# terms

id: GO:2000509
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dendritic cell chemotaxis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte chemotaxis","termid":"GO:0002689"},{"relation_name":"is_a","term_name":"negative regulation of mononuclear cell migration","termid":"GO:0071676"},{"relation_name":"is_a","term_name":"regulation of dendritic cell chemotaxis","termid":"GO:2000508"},{"relation_name":"negatively_regulates","term_name":"dendritic cell chemotaxis","termid":"GO:0002407"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of dendritic cell chemotaxis","termid":"GO:2000509"}


id: FYPO:0002776
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 sumoylated protein measured in a cell is normal (i.e. indistinguishable from wild type). Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein level during vegetative growth","termid":"FYPO:0000833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal level of sumoylated protein in cell","synonyms":[{"name":"normal level of sumoylated protein during vegetative growth","type":"exact"},{"name":"normal level of sumoylated protein in cell during mitotic cell cycle","type":"related"},{"name":"normal sumoylated protein accumulation","type":"related"},{"name":"normal sumoylated protein level","type":"exact"}],"termid":"FYPO:0002776"}


id: FYPO:0003134
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 alpha-D-glucan measured in the cell wall is greater than normal during a cellular response to calcium starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cell wall alpha-glucan level","termid":"FYPO:0001084"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002946"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002946"],"is_obsolete":false,"name":"increased cell wall alpha-glucan level during cellular response to calcium starvation","synonyms":[{"name":"increased cell wall alpha-D-glucan level during cellular response to calcium starvation","type":"exact"},{"name":"increased cell wall alpha-glucan accumulation during cellular response to calcium starvation","type":"related"},{"name":"increased cell wall alpha-glucan level during cellular response to calcium starvation during mitotic cell cycle","type":"related"},{"name":"increased cell wall alpha-glucan level during cellular response to calcium starvation during vegetative growth","type":"exact"}],"termid":"FYPO:0003134"}


id: PBO:0029394
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleoplasm_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0029394"}


id: MONDO:0015417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"facial cleft","termid":"MONDO:0015411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tessier number 6 facial cleft","secondary_identifiers":["UMLS:C0432120","icd11.foundation:1934815559","GARD:19969","MEDGEN:609365","Orphanet:141265"],"termid":"MONDO:0015417","xrefs":{"Monarch":{"xref_id":"0015417"}}}


id: PBO:0017573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 Ubc6 (predicted)","termid":"PBO:0017573"}


id: MONDO:0015775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nonrhizomelic chondrodysplasia punctata is a form of chondrodysplasia punctata, a group of diseases in which the common characteristic is bone calcifications near joints from birth. Nonrhizomelic chondrodysplasia punctata is not an entity in itself but covers several diseases with variable clinical findings and modes of transmission.","definition_xrefs":["Orphanet:176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chondrodysplasia punctata","termid":"MONDO:0019701"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-rhizomelic chondrodysplasia punctata","secondary_identifiers":["UMLS:C5681009","GARD:18679","MEDGEN:1842643"],"termid":"MONDO:0015775","xrefs":{"Monarch":{"xref_id":"0015775"}}}


id: PR:P79007
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- php5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P79007"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional activator hap5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B8.02","synonyms":[{"name":"Spom972h-php5","type":"exact"}],"termid":"PR:P79007"}


id: GO:0044288
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small version of the zonula adherens type junction, characterized by a symmetrical adherent point between two cells.","definition_xrefs":["NIF_Subcellular:sao257629430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"zonula adherens","termid":"GO:0005915"}],"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":"puncta adhaerentia","termid":"GO:0044288"}


id: PBO:0088704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arf GEF","termid":"PBO:0088704"}


id: PBO:0076943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TCF3 fusion partner","termid":"PBO:0076943"}


id: MONDO:0022094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"intellectual disability","termid":"MONDO:0001071"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cartwright Nelson Fryns syndrome","secondary_identifiers":["MEDGEN:443968","UMLS:C2931062","MESH:C535917"],"synonyms":[{"name":"Growth retardation, severe intellectual disability, acral limb deficiencies with poorly keratinized nails","type":"related"},{"name":"Growth retardation, severe mental retardation, acral limb deficiencies with poorly keratinized nails","type":"related"}],"termid":"MONDO:0022094","xrefs":{"Monarch":{"xref_id":"0022094"}}}


id: GO:2000502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of natural killer cell chemotaxis.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lymphocyte chemotaxis","termid":"GO:1901624"},{"relation_name":"is_a","term_name":"regulation of natural killer cell chemotaxis","termid":"GO:2000501"},{"relation_name":"negatively_regulates","term_name":"natural killer cell chemotaxis","termid":"GO:0035747"}],"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 natural killer cell chemotaxis","termid":"GO:2000502"}


id: PBO:0087037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L18A; intron of RPL18A pre-mRNA forms stem-loop structures that are a target for Rnt1p cleavage leading to degradation; homologous to mammalian ribosomal protein L18, no bacterial homolog; RPL18A has a paralog, RPL18B, that arose from the whole genome duplication","termid":"PBO:0087037"}


id: GO:0032139
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a double-stranded DNA region containing a dinucleotide insertion or deletion.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA insertion or deletion binding","termid":"GO:0032135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003677","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"dinucleotide insertion or deletion binding","synonyms":[{"name":"dinucleotide insertion binding","type":"narrow"}],"termid":"GO:0032139"}


id: GO:0045680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of R8 cell differentiation.","definition_xrefs":["GOC:tb","GOC:go_curators","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of R8 cell differentiation","termid":"GO:0045679"},{"relation_name":"is_a","term_name":"negative regulation of compound eye photoreceptor cell differentiation","termid":"GO:0110118"},{"relation_name":"negatively_regulates","term_name":"R8 cell differentiation","termid":"GO:0045465"}],"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 R8 cell differentiation","synonyms":[{"name":"down regulation of R8 differentiation","type":"exact"},{"name":"down-regulation of R8 differentiation","type":"exact"},{"name":"downregulation of R8 differentiation","type":"exact"},{"name":"inhibition of R8 differentiation","type":"narrow"},{"name":"negative regulation of R8 differentiation","type":"exact"}],"termid":"GO:0045680"}


id: PBO:0075614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted phosphoprotein 2","termid":"PBO:0075614"}


id: MONDO:0019140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute ackee fruit intoxication (also referred to as Jamaican vomiting syndrome or sickness) is caused by the ingestion of unripe Blighia sapida fruits. It is a serious intoxication that is frequent in certain countries in the Caribbean and Western Africa. In contrast, it is rare in France and other Western countries. Intoxication leads to toxic hypoglycaemia and inhibition of neoglucogenesis. The hypoglycaemia is caused by the effect of hypoglycin A, which is found in the arils.","definition_xrefs":["Orphanet:73423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute ackee fruit intoxication","secondary_identifiers":["GARD:9299","SCTID:49434001","MESH:C537562","ICD9:988.2"],"synonyms":[{"name":"Jamaican vomiting sickness","type":"exact"},{"name":"Jamaican vomiting syndrome","type":"exact"},{"name":"ackee poisoning","type":"related"},{"name":"acute intoxication by Blighia sapida","type":"exact"}],"termid":"MONDO:0019140","xrefs":{"Monarch":{"xref_id":"0019140"}}}


id: PBO:0073558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHC adaptor protein 1 pseudogene 2","termid":"PBO:0073558"}


id: FYPO:0000385
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which macroautophagy is normal (i.e. indistinguishable from wild type). Macroautophagy is the major pathway by which cells digest parts of their own cytoplasm.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal metabolic process","termid":"FYPO:0002496"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal macroautophagy","synonyms":[{"name":"autophagy: normal","type":"broad"}],"termid":"FYPO:0000385"}


id: PBO:0004896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ/TPR domain protein DNAJC7 family","termid":"PBO:0004896"}


id: SO:0001346
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"5_2_prime_O_dimethyluridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_two_prime_O_dimethyluridine","secondary_identifiers":["RNAMOD:054"],"synonyms":[{"name":"5,2'-O-dimethyluridine","type":"exact"},{"name":"five two prime O dimethyluridine","type":"exact"},{"name":"m5Um","type":"exact"}],"termid":"SO:0001346"}


id: PBO:0055248
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 2675","termid":"PBO:0055248"}


id: GO:1990171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of the SCF ubiquitin ligase complex in response to cadmium stress.","definition_xrefs":["GOC:rb","PMID:23000173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"part_of","term_name":"cellular response to cadmium ion","termid":"GO:0071276"}],"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":"SCF complex disassembly in response to cadmium stress","termid":"GO:1990171"}


id: GO:0050075
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-malate = H2O + maleate.","definition_xrefs":["RHEA:23692","EC:4.2.1.31"],"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":"maleate hydratase activity","secondary_identifiers":["MetaCyc:MALEATE-HYDRATASE-RXN","KEGG_REACTION:R02419"],"synonyms":[{"name":"(R)-malate hydro-lyase (maleate-forming)","type":"related"},{"name":"(R)-malate hydro-lyase activity","type":"related"},{"name":"D-malate hydro-lyase activity","type":"related"},{"name":"malease activity","type":"related"}],"termid":"GO:0050075"}


id: PBO:0040724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL11 transcription factor B","termid":"PBO:0040724"}


id: GO:0032727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interferon-alpha production.","definition_xrefs":["PMID:15546383","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of type I interferon production","termid":"GO:0032481"},{"relation_name":"is_a","term_name":"regulation of interferon-alpha production","termid":"GO:0032647"},{"relation_name":"positively_regulates","term_name":"interferon-alpha production","termid":"GO:0032607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interferon-alpha production","secondary_identifiers":["GO:1902741","GO:0045356"],"synonyms":[{"name":"activation of interferon-alpha production","type":"narrow"},{"name":"positive regulation of interferon-alpha biosynthetic process","type":"narrow"},{"name":"positive regulation of interferon-alpha secretion","type":"narrow"},{"name":"stimulation of interferon-alpha production","type":"narrow"},{"name":"up regulation of interferon-alpha production","type":"exact"},{"name":"up-regulation of interferon-alpha production","type":"exact"},{"name":"upregulation of interferon-alpha production","type":"exact"}],"termid":"GO:0032727"}


id: GO:0050779
data:
  {"annotated_genes":["SJAG_01625","SJAG_04880","SJAG_04824","SJAG_05010","SJAG_04084","SJAG_02808","SJAG_01521","SJAG_03179","SJAG_00854","SJAG_01910","SJAG_02239","SJAG_04118","SJAG_00343","SJAG_04006","SJAG_03883","SJAG_02213","SJAG_01191","SJAG_00759","SJAG_05694","SJAG_01944","SJAG_03157","SJAG_05322","SJAG_02383","SJAG_02036","SJAG_02540","SJAG_04427","SJAG_00686","SJAG_03876","SJAG_04818","SJAG_16457","SJAG_01053","SJAG_03745","SJAG_04350","SJAG_04153","SJAG_00966","SJAG_01818","SJAG_04407","SJAG_02622","SJAG_00391","SJAG_02370","SJAG_04321","SJAG_03113","SJAG_00285","SJAG_04825","SJAG_03597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061158"},{"annotations":[109379,112971,109428,105626,111494,91035],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000290"},{"annotations":[117609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061157"},{"annotations":[91153],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0060212"},{"annotations":[92556,114941,117799,104754,95403,96737,115382,101583,106947,91733,105956,103905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071042"},{"annotations":[99427,114642,97635,97548,89173,110560,112819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000288"},{"annotations":[116663,93820,89263,91479,98011,116100,91418,108693,91983,102530,115154,92078,92889,90264,94994],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000289"},{"annotations":[91154],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"},{"annotations":[116725,90265,95111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990074"}]},"cv_name":"biological_process","definition":"Any process that decreases the stability of an RNA molecule, making it more vulnerable to degradative processes.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"regulation of RNA stability","termid":"GO:0043487"},{"relation_name":"is_a","term_name":"positive regulation of RNA metabolic process","termid":"GO:0051254"},{"relation_name":"positively_regulates","term_name":"RNA catabolic process","termid":"GO:0006401"}],"gene_count":45,"genes_by_uniquename":{"SJAG_00285":null,"SJAG_00343":null,"SJAG_00391":null,"SJAG_00686":null,"SJAG_00759":null,"SJAG_00854":null,"SJAG_00966":null,"SJAG_01053":null,"SJAG_01191":null,"SJAG_01521":null,"SJAG_01625":null,"SJAG_01818":null,"SJAG_01910":null,"SJAG_01944":null,"SJAG_02036":null,"SJAG_02213":null,"SJAG_02239":null,"SJAG_02370":null,"SJAG_02383":null,"SJAG_02540":null,"SJAG_02622":null,"SJAG_02808":null,"SJAG_03113":null,"SJAG_03157":null,"SJAG_03179":null,"SJAG_03597":null,"SJAG_03745":null,"SJAG_03876":null,"SJAG_03883":null,"SJAG_04006":null,"SJAG_04084":null,"SJAG_04118":null,"SJAG_04153":null,"SJAG_04321":null,"SJAG_04350":null,"SJAG_04407":null,"SJAG_04427":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04880":null,"SJAG_05010":null,"SJAG_05322":null,"SJAG_05694":null,"SJAG_16457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"RNA destabilization","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0050779","terms_by_termid":{"GO:0000288":null,"GO:0000289":null,"GO:0000290":null,"GO:0036450":null,"GO:0060212":null,"GO:0061157":null,"GO:0061158":null,"GO:0071042":null,"GO:1990074":null}}


id: PR:O74799
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- exg3 gene.","definition_xrefs":["UniProtKB:O74799","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":"glucan 1,3-beta-glucosidase 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2D10.05","synonyms":[{"name":"Exo-1,3-beta-glucanase 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-exg3","type":"exact"}],"termid":"PR:O74799"}


id: PBO:0000302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rrm RNA recognition motif","termid":"PBO:0000302"}


id: GO:0039617
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The protein coat that surrounds the infective nucleic acid in some virus particles where the subunits (capsomeres) are arranged to form an icosahedron with T=3 symmetry. The T=3 capsid is composed of 12 pentameric and 20 hexameric capsomeres.","definition_xrefs":["VZ:806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"icosahedral viral capsid","termid":"GO:0019030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"T=3 icosahedral viral capsid","termid":"GO:0039617"}


id: PBO:0048370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase activating protein and VPS9 domains 1","termid":"PBO:0048370"}


id: MONDO:0017295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Juvenile glycerol kinase deficiency (GKD) is an uncommon form of GKD characterized by Reye-like clinical manifestations including episodic vomiting, acidemia, and disorders of consciousness.","definition_xrefs":["Orphanet:284411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated glycerol kinase deficiency","termid":"MONDO:0018459"},{"relation_name":"is_a","term_name":"disorder of gluconeogenesis","termid":"MONDO:0019225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"glycerol kinase deficiency, juvenile form","secondary_identifiers":["MEDGEN:1842281","GARD:17316","UMLS:C5681029"],"termid":"MONDO:0017295","xrefs":{"Monarch":{"xref_id":"0017295"}}}


id: GO:0035657
data:
  {"annotated_genes":["SJAG_04890","SJAG_03949"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[95702,95964],"is_not":false,"summary":null,"term":"GO:0035657"}]},"cv_name":"cellular_component","definition":"A protein complex required for the methylation of a glutamine (Gln) residue in the protein release factor eRF1. In S. cerevisiae, this complex consists of at least Trm112p and Mtq2p.","definition_xrefs":["PMID:20400505","PMID:17008308","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase complex","termid":"GO:0034708"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03949":null,"SJAG_04890":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"eRF1 methyltransferase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"eRF1 MTase complex","type":"exact"}],"termid":"GO:0035657","terms_by_termid":{"GO:0035657":null}}


id: MONDO:0004944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of the brain or spinal cord by Treponema pallidum. It occurs many years following the original infection which remained untreated. Signs and symptoms include abnormal gait, blindness, depression, paralysis, seizures and dementia.","definition_xrefs":["NCIT:C84935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tertiary syphilis","termid":"MONDO:0004497"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurosyphilis","secondary_identifiers":["MEDGEN:14360","SCTID:26039008","ICD9:094.89","MESH:D009494","ICD9:094.9","ICD10CM:A52.3","icd11.foundation:2118246468","UMLS:C0027927","GARD:8729","DOID:9988","ICD9:094"],"synonyms":[{"name":"late neurosyphilis","type":"exact"},{"name":"neurosyphilis","type":"exact"},{"name":"tertiary neurosyphilis","type":"exact"}],"termid":"MONDO:0004944","xrefs":{"Monarch":{"xref_id":"0004944"}}}


id: PBO:0050340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 42","termid":"PBO:0050340"}


id: MONDO:1012910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cerebellar ataxia that occurs in white-tufted-ear marmoset due to a mutation in the ATXN3 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary cerebellar ataxia, non-human animal","termid":"MONDO:1012960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinocerebellar ataxia, ATXN3-related, white-tufted-ear marmoset","secondary_identifiers":["OMIA:002473-9483"],"synonyms":[{"name":"ataxia, spinocerebellar, ATXN3-related, white-tufted-ear marmoset","type":"exact"}],"termid":"MONDO:1012910","xrefs":{"Monarch":{"xref_id":"1012910"}}}


id: PBO:0071310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 33","termid":"PBO:0071310"}


id: PR:P52890
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atf1 gene.","definition_xrefs":["UniProtKB:P52890","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":"transcription factor atf1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29B5.01","synonyms":[{"name":"Spom972h-atf1","type":"exact"},{"name":"protein sss1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"transcription factor mts1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P52890"}


id: PBO:0005771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human CTD-binding SR-like protein rA9 homolog (predicted)","termid":"PBO:0005771"}


id: MONDO:0019669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"achondrogenesis","termid":"MONDO:0019648"},{"relation_name":"is_a","term_name":"type 2 collagenopathy","termid":"MONDO:0022800"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"hypochondrogenesis","secondary_identifiers":["DOID:0080044","GARD:16815","MEDGEN:107448","Orphanet:93297","UMLS:C0542428","NANDO:2201346","icd11.foundation:1494246635","MESH:C563007"],"termid":"MONDO:0019669","xrefs":{"Monarch":{"xref_id":"0019669"}}}


id: MONDO:0006940
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A peripheral nerve lesion that involves the radial nerve.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radial neuropathy","termid":"MONDO:0001459"},{"relation_name":"is_a","term_name":"neuritis of upper limb","termid":"MONDO:0003607"},{"relation_name":"is_a","term_name":"brachial plexus neuritis","termid":"MONDO:0006682"},{"relation_name":"is_a","term_name":"peripheral nerve lesion","termid":"MONDO:0024334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"radial nerve lesion","secondary_identifiers":["EFO:1001143","MedDRA:10061477","SCTID:193137006","ICD9:354.3","MEDGEN:102317","DOID:12170","UMLS:C0154744"],"synonyms":[{"name":"lesion of radial nerve","type":"exact"},{"name":"peripheral nerve lesion of radial nerve","type":"exact"},{"name":"radial nerve lesions","type":"exact"},{"name":"radial nerve peripheral nerve lesion","type":"exact"}],"termid":"MONDO:0006940","xrefs":{"Monarch":{"xref_id":"0006940"}}}


id: PBO:0074841
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 34","termid":"PBO:0074841"}


id: PBO:0086983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory subunit of trehalose-6-phosphate synthase/phosphatase; involved in synthesis of storage carbohydrate trehalose; expression is induced by stress conditions and repressed by the Ras-cAMP pathway; TPS3 has a paralog, TSL1, that arose from the whole genome duplication","termid":"PBO:0086983"}


id: PBO:0076748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tectonic family member 3","termid":"PBO:0076748"}


id: GO:0043223
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ubiquitin ligase complex, located in the cytoplasm, in which a cullin from the Cul1 subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by a Skp1 adaptor and an F-box protein. SCF complexes are involved in targeting proteins for degradation by the proteasome. The best characterized complexes are those from yeast and mammals (with core subunits named Cdc53/Cul1, Rbx1/Hrt1/Roc1).","definition_xrefs":["PMID:15571813","PMID:15688063"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic ubiquitin ligase complex","termid":"GO:0000153"},{"relation_name":"is_a","term_name":"SCF ubiquitin ligase complex","termid":"GO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"cytoplasmic SCF ubiquitin ligase complex","synonyms":[{"name":"cytoplasmic SCF complex","type":"exact"},{"name":"cytoplasmic Skp1/Cul1/F-box protein complex","type":"exact"},{"name":"cytoplasmic cullin complex","type":"exact"}],"termid":"GO:0043223"}


id: MONDO:0005207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant tumor arising from trophoblastic cells. The vast majority of cases arise in the uterus and represent gestational choriocarcinomas that derive from placental trophoblastic cells. Approximately half of the cases develop from a complete hydatidiform mole. A minority of cases arise in the testis or the ovaries. There is often marked elevation of human chorionic gonadotropin (hCG) in the blood. Choriocarcinomas disseminate rapidly through the hematogenous route; the lungs are most frequently affected.","definition_xrefs":["NCIT:C2948"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"placenta cancer","termid":"MONDO:0002178"},{"relation_name":"excluded_subClassOf","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"trophoblastic neoplasm","termid":"MONDO:0002872"},{"relation_name":"is_a","term_name":"germ cell tumor","termid":"MONDO:0005040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choriocarcinoma","secondary_identifiers":["ONCOTREE:BCCA","SCTID:188188009","DOID:3594","EFO:0002893","NANDO:2200070","ICDO:9100/3","MESH:D002822","UMLS:C0008497","GARD:6059","HP:0100768","MEDGEN:40278"],"synonyms":[{"name":"chorioblastoma","type":"exact"},{"name":"choriocarcinoma","type":"exact"},{"name":"choriocarcinoma (disease)","type":"exact"},{"name":"choriocarcinoma, malignant","type":"exact"},{"name":"chorioepithelioma","type":"exact"},{"name":"chorion carcinoma","type":"exact"},{"name":"chorionic carcinoma","type":"exact"}],"termid":"MONDO:0005207","xrefs":{"Monarch":{"xref_id":"0005207"}}}


id: GO:0061830
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The concave part of the late spermatid head or spermatozoon head that forms the ventral portion of the head, particularly in some rodent species.","definition_xrefs":["PMID:23403943","PMID:26990065","PMID:22332112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"sperm head","termid":"GO:0061827"}],"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":"concave side of sperm head","termid":"GO:0061830"}


