SJAG_00786":null,"SJAG_01528":null,"SJAG_01942":null,"SJAG_02026":null,"SJAG_02244":null,"SJAG_02592":null,"SJAG_02638":null,"SJAG_03048":null,"SJAG_03501":null,"SJAG_03869":null,"SJAG_04291":null,"SJAG_05000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0032269"],"synonyms":[{"name":"down regulation of cellular protein metabolic process","type":"exact"},{"name":"down regulation of protein metabolic process","type":"exact"},{"name":"down-regulation of cellular protein metabolic process","type":"exact"},{"name":"down-regulation of protein metabolic process","type":"exact"},{"name":"downregulation of cellular protein metabolic process","type":"exact"},{"name":"downregulation of protein metabolic process","type":"exact"},{"name":"inhibition of cellular protein metabolic process","type":"narrow"},{"name":"inhibition of protein metabolic process","type":"narrow"},{"name":"negative regulation of cellular protein metabolic process","type":"exact"},{"name":"negative regulation of cellular protein metabolism","type":"exact"},{"name":"negative regulation of protein metabolism","type":"exact"}],"termid":"GO:0051248","terms_by_termid":{"GO:0032435":null,"GO:0141014":null,"GO:1904293":null,"GO:1904689":null,"GO:1905785":null,"GO:1990625":null,"GO:2000766":null,"GO:2001125":null}}


id: SO:0001343
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"N2_7_2prirme_O_trimethylguanosine 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":"N2_7_2prirme_O_trimethylguanosine","secondary_identifiers":["RNAMOD:106"],"synonyms":[{"name":"N2 7 2prirme O trimethylguanosine","type":"exact"},{"name":"N2,7,2'-O-trimethylguanosine","type":"exact"},{"name":"m2,7Gm","type":"exact"}],"termid":"SO:0001343"}


id: PBO:0005705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"notchless-like protein (predicted)","termid":"PBO:0005705"}


id: FYPO:0008127
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype where a ribosome is mislocalized to the nucleoplasm in the vegetative growth phase of the life cycle.","definition_xrefs":["PMID:37783794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal organelle localization","termid":"FYPO:0006329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"ribosome mislocalized to nucleoplasm","termid":"FYPO:0008127"}


id: PBO:0001943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAD-dependent amino acid oxidase (predicted)","termid":"PBO:0001943"}


id: PBO:0056657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 24","termid":"PBO:0056657"}


id: PBO:0054715
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 2124","termid":"PBO:0054715"}


id: GO:1905649
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of shell calcification.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:14648763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biomineral tissue development","termid":"GO:0070168"},{"relation_name":"is_a","term_name":"regulation of shell calcification","termid":"GO:1905648"},{"relation_name":"negatively_regulates","term_name":"shell calcification","termid":"GO:0031215"}],"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 shell calcification","synonyms":[{"name":"down regulation of shell calcification","type":"exact"},{"name":"down-regulation of shell calcification","type":"exact"},{"name":"downregulation of shell calcification","type":"exact"},{"name":"inhibition of shell calcification","type":"narrow"}],"termid":"GO:1905649"}


id: PBO:0059809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 35","termid":"PBO:0059809"}


id: GO:0016095
data:
  {"annotated_genes":["SJAG_04954"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61241],"is_not":false,"summary":null,"term":"GO:0016095"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of polyprenols, prenols with more than 4 isoprenoid residues, which may be all-trans, or a mixture of cis and trans.","definition_xrefs":["GOC:go_curators","Wikipedia:Polyprenol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid catabolic process","termid":"GO:0008300"},{"relation_name":"is_a","term_name":"polyprenol metabolic process","termid":"GO:0016093"},{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04954":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"polyprenol catabolic process","references_by_uniquename":{"GO_REF:0000104":null},"synonyms":[{"name":"polyprenol breakdown","type":"exact"},{"name":"polyprenol catabolism","type":"exact"},{"name":"polyprenol degradation","type":"exact"}],"termid":"GO:0016095","terms_by_termid":{"GO:0016095":null}}


