# terms

id: PBO:0003047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferric-chelate reductase Frp1","termid":"PBO:0003047"}


id: GO:0001848
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a component or product of the complement cascade.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"complement binding","termid":"GO:0001848"}


id: GO:0000800
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A proteinaceous core found between sister chromatids during meiotic prophase.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"synaptonemal complex","termid":"GO:0000795"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0005694"],"is_obsolete":false,"name":"lateral element","synonyms":[{"name":"axial element","type":"exact"}],"termid":"GO:0000800"}


id: PATO:0001293
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A scalar EM radiation quality which obtains by the capacity of the bearer to retain radiation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"full-spectrum EM radiation quality","termid":"PATO:0001292"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"absorption quality","termid":"PATO:0001293"}


id: MONDO:0014897
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete portal hypertension, noncirrhotic (obsolete MONDO:0014897)","termid":"MONDO:0014897","xrefs":{"Monarch":{"xref_id":"0014897"}}}


id: PBO:0055709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"limb development membrane protein 1","termid":"PBO:0055709"}


id: MONDO:0006320
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Melanoma is a malignant tumor of melanocytes, cells that are derived from the neural crest. Although most melanomas arise in the skin, they also may arise from mucosal surfaces or at other sites to which neural crest cells migrate. (PDQ)","definition_xrefs":["NCIT:C8711"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-cutaneous melanoma","secondary_identifiers":["EFO:1000397","MEDGEN:233761","UMLS:C1334974"],"synonyms":[{"name":"extracutaneous melanoma","type":"exact"},{"name":"non-cutaneous melanoma","type":"exact"}],"termid":"MONDO:0006320","xrefs":{"Monarch":{"xref_id":"0006320"}}}


id: MONDO:0007487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyslexia, susceptibility to, 1","secondary_identifiers":["UMLS:C1851967","MEDGEN:338828","OMIM:127700"],"synonyms":[{"name":"DYX1","type":"related"},{"name":"Word-blindness, congenital","type":"related"},{"name":"dyslexia, susceptibility to, 1","type":"exact"},{"name":"dyslexia, susceptibility to, 4","type":"related"},{"name":"dyslexia, susceptibility to, 7","type":"related"},{"name":"dyslexia, susceptibility to, type 1","type":"exact"},{"name":"reading disability, specific, 1","type":"related"},{"name":"susceptibility to dyslexia 1","type":"related"}],"termid":"MONDO:0007487","xrefs":{"Monarch":{"xref_id":"0007487"}}}


id: GO:0097174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 1,6-anhydro-N-acetyl-beta-muramic acid, the 1,6-anhydro-derivative of N-acetyl-beta-muramic acid.","definition_xrefs":["GOC:yaf","PMID:15901686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"1,6-anhydro-N-acetyl-beta-muramic acid metabolic process","synonyms":[{"name":"1,6-anhydro-N-acetyl-beta-muramate metabolic process","type":"exact"},{"name":"1,6-anhydro-N-acetyl-beta-muramate metabolism","type":"exact"},{"name":"1,6-anhydro-N-acetyl-beta-muramic acid metabolism","type":"exact"},{"name":"1,6-anhydro-N-acetylmuramic acid metabolic process","type":"exact"},{"name":"1,6-anhydro-N-acetylmuramic acid metabolism","type":"exact"}],"termid":"GO:0097174"}


id: PBO:0059069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molybdenum cofactor sulfurase","termid":"PBO:0059069"}


id: PATO:0000763
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A behavioral quality inhering in a bearer by virtue of the bearer's being affected by loss of the ability to move a body part.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement behavioral quality","termid":"PATO:0002076"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paralysed","synonyms":[{"name":"palsy","type":"narrow"}],"termid":"PATO:0000763"}


id: MONDO:0004950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the stomach.","direct_ancestors":[{"relation_name":"is_a","term_name":"gastric cancer","termid":"MONDO:0001056"},{"relation_name":"is_a","term_name":"digestive system carcinoma","termid":"MONDO:0006181"}],"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":"gastric carcinoma","secondary_identifiers":["UMLS:C0699791","ICD9:151.3","MEDGEN:147066","SCTID:92756002","EFO:0000178","NCIT:C4911","ICD9:230.2","DOID:10538","SCTID:187741001","DOID:5517"],"synonyms":[{"name":"Ca fundus - stomach","type":"narrow"},{"name":"cancer of fundus of stomach","type":"narrow"},{"name":"cancer of stomach","type":"broad"},{"name":"cancer of the stomach","type":"broad"},{"name":"carcinoma of stomach","type":"exact"},{"name":"carcinoma of the stomach","type":"exact"},{"name":"fundus of stomach cancer","type":"narrow"},{"name":"gastric (stomach) cancer","type":"broad"},{"name":"gastric cancer","type":"broad"},{"name":"gastric cancer, NOS","type":"broad"},{"name":"gastric carcinoma","type":"exact"},{"name":"gastric fundus cancer","type":"narrow"},{"name":"malignant fundus of stomach neoplasm","type":"narrow"},{"name":"malignant neoplasm of fundus of stomach","type":"narrow"},{"name":"malignant tumor of fundus of stomach","type":"narrow"},{"name":"malignant tumour of fundus of stomach","type":"narrow"},{"name":"stomach cancer","type":"broad"},{"name":"stomach carcinoma","type":"exact"}],"termid":"MONDO:0004950","xrefs":{"Monarch":{"xref_id":"0004950"}}}


id: GO:0015488
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: glucuronide(out) + monovalent cation(out) = glucuronide(in) + monovalent cation(in).","definition_xrefs":["TC:2.A.2.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucuronoside transmembrane transporter activity","termid":"GO:0015164"},{"relation_name":"is_a","term_name":"glycoside-pentoside-hexuronide:cation symporter activity","termid":"GO:0015486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"glucuronide:cation symporter activity","synonyms":[{"name":"glucuronide:monovalent cation symporter activity","type":"exact"},{"name":"glucuronoside permease activity","type":"related"}],"termid":"GO:0015488"}


id: GO:0071628
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of a fungal-type vacuole membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of fungal-type vacuolar membrane (obsolete GO:0071628)","termid":"GO:0071628"}


id: GO:1990658
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transferase complex which is capable of transferring nitrogenous groups from one component to another.","definition_xrefs":["PMID:25417112","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"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:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"transnitrosylase complex","synonyms":[{"name":"transferase complex, transferring nitrogenous groups","type":"exact"}],"termid":"GO:1990658"}


id: PBO:0073861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 9 member A9","termid":"PBO:0073861"}


id: PBO:0076801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tektin 2","termid":"PBO:0076801"}


id: GO:0120158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of collagen catabolism. Collagen catabolism is the proteolytic chemical reactions and pathways resulting in the breakdown of collagen in the extracellular matrix.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"regulation of collagen catabolic process","termid":"GO:0010710"},{"relation_name":"is_a","term_name":"positive regulation of collagen metabolic process","termid":"GO:0010714"},{"relation_name":"positively_regulates","term_name":"collagen catabolic process","termid":"GO:0030574"}],"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 collagen catabolic process","synonyms":[{"name":"activation of collagen catabolic process","type":"narrow"},{"name":"positive regulation of collagen breakdown","type":"exact"},{"name":"positive regulation of collagen catabolism","type":"exact"},{"name":"positive regulation of collagen degradation","type":"exact"},{"name":"up regulation of collagen catabolic process","type":"exact"},{"name":"up-regulation of collagen catabolic process","type":"exact"},{"name":"upregulation of collagen catabolic process","type":"exact"}],"termid":"GO:0120158"}


id: FYPO:0007372
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of chlorpromazine than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000139","FYPO:0002682","FYPO:0000003"],"is_obsolete":false,"name":"resistance to chlorpromazine","synonyms":[{"name":"resistance to chlorpromazine during mitotic cell cycle","type":"related"},{"name":"resistance to chlorpromazine during vegetative growth","type":"exact"},{"name":"resistant to chlorpromazine","type":"exact"}],"termid":"FYPO:0007372"}


id: MONDO:0013292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The 4q21 microdeletion syndrome is a newly described syndrome associated with facial dysmorphism, progressive growth restriction, severe intellectual deficit and absent or severely delayed speech.","definition_xrefs":["Orphanet:238750"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 4","termid":"MONDO:0016903"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 4q21 deletion syndrome","secondary_identifiers":["GARD:17181","MEDGEN:462106","OMIM:613509","UMLS:C3150756","SCTID:719660008","DOID:0060420"],"synonyms":[{"name":"4q21 microdeletion syndrome","type":"exact"},{"name":"Del(4)(q21)","type":"exact"},{"name":"chromosome 4q21 deletion syndrome","type":"exact"},{"name":"chromosome 4q21 deletion syndrome, isolated cases","type":"exact"},{"name":"monosomy 4q21","type":"exact"}],"termid":"MONDO:0013292","xrefs":{"Monarch":{"xref_id":"0013292"}}}


id: PBO:0066864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 164","termid":"PBO:0066864"}


id: PBO:0073811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC6A14 pseudogene 2","termid":"PBO:0073811"}


id: MONDO:0012307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.","definition_xrefs":["Orphanet:168624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial scaphocephaly syndrome","termid":"MONDO:0015704"}],"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":"familial scaphocephaly syndrome, McGillivray type","secondary_identifiers":["GARD:3426","icd11.foundation:512057922","MESH:C566511","MEDGEN:355365","UMLS:C1865070","OMIM:609579"],"synonyms":[{"name":"scaphocephaly, maxillary retrusion, and intellectual disability","type":"related"},{"name":"scaphocephaly, maxillary retrusion, and mental retardation","type":"related"},{"name":"scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome","type":"exact"}],"termid":"MONDO:0012307","xrefs":{"Monarch":{"xref_id":"0012307"}}}


id: PBO:0059977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 22","termid":"PBO:0059977"}


id: PBO:0085759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase involved in response to oxidative and osmotic stress; identified as suppressor of S. pombe cell cycle checkpoint mutations; similar to CaM (calmodulin) kinases; RCK2 has a paralog, RCK1, that arose from the whole genome duplication","termid":"PBO:0085759"}


id: PBO:0066959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 261","termid":"PBO:0066959"}


id: GO:0044739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism positively regulates the activity of a voltage-gated sodium channel in another organism.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of acid-sensing ion channel in another organism","termid":"GO:0044737"}],"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 acid-sensing ion channel in another organism","synonyms":[{"name":"positive regulation of ASIC channel in other organism","type":"exact"},{"name":"positive regulation of acid-sensing ion channel in other organism","type":"exact"}],"termid":"GO:0044739"}


id: PBO:0088038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-conjugating enzyme; key E2 partner with Ubc4p for the anaphase-promoting complex (APC); mediates selective degradation of short-lived and abnormal proteins; plays a role in vesicle biogenesis and ER-associated protein degradation (ERAD); component of the cellular stress response; protein abundance increases in response to DNA replication stress key E2 partner with Ubc4p for the anaphase-promoting complex (APC)","termid":"PBO:0088038"}


id: PBO:0109055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat protein Ank1","termid":"PBO:0109055"}


id: MONDO:0004481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pancreatic intraductal papillary mucinous neoplasm characterized by the presence of a focal or multifocal invasive carcinomatous component. The invasive carcinoma is either colloid or ductal adenocarcinoma.","definition_xrefs":["NCIT:C5726"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic intraductal papillary-mucinous carcinoma","termid":"MONDO:0004285"},{"relation_name":"is_a","term_name":"pancreatic intraductal papillary-mucinous neoplasm","termid":"MONDO:0004286"},{"relation_name":"is_a","term_name":"pancreatic adenocarcinoma","termid":"MONDO:0006047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma","secondary_identifiers":["UMLS:C1518871","DOID:8150","MEDGEN:275329","ICDO:8453/3"],"synonyms":[{"name":"pancreatic intraductal papillary mucinous neoplasm with an associated invasive carcinoma","type":"exact"},{"name":"pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma","type":"exact"},{"name":"pancreatic invasive intraductal papillary-mucinous carcinoma","type":"exact"}],"termid":"MONDO:0004481","xrefs":{"Monarch":{"xref_id":"0004481"}}}


id: GO:0009243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the O side chain of a lipopolysaccharide, which determines the antigenic specificity of the organism. It is made up of about 50 repeating units of a branched tetrasaccharide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide biosynthetic process","termid":"GO:0000271"},{"relation_name":"is_a","term_name":"O antigen metabolic process","termid":"GO:0046402"},{"relation_name":"part_of","term_name":"lipopolysaccharide biosynthetic process","termid":"GO:0009103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"O antigen biosynthetic process","synonyms":[{"name":"O antigen anabolism","type":"exact"},{"name":"O antigen biosynthesis","type":"exact"},{"name":"O antigen formation","type":"exact"},{"name":"O antigen synthesis","type":"exact"}],"termid":"GO:0009243"}


id: MONDO:0000725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Simpson-Golabi-Behmel syndrome (obsolete MONDO:0000725)","termid":"MONDO:0000725","xrefs":{"Monarch":{"xref_id":"0000725"}}}


id: PBO:0113563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase complex subunit, Ost4","termid":"PBO:0113563"}


id: PBO:0057489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 607","termid":"PBO:0057489"}


id: GO:0140525
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The pole of the kinetoplast associated with kinetoplast DNA replication. The antipodal sites flank the kinetoplast DNA disk and are positioned approximately 180 degrees apart. In Trypanosoma brucei and Crithidia fasciculata, minicircles are attached at antipodal sites and they contain enzymes that catalyse some of the later reactions in minicircle replication.","definition_xrefs":["PMID:17462016","PMID:8045928","PMID:12455998"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinetoplast","termid":"GO:0020023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005739","GO:0005737"],"is_obsolete":false,"name":"antipodal site","synonyms":[{"name":"antipodal zone","type":"exact"}],"termid":"GO:0140525"}


id: GO:0071951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification process that results in the conversion of methionine charged on a tRNA(fMet) to N-formyl-methionine-tRNA(fMet).","definition_xrefs":["GOC:jsg","PMID:5337045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"charged-tRNA amino acid modification","termid":"GO:0019988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0006399","GO:0010467"],"is_obsolete":false,"name":"conversion of methionyl-tRNA to N-formyl-methionyl-tRNA","termid":"GO:0071951"}


id: MONDO:0017053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intermittent maple syrup urine disease (intermittent MSUD) is a mild form of MSUD where patients (when well) are asymptomatic with normal levels of branched-chain amino acids (BCAAs) but with catabolic stress are at risk of acute decompensation with ketoacidosis, which can lead to cerebral edema and coma if untreated.","definition_xrefs":["Orphanet:268173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maple syrup urine disease","termid":"MONDO:0009563"}],"gene_count":0,"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":"intermittent maple syrup urine disease","secondary_identifiers":["GARD:17265","NANDO:2201080","MEDGEN:78690","SCTID:405288003","UMLS:C0268569"],"synonyms":[{"name":"intermittent BCKD deficiency","type":"exact"},{"name":"intermittent MSUD","type":"exact"},{"name":"intermittent branched-chain 2-ketoacid dehydrogenase deficiency","type":"exact"},{"name":"intermittent branched-chain alpha-ketoacid dehydrogenase deficiency","type":"exact"},{"name":"intermittent maple syrup urine disease","type":"exact"}],"termid":"MONDO:0017053","xrefs":{"Monarch":{"xref_id":"0017053"}}}


id: GO:0034680
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integrin complex that comprises one alpha10 subunit and one beta1 subunit.","definition_xrefs":["PMID:12297042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integrin complex","termid":"GO:0008305"}],"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:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"integrin alpha10-beta1 complex","synonyms":[{"name":"ITGA10-ITGB1 complex","type":"narrow"},{"name":"alpha10-beta1 integrin complex","type":"exact"}],"termid":"GO:0034680"}


id: GO:0015726
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which L-idonate is transported across a lipid bilayer, from one side of a membrane to the other. L-idonate is an aldonic acid derived from L-idose, an aldohexose which is epimeric with D-glucose.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transport","termid":"GO:0034219"},{"relation_name":"is_a","term_name":"aldonate transmembrane transport","termid":"GO:0042873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"L-idonate transmembrane transport","synonyms":[{"name":"L-idonate transport","type":"related"}],"termid":"GO:0015726"}


id: PBO:0029778
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_branched,_curved,_elongated_vegetative_cell","termid":"PBO:0029778"}


id: MONDO:0010870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A distal myopathy characterized by weakness of the muscles of the anterior compartment of lower limbs, appearing in the fourth to seventh decade of life.","definition_xrefs":["Orphanet:609"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant distal myopathy","termid":"MONDO:0016108"},{"relation_name":"is_a","term_name":"autosomal dominant titinopathy","termid":"MONDO:0100494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0000426","MONDO:0005336"],"is_obsolete":false,"name":"tibial muscular dystrophy","secondary_identifiers":["MEDGEN:333047","DOID:0111078","SCTID:698846009","UMLS:C1838244","OMIM:600334","GARD:13154"],"synonyms":[{"name":"Finnish tibial muscular dystrophy","type":"exact"},{"name":"TMD","type":"exact"},{"name":"Tmd","type":"related"},{"name":"Udd myopathy","type":"exact"},{"name":"Udd type distal myopathy","type":"exact"},{"name":"distal myopathy, Udd type","type":"exact"},{"name":"distal titinopathy","type":"exact"},{"name":"tardive tibial muscular dystrophy","type":"exact"},{"name":"tibial muscular dystrophy, tardive","type":"related"}],"termid":"MONDO:0010870","xrefs":{"Monarch":{"xref_id":"0010870"}}}


id: MONDO:0000104
data:
  {"annotated_genes":["SJAG_01007"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008787"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypochromic microcytic anemia","termid":"MONDO:0000387"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01007":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"anemia, hypochromic microcytic with iron overload","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C2673913","OMIMPS:206100","MESH:C567144","MEDGEN:388759"],"synonyms":[{"name":"anemia, hypochromic microcytic, with iron overload","type":"exact"}],"termid":"MONDO:0000104","terms_by_termid":{"MONDO:0008787":null},"xrefs":{"Monarch":{"xref_id":"0000104"}}}


id: GO:1904784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a NLRP1 inflammasome complex.","definition_xrefs":["GO_REF:0000079","GOC:TermGenie","PMID:19124602"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canonical inflammasome complex assembly","termid":"GO:0140632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0065003","GO:0023052"],"is_obsolete":false,"name":"NLRP1 inflammasome complex assembly","synonyms":[{"name":"NALP1 inflammasome complex assembly","type":"exact"},{"name":"NALP1 inflammasome complex formation","type":"exact"},{"name":"NLRP1 inflammasome complex formation","type":"exact"}],"termid":"GO:1904784"}


id: GO:0051723
data:
  {"annotated_genes":["SJAG_01628"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051722"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: protein amino acid methyl ester + H2O = protein amino acid + methanol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01628":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0016787","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"protein methylesterase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5367022"],"synonyms":[{"name":"PME activity","type":"related"},{"name":"protein carboxyl methylesterase activity","type":"related"},{"name":"protein carboxylic ester hydrolase activity","type":"exact"},{"name":"protein methyl-esterase activity","type":"related"}],"termid":"GO:0051723","terms_by_termid":{"GO:0051722":null}}


id: MONDO:0004435
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually aggressive malignant neoplasm arising from the liver. It is characterized by the presence of spindle-shaped fibroblasts and collagenous stroma formation in a herringbone growth pattern.","definition_xrefs":["NCIT:C5832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver sarcoma","termid":"MONDO:0002397"},{"relation_name":"is_a","term_name":"fibrosarcoma","termid":"MONDO:0005164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"liver fibrosarcoma","secondary_identifiers":["MEDGEN:232274","UMLS:C1333966","DOID:8022"],"synonyms":[{"name":"fibrosarcoma of liver","type":"exact"},{"name":"fibrosarcoma of the liver","type":"exact"},{"name":"hepatic fibrosarcoma","type":"exact"},{"name":"liver fibrosarcoma","type":"exact"},{"name":"liver fibrosarcoma (disease)","type":"exact"}],"termid":"MONDO:0004435","xrefs":{"Monarch":{"xref_id":"0004435"}}}


id: MONDO:0019215
data:
  {"annotated_genes":["SJAG_00737","SJAG_02641","SJAG_03560","SJAG_03069","SJAG_01199","SJAG_00944","SJAG_03258","SJAG_00413","SJAG_01597","SJAG_00947"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009603"},{"annotations":[86452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009787"},{"annotations":[84878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012435"},{"annotations":[86528,86529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044723"},{"annotations":[84816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044724"},{"annotations":[86547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008760"},{"annotations":[85187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013661"},{"annotations":[85808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009666"},{"annotations":[86208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn organic aciduria","termid":"MONDO:0000688"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00413":null,"SJAG_00737":null,"SJAG_00944":null,"SJAG_00947":null,"SJAG_01199":null,"SJAG_01597":null,"SJAG_02641":null,"SJAG_03069":null,"SJAG_03258":null,"SJAG_03560":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:0004736","MONDO:0005066"],"is_obsolete":false,"name":"classic organic aciduria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842457","Orphanet:79163","UMLS:C5681291","GARD:18947","icd11.foundation:1879509617"],"termid":"MONDO:0019215","terms_by_termid":{"MONDO:0008760":null,"MONDO:0009603":null,"MONDO:0009666":null,"MONDO:0009787":null,"MONDO:0010184":null,"MONDO:0012435":null,"MONDO:0013661":null,"MONDO:0044723":null,"MONDO:0044724":null},"xrefs":{"Monarch":{"xref_id":"0019215"}}}


id: MONDO:1010084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dermatomyositis characterized by the presence of anti-NXP2 autoantibodies.","definition_xrefs":["PMID:31279808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatomyositis","termid":"MONDO:0016367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005336"],"is_obsolete":false,"name":"anti-NXP2 dermatomyositis","synonyms":[{"name":"anti-nuclear matrix protein 2 dermatomyositis","type":"exact"}],"termid":"MONDO:1010084","xrefs":{"Monarch":{"xref_id":"1010084"}}}


id: GO:0090562
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + N,N'-diacetylchitobiose(out) = protein histidine + N,N'-diacetylchitobiose phosphate(in).","definition_xrefs":["GOC:am","PMID:10913119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"}],"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:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0005215","GO:0022857","GO:0003824"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-N,N'-diacetylchitobiose phosphotransferase system transporter activity","termid":"GO:0090562"}


id: PBO:0025432
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid metabolism disorders","termid":"PBO:0025432"}


id: GO:1903508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of nucleic acid-templated transcription.","definition_xrefs":["GOC:vw","GOC:TermGenie","GO_REF:0000058","GOC:pr","GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of nucleic acid-templated transcription (obsolete GO:1903508)","synonyms":[{"name":"activation of nucleic acid-templated transcription","type":"narrow"},{"name":"up regulation of nucleic acid-templated transcription","type":"exact"},{"name":"up-regulation of nucleic acid-templated transcription","type":"exact"},{"name":"upregulation of nucleic acid-templated transcription","type":"exact"}],"termid":"GO:1903508"}


id: PBO:0059697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO2 pseudogene 5","termid":"PBO:0059697"}


id: GO:1990471
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to uni-strand piRNA clusters, double-stranded DNA regions that give rise to PIWI-interacting RNAs (piRNAs) that map predominantly to only one strand and exhibit hallmarks of canonical Pol II transcription. Uni-strand piRNA clusters are found in many taxa.","definition_xrefs":["GOC:bhm","PMID:24906153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"piRNA cluster binding","termid":"GO:1990470"}],"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:0005488","GO:0003677","GO:0003674"],"is_obsolete":false,"name":"piRNA uni-strand cluster binding","termid":"GO:1990471"}


id: SO:0001989
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A 5' UTR variant where a premature start codon is lost.","definition_xrefs":["SANGER:am"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5_prime_UTR_premature_start_codon_variant","termid":"SO:0001983"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_prime_UTR_premature_start_codon_loss_variant","termid":"SO:0001989"}


id: PBO:0001779
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disruption of interaction between Cdc27 and Pcn1 makes Cdc24-Dna2 complex dispensible","termid":"PBO:0001779"}


id: MONDO:0007079
data:
  {"annotated_genes":["SJAG_01457"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86845],"is_not":false,"summary":null,"term":"MONDO:0007079"}]},"cv_name":"mondo","definition":"Physical and psychological dependence on alcohol.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"drug dependence","termid":"MONDO:0005303"},{"relation_name":"is_a","term_name":"alcohol-related disorders","termid":"MONDO:0021698"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01457":null},"genotype_count":0,"is_obsolete":false,"name":"alcohol dependence","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1580466198","MESH:D019973","NCIT:C3325","SCTID:66590003","OMIM:103780","DOID:0050741","ICD9:303.90","MEDGEN:1801","MESH:D010610","UMLS:C0001973","NCIT:C93040","ICD9:305.0","MESH:D000437"],"synonyms":[{"name":"aerodigestive tract cancer, squamous cell, alcohol-related, protection against","type":"related"},{"name":"alcohol dependence","type":"exact"},{"name":"alcohol dependence, protection against","type":"related"},{"name":"alcohol dependence, susceptibility to","type":"related"},{"name":"alcoholism","type":"exact"}],"termid":"MONDO:0007079","terms_by_termid":{"MONDO:0007079":null},"xrefs":{"Monarch":{"xref_id":"0007079"}}}