id: GO:0043039
data:
  {"annotated_genes":["SJAG_01259","SJAG_04856","SJAG_00443","SJAG_03545","SJAG_16456","SJAG_02721","SJAG_01235","SJAG_04738","SJAG_01577","SJAG_04409","SJAG_02615","SJAG_04094","SJAG_02206","SJAG_00103","SJAG_00488","SJAG_02015","SJAG_01159","SJAG_02263","SJAG_04762","SJAG_02517","SJAG_03071","SJAG_00243","SJAG_00420","SJAG_01797","SJAG_03626","SJAG_04285","SJAG_04840","SJAG_03585","SJAG_03277","SJAG_01352","SJAG_02428","SJAG_01522","SJAG_01197","SJAG_05560","SJAG_00653","SJAG_04482","SJAG_02977","SJAG_04473","SJAG_02236"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101770,104565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006421"},{"annotations":[113544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006422"},{"annotations":[95055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006423"},{"annotations":[93202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990762"},{"annotations":[104164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061475"},{"annotations":[108785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006425"},{"annotations":[117895,96146,110780],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070681"},{"annotations":[89801,100955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006424"},{"annotations":[96495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006426"},{"annotations":[107858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006427"},{"annotations":[112132,115541],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006428"},{"annotations":[97578,94528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006429"},{"annotations":[115172,104863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006430"},{"annotations":[104700,94727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006431"},{"annotations":[93203],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070143"},{"annotations":[106708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070144"},{"annotations":[117552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070146"},{"annotations":[96496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070150"},{"annotations":[94151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070158"},{"annotations":[96783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070183"},{"annotations":[97160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070185"},{"annotations":[117539,93110,96697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006432"},{"annotations":[105414,106604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006433"},{"annotations":[94917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006434"},{"annotations":[93958,106776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006435"},{"annotations":[95573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006418"},{"annotations":[95390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006436"},{"annotations":[116895,114534],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006437"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways by which the various amino acids become bonded to their corresponding tRNAs. The most common route for synthesis of aminoacyl tRNA is by the formation of an ester bond between the 3'-hydroxyl group of the most 3' adenosine of the tRNA and the alpha carboxylic acid group of an amino acid, usually catalyzed by the cognate aminoacyl-tRNA ligase. A given aminoacyl-tRNA ligase aminoacylates all species of an isoaccepting group of tRNA molecules.","definition_xrefs":["GOC:mah","GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA metabolic process","termid":"GO:0006399"},{"relation_name":"is_a","term_name":"amino acid activation","termid":"GO:0043038"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00103":null,"SJAG_00243":null,"SJAG_00420":null,"SJAG_00443":null,"SJAG_00488":null,"SJAG_00653":null,"SJAG_01159":null,"SJAG_01197":null,"SJAG_01235":null,"SJAG_01259":null,"SJAG_01352":null,"SJAG_01522":null,"SJAG_01577":null,"SJAG_01797":null,"SJAG_02015":null,"SJAG_02206":null,"SJAG_02236":null,"SJAG_02263":null,"SJAG_02428":null,"SJAG_02517":null,"SJAG_02615":null,"SJAG_02721":null,"SJAG_02977":null,"SJAG_03071":null,"SJAG_03277":null,"SJAG_03545":null,"SJAG_03585":null,"SJAG_03626":null,"SJAG_04094":null,"SJAG_04285":null,"SJAG_04409":null,"SJAG_04473":null,"SJAG_04482":null,"SJAG_04738":null,"SJAG_04762":null,"SJAG_04840":null,"SJAG_04856":null,"SJAG_05560":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0006399"],"is_obsolete":false,"name":"tRNA aminoacylation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"aminoacyl-tRNA biosynthesis","type":"exact"},{"name":"aminoacyl-tRNA biosynthetic process","type":"exact"},{"name":"tRNA charging","type":"exact"}],"termid":"GO:0043039","terms_by_termid":{"GO:0006418":null,"GO:0006421":null,"GO:0006422":null,"GO:0006423":null,"GO:0006424":null,"GO:0006425":null,"GO:0006426":null,"GO:0006427":null,"GO:0006428":null,"GO:0006429":null,"GO:0006430":null,"GO:0006431":null,"GO:0006432":null,"GO:0006433":null,"GO:0006434":null,"GO:0006435":null,"GO:0006436":null,"GO:0006437":null,"GO:0061475":null,"GO:0070143":null,"GO:0070144":null,"GO:0070146":null,"GO:0070150":null,"GO:0070158":null,"GO:0070183":null,"GO:0070185":null,"GO:0070681":null,"GO:1990762":null}}


id: PBO:0040358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit g pseudogene 7","termid":"PBO:0040358"}


id: PBO:0087846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Topoisomerase I; nuclear enzyme that relieves torsional strain in DNA by cleaving and re-sealing the phosphodiester backbone; relaxes both positively and negatively supercoiled DNA; functions in replication, transcription, and recombination; role in processing ribonucleoside monophosphates in genomic DNA into irreversible single-strand breaks; enzymatic activity and interaction with Nsr1p are negatively regulated by polyphosphorylation","termid":"PBO:0087846"}


id: GO:0097094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which any suture between cranial and/or facial bones is generated and organized.","definition_xrefs":["Wikipedia:Cranial_sutures","GOC:pr","GOC:sl","Wikipedia:Head_and_neck_anatomy#Musculoskeletal_system"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"bone morphogenesis","termid":"GO:0060349"},{"relation_name":"part_of","term_name":"cranial skeletal system development","termid":"GO:1904888"}],"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":"craniofacial suture morphogenesis","termid":"GO:0097094"}


id: PBO:0028773
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_nitric_oxide_level","termid":"PBO:0028773"}


id: PBO:0081694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 616","termid":"PBO:0081694"}


id: PR:P25009
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- puc1 gene.","definition_xrefs":["UniProtKB:P25009","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":"cyclin puc1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19F5.01c","synonyms":[{"name":"Spom972h-puc1","type":"exact"}],"termid":"PR:P25009"}


id: GO:0097200
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of internal, alpha-peptide bonds in a polypeptide chain by a mechanism in which the sulfhydryl group of a cysteine residue at the active center acts as a nucleophile, and contributing to the execution phase of apoptosis.","definition_xrefs":["GOC:mtg_apoptosis","Wikipedia:Caspase"],"gene_count":0,"genotype_count":0,"name":"obsolete cysteine-type endopeptidase activity involved in execution phase of apoptosis (obsolete GO:0097200)","synonyms":[{"name":"effector caspase activity","type":"narrow"},{"name":"executioner caspase activity","type":"narrow"}],"termid":"GO:0097200"}


id: PBO:0064532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit K","termid":"PBO:0064532"}


id: MONDO:0032893
data:
  {"annotated_genes":["SJAG_03835"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86299],"is_not":false,"summary":null,"term":"MONDO:0032893"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03835":null},"genotype_count":0,"is_obsolete":false,"name":"pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1684879","DOID:0081266","OMIM:618737","UMLS:C5231486"],"synonyms":[{"name":"PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES","type":"related"},{"name":"PAMDDFS","type":"related"}],"termid":"MONDO:0032893","terms_by_termid":{"MONDO:0032893":null},"xrefs":{"Monarch":{"xref_id":"0032893"}}}


id: GO:0034603
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyruvate + CoA + NAD(P)+ = acetyl-CoA + CO2 + NAD(P)H.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase activity","termid":"GO:0004738"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"pyruvate dehydrogenase [NAD(P)+] activity","termid":"GO:0034603"}


id: PBO:0055823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRAT domain containing 1","termid":"PBO:0055823"}


id: PBO:0076113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STX18 antisense RNA 1 (head to head)","termid":"PBO:0076113"}


id: PBO:0002676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prohibitin Phb1 (predicted)","termid":"PBO:0002676"}


id: GO:0018484
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-hydroxybenzaldehyde + NAD+ + H2O = 4-hydroxybenzoate + NADH + H+.","definition_xrefs":["EC:1.2.1.64"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"4-hydroxybenzaldehyde dehydrogenase (NAD+) activity","secondary_identifiers":["UM-BBD_reactionID:r0273","RHEA:20305","MetaCyc:HYDROXYBENZALDEHYDE-OXIDATION-NAD-RXN","Reactome:R-HSA-9856794"],"synonyms":[{"name":"3-hydroxybenzaldehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"p-hydroxybenzaldehyde dehydrogenase activity","type":"related"}],"termid":"GO:0018484"}


id: GO:1904843
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 nitroglycerin stimulus.","definition_xrefs":["PMID:25626975","GO_REF:0000071","GOC:TermGenie"],"direct_ancestors":[{"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"},{"relation_name":"is_a","term_name":"response to nitroglycerin","termid":"GO:1904842"}],"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 nitroglycerin","synonyms":[{"name":"cellular response to nitroglycerine","type":"exact"},{"name":"cellular response to nitroglycerol","type":"exact"},{"name":"cellular response to trinitroglycerin","type":"exact"},{"name":"cellular response to trinitroglycerol","type":"exact"}],"termid":"GO:1904843"}


id: SO:0000750
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An origin_of_replication that is used for the amplification of a chromosomal nucleic acid sequence.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"origin_of_replication","termid":"SO:0000296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amplification_origin","synonyms":[{"name":"amplification origin","type":"exact"}],"termid":"SO:0000750"}


id: GO:0048262
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Determination of asymmetry from the dorsal to the ventral side; as, the dorsoventral axis.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"determination of bilateral symmetry","termid":"GO:0009855"},{"relation_name":"part_of","term_name":"dorsal/ventral pattern formation","termid":"GO:0009953"}],"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":"determination of dorsal/ventral asymmetry","synonyms":[{"name":"determination of adaxial/abaxial asymmetry","type":"related"},{"name":"determination of dorsal-ventral asymmetry","type":"exact"},{"name":"determination of dorsoventral asymmetry","type":"exact"}],"termid":"GO:0048262"}


id: MONDO:0018690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare syndrome characterized by an abnormally dilated pupil, hypoflexia, and diaphoresis. The syndrome is usually caused by a viral or bacterial infection. The abnormally dilated pupil is caused by damage to postganglionic parasympathetic fibers innervating the eye.","definition_xrefs":["NCIT:C34357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Holmes-Adie syndrome","secondary_identifiers":["UMLS:C0001519","EFO:0004126","GARD:5749","MEDGEN:138","DOID:11549","MESH:D000270","NORD:735","Orphanet:454718","SCTID:24225004","OMIM:103100"],"synonyms":[{"name":"Adie Syndrome","type":"exact"},{"name":"Adie pupil","type":"exact"},{"name":"Adie syndrome","type":"exact"},{"name":"Adie's pupil","type":"exact"},{"name":"Adie's pupil or syndrome","type":"exact"},{"name":"Adie's pupil syndrome","type":"exact"},{"name":"Adie's syndrome","type":"exact"},{"name":"Holmes-Adie syndrome","type":"exact"},{"name":"poorly Reacting pupils","type":"related"},{"name":"tonic pupil","type":"exact"},{"name":"tonic pupil-tendon areflexia syndrome","type":"exact"},{"name":"tonic, sluggishly reacting pupil and hypoactive or absent tendon reflexes","type":"related"}],"termid":"MONDO:0018690","xrefs":{"Monarch":{"xref_id":"0018690"}}}


id: PBO:0044442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 11","termid":"PBO:0044442"}


id: PBO:0017988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochindrial dynamin family GTPase Dnm1","termid":"PBO:0017988"}


id: PBO:0025553
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA modification, acetylated cytidines","termid":"PBO:0025553"}


id: PBO:0027937
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_oxygen_consumption_during_vegetative_growth","termid":"PBO:0027937"}


id: PBO:0003425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VRR-NUC nuclease associated domain, human MTMR15 homolog","termid":"PBO:0003425"}


id: MONDO:0012455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic disorder characterized by intellectual disability, childhood hypotonia, severe expressive speech delay and a distinctive facial appearance with a spectrum of additional clinical features.","definition_xrefs":["Orphanet:261494"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kleefstra syndrome","secondary_identifiers":["icd11.foundation:1997337437","UMLS:C4551771","NORD:184097","DOID:0080597","GARD:8672","OMIMPS:610253","MEDGEN:1684615","NANDO:1200959"],"synonyms":[{"name":"9Q subtelomeric deletion syndrome","type":"exact"},{"name":"9Q- syndrome","type":"exact"},{"name":"9q-syndrome","type":"exact"},{"name":"9q34 deletion syndrome","type":"exact"},{"name":"9q34.3 microdeletion syndrome","type":"exact"},{"name":"Kleefstra syndrome","type":"exact"},{"name":"chromosome 9Q34.3 deletion syndrome","type":"exact"},{"name":"chromosome 9q deletion syndrome","type":"exact"}],"termid":"MONDO:0012455","xrefs":{"Monarch":{"xref_id":"0012455"}}}


id: GO:1902655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of aromatic primary alcohol.","definition_xrefs":["PMID:19219878","GO_REF:0000068","GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"aromatic primary alcohol metabolic process","termid":"GO:1902654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"aromatic primary alcohol biosynthetic process","synonyms":[{"name":"aromatic primary alcohol anabolism","type":"exact"},{"name":"aromatic primary alcohol biosynthesis","type":"exact"},{"name":"aromatic primary alcohol formation","type":"exact"},{"name":"aromatic primary alcohol synthesis","type":"exact"}],"termid":"GO:1902655"}


id: GO:0002550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of the plasma kallikrein-kinin cascade.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of kinin cascade","termid":"GO:0002258"},{"relation_name":"is_a","term_name":"regulation of plasma kallikrein-kinin cascade","termid":"GO:0002529"},{"relation_name":"positively_regulates","term_name":"plasma kallikrein-kinin cascade","termid":"GO:0002353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0051604"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0051604","GO:0008150"],"is_obsolete":false,"name":"positive regulation of plasma kallikrein-kinin cascade","synonyms":[{"name":"activation of plasma kallikrein-kinin cascade","type":"narrow"},{"name":"stimulation of plasma kallikrein-kinin cascade","type":"narrow"},{"name":"up regulation of plasma kallikrein-kinin cascade","type":"exact"},{"name":"up-regulation of plasma kallikrein-kinin cascade","type":"exact"},{"name":"upregulation of plasma kallikrein-kinin cascade","type":"exact"}],"termid":"GO:0002550"}


id: GO:0031686
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an A1 adenosine receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosine receptor binding","termid":"GO:0031685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"A1 adenosine receptor binding","synonyms":[{"name":"A1 adenosine receptor ligand","type":"narrow"}],"termid":"GO:0031686"}


id: MONDO:1011849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myasthenia, non-human animal","secondary_identifiers":["OMIA:000684"],"termid":"MONDO:1011849","xrefs":{"Monarch":{"xref_id":"1011849"}}}


id: MONDO:0100201
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A vertebral column disorder caused by degeneration of intervertebral disks of the lumbar spine. One of the most common musculoskeletal disorders, it has strong genetic determinants.","definition_xrefs":["OMIM:603932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lumbar disk disease","secondary_identifiers":["MEDGEN:67462","UMLS:C0221775"],"termid":"MONDO:0100201","xrefs":{"Monarch":{"xref_id":"0100201"}}}


id: MONDO:0030639
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":"Teebi hypertelorism syndrome","secondary_identifiers":["DOID:0081073","OMIMPS:145420","UMLS:C0796179","MEDGEN:208673"],"termid":"MONDO:0030639","xrefs":{"Monarch":{"xref_id":"0030639"}}}


id: PBO:0041311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 50","termid":"PBO:0041311"}


id: PBO:0065155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein arginine methyltransferase 5 pseudogene 1","termid":"PBO:0065155"}


id: GO:0033185
data:
  {"annotated_genes":["SJAG_05219","SJAG_00831","SJAG_02903"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[95907,103270,106206],"is_not":false,"summary":null,"term":"GO:0033185"}]},"cv_name":"cellular_component","definition":"A protein complex that possesses dolichyl-phosphate beta-D-mannosyltransferase activity; contains a catalytic subunit, a regulatory subunit, and a third subunit that stabilizes the complex. In human and several other metazoa, the subunits are named DPM1, DPM2 and DPM3, respectively.","definition_xrefs":["PMID:10835346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosyltransferase complex","termid":"GO:0031501"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00831":null,"SJAG_02903":null,"SJAG_05219":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"dolichol-phosphate-mannose synthase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DPM synthase complex","type":"exact"},{"name":"dolichyl-phosphate beta-D-mannosyltransferase complex","type":"exact"}],"termid":"GO:0033185","terms_by_termid":{"GO:0033185":null}}


id: PBO:0062007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily J member 1","termid":"PBO:0062007"}


id: GO:0016306
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A phosphoinositide 3-kinase which can only phosphorylate phosphatidylinositol.","definition_xrefs":["PMID:9759495"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphatidylinositol 3-kinase activity, class III (obsolete GO:0016306)","synonyms":[{"name":"phosphatidylinositol 3-kinase activity, class III","type":"exact"}],"termid":"GO:0016306"}


id: PBO:0082298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Aromatic aminotransferase I; expression is regulated by general control of amino acid biosynthesis; involved with Aro9p in production of kynurenic acid to detoxify excess tryptophan","termid":"PBO:0082298"}


id: GO:0042934
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of achromobactin, a citrate siderophore, from one side of a membrane to the other.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore-iron transmembrane transporter activity","termid":"GO:0015343"},{"relation_name":"is_a","term_name":"amide transmembrane transporter activity","termid":"GO:0042887"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"achromobactin transmembrane transporter activity","synonyms":[{"name":"achromobactin transporter activity","type":"related"}],"termid":"GO:0042934"}


id: FYPO:0007809
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, and morphology of cytoplasmic microtubules is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component","termid":"FYPO:0001233"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cytoplasmic microtubules","synonyms":[{"name":"normal cytoplasmic microtubule morphology","type":"exact"},{"name":"normal cytoplasmic microtubule structure","type":"narrow"}],"termid":"FYPO:0007809"}


id: GO:0005092
data:
  {"annotated_genes":["SJAG_03361","SJAG_02063","SJAG_02422","SJAG_02390","SJAG_02831"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95356,103023],"is_not":false,"summary":null,"term":"GO:0005092"},{"annotations":[92983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005093"},{"annotations":[99037,110292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005094"}]},"cv_name":"molecular_function","definition":"Prevents the dissociation of GDP from a GTPase, thereby preventing GTP from binding.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTPase regulator activity","termid":"GO:0030695"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02063":null,"SJAG_02390":null,"SJAG_02422":null,"SJAG_02831":null,"SJAG_03361":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"GDP-dissociation inhibitor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"GDI","type":"exact"}],"termid":"GO:0005092","terms_by_termid":{"GO:0005092":null,"GO:0005093":null,"GO:0005094":null}}


id: PBO:0047132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 171 member A1","termid":"PBO:0047132"}


id: GO:0034964
data:
  {"annotated_genes":["SJAG_04754"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000495"}]},"cv_name":"biological_process","definition":"Any process involved in the conversion of a primary box H/ACA type small RNA transcript into a mature box H/ACA RNA.","definition_xrefs":["GOC:mah","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"box H/ACA sno(s)RNA metabolic process","termid":"GO:0033979"},{"relation_name":"is_a","term_name":"sno(s)RNA processing","termid":"GO:0043144"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016074"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0016074","GO:0010467"],"is_obsolete":false,"name":"box H/ACA sno(s)RNA processing","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"box H/ACA sRNA processing","type":"narrow"},{"name":"box H/ACA snoRNA processing","type":"narrow"}],"termid":"GO:0034964","terms_by_termid":{"GO:0000495":null}}


id: SO:0000806
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"When two regions of DNA are joined together that are not normally together.","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_attribute","termid":"SO:0000733"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fusion","termid":"SO:0000806"}


id: FYPO:0003807
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 mitochondria form branched structures.","definition_xrefs":["PMID:19373772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial morphology","termid":"FYPO:0000359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"net-like mitochondrial morphology","synonyms":[{"name":"branched mitochondria","type":"exact"},{"name":"branched mitochondria during vegetative growth","type":"exact"},{"name":"branched mitochondrion","type":"exact"}],"termid":"FYPO:0003807"}


id: PBO:0034438
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_phosphorylation_during_cellular_response_to_bleomycin","termid":"PBO:0034438"}


id: PR:O13814
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mdm10 gene.","definition_xrefs":["UniProtKB:O13814","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial distribution and morphology protein 10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.17c","synonyms":[{"name":"Spom972h-mdm10","type":"exact"},{"name":"mitochondrial inheritance component mdm10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13814"}


id: PBO:0068649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 30, pseudogene","termid":"PBO:0068649"}


id: PBO:0045892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 gamma pseudogene 4","termid":"PBO:0045892"}


id: MONDO:0004328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma that arises from the maxillary sinus. It is classified as intestinal-type or non-intestinal-type adenocarcinoma. Nasal obstruction and epistaxis are the presenting signs.","definition_xrefs":["NCIT:C6240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maxillary sinus carcinoma","termid":"MONDO:0001748"},{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"maxillary sinus adenocarcinoma","secondary_identifiers":["DOID:7684","MEDGEN:233167","SCTID:707339009","UMLS:C1334642"],"synonyms":[{"name":"adenocarcinoma of maxillary sinus","type":"related"},{"name":"adenocarcinoma of the maxillary sinus","type":"exact"},{"name":"maxillary sinus adenocarcinoma","type":"exact"}],"termid":"MONDO:0004328","xrefs":{"Monarch":{"xref_id":"0004328"}}}


id: PBO:0070365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY5 pseudogene 3","termid":"PBO:0070365"}


id: PBO:0048340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 51","termid":"PBO:0048340"}


id: GO:0035192
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The symmetric outward movement of the syncytial nuclei from their positions in the ellipsoid toward the periphery of the embryo, during mitotic cycles 8 and 9. This movement results in the placement of nuclei in a uniform monolayer at the cortex of the developing embryo.","definition_xrefs":["PMID:8314839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syncytial nuclear migration","termid":"GO:0035190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"nuclear cortical migration","termid":"GO:0035192"}


id: PBO:0091686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBAP2/UBAP2L","termid":"PBO:0091686"}


id: PBO:0082818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Conserved NAD+ dependent histone deacetylase of the Sirtuin family; deacetylation targets are primarily nuclear proteins; required for telomere hypercluster formation in quiescent yeast cells; involved in regulation of lifespan; plays roles in silencing at HML, HMR, telomeres, and rDNA; negatively regulates initiation of DNA replication; functions as regulator of autophagy like mammalian homolog SIRT1, and also of mitophagy","termid":"PBO:0082818"}


id: PBO:0041373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 4 open reading frame 47","termid":"PBO:0041373"}


id: GO:0031867
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an EP4 subtype prostaglandin E2 receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostanoid receptor binding","termid":"GO:0031862"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"EP4 subtype prostaglandin E2 receptor binding","synonyms":[{"name":"EP4 subtype prostaglandin E2 receptor ligand","type":"narrow"},{"name":"prostanoid EP4 receptor binding","type":"exact"}],"termid":"GO:0031867"}


id: PBO:0060483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nanog homeobox pseudogene 5","termid":"PBO:0060483"}


id: GO:0070982
data:
  {"annotated_genes":["SJAG_04549"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070981"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-asparagine, (2S)-2-amino-3-carbamoylpropanoic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asparagine metabolic process","termid":"GO:0006528"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04549":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"L-asparagine metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-asparagine metabolism","type":"exact"}],"termid":"GO:0070982","terms_by_termid":{"GO:0070981":null}}


id: PBO:0083874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein subunit of SCF ubiquitin ligase complex; substrate-specific adaptor subunit that recruits substrates to a core ubiquitination complex","termid":"PBO:0083874"}


id: GO:0047526
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: vestitone + NADP+ = 2'-hydroxyformononetin + NADPH + H+.","definition_xrefs":["RHEA:22560"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"2'-hydroxyisoflavone reductase activity","secondary_identifiers":["EC:1.3.1.45","MetaCyc:RXN-3562"],"synonyms":[{"name":"2',7-dihydroxy-4',5'-methylenedioxyisoflavone reductase activity","type":"related"},{"name":"NADPH:2'-hydroxyisoflavone oxidoreductase activity","type":"related"},{"name":"isoflavone reductase activity","type":"related"},{"name":"vestitone:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047526"}