id: GO:0000122
data:
  {"annotated_genes":["SJAG_00792","SJAG_04613","SJAG_04039","SJAG_03081","SJAG_02385","SJAG_04249","SJAG_00969","SJAG_01254","SJAG_02981","SJAG_02444","SJAG_04584","SJAG_00142","SJAG_00410","SJAG_04381","SJAG_00441","SJAG_00987","SJAG_04312","SJAG_01157","SJAG_01230","SJAG_03067","SJAG_03319","SJAG_00926","SJAG_04268","SJAG_00802","SJAG_01000","SJAG_01804","SJAG_00124","SJAG_00290","SJAG_01799","SJAG_00163","SJAG_02752","SJAG_02846","SJAG_01311","SJAG_03473","SJAG_00861","SJAG_04026","SJAG_01728","SJAG_00266","SJAG_03143","SJAG_04539","SJAG_01680","SJAG_03845","SJAG_02858","SJAG_02730","SJAG_04607","SJAG_00996","SJAG_04921","SJAG_02104","SJAG_01199","SJAG_02255"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69925,70210,71475,71968,72897,73381,73474,73650,73828,75090,76508,76707,79359,80192,87337,90939,91011,91894,91918,93055,93153,93499,93641,93989,94401,94484,96047,98671,100784,101638,103344,103744,104047,105614,105707,106052,106294,106527,106547,107772,108033,108376,108816,110519,110940,111889,112776,113632,114066,117180],"is_not":false,"summary":null,"term":"GO:0000122"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II.","definition_xrefs":["GOC:go_curators","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transcription by RNA polymerase II","termid":"GO:0006357"},{"relation_name":"is_a","term_name":"negative regulation of DNA-templated transcription","termid":"GO:0045892"},{"relation_name":"negatively_regulates","term_name":"transcription by RNA polymerase II","termid":"GO:0006366"}],"gene_count":50,"genes_by_uniquename":{"SJAG_00124":null,"SJAG_00142":null,"SJAG_00163":null,"SJAG_00266":null,"SJAG_00290":null,"SJAG_00410":null,"SJAG_00441":null,"SJAG_00792":null,"SJAG_00802":null,"SJAG_00861":null,"SJAG_00926":null,"SJAG_00969":null,"SJAG_00987":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01157":null,"SJAG_01199":null,"SJAG_01230":null,"SJAG_01254":null,"SJAG_01311":null,"SJAG_01680":null,"SJAG_01728":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_02104":null,"SJAG_02255":null,"SJAG_02385":null,"SJAG_02444":null,"SJAG_02730":null,"SJAG_02752":null,"SJAG_02846":null,"SJAG_02858":null,"SJAG_02981":null,"SJAG_03067":null,"SJAG_03081":null,"SJAG_03143":null,"SJAG_03319":null,"SJAG_03473":null,"SJAG_03845":null,"SJAG_04026":null,"SJAG_04039":null,"SJAG_04249":null,"SJAG_04268":null,"SJAG_04312":null,"SJAG_04381":null,"SJAG_04539":null,"SJAG_04584":null,"SJAG_04607":null,"SJAG_04613":null,"SJAG_04921":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006351","GO:0006355","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of transcription by RNA polymerase II","references_by_uniquename":{"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2173795","GO:0045816","GO:0010553","Reactome:R-HSA-8866904"],"synonyms":[{"name":"down regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"down regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"down-regulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"down-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"downregulation of global transcription from RNA polymerase II promoter","type":"related"},{"name":"downregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"inhibition of global transcription from RNA polymerase II promoter","type":"related"},{"name":"inhibition of transcription from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"negative regulation of global transcription from Pol II promoter","type":"related"},{"name":"negative regulation of transcription from Pol II promoter","type":"exact"},{"name":"negative regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of transcription from RNA polymerase II promoter, global","type":"related"}],"termid":"GO:0000122","terms_by_termid":{"GO:0000122":null}}


id: GO:0072493
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membranes of the host cell endosome.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell cytoplasm part","termid":"GO:0033655"},{"relation_name":"part_of","term_name":"host cell endosome","termid":"GO:0044174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell endosome lumen","synonyms":[{"name":"host endosome lumen","type":"exact"}],"termid":"GO:0072493"}