id: PBO:0012293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome segregation impaired protein 1","termid":"PBO:0012293"}


id: PBO:0109831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex alpha subunit Apl3","termid":"PBO:0109831"}


id: FYPO:0006019
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 excess endoplasmic reticulum (ER) membrane forms stacks adjacent to the nucleus, known as karmellae.","definition_xrefs":["PMID:16607018","PomBase:mah","PMID:28242692"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear envelope morphology during vegetative growth","termid":"FYPO:0000769"},{"relation_name":"is_a","term_name":"excess endoplasmic reticulum membrane present","termid":"FYPO:0001784"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002403"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002403","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"karmellae present","synonyms":[{"name":"karmellae formation","type":"related"}],"termid":"FYPO:0006019"}


id: MONDO:0010308
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An X-linked condition caused by mutation(s) in the GATA1 gene, encoding erythroid transcription factor. It is characterized by thrombocytopenia, as well as abnormal platelet function and morphology. Dyserythropoietic anemia of variable severity may also be present.","definition_xrefs":["NCIT:C136653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombocytopenia","termid":"MONDO:0100241"}],"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":"thrombocytopenia, X-linked, with or without dyserythropoietic anemia","secondary_identifiers":["MEDGEN:763703","OMIM:300367","UMLS:C3550789"],"synonyms":[{"name":"X-linked thrombocytopenia, with or without dyserythropoietic Anaemia","type":"exact"},{"name":"X-linked thrombocytopenia, with or without dyserythropoietic Anemia","type":"exact"},{"name":"XLTDA","type":"related"},{"name":"thrombocytopenia, X-linked, with or without dyserythropoietic anemia","type":"exact"},{"name":"thrombocytopenia, X-linked, with or without dyserythropoietic anemia, X-linked recessive","type":"exact"}],"termid":"MONDO:0010308","xrefs":{"Monarch":{"xref_id":"0010308"}}}


id: GO:1903378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of oxidative stress-induced neuron intrinsic apoptotic signaling pathway.","definition_xrefs":["GOC:bf","GOC:PARL","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of neuron apoptotic process","termid":"GO:0043525"},{"relation_name":"is_a","term_name":"positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway","termid":"GO:1902177"},{"relation_name":"is_a","term_name":"regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway","termid":"GO:1903376"},{"relation_name":"positively_regulates","term_name":"neuron intrinsic apoptotic signaling pathway in response to oxidative stress","termid":"GO:0036480"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway","synonyms":[{"name":"activation of neuron apoptosis in response to oxidative stress","type":"related"},{"name":"activation of neuron intrinsic apoptotic signaling pathway in response to oxidative stress","type":"narrow"},{"name":"positive regulation of neuron apoptosis in response to oxidative stress","type":"related"},{"name":"positive regulation of neuron intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"},{"name":"up regulation of neuron apoptosis in response to oxidative stress","type":"related"},{"name":"up regulation of neuron intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"},{"name":"up-regulation of neuron apoptosis in response to oxidative stress","type":"related"},{"name":"up-regulation of neuron intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"},{"name":"upregulation of neuron apoptosis in response to oxidative stress","type":"related"},{"name":"upregulation of neuron intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"}],"termid":"GO:1903378"}


id: GO:0061278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of epithelial cells within a renal tubule that contributes to mesonephric nephron tubule morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration involved in nephron tubule morphogenesis","termid":"GO:0072155"},{"relation_name":"part_of","term_name":"mesonephric nephron tubule morphogenesis","termid":"GO:0061240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"epithelial cell migration involved in mesonephric nephron tubule morphogenesis","termid":"GO:0061278"}


id: PR:O74895
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl15 gene.","definition_xrefs":["UniProtKB:O74895","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":"60S ribosomal protein L15-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC576.11","synonyms":[{"name":"Spom972h-rpl15","type":"exact"}],"termid":"PR:O74895"}


id: FYPO:0002551
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which cells show increased sensitivity to ultraviolet light during G0 phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to UV","termid":"FYPO:0002550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to UV during G0","synonyms":[{"name":"decreased cell population growth during cellular response to UV during G0","type":"exact"},{"name":"decreased growth during cellular response to UV during G0","type":"exact"},{"name":"hypersensitive to UV during G0","type":"exact"},{"name":"increased sensitivity to UV irradiation during G0","type":"exact"},{"name":"sensitive to UV during cell quiescence","type":"exact"},{"name":"sensitive to UV during quiescence","type":"exact"},{"name":"sensitive to ultraviolet light during G0","type":"exact"}],"termid":"FYPO:0002551"}


id: GO:0031236
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of a plasma membrane consisting of gene products and protein complexes that are loosely bound to its periplasmic surface, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:dos","GOC:mtg_sensu","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of external side of plasma membrane","termid":"GO:0031232"},{"relation_name":"part_of","term_name":"periplasmic side of plasma membrane","termid":"GO:0098567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0009986"],"is_obsolete":false,"name":"extrinsic component of periplasmic side of plasma membrane","secondary_identifiers":["GO:0031238"],"synonyms":[{"name":"extrinsic to external leaflet of plasma membrane, in periplasmic space","type":"narrow"},{"name":"extrinsic to external side of plasma membrane, in periplasmic space","type":"narrow"}],"termid":"GO:0031236"}


id: PBO:0082300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arsenate reductase required for arsenate resistance; converts arsenate to arsenite which can then be exported from cells by Arr3p","termid":"PBO:0082300"}


id: PBO:0057718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1302-3","termid":"PBO:0057718"}


id: PR:000085731
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe) that has been methylated on Lys-9 but not phosphorylated on Ser-10. UniProtKB:P10651, 2-136, Lys-10, MOD:00663|Ser-11, PR:000026291.","definition_xrefs":["PomBase:VW","PMID:19362535","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht3/Me(K9),UnPhos(S10)","pombase_gene_id":"SPBC1105.11c","synonyms":[{"name":"PRO_0000221367, Lys-10, MOD:00663|Ser-11, PR:000026291","type":"exact"},{"name":"PomBase_original_PRO_term_name: histone H3.3, initiator methionine removed K9-methylated and unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht3/InitMet-/K9MeUnPhos:1","type":"exact"},{"name":"UniProtKB:P10651, 2-136, Lys-10, MOD:00663|Ser-11, PR:000026291","type":"exact"},{"name":"hht3/Me(K9),UnPhos(S10)","type":"exact"}],"termid":"PR:000085731"}


id: GO:0000313
data:
  {"annotated_genes":["SJAG_03040","SJAG_05218","SJAG_01591","SJAG_05320","SJAG_04281","SJAG_02762","SJAG_03176","SJAG_04490","SJAG_01630","SJAG_00782","SJAG_00148","SJAG_01829","SJAG_02067","SJAG_01727","SJAG_04893","SJAG_03192","SJAG_03402","SJAG_02836","SJAG_02324","SJAG_05573","SJAG_03459","SJAG_05244","SJAG_01478","SJAG_07009","SJAG_04378","SJAG_01734","SJAG_06253","SJAG_01520","SJAG_00060","SJAG_04019","SJAG_01468","SJAG_00315","SJAG_01463","SJAG_01413","SJAG_04173","SJAG_02643","SJAG_04216","SJAG_03284","SJAG_04493","SJAG_04788","SJAG_04753","SJAG_03297","SJAG_01767","SJAG_04244","SJAG_02452","SJAG_01473","SJAG_00944","SJAG_04207","SJAG_05270","SJAG_05221","SJAG_00105","SJAG_00799","SJAG_01045","SJAG_00860","SJAG_00889","SJAG_03584","SJAG_00513","SJAG_04494","SJAG_00844","SJAG_04164","SJAG_01719","SJAG_03649","SJAG_02777","SJAG_04918","SJAG_03053","SJAG_03065","SJAG_03636","SJAG_02071","SJAG_02359","SJAG_01303","SJAG_06110","SJAG_02201","SJAG_00086","SJAG_00497","SJAG_04889","SJAG_04689","SJAG_00628"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[109300,107542,105172,114860,97460,112338,90975,95763,110550,97481,98598,114036,107687,103846,102815,114679,88537,100585,111904,112889,114155,116441,104335,96398,102924,98153,103171,115598,111668,107640,102104,114813,117357,96097,110225,87866,106220,88987,95726,115708,112163,105322,113752,101423,116556],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005762"},{"annotations":[103418,91586,101799,103487,95428,108815,96130,93995,97485,97722,115033,105863,94847,89441,105498,93982,107406,97484,107799,108046,89388,102843,93697,109836,117514,93156,109589,115457,102563,107546,110115,111804],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005763"}]},"cv_name":"cellular_component","definition":"A ribosome contained within a subcellular membrane-bounded organelle.","definition_xrefs":["GOC:mcc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribosome","termid":"GO:0005840"},{"relation_name":"part_of","term_name":"organelle","termid":"GO:0043226"}],"gene_count":77,"genes_by_uniquename":{"SJAG_00060":null,"SJAG_00086":null,"SJAG_00105":null,"SJAG_00148":null,"SJAG_00315":null,"SJAG_00497":null,"SJAG_00513":null,"SJAG_00628":null,"SJAG_00782":null,"SJAG_00799":null,"SJAG_00844":null,"SJAG_00860":null,"SJAG_00889":null,"SJAG_00944":null,"SJAG_01045":null,"SJAG_01303":null,"SJAG_01413":null,"SJAG_01463":null,"SJAG_01468":null,"SJAG_01473":null,"SJAG_01478":null,"SJAG_01520":null,"SJAG_01591":null,"SJAG_01630":null,"SJAG_01719":null,"SJAG_01727":null,"SJAG_01734":null,"SJAG_01767":null,"SJAG_01829":null,"SJAG_02067":null,"SJAG_02071":null,"SJAG_02201":null,"SJAG_02324":null,"SJAG_02359":null,"SJAG_02452":null,"SJAG_02643":null,"SJAG_02762":null,"SJAG_02777":null,"SJAG_02836":null,"SJAG_03040":null,"SJAG_03053":null,"SJAG_03065":null,"SJAG_03176":null,"SJAG_03192":null,"SJAG_03284":null,"SJAG_03297":null,"SJAG_03402":null,"SJAG_03459":null,"SJAG_03584":null,"SJAG_03636":null,"SJAG_03649":null,"SJAG_04019":null,"SJAG_04164":null,"SJAG_04173":null,"SJAG_04207":null,"SJAG_04216":null,"SJAG_04244":null,"SJAG_04281":null,"SJAG_04378":null,"SJAG_04490":null,"SJAG_04493":null,"SJAG_04494":null,"SJAG_04689":null,"SJAG_04753":null,"SJAG_04788":null,"SJAG_04889":null,"SJAG_04893":null,"SJAG_04918":null,"SJAG_05218":null,"SJAG_05221":null,"SJAG_05244":null,"SJAG_05270":null,"SJAG_05320":null,"SJAG_05573":null,"SJAG_06110":null,"SJAG_06253":null,"SJAG_07009":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"organellar ribosome","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000313","terms_by_termid":{"GO:0005762":null,"GO:0005763":null}}


id: GO:0002801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of antifungal peptide secretion.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of antifungal peptide production","termid":"GO:0002789"},{"relation_name":"is_a","term_name":"negative regulation of antimicrobial peptide secretion","termid":"GO:0002795"},{"relation_name":"is_a","term_name":"regulation of antifungal peptide secretion","termid":"GO:0002800"},{"relation_name":"negatively_regulates","term_name":"antifungal peptide secretion","termid":"GO:0002782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006810"],"is_obsolete":false,"name":"negative regulation of antifungal peptide secretion","synonyms":[{"name":"down regulation of antifungal peptide secretion","type":"exact"},{"name":"down-regulation of antifungal peptide secretion","type":"exact"},{"name":"downregulation of antifungal peptide secretion","type":"exact"},{"name":"inhibition of antifungal peptide secretion","type":"narrow"}],"termid":"GO:0002801"}


id: MONDO:0957211
data:
  {"annotated_genes":["SJAG_04246","SJAG_01493"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86044,86045],"is_not":false,"summary":null,"term":"MONDO:0957211"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01493":null,"SJAG_04246":null},"genotype_count":0,"is_obsolete":false,"name":"neurodegeneration and seizures due to copper transport defect","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620306","MEDGEN:1841021","UMLS:C5830385"],"termid":"MONDO:0957211","terms_by_termid":{"MONDO:0957211":null},"xrefs":{"Monarch":{"xref_id":"0957211"}}}


id: PBO:0052045
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 1 pseudogene 1","termid":"PBO:0052045"}


id: GO:1900338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of methane biosynthetic process from carbon monoxide.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of methane biosynthetic process from carbon monoxide","termid":"GO:1900336"},{"relation_name":"is_a","term_name":"positive regulation of alkane biosynthetic process","termid":"GO:1901579"},{"relation_name":"is_a","term_name":"positive regulation of cellular respiration","termid":"GO:1901857"},{"relation_name":"positively_regulates","term_name":"methane biosynthetic process from carbon monoxide","termid":"GO:2001134"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"positively_regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"positive regulation of methane biosynthetic process from carbon monoxide","synonyms":[{"name":"activation of methane biosynthetic process from carbon monoxide","type":"narrow"},{"name":"up regulation of methane biosynthetic process from carbon monoxide","type":"exact"},{"name":"up-regulation of methane biosynthetic process from carbon monoxide","type":"exact"},{"name":"upregulation of methane biosynthetic process from carbon monoxide","type":"exact"}],"termid":"GO:1900338"}


id: GO:2001007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellulose biosynthetic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macromolecule biosynthetic process","termid":"GO:0010558"},{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"regulation of cellulose biosynthetic process","termid":"GO:2001006"},{"relation_name":"negatively_regulates","term_name":"cellulose biosynthetic process","termid":"GO:0030244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cellulose biosynthetic process","synonyms":[{"name":"negative regulation of cellulose anabolism","type":"exact"},{"name":"negative regulation of cellulose biosynthesis","type":"exact"},{"name":"negative regulation of cellulose formation","type":"exact"},{"name":"negative regulation of cellulose synthesis","type":"exact"}],"termid":"GO:2001007"}


id: PBO:0086030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; YLL033W is not an essential gene but mutant is defective in spore formation; null mutant displays increased levels of spontaneous Rad52p foci","termid":"PBO:0086030"}


id: PBO:0035932
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_trimethylation_at_centromere_during_vegetative_growth","termid":"PBO:0035932"}


id: MONDO:0003739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A broad classification of dysgammaglobulinemias characterized by low or undetectable serum levels of one of the five immunoglobulin classes. Deficiencies of immunoglobulins present variably according to isotype. Selective deficiencies may be caused by decreased or inefficient production from progenitor B cells without any corresponding decreases in the other isotypes. The clinical course and prognosis is dependent upon the severity of the selective deficiency and associated morbidity.","definition_xrefs":["NCIT:C27870"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell deficiency","termid":"MONDO:0002211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"selective immunoglobulin deficiency disease","secondary_identifiers":["DOID:6025","UMLS:C1335942","MEDGEN:235584"],"synonyms":[{"name":"selective Immunoglobulin isotype deficiency","type":"exact"}],"termid":"MONDO:0003739","xrefs":{"Monarch":{"xref_id":"0003739"}}}


id: GO:0097381
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Stack of disc membranes located inside a photoreceptor outer segment, and containing densely packed molecules of photoreceptor proteins that traverse the lipid bilayer. Disc membranes arise as evaginations of the ciliary membrane during the development of the outer segment and may or may not remain contiguous with the ciliary membrane.","definition_xrefs":["GOC:bj","PMID:6771304","GOC:krc","PMID:11826267","PMID:26574505","GOC:pde","PMID:19501669","PMID:2537204","PMID:7507907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle membrane","termid":"GO:0031090"},{"relation_name":"part_of","term_name":"photoreceptor outer segment","termid":"GO:0001750"}],"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":"photoreceptor disc membrane","termid":"GO:0097381"}


id: PBO:0087213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine-homocysteine methyltransferase; functions along with Mht1p in the conversion of S-adenosylmethionine (AdoMet) to methionine to control the methionine/AdoMet ratio; SAM4 has a paralog, YMR321C, that arose from a single-locus duplication","termid":"PBO:0087213"}


id: PATO:0002157
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being slightly out of its usual or proper place, or position.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dislocated","termid":"PATO:0001852"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partially dislocated","secondary_identifiers":["PATO:0002160"],"synonyms":[{"name":"partial dislocated towards","type":"exact"},{"name":"subluxation","type":"exact"},{"name":"suluxated towards","type":"exact"}],"termid":"PATO:0002157"}


id: FYPO:0006992
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing at the right outer repeat region (otr1R) of the centromere is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:26518661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin silencing at centromere outer repeat","termid":"FYPO:0004742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal chromatin silencing at centromere otr1R","synonyms":[{"name":"normal centromere outer repeat region chromatin silencing at otr1R","type":"exact"},{"name":"normal chromatin silencing at centromere otr1R during mitotic cell cycle","type":"related"},{"name":"normal chromatin silencing at centromere otr1R during vegetative growth","type":"exact"},{"name":"normal chromatin silencing at centromere otr1R region","type":"exact"},{"name":"normal chromatin silencing at centromeric otr1R","type":"exact"},{"name":"normal chromatin silencing at pericentric region otr1R","type":"related"},{"name":"normal chromatin silencing at pericentromeric region otr1R","type":"related"},{"name":"normal heterochromatic silencing at centromere otr1R","type":"exact"},{"name":"normal heterochromatin silencing at centromere otr1R","type":"exact"}],"termid":"FYPO:0006992"}


id: PBO:0014243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERMES complex subunit Mdm10 (predicted)","termid":"PBO:0014243"}


id: GO:0071072
data:
  {"annotated_genes":["SJAG_01187","SJAG_01906","SJAG_03940","SJAG_00053","SJAG_02380","SJAG_03170"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109190,112188],"is_not":false,"summary":null,"term":"GO:0071072"},{"annotations":[89923,103860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[114923,110824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of phospholipids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"regulation of phospholipid biosynthetic process","termid":"GO:0071071"},{"relation_name":"is_a","term_name":"negative regulation of phospholipid metabolic process","termid":"GO:1903726"},{"relation_name":"negatively_regulates","term_name":"phospholipid biosynthetic process","termid":"GO:0008654"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01187":null,"SJAG_01906":null,"SJAG_02380":null,"SJAG_03170":null,"SJAG_03940":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of phospholipid biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of phospholipid biosynthetic process","type":"exact"},{"name":"down-regulation of phospholipid biosynthetic process","type":"exact"},{"name":"downregulation of phospholipid biosynthetic process","type":"exact"},{"name":"inhibition of phospholipid biosynthetic process","type":"narrow"},{"name":"negative regulation of phospholipid anabolism","type":"exact"},{"name":"negative regulation of phospholipid biosynthesis","type":"exact"},{"name":"negative regulation of phospholipid formation","type":"exact"},{"name":"negative regulation of phospholipid synthesis","type":"exact"}],"termid":"GO:0071072","terms_by_termid":{"GO:0071072":null,"GO:1902647":null,"GO:2001211":null}}


id: GO:0001410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the chlamydospore over time, from its formation to the mature structure. A chlamydospores is a mitotic (asexual) one-celled spore, produced primarily for survival, not dispersal, originating endogenously and singly within part of a pre-existing cell and possessing an inner secondary and often thickened cell wall. An example of this is found in Candida albicans.","definition_xrefs":["GOC:mtg_sensu","PMID:14663094","ISBN:085199377X","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043936"},{"relation_name":"is_a","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":"chlamydospore formation","secondary_identifiers":["GO:0055027"],"synonyms":[{"name":"chlamydospore development","type":"exact"}],"termid":"GO:0001410"}


id: GO:0043845
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A subcomplex of DNA polymerase III composed of the epsilon subunit which has proofreading activity, and the theta subunit which enhances the epsilon subunit's proofreading activity.","definition_xrefs":["Wikipedia:Pol_III","PMID:16973612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"DNA polymerase III, core complex","termid":"GO:0044776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"DNA polymerase III, proofreading complex","synonyms":[{"name":"DNA polymerase III, proof-reading complex","type":"exact"},{"name":"DNA polymerase III, proof-reading subcomplex","type":"exact"},{"name":"DNA polymerase III, proofreading subcomplex","type":"exact"}],"termid":"GO:0043845"}


id: GO:0140846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that activates or increases the frequency, rate or extent of the transition from the initiation to the elongation phases of transcription by RNA polymerase II.","definition_xrefs":["PMID:28248323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of promoter clearance from RNA polymerase II promoter","termid":"GO:0140845"},{"relation_name":"is_a","term_name":"positive regulation of RNA biosynthetic process","termid":"GO:1902680"},{"relation_name":"positively_regulates","term_name":"RNA polymerase II promoter clearance","termid":"GO:0001111"}],"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 promoter clearance from RNA polymerase II promoter","termid":"GO:0140846"}


id: MONDO:0011276
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"orofacial cleft","termid":"MONDO:0000358"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orofacial cleft 2","secondary_identifiers":["UMLS:C1864323","DOID:0080396","MESH:C566419","MEDGEN:400499","OMIM:602966"],"synonyms":[{"name":"OFC2","type":"exact"},{"name":"cleft lip with or without cleft palate, nonsyndromic, 2","type":"related"},{"name":"orofacial cleft 2","type":"exact"}],"termid":"MONDO:0011276","xrefs":{"Monarch":{"xref_id":"0011276"}}}


id: MONDO:0032901
data:
  {"annotated_genes":["SJAG_00143"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86220],"is_not":false,"summary":null,"term":"MONDO:0032901"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00143":null},"genotype_count":0,"is_obsolete":false,"name":"Catifa syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1684686","UMLS:C5231492","OMIM:618761"],"synonyms":[{"name":"CATIFA","type":"related"},{"name":"CATIFA SYNDROME","type":"related"},{"name":"Cleft Lip, Cataract, Tooth Abnormality, Impaired Intellectual Development, Facial Dysmorphism, and Attention-Deficit Hyperactivity Disorder","type":"related"}],"termid":"MONDO:0032901","terms_by_termid":{"MONDO:0032901":null},"xrefs":{"Monarch":{"xref_id":"0032901"}}}


id: PBO:0067967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 269","termid":"PBO:0067967"}


id: PBO:0046924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 41 member C","termid":"PBO:0046924"}


id: PR:O74374
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phosphoglucomutase-1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR22573:SF5","PRO:DNx","OMA:SCHPO03429"],"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":"phosphoglucomutase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC32F12.10","secondary_identifiers":["UniProtKB:O74374"],"synonyms":[{"name":"PGM (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PGM1","type":"exact"},{"name":"glucose phosphomutase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74374"}


id: PBO:0040563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,4-N-acetyl-galactosaminyltransferase 3","termid":"PBO:0040563"}


id: PBO:0048077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin heavy chain like 17","termid":"PBO:0048077"}


id: PBO:0067709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal 7","termid":"PBO:0067709"}


id: PR:O13775
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gus1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13775"],"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":"glutamate--tRNA ligase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17A5.15c","synonyms":[{"name":"GluRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gus1","type":"exact"},{"name":"glutamyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13775"}


id: FYPO:0002845
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is inviable, is swollen, is elongated, and contains one or more septa. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"inviable swollen elongated vegetative cell","termid":"FYPO:0002251"},{"relation_name":"is_a","term_name":"inviable swollen vegetative cell with abnormal cell shape","termid":"FYPO:0002415"},{"relation_name":"is_a","term_name":"inviable septated vegetative cell with abnormal cell morphology","termid":"FYPO:0002452"},{"relation_name":"is_a","term_name":"elongated septated vegetative cell","termid":"FYPO:0004750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000005","FYPO:0001985","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"inviable swollen elongated septated vegetative cell","synonyms":[{"name":"inviable enlarged elongated septated vegetative cell with enlarged nucleus","type":"related"},{"name":"inviable large elongated septated vegetative cell","type":"related"},{"name":"lethal; swollen elongated septated vegetative cell","type":"exact"}],"termid":"FYPO:0002845"}


id: GO:0008500
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete glycine-, glutamate-, thienylcyclohexylpiperidine binding (obsolete GO:0008500)","synonyms":[{"name":"glycine-, glutamate-, thienylcyclohexylpiperidine binding","type":"exact"}],"termid":"GO:0008500"}


id: PBO:0002990
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae CAN1","termid":"PBO:0002990"}


id: PBO:0044916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol O-acyltransferase 2 like 7, pseudogene","termid":"PBO:0044916"}


id: PBO:0002266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase Stp1","termid":"PBO:0002266"}


id: PBO:0045042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dickkopf WNT signaling pathway inhibitor 2","termid":"PBO:0045042"}