id: PBO:0005148
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.6.1.17","termid":"PBO:0005148"}


id: PBO:0068186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 493","termid":"PBO:0068186"}


id: PBO:0042705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CUGBP Elav-like family member 4","termid":"PBO:0042705"}


id: MONDO:0020768
data:
  {"annotated_genes":["SJAG_03811","SJAG_02016","SJAG_04882"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84872,84873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010577"},{"annotations":[86663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010378"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"hearing loss disorder","termid":"MONDO:0005365"},{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02016":null,"SJAG_03811":null,"SJAG_04882":null},"genotype_count":0,"is_obsolete":false,"name":"X-linked deafness","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:304500"],"synonyms":[{"name":"DFNX","type":"exact"},{"name":"X-linked deafness","type":"exact"},{"name":"deafness, X-linked","type":"exact"},{"name":"deafness, X-linked, DFN","type":"exact"}],"termid":"MONDO:0020768","terms_by_termid":{"MONDO:0010378":null,"MONDO:0010577":null},"xrefs":{"Monarch":{"xref_id":"0020768"}}}


id: PBO:0066663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor interacting serine/threonine kinase 4","termid":"PBO:0066663"}


id: MONDO:0000998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete parotid disease (obsolete MONDO:0000998)","termid":"MONDO:0000998","xrefs":{"Monarch":{"xref_id":"0000998"}}}


id: PBO:0045985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EHMT2 and SLC44A4 antisense RNA 1","termid":"PBO:0045985"}


id: MONDO:0017289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pleuropulmonary blastoma","termid":"MONDO:0011014"}],"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":"fetal lung interstitial tumor","secondary_identifiers":["UMLS:C5679952","GARD:21118","MEDGEN:1830091","Orphanet:284362"],"synonyms":[{"name":"FLIT","type":"exact"},{"name":"flit","type":"exact"},{"name":"immature interstitial mesenchymal tumor","type":"exact"},{"name":"immature interstitial mesenchymal tumour","type":"exact"}],"termid":"MONDO:0017289","xrefs":{"Monarch":{"xref_id":"0017289"}}}


id: MONDO:0010468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intracranial berry aneurysm","termid":"MONDO:0016483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneurysm, intracranial berry, 5","secondary_identifiers":["MEDGEN:324377","DOID:0080968","GARD:18321","MESH:C563670","OMIM:300870","UMLS:C1835857"],"synonyms":[{"name":"ANIB5","type":"exact"},{"name":"aneurysm, intracranial BERRY, 5","type":"related"}],"termid":"MONDO:0010468","xrefs":{"Monarch":{"xref_id":"0010468"}}}


id: PBO:0004660
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIRA Interacting Protein","termid":"PBO:0004660"}


id: PBO:0088329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase Pyp3","termid":"PBO:0088329"}


id: GO:0006637
data:
  {"annotated_genes":["SJAG_03313","SJAG_03731","SJAG_01402","SJAG_03909","SJAG_03064","SJAG_04895","SJAG_00982","SJAG_00902","SJAG_03715","SJAG_03813","SJAG_02741","SJAG_01989","SJAG_02380","SJAG_03471","SJAG_03310","SJAG_01139","SJAG_01474","SJAG_04499","SJAG_03290","SJAG_02769","SJAG_03349","SJAG_00947","SJAG_01524","SJAG_04865","SJAG_04007","SJAG_01187","SJAG_00866","SJAG_02006","SJAG_02158"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96306,108199],"is_not":false,"summary":null,"term":"GO:0006637"},{"annotations":[92738,97877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006085"},{"annotations":[115593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019427"},{"annotations":[116545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990181"},{"annotations":[86903,113732,117956,108080,94488,87329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006086"},{"annotations":[90924,115258,113838,97531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006084"},{"annotations":[114398,93929,96080,88174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019287"},{"annotations":[106963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035338"},{"annotations":[105088,112915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035336"},{"annotations":[97857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001295"},{"annotations":[114976,110863],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2001211"},{"annotations":[98532],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010510"},{"annotations":[89392,114466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006104"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving acyl-CoA, any derivative of coenzyme A in which the sulfhydryl group is in thiolester linkage with an acyl group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside phosphate metabolic process","termid":"GO:0006753"},{"relation_name":"is_a","term_name":"thioester metabolic process","termid":"GO:0035383"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"},{"relation_name":"is_a","term_name":"purine-containing compound metabolic process","termid":"GO:0072521"}],"gene_count":29,"genes_by_uniquename":{"SJAG_00866":null,"SJAG_00902":null,"SJAG_00947":null,"SJAG_00982":null,"SJAG_01139":null,"SJAG_01187":null,"SJAG_01402":null,"SJAG_01474":null,"SJAG_01524":null,"SJAG_01989":null,"SJAG_02006":null,"SJAG_02158":null,"SJAG_02380":null,"SJAG_02741":null,"SJAG_02769":null,"SJAG_03064":null,"SJAG_03290":null,"SJAG_03310":null,"SJAG_03313":null,"SJAG_03349":null,"SJAG_03471":null,"SJAG_03715":null,"SJAG_03731":null,"SJAG_03813":null,"SJAG_03909":null,"SJAG_04007":null,"SJAG_04499":null,"SJAG_04865":null,"SJAG_04895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150","GO:0006790"],"is_obsolete":false,"name":"acyl-CoA metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"acyl-CoA metabolism","type":"exact"}],"termid":"GO:0006637","terms_by_termid":{"GO:0006084":null,"GO:0006085":null,"GO:0006086":null,"GO:0006104":null,"GO:0006637":null,"GO:0010510":null,"GO:0019287":null,"GO:0019427":null,"GO:0035336":null,"GO:0035338":null,"GO:1990181":null,"GO:2001211":null,"GO:2001295":null}}


id: MONDO:0005210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm arising from the wall of the uterine corpus (uterine body). The most representative examples are leiomyosarcoma and endometrial stromal sarcoma.","definition_xrefs":["NCIT:C6339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"},{"relation_name":"is_a","term_name":"uterine corpus cancer","termid":"MONDO:0006003"}],"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":"uterine corpus sarcoma","secondary_identifiers":["ONCOTREE:USARC","DOID:5165","MedDRA:10039497","Orphanet:213620","GARD:20476","SCTID:254877001","UMLS:C0338113","EFO:0002914","MONDO:0021422","MEDGEN:137837"],"synonyms":[{"name":"body of uterus sarcoma","type":"exact"},{"name":"corpus uteri sarcoma","type":"exact"},{"name":"sarcoma of body of uterus","type":"exact"},{"name":"sarcoma of corpus uteri","type":"exact"},{"name":"sarcoma of the body of uterus","type":"exact"},{"name":"sarcoma of the corpus uteri","type":"exact"},{"name":"sarcoma of the uterine body","type":"exact"},{"name":"sarcoma of the uterine corpus","type":"exact"},{"name":"sarcoma of the uterus","type":"related"},{"name":"sarcoma of uterine body","type":"exact"},{"name":"sarcoma of uterine corpus","type":"exact"},{"name":"sarcoma of uterus","type":"exact"},{"name":"uterine body sarcoma","type":"exact"},{"name":"uterine sarcoma","type":"related"},{"name":"uterine sarcoma/mesenchymal","type":"related"},{"name":"uterus sarcoma","type":"exact"}],"termid":"MONDO:0005210","xrefs":{"Monarch":{"xref_id":"0005210"}}}


id: PR:Q10134
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fep1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10134"],"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":"iron-sensing transcription factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23E2.01","synonyms":[{"name":"Gaf-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-fep1","type":"exact"},{"name":"transcription factor gaf2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10134"}


id: FYPO:0001009
data:
  {"alleles_by_uniquename":{"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118702,118637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"}]},"cv_name":"fission_yeast_phenotype","definition":"A cytokinesis phenotype observed in the vegetative growth phase of the life cycle in which the assembly and distribution of actin filaments and associated proteins does not occur, resulting in the failure to form an actomyosin contractile ring.","definition_xrefs":["PomBase:mah","PMID:19713940"],"direct_ancestors":[{"relation_name":"has_output","term_name":"actomyosin contractile ring absent","termid":"FYPO:0001008"},{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring assembly","termid":"FYPO:0000161"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02592":null},"genotype_count":1,"genotypes_by_uniquename":{"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0004803","FYPO:0005447","FYPO:0000002","FYPO:0000032","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"abolished actomyosin contractile ring assembly","references_by_uniquename":{"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_02592"],"single_locus_genotype_uniquenames":["sty1delta"],"synonyms":[{"name":"abolished actomyosin contractile ring assembly during mitotic cell cycle","type":"related"},{"name":"abolished actomyosin contractile ring assembly during vegetative growth","type":"exact"},{"name":"abolished actomyosin contractile ring formation","type":"related"},{"name":"abolished contractile ring assembly","type":"exact"},{"name":"abolished cytokinetic contractile ring assembly","type":"exact"},{"name":"abolished cytokinetic ring assembly","type":"related"},{"name":"abolished cytokinetic ring formation","type":"related"},{"name":"abolished mitotic contractile ring assembly","type":"exact"},{"name":"actomyosin contractile ring assembly abolished","type":"exact"},{"name":"cytokinesis defects, contractile ring actin, absent","type":"related"}],"termid":"FYPO:0001009","terms_by_termid":{"FYECO:0000248":null,"FYPO:0002998":null,"FYPO_EXT:0000001":null}}


id: PBO:0074135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 34 member 3","termid":"PBO:0074135"}


id: PBO:0116276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic delta 1-pyrroline-5-carboxylate reductase; catalyzes the last step in proline biosynthesis","termid":"PBO:0116276"}


id: MONDO:0003606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the adrenal medulla","direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal gland cancer","termid":"MONDO:0002817"},{"relation_name":"is_a","term_name":"adrenal medulla neoplasm","termid":"MONDO:0021237"}],"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":"adrenal medulla cancer","secondary_identifiers":["GARD:5755","NCIT:C4396","SCTID:371965009","DOID:5719","MEDGEN:87485","UMLS:C0344456"],"synonyms":[{"name":"adrenal medulla cancer","type":"exact"},{"name":"adrenal medulla neoplasm","type":"broad"},{"name":"adrenal medulla tumor","type":"broad"},{"name":"adrenal medulla tumour","type":"broad"},{"name":"cancer of adrenal medulla","type":"exact"},{"name":"malignant adrenal medulla neoplasm","type":"exact"},{"name":"malignant adrenal medulla tumor","type":"exact"},{"name":"malignant adrenal medulla tumour","type":"exact"},{"name":"malignant neoplasm of adrenal medulla","type":"exact"},{"name":"malignant neoplasm of the adrenal medulla","type":"exact"},{"name":"malignant tumor of adrenal medulla","type":"exact"},{"name":"malignant tumor of the adrenal medulla","type":"exact"},{"name":"malignant tumour of adrenal medulla","type":"exact"},{"name":"malignant tumour of the adrenal medulla","type":"exact"}],"termid":"MONDO:0003606","xrefs":{"Monarch":{"xref_id":"0003606"}}}


id: PBO:0091461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal-ubiquitin fusion protein Ubi3","termid":"PBO:0091461"}


id: MONDO:1011345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Poisoning that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poisoning, non-human animal","termid":"MONDO:1011345","xrefs":{"Monarch":{"xref_id":"1011345"}}}


id: PBO:0044264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine ligand 2","termid":"PBO:0044264"}


id: MONDO:0007239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare keratinopathic ichthyosis (KPI), that is characterized by a blistering phenotype at birth which progressively becomes hyperkeratotic.","definition_xrefs":["Orphanet:312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratinopathic ichthyosis","termid":"MONDO:0017266"},{"relation_name":"is_a","term_name":"keratinization disease","termid":"MONDO:0045011"}],"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":"epidermolytic ichthyosis","secondary_identifiers":["DOID:4603","MEDGEN:38179","MESH:D017488","NORD:1100","OMIMPS:113800","SCTID:254167000","UMLS:C0079153","icd11.foundation:1183730789"],"synonyms":[{"name":"BCIE","type":"exact"},{"name":"EHK","type":"exact"},{"name":"EI","type":"exact"},{"name":"autosomal dominant epidermolytic ichthyosis","type":"narrow"},{"name":"bullous congenital ichthyosiform erythroderma","type":"exact"},{"name":"bullous congenital ichthyosiform erythroderma of Brock","type":"exact"},{"name":"bullous erythroderma Ichthyosiformis congenita of Brocq","type":"related"},{"name":"bullous ichthyosiform erythroderma","type":"related"},{"name":"bullous ichthyosiform erythroderma congenita","type":"related"},{"name":"bullous ichthyosis","type":"exact"},{"name":"congenital bullous ichthyosiform erythroderma","type":"related"},{"name":"epidermolytic hyperkeratosis","type":"exact"},{"name":"epidermolytic ichthyosis","type":"exact"},{"name":"epidermolytic palmoplantar hyperkeratosis","type":"exact"},{"name":"ichthyosis hystrix Brocq type","type":"exact"}],"termid":"MONDO:0007239","xrefs":{"Monarch":{"xref_id":"0007239"}}}


id: PR:O13912
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC23C11.06c gene.","definition_xrefs":["UniProtKB:O13912","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C23C11.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23C11.06c","synonyms":[{"name":"Spom972h-SPAC23C11.06c","type":"exact"}],"termid":"PR:O13912"}


id: MONDO:0001678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tuberculosis that involves the intestine.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastroenteritis","termid":"MONDO:0002269"},{"relation_name":"is_a","term_name":"gastrointestinal tuberculosis","termid":"MONDO:0005768"}],"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":"intestinal tuberculosis","secondary_identifiers":["MEDGEN:546943","UMLS:C0275911","ICD9:014.80","ICD9:014.8","SCTID:60136008","DOID:13282"],"synonyms":[{"name":"intestine tuberculosis","type":"exact"},{"name":"tuberculosis of intestine","type":"exact"}],"termid":"MONDO:0001678","xrefs":{"Monarch":{"xref_id":"0001678"}}}


id: MONDO:0008891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A progressive motor neuron disorder characterized by respiratory insufficiency, sensorineural deafness and progressive ponto-bulbar palsy.","definition_xrefs":["Orphanet:97229"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete bulbospinal muscular atrophy of childhood (obsolete MONDO:0016114)","termid":"MONDO:0016114"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic genetic hearing loss (obsolete MONDO:0019589)","termid":"MONDO:0019589"},{"relation_name":"is_a","term_name":"hereditary motor neuron disease","termid":"MONDO:0024257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"riboflavin transporter deficiency","secondary_identifiers":["GARD:9993","MEDGEN:1634394","OMIMPS:211530","SCTID:699866005","MESH:C537111","DOID:0050694","NORD:1960","UMLS:C4551777"],"synonyms":[{"name":"BVVLS","type":"related"},{"name":"BVVLS1","type":"related"},{"name":"Brown-Vialetto-Van Laere syndrome 1","type":"narrow"},{"name":"Brown-Vialetto-van Laere syndrome","type":"exact"},{"name":"Fazio-Londe syndrome","type":"exact"},{"name":"disorder of riboflavin transmembrane transporter activity","type":"exact"},{"name":"pontobulbar palsy and neurosensory deafness","type":"related"},{"name":"progressive bulbar palsy with sensorineural deafness","type":"related"},{"name":"riboflavin transmembrane transporter activity disease","type":"exact"},{"name":"sensorineural hearing loss-pontobulbar palsy syndrome","type":"exact"}],"termid":"MONDO:0008891","xrefs":{"Monarch":{"xref_id":"0008891"}}}


id: MONDO:0035605
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"precursor lymphoblastic lymphoma/leukemia","termid":"MONDO:0003538"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality","secondary_identifiers":["Orphanet:585877","MEDGEN:396322","UMLS:C2698313","ICD10CM:C91.0","NCIT:C80328","GARD:22341"],"termid":"MONDO:0035605","xrefs":{"Monarch":{"xref_id":"0035605"}}}


id: GO:0009321
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An enzyme complex, usually a homodimer, which directly reduces cellular levels of organic hydroperoxides.","definition_xrefs":["GOC:jl","PMID:2649484"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"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:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"alkyl hydroperoxide reductase complex","termid":"GO:0009321"}


id: PBO:0059960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 5","termid":"PBO:0059960"}


id: PATO:0000915
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A 1-D extent quality which is equal to the dimension through an object as opposed to its length or width.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1-D extent","termid":"PATO:0001708"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thickness","termid":"PATO:0000915"}


id: GO:0009078
data:
  {"annotated_genes":["SJAG_02841","SJAG_03562","SJAG_04098","SJAG_06635","SJAG_04149","SJAG_03985","SJAG_03243","SJAG_00396","SJAG_04145"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042853"},{"annotations":[90167,102796,105673,109927,109569,112748,100323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009098"},{"annotations":[110586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006551"},{"annotations":[110587,102797,109928,112749,90168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009099"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving any amino acid that requires pyruvate for its synthesis, e.g. alanine.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-amino acid metabolic process","termid":"GO:0170033"},{"relation_name":"is_a","term_name":"proteinogenic amino acid metabolic process","termid":"GO:0170039"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00396":null,"SJAG_02841":null,"SJAG_03243":null,"SJAG_03562":null,"SJAG_03985":null,"SJAG_04098":null,"SJAG_04145":null,"SJAG_04149":null,"SJAG_06635":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"pyruvate family amino acid metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8964540"],"synonyms":[{"name":"pyruvate family amino acid metabolism","type":"exact"}],"termid":"GO:0009078","terms_by_termid":{"GO:0006551":null,"GO:0009098":null,"GO:0009099":null,"GO:0042853":null}}


id: PBO:0026640
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_vegetative_cell_during_cellular_response_to_UV","termid":"PBO:0026640"}


id: MONDO:1012279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tremor, non-human animal","termid":"MONDO:1011861"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tremor, dog","secondary_identifiers":["OMIA:001016-9615"],"termid":"MONDO:1012279","xrefs":{"Monarch":{"xref_id":"1012279"}}}


id: GO:1990220
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Bacterial chaperonin complex consisting of a heptameric 10kDa chaperonin subunit GroES and a tetradecameric (2x7) 60kDa chaperonin subunit GroEL. The 60kDa subunit possesses ATPase activity while the holo-enzyme is responsible for the correct folding of proteins.","definition_xrefs":["GOC:bhm","PMID:15313620"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chaperonin ATPase complex","termid":"GO:0016465"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005829","GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"GroEL-GroES complex","synonyms":[{"name":"bacterial chaperonin ATPase complex","type":"related"},{"name":"bacterial chaperonin complex","type":"related"}],"termid":"GO:1990220"}


id: GO:0072532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the meta-hydroxylation of any of the three phenolic rings on triferuloyl spermidine or any of its mono- or di-(hydroxyferuloyl)-spermidine derivatives.","definition_xrefs":["PMID:19779199","GOC:kad"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"tri-(feruloyl or hydroxyferuloyl) spermidine meta-hydroxylase activity","termid":"GO:0072532"}


id: PBO:0057504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 622","termid":"PBO:0057504"}


id: GO:0010080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in maintaining the size and shape of a floral meristem.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of meristem growth","termid":"GO:0010075"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"floral meristem growth","termid":"GO:0010451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of floral meristem growth","synonyms":[{"name":"regulation of floral meristem size","type":"exact"}],"termid":"GO:0010080"}


id: GO:0060421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or extent of heart growth. Heart growth is the increase in size or mass of the heart.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organ growth","termid":"GO:0046622"},{"relation_name":"is_a","term_name":"regulation of heart growth","termid":"GO:0060420"},{"relation_name":"positively_regulates","term_name":"heart growth","termid":"GO:0060419"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of heart growth","termid":"GO:0060421"}


id: GO:0006785
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of heme B, a Fe(II) porphyrin complex readily isolated from the hemoglobin of beef blood, but also found in other proteins including other hemoglobins, myoglobins, cytochromes P-450, catalases, peroxidases as well as b type cytochromes.","definition_xrefs":["GOC:yaf","PMID:29414780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme biosynthetic process","termid":"GO:0006783"},{"relation_name":"is_a","term_name":"heme B metabolic process","termid":"GO:0046492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"heme B biosynthetic process","synonyms":[{"name":"haem B biosynthesis","type":"exact"},{"name":"haem B biosynthetic process","type":"exact"},{"name":"heme B anabolism","type":"exact"},{"name":"heme B biosynthesis","type":"exact"},{"name":"heme B formation","type":"exact"},{"name":"heme B synthesis","type":"exact"},{"name":"protoheme biosynthesis","type":"exact"},{"name":"protoheme biosynthetic process","type":"exact"}],"termid":"GO:0006785"}


id: GO:1900360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pentasaccharide transport.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"pentasaccharide transport","termid":"GO:2001100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of pentasaccharide transport","termid":"GO:1900360"}


id: PBO:0068305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 10","termid":"PBO:0068305"}


id: GO:0021767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mammillary body over time from its initial formation until its mature state. The mammillary body is a protrusion at the posterior end of the hypothalamus that contains hypothalamic nuclei.","definition_xrefs":["GOC:jid","GOC:cls","GO_REF:0000021","GOC:dgh","GOC:dph","ISBN:0878937420"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"diencephalon development","termid":"GO:0021536"},{"relation_name":"part_of","term_name":"limbic system development","termid":"GO:0021761"}],"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":"mammillary body development","termid":"GO:0021767"}


id: FYPO:0004764
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the meiotic spindle pole body is normal (i.e. indistinguishable from wild type) during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to meiotic spindle pole body","termid":"FYPO:0003541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to meiotic spindle pole body during meiosis I","synonyms":[{"name":"normal protein localisation to meiotic spindle pole body during meiosis I","type":"exact"},{"name":"normal protein localization to meiotic SPB during meiosis I","type":"exact"},{"name":"normal protein localization to meiotic spindle pole body during first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0004764"}


id: PBO:0078800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (GTT) 18-1","termid":"PBO:0078800"}


id: PBO:0074729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 87","termid":"PBO:0074729"}


id: GO:0071223
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 lipoteichoic acid stimulus; lipoteichoic acid is a major component of the cell wall of gram-positive bacteria and typically consists of a chain of glycerol-phosphate repeating units linked to a glycolipid anchor.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipoteichoic acid","termid":"GO:0070391"},{"relation_name":"is_a","term_name":"cellular response to molecule of bacterial origin","termid":"GO:0071219"},{"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 lipoteichoic acid","synonyms":[{"name":"cellular response to LTA","type":"exact"}],"termid":"GO:0071223"}


id: PBO:0113443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Substrate-recruiting cofactor of the Cdc48p-Npl4p-Ufd1p segregase; K48-specific Ub chain binding receptor that assists Cdc48p in the dislocation of misfolded, polyubiquitinated ERAD substrates destined for proteasomal degradation; role in regulated destruction of ER membrane proteins, like HMG-CoA reductase (Hmg1/2p), cytosolic proteins (Fbp1p) and mislocalized proteins (Cse4p); mobilizes membrane-bound transcription factors by regulated Ub/proteasome-dependent processing; contains a UBX domain","termid":"PBO:0113443"}


id: PBO:0084388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low-affinity phosphate transporter; acts upstream of Pho81p in regulation of the PHO pathway; deletion of pho84, pho87, pho89, pho90, and pho91 causes synthetic lethality; transcription independent of Pi and Pho4p activity; overexpression results in vigorous growth; PHO90 has a paralog, PHO87, that arose from the whole genome duplication","termid":"PBO:0084388"}


id: MONDO:1010920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myositis ossificans that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myositis ossificans, non-human animal","termid":"MONDO:1010197"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myositis ossificans, pig","secondary_identifiers":["OMIA:000697-9823"],"termid":"MONDO:1010920","xrefs":{"Monarch":{"xref_id":"1010920"}}}


id: FYPO:0005379
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the spindle pole bodies are normal (i.e. indistinguishable from wild type) with respect to structure, composition, location, and orientation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component","termid":"FYPO:0001233"},{"relation_name":"output_of","term_name":"normal spindle pole body organization","termid":"FYPO:0005378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"output_of","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal spindle pole body","synonyms":[{"name":"normal SPB","type":"exact"}],"termid":"FYPO:0005379"}


id: GO:2001134
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a methane from a carbon monoxide.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methanogenesis","termid":"GO:0015948"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"methane biosynthetic process from carbon monoxide","termid":"GO:2001134"}


id: PR:Q9UUG3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dph4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUG3"],"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":"diphthamide biosynthesis protein 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC926.05c","synonyms":[{"name":"Spom972h-dph4","type":"exact"}],"termid":"PR:Q9UUG3"}