id: MONDO:8000004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Discitis caused by infection with Salmonella.","definition_xrefs":["PMID:27070599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salmonellosis","termid":"MONDO:0000827"},{"relation_name":"is_a","term_name":"bacterial arthritis","termid":"MONDO:0004471"},{"relation_name":"is_a","term_name":"infectious discitis","termid":"MONDO:8000000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salmonella discitis","termid":"MONDO:8000004","xrefs":{"Monarch":{"xref_id":"8000004"}}}


id: PBO:0059017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix metallopeptidase 3","termid":"PBO:0059017"}


id: PBO:0047237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 230 member I","termid":"PBO:0047237"}


id: GO:0033538
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ajugose, the hexasaccharide beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside, by a pathway in which galactan:galactan galactosyltransferase catalyzes chain elongation by transferring the alpha-galactosyl residue of one raffinose-family oligosaccharide to another.","definition_xrefs":["GOC:mah","MetaCyc:PWY-5343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ajugose biosynthetic process","termid":"GO:0033536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"ajugose biosynthetic process using galactan:galactan galactosyltransferase","synonyms":[{"name":"ajugose anabolism using galactan:galactan galactosyltransferase","type":"exact"},{"name":"ajugose biosynthesis using galactan:galactan galactosyltransferase","type":"exact"},{"name":"ajugose formation using galactan:galactan galactosyltransferase","type":"exact"},{"name":"ajugose synthesis using galactan:galactan galactosyltransferase","type":"exact"}],"termid":"GO:0033538"}


id: MOD:00447
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a glucuronic acid either through a carboxyl group amide or ester bond, or through C1-glycosylation.","definition_xrefs":["Unimod:54#N-term","PubMed:7398618","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoconjugated residue","termid":"MOD:00764"}],"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":"N-glucuronylated residue","synonyms":[{"name":"Glucuronyl","type":"related"},{"name":"N-Glucuronyl (N terminus)","type":"exact"},{"name":"N-glucuronylation","type":"related"}],"termid":"MOD:00447"}


id: PBO:0041968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 12","termid":"PBO:0041968"}


id: PBO:0051087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy constant gamma P (non-functional)","termid":"PBO:0051087"}


id: MONDO:0004647
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant epithelial neoplasm which is confined to the epithelial layer without evidence of further tissue invasion.","definition_xrefs":["NCIT:C2917"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pre-malignant neoplasm","termid":"MONDO:0000611"},{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"},{"relation_name":"is_a","term_name":"high grade malignant neoplasm","termid":"MONDO:0020665"},{"relation_name":"is_a","term_name":"precancerous condition","termid":"MONDO:0021074"}],"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":"in situ carcinoma","secondary_identifiers":["ICD9:230-234.99","DOID:8719","ICD9:234.8","ICD9:234.9","MEDGEN:763","MESH:D002278","UMLS:C0007099","SCTID:109355002","ICDO:8010/2"],"synonyms":[{"name":"CIS","type":"broad"},{"name":"carcinoma in situ","type":"exact"},{"name":"carcinoma, in situ, malignant","type":"exact"},{"name":"epithelial tumor, in situ, malignant","type":"exact"},{"name":"intraepithelial carcinoma","type":"exact"},{"name":"non-invasive carcinoma","type":"exact"},{"name":"stage 0 disease","type":"exact"}],"termid":"MONDO:0004647","xrefs":{"Monarch":{"xref_id":"0004647"}}}


id: PBO:0059754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 28","termid":"PBO:0059754"}


id: GO:0070046
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptobrevin 2 (VAMP2), SNAP-25, and syntaxin 3 (or orthologs thereof).","definition_xrefs":["PMID:10336434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"synaptobrevin 2-SNAP-25-syntaxin-3 complex","synonyms":[{"name":"SNARE complex (Stx3, Snap25, Vamp2)","type":"narrow"},{"name":"Stx3-Snap25-Vamp2 complex","type":"narrow"}],"termid":"GO:0070046"}


id: PATO:0002246
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A force which is relative low.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"force","termid":"PATO:0001035"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased force","synonyms":[{"name":"decreased force amplitude","type":"exact"}],"termid":"PATO:0002246"}


id: PBO:0044737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 18 pseudogene 5","termid":"PBO:0044737"}