id: FYPO:0003377
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to nitrosative stress is lower than normal. Total RNA or a specific RNA may be affected. Nitrosative stress often results from exposure to high levels of nitric oxide (NO) or the highly reactive oxidant peroxynitrite, which is produced following interaction of NO with superoxide anions.","definition_xrefs":["GO:0071500","PomBase:mah","PMID:20204527"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"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"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased RNA level during cellular response to nitrosative stress","synonyms":[{"name":"decreased RNA accumulation during cellular response to nitrosative stress","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to nitrosative stress","type":"narrow"},{"name":"decreased transcript level during cellular response to nitrosative stress","type":"exact"},{"name":"reduced RNA level during cellular response to nitrosative stress","type":"exact"}],"termid":"FYPO:0003377"}


id: PBO:0116252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane leptomycin transmembrane transporter Pmd1","termid":"PBO:0116252"}


id: GO:0102501
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-mannonate + NADP = NADPH + H+ + D-fructuronate.","definition_xrefs":["PMID:22925190","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"D-fructuronate reductase activity","secondary_identifiers":["MetaCyc:RXN-14368"],"termid":"GO:0102501"}


id: PBO:0073909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC16A1 antisense RNA 1","termid":"PBO:0073909"}


id: PBO:0087421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit 9 of ubiquinol cytochrome-c reductase (Complex III); Complex III is a component of the mitochondrial inner membrane electron transport chain; required for electron transfer at the ubiquinol oxidase site of the complex","termid":"PBO:0087421"}


id: GO:0047080
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2'-deoxyuridine + 2-oxoglutarate + O2 = CO2 + succinate + uridine.","definition_xrefs":["EC:1.14.11.3","RHEA:21076"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"deoxyuridine 2'-dioxygenase activity","secondary_identifiers":["MetaCyc:1.14.11.3-RXN","KEGG_REACTION:R01879"],"synonyms":[{"name":"2'-deoxyuridine,2-oxoglutarate:oxygen oxidoreductase (2'-hydroxylating)","type":"related"},{"name":"deoxyuridine 2'-hydroxylase activity","type":"related"},{"name":"pyrimidine deoxyribonucleoside 2'-hydroxylase activity","type":"broad"},{"name":"pyrimidine-deoxynucleoside 2'-dioxygenase activity","type":"broad"},{"name":"pyrimidine-deoxynucleoside,2-oxoglutarate 2'-dioxygenase activity","type":"broad"},{"name":"thymidine 2'-dioxygenase activity","type":"narrow"},{"name":"thymidine 2'-hydroxylase activity","type":"related"},{"name":"thymidine 2-oxoglutarate dioxygenase activity","type":"related"},{"name":"thymidine dioxygenase activity","type":"related"}],"termid":"GO:0047080"}


id: PATO:0002451
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's exhibiting a phenotypic difference between males and females of the same species.","definition_xrefs":["PATOC:WC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organismal quality","termid":"PATO:0001995"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sexually dimorphic","termid":"PATO:0002451"}


id: PBO:0067778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 78","termid":"PBO:0067778"}


id: GO:0140039
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of one cell to another cell via adhesion molecules as a result of an extracellular stimulus.","definition_xrefs":["PMID:14996911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion","termid":"GO:0098609"},{"relation_name":"part_of","term_name":"cellular response to stimulus","termid":"GO:0051716"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"cell-cell adhesion in response to extracellular stimulus","termid":"GO:0140039"}


id: MONDO:0017314
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.","definition_xrefs":["Orphanet:286"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, vascular type","secondary_identifiers":["icd11.foundation:1202686415","NANDO:2201258","GARD:2082","NANDO:1200648","UMLS:C0268338","SCTID:17025000","NCIT:C125699","MEDGEN:82790"],"synonyms":[{"name":"EDS IV","type":"exact"},{"name":"EDS IV (formerly)","type":"related"},{"name":"EDS type 4","type":"exact"},{"name":"EDS type 4 (formerly)","type":"related"},{"name":"EDS4 (formerly)","type":"related"},{"name":"Ehlers Danlos syndrome, arterial type","type":"related"},{"name":"Ehlers Danlos syndrome, ecchymotic type","type":"related"},{"name":"Ehlers Danlos syndrome, sack-Barabas type","type":"related"},{"name":"Ehlers-Danlos syndrome type 4","type":"exact"},{"name":"Ehlers-Danlos syndrome type 4 (formerly)","type":"related"},{"name":"Ehlers-Danlos syndrome type IV","type":"exact"},{"name":"Ehlers-Danlos syndrome type IV (formerly)","type":"related"},{"name":"Ehlers-Danlos syndrome, type IV","type":"exact"},{"name":"Ehlers-Danlos syndrome, vascular type","type":"exact"},{"name":"sack-Barabas syndrome","type":"exact"},{"name":"vEDS","type":"related"},{"name":"vascular EDS","type":"related"},{"name":"vascular Ehlers-Danlos syndrome","type":"related"}],"termid":"MONDO:0017314","xrefs":{"Monarch":{"xref_id":"0017314"}}}


id: PBO:0049696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan and proteoglycan link protein 2","termid":"PBO:0049696"}


id: GO:0070785
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the process in which cells remain attached after division and form thread-like filaments that may penetrate into a solid growth medium.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of growth of unicellular organism as a thread of attached cells","termid":"GO:0070784"},{"relation_name":"is_a","term_name":"negative regulation of filamentous growth of a population of unicellular organisms","termid":"GO:1900429"},{"relation_name":"negatively_regulates","term_name":"growth of unicellular organism as a thread of attached cells","termid":"GO:0070783"}],"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 growth of unicellular organism as a thread of attached cells","termid":"GO:0070785"}


id: PBO:0066841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 141","termid":"PBO:0066841"}


id: PBO:0027176
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_spatial_extent_of_telomeric_heterochromatin_assembly","termid":"PBO:0027176"}


id: PBO:0040991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bolA family member 2 pseudogene 1","termid":"PBO:0040991"}


id: MONDO:1011803
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":"muscular dystrophy-dystroglycanopathy (limb-girdle), non-human animal","secondary_identifiers":["OMIA:001621"],"termid":"MONDO:1011803","xrefs":{"Monarch":{"xref_id":"1011803"}}}


id: MONDO:0013951
data:
  {"annotated_genes":["SJAG_03781"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86766],"is_not":false,"summary":null,"term":"MONDO:0013951"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"peroxisome biogenesis disorder","termid":"MONDO:0019234"},{"relation_name":"is_a","term_name":"peroxisome biogenesis disorder due to PEX19 defect","termid":"MONDO:0100270"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03781":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0005244","MONDO:0019053","MONDO:0006025"],"is_obsolete":false,"name":"peroxisome biogenesis disorder 12A (Zellweger)","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15876","DOID:0080486","OMIM:614886","UMLS:C3554002","MEDGEN:766916"],"synonyms":[{"name":"Cg14","type":"related"},{"name":"Cgj","type":"related"},{"name":"PBD12A","type":"related"},{"name":"peroxisome biogenesis disorder 12A (Zellweger)","type":"exact"},{"name":"peroxisome biogenesis disorder, complementation group 14","type":"related"},{"name":"peroxisome biogenesis disorder, complementation group J","type":"related"}],"termid":"MONDO:0013951","terms_by_termid":{"MONDO:0013951":null},"xrefs":{"Monarch":{"xref_id":"0013951"}}}


id: MONDO:1010828
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndactyly that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndactyly, non-human animal","termid":"MONDO:1010160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndactyly, sheep","secondary_identifiers":["OMIA:000963-9940"],"termid":"MONDO:1010828","xrefs":{"Monarch":{"xref_id":"1010828"}}}


id: MONDO:0020018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cranial malformation (obsolete MONDO:0020018)","secondary_identifiers":["Orphanet:98038"],"termid":"MONDO:0020018","xrefs":{"Monarch":{"xref_id":"0020018"}}}


id: PBO:0004264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Ypt1","termid":"PBO:0004264"}


id: PATO:0001380
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A polyploidy quality inhering in a bearer by virtue of the bearer's having an ancient polyploid ancestor.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Paleopolyploid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyploid","termid":"PATO:0001377"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paleopolyploid","termid":"PATO:0001380"}


id: PBO:0013771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA m(1)G methyltransferase Trm10","termid":"PBO:0013771"}


id: MONDO:0012693
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glycogen storage disease characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase.","definition_xrefs":["Orphanet:137625"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of glycogen metabolism","termid":"MONDO:0002412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"glycogen storage disease due to muscle and heart glycogen synthase deficiency","secondary_identifiers":["MESH:C566917","OMIM:611556","MEDGEN:409741","SCTID:725027004","NANDO:2201152","UMLS:C1969054","GARD:10760"],"synonyms":[{"name":"GSD 0B","type":"related"},{"name":"GSD due to muscle and heart glycogen synthase deficiency","type":"exact"},{"name":"GSD type 0b","type":"exact"},{"name":"GSD0B","type":"related"},{"name":"glycogen storage disease 0, muscle","type":"related"},{"name":"glycogen storage disease due to glycogen synthase deficiency of heart","type":"exact"},{"name":"glycogen storage disease type 0, muscle","type":"related"},{"name":"glycogen storage disease type 0b","type":"exact"},{"name":"glycogenosis due to muscle and heart glycogen synthase deficiency","type":"exact"},{"name":"glycogenosis type 0b","type":"exact"},{"name":"heart glycogen storage disease due to glycogen synthase deficiency","type":"exact"},{"name":"muscle glycogen storage disease 0","type":"related"},{"name":"muscle glycogen synthase deficiency","type":"related"}],"termid":"MONDO:0012693","xrefs":{"Monarch":{"xref_id":"0012693"}}}


id: PR:P0CT78
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1102 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT78"],"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":"60S ribosomal protein L11-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17G9.10","synonyms":[{"name":"Spom972h-rpl1102","type":"exact"}],"termid":"PR:P0CT78"}


id: PR:Q9UT05
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tripeptidyl-peptidase 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02216","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":"tripeptidyl-peptidase 2 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP8A3.12c","secondary_identifiers":["UniProtKB:Q9UT05"],"synonyms":[{"name":"Spom972h-TPP2","type":"exact"},{"name":"TPP-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"multicorn protease (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT05"}


id: PBHQ:002
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_has_qualifier_range","direct_ancestors":[{"relation_name":"is_a","term_name":"has_qualifier_range","termid":"PBHQ:001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOT","termid":"PBHQ:002"}


id: PBO:0083410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the dubious ORF YML089C; exhibits growth defect on a non-fermentable (respiratory) carbon source","termid":"PBO:0083410"}


id: PBO:0051481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable (VI)-22-1 (pseudogene)","termid":"PBO:0051481"}


id: SO:0001001
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Cytosolic 23S rRNA is an RNA component of the large subunit of cytosolic ribosomes in prokaryotes.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"cytosolic_rRNA_23S_gene","termid":"SO:0002243"},{"relation_name":"is_a","term_name":"cytosolic_LSU_rRNA","termid":"SO:0000651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_23S_rRNA","synonyms":[{"name":"cytosolic 23S LSU rRNA","type":"exact"},{"name":"cytosolic 23S rRNA","type":"exact"},{"name":"cytosolic 23S ribosomal RNA","type":"related"},{"name":"cytosolic rRNA 23S","type":"exact"}],"termid":"SO:0001001"}


id: PBO:0059939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 25","termid":"PBO:0059939"}


id: MONDO:0017291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Reversible cerebral vasoconstriction syndrome (RCVS) is an infrequent cerebrovascular disorder characterized by severe headaches with or without focal neurological deficits or seizures, and a reversible segmental and multifocal vasoconstriction of cerebral arteries.","definition_xrefs":["Orphanet:284388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"headache disorder","termid":"MONDO:0021146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reversible cerebral vasoconstriction syndrome","secondary_identifiers":["ICD9:437.8","SCTID:700467001","UMLS:C3544214","GARD:12768","icd11.foundation:1474881372","MEDGEN:811291"],"synonyms":[{"name":"RCVS","type":"exact"}],"termid":"MONDO:0017291","xrefs":{"Monarch":{"xref_id":"0017291"}}}


id: GO:0031735
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a CCR10 chemokine receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CCR chemokine receptor binding","termid":"GO:0048020"}],"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:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"CCR10 chemokine receptor binding","synonyms":[{"name":"CCR10 chemokine receptor ligand","type":"narrow"}],"termid":"GO:0031735"}


id: FYPO:0001023
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing cisplatin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0002058","FYPO:0000139","FYPO:0002057","FYPO:0000003","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on cisplatin","synonyms":[{"name":"normal cell population growth in presence of cisplatin","type":"exact"},{"name":"normal cell population growth on cisplatin","type":"exact"},{"name":"normal cellular response to cisplatin","type":"related"},{"name":"normal growth on cis-DDP","type":"exact"},{"name":"normal vegetative cell population growth on cisplatin","type":"exact"}],"termid":"FYPO:0001023"}


id: PBO:0082995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic leucyl tRNA synthetase; ligates leucine to the appropriate tRNA; human homolog LARS can complement yeast temperature-sensitive mutant at restrictive temperature","termid":"PBO:0082995"}


id: MONDO:0019030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Acanthamoeba keratitis (obsolete MONDO:0019030)","termid":"MONDO:0019030","xrefs":{"Monarch":{"xref_id":"0019030"}}}


id: GO:0007443
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the Malpighian tubule are generated and organized. This process takes place entirely during the embryonic phase. A Malpighian tubule is a fine, thin-walled excretory tubule in insects which leads into the posterior part of the gut.","definition_xrefs":["GOC:bf","ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"is_a","term_name":"renal tubule morphogenesis","termid":"GO:0061333"},{"relation_name":"part_of","term_name":"embryonic hindgut morphogenesis","termid":"GO:0048619"},{"relation_name":"part_of","term_name":"Malpighian tubule development","termid":"GO:0072002"}],"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":"Malpighian tubule morphogenesis","termid":"GO:0007443"}


id: SO:0000053
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence_variant_effect which changes the regulatory region of a gene.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000053 sequence_variant_affecting_regulatory_region (obsolete SO:0000053)","synonyms":[{"name":"mutation affecting regulatory region","type":"related"},{"name":"sequence variant affecting regulatory region","type":"exact"}],"termid":"SO:0000053"}


id: MONDO:0021193
data:
  {"annotated_genes":["SJAG_01111","SJAG_04213"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86838,86839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024517"}]},"cv_name":"mondo","definition":"A neoplasm of the nervous system that arises from the neuroepithelial tissues. Representative examples include astrocytic tumors, oligodendroglial tumors, ependymal tumors, and primitive neuroectodermal tumors.","definition_xrefs":["NCIT:C3787"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system neoplasm","termid":"MONDO:0021248"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01111":null,"SJAG_04213":null},"genotype_count":0,"is_obsolete":false,"name":"neuroepithelial neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0206715","MESH:D018302","MEDGEN:60215","ONCOTREE:PRNET"],"synonyms":[{"name":"neoplasm of neuroepithelial tissue","type":"exact"},{"name":"neoplasm of neuroepithelium","type":"exact"},{"name":"neoplasm of the neuroepithelium","type":"exact"},{"name":"neuroepithelial neoplasm","type":"exact"},{"name":"neuroepithelial neoplasms","type":"exact"},{"name":"neuroepithelial tissue neoplasm","type":"exact"},{"name":"neuroepithelial tissue tumor","type":"exact"},{"name":"neuroepithelial tissue tumour","type":"exact"},{"name":"neuroepithelial tumor","type":"exact"},{"name":"neuroepithelial tumors","type":"exact"},{"name":"neuroepithelial tumour","type":"exact"},{"name":"neuroepithelial tumours","type":"exact"},{"name":"primary neuroepithelial tumor","type":"related"},{"name":"primary neuroepithelial tumour","type":"related"},{"name":"tumor of neuroepithelial tissue","type":"exact"},{"name":"tumor of neuroepithelium","type":"exact"},{"name":"tumor of the neuroepithelium","type":"exact"},{"name":"tumour of neuroepithelial tissue","type":"exact"},{"name":"tumour of neuroepithelium","type":"exact"},{"name":"tumour of the neuroepithelium","type":"exact"}],"termid":"MONDO:0021193","terms_by_termid":{"MONDO:0024517":null},"xrefs":{"Monarch":{"xref_id":"0021193"}}}


id: MONDO:0019092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infantile apnea is a cessation of respiratory air flow that may affect newborns or older children because of neurological impairment of the respiratory rhythm or obstruction of air flow through the air passages. The symptoms include cyanosis, pallor or bradycardia and snoring in case of obstructive apnea.","definition_xrefs":["Orphanet:70590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infantile apnea","secondary_identifiers":["SCTID:724229002","UMLS:C0745261","GARD:6779","MEDGEN:1378556"],"synonyms":[{"name":"apnea of infancy","type":"exact"}],"termid":"MONDO:0019092","xrefs":{"Monarch":{"xref_id":"0019092"}}}


id: PBO:0065363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoserine aminotransferase 1 pseudogene 4","termid":"PBO:0065363"}


id: PBO:0073700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SKAP1 antisense RNA 1","termid":"PBO:0073700"}


id: PBO:0063184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PBX homeobox 4","termid":"PBO:0063184"}


id: PBO:0088573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex cyclin subunit Srb11","termid":"PBO:0088573"}


id: GO:0060305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the diameter of a cell, the length of a line segment that crosses through the center of a circular section through a cell.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell size","termid":"GO:0008361"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell diameter","synonyms":[{"name":"regulation of cell width","type":"broad"}],"termid":"GO:0060305"}


id: FYPO:0004247
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the fungal-type vacuole is normal (i.e. indistinguishable from wild type)..","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal vacuolar morphology during vegetative growth","synonyms":[{"name":"normal vacuolar morphology during mitotic cell cycle","type":"related"},{"name":"normal vacuole morphology during vegetative growth","type":"exact"}],"termid":"FYPO:0004247"}


id: MONDO:0016210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"alternating hemiplegia","secondary_identifiers":["MEDGEN:124456","SCTID:404689008","icd11.foundation:774373615","UMLS:C0278110","GARD:20446","Orphanet:209978"],"termid":"MONDO:0016210","xrefs":{"Monarch":{"xref_id":"0016210"}}}


id: PBO:0089185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trehalose-phosphate synthase Tps2","termid":"PBO:0089185"}


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


id: PBO:0057907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3610","termid":"PBO:0057907"}


id: PATO:0002632
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality in which the effect or outcome is not primary or the focus of the observation.","definition_xrefs":["PATO:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative","termid":"PATO:0000068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary","termid":"PATO:0002632"}


id: PBO:0046501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERI1 exoribonuclease family member 2","termid":"PBO:0046501"}


id: PR:O74917
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC757.06 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74917"],"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 C757.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC757.06","synonyms":[{"name":"Spom972h-SPCC757.06","type":"exact"}],"termid":"PR:O74917"}


id: PBO:0058706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6834","termid":"PBO:0058706"}


id: GO:1902178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An apoptotic signaling pathway that starts with a ligand binding to, or being withdrawn from, a fibroblast growth factor receptor (FGFR).","definition_xrefs":["GOC:mtg_apoptosis","GOC:TermGenie","PMID:17561467","GOC:pm","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblast growth factor receptor signaling pathway","termid":"GO:0008543"},{"relation_name":"is_a","term_name":"extrinsic apoptotic signaling pathway","termid":"GO:0097191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"fibroblast growth factor receptor apoptotic signaling pathway","synonyms":[{"name":"FGF receptor signaling pathway involved in apoptosis","type":"narrow"},{"name":"FGF receptor signaling pathway involved in apoptotic cell death","type":"exact"},{"name":"FGF receptor signaling pathway involved in apoptotic process","type":"exact"},{"name":"FGF receptor signaling pathway involved in apoptotic program","type":"narrow"},{"name":"FGF receptor signaling pathway involved in apoptotic programmed cell death","type":"exact"},{"name":"FGF receptor signaling pathway involved in programmed cell death by apoptosis","type":"exact"},{"name":"FGF receptor signaling pathway involved in signaling (initiator) caspase activity","type":"related"},{"name":"FGF receptor signaling pathway involved in type I programmed cell death","type":"narrow"},{"name":"FGF receptor signalling pathway involved in apoptosis","type":"narrow"},{"name":"FGF receptor signalling pathway involved in apoptotic cell death","type":"exact"},{"name":"FGF receptor signalling pathway involved in apoptotic process","type":"exact"},{"name":"FGF receptor signalling pathway involved in apoptotic program","type":"narrow"},{"name":"FGF receptor signalling pathway involved in apoptotic programmed cell death","type":"exact"},{"name":"FGF receptor signalling pathway involved in programmed cell death by apoptosis","type":"exact"},{"name":"FGF receptor signalling pathway involved in signaling (initiator) caspase activity","type":"related"},{"name":"FGF receptor signalling pathway involved in type I programmed cell death","type":"narrow"},{"name":"FGFR signaling pathway involved in apoptosis","type":"narrow"},{"name":"FGFR signaling pathway involved in apoptotic cell death","type":"exact"},{"name":"FGFR signaling pathway involved in apoptotic process","type":"exact"},{"name":"FGFR signaling pathway involved in apoptotic program","type":"narrow"},{"name":"FGFR signaling pathway involved in apoptotic programmed cell death","type":"exact"},{"name":"FGFR signaling pathway involved in programmed cell death by apoptosis","type":"exact"},{"name":"FGFR signaling pathway involved in signaling (initiator) caspase activity","type":"related"},{"name":"FGFR signaling pathway involved in type I programmed cell death","type":"narrow"},{"name":"fibroblast growth factor receptor signaling pathway involved in apoptosis","type":"narrow"},{"name":"fibroblast growth factor receptor signaling pathway involved in apoptotic cell death","type":"exact"},{"name":"fibroblast growth factor receptor signaling pathway involved in apoptotic process","type":"exact"},{"name":"fibroblast growth factor receptor signaling pathway involved in apoptotic program","type":"narrow"},{"name":"fibroblast growth factor receptor signaling pathway involved in apoptotic programmed cell death","type":"exact"},{"name":"fibroblast growth factor receptor signaling pathway involved in programmed cell death by apoptosis","type":"exact"},{"name":"fibroblast growth factor receptor signaling pathway involved in signaling (initiator) caspase activity","type":"related"},{"name":"fibroblast growth factor receptor signaling pathway involved in type I programmed cell death","type":"narrow"},{"name":"fibroblast growth factor receptor signalling pathway involved in apoptosis","type":"narrow"},{"name":"fibroblast growth factor receptor signalling pathway involved in apoptotic cell death","type":"exact"},{"name":"fibroblast growth factor receptor signalling pathway involved in apoptotic process","type":"exact"},{"name":"fibroblast growth factor receptor signalling pathway involved in apoptotic program","type":"narrow"},{"name":"fibroblast growth factor receptor signalling pathway involved in apoptotic programmed cell death","type":"exact"},{"name":"fibroblast growth factor receptor signalling pathway involved in programmed cell death by apoptosis","type":"exact"},{"name":"fibroblast growth factor receptor signalling pathway involved in signaling (initiator) caspase activity","type":"related"},{"name":"fibroblast growth factor receptor signalling pathway involved in type I programmed cell death","type":"narrow"}],"termid":"GO:1902178"}


id: GO:0021644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the vagus nerve is generated and organized. This nerve is primarily sensory but also has visceromotor components. It originates in the brain stem and controls many autonomic functions of the heart, lungs, stomach, pharynx, larynx, trachea, esophagus and other gastrointestinal tract components. It controls some motor functions such as speech. The sensory branches mediate sensation from the pharynx, larynx, thorax and abdomen; it also innervates taste buds in the epiglottis.","definition_xrefs":["GOC:dph","GOC:jid","ISBN:0838580343","GOC:dgh","GO_REF:0000021","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve morphogenesis","termid":"GO:0021602"},{"relation_name":"part_of","term_name":"vagus nerve development","termid":"GO:0021564"}],"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":"vagus nerve morphogenesis","synonyms":[{"name":"CN X morphogenesis","type":"related"}],"termid":"GO:0021644"}


id: PBO:0065619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase domain containing 1","termid":"PBO:0065619"}


id: PBO:0005733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Helicase Required for RNAi-mediated heterochromatin assembly Hrr1","termid":"PBO:0005733"}


id: GO:0002809
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of antibacterial peptide biosynthesis.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of antibacterial peptide production","termid":"GO:0002787"},{"relation_name":"is_a","term_name":"negative regulation of antimicrobial peptide biosynthetic process","termid":"GO:0002806"},{"relation_name":"is_a","term_name":"regulation of antibacterial peptide biosynthetic process","termid":"GO:0002808"},{"relation_name":"negatively_regulates","term_name":"antibacterial peptide biosynthetic process","termid":"GO:0002780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of antibacterial peptide biosynthetic process","synonyms":[{"name":"down regulation of antibacterial peptide biosynthetic process","type":"exact"},{"name":"down-regulation of antibacterial peptide biosynthetic process","type":"exact"},{"name":"downregulation of antibacterial peptide biosynthetic process","type":"exact"},{"name":"inhibition of antibacterial peptide biosynthetic process","type":"narrow"}],"termid":"GO:0002809"}


id: PR:Q9P7F4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC2E1P3.01 gene.","definition_xrefs":["UniProtKB:Q9P7F4","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc-type alcohol dehydrogenase-like protein C2E1P3.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2E1P3.01","synonyms":[{"name":"Spom972h-SPAC2E1P3.01","type":"exact"}],"termid":"PR:Q9P7F4"}