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


id: GO:0009890
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id: PBO:0087304
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id: GO:0034908
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id: PBO:0071071
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id: PBO:0076727
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id: PATO:0001928
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id: PBO:0075649
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id: MONDO:0017529
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id: PBO:0075258
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id: GO:0100008
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id: GO:0002504
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id: PBO:0002472
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id: GO:0051574
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id: PBO:0047208
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id: PBO:0084269
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id: SO:0000176
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id: GO:0002834
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id: MONDO:0003977
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id: PBO:0047883
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id: MONDO:1011979
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id: PR:Q9USR5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A THO complex subunit 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13375:SF3","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized THOC5 family protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC577.04","secondary_identifiers":["UniProtKB:Q9USR5"],"synonyms":[{"name":"Spom972h-THOC5","type":"exact"}],"termid":"PR:Q9USR5"}


id: PBO:0047495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fem-1 homolog A pseudogene 3","termid":"PBO:0047495"}


id: PR:O13737
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC16E8.02 gene.","definition_xrefs":["UniProtKB:O13737","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized endoplasmic reticulum membrane protein C16E8.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.02","synonyms":[{"name":"Spom972h-SPAC16E8.02","type":"exact"}],"termid":"PR:O13737"}


id: PBO:0080319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 83 pseudogene","termid":"PBO:0080319"}


id: MONDO:0030263
data:
  {"annotated_genes":["SJAG_03761"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86002],"is_not":false,"summary":null,"term":"MONDO:0030263"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03761":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukodystrophy, hypomyelinating, 21","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070407","MEDGEN:1778269","OMIM:619310","UMLS:C5543334"],"synonyms":[{"name":"HLD21","type":"exact"},{"name":"leukodystrophy, hypomyelinating, 21","type":"exact"}],"termid":"MONDO:0030263","terms_by_termid":{"MONDO:0030263":null},"xrefs":{"Monarch":{"xref_id":"0030263"}}}


id: PBO:0075419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPAG5 antisense RNA 1","termid":"PBO:0075419"}


id: MONDO:0060768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic nodular lesion that arises from the gingiva. It is composed of epithelial cells lining connective tissue stroma.","definition_xrefs":["NCIT:C4693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epulis","termid":"MONDO:0003396"},{"relation_name":"is_a","term_name":"fibroepithelial polyp","termid":"MONDO:0060765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gingival fibroepithelial polyp","secondary_identifiers":["icd11.foundation:1520492305","MEDGEN:98314","SCTID:235001002","UMLS:C0399441"],"synonyms":[{"name":"fibroepithelial polyp of gingiva","type":"exact"},{"name":"fibroepithelial polyp of gum","type":"exact"},{"name":"fibroepithelial polyp of the gingiva","type":"exact"},{"name":"fibroepithelial polyp of the gum","type":"exact"},{"name":"gingival fibroepithelial polyp","type":"exact"},{"name":"gum fibroepithelial polyp","type":"exact"}],"termid":"MONDO:0060768","xrefs":{"Monarch":{"xref_id":"0060768"}}}


id: MONDO:0004991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solitary adenocarcinoma arising from the lung measuring 3 cm or less. It is characterized by a predominantly lepidic pattern and 5 mm or less invasion in greatest dimension. It is usually a non-mucinous adenocarcinoma, but rarely may be mucinous.","definition_xrefs":["NCIT:C2923","NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung adenocarcinoma","termid":"MONDO:0005061"}],"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":"minimally invasive lung adenocarcinoma","secondary_identifiers":["SCTID:373627005","ICDO:8251/3","EFO:0000308","ICD9:162.9","DOID:4926","UMLS:C0007120","ICDO:8250/3","MEDGEN:2871","MESH:D002282"],"synonyms":[{"name":"BAC","type":"exact"},{"name":"bac","type":"exact"},{"name":"bronchioalveolar adenocarcinoma of lung","type":"exact"},{"name":"bronchioalveolar adenocarcinoma of the lung","type":"exact"},{"name":"bronchioalveolar lung carcinoma","type":"exact"},{"name":"bronchiolo-alveolar adenocarcinoma","type":"related"},{"name":"bronchiolo-alveolar carcinoma of lung","type":"exact"},{"name":"bronchiolo-alveolar carcinoma of the lung","type":"exact"},{"name":"bronchiolo-alveolar lung carcinoma","type":"exact"},{"name":"bronchioloalveolar adenocarcinoma of lung","type":"exact"},{"name":"bronchioloalveolar adenocarcinoma of the lung","type":"exact"},{"name":"bronchioloalveolar carcinoma","type":"exact"},{"name":"bronchioloalveolar lung adenocarcinoma","type":"exact"},{"name":"carcinoma, bronchioloalveolar, malignant","type":"exact"},{"name":"minimally invasive lung adenocarcinoma","type":"exact"}],"termid":"MONDO:0004991","xrefs":{"Monarch":{"xref_id":"0004991"}}}


id: GO:0090261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of inclusion body assembly. Inclusion body assembly is the aggregation, arrangement and bonding together of a set of components to form an inclusion body.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component biogenesis","termid":"GO:0044089"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of inclusion body assembly","termid":"GO:0090083"},{"relation_name":"positively_regulates","term_name":"inclusion body assembly","termid":"GO:0070841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of inclusion body assembly","termid":"GO:0090261"}


id: SO:0002383
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant that has been found to be pathogenic in the context of a neoplastic disease.","definition_xrefs":["PMID:35101336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disease_associated_variant","termid":"SO:0001771"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oncogenic_variant","termid":"SO:0002383"}


id: FYECO:0000268
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which trichostatin A was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ trichostatin A","termid":"FYECO:0000268"}


id: PBO:0084037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-anchored cell wall protein involved in weak acid resistance; basal expression requires Msn2p/Msn4p; expression is induced under conditions of stress and during the diauxic shift; SPI1 has a paralog, SED1, that arose from the whole genome duplication","termid":"PBO:0084037"}


id: SO:0002378
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that codes for U3_snoRNA. U3 snoRNA is a member of the box C/D class of small nucleolar RNAs. The U3 snoRNA secondary structure is characterised by a small 5' domain (with boxes A and A'), and a larger 3' domain (with boxes B, C, C', and D), the two domains being linked by a single-stranded hinge. Boxes B and C form the B/C motif, which appears to be exclusive to U3 snoRNAs, and boxes C' and D form the C'/D motif. The latter is functionally similar to the C/D motifs found in other snoRNAs. The 5' domain and the hinge region act as a pre-rRNA-binding domain. The 3' domain has conserved protein-binding sites. Both the box B/C and box C'/D motifs are sufficient for nuclear retention of U3 snoRNA. The box C'/D motif is also necessary for nucleolar localization, stability and hypermethylation of U3 snoRNA. Both box B/C and C'/D motifs are involved in specific protein interactions and are necessary for the rRNA processing functions of U3 snoRNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"C_D_box_snoRNA_gene","termid":"SO:0002375"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3_snoRNA_gene","synonyms":[{"name":"small nucleolar RNA U3 gene, snoRNA U3 gene, U3 small nucleolar RNA gene, U3 snoRNA gene","type":"exact"}],"termid":"SO:0002378"}


id: GO:0018675
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (4S)-limonene + O2 + reduced [NADPH--hemoprotein reductase] = (1S,5R)-carveol + H+ + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:17945"],"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"},{"relation_name":"is_a","term_name":"limonene monooxygenase activity","termid":"GO:0019113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"(S)-limonene 6-monooxygenase activity","secondary_identifiers":["UM-BBD_reactionID:r0713","EC:1.14.14.51","MetaCyc:--LIMONENE-6-MONOOXYGENASE-RXN"],"synonyms":[{"name":"(-)-limonene 6-hydroxylase activity","type":"related"},{"name":"(-)-limonene 6-monooxygenase activity","type":"exact"},{"name":"(-)-limonene,NADPH:oxygen oxidoreductase (6-hydroxylating) activity","type":"related"},{"name":"(S)-limonene,NADPH:oxygen oxidoreductase (6-hydroxylating)","type":"related"},{"name":"limonene 6-hydroxylase activity","type":"exact"}],"termid":"GO:0018675"}


id: PBO:0069465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 730, pseudogene","termid":"PBO:0069465"}


id: PATO:0000891
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A male fertility quality inhering in a male by virtue of the bearer's being capable of initiating, sustaining, or supporting reproduction.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male fertility","termid":"PATO:0000279"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male fertile","termid":"PATO:0000891"}


id: FYPO:0003916
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 degradation of messenger RNA (mRNA) molecules that contain nonsense mutations is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression regulation phenotype during vegetative growth","termid":"FYPO:0001333"},{"relation_name":"is_a","term_name":"abnormal RNA catabolic process during vegetative growth","termid":"FYPO:0002136"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0000294"],"is_obsolete":false,"name":"abnormal nonsense-mediated decay","synonyms":[{"name":"abnormal NMD","type":"exact"},{"name":"abnormal nonsense-mediated decay during mitotic cell cycle","type":"related"},{"name":"abnormal nonsense-mediated decay during vegetative growth","type":"exact"},{"name":"abnormal nuclear-transcribed mRNA catabolic process, nonsense-mediated decay","type":"exact"}],"termid":"FYPO:0003916"}


id: PBO:0113160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSP70 family ATP-binding protein; role in protein folding and vacuolar protein import; required for Ub-dependent degradation of short-lived proteins; associated with the chaperonin-containing T-complex; unique specificity in propagation of [URE3] prions and vacuolar degradation of gluconeogenic enzymes; contributes to tRNA nuclear import during starvation; targeted to vacuoles via the AP-3 pathway; localizes to exosomes during heat stress with a role in thermotolerance; 98% identity with Ssa1p","termid":"PBO:0113160"}


id: PBO:0073070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SDCBP2 antisense RNA 1","termid":"PBO:0073070"}


id: GO:0033574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a testosterone stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"relation_name":"is_a","term_name":"response to ketone","termid":"GO:1901654"}],"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 testosterone","synonyms":[{"name":"response to testosterone stimulus","type":"exact"}],"termid":"GO:0033574"}


id: PBO:0005404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial morphology protein (predicted)","termid":"PBO:0005404"}


id: PBO:0045007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iodothyronine deiodinase 2","termid":"PBO:0045007"}


id: GO:0006730
data:
  {"annotated_genes":["SJAG_01616","SJAG_03224","SJAG_03712","SJAG_00106","SJAG_03914","SJAG_04156","SJAG_06611","SJAG_01466","SJAG_01126","SJAG_01766"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104248,111904,112999],"is_not":false,"summary":null,"term":"GO:0006730"},{"annotations":[104091,93971,96130,90786,97908,104285,107833,111905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035999"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving the transfer of one-carbon units in various oxidation states.","definition_xrefs":["GOC:mah","GOC:pde","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule metabolic process","termid":"GO:0044281"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_01126":null,"SJAG_01466":null,"SJAG_01616":null,"SJAG_01766":null,"SJAG_03224":null,"SJAG_03712":null,"SJAG_03914":null,"SJAG_04156":null,"SJAG_06611":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"one-carbon metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["UM-BBD_pathwayID:C1cyc","GO:0019753","GO:0019754"],"synonyms":[{"name":"one carbon metabolic process","type":"exact"},{"name":"one carbon metabolism","type":"exact"},{"name":"one-carbon metabolism","type":"exact"},{"name":"one-carbon transfer metabolic process","type":"exact"},{"name":"one-carbon transfer metabolism","type":"exact"}],"termid":"GO:0006730","terms_by_termid":{"GO:0006730":null,"GO:0035999":null}}


id: GO:2000817
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any regulation of histone H3-T3 phosphorylation that is involved in chromosome passenger complex localization to kinetochore.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H3-T3 phosphorylation involved in chromosome passenger complex localization to kinetochore (obsolete GO:2000817)","synonyms":[{"name":"regulation of histone H3-T3 phosphorylation involved in CPC complex localization to kinetochore","type":"exact"},{"name":"regulation of histone H3-T3 phosphorylation involved in CPC localization to kinetochore","type":"exact"},{"name":"regulation of histone H3-T3 phosphorylation involved in chromosomal passenger complex localization to kinetochore","type":"exact"},{"name":"regulation of histone H3-T3 phosphorylation involved in chromosome passenger complex localisation to kinetochore","type":"related"}],"termid":"GO:2000817"}


id: MONDO:0000639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer involving a cartilage tissue.","definition_xrefs":["MONDO:patterns/cancer"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone cancer","termid":"MONDO:0002129"}],"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":"cartilage cancer","secondary_identifiers":["MEDGEN:1843449","DOID:0060102","GARD:6004","UMLS:C4290064"],"synonyms":[{"name":"cancer of cartilage tissue","type":"exact"},{"name":"cartilage tissue cancer","type":"exact"},{"name":"cartilaginous cancer","type":"exact"},{"name":"malignant cartilage tissue neoplasm","type":"exact"},{"name":"malignant neoplasm of cartilage tissue","type":"exact"}],"termid":"MONDO:0000639","xrefs":{"Monarch":{"xref_id":"0000639"}}}


id: FYPO:0005504
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which galactose-specific flocculation does not occur. Galactose-specific flocculation is the non-sexual aggregation of single cells, mediated by the binding of cell wall proteins on one cell to galactose residues on the other.","definition_xrefs":["PMID:23236291","PomBase:mah","GO:0036349"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell adhesion","termid":"FYPO:0001872"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"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"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished galactose-specific flocculation","synonyms":[{"name":"abolished flocculation","type":"broad"},{"name":"galactose-specific flocculation abolished","type":"exact"}],"termid":"FYPO:0005504"}


id: FYPO:0006386
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that normally localizes to a compact region at the tip of a shmoo, or mating projection, is more dispersed than normal.","definition_xrefs":["PomBase:mah","PMID:19627505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to shmoo tip","termid":"FYPO:0004802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"protein abnormally dispersed at shmoo tip","synonyms":[{"name":"abnormally dispersed protein localization at shmoo tip","type":"exact"},{"name":"protein abnormally dispersed at mating projection tip","type":"exact"},{"name":"protein abnormally dispersed at shmoo projection","type":"related"}],"termid":"FYPO:0006386"}


id: MONDO:0010007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microbrachycephaly-ptosis-cleft lip syndrome is characterized by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis. It has been described in two Brazilian sisters. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:2511"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microbrachycephaly-ptosis-cleft lip syndrome","secondary_identifiers":["OMIM:268850","MEDGEN:162914","UMLS:C0796142","GARD:3596"],"synonyms":[{"name":"Richieri Costa-Guion Almeida-Ramos syndrome","type":"exact"},{"name":"Richieri-COSTA/Guion-Almeida syndrome","type":"related"},{"name":"microbrachycephaly ptosis cleft lip","type":"related"},{"name":"sao Paulo MCA/Mr syndrome","type":"related"},{"name":"short stature, intellectual disability, eye anomalies, and cleft Lip/palate","type":"related"},{"name":"short stature, mental retardation, eye anomalies, and cleft Lip/palate","type":"related"}],"termid":"MONDO:0010007","xrefs":{"Monarch":{"xref_id":"0010007"}}}


id: GO:1901163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of trophoblast cell migration.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"regulates","term_name":"trophoblast cell migration","termid":"GO:0061450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of trophoblast cell migration","termid":"GO:1901163"}


id: MONDO:0033480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type III","termid":"MONDO:0019793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"spinocerebellar ataxia 45","secondary_identifiers":["MEDGEN:1622156","DOID:0080287","GARD:22353","OMIM:617769","Orphanet:589527","UMLS:C4540400"],"synonyms":[{"name":"SCA45","type":"related"},{"name":"spinocerebellar ataxia 45","type":"exact"}],"termid":"MONDO:0033480","xrefs":{"Monarch":{"xref_id":"0033480"}}}


id: PATO:0001268
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of brown hue and low saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brown","termid":"PATO:0000952"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desaturated brown","synonyms":[{"name":"pale brown","type":"exact"}],"termid":"PATO:0001268"}


id: PBO:0039699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apoptosis inhibitor 5","termid":"PBO:0039699"}


id: MONDO:0024282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive malignant neoplasm that arises from the ovary and is characterized by the presence of malignant epithelial cells that contain intracytoplasmic mucin and may resemble the epithelial cells of the endocervix or gastrointestinal tract. It includes mucinous adenocarcinoma and mucinous adenocarcinofibroma.","definition_xrefs":["NCIT:C40033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian mucinous neoplasm","termid":"MONDO:0003756"},{"relation_name":"is_a","term_name":"malignant epithelial tumor of ovary","termid":"MONDO:0018364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"mucinous ovarian cancer","secondary_identifiers":["MEDGEN:274767","ONCOTREE:MOV","UMLS:C1518233"],"synonyms":[{"name":"malignant ovarian mucinous neoplasm","type":"exact"},{"name":"malignant ovarian mucinous tumor","type":"exact"},{"name":"malignant ovarian mucinous tumour","type":"exact"},{"name":"ovarian mucinous neoplasm, malignant","type":"exact"}],"termid":"MONDO:0024282","xrefs":{"Monarch":{"xref_id":"0024282"}}}


id: PBO:0044786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"differentially expressed in FDCP 8 homolog","termid":"PBO:0044786"}


id: MONDO:0017892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive myogenic arthrogryposis multiplex congenita is a rare inherited neuromuscular disease characterized by prenatal presentation (usually in the second trimester) of reduced fetal movements and abnormal positioning resulting in joint abnormalities that may involve both lower and upper extremities and is usually symmetric, severe hypotonia at birth with bilateral club foot, motor development delay, mild facial weakness without opthalmoplegia, absent deep tendon reflexes, normal motor and sensory nerve conduction velocities, no cerebellar or pyramidal involvement, and progressive disease course with loss of ambulation after the first decade of life.","definition_xrefs":["Orphanet:319332"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"},{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"autosomal recessive myogenic arthrogryposis multiplex congenita","secondary_identifiers":["MEDGEN:1647450","UMLS:C4707155","SCTID:764812008","GARD:17447"],"synonyms":[{"name":"SYNE1-related AMC","type":"exact"},{"name":"SYNE1-related arthrogryposis multiplex congenita","type":"exact"},{"name":"autosomal recessive myogenic AMC","type":"exact"}],"termid":"MONDO:0017892","xrefs":{"Monarch":{"xref_id":"0017892"}}}


id: GO:0047240
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-galactosyl-(1->4)-beta-D-glucosyl-R + UDP-D-galactose = D-galactosyl-(1->3)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-R + H+ + UDP.","definition_xrefs":["RHEA:18413","EC:2.4.1.179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"},{"relation_name":"is_a","term_name":"beta-1,3-galactosyltransferase activity","termid":"GO:0048531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"lactosylceramide beta-1,3-galactosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04431","MetaCyc:2.4.1.179-RXN"],"synonyms":[{"name":"UDP-galactose:D-galactosyl-1,4-beta-D-glucosyl-R beta-1,3-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:D-galactosyl-1,4-beta-D-glucosyl-R beta-1,3-galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-lactosylceramide beta1->3-galactosyltransferase activity","type":"related"}],"termid":"GO:0047240"}


id: GO:0060489
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a lung bud bifurcates parallel to the plane of the previous bud.","definition_xrefs":["GOC:dph","GOC:mtg_lung"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dichotomous subdivision of terminal units involved in lung branching","termid":"GO:0060448"}],"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":"planar dichotomous subdivision of terminal units involved in lung branching morphogenesis","termid":"GO:0060489"}


id: PBO:0001548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial TOM complex subunit Tom70 (predicted)","termid":"PBO:0001548"}


id: PBO:0003902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation initiation factor (predicted)","termid":"PBO:0003902"}


id: GO:0034925
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: pyrene + O2 + 2 H+ + 2 e- = pyrene-4,5-oxide + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrene 4,5-monooxygenase activity (obsolete GO:0034925)","termid":"GO:0034925"}


id: GO:0002817
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of biosynthesis of antibacterial peptides active against Gram-positive bacteria.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of antibacterial peptide biosynthetic process","termid":"GO:0002809"},{"relation_name":"is_a","term_name":"regulation of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","termid":"GO:0002816"},{"relation_name":"negatively_regulates","term_name":"biosynthetic process of antibacterial peptides active against Gram-positive bacteria","termid":"GO:0002815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","synonyms":[{"name":"down regulation of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","type":"exact"},{"name":"down-regulation of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","type":"exact"},{"name":"downregulation of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","type":"exact"},{"name":"inhibition of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","type":"narrow"}],"termid":"GO:0002817"}


id: FYPO:0000570
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of mating projection assembly is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal shmoo formation","termid":"FYPO:0000568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000301"}],"interesting_parent_ids":["FYPO:0000301","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased shmoo formation","synonyms":[{"name":"decreased conjugation tube formation","type":"exact"},{"name":"decreased mating projection assembly","type":"exact"},{"name":"decreased mating projection formation","type":"exact"},{"name":"decreased shmoo assembly","type":"exact"},{"name":"reduced shmoo formation","type":"exact"},{"name":"shmoo formation: decreased","type":"related"}],"termid":"FYPO:0000570"}


id: PBO:0083208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the verified ORF FRT1","termid":"PBO:0083208"}