id: MONDO:0001322
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the pericardium.","direct_ancestors":[{"relation_name":"is_a","term_name":"heart cancer","termid":"MONDO:0001340"},{"relation_name":"is_a","term_name":"neoplasm of pericardium","termid":"MONDO:0021381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0004992"],"is_obsolete":false,"name":"pericardium cancer","secondary_identifiers":["MEDGEN:87561","DOID:116","NCIT:C4567","UMLS:C0346609"],"synonyms":[{"name":"cancer of pericardium","type":"exact"},{"name":"malignant neoplasm of pericardium","type":"exact"},{"name":"malignant neoplasm of the pericardium","type":"exact"},{"name":"malignant pericardial neoplasm","type":"exact"},{"name":"malignant pericardial tumor","type":"exact"},{"name":"malignant pericardial tumour","type":"exact"},{"name":"malignant pericardium neoplasm","type":"exact"},{"name":"malignant tumor of pericardium","type":"exact"},{"name":"malignant tumor of the pericardium","type":"exact"},{"name":"malignant tumour of pericardium","type":"exact"},{"name":"malignant tumour of the pericardium","type":"exact"},{"name":"pericardial tumor","type":"broad"},{"name":"pericardial tumour","type":"broad"},{"name":"pericardium cancer","type":"exact"}],"termid":"MONDO:0001322","xrefs":{"Monarch":{"xref_id":"0001322"}}}


id: GO:0018672
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: anthranilate + 2 H+ + NADPH + O2 = 2,3-dihydroxybenzoate + NADP+ + NH4.","definition_xrefs":["EC:1.14.13.35","RHEA:21236"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"anthranilate 3-monooxygenase (deaminating) activity","secondary_identifiers":["UM-BBD_reactionID:r0578","MetaCyc:1.14.13.35-RXN","KEGG_REACTION:R00980"],"synonyms":[{"name":"anthranilate 2,3-dioxygenase (deaminating)","type":"related"},{"name":"anthranilate 2,3-hydroxylase (deaminating) activity","type":"related"},{"name":"anthranilate hydroxylase (deaminating) activity","type":"exact"},{"name":"anthranilate hydroxylase activity","type":"broad"},{"name":"anthranilate,NADPH:oxygen oxidoreductase (3-hydroxylating, deaminating)","type":"related"}],"termid":"GO:0018672"}


id: PBO:0057325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 519e","termid":"PBO:0057325"}


id: PBO:0068365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 148","termid":"PBO:0068365"}


id: GO:0008337
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A class of cell adhesion molecules that bind to carbohydrate via a lectin-like domain; integral membrane glycoproteins.","definition_xrefs":["ISBN:0124325653"],"gene_count":0,"genotype_count":0,"name":"obsolete selectin (obsolete GO:0008337)","synonyms":[{"name":"selectin","type":"exact"}],"termid":"GO:0008337"}


id: GO:1905622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of leaf development.","definition_xrefs":["PMID:11606552","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of leaf development","termid":"GO:2000024"},{"relation_name":"negatively_regulates","term_name":"leaf development","termid":"GO:0048366"}],"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 leaf development","synonyms":[{"name":"down regulation of leaf development","type":"exact"},{"name":"down-regulation of leaf development","type":"exact"},{"name":"downregulation of leaf development","type":"exact"},{"name":"inhibition of leaf development","type":"narrow"}],"termid":"GO:1905622"}


id: FYPO:0005737
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which prospore membrane formation begins later than normal.","definition_xrefs":["PMID:27630265","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal prospore membrane formation","termid":"FYPO:0001914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000121"}],"interesting_parent_ids":["FYPO:0000121","FYPO:0005447","FYPO:0001985","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"delayed onset of prospore membrane formation","synonyms":[{"name":"delayed onset of ascospore-type prospore membrane assembly","type":"exact"},{"name":"delayed onset of forespore membrane formation","type":"exact"},{"name":"delayed prospore membrane formation","type":"exact"}],"termid":"FYPO:0005737"}