id: GO:1990069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of opening of stomata, pores in the epidermis of leaves and stems bordered by two guard cells and serving in gas exchange.","definition_xrefs":["PMID:21749899"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stomatal movement","termid":"GO:0010118"}],"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":"stomatal opening","termid":"GO:1990069"}


id: PBO:0091619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-aminocyclopropane-1-carboxylate deaminase","termid":"PBO:0091619"}


id: PBO:0049251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-rich RNA sequence binding factor 1","termid":"PBO:0049251"}


id: GO:0006705
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mineralocorticoids, hormonal C21 corticosteroids synthesized from cholesterol.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mineralocorticoid metabolic process","termid":"GO:0008212"},{"relation_name":"is_a","term_name":"hormone biosynthetic process","termid":"GO:0042446"},{"relation_name":"is_a","term_name":"steroid hormone biosynthetic process","termid":"GO:0120178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"mineralocorticoid biosynthetic process","secondary_identifiers":["Reactome:R-HSA-193993"],"synonyms":[{"name":"mineralocorticoid anabolism","type":"exact"},{"name":"mineralocorticoid biosynthesis","type":"exact"},{"name":"mineralocorticoid formation","type":"exact"},{"name":"mineralocorticoid synthesis","type":"exact"}],"termid":"GO:0006705"}


id: PBO:0061781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OCIA domain containing 2","termid":"PBO:0061781"}


id: PBO:0004039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF2 alpha kinase Gcn2","termid":"PBO:0004039"}


id: FYECO:0000135
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"The assay, or growth of cells, was conducted under semi-anaerobic conditions, where the level of oxygen is lower than normal.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping experimental environment","termid":"FYECO:0000132"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semi-aerobic environment","synonyms":[{"name":"hypoxia","type":"related"},{"name":"hypoxic environment","type":"related"},{"name":"limited O atoms","type":"related"},{"name":"limited oxygen","type":"related"},{"name":"reduced oxygen level","type":"related"},{"name":"semi aerobic environment","type":"exact"},{"name":"semi-anaerobic environment","type":"exact"},{"name":"semiaerobic environment","type":"exact"},{"name":"semianaerobic environment","type":"exact"}],"termid":"FYECO:0000135"}


id: PR:O94373
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atp4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94373"],"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":"ATP synthase subunit 4, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.07","synonyms":[{"name":"Spom972h-atp4","type":"exact"}],"termid":"PR:O94373"}


id: PBO:0064332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid scramblase 2","termid":"PBO:0064332"}


id: GO:1905852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of backward locomotion.","definition_xrefs":["PMID:11717360","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of locomotion","termid":"GO:0040017"},{"relation_name":"is_a","term_name":"regulation of backward locomotion","termid":"GO:0043058"},{"relation_name":"positively_regulates","term_name":"backward locomotion","termid":"GO:0043057"}],"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 backward locomotion","synonyms":[{"name":"activation of backward locomotion","type":"narrow"},{"name":"up regulation of backward locomotion","type":"exact"},{"name":"up-regulation of backward locomotion","type":"exact"},{"name":"upregulation of backward locomotion","type":"exact"}],"termid":"GO:1905852"}


id: GO:0061692
data:
  {"annotated_genes":["SJAG_04953","SJAG_04823","SJAG_00141","SJAG_02515","SJAG_01199","SJAG_01216"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94696,99493,104511,108291,116810,117725],"is_not":false,"summary":null,"term":"GO:0061692"}]},"cv_name":"biological_process","definition":"Any process that reduces or removes the toxicity of hydrogen peroxide in a cell. These include transport of hydrogen peroxide away from sensitive areas and to compartments or complexes whose purpose is sequestration.","definition_xrefs":["GOC:vw","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification of hydrogen peroxide","termid":"GO:0061691"},{"relation_name":"is_a","term_name":"cellular oxidant detoxification","termid":"GO:0098869"},{"relation_name":"part_of","term_name":"cellular response to hydrogen peroxide","termid":"GO:0070301"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00141":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_02515":null,"SJAG_04823":null,"SJAG_04953":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"cellular detoxification of hydrogen peroxide","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061692","terms_by_termid":{"GO:0061692":null}}


id: GO:0004365
data:
  {"annotated_genes":["SJAG_02135","SJAG_06621","SJAG_02945","SJAG_03903","SJAG_03828","SJAG_06622","SJAG_00027"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108405,108406,108407,108408,108409,108410,108411,108855,108856,108857,108858,108859,108860,108861],"is_not":false,"summary":null,"term":"GO:0004365"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glyceraldehyde 3-phosphate + phosphate + NAD+ = 3-phospho-D-glyceroyl phosphate + NADH + H+.","definition_xrefs":["EC:1.2.1.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glyceraldehyde-3-phosphate dehydrogenase [NAD(P)+] (phosphorylating) activity","termid":"GO:0043891"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_02135":null,"SJAG_02945":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-70482","RHEA:10300","Reactome:R-HSA-70449","MetaCyc:GAPOXNPHOSPHN-RXN"],"synonyms":[{"name":"3-phosphoglyceraldehyde dehydrogenase activity","type":"related"},{"name":"D-glyceraldehyde-3-phosphate:NAD+ oxidoreductase (phosphorylating)","type":"related"},{"name":"GAPDH activity","type":"related"},{"name":"NAD-dependent glyceraldehyde phosphate dehydrogenase activity","type":"related"},{"name":"NAD-dependent glyceraldehyde-3-phosphate dehydrogenase activity","type":"related"},{"name":"NADH-glyceraldehyde phosphate dehydrogenase activity","type":"related"},{"name":"dehydrogenase, glyceraldehyde phosphate","type":"related"},{"name":"glyceraldehyde phosphate dehydrogenase (NAD)","type":"related"},{"name":"glyceraldehyde-3-P-dehydrogenase activity","type":"related"},{"name":"phosphoglyceraldehyde dehydrogenase activity","type":"related"},{"name":"triosephosphate dehydrogenase activity","type":"broad"}],"termid":"GO:0004365","terms_by_termid":{"GO:0004365":null}}


id: MONDO:0017499
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital absence of both forearm and hand, bilateral is a rare developmental defect during embryogenesis characterized by a bilateral, transverse absence of the radius and ulna (of varying terminal lengths), as well as all the elements composing the hand.","definition_xrefs":["Orphanet:295095"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital absence of both forearm and hand","termid":"MONDO:0017443"}],"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":"congenital absence of both forearm and hand, bilateral","secondary_identifiers":["icd11.foundation:1524444518","UMLS:C2910270","ICD10CM:Q71.23","MEDGEN:1843505"],"synonyms":[{"name":"radio-ulnar terminal transverse meromelia, bilateral","type":"exact"}],"termid":"MONDO:0017499","xrefs":{"Monarch":{"xref_id":"0017499"}}}


id: MONDO:0022465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by anotia (congenital absence of the pinna) with a normal cochlea and vestibular apparatus, with facial paralysis caused by congenital absence of the entire right facial nerve, and congenital heart disease, which may present as atrioventricular septal defects or variations of tetralogy of Fallot.","definition_xrefs":["PMID:6470867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anotia facial palsy cardiac defect","termid":"MONDO:0022465","xrefs":{"Monarch":{"xref_id":"0022465"}}}


id: GO:0036378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Conversion of vitamin D3 from its largely inactive form (calciol, also called cholecalciferol) into a hormonally active form (calcitriol). Conversion requires 25-hydroxylation of calciol in the liver to form calcidiol, and subsequent 1,alpha-hydroxylation of calcidiol in the kidney to form calcitriol.","definition_xrefs":["PMID:20511049","PMID:17426122","GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin D biosynthetic process","termid":"GO:0042368"},{"relation_name":"is_a","term_name":"polyol biosynthetic process","termid":"GO:0046173"},{"relation_name":"is_a","term_name":"vitamin D3 metabolic process","termid":"GO:0070640"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006766","GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"calcitriol biosynthetic process from calciol","synonyms":[{"name":"1alpha,25(OH)2D3 biosynthesis","type":"broad"},{"name":"1alpha,25-dihydroxycholecalciferol biosynthesis","type":"broad"},{"name":"1alpha,25-dihydroxyvitamin D3 biosynthesis","type":"broad"},{"name":"calcitriol biosynthesis from calciol","type":"exact"},{"name":"vitamin D3 activation","type":"exact"}],"termid":"GO:0036378"}


id: GO:0141111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of of cGAS/STING signaling pathway.","definition_xrefs":["PMID:37802025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039531"},{"relation_name":"is_a","term_name":"positive regulation of pattern recognition receptor signaling pathway","termid":"GO:0062208"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"cGAS/STING signaling pathway","termid":"GO:0140896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of cGAS/STING signaling pathway","termid":"GO:0141111"}


id: PBO:0082403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta subunit of the mitochondrial processing protease (MPP); essential processing enzyme that cleaves the N-terminal targeting sequences from mitochondrially imported proteins","termid":"PBO:0082403"}


id: MONDO:0007742
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":"5-hydroxytryptamine oxygenase regulator","secondary_identifiers":["UMLS:C3887951","OMIM:143460","MEDGEN:854659"],"synonyms":[{"name":"5-HYDROXYTRYPTAMINE oxygenase regulator","type":"related"},{"name":"5-hydroxytryptamine oxygenase regulator","type":"exact"},{"name":"HTOR","type":"related"}],"termid":"MONDO:0007742","xrefs":{"Monarch":{"xref_id":"0007742"}}}


id: GO:0033364
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a secretory granule in a mast cell. A secretory granule is a small subcellular vesicle, surrounded by a membrane, that is formed from the Golgi apparatus and contains a highly concentrated protein destined for secretion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule organization","termid":"GO:0033363"}],"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":"mast cell secretory granule organization","synonyms":[{"name":"mast cell secretory granule maturation","type":"related"},{"name":"mast cell secretory granule organisation","type":"exact"},{"name":"mast cell secretory granule organization and biogenesis","type":"related"}],"termid":"GO:0033364"}


id: GO:0036219
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GTP + H2O = GMP + H+ + diphosphate.","definition_xrefs":["PMID:22531138","RHEA:29391","GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate diphosphatase activity","termid":"GO:0047429"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0047429"}],"interesting_parent_ids":["GO:0003674","GO:0047429","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"GTP diphosphatase activity","secondary_identifiers":["KEGG_REACTION:R00426"],"synonyms":[{"name":"GTP diphosphohydrolase (diphosphate-forming); guanosine 5'-triphosphate pyrophosphohydrolase","type":"exact"},{"name":"GTP diphosphohydrolase activity","type":"exact"},{"name":"GTP pyrophosphatase activity","type":"exact"}],"termid":"GO:0036219"}


id: PBO:0073237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenophosphate synthetase 1 pseudogene 1","termid":"PBO:0073237"}


id: PBO:0085484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Probable type-III integral membrane protein of unknown function; has regions of similarity to mitochondrial electron transport proteins","termid":"PBO:0085484"}


id: SO:0000190
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intron that is the most 5-prime in a given transcript.","direct_ancestors":[{"relation_name":"is_a","term_name":"intron","termid":"SO:0000188"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_intron","synonyms":[{"name":"5' intron","type":"exact"},{"name":"5' intron sequence","type":"exact"},{"name":"five prime intron","type":"exact"}],"termid":"SO:0000190"}


id: PBO:0051900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha 8","termid":"PBO:0051900"}


id: MONDO:0004330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sarcoma arising from the leptomeninges.","definition_xrefs":["NCIT:C8312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant leptomeningeal tumor","termid":"MONDO:0003762"},{"relation_name":"is_a","term_name":"meningeal sarcoma","termid":"MONDO:0004308"}],"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":"leptomeningeal sarcoma","secondary_identifiers":["DOID:7689","MEDGEN:235139","UMLS:C1384416"],"synonyms":[{"name":"leptomeningeal sarcoma","type":"exact"},{"name":"leptomeninges sarcoma","type":"related"},{"name":"leptomeninx sarcoma","type":"exact"},{"name":"sarcoma of leptomeninges","type":"exact"},{"name":"sarcoma of leptomeninx","type":"exact"},{"name":"sarcoma of the leptomeninges","type":"exact"},{"name":"sarcoma, leptomeningeal, malignant","type":"exact"},{"name":"sarcoma, meningeal","type":"exact"}],"termid":"MONDO:0004330","xrefs":{"Monarch":{"xref_id":"0004330"}}}


id: PBO:0043603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collectin subfamily member 12","termid":"PBO:0043603"}


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


id: GO:0030115
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A crystalline protein layer surrounding some bacteria.","definition_xrefs":["ISBN:0815108893","GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external encapsulating structure","termid":"GO:0030312"}],"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":"S-layer","secondary_identifiers":["Wikipedia:S-layer"],"termid":"GO:0030115"}


id: PBO:0088569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP-independent ER targeting protein Snd3a","termid":"PBO:0088569"}


id: GO:0046091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of deoxyadenosine, 2-deoxyribosyladenine, one of the four major nucleosides of DNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyadenosine metabolic process","termid":"GO:0046090"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside biosynthetic process","termid":"GO:0046123"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"deoxyadenosine biosynthetic process","synonyms":[{"name":"deoxyadenosine anabolism","type":"exact"},{"name":"deoxyadenosine biosynthesis","type":"exact"},{"name":"deoxyadenosine formation","type":"exact"},{"name":"deoxyadenosine synthesis","type":"exact"}],"termid":"GO:0046091"}


id: PBO:0002130
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.5.1.58","termid":"PBO:0002130"}


id: PR:O13703
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A vacuolar protein sorting-associated protein VTA1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12741:SF4","OMA:SCHPO00899","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":"vacuolar protein sorting-associated protein vts1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13F5.04c","secondary_identifiers":["UniProtKB:O13703"],"synonyms":[{"name":"Spom972h-VTA1","type":"exact"},{"name":"VPS20-associated protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13703"}


id: PBO:0000861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyruvate dehydrogenase (lipoamide) phosphatase (predicted)","termid":"PBO:0000861"}


id: MONDO:0011880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chronic mucocutaneous candidiasis","termid":"MONDO:0015279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"candidiasis, familial, 3","secondary_identifiers":["UMLS:C1843306","GARD:15418","MEDGEN:335927","MESH:C564361","OMIM:607644"],"synonyms":[{"name":"CANDF3","type":"exact"},{"name":"Fcnc","type":"related"},{"name":"candidiasis, familial chronic nail, with Icam1 deficiency","type":"related"},{"name":"candidiasis, familial, 3","type":"exact"}],"termid":"MONDO:0011880","xrefs":{"Monarch":{"xref_id":"0011880"}}}


id: GO:0102711
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A25 + 2-oxoglutarate + O2 = gibberellin A13 + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A25,oxoglutarate:oxygen oxidoreductase activity (obsolete GO:0102711)","termid":"GO:0102711"}


id: PBO:0064082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylserine decarboxylase","termid":"PBO:0064082"}


id: GO:1990208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of the RNA levels in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:18703740","PMID:12182338"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of RNA levels in host (obsolete GO:1990208)","termid":"GO:1990208"}


id: PBO:0039291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG6 alpha-1,3-glucosyltransferase","termid":"PBO:0039291"}


id: PR:Q9US46
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An E3 ubiquitin-protein ligase RNF14 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00750"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E3 ubiquitin-protein ligase itt1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1002.14","secondary_identifiers":["UniProtKB:Q9US46"],"synonyms":[{"name":"RING finger protein itt1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RNF14","type":"exact"}],"termid":"PR:Q9US46"}


id: PBO:0074821
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 19","termid":"PBO:0074821"}


id: PBO:0044146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitobiase","termid":"PBO:0044146"}


id: PBO:0051160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-41 (pseudogene)","termid":"PBO:0051160"}


id: FYPO:0001524
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of L-thialysine than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0000139","FYPO:0002682","FYPO:0005447"],"is_obsolete":false,"name":"resistance to L-thialysine","synonyms":[{"name":"resistance to L-thialysine during mitotic cell cycle","type":"related"},{"name":"resistance to L-thialysine during vegetative growth","type":"exact"},{"name":"resistance to thialysine","type":"broad"},{"name":"resistant to L-thialysine","type":"exact"}],"termid":"FYPO:0001524"}


id: PBO:0013018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triacylglycerol lipase ptl3","termid":"PBO:0013018"}


id: PBO:0069742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1023, pseudogene","termid":"PBO:0069742"}


id: PBO:0002747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fusion cytochrome c oxidase assembly protein Cox1102, mitochondrial ribosomal protein Rsm2202 (predicted)","termid":"PBO:0002747"}


id: GO:0021801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The radial migration of neuronal or glial precursor cells along radial glial cells during the development of the cerebral cortex.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:dgh","GOC:dph","PMID:12626695","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cortex radially oriented cell migration","termid":"GO:0021799"},{"relation_name":"is_a","term_name":"telencephalon glial cell migration","termid":"GO:0022030"}],"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":"cerebral cortex radial glia-guided migration","synonyms":[{"name":"cerebral cortex radial glia guided migration","type":"exact"},{"name":"cerebral cortex radial glia-dependent cell migration","type":"exact"},{"name":"glial-guided locomotion","type":"related"}],"termid":"GO:0021801"}


id: GO:0034761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of iron ions from one side of a membrane to the other by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of iron ion transport","termid":"GO:0034758"},{"relation_name":"is_a","term_name":"regulation of iron ion transmembrane transport","termid":"GO:0034759"},{"relation_name":"is_a","term_name":"positive regulation of cation transmembrane transport","termid":"GO:1904064"},{"relation_name":"positively_regulates","term_name":"iron ion transmembrane transport","termid":"GO:0034755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of iron ion transmembrane transport","synonyms":[{"name":"activation of transmembrane iron ion transport","type":"narrow"},{"name":"positive regulation of iron ion membrane transport","type":"exact"},{"name":"positive regulation of transmembrane iron ion transport","type":"exact"},{"name":"positive regulation of transmembrane iron transport","type":"exact"},{"name":"stimulation of transmembrane iron ion transport","type":"narrow"},{"name":"up regulation of transmembrane iron ion transport","type":"exact"},{"name":"up-regulation of transmembrane iron ion transport","type":"exact"},{"name":"upregulation of transmembrane iron ion transport","type":"exact"}],"termid":"GO:0034761"}


id: PBO:0001308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallopeptidase","termid":"PBO:0001308"}


id: SO:0000228
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding tryptophanyl tRNA (SO:000271).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptophan_tRNA_primary_transcript","synonyms":[{"name":"tryptophan tRNA primary transcript","type":"exact"}],"termid":"SO:0000228"}


id: GO:2000290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myotome development.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"myotome development","termid":"GO:0061055"}],"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 myotome development","termid":"GO:2000290"}


id: MONDO:0700059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Actinobacillus infectious disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease, non-human animal","termid":"MONDO:0700050"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actinobacillus infectious disease, non-human animal","termid":"MONDO:0700059","xrefs":{"Monarch":{"xref_id":"0700059"}}}


id: PBO:0034484
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_cohesin_loading","termid":"PBO:0034484"}


id: PR:O59792
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cif1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59792"],"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":"calnexin-independence factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC364.01","synonyms":[{"name":"Spom972h-cif1","type":"exact"}],"termid":"PR:O59792"}


id: PBO:0029699
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_septated_mononucleate_vegetative_cell","termid":"PBO:0029699"}


id: MONDO:0033927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic complex vascular malformation with associated anomalies (obsolete MONDO:0033927)","secondary_identifiers":["Orphanet:459537"],"termid":"MONDO:0033927","xrefs":{"Monarch":{"xref_id":"0033927"}}}


id: MONDO:0017225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The null syndrome is part of the Pelizaeus-Merzbacher disease (PMD) spectrum and is characterized by mild PMD features associated with demyelinating peripheral neuropathy.","definition_xrefs":["Orphanet:280234"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Pelizeaus-Merzbacher spectrum disorder","termid":"MONDO:0010714"}],"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":"null syndrome","secondary_identifiers":["GARD:17292","icd11.foundation:1663254692","MEDGEN:1740046","UMLS:C5439441"],"synonyms":[{"name":"PLP1 null syndrome","type":"exact"},{"name":"Pelizaeus-Merzbacher disease, null syndrome","type":"exact"}],"termid":"MONDO:0017225","xrefs":{"Monarch":{"xref_id":"0017225"}}}


id: MONDO:0010381
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":"Tn polyagglutination syndrome","secondary_identifiers":["MESH:C562719","UMLS:C0272137","DOID:0080520","MEDGEN:82896","OMIM:300622"],"synonyms":[{"name":"TNPS","type":"related"},{"name":"Tn polyagglutination syndrome","type":"exact"},{"name":"Tn polyagglutination syndrome, somatic","type":"exact"},{"name":"galactosyltransferase deficiency","type":"related"}],"termid":"MONDO:0010381","xrefs":{"Monarch":{"xref_id":"0010381"}}}


id: GO:0044870
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a host organism modulates the frequency, rate or extent of viral glycoprotein metabolic process.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation by host of viral process","termid":"GO:0044788"},{"relation_name":"regulates","term_name":"glycoprotein metabolic process","termid":"GO:0009100"}],"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 by host of viral glycoprotein metabolic process","termid":"GO:0044870"}


id: GO:0044495
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which one organism modulates the force with which blood travels through the circulatory system of another organism.","definition_xrefs":["PMID:19837656","GOC:jl","GOC:fj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of biological quality in another organism","termid":"GO:0044553"}],"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 blood pressure in another organism","synonyms":[{"name":"modulation of blood pressure in other organism","type":"exact"},{"name":"regulation of blood pressure in other organism","type":"exact"}],"termid":"GO:0044495"}


id: PBO:0086071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function that may interact with ribosomes; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and to COPI-coated vesicles (early Golgi); mtc1 is synthetically lethal with cdc13-1","termid":"PBO:0086071"}


id: PBO:0004613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HDEL receptor (predicted)","termid":"PBO:0004613"}


id: PBO:0081277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 44","termid":"PBO:0081277"}


id: MONDO:0001667
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"gram-negative bacterial infections","termid":"MONDO:0021678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"streptobacillus infectious disease","secondary_identifiers":["MEDGEN:923114","SCTID:721738002","UMLS:C0947939"],"synonyms":[{"name":"infection caused by streptobacillus","type":"exact"},{"name":"streptobacillus infection","type":"related"}],"termid":"MONDO:0001667","xrefs":{"Monarch":{"xref_id":"0001667"}}}


id: MONDO:0001166
data:
  {"annotated_genes":["SJAG_03994"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013898"}]},"cv_name":"mondo","definition":"Inflammation of renal tissue.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03994":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephritis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:14328","EFO:1002050","NCIT:C26833","SCTID:52845002","MESH:D009393","ICD9:583.89","UMLS:C0027697","DOID:10952","ICD9:583.7","ICD9:583.9"],"synonyms":[{"name":"inflammation of kidney","type":"exact"},{"name":"kidney inflammation","type":"exact"}],"termid":"MONDO:0001166","terms_by_termid":{"MONDO:0013898":null},"xrefs":{"Monarch":{"xref_id":"0001166"}}}


id: PBO:0066640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal modification protein rimK like family member B pseudogene 1","termid":"PBO:0066640"}


id: GO:0006457
data:
  {"annotated_genes":["SJAG_03601","SJAG_03166","SJAG_02016","SJAG_00564","SJAG_04567","SJAG_00353","SJAG_04352","SJAG_03237","SJAG_01626","SJAG_02014","SJAG_00983","SJAG_01641","SJAG_02825","SJAG_04741","SJAG_02308","SJAG_00505","SJAG_03784","SJAG_01002","SJAG_00602","SJAG_00753","SJAG_01747","SJAG_01038","SJAG_02461","SJAG_01545","SJAG_05189","SJAG_04046","SJAG_02270","SJAG_04602","SJAG_03794","SJAG_03030","SJAG_03022","SJAG_01684","SJAG_02413","SJAG_00524","SJAG_03570","SJAG_00288","SJAG_03320","SJAG_00893","SJAG_01052","SJAG_04074","SJAG_02919","SJAG_00790","SJAG_01246","SJAG_03414","SJAG_01664","SJAG_04784","SJAG_00403","SJAG_05206","SJAG_03052","SJAG_03815","SJAG_03135","SJAG_03955","SJAG_02926","SJAG_04518","SJAG_04187","SJAG_02672","SJAG_02489","SJAG_04055","SJAG_05414","SJAG_00436","SJAG_00574","SJAG_02378","SJAG_03992","SJAG_04371","SJAG_04844","SJAG_00750","SJAG_04197","SJAG_01733","SJAG_04817","SJAG_00196","SJAG_00954","SJAG_01737","SJAG_01647","SJAG_01874","SJAG_04014","SJAG_03238","SJAG_02620","SJAG_04121","SJAG_01510","SJAG_04012","SJAG_04511","SJAG_00558","SJAG_04336","SJAG_02032","SJAG_04228","SJAG_02367","SJAG_02694","SJAG_01121","SJAG_01714","SJAG_05191","SJAG_00447","SJAG_01615","SJAG_01186","SJAG_01914","SJAG_02827","SJAG_02301","SJAG_00609","SJAG_03717","SJAG_01160","SJAG_03267","SJAG_02875","SJAG_03094","SJAG_01526","SJAG_03463","SJAG_00112"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58611,62563,64921,67088,67577,77443,88363,89679,90401,90754,91488,91632,92270,92421,92450,92764,94022,95240,96258,96466,97011,97342,97950,98985,100201,100377,101316,102322,103827,103901,103968,104154,104283,105485,105692,105714,105952,106803,107103,107496,108680,108978,109337,109468,109469,110307,110805,112362,112912,115181,115781,116232,116688,116754,117378,118016],"is_not":false,"summary":null,"term":"GO:0006457"},{"annotations":[104159,106766,117080,100200,103207,98067,117180,97065,97411,87002,104563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051083"},{"annotations":[88814,95113,95840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006458"},{"annotations":[116231,117280,93355,94543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061077"},{"annotations":[94554,97996,96638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160203"},{"annotations":[96056,92992,100059,101937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007023"},{"annotations":[91845,110280,109498,102670,117837,88130,91821,95841,104683,95217,113097,90402,102587,109438,114225,102413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034975"},{"annotations":[102414,98744,103694,109737,87848,116602,88262,101814,114943,104466,102671,104160,75451,110285,110391,88261,116171,92602,87426,98068,114944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042026"}]},"cv_name":"biological_process","definition":"The process of assisting in the covalent and noncovalent assembly of single chain polypeptides or multisubunit complexes into the correct tertiary structure.","definition_xrefs":["GOC:rb","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"},{"relation_name":"part_of","term_name":"protein 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pathway","type":"related"}],"termid":"GO:0006457","terms_by_termid":{"GO:0006457":null,"GO:0006458":null,"GO:0007023":null,"GO:0034975":null,"GO:0042026":null,"GO:0051083":null,"GO:0061077":null,"GO:0160203":null}}