id: FYPO:0003042
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 nuclear exosome foci does not occur. Nuclear exosome foci, also called Mmi1 nuclear foci, are small structures that form within the nucleus, and contain proteins involved in degrading meiosis-specific RNAs during the mitotic cell cycle, such as Mmi1, Iss10, and Red1.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"},{"relation_name":"is_a","term_name":"abnormal protein localization to nuclear exosome focus","termid":"FYPO:0002963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to nuclear exosome focus","synonyms":[{"name":"abolished protein localisation to nuclear exosome focus","type":"exact"},{"name":"abolished protein localization to Mmi1 focus","type":"exact"},{"name":"abolished protein localization to Mmi1 nuclear focus","type":"exact"},{"name":"abolished protein localization to nuclear exosome focus during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to nuclear exosome focus during vegetative growth","type":"exact"},{"name":"protein localization to nuclear exosome focus abolished","type":"exact"}],"termid":"FYPO:0003042"}


id: GO:0140255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to phosphate starvation.","definition_xrefs":["PMID:29414789"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to phosphate starvation","termid":"GO:0016036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cellular response to phosphate starvation","termid":"GO:0140255"}


id: PBO:0027619
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitosis_following_normal_mitosis","termid":"PBO:0027619"}


id: PBO:0052046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KN motif and ankyrin repeat domains 2","termid":"PBO:0052046"}


id: PBO:0111527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIFK pseudogene 7","termid":"PBO:0111527"}


id: MONDO:0010425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lisch epithelial corneal dystrophy (LECD) is a very rare form of superficial corneal dystrophy characterized by feather-shaped opacities and microcysts in the corneal epithelium arranged in a band-shaped and sometimes whorled pattern, occasionally with impaired vision.","definition_xrefs":["Orphanet:98955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial and subepithelial corneal dystrophy","termid":"MONDO:0000763"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"superficial corneal dystrophy","termid":"MONDO:0020212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"Lisch epithelial corneal dystrophy","secondary_identifiers":["GARD:16877","icd11.foundation:1571503165","UMLS:C2749050","SCTID:724175002","OMIM:620763","DOID:0060450","MEDGEN:411737","OMIM:300778","MESH:C567588"],"synonyms":[{"name":"LECD","type":"exact"},{"name":"Lisch epithelial corneal dystrophy","type":"exact"},{"name":"band-Shaped and whorled microcystic corneal epithelial dystrophy","type":"related"},{"name":"band-shaped and whorled microcystic","type":"exact"},{"name":"band-shaped and whorled microcystic dystrophy of the corneal epithelium","type":"exact"},{"name":"corneal dystrophy, Lisch epithelial","type":"related"},{"name":"corneal dystrophy, Lisch epithelial, X-linked dominant","type":"exact"}],"termid":"MONDO:0010425","xrefs":{"Monarch":{"xref_id":"0010425"}}}


id: GO:0007120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of defining the next site of bud emergence adjacent to the last site of bud emergence on a budding cell.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular bud site selection","termid":"GO:0000282"},{"relation_name":"is_a","term_name":"cell budding","termid":"GO:0007114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150","GO:0000281","GO:0007049"],"is_obsolete":false,"name":"axial cellular bud site selection","synonyms":[{"name":"axial bud site selection","type":"exact"},{"name":"axial budding","type":"broad"}],"termid":"GO:0007120"}


id: GO:0042217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 1-aminocyclopropane-1-carboxylate, a natural product found in plant tissues. It is a key intermediate in the biosynthesis of ethylene (ethene), a fruit-ripening hormone in plants.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1-aminocyclopropane-1-carboxylate metabolic process","termid":"GO:0018871"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid catabolic process","termid":"GO:0170044"},{"relation_name":"is_a","term_name":"alpha-amino acid catabolic process","termid":"GO:1901606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044248","GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"1-aminocyclopropane-1-carboxylate catabolic process","synonyms":[{"name":"1-aminocyclopropane-1-carboxylate breakdown","type":"exact"},{"name":"1-aminocyclopropane-1-carboxylate catabolism","type":"exact"},{"name":"1-aminocyclopropane-1-carboxylate degradation","type":"exact"}],"termid":"GO:0042217"}


id: FYPO:0002134
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which an interaction between a protein and RNA is decreased. One of the relevant gene products may be encoded by the mutated gene, or both the RNA and protein may be encoded by genes other than the mutated one.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-RNA interaction","termid":"FYPO:0002132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002131"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002131","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased protein-RNA interaction","synonyms":[{"name":"decreased RNA binding","type":"exact"},{"name":"decreased RNA-protein interaction","type":"exact"},{"name":"reduced RNA binding","type":"exact"}],"termid":"FYPO:0002134"}


id: PBO:0084457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannosyltransferase in the N-linked glycosylation pathway; catalyzes two consecutive steps in N-linked glycosylation pathway; mutants exhibit temperature-sensitive growth and abnormal accumulation of lipid-linked oligosaccharide Man2GlcNAc2-PP-Dol; mutations of human ALG2 cause congenital myasthenic syndrome; human ALG2 complements temperature sensitivity and dolichol-linked oligosaccharide biosynthesis defect of alg2-1 mutant, but mutant form from a patient with CDG-Ii fails to complement","termid":"PBO:0084457"}


id: MOD:00557
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other","definition_xrefs":["PubMed:10825247","PubMed:15541752","Unimod:206"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Unimod","termid":"MOD:00003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acrolein addition +56","synonyms":[{"name":"Acrolein addition +56","type":"related"},{"name":"Delta:H(4)C(3)O(1)","type":"related"}],"termid":"MOD:00557"}


id: GO:0010623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The activation of endogenous cellular processes that result in the death of a cell as part of its development.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"programmed cell death","termid":"GO:0012501"},{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"},{"relation_name":"part_of","term_name":"cell development","termid":"GO:0048468"}],"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":"programmed cell death involved in cell development","synonyms":[{"name":"developmental programmed cell death","type":"broad"},{"name":"programmed cell death involved in development","type":"broad"}],"termid":"GO:0010623"}


id: MONDO:1011806
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immune-mediated myositis, non-human animal","secondary_identifiers":["OMIA:002141"],"termid":"MONDO:1011806","xrefs":{"Monarch":{"xref_id":"1011806"}}}


id: GO:0052164
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts either the host signal transduction pathways leading to the production of reactive oxygen species as part of the host innate immune response.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to oxidative stress","termid":"GO:0034599"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host innate immune response","termid":"GO:0052167"}],"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 defense to host-produced reactive oxygen species","secondary_identifiers":["GO:0052550","GO:0052303","GO:0052567","GO:0052059","GO:0052385","Reactome:R-HSA-1222387"],"synonyms":[{"name":"evasion by symbiont of cellular damage caused by host oxidative burst","type":"narrow"},{"name":"evasion or tolerance by organism of host-produced reactive oxygen species","type":"exact"},{"name":"evasion or tolerance by organism of reactive oxygen species produced by other organism involved in symbiotic interaction","type":"broad"},{"name":"evasion or tolerance by organism of reactive oxygen species produced during host defense response","type":"exact"},{"name":"evasion or tolerance by symbiont of host-produced reactive oxygen species","type":"exact"},{"name":"evasion or tolerance by symbiont of reactive oxygen species produced by other organism involved in symbiotic interaction","type":"broad"},{"name":"evasion or tolerance of defense-related host metabolic burst","type":"exact"},{"name":"evasion or tolerance of defense-related host oxidative burst","type":"exact"},{"name":"evasion or tolerance of defense-related host respiratory burst","type":"exact"},{"name":"evasion or tolerance of host-produced AOS","type":"exact"},{"name":"evasion or tolerance of host-produced ROIs","type":"exact"},{"name":"evasion or tolerance of host-produced ROS","type":"exact"},{"name":"evasion or tolerance of host-produced active oxygen species","type":"exact"},{"name":"evasion or tolerance of host-produced reactive oxygen intermediates","type":"exact"},{"name":"evasion or tolerance of reactive oxygen species produced by host","type":"exact"},{"name":"modulation by organism of defense-related host AOS production","type":"exact"},{"name":"modulation by organism of defense-related host ROI production","type":"exact"},{"name":"modulation by organism of defense-related host ROS production","type":"exact"},{"name":"modulation by organism of defense-related host active oxygen species production","type":"exact"},{"name":"modulation by organism of defense-related host metabolic burst","type":"exact"},{"name":"modulation by organism of defense-related host oxidative burst","type":"exact"},{"name":"modulation by organism of defense-related host reactive oxidative species production","type":"exact"},{"name":"modulation by organism of defense-related host reactive oxygen intermediate production","type":"exact"},{"name":"modulation by organism of defense-related host respiratory burst","type":"exact"},{"name":"modulation by organism of defense-related reactive oxygen species production in other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of defense-related host reactive oxygen species production","type":"related"},{"name":"response to defense-related host reactive oxygen species production","type":"related"},{"name":"response to defense-related reactive oxygen species production by other organism involved in symbiotic interaction","type":"broad"}],"termid":"GO:0052164"}


id: MONDO:0971058
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare bacterial infectious disease characterized by development of endothelial cell-derived, blood-filled tumors on the surface of the skin during the chronic phase of infection with Bartonella bacilliformis. The lesions can persist for months to years and may cause pain and scarring due to ulceration. They are classified as miliary (multiple red papules of <3 mm in diameter), mular (blood-filled nodules), and diffuse (groups of subdermal nodules >5 mm in diameter). Eruptions may be accompanied by fever and malaise, lymphadenopathy, acute bone and joint pains, and headache. Fatality rates during this phase are low.","definition_xrefs":["Orphanet:659759"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Oroya fever","termid":"MONDO:0018984"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"verruga peruana","termid":"MONDO:0971058","xrefs":{"Monarch":{"xref_id":"0971058"}}}


id: GO:0070394
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving lipoteichoic acid, which is a major component of the cell wall of gram-positive bacteria and typically consists of a chain of glycerol-phosphate repeating units linked to a glycolipid anchor.","definition_xrefs":["GOC:add","PMID:14665680","PMID:16020688"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid metabolic process","termid":"GO:0046374"}],"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":"lipoteichoic acid metabolic process","synonyms":[{"name":"LTA metabolic process","type":"exact"},{"name":"lipoteichoic acid metabolism","type":"exact"}],"termid":"GO:0070394"}


id: GO:0071159
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of a homo- or heterodimer of members of a family of structurally related proteins that contain a conserved N-terminal region called the Rel homology domain (RHD). In the nucleus, NF-kappaB complexes act as transcription factors. In unstimulated cells, NF-kappaB dimers are sequestered in the cytoplasm by IkappaB monomers; signals that induce NF-kappaB activity cause degradation of IkappaB, allowing NF-kappaB dimers to translocate to the nucleus and induce gene expression.","definition_xrefs":["ISBN:0849327946"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"NF-kappaB complex","termid":"GO:0071159"}


id: GO:0051044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of membrane protein ectodomain peptidolysis.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein catabolic process","termid":"GO:0045732"},{"relation_name":"is_a","term_name":"positive regulation of proteolysis","termid":"GO:0045862"},{"relation_name":"is_a","term_name":"regulation of membrane protein ectodomain proteolysis","termid":"GO:0051043"},{"relation_name":"positively_regulates","term_name":"membrane protein ectodomain proteolysis","termid":"GO:0006509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0030163"},{"rel_name":"regulates","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"positive regulation of membrane protein ectodomain proteolysis","synonyms":[{"name":"activation of membrane protein ectodomain proteolysis","type":"narrow"},{"name":"stimulation of membrane protein ectodomain proteolysis","type":"narrow"},{"name":"up regulation of membrane protein ectodomain proteolysis","type":"exact"},{"name":"up-regulation of membrane protein ectodomain proteolysis","type":"exact"},{"name":"upregulation of membrane protein ectodomain proteolysis","type":"exact"}],"termid":"GO:0051044"}


id: MOD:01993
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks two residues by formation of a thioether bond between a cysteine thiol and the beta-carbon of another amino acid residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thioether crosslinked residues","termid":"MOD:00687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"beta-carbon thioether crosslinked residues","termid":"MOD:01993"}


id: MONDO:1010731
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any severe combined immunodeficiency disease in dogs in which the cause of the disease is a mutation in the IL2RG gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"severe combined immunodeficiency disease, dog","termid":"MONDO:1011596"},{"relation_name":"is_a","term_name":"X-linked disease, non-human animal","termid":"MONDO:1012575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked severe combined immunodeficiency disease, IL2RG-related, dog","secondary_identifiers":["OMIA:000899-9615"],"termid":"MONDO:1010731","xrefs":{"Monarch":{"xref_id":"1010731"}}}


id: GO:0016545
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process during courtship where the male insect vibrates his wings. An example of this is found in Drosophila melanogaster.","definition_xrefs":["PMID:11092827","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male courtship behavior, veined wing extension","termid":"GO:0048065"}],"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":"male courtship behavior, veined wing vibration","synonyms":[{"name":"male courtship behavior, wing vibration","type":"related"},{"name":"male courtship behaviour, veined wing vibration","type":"exact"},{"name":"male courtship behaviour, wing vibration","type":"related"}],"termid":"GO:0016545"}


id: GO:0034083
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A polyketide synthase complex that consists of two identical ketosynthase polypeptides.","definition_xrefs":["GOC:cb","PMID:12636085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide synthase complex","termid":"GO:0034081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"type III polyketide synthase complex","synonyms":[{"name":"type III PKS","type":"exact"},{"name":"type III PKS complex","type":"exact"},{"name":"type III polyketide synthase","type":"exact"}],"termid":"GO:0034083"}


id: MONDO:0018724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0020022","MONDO:0005497"],"is_obsolete":false,"name":"X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome","secondary_identifiers":["GARD:17815","Orphanet:459070","MEDGEN:1811349","UMLS:C5687848"],"termid":"MONDO:0018724","xrefs":{"Monarch":{"xref_id":"0018724"}}}


id: PR:Q09896
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A brain protein 44 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR14154:SF2","PRO:DNx","OMA:SCHPO00081"],"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 pyruvate carrier 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.09","secondary_identifiers":["UniProtKB:Q09896"],"synonyms":[{"name":"MPC2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MPC2","type":"exact"}],"termid":"PR:Q09896"}


id: MONDO:0600014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare form of interstitial and vascular lung disease that presents as severe pulmonary hypertension and refractory hypoxemia early in life that is characterized by a lack of misalignment of the pulmonary veins.","definition_xrefs":["PMID:33766794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital pulmonary veins anomaly","termid":"MONDO:0020295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"alveolar capillary dysplasia without misalignment of pulmonary veins","synonyms":[{"name":"ACD without misalignment","type":"exact"}],"termid":"MONDO:0600014","xrefs":{"Monarch":{"xref_id":"0600014"}}}


id: FYPO:0007296
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 biosynthesis of UDP-galactose does not occur.","definition_xrefs":["GO:0052574","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal metabolic process","termid":"FYPO:0000860"},{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"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:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abolished UDP-galactose biosynthetic process","synonyms":[{"name":"UDP-galactose biosynthetic process abolished","type":"exact"},{"name":"abolished UDP-D-galactopyranose biosynthesis","type":"exact"},{"name":"abolished UDP-D-galactose biosynthesis","type":"exact"},{"name":"abolished UDP-galactose biosynthesis","type":"exact"},{"name":"abolished UDP-galactose biosynthetic process during mitotic cell cycle","type":"related"},{"name":"abolished UDP-galactose biosynthetic process during vegetative growth","type":"exact"}],"termid":"FYPO:0007296"}


id: PBO:0067478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 610, pseudogene","termid":"PBO:0067478"}


id: GO:0016502
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a nucleotide and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity. A nucleotide is a compound that consists of a nucleoside esterified with a phosphate molecule.","definition_xrefs":["ISBN:0198506732","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"nucleotide receptor activity","termid":"GO:0016502"}


id: GO:0047555
data:
  {"annotated_genes":["SJAG_02481"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115883],"is_not":false,"summary":null,"term":"GO:0047555"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 3',5'-cyclic GMP + H2O = GMP + H+.","definition_xrefs":["RHEA:16957"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3',5'-cyclic-nucleotide phosphodiesterase activity","termid":"GO:0004114"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02481":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"3',5'-cyclic-GMP phosphodiesterase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0004116","EC:3.1.4.35","MetaCyc:35-CYCLIC-GMP-PHOSPHODIESTERASE-RXN","Reactome:R-HSA-4086392","Reactome:R-HSA-74059","Reactome:R-HSA-418456"],"synonyms":[{"name":"3',5' cyclic-GMP phosphodiesterase activity","type":"exact"},{"name":"3',5'-cyclic-GMP 5'-nucleotidohydrolase activity","type":"related"},{"name":"cGMP phosphodiesterase activity","type":"exact"},{"name":"cGMP-PDE","type":"related"},{"name":"cGMP-specific phosphodiesterase activity","type":"exact"},{"name":"cyclic 3',5'-GMP phosphodiesterase activity","type":"related"},{"name":"cyclic GMP phosphodiesterase activity","type":"exact"},{"name":"cyclic guanosine 3',5'-monophosphate phosphodiesterase activity","type":"related"},{"name":"cyclic guanosine 3',5'-phosphate phosphodiesterase activity","type":"related"},{"name":"guanosine cyclic 3',5'-phosphate phosphodiesterase activity","type":"exact"}],"termid":"GO:0047555","terms_by_termid":{"GO:0047555":null}}


id: GO:0031788
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a motilin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"motilin receptor binding","synonyms":[{"name":"motilin receptor ligand","type":"narrow"}],"termid":"GO:0031788"}


id: GO:0051801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The killing by an organism of a cell in a second organism by means of the rupture of cell membranes and the loss of cytoplasm, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete cytolysis in other organism involved in symbiotic interaction (obsolete GO:0051801)","synonyms":[{"name":"cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"cytolysis of cells in other organism involved in symbiotic interaction","type":"exact"}],"termid":"GO:0051801"}


id: PBO:0040631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRCA1 associated RING domain 1","termid":"PBO:0040631"}


id: PBO:0053609
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 642","termid":"PBO:0053609"}


id: GO:1905483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of motor neuron migration.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:16516839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neuron migration","termid":"GO:2001222"},{"relation_name":"regulates","term_name":"motor neuron migration","termid":"GO:0097475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of motor neuron migration","termid":"GO:1905483"}


id: PBO:0077049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone receptor beta","termid":"PBO:0077049"}


id: GO:1905062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardioblast proliferation.","definition_xrefs":["GOC:BHF","GO_REF:0000058","GOC:bc","GOC:BHF_miRNA","PMID:24236097","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardioblast proliferation","termid":"GO:0003264"},{"relation_name":"is_a","term_name":"positive regulation of cell proliferation involved in heart morphogenesis","termid":"GO:2000138"},{"relation_name":"positively_regulates","term_name":"cardioblast proliferation","termid":"GO:0003263"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cardioblast proliferation","synonyms":[{"name":"activation of cardioblast proliferation","type":"narrow"},{"name":"up regulation of cardioblast proliferation","type":"exact"},{"name":"up-regulation of cardioblast proliferation","type":"exact"},{"name":"upregulation of cardioblast proliferation","type":"exact"}],"termid":"GO:1905062"}


id: PBO:0075367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SOX5 pseudogene 1","termid":"PBO:0075367"}


id: GO:0047479
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: reduced glutathione + glutathionylspermidine + ATP = trypanothione + ADP + phosphate.","definition_xrefs":["EC:6.3.1.9","MetaCyc:6.3.1.9-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-ammonia (or amide) ligase activity","termid":"GO:0016880"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"trypanothione synthase activity","secondary_identifiers":["RHEA:21532"],"synonyms":[{"name":"TSR synthetase activity","type":"related"},{"name":"glutathionylspermidine:glutathione ligase (ADP-forming)","type":"related"}],"termid":"GO:0047479"}


id: PBO:0084971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAD(+)-dependent glutamate synthase (GOGAT); synthesizes glutamate from glutamine and alpha-ketoglutarate; with Gln1p, forms the secondary pathway for glutamate biosynthesis from ammonia; expression regulated by nitrogen source; assembles into filaments as cells approach stationary phase and under cytosolic acidification and starvation conditions","termid":"PBO:0084971"}


id: PR:O94245
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC737.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94245"],"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":"UPF0300 protein C737.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC737.04","synonyms":[{"name":"Spom972h-SPCC737.04","type":"exact"}],"termid":"PR:O94245"}


id: GO:0019506
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phenylmercury acetate, an organomercurial compound composed of a mercury atom attached to a benzene ring and an acetate group.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"phenylmercury acetate metabolic process","termid":"GO:0046412"}],"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":"phenylmercury acetate catabolic process","secondary_identifiers":["MetaCyc:P641-PWY"],"synonyms":[{"name":"phenylmercury acetate breakdown","type":"exact"},{"name":"phenylmercury acetate catabolism","type":"exact"},{"name":"phenylmercury acetate degradation","type":"exact"}],"termid":"GO:0019506"}


id: GO:0006738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nicotinamide riboside, the product of the formation of a glycosidic bond between ribose and nicotinamide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nicotinamide riboside metabolic process","termid":"GO:0046495"},{"relation_name":"is_a","term_name":"pyridine nucleoside catabolic process","termid":"GO:0070638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"nicotinamide riboside catabolic process","synonyms":[{"name":"N-ribosylnicotinamide catabolic process","type":"exact"},{"name":"nicotinamide riboside breakdown","type":"exact"},{"name":"nicotinamide riboside catabolism","type":"exact"},{"name":"nicotinamide riboside degradation","type":"exact"}],"termid":"GO:0006738"}


id: PBO:0080924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 2","termid":"PBO:0080924"}


id: PR:Q10281
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A guanine nucleotide-binding protein subunit beta-2-like 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01018","PANTHER:PTHR19868: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":"guanine nucleotide-binding protein subunit beta-like protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6B12.15","secondary_identifiers":["UniProtKB:Q10281"],"synonyms":[{"name":"Spom972h-GNB2L1","type":"exact"},{"name":"receptor of activated protein kinase C (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10281"}


id: PR:O42967
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1E8.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized ubiquitin-like protein C1E8.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1E8.02","synonyms":[{"name":"Spom972h-SPBC1E8.02","type":"exact"}],"termid":"PR:O42967"}


id: MONDO:0009907
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":"Prepapillary vascular loops","secondary_identifiers":["SCTID:424728002","OMIM:264060","MESH:C563287","UMLS:C1828066","MEDGEN:316814"],"synonyms":[{"name":"Prepapillary vascular loops","type":"exact"},{"name":"preretinal vascular loops","type":"related"}],"termid":"MONDO:0009907","xrefs":{"Monarch":{"xref_id":"0009907"}}}


id: GO:0098543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus from another organism is received and converted into a molecular signal.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to other organism","termid":"GO:0051707"},{"relation_name":"is_a","term_name":"detection of external biotic stimulus","termid":"GO:0098581"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of other organism","secondary_identifiers":["GO:0051824"],"synonyms":[{"name":"recognition of other organism during symbiotic interaction","type":"narrow"},{"name":"recognition of other organism involved in symbiotic interaction","type":"narrow"}],"termid":"GO:0098543"}


id: PBO:0091073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytidylyltransferase","termid":"PBO:0091073"}


id: GO:0018412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a protein by glucuronidation on an amino acid oxygen atom.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete protein O-glucuronidation (obsolete GO:0018412)","synonyms":[{"name":"protein amino acid O-glucuronidation","type":"exact"}],"termid":"GO:0018412"}


id: GO:0006812
data:
  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id: PBO:0062349
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id: MONDO:0010960
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id: GO:0071830
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id: MONDO:0015757
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id: PBO:0004001
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id: PBO:0049873
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEN methyltransferase 1","termid":"PBO:0049873"}