id: MONDO:0016662
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare autoinflammatory syndrome defined as recurrence of pericardial inflammation of unknown origin following the first episode of acute pericarditis and a symptom-free interval of 4-6 weeks or longer. Recurrent attacks of chest pain may be the sole presentation or the chest pain may be accompanied by pericardial friction rub, electrocardiographic or echocardiographic changes, pericardial effusion and increased C-reactive protein. Cardiac tamponade is a rare, life-threatening complication.","definition_xrefs":["Orphanet:251307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic recurrent pericarditis","secondary_identifiers":["MEDGEN:1642945","SCTID:766704005","GARD:20695","ICD10CM:I09.2","UMLS:C4707790"],"synonyms":[{"name":"idiopathic relapsing pericarditis","type":"exact"}],"termid":"MONDO:0016662","xrefs":{"Monarch":{"xref_id":"0016662"}}}


id: GO:0021666
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to rhombomere 5. This process pertains to the initial formation of a structure from unspecified parts. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in anterior to posterior order.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:dgh","GOC:jid","GOC:dph","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere formation","termid":"GO:0021594"},{"relation_name":"part_of","term_name":"rhombomere 5 morphogenesis","termid":"GO:0021664"}],"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 5 formation","termid":"GO:0021666"}


id: PBO:0087866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional activator of the pleiotropic drug resistance network; regulates expression of ATP-binding cassette (ABC) transporters through binding to cis-acting PDRE sites (PDR responsive elements); has a role in response to drugs and organic solvents; post-translationally up-regulated in cells lacking functional mitochondrial genome; involved in diauxic shift; relative distribution to nucleus increases upon DNA replication stress; APCC(Cdh1) substrate","termid":"PBO:0087866"}


id: PBO:0046887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 9 member C","termid":"PBO:0046887"}


id: PBO:0018196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AMP-activated protein serine/threonine kinase alpha subunit Ssp2","termid":"PBO:0018196"}


id: GO:0052511
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the ethylene-mediated defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of symbiont ethylene-mediated defense response (obsolete GO:0052511)","synonyms":[{"name":"activation by organism of symbiont ethylene-mediated defense response","type":"narrow"},{"name":"induction by organism of symbiont ethylene-mediated defense response","type":"narrow"},{"name":"positive regulation by organism of symbiont ethylene-mediated defense response","type":"exact"},{"name":"upregulation by organism of symbiont ethylene-mediated defense response","type":"narrow"}],"termid":"GO:0052511"}


id: PBO:0083821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential subunit of the Dam1 complex (aka DASH complex); complex couples kinetochores to the force produced by MT depolymerization thereby aiding in chromosome segregation; also localized to nuclear side of spindle pole body","termid":"PBO:0083821"}


id: GO:0072077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the renal vesicle are generated and organized. The renal vesicle is the primordial structure of the nephron epithelium, and is formed by the condensation of mesenchymal cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"part_of","term_name":"renal vesicle development","termid":"GO:0072087"},{"relation_name":"part_of","term_name":"nephron epithelium morphogenesis","termid":"GO:0072088"}],"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":"renal vesicle morphogenesis","termid":"GO:0072077"}


id: FYPO:0003637
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ADP binding by a gene product (usually a protein) in a mutant is abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"},{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"abnormal ADP binding","termid":"FYPO:0003637"}


id: MONDO:0018668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fungal infectious disease","termid":"MONDO:0002041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scedosporiosis","secondary_identifiers":["MEDGEN:1713603","Orphanet:449280","MESH:C000656924","UMLS:C1142170","icd11.foundation:807637046","GARD:21880"],"termid":"MONDO:0018668","xrefs":{"Monarch":{"xref_id":"0018668"}}}


id: GO:0102434
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 10-formyltetrahydrofolate-4a-carbinolamine = H2O + a 10-formyldihydrofolate.","definition_xrefs":["PMID:20959559","PMID:18245455","GOC:pz"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"pterin-4alpha-carbinolamine dehydratase activity","secondary_identifiers":["MetaCyc:RXN-13908"],"termid":"GO:0102434"}


id: PBO:0043067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor muscarinic 3","termid":"PBO:0043067"}