id: GO:0099140
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures comprising actin filaments and their associated proteins in the presynaptic actin cytoskeleton.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin cytoskeleton organization","termid":"GO:0030036"},{"relation_name":"is_a","term_name":"presynaptic cytoskeleton organization","termid":"GO:0099187"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0030036"],"is_obsolete":false,"name":"presynaptic actin cytoskeleton organization","termid":"GO:0099140"}


id: GO:0090348
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the chemical reactions and pathways involving organofluorine compounds, as carried out by individual cells.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organohalogen metabolic process","termid":"GO:0090347"},{"relation_name":"regulates","term_name":"organofluorine metabolic process","termid":"GO:0090346"}],"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 organofluorine metabolic process","termid":"GO:0090348"}


id: PBO:0056240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGOH divergent transcript","termid":"PBO:0056240"}


id: MONDO:0017358
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete organic aciduria (obsolete MONDO:0017358)","termid":"MONDO:0017358","xrefs":{"Monarch":{"xref_id":"0017358"}}}


id: GO:1990246
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A calcium channel complex in the mitochondrial inner membrane capable of highly-selective calcium channel activity. Its components include the EF-hand-containing proteins mitochondrial calcium uptake 1 (MICU1) and MICU2, the pore-forming subunit mitochondrial calcium uniporter (MCU) and its paralog MCUb, and the MCU regulator EMRE.","definition_xrefs":["PMID:24231807"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium channel complex","termid":"GO:0034704"},{"relation_name":"is_a","term_name":"inner mitochondrial membrane protein complex","termid":"GO:0098800"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005739","GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"uniplex complex","synonyms":[{"name":"mitochondrial uniporter complex","type":"exact"},{"name":"mitochondrial uniporter holocomplex","type":"exact"}],"termid":"GO:1990246"}


id: GO:0052113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The responsive adjustment of an organism to the osmotic conditions in or around its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete adaptation to host osmotic environment (obsolete GO:0052113)","synonyms":[{"name":"adaptation to host osmotic environment","type":"exact"},{"name":"osmotic tolerance to host environment","type":"exact"}],"termid":"GO:0052113"}


id: PBO:0089457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA queuosine modification protein Qtr3-like","termid":"PBO:0089457"}


id: MONDO:0009772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculorenocerebellar syndrome","secondary_identifiers":["Orphanet:2715","MEDGEN:340516","UMLS:C1850331","GARD:4050","MESH:C537739","OMIM:257970"],"synonyms":[{"name":"ORC syndrome","type":"related"},{"name":"absence of the cerebellar granular layer, intellectual disability, tapetoretinal degeneration and progressive glomerulopathy","type":"related"},{"name":"absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy","type":"related"},{"name":"oculorenocerebellar syndrome","type":"exact"}],"termid":"MONDO:0009772","xrefs":{"Monarch":{"xref_id":"0009772"}}}


id: GO:0071194
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A voltage-gated potassium channel complex that contains the Kv channel interacting protein KChIP3 associated with the channel via interaction with the Kv alpha subunit 4.2.","definition_xrefs":["PMID:15356203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Kv4.2-KChIP3 channel complex","secondary_identifiers":["CORUM:608"],"termid":"GO:0071194"}


id: PBO:0073356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family D member 1","termid":"PBO:0073356"}


id: GO:0060846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of a cell to a blood vessel endothelial cell fate and its capacity to differentiate into a blood vessel endothelial cell.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell fate commitment","termid":"GO:0060839"},{"relation_name":"part_of","term_name":"blood vessel endothelial cell differentiation","termid":"GO:0060837"}],"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":"blood vessel endothelial cell fate commitment","termid":"GO:0060846"}


id: MOD:01580
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group.","definition_xrefs":["Unimod:731#Y"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"iTRAQ8plex-121 reporter+balance reagent acylated residue","termid":"MOD:01577"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent O-acylated residue","termid":"MOD:01714"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-121 reporter+balance reagent O4'-acylated tyrosine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Accurate mass for 115, 118, 119 & 121","type":"related"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"iTRAQ8plex:13C(6)15N(2)","type":"related"}],"termid":"MOD:01580"}


id: PBO:0042241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine receptor 4","termid":"PBO:0042241"}


id: FYPO:0002920
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 methylation of lysine at position 36 of histone H3 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal histone H3-K36 methylation during vegetative growth","synonyms":[{"name":"normal histone H3 K36 methylation during vegetative growth","type":"exact"},{"name":"normal histone H3-K36 methylation during mitotic cell cycle","type":"related"},{"name":"normal histone H3K36me during vegetative growth","type":"exact"},{"name":"normal histone lysine H3 K36 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002920"}


id: PBO:0050556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HR lysine demethylase and nuclear receptor corepressor","termid":"PBO:0050556"}


id: MONDO:0027353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dyskeratosis congenita that has material basis in an autosomal recessive mutation of TERT on chromosome 5p15.33.","definition_xrefs":["DOID:0070021"],"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":"autosomal recessive dyskeratosis congenita 4","secondary_identifiers":["UMLS:C3151444","MEDGEN:462794"],"synonyms":[{"name":"DKCB4","type":"exact"},{"name":"dyskeratosis congenita, autosomal recessive 4","type":"exact"}],"termid":"MONDO:0027353","xrefs":{"Monarch":{"xref_id":"0027353"}}}


id: PBO:0072439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 3","termid":"PBO:0072439"}


id: PBO:0002607
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.7.25","termid":"PBO:0002607"}


id: PBO:0069085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 332, pseudogene","termid":"PBO:0069085"}


id: PBO:0055368
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 2797","termid":"PBO:0055368"}


id: FYPO:0001103
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of hydrogen peroxide than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000139","FYPO:0002682","FYPO:0000003"],"is_obsolete":false,"name":"resistance to hydrogen peroxide","synonyms":[{"name":"resistance to H2O2","type":"exact"},{"name":"resistance to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"resistance to hydrogen peroxide during vegetative growth","type":"exact"},{"name":"resistant to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0001103"}


id: GO:0052704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pathway resulting in the formation of ergothioneine from histidine via a set of steps in which gamma-glutamyl-hercynylcysteine sulfoxide is formed as an intermediate.","definition_xrefs":["PMID:5484456","PMID:4276459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ergothioneine biosynthetic process","termid":"GO:0052699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"ergothioneine biosynthesis from histidine via gamma-glutamyl-hercynylcysteine sulfoxide","secondary_identifiers":["Wikipedia:Ergothioneine"],"synonyms":[{"name":"ergothioneine biosynthesis from histidine via N-alpha,N-alpha,N-alpha-trimethyl-L-histidine","type":"broad"}],"termid":"GO:0052704"}


id: FYECO:0000137
data:
  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medium","type":"related"},{"name":"glucose rich medium","type":"exact"},{"name":"normal glucose rich medium","type":"exact"},{"name":"standard dextrose rich medium","type":"exact"},{"name":"standard glucose rich medium","type":"exact"}],"termid":"FYECO:0000137","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000006":null,"FYECO:0000102":null,"FYECO:0000103":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000314":null,"FYECO:0000338":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"FYPO_EXT:0000003":null}}


id: PBO:0059417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S36 pseudogene 3","termid":"PBO:0059417"}


id: MONDO:0005894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A systemic fungal infection caused by Paracoccidioides brasiliensis that is most often seen in immunocompromised patients. It affects the mucous membranes, lymph nodes, lungs and bones.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary systemic mycosis","termid":"MONDO:0000308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paracoccidioidomycosis","secondary_identifiers":["NORD:1553","MEDGEN:14601","Orphanet:73260","SCTID:36866003","MESH:D010229","NCIT:C34891","UMLS:C0030409","GARD:7323","ICD9:116.1","MedDRA:10061906","DOID:12662","EFO:0007417","icd11.foundation:268777657","ICD10CM:B41"],"synonyms":[{"name":"Lutz-Splendore-Almeida disease","type":"related"},{"name":"PCM","type":"related"},{"name":"Paracoccidioidal granuloma","type":"related"},{"name":"South American blastomycosis","type":"related"},{"name":"lobo disease","type":"related"},{"name":"mucocutaneous-lymphangitic paracoccidioidomycosis","type":"exact"},{"name":"paracoccidioidal mycosis","type":"exact"}],"termid":"MONDO:0005894","xrefs":{"Monarch":{"xref_id":"0005894"}}}


id: PBO:0004537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homocitrate synthase (predicted)","termid":"PBO:0004537"}


id: PBO:0084071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase required for ribosomal subunit synthesis and rRNA processing; required for synthesis of 40S ribosomal subunits and for processing the 35S pre-rRNA at sites A0, A1, and A2; interacts with Rcl1p, which stimulates its GTPase and U3 snoRNA binding activities; has similarity to Tsr1p","termid":"PBO:0084071"}


id: GO:0047490
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a pectin = an oligosaccharide with 4-deoxy-6-O-methyl-alpha-D-galact-4-enuronate end + a pectin. This reaction is the eliminative cleavage of (1->4)-alpha-D-galacturonan methyl ester to give oligosaccharides with 4-deoxy-6-O-methyl-alpha-D-galact-4-enuronosyl groups at their nonreducing ends.","definition_xrefs":["EC:4.2.2.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on polysaccharides","termid":"GO:0016837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"pectin lyase activity","secondary_identifiers":["MetaCyc:RXN-19781"],"synonyms":[{"name":"(1->4)-6-O-methyl-alpha-D-galacturonan lyase activity","type":"related"},{"name":"PL activity","type":"related"},{"name":"PMGL activity","type":"related"},{"name":"PNL activity","type":"related"},{"name":"endo-pectin lyase activity","type":"related"},{"name":"pectin methyltranseliminase activity","type":"related"},{"name":"pectin trans-eliminase activity","type":"broad"},{"name":"pectolyase activity","type":"related"},{"name":"polymethylgalacturonic transeliminase activity","type":"related"}],"termid":"GO:0047490"}


id: GO:0019660
data:
  {"annotated_genes":["SJAG_03822","SJAG_03743","SJAG_00240","SJAG_05006","SJAG_04495","SJAG_01414","SJAG_03370"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97496],"is_not":false,"summary":null,"term":"GO:0019660"},{"annotations":[88021,98229,114058,114059,98230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019655"},{"annotations":[96079],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2001172"}]},"cv_name":"biological_process","definition":"Fermentation that includes the anaerobic conversion of glucose to pyruvate via the glycolytic pathway.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fermentation","termid":"GO:0006113"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00240":null,"SJAG_01414":null,"SJAG_03370":null,"SJAG_03743":null,"SJAG_03822":null,"SJAG_04495":null,"SJAG_05006":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"glycolytic fermentation","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:Pyruvate-Degradation"],"termid":"GO:0019660","terms_by_termid":{"GO:0019655":null,"GO:0019660":null,"GO:2001172":null}}


id: MONDO:0014801
data:
  {"annotated_genes":["SJAG_01615"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85326],"is_not":false,"summary":null,"term":"MONDO:0014801"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01615":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"even-plus syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:904613","Orphanet:496751","GARD:17913","OMIM:616854","UMLS:C4225180"],"synonyms":[{"name":"EVPLS","type":"exact"},{"name":"epiphyseal and vertebral dysplasia, microtia, and flat Nose, plus associated malformations","type":"related"},{"name":"epiphysial-vertebral-ear dysplasia-nose-plus associated findings syndrome","type":"exact"},{"name":"even-plus syndrome","type":"exact"}],"termid":"MONDO:0014801","terms_by_termid":{"MONDO:0014801":null},"xrefs":{"Monarch":{"xref_id":"0014801"}}}


id: SO:0000791
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000791 cloned_genomic (obsolete SO:0000791)","termid":"SO:0000791"}


id: FYPO:0000859
data:
  {"alleles_by_uniquename":{"SJAG_02621:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02621","name":"ago1delta","uniquename":"SJAG_02621:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118598,118599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}],"single_locus_phenotype":[{"annotations":[118591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which a cellular metabolic process is normal (i.e. indistinguishable from wild type). A metabolic process is any set of chemical reactions and pathways, including anabolism and catabolism, by which living organisms transform chemical substances.","definition_xrefs":["PomBase:mah","GO:0044237"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"},{"relation_name":"is_a","term_name":"normal metabolic process","termid":"FYPO:0002496"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03118":null,"SJAG_03689":null},"genotype_count":3,"genotypes_by_uniquename":{"ago1delta__leo1delta":{"display_name":"ago1delta leo1delta","display_uniquename":"ago1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02621:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]},"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]},"dcr1delta__leo1delta":{"display_name":"dcr1delta leo1delta","display_uniquename":"dcr1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03689","SJAG_02621","SJAG_03118"],"name":"normal metabolic process during vegetative growth","references_by_uniquename":{"PMID:35226668":null},"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"normal cellular metabolic process during vegetative growth","type":"exact"},{"name":"normal metabolic process during mitotic cell cycle","type":"related"},{"name":"normal metabolism during vegetative growth","type":"exact"}],"termid":"FYPO:0000859","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0006989":null}}


id: GO:1901178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving spheroidene.","definition_xrefs":["UniPathway:UPA00683","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll metabolic process","termid":"GO:0016122"},{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"spheroidene metabolic process","synonyms":[{"name":"spheroidene metabolism","type":"exact"}],"termid":"GO:1901178"}


id: PBO:0006170
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-during","termid":"PBO:0006170"}


id: PBO:0077778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of outer mitochondrial membrane 70","termid":"PBO:0077778"}


id: PBO:0039859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 23 pseudogene 1","termid":"PBO:0039859"}


id: GO:0031068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the removal of acetyl groups from histones in centromeric DNA.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone deacetylation at centromere (obsolete GO:0031068)","synonyms":[{"name":"activation of histone deacetylation at centromere","type":"narrow"},{"name":"stimulation of histone deacetylation at centromere","type":"narrow"},{"name":"up regulation of histone deacetylation at centromere","type":"exact"},{"name":"up-regulation of histone deacetylation at centromere","type":"exact"},{"name":"upregulation of histone deacetylation at centromere","type":"exact"}],"termid":"GO:0031068"}


id: PBO:0054775
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 2188","termid":"PBO:0054775"}


id: PBO:0114419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AIF family member 2","termid":"PBO:0114419"}


id: PBO:0079590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 D3 pseudogene 2","termid":"PBO:0079590"}


id: PBO:0085741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in translation; mutants have defects in biogenesis of nuclear ribosomes; sequence similar to prokaryotic ribosomal protein L36, may be a mitochondrial ribosomal protein; protein abundance increases in response to DNA replication stress","termid":"PBO:0085741"}


id: PBO:0046495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERGIC and golgi 2","termid":"PBO:0046495"}


id: GO:1900870
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of tatiopterin.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine-containing compound biosynthetic process","termid":"GO:0042559"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"},{"relation_name":"is_a","term_name":"tatiopterin metabolic process","termid":"GO:1900869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0042559"}],"interesting_parent_ids":["GO:0044281","GO:0042559","GO:0008150"],"is_obsolete":false,"name":"tatiopterin biosynthetic process","synonyms":[{"name":"tatiopterin anabolism","type":"exact"},{"name":"tatiopterin biosynthesis","type":"exact"},{"name":"tatiopterin formation","type":"exact"},{"name":"tatiopterin synthesis","type":"exact"}],"termid":"GO:1900870"}


id: PBO:0048641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gap junction protein beta 1","termid":"PBO:0048641"}


id: PBO:0045546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 1","termid":"PBO:0045546"}


id: FYPO:0007484
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype in which nucleation of microtubules from one or more microtubule organizing centers (MTOCs) is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"monopolar spindle during meiosis II","termid":"FYPO:0007486"},{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization","termid":"FYPO:0000054"},{"relation_name":"is_a","term_name":"abnormal cellular component assembly","termid":"FYPO:0000336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000054"],"is_obsolete":false,"name":"abnormal microtubule nucleation","synonyms":[{"name":"microtubule nucleation defects","type":"exact"}],"termid":"FYPO:0007484"}


id: GO:1990919
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together a proteasome complex and a nuclear inner membrane, to maintain the nuclear membrane localization of the proteasome.","definition_xrefs":["PMID:16096059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-membrane adaptor activity","termid":"GO:0043495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0030674","GO:0060090"],"is_obsolete":false,"name":"proteasome-nuclear membrane anchor activity","synonyms":[{"name":"nuclear membrane proteasome adaptor","type":"related"},{"name":"nuclear membrane proteasome anchor","type":"exact"},{"name":"nuclear membrane proteasome tether","type":"exact"},{"name":"nuclear membrane proteasome tether activity","type":"exact"},{"name":"nuclear membrane-proteasome anchor activity","type":"exact"},{"name":"nuclear membrane-proteasome tether activity","type":"exact"},{"name":"tethering factor for nuclear proteasome","type":"related"}],"termid":"GO:1990919"}


id: MONDO:0016963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete partial duplication of the long arm of chromosome 13 (obsolete MONDO:0016963)","termid":"MONDO:0016963","xrefs":{"Monarch":{"xref_id":"0016963"}}}


id: MONDO:0018387
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare male infertility due to adrenal disorder (obsolete MONDO:0018387)","secondary_identifiers":["Orphanet:399584"],"termid":"MONDO:0018387","xrefs":{"Monarch":{"xref_id":"0018387"}}}


id: GO:0010653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of cell communication via chemical coupling. Cell communication by chemical coupling is the process that mediates signaling interactions between one cell and another cell by the transfer of small, water-soluble molecules or metabolites between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:dph","GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication by chemical coupling","termid":"GO:0010645"},{"relation_name":"is_a","term_name":"negative regulation of cell communication","termid":"GO:0010648"},{"relation_name":"negatively_regulates","term_name":"cell communication by chemical coupling","termid":"GO:0010643"}],"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 cell communication by chemical coupling","termid":"GO:0010653"}


id: PR:Q9UT51
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- csn3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT51"],"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":"COP9 signalosome complex subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC222.16c","synonyms":[{"name":"CSN complex subunit 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SGN3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-csn3","type":"exact"}],"termid":"PR:Q9UT51"}


id: PBO:0070846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13a pseudogene 25","termid":"PBO:0070846"}


id: PBO:0053321
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 106","termid":"PBO:0053321"}


id: MONDO:0004687
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"background diabetic retinopathy","termid":"MONDO:0001661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"severe nonproliferative diabetic retinopathy","secondary_identifiers":["UMLS:C0730278","icd11.foundation:561966379","MEDGEN:676487","DOID:8946","SCTID:312905005","ICD9:362.06"],"synonyms":[{"name":"high risk non proliferative diabetic retinopathy","type":"exact"},{"name":"severe NPDR","type":"exact"},{"name":"severe nonproliferative diabetic retinopathy","type":"exact"},{"name":"severe nonproliferative retinopathy","type":"related"},{"name":"severe npdr","type":"related"}],"termid":"MONDO:0004687","xrefs":{"Monarch":{"xref_id":"0004687"}}}


id: PBO:0026911
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_rate_of_protein_localization_to_actomyosin_contractile_ring","termid":"PBO:0026911"}


id: MONDO:0012356
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete glomerulocystic kidney disease with hyperuricemia and isosthenuria (obsolete MONDO:0012356)","termid":"MONDO:0012356","xrefs":{"Monarch":{"xref_id":"0012356"}}}


id: MONDO:0008069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Leigh syndrome","termid":"MONDO:0009723"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"necrotizing encephalomyelopathy, subacute, of Leigh, adult","secondary_identifiers":["MEDGEN:331718","UMLS:C1834340","OMIM:161700","MESH:C563530"],"synonyms":[{"name":"Leigh syndrome, adult","type":"related"},{"name":"necrotizing encephalomyelopathy, subacute, of Leigh, adult","type":"exact"}],"termid":"MONDO:0008069","xrefs":{"Monarch":{"xref_id":"0008069"}}}


id: PBO:0062276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily H member 7 pseudogene","termid":"PBO:0062276"}


id: GO:0021909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that results in the spatial identity of regions along the anterior-posterior axis of the spinal cord.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:cls","PMID:11262869","GOC:dph","GO_REF:0000021"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in spinal cord anterior-posterior patterning (obsolete GO:0021909)","termid":"GO:0021909"}


id: PR:O14291
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC9E9.05 gene.","definition_xrefs":["UniProtKB:O14291","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 C9E9.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9E9.05","synonyms":[{"name":"Spom972h-SPAC9E9.05","type":"exact"}],"termid":"PR:O14291"}


id: GO:0061917
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"That part of the dendritic growth cone which represents the distal part of the structure.","definition_xrefs":["PMID:16098134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth cone leading edge","termid":"GO:0061850"},{"relation_name":"part_of","term_name":"dendritic growth cone","termid":"GO:0044294"}],"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":"leading edge of dendritic growth cone","synonyms":[{"name":"dendritic growth cone leading edge","type":"exact"},{"name":"distal tip of dendritic growth cone","type":"exact"}],"termid":"GO:0061917"}


id: PBO:0076774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis development related 1","termid":"PBO:0076774"}


id: PBO:0041389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 5 open reading frame 52","termid":"PBO:0041389"}


id: PBO:0051649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 1 pseudogene 4","termid":"PBO:0051649"}


id: RO:0002331
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c involved_in p if and only if c enables some process p', and p' is part of p","direct_ancestors":[{"relation_name":"is_a","term_name":"involved_in_or_involved_in_regulation_of","termid":"RO:0002431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involved_in","termid":"RO:0002331"}


id: PBO:0059691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 57","termid":"PBO:0059691"}


id: PBO:0028959
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_UDP-galactose_transmembrane_transport","termid":"PBO:0028959"}


id: GO:0034279
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9-alpha-copalyl diphosphate = 9-beta-pimara-7,15-diene + diphosphate.","definition_xrefs":["RHEA:25560"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"syn-pimara-7,15-diene synthase activity","secondary_identifiers":["EC:4.2.3.35","KEGG_REACTION:R09117","MetaCyc:RXN-4883"],"synonyms":[{"name":"9alpha-copalyl-diphosphate diphosphate-lyase (9beta-pimara-7,15-diene-forming) activity","type":"exact"}],"termid":"GO:0034279"}


id: PBO:0001643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"steroid dehydrogenase (predicted)","termid":"PBO:0001643"}


id: PBO:0087507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of HDA1 histone deacetylase complex; tetrameric trichostatin A-sensitive class II histone deacetylase complex contains Hda1p homodimer and an Hda2p-Hda3p heterodimer; required for activity of complex; relocalizes to cytosol in response to hypoxia; similar to Hda2p; the HDA1 histone deacetylase complex regulates aging through trehalose metabolism","termid":"PBO:0087507"}


id: GO:0104005
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A function that was not selected for in the evolution of an organism, but arises from co-option by another organism, e.g. a human protein used as a virus receptor.","definition_xrefs":["GOC:pdt"],"gene_count":0,"genotype_count":0,"name":"obsolete hijacked molecular function (obsolete GO:0104005)","termid":"GO:0104005"}


id: PBO:0079468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"twinfilin actin binding protein 1","termid":"PBO:0079468"}


id: PBO:0066045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAP1B pseudogene 1","termid":"PBO:0066045"}