id: MONDO:0030260
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id: PBO:0003619
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  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.3.4.-","termid":"PBO:0003619"}


id: PBO:0057450
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id: GO:0006313
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id: GO:0060809
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The epithelial to mesenchymal transition process in which a mesodermal cell loses apical/basolateral polarity, severs intercellular adhesive junctions, degrades basement membrane components and becomes a migratory mesenchymal cell as part of the process of gastrulation.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial to mesenchymal transition","termid":"GO:0001837"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"gastrulation","termid":"GO:0007369"}],"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":"mesodermal to mesenchymal transition involved in gastrulation","termid":"GO:0060809"}


id: PBO:0044311
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b561","termid":"PBO:0044311"}


id: GO:0071961
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which the sister chromatids of a replicated chromosome are joined along the length of the chromosome arms during mitosis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic sister chromatid cohesion","termid":"GO:0007064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"mitotic sister chromatid cohesion, arms","synonyms":[{"name":"mitotic sister chromatid cohesion along arms","type":"exact"},{"name":"sister chromatid cohesion along arms at mitosis","type":"exact"}],"termid":"GO:0071961"}


id: FYPO:0006847
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id: GO:0007042
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id: GO:1904202
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id: PBO:0062758
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id: PBO:0004843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-B homolog Cbh2","termid":"PBO:0004843"}


id: GO:2000107
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of leukocyte apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of apoptotic process","termid":"GO:0043066"},{"relation_name":"is_a","term_name":"regulation of leukocyte apoptotic process","termid":"GO:2000106"},{"relation_name":"negatively_regulates","term_name":"leukocyte apoptotic process","termid":"GO:0071887"}],"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 leukocyte apoptotic process","synonyms":[{"name":"negative regulation of leukocyte apoptosis","type":"narrow"}],"termid":"GO:2000107"}


id: GO:0039722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts a toll-like receptor signaling pathway in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:18327267","PMID:17299722","PMID:15944308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host signal transduction pathway","termid":"GO:0052029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host toll-like receptor signaling pathway","synonyms":[{"name":"inhibition of host TLR pathway by virus","type":"narrow"},{"name":"suppression by virus of host TLR signaling pathway","type":"narrow"},{"name":"suppression by virus of host toll-like receptor signaling pathway","type":"narrow"}],"termid":"GO:0039722"}


id: PBO:0085842
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 cytoplasm and to the nucleus; protein abundance increases in response to DNA replication stress","termid":"PBO:0085842"}


id: PBO:0086342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pseudouridine synthase; catalyzes only the formation of pseudouridine-55 (Psi55), a highly conserved tRNA modification, in mitochondrial and cytoplasmic tRNAs; also responsible for pseudouracil modification of some mRNAs; PUS4 overexpression leads to translational derepression of GCN4 (Gcd- phenotype)","termid":"PBO:0086342"}


id: GO:0030972
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The proteolytic degradation of proteins in the cytosol that contributes to apoptosis.","definition_xrefs":["GOC:mah","GOC:mtg_apoptosis","GOC:tb","GOC:dph","ISBN:0815332181"],"gene_count":0,"genotype_count":0,"name":"obsolete cleavage of cytosolic proteins involved in execution phase of apoptosis (obsolete GO:0030972)","synonyms":[{"name":"apoptotic cleavage of cytosolic proteins","type":"exact"},{"name":"cleavage of cytosolic proteins involved in apoptosis","type":"broad"},{"name":"cleavage of cytosolic proteins involved in execution phase of apoptosis","type":"exact"}],"termid":"GO:0030972"}


id: PBO:0086470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative mitochondrial protein of unknown function","termid":"PBO:0086470"}


id: MONDO:0012978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the RSPH4A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 11","secondary_identifiers":["OMIM:612649","UMLS:C2675229","DOID:0110602","MESH:C567212","MEDGEN:390741","GARD:15574"],"synonyms":[{"name":"CILD11","type":"exact"},{"name":"RSPH4A primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 11","type":"related"},{"name":"ciliary dyskinesia, primary, 11, without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 11","type":"exact"},{"name":"primary ciliary dyskinesia 11","type":"exact"},{"name":"primary ciliary dyskinesia 11 without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in RSPH4A","type":"exact"},{"name":"primary ciliary dyskinesia type 11","type":"exact"}],"termid":"MONDO:0012978","xrefs":{"Monarch":{"xref_id":"0012978"}}}


id: GO:0048355
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mucilage that occur in the root cap; mucilage is normally synthesized during root growth.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucilage biosynthetic process","termid":"GO:0010192"},{"relation_name":"part_of","term_name":"root cap mucilage metabolic process","termid":"GO:0048360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"root cap mucilage biosynthetic process","synonyms":[{"name":"root cap mucilage anabolism","type":"exact"},{"name":"root cap mucilage biosynthesis","type":"exact"},{"name":"root cap mucilage formation","type":"exact"},{"name":"root cap mucilage synthesis","type":"exact"}],"termid":"GO:0048355"}


id: GO:0034518
data:
  {"annotated_genes":["SJAG_01830","SJAG_04772","SJAG_01954","SJAG_00507","SJAG_04360","SJAG_03223","SJAG_01064"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87000,89836,89378,104253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016281"},{"annotations":[102487,114871,99270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005846"}]},"cv_name":"cellular_component","definition":"A protein complex that binds to an RNA cap structure to mediate RNA processing and/or translation initiation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00507":null,"SJAG_01064":null,"SJAG_01830":null,"SJAG_01954":null,"SJAG_03223":null,"SJAG_04360":null,"SJAG_04772":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"RNA cap binding complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0034518","terms_by_termid":{"GO:0005846":null,"GO:0016281":null}}


id: FYPO:0005104
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of Lys63-specific deubiquitinase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal ubiquitinyl hydrolase activity","termid":"FYPO:0003111"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000707"],"is_obsolete":false,"name":"abnormal Lys63-specific deubiquitinase activity","termid":"FYPO:0005104"}


id: PR:O74927
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- met11 gene.","definition_xrefs":["UniProtKB:O74927","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":"methylenetetrahydrofolate reductase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC343.10","synonyms":[{"name":"Spom972h-met11","type":"exact"}],"termid":"PR:O74927"}


id: MONDO:0014109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete NGLY1-deficiency (obsolete MONDO:0014109)","termid":"MONDO:0014109","xrefs":{"Monarch":{"xref_id":"0014109"}}}


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


id: SO:0002191
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A regulatory region that controls epigenetic imprinting and affects the expression of target genes in an allele- or parent-of-origin-specific manner. Associated regulatory elements may include differentially methylated regions and non-coding RNAs.","direct_ancestors":[{"relation_name":"is_a","term_name":"epigenetically_modified_region","termid":"SO:0001720"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"imprinting_control_region","synonyms":[{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:imprinting_control_region","type":"exact"},{"name":"imprinting control region","type":"exact"}],"termid":"SO:0002191"}


id: PBO:0051881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ISY1-RAB43 readthrough","termid":"PBO:0051881"}


id: PBO:0061212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein 4 like","termid":"PBO:0061212"}


id: PBO:0053230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing G protein-coupled receptor 6","termid":"PBO:0053230"}


id: GO:1905486
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of anterior/posterior axon guidance.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:16516839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of axon guidance","termid":"GO:1902667"},{"relation_name":"regulates","term_name":"anterior/posterior axon guidance","termid":"GO:0033564"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of anterior/posterior axon guidance","synonyms":[{"name":"regulation of anterior-posterior axon guidance","type":"exact"},{"name":"regulation of anterior/posterior axon pathfinding","type":"exact"}],"termid":"GO:1905486"}


id: PBO:0053370
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 293","termid":"PBO:0053370"}


id: FYPO:0002858
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 (1->3)-beta-D-glucan measured at the cell tip is greater than normal.","definition_xrefs":["PMID:17581129","PMID:21652630","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased (1->3)-beta-D-glucan level","termid":"FYPO:0007949"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased (1->3)-beta-D-glucan level at cell tip","synonyms":[{"name":"increased (1,3)beta-D-glucan level at cell tip","type":"exact"},{"name":"increased (1->3)-beta-D-glucan accumulation at cell tip","type":"related"},{"name":"increased (1->3)-beta-D-glucan level at cell end","type":"exact"},{"name":"increased (1->3)-beta-D-glucan level at cell tip during mitotic cell cycle","type":"related"},{"name":"increased (1->3)-beta-D-glucan level at cell tip during vegetative growth","type":"exact"},{"name":"increased 1,3-beta-D-glucan level at cell tip","type":"exact"},{"name":"increased level of (1->3)-beta-D-glucan at cell tip","type":"exact"},{"name":"septal material present at cell tip","type":"related"},{"name":"septum material present at cell tip","type":"related"}],"termid":"FYPO:0002858"}


id: PBO:0079101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed basic protein 1","termid":"PBO:0079101"}


id: GO:1903213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a subtelomeric heterochromatin.","definition_xrefs":["SO:0001997","GO_REF:0000087","GOC:TermGenie","PMID:21300781"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to chromosome, telomeric region","termid":"GO:0070198"},{"relation_name":"is_a","term_name":"protein localization to heterochromatin","termid":"GO:0097355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to subtelomeric heterochromatin","secondary_identifiers":["GO:1990152"],"synonyms":[{"name":"protein localisation in subtelomeric heterochromatin","type":"exact"},{"name":"protein localisation to subtelomeric heterochromatin","type":"exact"},{"name":"protein localisation to telomeric heterochromatin","type":"related"},{"name":"protein localization in subtelomeric heterochromatin","type":"exact"},{"name":"protein localization to telomeric heterochromatin","type":"related"}],"termid":"GO:1903213"}


id: GO:0080082
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of glucosidic link in esculin.","definition_xrefs":["PMID:15604686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-glucosidase activity","termid":"GO:0008422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"esculin beta-glucosidase activity","termid":"GO:0080082"}


id: PR:P30821
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A flavoprotein wrbA that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00863"],"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":"P25 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3C7.14c","secondary_identifiers":["UniProtKB:P30821"],"synonyms":[{"name":"Spom972h-wrbA","type":"exact"},{"name":"brefeldin A resistance protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P30821"}


id: MONDO:0017306
data:
  {"annotated_genes":["SJAG_03275","SJAG_03098"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012994"},{"annotations":[84548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007495"},{"annotations":[84910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100186"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid and other organic acid metabolism","termid":"MONDO:0019189"},{"relation_name":"is_a","term_name":"inborn disorder of phenylalanine and tyrosine metabolism","termid":"MONDO:0019235"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03098":null,"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"disorder of phenylalanine metabolism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:541325","SCTID:12957008","ICD9:270.8","UMLS:C0268461","Orphanet:284814","GARD:21126"],"termid":"MONDO:0017306","terms_by_termid":{"MONDO:0007495":null,"MONDO:0012994":null,"MONDO:0100186":null},"xrefs":{"Monarch":{"xref_id":"0017306"}}}


id: PBO:0017697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycosylceramide biosynthesis protein Cwh43 (predicted)","termid":"PBO:0017697"}


id: PR:O59747
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59747"],"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":"palmitoyl-protein thioesterase-dolichyl pyrophosphate phosphatase fusion 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.12c","synonyms":[{"name":"Spom972h-pdf1","type":"exact"}],"termid":"PR:O59747"}


id: GO:0102687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + dihydrozeatin = H+ + dihydrozeatin-7-N-glucose + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete UDP-glucose:dihydrozeatin 7-N-glucosyltransferase activity (obsolete GO:0102687)","termid":"GO:0102687"}


id: SO:0001154
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A motif of four consecutive peptide residues, of which the i+2 residue is proline, and that may contain one H-bond, which, if present, is between the main-chain CO of the first residue and the main-chain NH of the fourth and is characterized by the dihedral angles: Residue(i+1): phi ~ -120 degrees, psi ~ 120 degrees. Residue(i+2): phi ~ -60 degrees, psi ~ 0 degrees.","definition_xrefs":["PMID:2371257","SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta_turn_type_six","termid":"SO:0001150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"beta_turn_type_six_b","synonyms":[{"name":"beta turn type six b","type":"exact"},{"name":"type VIb beta turn","type":"exact"},{"name":"type VIb turn","type":"exact"}],"termid":"SO:0001154"}


id: FYPO:0003432
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of a protein to histone H3 methylated on the lysine at position 9 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein-protein interaction","termid":"FYPO:0000703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal histone H3K9me binding","synonyms":[{"name":"normal K9-methylated histone H3 binding","type":"exact"},{"name":"normal methylated histone H3K9me binding","type":"exact"}],"termid":"FYPO:0003432"}


id: GO:0140204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of pyridoxal from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"pyridoxal transmembrane transport","termid":"GO:1903090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"pyridoxal import across plasma membrane","termid":"GO:0140204"}


id: MONDO:0019838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune disease of the pituitary gland which can present with varying degrees of pituitary hormonal impairment and/or with symptoms related to pituitary enlargement. It predominantly affects young women in pregnancy or the peripartum period.","definition_xrefs":["PMID:21592417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary hypophysitis","termid":"MONDO:0019835"},{"relation_name":"is_a","term_name":"anterior pituitary gland disorder","termid":"MONDO:0024468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"adenohypophysitis","secondary_identifiers":["GARD:19284","UMLS:C5190880","MEDGEN:1677203","Orphanet:95512"],"synonyms":[{"name":"adenohypophysis inflammation","type":"exact"},{"name":"anterior pituitary hypophysitis","type":"exact"},{"name":"inflammation of adenohypophysis","type":"exact"},{"name":"lymphocytic adenohypophysitis","type":"exact"}],"termid":"MONDO:0019838","xrefs":{"Monarch":{"xref_id":"0019838"}}}


id: GO:2000060
data:
  {"annotated_genes":["SJAG_00071","SJAG_00642","SJAG_03699","SJAG_03048","SJAG_02723","SJAG_01210"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[108380,106147,111205,116568,101885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ubiquitin-dependent protein catabolic process.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"positive regulation of proteolysis involved in protein catabolic process","termid":"GO:1903052"},{"relation_name":"is_a","term_name":"regulation of ubiquitin-dependent protein catabolic process","termid":"GO:2000058"},{"relation_name":"positively_regulates","term_name":"ubiquitin-dependent protein catabolic process","termid":"GO:0006511"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00642":null,"SJAG_01210":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of ubiquitin-dependent protein catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"positive regulation of protein degradation tagging activity","type":"related"},{"name":"positive regulation of protein ubiquitination during ubiquitin-dependent protein breakdown","type":"narrow"},{"name":"positive regulation of protein ubiquitination during ubiquitin-dependent protein catabolism","type":"narrow"},{"name":"positive regulation of protein ubiquitination during ubiquitin-dependent protein degradation","type":"narrow"},{"name":"positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"positive regulation of protein ubiquitinylation during ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"positive regulation of protein ubiquitinylation during ubiquitin-dependent protein catabolism","type":"narrow"},{"name":"positive regulation of protein ubiquitylation during ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"positive regulation of protein ubiquitylation during ubiquitin-dependent protein catabolism","type":"narrow"}],"termid":"GO:2000060","terms_by_termid":{"GO:0032436":null,"GO:1905786":null}}


id: PBO:0042858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 74","termid":"PBO:0042858"}


id: GO:1905421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of plant organ morphogenesis.","definition_xrefs":["GO_REF:0000058","GOC:tb","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"regulates","term_name":"plant organ morphogenesis","termid":"GO:1905392"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of plant organ morphogenesis","termid":"GO:1905421"}


id: PBO:0036119
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_spindle_assembly_checkpoint","termid":"PBO:0036119"}


id: PBO:0057296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 513a-1","termid":"PBO:0057296"}


id: PBO:0079501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TXNL4A pseudogene 1","termid":"PBO:0079501"}


id: PBO:0108897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 10","termid":"PBO:0108897"}


id: MONDO:0016279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Adenosarcoma of the cervix uteri is a rare subtype of malignant mixed epithelial and mesenchymal tumor composed of benign or mildly atypical glandular elements and a surrounding low-grade malignant stroma, often containing heterologous elements, such as areas of sex-cord-like or smooth muscle differentiation. It usually presents with vaginal bleeding or discharge, lower abdominal pain and/or a cervical mass or polyp. The tumor may arise from pre-existing endometriosis and patients may have a history of recurrent cervical polyps.","definition_xrefs":["Orphanet:213792"],"gene_count":0,"genotype_count":0,"name":"obsolete adenosarcoma of the cervix uteri (obsolete MONDO:0016279)","termid":"MONDO:0016279","xrefs":{"Monarch":{"xref_id":"0016279"}}}


id: GO:1900067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to alkalinity.","definition_xrefs":["PMID:17023428","GOC:dgf","GOC:TermGenie","PMID:12509465"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to stimulus","termid":"GO:0048583"},{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"cellular response to alkaline pH","termid":"GO:0071469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cellular response to alkaline pH","synonyms":[{"name":"regulation of cellular response to alkalinity","type":"broad"},{"name":"regulation of cellular response to basic pH","type":"exact"}],"termid":"GO:1900067"}


id: MONDO:0800467
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dyskeratosis congenita caused by impaired telomere maintenance resulting in short or very short telomeres. The phenotypic spectrum includes individuals with classic dyskeratosis congenita (DC) as well as those with very short telomeres and an isolated physical finding. Classic DC is characterized by a triad of dysplastic nails, lacy reticular pigmentation of the upper chest and/or neck, and oral leukoplakia, although this may not be present in all individuals. People with DC/TBD are at increased risk for progressive bone marrow failure (BMF), myelodysplastic syndrome or acute myelogenous leukemia, solid tumors (usually squamous cell carcinoma of the head/neck or anogenital cancer), and pulmonary fibrosis. Other findings can include eye abnormalities (epiphora, blepharitis, sparse eyelashes, ectropion, entropion, trichiasis), taurodontism, liver disease, gastrointestinal telangiectasias, and avascular necrosis of the hips or shoulders. Additional findings include cerebellar hypoplasia (Hoyeraal Hreidarsson syndrome) and bilateral exudative retinopathy and intracranial calcifications (Revesz syndrome and Coats plus syndrome). Onset and progression of manifestations of DC/TBD vary: at the mild end of the spectrum are those who have only minimal physical findings with normal bone marrow function, and at the severe end are those who have the diagnostic triad and early-onset BMF.","definition_xrefs":["PMID:20301779"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dyskeratosis congenita","termid":"MONDO:0015780"}],"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":"dyskeratosis congenita and related telomere biology disorder","synonyms":[{"name":"dyskeratosis congenita and related telomere biology disorder","type":"exact"}],"termid":"MONDO:0800467","xrefs":{"Monarch":{"xref_id":"0800467"}}}


id: PBO:0006177
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-requires_sequence_feature","termid":"PBO:0006177"}


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


id: PBO:0074014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 6 pseudogene 5","termid":"PBO:0074014"}


id: PBO:0049719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAUS augmin like complex subunit 4 pseudogene 1","termid":"PBO:0049719"}


id: GO:1900273
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of long-term synaptic potentiation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission","termid":"GO:0050806"},{"relation_name":"is_a","term_name":"regulation of long-term synaptic potentiation","termid":"GO:1900271"},{"relation_name":"positively_regulates","term_name":"long-term synaptic potentiation","termid":"GO:0060291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of long-term synaptic potentiation","synonyms":[{"name":"activation of LTP","type":"related"},{"name":"activation of long-term potentiation","type":"broad"},{"name":"activation of long-term synaptic potentiation","type":"narrow"},{"name":"positive regulation of LTP","type":"related"},{"name":"positive regulation of long-term potentiation","type":"broad"},{"name":"up regulation of LTP","type":"related"},{"name":"up regulation of long-term potentiation","type":"broad"},{"name":"up regulation of long-term synaptic potentiation","type":"exact"},{"name":"up-regulation of LTP","type":"related"},{"name":"up-regulation of long-term potentiation","type":"broad"},{"name":"up-regulation of long-term synaptic potentiation","type":"exact"},{"name":"upregulation of LTP","type":"related"},{"name":"upregulation of long-term potentiation","type":"broad"},{"name":"upregulation of long-term synaptic potentiation","type":"exact"}],"termid":"GO:1900273"}


id: PBO:0043233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride voltage-gated channel 4","termid":"PBO:0043233"}


id: PBO:0044749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 28","termid":"PBO:0044749"}


id: PBO:0085927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; member of the seripauperin multigene family encoded mainly in subtelomeric regions; SWAT-GFP fusion protein localizes to the endoplasmic reticulum and vacuole, while mCherry fusion localizes to just the vacuole; identical to Pau21p; encodes two proteins that are translated from two different start codons","termid":"PBO:0085927"}


id: PR:Q9P3V6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1348.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P3V6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized methyltransferase C1348.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1348.04","synonyms":[{"name":"Spom972h-SPBC1348.04","type":"exact"}],"termid":"PR:Q9P3V6"}


id: MONDO:0006050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, aggressive, high grade invasive ductal carcinoma, not otherwise specified. It is characterized by the presence of pleomorphic and bizarre malignant cells that constitute more than 50 percent of the malignant cellular infiltrate.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invasive ductal breast carcinoma","termid":"MONDO:0004953"}],"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":"pleomorphic breast carcinoma","secondary_identifiers":["NCIT:C5161","UMLS:C1514169","MEDGEN:307976","EFO:1000047"],"synonyms":[{"name":"anaplastic breast carcinoma","type":"exact"}],"termid":"MONDO:0006050","xrefs":{"Monarch":{"xref_id":"0006050"}}}


id: PATO:0000653
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000653 addictive substance value (obsolete PATO:0000653)","termid":"PATO:0000653"}


id: MONDO:0024530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Bethlem myopathy","termid":"MONDO:0008029"},{"relation_name":"is_a","term_name":"collagen 6-related myopathy","termid":"MONDO:0100225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"Bethlem myopathy 1A","secondary_identifiers":["OMIM:158810"],"synonyms":[{"name":"BTHLM1","type":"related"},{"name":"Bethlem myopathy","type":"related"},{"name":"Bethlem myopathy 1","type":"broad"},{"name":"muscular dystrophy, benign congenital","type":"related"},{"name":"myopathy, benign congenital, with contractures","type":"related"}],"termid":"MONDO:0024530","xrefs":{"Monarch":{"xref_id":"0024530"}}}


id: PBO:0061384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 44","termid":"PBO:0061384"}


id: PATO:0000583
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A weight which is relatively 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":"weight","termid":"PATO:0000128"},{"relation_name":"is_a","term_name":"decreased force","termid":"PATO:0002246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased weight","synonyms":[{"name":"light weight","type":"exact"},{"name":"low weight","type":"exact"}],"termid":"PATO:0000583"}


id: PBO:0038341
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-realized_in_response_to","termid":"PBO:0038341"}


id: GO:0060028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The morphogenetic process in which an epithelium narrows along one axis and lengthens in a perpendicular axis contributing to the lengthening of the axis of an organism.","definition_xrefs":["GOC:dph","PMID:12062082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"convergent extension","termid":"GO:0060026"},{"relation_name":"part_of","term_name":"axis elongation","termid":"GO:0003401"}],"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":"convergent extension involved in axis elongation","termid":"GO:0060028"}