id: GO:0102971
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + phosphinothricin = H+ + coenzyme A(4-) + N-acetylphosphinatothricinate.","definition_xrefs":["EC:2.3.1.183","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"phosphinothricin N-acetyltransferase activity","secondary_identifiers":["MetaCyc:RXN-9382","RHEA:12597"],"termid":"GO:0102971"}


id: GO:0099002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Entry of a symbiont's genome into the host cell through the host cell envelope via a short tail ejection system consisting a central tube, the connector which attaches the tail to the phage capsid and releases inner core proteins. Upon binding to the host cell surface, the phage displays a tube-like extension of its short tail that penetrates both host membranes. This tail extension comes from the release of viral core proteins with channel forming properties. Occurs in non-enveloped prokaryotic viruses.","definition_xrefs":["GOC:dos","PMID:22297513","VZ:3954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont genome ejection through host cell envelope","termid":"GO:0039678"}],"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 genome ejection through host cell envelope, short tail mechanism","synonyms":[{"name":"viral genome ejection through host cell envelope, short tail mechanism","type":"related"},{"name":"viral short tail ejection system","type":"exact"}],"termid":"GO:0099002"}


id: GO:0003257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter that contributes to the differentiation of a myocardial precursor cell.","definition_xrefs":["GOC:mtg_heart"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in myocardial precursor cell differentiation (obsolete GO:0003257)","termid":"GO:0003257"}


id: PBO:0077216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation machinery associated 7 homolog B","termid":"PBO:0077216"}


id: GO:0043226
data:
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id: PR:O74786
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74786"],"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":"protein transport protein sec9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC26H8.02c","synonyms":[{"name":"Spom972h-sec9","type":"exact"}],"termid":"PR:O74786"}


id: MONDO:0010683
data:
  {"annotated_genes":["SJAG_03248"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85209],"is_not":false,"summary":null,"term":"MONDO:0010683"}]},"cv_name":"mondo","definition":"A rare X-linked congenital myopathy characterized by numerous centrally placed nuclei on muscle biopsy and that presents at birth with marked weakness, hypotonia and respiratory failure.","definition_xrefs":["Orphanet:596"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"congenital structural myopathy","termid":"MONDO:0002921"},{"relation_name":"excluded_subClassOf","term_name":"obsolete qualitative or quantitative defects of myotubularin (obsolete MONDO:0016154)","termid":"MONDO:0016154"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"centronuclear myopathy","termid":"MONDO:0018947"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"X-linked myotubular myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:46804001","GARD:11925","OMIM:310400","UMLS:C0410203","MEDGEN:98374","DOID:0111225","NCIT:C118781"],"synonyms":[{"name":"CNMX","type":"related"},{"name":"MTM","type":"exact"},{"name":"X-linked centronuclear myopathy","type":"exact"},{"name":"X-linked myotubular myopathy","type":"exact"},{"name":"XLCNM","type":"exact"},{"name":"XLMTM","type":"exact"},{"name":"centronuclear myopathy, X-linked","type":"exact"},{"name":"myopathy, centronuclear, X-linked","type":"related"},{"name":"myotubular myopathy 1","type":"related"},{"name":"myotubular myopathy, X-linked","type":"related"},{"name":"myotubular myopathy, X-linked, X-linked recessive","type":"exact"}],"termid":"MONDO:0010683","terms_by_termid":{"MONDO:0010683":null},"xrefs":{"Monarch":{"xref_id":"0010683"}}}


id: PBO:0066972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 275","termid":"PBO:0066972"}


id: MONDO:0020447
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronary sinus atresia","secondary_identifiers":["GARD:19659","UMLS:C0344683","MEDGEN:576419","Orphanet:99118"],"termid":"MONDO:0020447","xrefs":{"Monarch":{"xref_id":"0020447"}}}


id: MONDO:0015235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arachnodactyly-intellectual disability-dysmorphism syndrome is characterized by moderate intellectual deficit, brachycephaly, typical facies (thin lips and microstomia), ectomorphic habitus with extremely long, thin fingers and toes, and hypoplastic external genitalia. It has been described in three patients.","definition_xrefs":["Orphanet:1130"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"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":"arachnodactyly-intellectual disability-dysmorphism syndrome","secondary_identifiers":["UMLS:C4304030","MEDGEN:929699","GARD:764","SCTID:720502000"],"synonyms":[{"name":"De Die-Smulders-Vles-Fryns syndrome","type":"exact"},{"name":"arachnodactyly - intellectual disability - dysmorphism","type":"related"},{"name":"die Smulders Vles Fryns syndrome","type":"exact"}],"termid":"MONDO:0015235","xrefs":{"Monarch":{"xref_id":"0015235"}}}