id: GO:0071792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving bacillithiol, the alpha-anomeric glycoside of L-cysteinyl-D-glucosamine with L-malic acid. Bacillithiol, produced widely in the Firmicutes and sporadically in other bacterial lineages, is a low-molecular-weight thiol analogous to mycothiol in the Actinomycetes and glutathione in many species.","definition_xrefs":["GOC:dh","PMID:20308541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"glycoside metabolic process","termid":"GO:0016137"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"bacillithiol metabolic process","synonyms":[{"name":"bacillithiol metabolism","type":"exact"}],"termid":"GO:0071792"}


id: FYPO:0006166
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, branched, has more than one nucleus, and has a larger volume and is longer, than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah","PomBase:jh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated multinucleate vegetative cell","termid":"FYPO:0001493"},{"relation_name":"is_a","term_name":"inviable branched, swollen, elongated vegetative cell","termid":"FYPO:0004494"},{"relation_name":"is_a","term_name":"branched, swollen, elongated, multinucleate vegetative cell","termid":"FYPO:0006165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0001985","FYPO:0000005","FYPO:0000004","FYPO:0001320","FYPO:0000032"],"is_obsolete":false,"name":"inviable branched, swollen, elongated, multinucleate vegetative cell","synonyms":[{"name":"inviable branched, elongated, swollen, multinucleate vegetative cell","type":"exact"},{"name":"inviable branched, swollen, elongated, multinucleate cell during vegetative growth","type":"exact"},{"name":"inviable branched, swollen, elongated, multinucleate vegetative cell during mitotic cell cycle","type":"related"},{"name":"lethal; branched, swollen, elongated, multinucleate vegetative cell","type":"exact"}],"termid":"FYPO:0006166"}


id: GO:0043642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of novobiocin, a coumarin antibiotic produced by the bacterium Gyrasestreptomyces spheroides, that acts by inhibiting DNA gyrase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coumarin biosynthetic process","termid":"GO:0009805"},{"relation_name":"is_a","term_name":"glycoside biosynthetic process","termid":"GO:0016138"},{"relation_name":"is_a","term_name":"antibiotic biosynthetic process","termid":"GO:0017000"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"novobiocin metabolic process","termid":"GO:0043641"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"novobiocin biosynthetic process","secondary_identifiers":["Wikipedia:Novobiocin"],"termid":"GO:0043642"}


id: MONDO:0004544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade II, usually recurring meningioma characterized by the predominance of tissues that are histologically similar to chordoma.","definition_xrefs":["NCIT:C6908"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"clear cell meningioma","termid":"MONDO:0002918"},{"relation_name":"is_a","term_name":"grade II meningioma","termid":"MONDO:0045056"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chordoid meningioma","secondary_identifiers":["ONCOTREE:CHOM","MEDGEN:235089","UMLS:C1370510","DOID:8368"],"synonyms":[{"name":"CHOM","type":"related"},{"name":"chordoid meningioma","type":"exact"},{"name":"meningioma, chordoid","type":"exact"},{"name":"meningioma, chordoid (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004544","xrefs":{"Monarch":{"xref_id":"0004544"}}}


id: GO:0004414
data:
  {"annotated_genes":["SJAG_00395"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110543],"is_not":false,"summary":null,"term":"GO:0004414"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-homoserine + acetyl-CoA = O-acetyl-L-homoserine + CoA.","definition_xrefs":["RHEA:13701","EC:2.3.1.31"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00395":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"homoserine O-acetyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:HOMOSERINE-O-ACETYLTRANSFERASE-RXN","KEGG_REACTION:R01776"],"synonyms":[{"name":"L-homoserine O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:L-homoserine O-acetyltransferase activity","type":"related"},{"name":"homoserine O-trans-acetylase activity","type":"related"},{"name":"homoserine acetyltransferase activity","type":"related"},{"name":"homoserine transacetylase activity","type":"broad"},{"name":"homoserine-O-transacetylase activity","type":"related"}],"termid":"GO:0004414","terms_by_termid":{"GO:0004414":null}}


id: PBO:0034506
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_frequency_of_meiotic_crossover_associated_with_gene_conversion","termid":"PBO:0034506"}


id: PBO:0065131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKG2 antisense RNA 1","termid":"PBO:0065131"}


id: GO:0099177
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of trans-synaptic signaling.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"is_a","term_name":"regulation of signaling","termid":"GO:0023051"},{"relation_name":"regulates","term_name":"trans-synaptic signaling","termid":"GO:0099537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of trans-synaptic signaling","termid":"GO:0099177"}


id: PBO:0072762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100 calcium binding protein A13","termid":"PBO:0072762"}


id: GO:0051895
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of focal adhesion assembly, the establishment and maturation of focal adhesions.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell-matrix adhesion","termid":"GO:0001953"},{"relation_name":"is_a","term_name":"regulation of focal adhesion assembly","termid":"GO:0051893"},{"relation_name":"is_a","term_name":"negative regulation of cell-substrate junction organization","termid":"GO:0150118"},{"relation_name":"is_a","term_name":"negative regulation of cell junction assembly","termid":"GO:1901889"},{"relation_name":"negatively_regulates","term_name":"focal adhesion assembly","termid":"GO:0048041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0007155","GO:0044085"],"is_obsolete":false,"name":"negative regulation of focal adhesion assembly","synonyms":[{"name":"down regulation of focal adhesion formation","type":"exact"},{"name":"down-regulation of focal adhesion formation","type":"exact"},{"name":"downregulation of focal adhesion formation","type":"exact"},{"name":"inhibition of focal adhesion formation","type":"narrow"}],"termid":"GO:0051895"}


id: MONDO:0010535
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bazex-Dupre-Christol syndrome is a rare genodermatosis (hereditary skin disease) with a predisposition to early-onset basal cell carcinomas.","definition_xrefs":["Orphanet:113"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited skin tumor (obsolete MONDO:0015950)","termid":"MONDO:0015950"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"excluded_subClassOf","term_name":"obsolete malignant tumor of palpebral epidermis (obsolete MONDO:0020175)","termid":"MONDO:0020175"},{"relation_name":"excluded_subClassOf","term_name":"obsolete congenital absence of the eyebrow/eyelashes (obsolete MONDO:0020188)","termid":"MONDO:0020188"},{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"Bazex-Dupre-Christol syndrome","secondary_identifiers":["Orphanet:166113","ICD9:757.39","UMLS:C0346104","SCTID:238640007","SCTID:254820002","GARD:838","OMIM:301845","MEDGEN:87539"],"synonyms":[{"name":"BDCS","type":"exact"},{"name":"BZX","type":"related"},{"name":"Bazex syndrome","type":"exact"},{"name":"Bazex syndrome, X-linked dominant","type":"exact"},{"name":"Bazex-Dupre-Christol syndrome","type":"exact"},{"name":"Bazex-Dupré-Christol syndrome","type":"exact"},{"name":"acrokeratosis of Bazex","type":"exact"},{"name":"acrokeratosis paraneoplastica","type":"exact"},{"name":"acrokeratosis paraneoplastica of Bazex","type":"exact"},{"name":"follicular atrophoderma and basal cell carcinomas","type":"exact"},{"name":"follicular atrophoderma-basal cell carcinoma syndrome","type":"related"},{"name":"follicular atrophoderma-basocellular proliferations-hypotrichosis syndrome","type":"related"}],"termid":"MONDO:0010535","xrefs":{"Monarch":{"xref_id":"0010535"}}}


id: PATO:0001978
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being regularly divided by deep incisions.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cut","synonyms":[{"name":"incised","type":"exact"}],"termid":"PATO:0001978"}


id: PR:000029999
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tumor suppressor p53-binding protein 1 that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair protein Crb2 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC342.05","synonyms":[{"name":"DNA repair protein rhp9 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-TP53BP1","type":"exact"}],"termid":"PR:000029999"}


id: PBO:0041199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BUD23 rRNA methyltransferase and ribosome maturation factor","termid":"PBO:0041199"}


id: GO:0052239
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism towards a lower concentration of a specific chemical within a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative chemotaxis in other organism involved in symbiotic interaction (obsolete GO:0052239)","synonyms":[{"name":"negative chemotaxis in other organism during symbiotic interaction","type":"related"},{"name":"negative chemotaxis within other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052239"}


id: GO:0015108
data:
  {"annotated_genes":["SJAG_01168","SJAG_03401"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005254"},{"annotations":[105171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015379"}]},"cv_name":"molecular_function","definition":"Enables the transfer of chloride ions from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic anion transmembrane transporter activity","termid":"GO:0008509"},{"relation_name":"is_a","term_name":"inorganic anion transmembrane transporter activity","termid":"GO:0015103"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01168":null,"SJAG_03401":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"chloride transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5678992","Reactome:R-HSA-5678822","Reactome:R-HSA-5678863","GO:0008555"],"synonyms":[{"name":"ATP-dependent chloride transmembrane transporter activity","type":"narrow"},{"name":"ATPase-coupled chloride transmembrane transporter activity","type":"narrow"},{"name":"chloride ABC transporter","type":"narrow"},{"name":"chloride ion transmembrane transporter activity","type":"exact"},{"name":"chloride transporting ATPase activity","type":"narrow"},{"name":"chloride-transporting ATPase activity","type":"narrow"}],"termid":"GO:0015108","terms_by_termid":{"GO:0005254":null,"GO:0015379":null}}


id: FYPO:0001042
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell of normal morphology that undergoes one or two rounds of cell division, and then dies.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination","termid":"FYPO:0000316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination, single or double cell division","synonyms":[{"name":"inviable following spore germination, single or double cell division","type":"exact"},{"name":"inviable germinated spore, single or double cell division","type":"exact"},{"name":"lethal after spore germination, single or double cell division","type":"exact"}],"termid":"FYPO:0001042"}


id: GO:1905220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of platelet formation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:10606160"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of myeloid cell differentiation","termid":"GO:0045638"},{"relation_name":"is_a","term_name":"regulation of platelet formation","termid":"GO:1905219"},{"relation_name":"negatively_regulates","term_name":"platelet formation","termid":"GO:0030220"}],"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 platelet formation","synonyms":[{"name":"down regulation of platelet extrusion","type":"exact"},{"name":"down regulation of platelet formation","type":"exact"},{"name":"down-regulation of platelet extrusion","type":"exact"},{"name":"down-regulation of platelet formation","type":"exact"},{"name":"downregulation of platelet extrusion","type":"exact"},{"name":"downregulation of platelet formation","type":"exact"},{"name":"inhibition of platelet extrusion","type":"narrow"},{"name":"inhibition of platelet formation","type":"narrow"},{"name":"negative regulation of platelet extrusion","type":"exact"}],"termid":"GO:1905220"}


id: PATO:0000712
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000712 bouts value (obsolete PATO:0000712)","termid":"PATO:0000712"}


id: PBO:0083494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene YJL121C/RPE1; deletion confers sensitivity to GSAO","termid":"PBO:0083494"}


id: PBO:0077254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 5","termid":"PBO:0077254"}


id: MONDO:0100454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inherited retinal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"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":"GUCY2D retinopathy","synonyms":[{"name":"retinopathy caused by mutation in GUCY2D","type":"exact"}],"termid":"MONDO:0100454","xrefs":{"Monarch":{"xref_id":"0100454"}}}


id: PBO:0069656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 933, pseudogene","termid":"PBO:0069656"}


id: MONDO:0001662
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete right bundle branch block (obsolete MONDO:0001662)","secondary_identifiers":["SCTID:59118001","ICD9:426.51","HP:0011712","DOID:13209","ICD9:426.4"],"synonyms":[{"name":"obsolete right bundle branch block (disease)","type":"exact"},{"name":"right bundle branch block","type":"exact"},{"name":"right bundle branch block with left posterior fascicular block","type":"exact"}],"termid":"MONDO:0001662","xrefs":{"Monarch":{"xref_id":"0001662"}}}


id: PBO:0061286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore associated protein 1 pseudogene 7","termid":"PBO:0061286"}


id: PBO:0076165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1A member 1","termid":"PBO:0076165"}


id: PBO:0052613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KRAB box domain containing 5","termid":"PBO:0052613"}


id: FYPO:0005181
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein degradation is normal (i.e. indistinguishable from wild type) when the cell is exposed to ultraviolet light. Protein degradation, also known as protein catabolism, is any metabolic process that results in the destruction of the native, active configuration of a protein, with or without the hydrolysis of peptide bonds.","definition_xrefs":["GO:0030163","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein degradation during vegetative growth","termid":"FYPO:0002800"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein degradation during cellular response to UV","synonyms":[{"name":"normal protein breakdown during cellular response to UV","type":"exact"},{"name":"normal protein catabolic process during cellular response to UV","type":"exact"},{"name":"normal protein catabolism during cellular response to UV","type":"exact"},{"name":"normal protein degradation during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"normal protein degradation during cellular response to UV during vegetative growth","type":"exact"},{"name":"normal protein degradation during cellular response to ultraviolet light","type":"exact"}],"termid":"FYPO:0005181"}


id: FYPO:0005192
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A stress response phenotype in which the response to nitrogen starvation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to stress","termid":"FYPO:0005191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0000298"],"is_obsolete":false,"name":"normal cellular response to nitrogen starvation","synonyms":[{"name":"normal cellular response to nitrogen depletion","type":"exact"},{"name":"normal cellular response to nitrogen deprivation","type":"exact"}],"termid":"FYPO:0005192"}


id: PR:000037030
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the rho3 gene in Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding protein rho3 (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC23C4.08","synonyms":[{"name":"Spom-rho3","type":"exact"}],"termid":"PR:000037030"}


id: PBO:0040721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL10 immune signaling adaptor","termid":"PBO:0040721"}


id: GO:1904329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of myofibroblast contraction.","definition_xrefs":["PMID:19239477","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"regulation of myofibroblast contraction","termid":"GO:1904328"},{"relation_name":"negatively_regulates","term_name":"myofibroblast contraction","termid":"GO:1990764"}],"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 myofibroblast contraction","synonyms":[{"name":"down regulation of MF contraction","type":"exact"},{"name":"down regulation of MFB contraction","type":"exact"},{"name":"down regulation of myofibroblast contraction","type":"exact"},{"name":"down-regulation of MF contraction","type":"exact"},{"name":"down-regulation of MFB contraction","type":"exact"},{"name":"down-regulation of myofibroblast contraction","type":"exact"},{"name":"downregulation of MF contraction","type":"exact"},{"name":"downregulation of MFB contraction","type":"exact"},{"name":"downregulation of myofibroblast contraction","type":"exact"},{"name":"inhibition of MF contraction","type":"narrow"},{"name":"inhibition of MFB contraction","type":"narrow"},{"name":"inhibition of myofibroblast contraction","type":"narrow"},{"name":"negative regulation of MF contraction","type":"exact"},{"name":"negative regulation of MFB contraction","type":"exact"}],"termid":"GO:1904329"}


id: MONDO:0700127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 21 characterized by the presence of an extra chromosome 21 in some of the cells of the organism.","definition_xrefs":["PMID:29218069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trisomy 21","termid":"MONDO:0700126"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mosaic trisomy 21","secondary_identifiers":["MEDGEN:419386","UMLS:C2931324"],"termid":"MONDO:0700127","xrefs":{"Monarch":{"xref_id":"0700127"}}}


id: GO:0044013
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H2B L-lysine = CoA + histone H2B N6-acetyl-L-lysine.","definition_xrefs":["PMID:19056256"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone acetyltransferase activity","termid":"GO:0004402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0034212"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0016740","GO:0034212","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"histone H2B acetyltransferase activity","synonyms":[{"name":"H2B histone acetylase activity","type":"exact"},{"name":"H2B histone acetyltransferase activity","type":"exact"},{"name":"H2B histone lysine N-acetyltransferase activity","type":"exact"}],"termid":"GO:0044013"}


id: PBO:0071849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 44","termid":"PBO:0071849"}


id: GO:0140164
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a Golgi transport complex, a multisubunit tethering complex of the CATCHR family.","definition_xrefs":["PMID:28100664","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"Golgi transport complex binding","synonyms":[{"name":"COG complex binding","type":"exact"}],"termid":"GO:0140164"}


id: FYPO:0004304
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a phosphatase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal phosphatase activity","termid":"FYPO:0004302"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0001985","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"decreased phosphatase activity","synonyms":[{"name":"reduced phosphatase activity","type":"exact"}],"termid":"FYPO:0004304"}


id: PBO:0005318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RSC complex subunit Sfh1","termid":"PBO:0005318"}


id: PBO:0087151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA duplex-sensing translocase; ATP-dependent 3'-5' RNA helicase of the DExD/H family; involved in nuclear RNA processing and degradation as a component of TRAMP complex and in TRAMP-independent processes; TRAMP unwinds RNA duplexes, with Mtr4p unwinding activity stimulated by Pap2p/Air2p but not dependent on ongoing polyadenylation; contains an arch domain, with two coiled-coil arms/stalks and a globular fist/KOW domain, which has RNA binding activity and is required for 5.8S rRNA processing","termid":"PBO:0087151"}


id: MONDO:0011933
data:
  {"annotated_genes":["SJAG_03056"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86397],"is_not":false,"summary":null,"term":"MONDO:0011933"},{"annotations":[84940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014543"}]},"cv_name":"mondo","definition":"A form of congenital disorders of N-linked glycosylation characterized by iris coloboma, cataract, infantile spasms, developmental delay and abnormal coagulation factors. The disease is caused by loss-of-function mutations in the gene ALG2 (9q31.1). Transmission is autosomal recessive.","definition_xrefs":["Orphanet:79326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type I","termid":"MONDO:0005500"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03056":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"ALG2-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:9836","MEDGEN:334618","DOID:0080561","OMIM:607906","UMLS:C1842836"],"synonyms":[{"name":"ALG2-CDG","type":"exact"},{"name":"ALG2-CDG (CDG-II)","type":"related"},{"name":"ALG2-congenital disorder of glycosylation","type":"exact"},{"name":"CDG 1I","type":"exact"},{"name":"CDG Ii","type":"exact"},{"name":"CDG syndrome type Ii","type":"exact"},{"name":"CDG1I","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type Ii","type":"exact"},{"name":"carbohydrate-deficient glycoprotein syndrome type 1I","type":"related"},{"name":"congenital disorder of glycosylation type 1i","type":"exact"},{"name":"congenital disorder of glycosylation type Ii","type":"exact"},{"name":"congenital disorder of glycosylation, type Ii","type":"exact"},{"name":"mannosyltransferase 2 deficiency","type":"exact"}],"termid":"MONDO:0011933","terms_by_termid":{"MONDO:0011933":null,"MONDO:0014543":null},"xrefs":{"Monarch":{"xref_id":"0011933"}}}


id: PBO:0039794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARAP1 antisense RNA 1","termid":"PBO:0039794"}


id: PBO:0072446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 10","termid":"PBO:0072446"}


id: GO:0016498
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with neuromedin K, the peptide Asp-Met-His-Asp-Phe-Phe-Val-Gly-Leu-Met to initiate a change in cell activity.","definition_xrefs":["ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tachykinin receptor activity","termid":"GO:0004995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"neuromedin K receptor activity","synonyms":[{"name":"neurokinin B receptor activity","type":"exact"}],"termid":"GO:0016498"}


id: PR:O60093
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ber1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60093"],"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":"SRR1-like protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC14C8.13","synonyms":[{"name":"Spom972h-ber1","type":"exact"}],"termid":"PR:O60093"}


id: GO:0048074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of establishment of a pattern of pigment in the eye of an organism.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of eye pigmentation","termid":"GO:0048073"},{"relation_name":"is_a","term_name":"negative regulation of developmental pigmentation","termid":"GO:0048086"},{"relation_name":"negatively_regulates","term_name":"eye pigmentation","termid":"GO:0048069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of eye pigmentation","synonyms":[{"name":"down regulation of eye pigmentation","type":"exact"},{"name":"down-regulation of eye pigmentation","type":"exact"},{"name":"downregulation of eye pigmentation","type":"exact"},{"name":"inhibition of eye pigmentation","type":"narrow"}],"termid":"GO:0048074"}


id: GO:0072142
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a juxtaglomerulus cell over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"juxtaglomerulus cell differentiation","termid":"GO:0072052"}],"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":"juxtaglomerulus cell development","termid":"GO:0072142"}


id: GO:1905092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a diosgenin stimulus.","definition_xrefs":["GOC:bc","GO_REF:0000071","GOC:BHF_miRNA","GOC:BHF","GOC:TermGenie","PMID:25765596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to sterol","termid":"GO:0036314"},{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"},{"relation_name":"is_a","term_name":"response to triterpenoid","termid":"GO:1905836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to diosgenin","termid":"GO:1905092"}


id: PBO:0114377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma calcium permeable gated cation channel","termid":"PBO:0114377"}


id: PBO:0041433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 8 open reading frame 90","termid":"PBO:0041433"}


id: PBO:0081792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 722","termid":"PBO:0081792"}


id: MONDO:1012421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuroaxonal dystrophy with cerebellar abiotrophy, non-human animal","termid":"MONDO:1011886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroaxonal dystrophy with cerebellar abiotrophy, domestic cat","secondary_identifiers":["OMIA:001606-9685"],"termid":"MONDO:1012421","xrefs":{"Monarch":{"xref_id":"1012421"}}}


id: PBO:0057484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 602","termid":"PBO:0057484"}


id: PBO:0090464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-coenzyme A thioesterase The4","termid":"PBO:0090464"}


id: PBO:0064408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNMA family member 3","termid":"PBO:0064408"}


id: GO:0015736
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which hexuronate is transported across a lipid bilayer, from one side of a membrane to the other. A hexuronate is any monocarboxylic acid derived from a hexose by oxidation of C-6.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uronic acid transmembrane transport","termid":"GO:0015735"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"hexuronate transmembrane transport","synonyms":[{"name":"hexuronate transport","type":"related"}],"termid":"GO:0015736"}


id: GO:0016080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which synaptic vesicles are directed to specific destination membranes, mediated by molecules at the vesicle membrane and target membrane surfaces.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle targeting","termid":"GO:0006903"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"},{"relation_name":"part_of","term_name":"synaptic vesicle exocytosis","termid":"GO:0016079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"synaptic vesicle targeting","termid":"GO:0016080"}


id: PBO:0029529
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_alpha-glucanase","termid":"PBO:0029529"}


id: PBO:0091312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNA primary transcript","termid":"PBO:0091312"}


id: MONDO:1012271
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thrombasthenia, non-human animal","termid":"MONDO:1011694"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombasthenia, domestic cat","secondary_identifiers":["OMIA:001000-9685"],"termid":"MONDO:1012271","xrefs":{"Monarch":{"xref_id":"1012271"}}}


id: MONDO:0000169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete microphthalmia, isolated, with cataract (obsolete MONDO:0000169)","secondary_identifiers":["OMIMPS:156850"],"termid":"MONDO:0000169","xrefs":{"Monarch":{"xref_id":"0000169"}}}


id: GO:0036207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of expression of a histone-encoding gene. Gene expression is the process in which a gene's coding sequence is converted into a mature gene product or products (proteins or RNA). This includes the production of an RNA transcript as well as any processing to produce a mature RNA product or an mRNA (for protein-coding genes) and the translation of that mRNA into protein.","definition_xrefs":["GOC:bf","GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone gene expression (obsolete GO:0036207)","synonyms":[{"name":"activation of histone gene expression","type":"narrow"},{"name":"positive regulation of expression of histone-encoding gene","type":"exact"},{"name":"up-regulation of histone gene expression","type":"exact"},{"name":"upregulation of histone gene expression","type":"exact"}],"termid":"GO:0036207"}


id: MONDO:0015238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arhinia-choanal atresia-microphthalmia is a malformation disorder characterized by complete or incomplete absence of nose (arrhinia), choanal atresia, microphthalmia, anophthalmia and cleft or high palate.","definition_xrefs":["Orphanet:1135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrhinia-choanal atresia-microphthalmia syndrome","secondary_identifiers":["GARD:8755","NORD:1909"],"synonyms":[{"name":"Bosma Arhinia Microphthalmia Syndrome","type":"exact"},{"name":"Bosma Henkin Christiansen syndrome","type":"related"},{"name":"Bosma arhinia microphthalmia syndrome","type":"related"},{"name":"arhinia choanal atresia microphthalmia","type":"related"},{"name":"congenital absence of nose and anterior nasopharynx","type":"related"}],"termid":"MONDO:0015238","xrefs":{"Monarch":{"xref_id":"0015238"}}}


id: GO:2000855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mineralocorticoid secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of corticosteroid hormone secretion","termid":"GO:2000846"},{"relation_name":"regulates","term_name":"mineralocorticoid secretion","termid":"GO:0035931"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"regulation of mineralocorticoid secretion","termid":"GO:2000855"}