id: PBO:0083147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; almost completely overlaps ORF GND1/YHR183W","termid":"PBO:0083147"}


id: PBO:0033751
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_intergenic_meiotic_recombination","termid":"PBO:0033751"}


id: GO:0072484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about spindle assembly is received and converted into a molecular signal, contributing to a spindle assembly checkpoint.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in spindle assembly checkpoint (obsolete GO:0072484)","synonyms":[{"name":"sensing involved in spindle assembly checkpoint","type":"related"},{"name":"spindle assembly checkpoint sensor mechanism","type":"related"},{"name":"spindle assembly checkpoint sensor process","type":"related"}],"termid":"GO:0072484"}


id: GO:0061211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a collecting duct in the mesonephros over time, from its formation to the mature structure. The collecting duct regulates water, electrolyte and acid-base balance. The collecting duct is the final common path through which urine flows before entering the ureter and then emptying into the bladder.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collecting duct development","termid":"GO:0072044"},{"relation_name":"part_of","term_name":"mesonephros development","termid":"GO:0001823"}],"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":"mesonephric collecting duct development","termid":"GO:0061211"}


id: MONDO:0009975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An antiquated term that refers to a non-Hodgkin lymphoma composed of diffuse infiltrates of large, often anaplastic lymphocytes.","definition_xrefs":["NCIT:C27824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphatic system cancer","termid":"MONDO:0000612"},{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"},{"relation_name":"is_a","term_name":"dendritic cell tumor","termid":"MONDO:0020082"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"reticulum cell sarcoma","secondary_identifiers":["ICD9:200.7","GARD:16765","DOID:8538","EFO:0005287","Orphanet:86900","MEDGEN:44224","ICD9:200.0","MedDRA:10038804","MESH:D054739","OMIM:267730","ICD9:200.00","SCTID:373168002","MESH:D008228","UMLS:C0024302"],"synonyms":[{"name":"Reticulum cell sarcoma","type":"exact"},{"name":"histiocytic lymphoma","type":"exact"},{"name":"interdigitating cell sarcoma","type":"exact"},{"name":"large-cell Lymphomas","type":"exact"},{"name":"reticular cell sarcoma","type":"exact"},{"name":"reticulosarcoma","type":"exact"},{"name":"reticulum cell sarcoma","type":"exact"},{"name":"sarcoma of reticular cell","type":"exact"}],"termid":"MONDO:0009975","xrefs":{"Monarch":{"xref_id":"0009975"}}}


id: PBO:0074913
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 83B","termid":"PBO:0074913"}


id: GO:0002256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the kinin cascade.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of acute inflammatory response","termid":"GO:0002673"},{"relation_name":"is_a","term_name":"regulation of protein activation cascade","termid":"GO:2000257"},{"relation_name":"regulates","term_name":"kinin cascade","termid":"GO:0002254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"regulation of kinin cascade","termid":"GO:0002256"}


id: GO:1902721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of prolactin secretion.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:16159377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein secretion","termid":"GO:0050709"},{"relation_name":"is_a","term_name":"negative regulation of peptide hormone secretion","termid":"GO:0090278"},{"relation_name":"negatively_regulates","term_name":"prolactin secretion","termid":"GO:0070459"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of prolactin secretion","synonyms":[{"name":"down regulation of prolactin secretion","type":"exact"},{"name":"down-regulation of prolactin secretion","type":"exact"},{"name":"downregulation of prolactin secretion","type":"exact"},{"name":"inhibition of prolactin secretion","type":"narrow"}],"termid":"GO:1902721"}


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


id: MONDO:0017272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal ichthyosis syndrome with prominent neurologics signs (obsolete MONDO:0017272)","secondary_identifiers":["Orphanet:281238"],"synonyms":[{"name":"autosomal ichthyosis syndrome with prominent neurologic signs","type":"related"}],"termid":"MONDO:0017272","xrefs":{"Monarch":{"xref_id":"0017272"}}}


id: PBO:0045060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"discs large MAGUK scaffold protein 2","termid":"PBO:0045060"}


id: GO:0018546
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N-phenylhydroxylamine + 2 NADP+ = 2 H+ + 2 NADPH + nitrobenzene.","definition_xrefs":["PMID:16517619","RHEA:52884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"nitrobenzene nitroreductase activity","secondary_identifiers":["EC:1.7.1.16","UM-BBD_enzymeID:r0303","MetaCyc:RXN-8815"],"termid":"GO:0018546"}


id: GO:0102237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,-6-trans-farnesol + ATP = 2-trans,-6-trans-farnesyl monophosphate + ADP + H+.","definition_xrefs":["RHEA:61656","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenol kinase activity","termid":"GO:0052673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"ATP:farnesol kinase activity","secondary_identifiers":["MetaCyc:RXN-12304"],"synonyms":[{"name":"ATP-dependent farnesol kinase activity","type":"related"}],"termid":"GO:0102237"}


id: GO:0035565
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the size of a pronephric kidney.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of kidney size","termid":"GO:0035564"},{"relation_name":"part_of","term_name":"pronephros morphogenesis","termid":"GO:0072114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of pronephros size","synonyms":[{"name":"regulation of pronephric kidney size","type":"exact"}],"termid":"GO:0035565"}


id: GO:0001664
data:
  {"annotated_genes":["SJAG_02233","SJAG_02444"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73814,79817],"is_not":false,"summary":null,"term":"GO:0001664"}]},"cv_name":"molecular_function","definition":"Binding to a G protein-coupled receptor.","definition_xrefs":["GOC:ceb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02233":null,"SJAG_02444":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled receptor binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-500717"],"synonyms":[{"name":"G protein coupled receptor binding","type":"exact"},{"name":"G protein coupled receptor ligand","type":"narrow"},{"name":"G-protein coupled receptor binding","type":"exact"},{"name":"G-protein-coupled receptor ligand","type":"narrow"}],"termid":"GO:0001664","terms_by_termid":{"GO:0001664":null}}


id: PR:O13820
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erg5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13820"],"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":"cytochrome P450 61 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19A8.04","synonyms":[{"name":"C-22 sterol desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-erg5","type":"exact"}],"termid":"PR:O13820"}


id: PATO:0000699
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000699 glutinous (obsolete PATO:0000699)","termid":"PATO:0000699"}


id: PBO:0066221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBM25 antisense RNA 1","termid":"PBO:0066221"}


id: GO:0034470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in the conversion of one or more primary non-coding RNA (ncRNA) transcripts into one or more mature ncRNA molecules.","definition_xrefs":["PMID:27573892","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete ncRNA processing (obsolete GO:0034470)","termid":"GO:0034470"}


id: PBO:0084628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Methylglyoxalase that converts methylglyoxal to D-lactate; involved in oxidative stress resistance, diauxic shift, and stationary phase survival; has similarity to E. coli Hsp31 and C. albicans Glx3p; member of the DJ-1/ThiJ/PfpI superfamily, which includes human DJ-1 involved in Parkinson's disease and cancer; exists as a dimer and contains a putative metal-binding site; protein abundance increases in response to DNA replication stress","termid":"PBO:0084628"}


id: PBO:0030103
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_threonine_level","termid":"PBO:0030103"}


id: PBO:0029599
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sodium:hydrogen_antiporter_activity","termid":"PBO:0029599"}


id: PBO:0076136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUCLA2 pseudogene 1","termid":"PBO:0076136"}


id: PBO:0040240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activating transcription factor 7 interacting protein 2","termid":"PBO:0040240"}


id: GO:0080108
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the conversion of a S-alkylthiohydroximate to a thiohydroximate.","definition_xrefs":["PMID:14871316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"S-alkylthiohydroximate lyase activity","synonyms":[{"name":"S-alkylthiohydroximate C-S lyase activity","type":"narrow"}],"termid":"GO:0080108"}


id: PBO:0057327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 520b","termid":"PBO:0057327"}


id: GO:1902973
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any DNA ligation involved in mitotic cell cycle DNA replication.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete mitotic DNA replication DNA ligation (obsolete GO:1902973)","synonyms":[{"name":"DNA ligation involved in mitotic DNA replication","type":"exact"},{"name":"DNA ligation involved in mitotic cell cycle DNA replication","type":"exact"}],"termid":"GO:1902973"}


id: GO:0014703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within oscillatory skeletal muscle tissue, resulting in a change in muscle geometry. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. Oscillatory muscle contraction occurs in insect wing muscles and is characterized by asynchrony between action potential and contraction and by stretch activation.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voluntary skeletal muscle contraction","termid":"GO:0003010"}],"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":"oscillatory muscle contraction","termid":"GO:0014703"}


id: PATO:0000776
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000776 memory value (obsolete PATO:0000776)","termid":"PATO:0000776"}


id: PBO:0035898
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_anaerobic_cell_population_growth","termid":"PBO:0035898"}


id: GO:0047628
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ADP + thymidine = AMP + thymidine 5'-phosphate.","definition_xrefs":["MetaCyc:ADP--THYMIDINE-KINASE-RXN","EC:2.7.1.118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016301","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"ADP-thymidine kinase activity","secondary_identifiers":["RHEA:13413"],"synonyms":[{"name":"ADP:dThd phosphotransferase activity","type":"related"},{"name":"ADP:thymidine 5'-phosphotransferase activity","type":"related"},{"name":"adenosine diphosphate-thymidine phosphotransferase activity","type":"related"}],"termid":"GO:0047628"}


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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","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: MONDO:0035776
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"combined deficiency of factor VII and factor X","secondary_identifiers":["GARD:22418","Orphanet:600691","UMLS:C5681529","MEDGEN:1843297"],"termid":"MONDO:0035776","xrefs":{"Monarch":{"xref_id":"0035776"}}}


id: MONDO:0004313
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the trigeminal ganglion.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gasserian ganglion meningioma","secondary_identifiers":["MEDGEN:232542","NCIT:C6779","UMLS:C1333760","DOID:7635"],"synonyms":[{"name":"Gasserian meningioma","type":"exact"},{"name":"gasserian ganglion meningioma (disease)","type":"exact"},{"name":"meningioma (disease) of gasserian ganglion","type":"exact"},{"name":"meningioma of Gasserian ganglion","type":"exact"},{"name":"meningioma of the Gasserian ganglion","type":"exact"}],"termid":"MONDO:0004313","xrefs":{"Monarch":{"xref_id":"0004313"}}}


id: GO:1905135
data:
  {"annotated_genes":["SJAG_02780","SJAG_02779"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71319,91544],"is_not":false,"summary":null,"term":"GO:1905135"}]},"cv_name":"biological_process","definition":"The directed movement of biotin from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:12557275","GOC:TermGenie","GO_REF:0000075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biotin transport","termid":"GO:0015878"},{"relation_name":"is_a","term_name":"vitamin transmembrane transport","termid":"GO:0035461"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02779":null,"SJAG_02780":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"biotin import across plasma membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0044756","GO:1901689"],"synonyms":[{"name":"biotin import","type":"related"},{"name":"biotin import into cell","type":"exact"}],"termid":"GO:1905135","terms_by_termid":{"GO:1905135":null}}


id: PBO:0052422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIRREL3 antisense RNA 1","termid":"PBO:0052422"}


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


id: PBO:0029683
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_oxygen","termid":"PBO:0029683"}


id: GO:0042811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of pheromones, a substance that is secreted and released by an organism and detected by a second organism of the same or a closely related species, in which it causes a specific reaction, such as a definite behavioral reaction or a developmental process.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone biosynthetic process","termid":"GO:0042446"},{"relation_name":"is_a","term_name":"pheromone metabolic process","termid":"GO:0042810"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"pheromone biosynthetic process","synonyms":[{"name":"pheromone anabolism","type":"exact"},{"name":"pheromone biosynthesis","type":"exact"},{"name":"pheromone formation","type":"exact"},{"name":"pheromone synthesis","type":"exact"}],"termid":"GO:0042811"}


id: PBO:0047285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FA complementation group L","termid":"PBO:0047285"}


id: GO:0043966
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of an acetyl group.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3 acetylation (obsolete GO:0043966)","termid":"GO:0043966"}


id: GO:0044466
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: glutaryl-CoA + H2O = CoA + glutarate.","definition_xrefs":["GOC:pm","PMID:16141203"],"gene_count":0,"genotype_count":0,"name":"obsolete glutaryl-CoA hydrolase activity (obsolete GO:0044466)","synonyms":[{"name":"glutaryl-CoA thioesterase activity","type":"exact"}],"termid":"GO:0044466"}


id: PBO:0072159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 36","termid":"PBO:0072159"}


id: PR:P48011
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerases I, II, and III subunit RPABC4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12056:SF0","PRO:DNx","OMA:SCHPO02953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerases I, II, and III subunit RPABC4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.03","secondary_identifiers":["UniProtKB:P48011"],"synonyms":[{"name":"ABC10-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerases I, II, and III subunit ABC4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLR2K","type":"exact"}],"termid":"PR:P48011"}


id: GO:0003055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the suprachiasmatic nucleus modulates heart rate at different values with a regularity of approximately 24 hours.","definition_xrefs":["GOC:rl","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circadian regulation of heart rate","termid":"GO:0003053"}],"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":"circadian regulation of heart rate by the suprachiasmatic nucleus","synonyms":[{"name":"SCN regulation of heart rate","type":"exact"},{"name":"circadian regulation of heart contraction rate by the suprachiasmatic nucleus","type":"related"},{"name":"master pacemaker clock regulation of heart rate","type":"exact"}],"termid":"GO:0003055"}


id: GO:0000444
data:
  {"annotated_genes":["SJAG_02346","SJAG_01228","SJAG_00418","SJAG_03220"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[95043,98766,109803,109849],"is_not":false,"summary":null,"term":"GO:0000444"}]},"cv_name":"cellular_component","definition":"A multiprotein kinetochore subcomplex that binds to centromeric chromatin and forms part of the outer kinetochore. It helps to recruit outer kinetochore subunits that will bind to microtubules. In humans, it consists of MIS12, DSN1, NSL1 and PMF1.","definition_xrefs":["PMID:14633972","GOC:krc","PMID:16585270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"outer kinetochore","termid":"GO:0000940"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00418":null,"SJAG_01228":null,"SJAG_02346":null,"SJAG_03220":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000776"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991","GO:0000776"],"is_obsolete":false,"name":"MIS12/MIND type complex","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000818"],"synonyms":[{"name":"MIND complex","type":"exact"},{"name":"Mis12 complex","type":"narrow"},{"name":"Mtw1p Including Nnf1p-Nsl1p-Dsn1p complex","type":"related"},{"name":"nuclear MIS12/MIND complex","type":"related"}],"termid":"GO:0000444","terms_by_termid":{"GO:0000444":null}}


id: MONDO:0040870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of polydipsia characterized by excessive fluid intake in the absence of physiological stimuli to drink.","definition_xrefs":["Wikipedia:Primary_polydipsia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impulse control disorder","termid":"MONDO:0001162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary polydipsia","termid":"MONDO:0040870","xrefs":{"Monarch":{"xref_id":"0040870"}}}


id: PBO:0086305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with DNA-dependent ATPase and ssDNA annealing activities; involved in maintenance of genome; interacts functionally with DNA polymerase delta; homolog of human Werner helicase interacting protein (WHIP); forms nuclear foci upon DNA replication stress","termid":"PBO:0086305"}


id: PBO:0038587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA carboxylase alpha","termid":"PBO:0038587"}


id: FYPO:0005356
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 site-specific DNA replication termination at RTS1 barrier in the mating type region does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal site-specific DNA replication termination at RTS1 barrier","termid":"FYPO:0005355"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished site-specific DNA replication termination at RTS1 barrier","synonyms":[{"name":"abolished site-specific DNA replication termination at RTS1 barrier during mitotic cell cycle","type":"related"},{"name":"abolished site-specific DNA replication termination at RTS1 barrier during vegetative growth","type":"exact"},{"name":"site-specific DNA replication termination at RTS1 barrier abolished","type":"exact"}],"termid":"FYPO:0005356"}


id: PBO:0082538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cell wall mannoprotein; member of Srp1p/Tip1p family of serine-alanine-rich proteins; expressed under anaerobic conditions and required for anaerobic growth; TIR3 has a paralog, TIR2, that arose from the whole genome duplication","termid":"PBO:0082538"}


id: GO:0035027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to leading edge cell fate and their capacity to differentiate into leading edge cells. Leading edge cells are found at the front of a migrating epithelial sheet.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell fate commitment","termid":"GO:0072148"},{"relation_name":"part_of","term_name":"leading edge cell differentiation","termid":"GO:0035026"}],"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":"leading edge cell fate commitment","termid":"GO:0035027"}


id: MONDO:0014236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Ehlers-Danlos syndrome, musculocontractural type in which the cause of the disease is a mutation in the DSE gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, musculocontractural type","termid":"MONDO:0011142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066","MONDO:0005267"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, musculocontractural type 2","secondary_identifiers":["DOID:0080735","OMIM:615539","UMLS:C3809845","GARD:15982","DOID:0080737","MEDGEN:816175"],"synonyms":[{"name":"DSE Ehlers-Danlos syndrome, musculocontractural type","type":"exact"},{"name":"EDSMC2","type":"related"},{"name":"Ehlers-Danlos syndrome, musculocontractural type 2","type":"exact"},{"name":"Ehlers-Danlos syndrome, musculocontractural type caused by mutation in DSE","type":"exact"},{"name":"Ehlers-Danlos syndrome, musculocontractural type, 2","type":"related"}],"termid":"MONDO:0014236","xrefs":{"Monarch":{"xref_id":"0014236"}}}


id: PBO:0079145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 7","termid":"PBO:0079145"}


id: GO:0032586
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a protein storage vacuole.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant-type vacuole membrane","termid":"GO:0009705"},{"relation_name":"part_of","term_name":"protein storage vacuole","termid":"GO:0000326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005773"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005773"],"is_obsolete":false,"name":"protein storage vacuole membrane","termid":"GO:0032586"}


id: GO:0044001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directional movement of an organism from one place to another within its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:cc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in interaction with host","termid":"GO:0051701"}],"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":"migration in host","synonyms":[{"name":"migration within host","type":"exact"}],"termid":"GO:0044001"}


id: PBO:0030243
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_response_to_water_deprivation","termid":"PBO:0030243"}


id: MONDO:0010342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autism, susceptibility to, X-linked 3","secondary_identifiers":["OMIM:300496","UMLS:C1845336","MEDGEN:335161"],"synonyms":[{"name":"AUTSX3","type":"related"},{"name":"autism susceptibility, X-linked 3","type":"exact"},{"name":"autism, susceptibility to, X-linked 3","type":"exact"},{"name":"autism, susceptibility to, X-linked type 3","type":"exact"},{"name":"susceptibility to X-linked autism 3","type":"related"}],"termid":"MONDO:0010342","xrefs":{"Monarch":{"xref_id":"0010342"}}}


id: PBO:0081714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 639","termid":"PBO:0081714"}


id: MONDO:0014833
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":"heart and brain malformation syndrome","secondary_identifiers":["OMIM:616920","UMLS:C4310793","MEDGEN:934760"],"synonyms":[{"name":"HBMS","type":"exact"},{"name":"heart and brain malformation syndrome","type":"exact"},{"name":"heart and brain malformation syndrome; HBMS","type":"exact"}],"termid":"MONDO:0014833","xrefs":{"Monarch":{"xref_id":"0014833"}}}


id: PBO:0060982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NGFR antisense RNA 1","termid":"PBO:0060982"}


id: PBO:0077481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 201","termid":"PBO:0077481"}


id: GO:0042969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of lactone from one side of a membrane to the other. A lactone is a cyclic ester of a hydroxy carboxylic acid, containing a 1-oxacycloalkan-2-one structure, or an analogue having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete lactone transport (obsolete GO:0042969)","termid":"GO:0042969"}


id: PBO:0001736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nedd4/Rsp5 family","termid":"PBO:0001736"}


id: MONDO:0007548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Transient bullous dermolysis of the newborn is a rare subtype of dystrophic epidermolysis bullosa (DEB) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life.","definition_xrefs":["Orphanet:79411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa dystrophica","termid":"MONDO:0006543"}],"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":"transient bullous dermolysis of the newborn","secondary_identifiers":["OMIM:131705","UMLS:C1851573","DOID:0111345","MESH:C536979","GARD:10010","MEDGEN:343607"],"synonyms":[{"name":"DEB, bullous dermolysis of the newborn","type":"exact"},{"name":"DEB-BDN","type":"exact"},{"name":"MONDON","type":"related"},{"name":"TBDN","type":"related"},{"name":"dystrophic epidermolysis bullosa, neonatal","type":"related"},{"name":"epidermolysis bullosa dystrophica, dominant neonatal form","type":"related"},{"name":"epidermolysis bullosa dystrophica, neonatal form","type":"related"},{"name":"transient bullous dermolysis of the newborn","type":"exact"},{"name":"transient bullous of the newborn","type":"exact"}],"termid":"MONDO:0007548","xrefs":{"Monarch":{"xref_id":"0007548"}}}


id: GO:0099063
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic recycling endosome membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of postsynaptic recycling endosome membrane (obsolete GO:0099063)","termid":"GO:0099063"}


id: MONDO:1012486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spinal intradural arachnoid cyst, non-human animal","termid":"MONDO:1011892"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal intradural arachnoid cyst, dog","secondary_identifiers":["OMIA:001923-9615"],"termid":"MONDO:1012486","xrefs":{"Monarch":{"xref_id":"1012486"}}}