id: FYPO:0001794
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to purvalanol A is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal RNA level during cellular response to purvalanol A","synonyms":[{"name":"normal RNA accumulation during cellular response to purvalanol A","type":"related"},{"name":"normal RNA level during cellular response to purvalanol A during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to purvalanol A during vegetative growth","type":"exact"},{"name":"normal mRNA level during cellular response to purvalanol A","type":"narrow"},{"name":"normal transcript level during cellular response to purvalanol A","type":"exact"}],"termid":"FYPO:0001794"}


id: PBO:0035770
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H4-K16_acetylation_at_telomere_during_vegetative_growth","termid":"PBO:0035770"}


id: FYPO:0000256
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 higher frequency than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered mutation rate","termid":"FYPO:0007431"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"mutator","synonyms":[{"name":"increased mutation rate","type":"exact"},{"name":"mutator during mitotic cell cycle","type":"related"},{"name":"mutator during vegetative growth","type":"exact"}],"termid":"FYPO:0000256"}


id: GO:0032496
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a lipopolysaccharide stimulus; lipopolysaccharide is a major component of the cell wall of gram-negative bacteria.","definition_xrefs":["GOC:add","ISBN:0721601464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to molecule of bacterial origin","termid":"GO:0002237"},{"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 lipopolysaccharide","synonyms":[{"name":"response to LPS","type":"exact"},{"name":"response to endotoxin","type":"broad"}],"termid":"GO:0032496"}


id: PBO:0057277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 499b","termid":"PBO:0057277"}


id: GO:0098508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The generation of hematopoietic stem cells from hemogenic endothelial cells by a process that includes tight-junction dissolution and loss of cell polarity followed by delamination from the endothelium.","definition_xrefs":["PMID:20154732","PMID:22521721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"is_a","term_name":"delamination","termid":"GO:0060232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"endothelial to hematopoietic transition","termid":"GO:0098508"}


id: PBO:0003486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aromatic ring-opening dioxygenase (predicted)","termid":"PBO:0003486"}


id: PBO:0027055
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-curved_microtubules","termid":"PBO:0027055"}


id: PBO:0109088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm microtubule inner protein 2","termid":"PBO:0109088"}


id: GO:0016338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of one cell to another cell via adhesion molecules that do not require the presence of calcium for the interaction.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules","synonyms":[{"name":"calcium-independent cell adhesion molecule activity","type":"related"}],"termid":"GO:0016338"}


id: MONDO:0021932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trypanosomiasis caused by infection by Trypanosoma brucei gambiense.","definition_xrefs":["NCIT:C35084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human African trypanosomiasis","termid":"MONDO:0005459"},{"relation_name":"is_a","term_name":"skin infection","termid":"MONDO:0021201"},{"relation_name":"is_a","term_name":"parasitic skin disorder","termid":"MONDO:0024610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"infection by Trypanosoma gambiense","secondary_identifiers":["SCTID:75809006","MEDGEN:11933","UMLS:C0041232","ICD9:086.3"],"synonyms":[{"name":"Gambian sleeping sickness","type":"related"},{"name":"Gambian trypanosomiasis","type":"related"},{"name":"Gambiense trypanosomiasis infection","type":"related"},{"name":"Infection by Trypanosoma gambiense","type":"exact"},{"name":"Infection caused by Trypanosoma gambiense","type":"related"},{"name":"chronic sleeping sickness","type":"related"}],"termid":"MONDO:0021932","xrefs":{"Monarch":{"xref_id":"0021932"}}}


id: GO:0031751
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a D4 dopamine receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dopamine receptor binding","termid":"GO:0050780"}],"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":"D4 dopamine receptor binding","synonyms":[{"name":"D4 dopamine receptor ligand","type":"narrow"}],"termid":"GO:0031751"}