id: GO:0032467
data:
  {"annotated_genes":["SJAG_02392","SJAG_02838","SJAG_03581","SJAG_04776","SJAG_01805","SJAG_04468","SJAG_04666","SJAG_05290","SJAG_00514","SJAG_03704","SJAG_04597","SJAG_00845","SJAG_01188","SJAG_03342","SJAG_03936","SJAG_03631","SJAG_01787","SJAG_01114","SJAG_00082"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89508,93917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[87052,109975,93918,94086,112803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903473"},{"annotations":[93304,89509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903490"},{"annotations":[90282,110217,118986,103189,95359],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903617"},{"annotations":[104650,88753,105852,112804,114914,106513,117331,89380,93305,91927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140281"},{"annotations":[93921,91928,87053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905758"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the division of the cytoplasm of a cell, and its separation into two daughter cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokinesis","termid":"GO:0032465"},{"relation_name":"is_a","term_name":"positive regulation of cell division","termid":"GO:0051781"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"positively_regulates","term_name":"cytokinesis","termid":"GO:0000910"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00514":null,"SJAG_00845":null,"SJAG_01114":null,"SJAG_01188":null,"SJAG_01787":null,"SJAG_01805":null,"SJAG_02392":null,"SJAG_02838":null,"SJAG_03342":null,"SJAG_03581":null,"SJAG_03631":null,"SJAG_03704":null,"SJAG_03936":null,"SJAG_04468":null,"SJAG_04597":null,"SJAG_04666":null,"SJAG_04776":null,"SJAG_05290":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"positive regulation of cytokinesis","references_by_uniquename":{"GO_REF:0000107":null,"PMID:25866389":null},"secondary_identifiers":["GO:0071777"],"synonyms":[{"name":"activation of cytokinesis","type":"narrow"},{"name":"positive regulation of cell cycle cytokinesis","type":"related"},{"name":"stimulation of cytokinesis","type":"narrow"},{"name":"up regulation of cytokinesis","type":"exact"},{"name":"up-regulation of cytokinesis","type":"exact"},{"name":"upregulation of cytokinesis","type":"exact"}],"termid":"GO:0032467","terms_by_termid":{"GO:0140281":null,"GO:1903473":null,"GO:1903490":null,"GO:1903501":null,"GO:1903617":null,"GO:1905758":null}}


id: PBO:0063777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHF5A pseudogene 4","termid":"PBO:0063777"}


id: MONDO:0016049
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paradas type congenital myopathy is an early-onset form of dysferlinopathy presenting with postnatal hypotonia, weakness in the proximal lower limbs and neck flexor muscles at birth and delayed motor development.","definition_xrefs":["Orphanet:199329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative defects of dysferlin","termid":"MONDO:0016145"},{"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":"congenital myopathy, Paradas type","secondary_identifiers":["MEDGEN:1388555","GARD:20335","UMLS:C4511057"],"termid":"MONDO:0016049","xrefs":{"Monarch":{"xref_id":"0016049"}}}


id: PBO:0069895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1186, pseudogene","termid":"PBO:0069895"}


id: FYPO:0002113
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is inviable, and is curved along the long axis. In a curved cell, the long axis follows a smooth bend rather than a straight line.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"curved vegetative cell","termid":"FYPO:0000016"},{"relation_name":"is_a","term_name":"curved vegetative cell","termid":"FYPO:0000016"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell morphology","termid":"FYPO:0002273"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell shape","termid":"FYPO:0002451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000005","FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"inviable curved vegetative cell","synonyms":[{"name":"curved inviable cell","type":"exact"},{"name":"inviable curved cell","type":"exact"},{"name":"inviable curved cell during vegetative growth","type":"exact"},{"name":"inviable curved vegetative cell during mitotic cell cycle","type":"related"},{"name":"lethal; curved vegetative cell","type":"exact"}],"termid":"FYPO:0002113"}


id: PBO:0001329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calnexin Cnx1","termid":"PBO:0001329"}


id: PBO:0043696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 5B pseudogene 2","termid":"PBO:0043696"}


id: MOD:01576
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ8plex-119 reporter+balance reagent acylated residue","termid":"MOD:01570"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent O-acylated residue","termid":"MOD:01714"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-119 reporter+balance reagent O3-acylated threonine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"}],"termid":"MOD:01576"}


id: PBO:0058839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8069","termid":"PBO:0058839"}


id: PR:Q9UTG3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1805.14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTG3"],"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 C1805.14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1805.14","synonyms":[{"name":"Spom972h-SPAC1805.14","type":"exact"}],"termid":"PR:Q9UTG3"}


id: PBO:0017636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc ion transmembrane transporter Zhf1","termid":"PBO:0017636"}


id: PR:O14176
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- usp104 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14176"],"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":"pre-mRNA-processing protein prp40 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.13","synonyms":[{"name":"Spom972h-usp104","type":"exact"}],"termid":"PR:O14176"}


id: PBO:0074128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 31 member 1","termid":"PBO:0074128"}


id: PBO:0052023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"junctophilin 1","termid":"PBO:0052023"}


id: GO:0016533
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that has protein serine/threonine kinase activity; in mammals composed of catalytic subunit CDK5 and regulatory subunits CDK5R1 or CDK5R2. Contrary to its gene symbol, CDK5 is not cyclin-dependent.","definition_xrefs":["PMID:15689152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine/threonine protein kinase complex","termid":"GO:1902554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"protein kinase 5 complex","synonyms":[{"name":"cyclin-dependent protein kinase 5 holoenzyme complex","type":"related"}],"termid":"GO:0016533"}


id: FYPO:0000084
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to 6-azauracil. Cells stop growing (and may die) at a concentration of 6-azauracil that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0002683","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to 6-azauracil","synonyms":[{"name":"hypersensitive to 6-azauracil","type":"exact"},{"name":"sensitive to 6-azauracil during mitotic cell cycle","type":"related"},{"name":"sensitive to 6-azauracil during vegetative growth","type":"exact"}],"termid":"FYPO:0000084"}


id: GO:0072140
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a distal convoluted tubule cell over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"DCT cell differentiation","termid":"GO:0072069"}],"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":"DCT cell development","synonyms":[{"name":"distal convoluted tubule cell development","type":"exact"}],"termid":"GO:0072140"}


id: PBO:0000884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-glycosylation protein (predicted)","termid":"PBO:0000884"}


id: GO:0003274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell-cell adhesion process of mesenchymal cardiac cushion cells that contributes to the process of cushion shaping.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell adhesion involved in heart morphogenesis","termid":"GO:0061343"},{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"},{"relation_name":"part_of","term_name":"endocardial cushion morphogenesis","termid":"GO:0003203"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"endocardial cushion fusion","termid":"GO:0003274"}


id: GO:0140509
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The organization of a polarized cell layer during morphogenesis in protozoa; an example is found during culmination in D. discoideum, involving alpha and beta catenins.","definition_xrefs":["PMID:21393547","PMID:22902739"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"}],"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":"epithelium-like organization","termid":"GO:0140509"}


id: FYPO:0004514
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell phenotype in which a cell has no septum, is elongated, and is viable.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete viable elongated aseptate vegetative cell (obsolete FYPO:0004514)","synonyms":[{"name":"viable elongated aseptate cell during mitotic cell cycle","type":"related"},{"name":"viable elongated aseptate cell during vegetative growth","type":"exact"},{"name":"viable long aseptate cell","type":"exact"}],"termid":"FYPO:0004514"}


id: GO:1903862
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of oxidative phosphorylation.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:10225962"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of oxidative phosphorylation","termid":"GO:0002082"},{"relation_name":"is_a","term_name":"positive regulation of cellular respiration","termid":"GO:1901857"},{"relation_name":"positively_regulates","term_name":"oxidative phosphorylation","termid":"GO:0006119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"positively_regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"positive regulation of oxidative phosphorylation","synonyms":[{"name":"activation of oxidative phosphorylation","type":"narrow"},{"name":"activation of respiratory-chain phosphorylation","type":"narrow"},{"name":"positive regulation of respiratory-chain phosphorylation","type":"exact"},{"name":"up regulation of oxidative phosphorylation","type":"exact"},{"name":"up regulation of respiratory-chain phosphorylation","type":"exact"},{"name":"up-regulation of oxidative phosphorylation","type":"exact"},{"name":"up-regulation of respiratory-chain phosphorylation","type":"exact"},{"name":"upregulation of oxidative phosphorylation","type":"exact"},{"name":"upregulation of respiratory-chain phosphorylation","type":"exact"}],"termid":"GO:1903862"}


id: MONDO:0024615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoid neoplasm","termid":"MONDO:0005157"}],"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":"T-cell and NK-cell neoplasm","secondary_identifiers":["NCIT:C27908","MEDGEN:277781","UMLS:C1336554"],"synonyms":[{"name":"T-cell and NK-cell neoplasm","type":"exact"},{"name":"T-cell neoplasm","type":"exact"}],"termid":"MONDO:0024615","xrefs":{"Monarch":{"xref_id":"0024615"}}}


id: PBO:0060012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 32","termid":"PBO:0060012"}


id: GO:0032179
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The slender tubular outgrowth first produced by most spores in germination.","definition_xrefs":["ISBN:0877799148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"germ tube","secondary_identifiers":["Wikipedia:Germ_tube"],"termid":"GO:0032179"}


id: RO:0002214
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has prototype y if and only if x is an instance of C and y is a prototypical instance of C. For example, every instance of heart, both normal and abnormal is related by the has prototype relation to some instance of a \\\"canonical\\\" heart, which participates in blood circulation.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_prototype","termid":"RO:0002214"}


id: PR:O42890
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cao2 gene.","definition_xrefs":["UniProtKB:O42890","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":"copper amine oxidase-like protein cao2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1289.16c","synonyms":[{"name":"Spom972h-cao2","type":"exact"}],"termid":"PR:O42890"}


id: PBO:0110971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human CREG1 ortholog, probable oxidase, implicated in lipid metabolism, vitamin metabolism or lipoylation","termid":"PBO:0110971"}


id: PBO:0067629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 801, pseudogene","termid":"PBO:0067629"}


id: GO:0008409
data:
  {"annotated_genes":["SJAG_04410","SJAG_05280","SJAG_01173","SJAG_02275","SJAG_04587","SJAG_03994","SJAG_03276","SJAG_01832","SJAG_03734","SJAG_01648"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102681],"is_not":false,"summary":null,"term":"GO:0008409"},{"annotations":[92506,87910,96629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035312"},{"annotations":[89826,90138,94465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004534"},{"annotations":[115128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033699"},{"annotations":[107225,96632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051908"},{"annotations":[96634,111039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045145"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within nucleic acids by removing nucleotide residues from the 5' end.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exonuclease activity","termid":"GO:0004527"}],"gene_count":10,"genes_by_uniquename":{"SJAG_01173":null,"SJAG_01648":null,"SJAG_01832":null,"SJAG_02275":null,"SJAG_03276":null,"SJAG_03734":null,"SJAG_03994":null,"SJAG_04410":null,"SJAG_04587":null,"SJAG_05280":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016788","GO:0003824","GO:0004527","GO:0016787"],"is_obsolete":false,"name":"5'-3' exonuclease activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5358619","Reactome:R-HSA-5358599"],"termid":"GO:0008409","terms_by_termid":{"GO:0004534":null,"GO:0008409":null,"GO:0033699":null,"GO:0035312":null,"GO:0045145":null,"GO:0051908":null}}


id: GO:1903057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of melanosome organization.","definition_xrefs":["GOC:TermGenie","GOC:BHF","GOC:rl","GO_REF:0000058","PMID:24769727"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle organization","termid":"GO:0010639"},{"relation_name":"is_a","term_name":"regulation of melanosome organization","termid":"GO:1903056"},{"relation_name":"negatively_regulates","term_name":"melanosome organization","termid":"GO:0032438"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of melanosome organization","synonyms":[{"name":"down regulation of melanosome organisation","type":"exact"},{"name":"down regulation of melanosome organization","type":"exact"},{"name":"down regulation of melanosome organization and biogenesis","type":"related"},{"name":"down-regulation of melanosome organisation","type":"exact"},{"name":"down-regulation of melanosome organization","type":"exact"},{"name":"down-regulation of melanosome organization and biogenesis","type":"related"},{"name":"downregulation of melanosome organisation","type":"exact"},{"name":"downregulation of melanosome organization","type":"exact"},{"name":"downregulation of melanosome organization and biogenesis","type":"related"},{"name":"inhibition of melanosome organisation","type":"narrow"},{"name":"inhibition of melanosome organization","type":"narrow"},{"name":"inhibition of melanosome organization and biogenesis","type":"related"},{"name":"negative regulation of melanosome organisation","type":"exact"},{"name":"negative regulation of melanosome organization and biogenesis","type":"related"}],"termid":"GO:1903057"}


id: PBO:0091949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf element Wtf12 (truncated)","termid":"PBO:0091949"}


id: GO:1902992
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of amyloid precursor protein catabolic process.","definition_xrefs":["GOC:PARL","GO_REF:0000058","GOC:rl","GOC:TermGenie","PMID:24499793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein metabolic process","termid":"GO:0051248"},{"relation_name":"is_a","term_name":"regulation of amyloid precursor protein catabolic process","termid":"GO:1902991"},{"relation_name":"negatively_regulates","term_name":"amyloid precursor protein catabolic process","termid":"GO:0042987"}],"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 amyloid precursor protein catabolic process","synonyms":[{"name":"down regulation of APP catabolic process","type":"exact"},{"name":"down regulation of APP catabolism","type":"exact"},{"name":"down regulation of amyloid precursor protein breakdown","type":"exact"},{"name":"down regulation of amyloid precursor protein catabolic process","type":"exact"},{"name":"down regulation of amyloid precursor protein catabolism","type":"exact"},{"name":"down regulation of amyloid precursor protein degradation","type":"exact"},{"name":"down-regulation of APP catabolic process","type":"exact"},{"name":"down-regulation of APP catabolism","type":"exact"},{"name":"down-regulation of amyloid precursor protein breakdown","type":"exact"},{"name":"down-regulation of amyloid precursor protein catabolic process","type":"exact"},{"name":"down-regulation of amyloid precursor protein catabolism","type":"exact"},{"name":"down-regulation of amyloid precursor protein degradation","type":"exact"},{"name":"downregulation of APP catabolic process","type":"exact"},{"name":"downregulation of APP catabolism","type":"exact"},{"name":"downregulation of amyloid precursor protein breakdown","type":"exact"},{"name":"downregulation of amyloid precursor protein catabolic process","type":"exact"},{"name":"downregulation of amyloid precursor protein catabolism","type":"exact"},{"name":"downregulation of amyloid precursor protein degradation","type":"exact"},{"name":"inhibition of APP catabolic process","type":"narrow"},{"name":"inhibition of APP catabolism","type":"narrow"},{"name":"inhibition of amyloid precursor protein breakdown","type":"narrow"},{"name":"inhibition of amyloid precursor protein catabolic process","type":"narrow"},{"name":"inhibition of amyloid precursor protein catabolism","type":"narrow"},{"name":"inhibition of amyloid precursor protein degradation","type":"narrow"},{"name":"negative regulation of APP catabolic process","type":"exact"},{"name":"negative regulation of APP catabolism","type":"exact"},{"name":"negative regulation of amyloid precursor protein breakdown","type":"exact"},{"name":"negative regulation of amyloid precursor protein catabolism","type":"exact"},{"name":"negative regulation of amyloid precursor protein degradation","type":"exact"}],"termid":"GO:1902992"}


id: MONDO:0018551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Patent urachus is a type of congenital urachal anomaly characterized by a persistent communication between the bladder and the umbilicus, secondary to non occlusion of the urachal lumen, manifesting as clear drainage from the umbilicus.","definition_xrefs":["Orphanet:431341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital urachal anomaly","termid":"MONDO:0018565"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patent urachus","secondary_identifiers":["HP:0010479","NCIT:C99005","SCTID:398316009","GARD:21798","icd11.foundation:1391202028","MEDGEN:75610","UMLS:C0266357"],"synonyms":[{"name":"patent urachus","type":"exact"},{"name":"patent urachus (disease)","type":"exact"}],"termid":"MONDO:0018551","xrefs":{"Monarch":{"xref_id":"0018551"}}}


id: GO:0009020
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + tRNA = S-adenosyl-L-homocysteine + tRNA containing 2'-O-methylguanosine.","definition_xrefs":["RHEA:20077","EC:2.1.1.34"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA (guanosine-2'-O-)-methyltransferase activity (obsolete GO:0009020)","termid":"GO:0009020"}


id: PBO:0078213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 7-6","termid":"PBO:0078213"}


id: PBO:0053394
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 323","termid":"PBO:0053394"}


id: PBO:0055235
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 2662","termid":"PBO:0055235"}


id: PR:Q10496
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A TBC1 domain family member 2B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase activating protein Gyp51 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26F1.09","secondary_identifiers":["UniProtKB:Q10496"],"synonyms":[{"name":"SPAC26F1.09","type":"related"},{"name":"Spom972h-TBC1D2B","type":"exact"}],"termid":"PR:Q10496"}


id: MONDO:0015188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A metabolic disease that involves the intestine.","definition_xrefs":["MONDO:patterns/location"],"gene_count":0,"genotype_count":0,"name":"obsolete metabolic disorder with intestinal involvement (obsolete MONDO:0015188)","secondary_identifiers":["Orphanet:104013"],"synonyms":[{"name":"intestine metabolic disease","type":"exact"},{"name":"metabolic disease of intestine","type":"exact"}],"termid":"MONDO:0015188","xrefs":{"Monarch":{"xref_id":"0015188"}}}


id: PBO:0047678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"filamin B","termid":"PBO:0047678"}


id: MONDO:0020702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"epidermolytic ichthyosis","termid":"MONDO:0007239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant epidermolytic ichthyosis","secondary_identifiers":["NANDO:1200611","NCIT:C62569","Orphanet:312","NANDO:2200988","GARD:1039"],"termid":"MONDO:0020702","xrefs":{"Monarch":{"xref_id":"0020702"}}}


id: GO:1904689
data:
  {"annotated_genes":["SJAG_02592","SJAG_02638","SJAG_00786","SJAG_00169","SJAG_00690","SJAG_02026","SJAG_01942","SJAG_03869"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90818,109133,111602],"is_not":false,"summary":null,"term":"GO:1904689"},{"annotations":[115059,92022,98834,92318,109134,93873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cytoplasmic translational initiation.","definition_xrefs":["GOC:TermGenie","PMID:12242291","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of translational initiation","termid":"GO:0045947"},{"relation_name":"is_a","term_name":"regulation of cytoplasmic translational initiation","termid":"GO:1904688"},{"relation_name":"negatively_regulates","term_name":"cytoplasmic translational initiation","termid":"GO:0002183"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00690":null,"SJAG_00786":null,"SJAG_01942":null,"SJAG_02026":null,"SJAG_02592":null,"SJAG_02638":null,"SJAG_03869":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0002181"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0002181","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cytoplasmic translational initiation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cytoplasmic translational initiation","type":"exact"},{"name":"down-regulation of cytoplasmic translational initiation","type":"exact"},{"name":"downregulation of cytoplasmic translational initiation","type":"exact"},{"name":"inhibition of cytoplasmic translational initiation","type":"narrow"}],"termid":"GO:1904689","terms_by_termid":{"GO:1904689":null,"GO:1990625":null}}


id: PBO:0111947
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-basic zinc finger","termid":"PBO:0111947"}


id: GO:1904611
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 3,3',4,4',5-pentachlorobiphenyl stimulus.","definition_xrefs":["GOC:TermGenie","PMID:23196670","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to organic cyclic compound","termid":"GO:0071407"},{"relation_name":"is_a","term_name":"response to 3,3',4,4',5-pentachlorobiphenyl","termid":"GO:1904610"}],"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 3,3',4,4',5-pentachlorobiphenyl","synonyms":[{"name":"cellular response to PCB 126","type":"exact"}],"termid":"GO:1904611"}


id: PR:P40847
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sap1 gene.","definition_xrefs":["UniProtKB:P40847","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":"switch-activating protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1672.02c","synonyms":[{"name":"Spom972h-sap1","type":"exact"}],"termid":"PR:P40847"}


id: MONDO:0700100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm, non-human animal","termid":"MONDO:0700098"},{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukemia, non-human animal","termid":"MONDO:0700100","xrefs":{"Monarch":{"xref_id":"0700100"}}}


id: MONDO:0015617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary gastro-esophageal disease (obsolete MONDO:0015617)","secondary_identifiers":["Orphanet:165658"],"synonyms":[{"name":"genetic gastro-esophageal disease","type":"exact"}],"termid":"MONDO:0015617","xrefs":{"Monarch":{"xref_id":"0015617"}}}


id: MONDO:0032813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 79","secondary_identifiers":["UMLS:C5231410","DOID:0112215","GARD:16366","MEDGEN:1684738","OMIM:618559"],"synonyms":[{"name":"DEE79","type":"exact"},{"name":"EIEE79","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 79","type":"exact"},{"name":"developmental and epileptic encephalopathy 79","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 79","type":"exact"}],"termid":"MONDO:0032813","xrefs":{"Monarch":{"xref_id":"0032813"}}}


id: GO:0042067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification of polarized ommatidia. Ommatidia occur in two chiral forms. The trapezoidal arrangement of photoreceptors in the dorsal part of the eye is the mirror image of that in the ventral part.","definition_xrefs":["GOC:tb","GOC:dph","PMID:3076112","PMID:3937883","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of planar polarity","termid":"GO:0001736"},{"relation_name":"is_a","term_name":"establishment or maintenance of cell polarity","termid":"GO:0007163"},{"relation_name":"part_of","term_name":"compound eye morphogenesis","termid":"GO:0001745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0008150","GO:0007163"],"is_obsolete":false,"name":"establishment of ommatidial planar polarity","synonyms":[{"name":"establishment of ommatidial polarity","type":"exact"}],"termid":"GO:0042067"}


id: FYPO:0002464
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells that are curved along the long axis, elongated, and branched (and septated). Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, branched, curved, elongated cells (obsolete FYPO:0002464)","synonyms":[{"name":"inviable microcolony, branched, curved, elongated, septated vegetative cells","type":"exact"},{"name":"inviable microcolony, curved, branched, elongated cells","type":"exact"}],"termid":"FYPO:0002464"}


id: PBO:0079635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2Q2 pseudogene 6","termid":"PBO:0079635"}


id: PBO:0011414
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_absence_of","termid":"PBO:0011414"}


id: MONDO:0044214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete androstenone, ability to smell (obsolete MONDO:0044214)","secondary_identifiers":["OMIM:105570"],"synonyms":[{"name":"ANDROSTENONE, ability to smell","type":"related"}],"termid":"MONDO:0044214","xrefs":{"Monarch":{"xref_id":"0044214"}}}


id: GO:0015386
data:
  {"annotated_genes":["SJAG_04616"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88831],"is_not":false,"summary":null,"term":"GO:0015386"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: K+(in) + H+(out) = K+(out) + H+(in).","definition_xrefs":["TC:2.A.37.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:potassium antiporter activity","termid":"GO:0022821"},{"relation_name":"is_a","term_name":"metal cation:proton antiporter activity","termid":"GO:0051139"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04616":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"potassium:proton antiporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:TRANS-RXN-42","RHEA:29467"],"synonyms":[{"name":"potassium:hydrogen antiporter activity","type":"exact"}],"termid":"GO:0015386","terms_by_termid":{"GO:0015386":null}}


id: PBO:0078783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 8-1","termid":"PBO:0078783"}


id: GO:0140867
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of ADP-ribose groups to the glutamate-18 residue of histone H2B (or an equivalent residue).","definition_xrefs":["PMID:28252050"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD+-protein-glutamate ADP-ribosyltransferase activity","termid":"GO:0140807"}],"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:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0016740","GO:0003674","GO:0016757"],"is_obsolete":false,"name":"NAD+-histone H2BE18 glutamate ADP-ribosyltransferase activity","synonyms":[{"name":"NAD+-histone H2B-E18 glutamate ADP-ribosyltransferase activity","type":"exact"},{"name":"NAD+-histone-glutamate ADP-ribosyltransferase activity (H2B-E18 specific)","type":"exact"}],"termid":"GO:0140867"}


id: PBO:0111292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fbp1 upstream regulatory lncRNA b","termid":"PBO:0111292"}


id: GO:1902426
data:
  {"annotated_genes":["SJAG_03353","SJAG_02169","SJAG_00883","SJAG_03126","SJAG_04259","SJAG_02336","SJAG_01679","SJAG_01297","SJAG_03681"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90237,99088,103377,106701,107713,111409,113221,113711,115344],"is_not":false,"summary":null,"term":"GO:1902426"}]},"cv_name":"biological_process","definition":"A positive regulation of the mitotic metaphase/anaphase transition that results from deactivation of the mitotic spindle assembly checkpoint.","definition_xrefs":["GOC:vw","GOC:TermGenie","PMID:19592249","PMID:19075002","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mitotic spindle assembly checkpoint signaling","termid":"GO:0140499"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044772"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0000070"},{"rel_name":"regulates","termid":"GO:0000070"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044772"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0044772","GO:0000070","GO:0023052"],"is_obsolete":false,"name":"deactivation of mitotic spindle assembly checkpoint","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of Mad2-dependent checkpoint","type":"related"},{"name":"down regulation of mitotic cell cycle spindle assembly checkpoint","type":"broad"},{"name":"down regulation of mitotic spindle assembly checkpoint","type":"broad"},{"name":"down-regulation of Mad2-dependent checkpoint","type":"related"},{"name":"down-regulation of mitotic cell cycle spindle assembly checkpoint","type":"broad"},{"name":"down-regulation of mitotic spindle assembly checkpoint","type":"broad"},{"name":"downregulation of Mad2-dependent checkpoint","type":"related"},{"name":"downregulation of mitotic cell cycle spindle assembly checkpoint","type":"broad"},{"name":"downregulation of mitotic spindle assembly checkpoint","type":"broad"},{"name":"inhibition of Mad2-dependent checkpoint","type":"related"},{"name":"inhibition of mitotic cell cycle spindle assembly checkpoint","type":"related"},{"name":"inhibition of mitotic spindle assembly checkpoint","type":"related"},{"name":"mitotic spindle assembly checkpoint silencing","type":"exact"},{"name":"mitotic spindle assembly deactivation","type":"exact"},{"name":"negative regulation of Mad2-dependent checkpoint","type":"related"},{"name":"negative regulation of mitotic cell cycle spindle assembly checkpoint","type":"broad"},{"name":"negative regulation of mitotic spindle assembly checkpoint","type":"broad"}],"termid":"GO:1902426","terms_by_termid":{"GO:1902426":null}}