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


id: MONDO:0023642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular motility disease","termid":"MONDO:0001584"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Weber syndrome","secondary_identifiers":["ICD9:344.89","GARD:8676","MEDGEN:96812","UMLS:C0455717","SCTID:24654003","icd11.foundation:1609214113"],"synonyms":[{"name":"Midbrain stroke syndromes","type":"related"},{"name":"Weber Syndrome","type":"related"},{"name":"Weber-Gubler syndrome","type":"exact"}],"termid":"MONDO:0023642","xrefs":{"Monarch":{"xref_id":"0023642"}}}


id: MONDO:0021452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the cornea.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cornea neoplasm","termid":"MONDO:0021238"},{"relation_name":"is_a","term_name":"benign neoplasm of eye","termid":"MONDO:0021454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"benign neoplasm of cornea","secondary_identifiers":["SCTID:92070006","NCIT:C3623","UMLS:C0154026","icd11.foundation:568257604","ICD9:224.4","MEDGEN:57579"],"synonyms":[{"name":"benign cornea neoplasm","type":"exact"},{"name":"benign cornea tumor","type":"exact"},{"name":"benign cornea tumour","type":"exact"},{"name":"benign corneal neoplasm","type":"exact"},{"name":"benign corneal tumor","type":"exact"},{"name":"benign corneal tumour","type":"exact"},{"name":"benign neoplasm of the cornea","type":"exact"},{"name":"benign tumor of cornea","type":"exact"},{"name":"benign tumor of the cornea","type":"exact"},{"name":"benign tumour of cornea","type":"exact"},{"name":"benign tumour of the cornea","type":"exact"},{"name":"cornea benign neoplasm","type":"exact"}],"termid":"MONDO:0021452","xrefs":{"Monarch":{"xref_id":"0021452"}}}


id: FYPO:0003100
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 heterochromatin assembly is normal (i.e. indistinguishable from wild type) in regions containing protein-coding genes. Heterochromatin assembly is the assembly of chromatin into a compact and highly condensed form that is often, but not always, transcriptionally silent.","definition_xrefs":["PMID:24095277","PomBase:mah","GO:0031507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal heterochromatin assembly","termid":"FYPO:0003099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal heterochromatin assembly at protein coding gene","synonyms":[{"name":"normal heterochromatin assembly at protein coding gene during mitotic cell cycle","type":"related"},{"name":"normal heterochromatin assembly at protein coding gene during vegetative growth","type":"exact"},{"name":"normal heterochromatin assembly at protein-coding gene","type":"exact"},{"name":"normal heterochromatin formation at protein coding gene","type":"exact"}],"termid":"FYPO:0003100"}


id: GO:0004977
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with melanocortin to initiate a change in cell activity.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled peptide receptor activity","termid":"GO:0008528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"melanocortin receptor activity","termid":"GO:0004977"}


id: PATO:0000641
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000641 deposition defective (obsolete PATO:0000641)","termid":"PATO:0000641"}


id: PBO:0027640
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-fragmented_spindle_during_meiosis_II","termid":"PBO:0027640"}


id: PBO:0073260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 7 pseudogene 4","termid":"PBO:0073260"}


id: GO:0035065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the addition of an acetyl group to a histone protein.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone acetylation (obsolete GO:0035065)","termid":"GO:0035065"}


id: PBO:0066820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 119","termid":"PBO:0066820"}


id: GO:0035916
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism effects a change in the frequency, rate or extent of the activity of a calcium channel in another organism.","definition_xrefs":["GOC:fj","PMID:20920515","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of ion channel activity in another organism","termid":"GO:0044561"}],"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":"modulation of calcium channel activity in another organism","synonyms":[{"name":"modulation of calcium channel activity in other organism","type":"exact"}],"termid":"GO:0035916"}


id: PBO:0030263
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_erythromycin","termid":"PBO:0030263"}


id: PBO:0044206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cathepsin L pseudogene 4","termid":"PBO:0044206"}


id: PBO:0072806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 3","termid":"PBO:0072806"}


id: PBO:0084844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; has similarity to E. coli L7/L12 and human MRPL7 ribosomal proteins; associates with the mitochondrial nucleoid; required for normal respiratory growth","termid":"PBO:0084844"}


id: PBO:0073112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short chain dehydrogenase/reductase family 42E, member 1","termid":"PBO:0073112"}


id: GO:0002483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses a peptide antigen of endogenous origin on its cell surface in association with an MHC protein complex. The peptide is typically a fragment of a larger endogenous protein which has been degraded within the cell.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation of endogenous antigen","termid":"GO:0019883"},{"relation_name":"is_a","term_name":"antigen processing and presentation of peptide antigen","termid":"GO:0048002"}],"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":"antigen processing and presentation of endogenous peptide antigen","synonyms":[{"name":"endogenous peptide antigen processing and presentation","type":"exact"}],"termid":"GO:0002483"}


id: MONDO:0008073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.","definition_xrefs":["Orphanet:209886"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal dominant medullary cystic kidney disease with or without hyperuricemia","termid":"MONDO:0008264"},{"relation_name":"is_a","term_name":"familial juvenile hyperuricemic nephropathy","termid":"MONDO:0000608"},{"relation_name":"is_a","term_name":"autosomal dominant medullary cystic kidney disease with or without hyperuricemia","termid":"MONDO:0008264"},{"relation_name":"is_a","term_name":"inborn disorder of purine metabolism","termid":"MONDO:0019236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005240","MONDO:0019254","MONDO:0005066"],"is_obsolete":false,"name":"familial juvenile hyperuricemic nephropathy type 1","secondary_identifiers":["MEDGEN:1645893","NORD:827","SCTID:445503007","UMLS:C4551496","OMIM:162000","OMIM:603860","GARD:10679","NCIT:C123172","OMIM:609886","Orphanet:88950","MESH:C563693"],"synonyms":[{"name":"ADMCKD2","type":"related"},{"name":"ADTKD-UMOD","type":"exact"},{"name":"Autosomal Dominant Tubulo-Interstitial Kidney Disease","type":"exact"},{"name":"FJHN type 1","type":"exact"},{"name":"HNFJ1","type":"exact"},{"name":"MCKD2","type":"related"},{"name":"UMOD familial juvenile hyperuricemic nephropathy","type":"exact"},{"name":"UMOD-associated FJHN","type":"exact"},{"name":"UMOD-associated familial juvenile hyperuricemic nephropathy","type":"exact"},{"name":"UMOD-related ADTKD","type":"exact"},{"name":"UMOD-related autosomal dominant tubulointerstitial kidney disease","type":"related"},{"name":"UMOD-related kidney disease","type":"exact"},{"name":"autosomal dominant medullary cystic kidney disease type 2","type":"exact"},{"name":"autosomal dominant medullary cystic kidney disease with hyperuricemia","type":"exact"},{"name":"autosomal dominant tubulointerstitial kidney disease - UMOD","type":"exact"},{"name":"autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD","type":"exact"},{"name":"familial juvenile gouty nephropathy","type":"broad"},{"name":"familial juvenile hyperuricaemic nephropathy","type":"related"},{"name":"familial juvenile hyperuricemic nephropathy caused by mutation in UMOD","type":"exact"},{"name":"familial nephropathy with gout","type":"broad"},{"name":"glomerulocystic kidney disease with hyperuricemia and isosthenuria","type":"exact"},{"name":"gouty nephropathy, familial juvenile","type":"broad"},{"name":"hyperuricemic nephropathy, familial juvenile","type":"broad"},{"name":"hyperuricemic nephropathy, familial juvenile, 1","type":"exact"},{"name":"hyperuricemic nephropathy, familial juvenile, type 1","type":"exact"},{"name":"medullary cystic kidney disease 2","type":"exact"},{"name":"medullary cystic kidney disease 2, autosomal dominant","type":"related"},{"name":"medullary cystic kidney disease type 2","type":"exact"},{"name":"medullary cystic kidney disease type II","type":"exact"},{"name":"nephropathy, familial, with gout","type":"broad"},{"name":"tubulointerstitial kidney disease, autosomal dominant, 1","type":"exact"},{"name":"uromodulin storage disease","type":"exact"},{"name":"uromodulin-associated kidney disease","type":"exact"}],"termid":"MONDO:0008073","xrefs":{"Monarch":{"xref_id":"0008073"}}}


id: GO:1900950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of 18-methylnonadec-1-ene biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of olefin biosynthetic process","termid":"GO:1900911"},{"relation_name":"is_a","term_name":"regulation of 18-methylnonadec-1-ene metabolic process","termid":"GO:1900953"},{"relation_name":"regulates","term_name":"18-methylnonadec-1-ene biosynthetic process","termid":"GO:1900881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of 18-methylnonadec-1-ene biosynthetic process","synonyms":[{"name":"regulation of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"regulation of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"regulation of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"regulation of 18-methylnonadec-1-ene synthesis","type":"exact"}],"termid":"GO:1900950"}


id: PATO:0001303
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's disposition to varying or changing.","definition_xrefs":["Dictionary:http://dictionary.reference.com/"],"direct_ancestors":[{"relation_name":"is_a","term_name":"process quality","termid":"PATO:0001236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variability","synonyms":[{"name":"variability of a physical quality","type":"related"}],"termid":"PATO:0001303"}


id: MONDO:0011068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing type 1 diabetes mellitus in which the cause of the disease is a mutation in the CTLA4 gene.","definition_xrefs":["MONDO:patterns/inherited_susceptibility","MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","termid":"MONDO:0010255"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus 12","secondary_identifiers":["OMIM:601388","UMLS:C1832392","DOID:0110751","MESH:C563326","MEDGEN:318618"],"synonyms":[{"name":"CTLA4 type 1 diabetes mellitus","type":"exact"},{"name":"IDDM12","type":"exact"},{"name":"diabetes mellitus, insulin-dependent, 12","type":"related"},{"name":"diabetes mellitus, insulin-dependent, type 12","type":"exact"},{"name":"insulin-dependent diabetes mellitus 12","type":"exact"},{"name":"type 1 diabetes mellitus caused by mutation in CTLA4","type":"exact"}],"termid":"MONDO:0011068","xrefs":{"Monarch":{"xref_id":"0011068"}}}


id: PBO:0079142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 5","termid":"PBO:0079142"}


id: PBO:0063532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ domain containing 1 pseudogene 1","termid":"PBO:0063532"}


id: MONDO:0001604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eyelid disorder","termid":"MONDO:0003382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"lagophthalmos","secondary_identifiers":["MEDGEN:57517","DOID:12959","ICD10CM:H02.2","ICD9:374.20","SCTID:60735000","ICD9:374.2","icd11.foundation:1200365909","UMLS:C0152226"],"termid":"MONDO:0001604","xrefs":{"Monarch":{"xref_id":"0001604"}}}


id: MONDO:0014809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary neoplastic syndrome in which the cause of the disease is a mutation in the DDX41 gene.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDX41-related hematologic malignancy predisposition syndrome","secondary_identifiers":["UMLS:C4225174","GARD:17899","OMIM:616871","MEDGEN:895780","Orphanet:488647"],"synonyms":[{"name":"DDX41 hereditary neoplastic syndrome","type":"exact"},{"name":"DDX41-related hematologic malignancy predisposition syndrome","type":"exact"},{"name":"MPLPF","type":"exact"},{"name":"hereditary neoplastic syndrome caused by mutation in DDX41","type":"exact"},{"name":"myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to","type":"exact"},{"name":"susceptibility to familial (multiple types) myeloproliferative/lymphoproliferative neoplasms","type":"related"}],"termid":"MONDO:0014809","xrefs":{"Monarch":{"xref_id":"0014809"}}}


id: GO:0075254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of uredospore formation, a process in which an asexual, dikaryotic, often rusty-colored spore, is formed in a structure called a uredinium.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043944"},{"relation_name":"is_a","term_name":"regulation of uredospore formation","termid":"GO:0075252"},{"relation_name":"negatively_regulates","term_name":"uredospore formation","termid":"GO:0075251"}],"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 uredospore formation","synonyms":[{"name":"negative regulation of ureidospore formation","type":"exact"}],"termid":"GO:0075254"}


id: PBO:0086889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transmembrane polyol transporter; supports growth on and uptake of mannitol, sorbitol and xylitol with moderate affinity when overexpressed in a strain deleted for hexose family members; minor hexose transport activity when overexpressed in a similar strain; similarity to hexose transporters; expression is induced by low levels of glucose and repressed by high levels of glucose","termid":"PBO:0086889"}


id: RO:HOM0000024
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Paralogy that results from a duplication preceding a given speciation event.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_paralogy_relationship_with","termid":"RO:HOM0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_out-paralogy_relationship_with","synonyms":[{"name":"alloparalogy","type":"exact"},{"name":"out-paralogous to","type":"exact"},{"name":"outparalogy","type":"exact"}],"termid":"RO:HOM0000024"}


id: MONDO:0001384
data:
  {"annotated_genes":["SJAG_03233","SJAG_04553"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032941"},{"annotations":[85532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012154"}]},"cv_name":"mondo","definition":"The condition in which the individual does not see far distances clearly.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"refractive error","termid":"MONDO:0004892"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03233":null,"SJAG_04553":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"myopia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["HP:0000545","SCTID:57190000","MESH:D009216","ICD10CM:H52.1","DOID:11830","icd11.foundation:1666440799","ICD9:367.1","MEDGEN:44558","UMLS:C0027092","OMIMPS:160700"],"synonyms":[{"name":"myopia","type":"exact"},{"name":"myopia (disease)","type":"exact"},{"name":"near vision","type":"exact"},{"name":"near-sightedness","type":"exact"},{"name":"short-sightedness","type":"exact"}],"termid":"MONDO:0001384","terms_by_termid":{"MONDO:0012154":null,"MONDO:0032941":null},"xrefs":{"Monarch":{"xref_id":"0001384"}}}


id: GO:0044378
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The activity of binding selectively and non-covalently to DNA in a sequence-independent manner and distorting the original structure of DNA, typically a straight helix, into a bend, or increasing the bend if the original structure was intrinsically bent due to its sequence.","definition_xrefs":["GOC:jl","GOC:vw","PMID:20123079"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA binding, bending","termid":"GO:0008301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0003677","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"non-sequence-specific DNA binding, bending","synonyms":[{"name":"DNA bending involving non-sequence-specific DNA binding","type":"exact"}],"termid":"GO:0044378"}


id: PBO:0062782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 56 subfamily B member 4","termid":"PBO:0062782"}


id: PBO:0052487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 2","termid":"PBO:0052487"}


id: PBO:0067759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 59","termid":"PBO:0067759"}


id: MONDO:0021039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spectrum of malignant tumors arising from the soft tissues, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. Pain and the presence of a mass are the most common clinical symptoms.","definition_xrefs":["NCIT:C27293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ewing sarcoma/peripheral primitive neuroectodermal tumor","termid":"MONDO:0021038"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor","secondary_identifiers":["MEDGEN:232170","DOID:4985","EFO:1000250","UMLS:C1333514"],"synonyms":[{"name":"extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumor","type":"exact"},{"name":"extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumour","type":"exact"},{"name":"extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor","type":"exact"},{"name":"extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumour","type":"exact"},{"name":"extraosseous Ewing's tumor","type":"related"},{"name":"extraosseous Ewing's tumour","type":"related"},{"name":"extraosseous Ewings sarcoma-primitive neuroepithelial tumor","type":"exact"},{"name":"extraosseous Ewings sarcoma-primitive neuroepithelial tumour","type":"exact"},{"name":"extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor","type":"exact"}],"termid":"MONDO:0021039","xrefs":{"Monarch":{"xref_id":"0021039"}}}


id: FYPO:0008314
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the initial release of duplicated spindle pole bodies that occurs as part of the first meiotic nuclear division, is normal (i.e. indistinguishable from wild type).","direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal initial meiotic spindle pole body separation in meiosis I","termid":"FYPO:0008314"}


id: PBO:0030259
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_chloramphenicol","termid":"PBO:0030259"}


id: GO:2000617
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone H3-K9 acetylation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone H3-K9 acetylation (obsolete GO:2000617)","synonyms":[{"name":"positive regulation of histone H3 acetylation at K9","type":"exact"},{"name":"positive regulation of histone H3K9 acetylation","type":"exact"}],"termid":"GO:2000617"}


id: PBO:0017811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipin, phosphatidate phosphatase Ned1","termid":"PBO:0017811"}


id: PBO:0030321
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_palmitoyl-CoA_ligase_activity","termid":"PBO:0030321"}


id: PBO:0080868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YJU2 splicing factor homolog","termid":"PBO:0080868"}


id: MONDO:0014815
data:
  {"annotated_genes":["SJAG_01991"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85306],"is_not":false,"summary":null,"term":"MONDO:0014815"}]},"cv_name":"mondo","definition":"Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LMAN2L gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01991":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0006025"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 52","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081215","MEDGEN:903181","UMLS:C4225168","GARD:22572","OMIM:616887"],"synonyms":[{"name":"LMAN2L autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"MRT52","type":"exact"},{"name":"autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L","type":"exact"},{"name":"intellectual developmental disorder, autosomal recessive 52","type":"exact"},{"name":"intellectual disability, autosomal recessive 52","type":"exact"},{"name":"intellectual disability, autosomal recessive type 52","type":"exact"},{"name":"mental retardation, autosomal recessive 52","type":"exact"},{"name":"mental retardation, autosomal recessive type 52","type":"exact"}],"termid":"MONDO:0014815","terms_by_termid":{"MONDO:0014815":null},"xrefs":{"Monarch":{"xref_id":"0014815"}}}


id: GO:0102424
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (+)-sesaminol 2-O-beta-D-gentiobioside + UDP-alpha-D-glucose = (+)-sesaminol 2-O-beta-D-gentiotrioside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete sesaminol-2-O-gentiobioside 1,6-glucosyltransferase activity (obsolete GO:0102424)","termid":"GO:0102424"}


id: GO:0017146
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An assembly of four or five subunits which form a structure with an extracellular N-terminus and a large loop that together form the ligand binding domain. The C-terminus is intracellular. The ionotropic glutamate receptor complex itself acts as a ligand gated ion channel; on binding glutamate, charged ions pass through a channel in the center of the receptor complex. NMDA receptors are composed of assemblies of NR1 subunits (Figure 3) and NR2 subunits, which can be one of four separate gene products (NR2A-D). Expression of both subunits are required to form functional channels. The glutamate binding domain is formed at the junction of NR1 and NR2 subunits. NMDA receptors are permeable to calcium ions as well as being permeable to other ions. Thus NMDA receptor activation leads to a calcium influx into the post-synaptic cells, a signal thought to be crucial for the induction of NMDA-receptor dependent LTP and LTD.","definition_xrefs":["PMID:8294079"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ionotropic glutamate receptor complex","termid":"GO:0008328"}],"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:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"NMDA selective glutamate receptor complex","synonyms":[{"name":"N-methyl-D-aspartate selective glutamate receptor complex","type":"exact"},{"name":"NMDA-selective glutamate receptor","type":"exact"}],"termid":"GO:0017146"}


id: PBO:0111901
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PINT/PCI domain","termid":"PBO:0111901"}


id: PBO:0067790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 92","termid":"PBO:0067790"}


id: PBO:0088382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multidomain vesicle coat component Sec16","termid":"PBO:0088382"}


id: PBO:0084660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial 15S rRNA-binding protein; required for intron removal of COB and COX1 pre-mRNAs; has separable roles in stabilizing mitochondrial 15S rRNA and in maturation of the COB and COX1 mRNAs; contains pentatricopeptide repeat (PPR) motifs; mutant is respiratory deficient and has defective plasma membrane electron transport","termid":"PBO:0084660"}


id: GO:0031391
data:
  {"annotated_genes":["SJAG_00729","SJAG_00272","SJAG_02182","SJAG_01010","SJAG_04150"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89047,93440,94748,111762,112317],"is_not":false,"summary":null,"term":"GO:0031391"}]},"cv_name":"cellular_component","definition":"A pentameric replication factor C (RLC) complex, which unloads the DNA polymerase processivity factor proliferating cell nuclear antigen (PCNA) from chromatin and has roles in telomere length regulation and other aspects of genome stability. In Saccharomyces the subunits are known as Elg1p, Rfc2p, Rfc3p, Rfc4p, and Rfc5p.","definition_xrefs":["PMID:14614842","PMID:27664980","PMID:23499004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00729":null,"SJAG_01010":null,"SJAG_02182":null,"SJAG_04150":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Elg1 RFC-like complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Elg1-RFC","type":"exact"},{"name":"Elg1-RLC","type":"exact"},{"name":"RFC (Elg1)","type":"exact"}],"termid":"GO:0031391","terms_by_termid":{"GO:0031391":null}}


id: GO:0022414
data:
  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id: MONDO:0015954
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  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic headache disorder (obsolete MONDO:0015954)","secondary_identifiers":["Orphanet:183509"],"synonyms":[{"name":"rare genetic headache","type":"exact"}],"termid":"MONDO:0015954","xrefs":{"Monarch":{"xref_id":"0015954"}}}


id: MONDO:0016653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"2q33.1 microdeletion syndrome is a rare chromosomal anomaly syndrome, resulting from the partial deletion of the long arm of chromosome 2, with a highly variable phenotype typically characterized by severe intellectual disability, moderate to severe developmental delay (particularly speech), feeding difficulties, failure to thrive, hypotonia, thin, sparse hair, various dental abnormalities and cleft/high-arched palate. Typical dysmorphic features include high, prominent forehead, down-slanting palpebral fissures and prominent nasal bridge with beaked nose. Various behavioral problems (e.g. hyperactivity, chaotic/repetitive behavior, touch avoidance) are also associated.","definition_xrefs":["Orphanet:251028"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 2","termid":"MONDO:0016901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2q33.1 microdeletion syndrome","secondary_identifiers":["DECIPHER:51","GARD:17204","SCTID:763062006","MEDGEN:1645054","UMLS:C4706258"],"synonyms":[{"name":"Del(2)(q33.1)","type":"exact"},{"name":"monosomy 2q33.1","type":"exact"}],"termid":"MONDO:0016653","xrefs":{"Monarch":{"xref_id":"0016653"}}}


id: PBO:0056025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSP1 pseudogene 3","termid":"PBO:0056025"}


id: PBO:0076967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGFB induced factor homeobox 2 like X-linked","termid":"PBO:0076967"}


id: PBO:0017884
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae FPR1","termid":"PBO:0017884"}


id: PBO:0078551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 41","termid":"PBO:0078551"}


id: GO:0032372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of sterols into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid transport","termid":"GO:0032369"},{"relation_name":"is_a","term_name":"regulation of sterol transport","termid":"GO:0032371"},{"relation_name":"negatively_regulates","term_name":"sterol transport","termid":"GO:0015918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of sterol transport","synonyms":[{"name":"down regulation of sterol transport","type":"exact"},{"name":"down-regulation of sterol transport","type":"exact"},{"name":"downregulation of sterol transport","type":"exact"},{"name":"inhibition of sterol transport","type":"narrow"}],"termid":"GO:0032372"}


id: GO:0003037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which information about the levels of hydrogen ions are received and are converted to a molecular signal by chemoreceptors in a carotid body.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of pH by chemoreceptor signaling","termid":"GO:0003022"},{"relation_name":"part_of","term_name":"detection of hypoxic conditions in blood by carotid body chemoreceptor signaling","termid":"GO:0003029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of pH by carotid body chemoreceptor signaling","synonyms":[{"name":"detection of pH by carotid body chemoreceptor signalling","type":"exact"}],"termid":"GO:0003037"}


id: GO:0008046
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an extracellular messenger and transmitting the signal from one side of the membrane to the other to results in a change in cellular activity involved in axon guidance.","definition_xrefs":["GOC:signaling","GOC:dph","PMID:15107857","PMID:15339666","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"axon guidance receptor activity","synonyms":[{"name":"receptor activity involved in axon guidance","type":"exact"}],"termid":"GO:0008046"}


id: MONDO:0859353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary dyskinesia, primary, 49, without situs inversus","secondary_identifiers":["MEDGEN:1824064","OMIM:620197","UMLS:C5774291"],"termid":"MONDO:0859353","xrefs":{"Monarch":{"xref_id":"0859353"}}}


id: PR:Q09739
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A meiotic nuclear division protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00227"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic coiled-coil protein 7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13A11.03","secondary_identifiers":["UniProtKB:Q09739"],"synonyms":[{"name":"Spom972h-MND1","type":"exact"},{"name":"meiotically up-regulated gene 32 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09739"}


id: PBO:0052220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel modifier subfamily V member 1","termid":"PBO:0052220"}


id: SO:0001774
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant within a gene that contributes to a quantitative trait such as height or weight.","direct_ancestors":[{"relation_name":"is_a","term_name":"variant_phenotype","termid":"SO:0001769"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quantitative_variant","synonyms":[{"name":"quantitative variant","type":"exact"}],"termid":"SO:0001774"}