id: PBO:0078576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 52","termid":"PBO:0078576"}


id: GO:1902898
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving fatty acid methyl ester.","definition_xrefs":["GOC:mengo_curators","PMID:16570218","GO_REF:0000068","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"fatty acid methyl ester metabolic process","synonyms":[{"name":"FAME metabolic process","type":"exact"},{"name":"fatty acid methyl ester metabolism","type":"exact"}],"termid":"GO:1902898"}


id: PBO:0071294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 17","termid":"PBO:0071294"}


id: PBO:0077591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane serine protease 2","termid":"PBO:0077591"}


id: PBO:0091114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase subunit Ost4","termid":"PBO:0091114"}


id: PBO:0029313
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_pre-autophagosomal_structure","termid":"PBO:0029313"}


id: GO:0100011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any prostaglandin secretion process that positively_regulates fever generation.","definition_xrefs":["GOC:obol","GOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of fever generation by prostaglandin secretion","termid":"GO:0100009"},{"relation_name":"positively_regulates","term_name":"fever generation","termid":"GO:0001660"}],"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":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"positive regulation of fever generation by prostaglandin secretion","termid":"GO:0100011"}


id: GO:0031601
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The core complex of a proteasome located in the nucleus of a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome core complex","termid":"GO:0005839"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear proteasome complex","termid":"GO:0031595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"nuclear proteasome core complex","termid":"GO:0031601"}


id: MONDO:0017993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare but serious cerebrovascular disorder involving thrombosis of the cerebral venous system. It affects children from the newborn period through childhood and adolescence. In childhood CSVT, acute infections of the head and neck such as mastoiditis are most common, followed by chronic underlying diseases such as nephrotic syndrome, cancer, and inflammatory bowel disease. Signs and symptoms are also age related. Seizures and altered mental status are the commonest manifestations in newborns. Headache, vomiting, and lethargy, sometimes with 6th nerve palsy, are the most common symptoms in children and adolescents.","definition_xrefs":["PMID:28798906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral sinovenous thrombosis","secondary_identifiers":["Orphanet:329217","GARD:21485"],"synonyms":[{"name":"CSVT","type":"exact"}],"termid":"MONDO:0017993","xrefs":{"Monarch":{"xref_id":"0017993"}}}


id: GO:0003318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell toward the midline that contributes to the progression of the heart over time.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration involved in heart development","termid":"GO:0060973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell migration to the midline involved in heart development","termid":"GO:0003318"}


id: PBO:0038788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosine deaminase 2","termid":"PBO:0038788"}


id: PBO:0084407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lysophosphatidic acid (LPA) phosphatase, nucleotidase; principle and physiological nucleotidase working on GMP, UMP and CMP; involved in LPA hydrolysis in response to phosphate starvation and ribose salvage pathway; phosphatase activity is soluble and Mg2+ dependent; expression is induced by low phosphate levels and by inactivation of Pho85p; repressed by Gcn4p under normal conditions; PHM8 has a paralog, SDT1, that arose from the whole genome duplication","termid":"PBO:0084407"}


id: PBO:0002056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpt5 (predicted)","termid":"PBO:0002056"}


id: PBO:0034131
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-directly_develops_from","termid":"PBO:0034131"}


id: MONDO:0007190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukemia, chronic lymphocytic, susceptibility to, 2","secondary_identifiers":["OMIM:109543","UMLS:C1868683","MEDGEN:358385"],"synonyms":[{"name":"B-cell malignancy, low-grade","type":"related"},{"name":"Clls2","type":"related"},{"name":"disrupted in B-cell malignancy","type":"related"},{"name":"leukemia, chronic lymphocytic, B-cell","type":"related"},{"name":"leukemia, chronic lymphocytic, susceptibility to, 2","type":"exact"},{"name":"leukemia, chronic lymphocytic, susceptibility to, type 2","type":"exact"}],"termid":"MONDO:0007190","xrefs":{"Monarch":{"xref_id":"0007190"}}}


id: PBO:0058951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muskelin 1","termid":"PBO:0058951"}


id: PBO:0055513
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 2947","termid":"PBO:0055513"}


id: MONDO:0013986
data:
  {"annotated_genes":["SJAG_02615"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86562],"is_not":false,"summary":null,"term":"MONDO:0013986"}]},"cv_name":"mondo","definition":"Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the FARS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02615":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:614946","DOID:0111477","Orphanet:319519","GARD:17455","UMLS:C4755312","MEDGEN:1663069"],"synonyms":[{"name":"COXPD14","type":"exact"},{"name":"FARS2 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 14","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in FARS2","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 14","type":"exact"}],"termid":"MONDO:0013986","terms_by_termid":{"MONDO:0013986":null},"xrefs":{"Monarch":{"xref_id":"0013986"}}}


id: SO:0000981
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcription terminator that is dependent upon Rho.","direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial_terminator","termid":"SO:0000614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rho_dependent_bacterial_terminator","synonyms":[{"name":"rho dependent bacterial terminator","type":"exact"}],"termid":"SO:0000981"}


id: GO:0033679
data:
  {"annotated_genes":["SJAG_00857","SJAG_00884","SJAG_04210"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105897,106716,114725],"is_not":false,"summary":null,"term":"GO:0033679"}]},"cv_name":"molecular_function","definition":"Unwinding of a DNA/RNA duplex in the 3' to 5' direction, driven by ATP hydrolysis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA/RNA helicase activity","termid":"GO:0033677"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00857":null,"SJAG_00884":null,"SJAG_04210":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140097","GO:0003824","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"3'-5' DNA/RNA helicase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0033681"],"synonyms":[{"name":"3' to 5' DNA/RNA helicase activity","type":"exact"},{"name":"ATP-dependent 3' to 5' DNA/RNA helicase activity","type":"exact"},{"name":"ATP-dependent 3'-5' DNA/RNA helicase activity","type":"exact"}],"termid":"GO:0033679","terms_by_termid":{"GO:0033679":null}}


id: FYPO:0005361
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the level of large Y-shaped DNA replication intermediates is greater than normal. Large Y-shaped intermediates are formed late in the passive replication of a DNA region by a replication fork moving from outside the region.","definition_xrefs":["PMID:19416828","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased level of large-Y replication intermediates","synonyms":[{"name":"increased level of large Y-shaped DNA replication intermediates","type":"exact"},{"name":"increased level of large-Y replication intermediates during mitotic cell cycle","type":"related"},{"name":"increased level of large-Y replication intermediates during vegetative growth","type":"exact"}],"termid":"FYPO:0005361"}


id: FYPO:0000244
data:
  {"alleles_by_uniquename":{"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005231"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable when cells are deprived of nutrients such as carbon or nitrogen.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"},{"relation_name":"is_a","term_name":"cell population viability","termid":"FYPO:0002057"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02527":null},"genotype_count":1,"genotypes_by_uniquename":{"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"loss of viability upon nutrient depletion","references_by_uniquename":{"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_02527"],"single_locus_genotype_uniquenames":["lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown"],"synonyms":[{"name":"decreased viability upon nutrient depletion","type":"exact"},{"name":"growth defect, required during nutrient depletion","type":"related"},{"name":"loss of cell population viability upon nutrient depletion","type":"exact"},{"name":"loss of viability upon nutrient starvation","type":"exact"},{"name":"reduced viability upon nutrient depletion","type":"exact"}],"termid":"FYPO:0000244","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0005231":null}}


id: PBO:0075069
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 118","termid":"PBO:0075069"}


id: PBO:0088780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysferlin-like membrane trafficking protein Mug65","termid":"PBO:0088780"}


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


id: PBO:0055557
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 2993","termid":"PBO:0055557"}


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


id: MONDO:0100443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A retinopathy caused by bialleleic variants in the RDH5 gene, often involving flecks in the retina.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"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":"RDH5-related retinopathy","synonyms":[{"name":"RDH5 retinopathy","type":"exact"},{"name":"fundus albipunctatus","type":"narrow"},{"name":"pigmentary retinal dystrophy","type":"narrow"},{"name":"retinitis punctata albescens","type":"narrow"}],"termid":"MONDO:0100443","xrefs":{"Monarch":{"xref_id":"0100443"}}}


id: GO:0061316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes that contributes to the progression of the heart over time. In this pathway, the activated receptor signals via downstream effectors that result in the inhibition of beta-catenin phosphorylation, thereby preventing degradation of beta-catenin. Stabilized beta-catenin can then accumulate and travel to the nucleus to trigger changes in transcription of target genes.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Wnt signaling pathway involved in heart development","termid":"GO:0003306"},{"relation_name":"is_a","term_name":"canonical Wnt signaling pathway","termid":"GO:0060070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"canonical Wnt signaling pathway involved in heart development","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in heart development","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in heart development","type":"exact"},{"name":"canonical Wnt-activated signaling pathway involved in heart development","type":"exact"}],"termid":"GO:0061316"}


id: GO:0002563
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which immune receptor genes are diversified through alternate splicing.","definition_xrefs":["GOC:add","ISBN:0781735149","PMID:16166509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immune receptors","termid":"GO:0002200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"somatic diversification of immune receptors via alternate splicing","termid":"GO:0002563"}


id: GO:0003910
data:
  {"annotated_genes":["SJAG_00198","SJAG_02527"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[92071,113337],"is_not":false,"summary":null,"term":"GO:0003910"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + deoxyribonucleotide(n) + deoxyribonucleotide(m) = AMP + diphosphate + deoxyribonucleotide(n+m).","definition_xrefs":["EC:6.5.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA ligase activity","termid":"GO:0003909"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00198":null,"SJAG_02527":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016874","GO:0140097","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"DNA ligase (ATP) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:DNA-LIGASE-ATP-RXN"],"synonyms":[{"name":"DNA joinase activity","type":"broad"},{"name":"DNA repair enzyme activity","type":"related"},{"name":"DNA-joining enzyme","type":"related"},{"name":"deoxyribonucleate ligase","type":"broad"},{"name":"deoxyribonucleic acid joinase","type":"broad"},{"name":"deoxyribonucleic acid ligase","type":"broad"},{"name":"deoxyribonucleic acid repair enzyme","type":"related"},{"name":"deoxyribonucleic acid-joining enzyme","type":"related"},{"name":"deoxyribonucleic joinase","type":"broad"},{"name":"deoxyribonucleic ligase","type":"broad"},{"name":"deoxyribonucleic repair enzyme","type":"related"},{"name":"deoxyribonucleic-joining enzyme","type":"related"},{"name":"poly(deoxyribonucleotide):poly(deoxyribonucleotide) ligase (AMP-forming)","type":"related"},{"name":"polydeoxyribonucleotide synthase (ATP) activity","type":"related"},{"name":"polynucleotide ligase","type":"broad"},{"name":"polynucleotide ligase (ATP) activity","type":"related"},{"name":"sealase activity","type":"related"}],"termid":"GO:0003910","terms_by_termid":{"GO:0003910":null}}


id: PBO:0068539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 142, pseudogene","termid":"PBO:0068539"}


id: PBO:0068231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 18S ribosomal 2","termid":"PBO:0068231"}


id: PATO:0001304
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A variability quality inhering in a bearer by virtue of whether the bearer exhibits temperature variation or change.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variability","termid":"PATO:0001303"},{"relation_name":"towards","term_name":"temperature","termid":"PATO:0000146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variability of temperature","termid":"PATO:0001304"}


id: PR:P0CT66
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps1801 gene.","definition_xrefs":["UniProtKB:P0CT66","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":"40S ribosomal protein S18-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.11c","synonyms":[{"name":"Spom972h-rps1801","type":"exact"}],"termid":"PR:P0CT66"}


id: FYPO:0001672
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a GTPase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0000257"],"is_obsolete":false,"name":"normal GTPase activity","termid":"FYPO:0001672"}


id: PBO:0043930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDP-L-ribitol pyrophosphorylase A","termid":"PBO:0043930"}


id: PBO:0059583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylthioadenosine phosphorylase","termid":"PBO:0059583"}


id: PBO:0071993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 22","termid":"PBO:0071993"}


id: PBO:0059483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methionine sulfoxide reductase A","termid":"PBO:0059483"}


id: FYPO:0004593
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype that shows detectable differences from normal at the level of an individual cell, when the cell is in the vegetative growth phase of the cell cycle, and after it has undergone a normal mitotic nuclear division and passed through the subsequent mitotic interphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal vegetative cell phenotype following normal mitosis","synonyms":[{"name":"abnormal cell phenotype following normal mitosis during vegetative growth","type":"exact"},{"name":"abnormal vegetative cell phenotype following normal mitosis and interphase","type":"exact"},{"name":"abnormal vegetative cell phenotype following normal mitosis and passage through mitotic G1 phase","type":"exact"},{"name":"abnormal vegetative cell phenotype following normal mitotic nuclear division","type":"exact"},{"name":"abnormal vegetative cell phenotype following normal nuclear division during mitotic cell cycle","type":"exact"}],"termid":"FYPO:0004593"}


id: MONDO:0004747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital abnormality consisting of one or more clefts (splits) in the upper lip, which may be accompanied by a cleft palate; it is the result of the failure of the embryonic parts of the lip to fuse.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orofacial cleft","termid":"MONDO:0000358"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleft lip","secondary_identifiers":["SCTID:80281008","ICD9:749.10","ICD9:749.11","MEDGEN:1370297","NCIT:C87175","HP:0410030","ICD9:749.1","MESH:D002971","UMLS:C4321245","DOID:9296"],"synonyms":[{"name":"cheiloschisis","type":"exact"},{"name":"cleft lip","type":"exact"},{"name":"cleft lip (disease)","type":"exact"},{"name":"cleft lip, unilateral, complete","type":"exact"},{"name":"complete unilateral cleft lip","type":"exact"},{"name":"hare lip","type":"exact"},{"name":"labium leporinum","type":"exact"}],"termid":"MONDO:0004747","xrefs":{"Monarch":{"xref_id":"0004747"}}}


id: FYPO:0006206
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 chromatin is decreased during a cellular response to phosphate starvation.","definition_xrefs":["PomBase:mah","PMID:19933844"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to chromatin during cellular response to phosphate starvation","synonyms":[{"name":"decreased protein localisation to chromatin during cellular response to phosphate starvation","type":"exact"},{"name":"decreased protein localization to chromatin during cellular response to phosphate ion starvation","type":"exact"},{"name":"decreased protein localization to chromatin during cellular response to phosphate starvation during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to chromatin during cellular response to phosphate starvation during vegetative growth","type":"exact"},{"name":"reduced protein localization to chromatin during cellular response to phosphate starvation","type":"exact"}],"termid":"FYPO:0006206"}


id: MONDO:0008426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Shprintzen-Goldberg syndrome (SGS) is a very rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability.","definition_xrefs":["Orphanet:2462"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"},{"relation_name":"is_a","term_name":"Marfan and Marfan-related disorder","termid":"MONDO:0017310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Shprintzen-Goldberg syndrome","secondary_identifiers":["SCTID:719069008","NCIT:C124840","OMIM:182212","UMLS:C1321551","GARD:4861","MEDGEN:231160","NORD:1908"],"synonyms":[{"name":"Marfanoid craniosynostosis syndrome","type":"exact"},{"name":"Marfanoid disorder with craniosynostosis type 1","type":"related"},{"name":"Marfanoid disorder with craniosynostosis, type 1","type":"related"},{"name":"Marfanoid-craniosynostosis syndrome","type":"related"},{"name":"SGS","type":"exact"},{"name":"Shprintzen Goldberg Syndrome","type":"exact"},{"name":"Shprintzen-Goldberg craniosynostosis syndrome","type":"related"},{"name":"Shprintzen-Goldberg marfanoid syndrome","type":"related"},{"name":"Shprintzen-Goldberg syndrome","type":"exact"},{"name":"craniosynostosis with arachnodactyly and abdominal hernias","type":"related"}],"termid":"MONDO:0008426","xrefs":{"Monarch":{"xref_id":"0008426"}}}


id: FYPO:0002139
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of threonine residues N-terminal to proline residues (i.e. in Thr-Pro sequences) does not occur.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete abolished protein threonine phosphorylation at Thr-Pro site during vegetative growth (obsolete FYPO:0002139)","synonyms":[{"name":"abolished protein threonine phosphorylation at TP site during vegetative growth","type":"exact"},{"name":"abolished protein threonine phosphorylation at Thr-Pro site during mitotic cell cycle","type":"related"},{"name":"abolished protein threonine phosphorylation at threonine-proline site during vegetative growth","type":"exact"}],"termid":"FYPO:0002139"}


id: SO:0000349
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A match against a protein sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"match","termid":"SO:0000343"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein_match","synonyms":[{"name":"protein match","type":"exact"}],"termid":"SO:0000349"}


id: PBO:0090080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase Alg13","termid":"PBO:0090080"}


id: GO:0051611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of the monoamine neurotransmitter serotonin into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotransmitter uptake","termid":"GO:0051580"},{"relation_name":"regulates","term_name":"serotonin uptake","termid":"GO:0051610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of serotonin uptake","synonyms":[{"name":"regulation of 5-HT uptake","type":"exact"},{"name":"regulation of 5-hydroxytryptamine uptake","type":"exact"},{"name":"regulation of 5HT uptake","type":"exact"},{"name":"regulation of serotonin import","type":"exact"}],"termid":"GO:0051611"}


id: PBO:0054451
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 1848","termid":"PBO:0054451"}


id: PBO:0083462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene KTR3","termid":"PBO:0083462"}


id: GO:2001126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of translational frameshifting.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of translational elongation","termid":"GO:0045901"},{"relation_name":"is_a","term_name":"regulation of translational frameshifting","termid":"GO:2001124"},{"relation_name":"positively_regulates","term_name":"translational frameshifting","termid":"GO:0006452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of translational frameshifting","termid":"GO:2001126"}


id: PBO:0049599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 2","termid":"PBO:0049599"}


id: MONDO:0700194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphoma that occurs in a chicken.","definition_xrefs":["NCIT:C135004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma, non-human animal","termid":"MONDO:0700102"},{"relation_name":"is_a","term_name":"chicken neoplasm","termid":"MONDO:0700189"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chicken lymphoma","termid":"MONDO:0700194","xrefs":{"Monarch":{"xref_id":"0700194"}}}


id: GO:0043822
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the endonucleolytic cleavage of RNA, removing 21 and 42 nucleotides, respectively, from the 5'- and 3'-termini of a 5S-rRNA precursor.","definition_xrefs":["PMID:402365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA endonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016891"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0140098","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"ribonuclease M5 activity","secondary_identifiers":["EC:3.1.26.8","MetaCyc:3.1.26.8-RXN"],"synonyms":[{"name":"5S ribosomal RNA maturation endonuclease activity","type":"exact"},{"name":"5S ribosomal maturation nuclease activity","type":"related"},{"name":"RNase M5 activity","type":"related"}],"termid":"GO:0043822"}


id: PBO:0029836
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-microtubule_bundles_present_in_increased_numbers","termid":"PBO:0029836"}


id: FYPO:0006827
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 zinc ion measured in the cytosol is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular zinc level","termid":"FYPO:0001534"},{"relation_name":"is_a","term_name":"decreased level of substance in cytosol","termid":"FYPO:0001605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased cytosolic zinc level","synonyms":[{"name":"decreased cytosolic zinc ion level","type":"exact"},{"name":"decreased cytosolic zinc ion level during vegetative growth","type":"exact"},{"name":"decreased cytosolic zinc level during mitotic cell cycle","type":"related"},{"name":"decreased level of zinc ions in cytosol","type":"exact"},{"name":"decreased levels of free cytosolic zinc","type":"exact"},{"name":"reduced cytosolic zinc level","type":"exact"}],"termid":"FYPO:0006827"}


id: MONDO:0015689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, malignant, neoplastic disease characterized by clonal proliferation of myeloid and/or lymphoid precursors harboring rearrangements in the PDGFRA gene, in the blood, bone marrow and often other tissues as well (spleen, lymph nodes, skin, etc.). It usually presents as chronic eosinophilic leukemia or, less commonly, as acute myeloid leukemia or T-lymphoblastic leukemia with eosinophilia. Patients usually present with eosinophilia, anemia, thrombocytopenia, neutrophilia, splenomegaly, lymphadenopathy, fever, sweating and/or weight loss. Tissue infiltration by eosinophils can manifest with skin rash, erythema, cough, neurological alterations, gastrointestinal symptoms or, rarely, endomyocardial fibrosis and restrictive cardiomyopathy.","definition_xrefs":["Orphanet:168947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2","termid":"MONDO:0015688"}],"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":"myeloid neoplasm associated with PDGFRA rearrangement","secondary_identifiers":["icd11.foundation:833355630","ONCOTREE:MLNPDGFRA","NCIT:C84275","SCTID:738527001","GARD:20106","UMLS:C4545381","ICDO:9965/3","MEDGEN:1620600","DOID:0080165"],"synonyms":[{"name":"myeloid and lymphoid neoplasms associated with PDGFRA rearrangement","type":"exact"},{"name":"myeloid and lymphoid neoplasms with PDGFRA rearrangement","type":"exact"},{"name":"myeloid/lymphoid neoplasm associated with PDGFRA rearrangement","type":"related"},{"name":"myeloid/lymphoid neoplasms with PDGFRA rearrangement","type":"exact"}],"termid":"MONDO:0015689","xrefs":{"Monarch":{"xref_id":"0015689"}}}


id: PBO:0049232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate metabotropic receptor 5","termid":"PBO:0049232"}


id: GO:0060830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Grouping of smoothened or patched receptors in a cilium, contributing to the smoothened signaling pathway.","definition_xrefs":["GOC:cilia","GOC:dph","GOC:sdb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor clustering","termid":"GO:0043113"},{"relation_name":"part_of","term_name":"smoothened signaling pathway","termid":"GO:0007224"}],"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":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0051179"],"is_obsolete":false,"name":"ciliary receptor clustering involved in smoothened signaling pathway","synonyms":[{"name":"ciliary receptor clustering involved in hedgehog signaling pathway","type":"exact"},{"name":"ciliary receptor clustering involved in hh signaling pathway","type":"exact"},{"name":"ciliary receptor clustering involved in smoothened signalling pathway","type":"exact"}],"termid":"GO:0060830"}


id: PBO:0000903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiamine diphosphokinase Tnr3","termid":"PBO:0000903"}


id: GO:0051373
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a member of the FATZ family of proteins, filamin-, actinin-, and telethonin-binding proteins of the Z-disc of striated muscle. FATZ proteins are located in the Z-disc of the sarcomere and are involved in a complex network of interactions with other Z-band components.","definition_xrefs":["PMID:10984498","PMID:11699871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeletal protein binding","termid":"GO:0008092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0008092"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0008092","GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"FATZ binding","secondary_identifiers":["GO:0051375","GO:0051374","GO:0051376"],"synonyms":[{"name":"FATZ 1 binding","type":"exact"},{"name":"FATZ 2 binding","type":"exact"},{"name":"FATZ 3 binding","type":"exact"},{"name":"calsarcin 1 binding","type":"exact"},{"name":"calsarcin 2 binding","type":"exact"},{"name":"calsarcin 3 binding","type":"exact"},{"name":"calsarcin binding","type":"exact"},{"name":"filamin-, actinin- and telethonin-binding protein of the Z-disc of striated muscle","type":"exact"}],"termid":"GO:0051373"}


id: PBO:0041674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell adhesion molecule 2","termid":"PBO:0041674"}


id: PBO:0064499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit C","termid":"PBO:0064499"}


id: MONDO:0010473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndromic X-linked intellectual disability characterized by intellectual disability, delayed psychomotor development, seizures, large joint contractures, cardiac abnormalities, and abnormal positioning of the thumbs that has material basis in mutation in the CLIC2 gene on chromosome Xq28.","definition_xrefs":["PMID:22814392","DOID:0060828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome","secondary_identifiers":["GARD:17485","MEDGEN:763827","Orphanet:324410","UMLS:C3550913","OMIM:300886"],"synonyms":[{"name":"MRXS32","type":"exact"},{"name":"intellectual developmental disorder, X-linked syndromic 32, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked, syndromic 32","type":"exact"},{"name":"intellectual disability, X-linked, syndromic type 32","type":"exact"},{"name":"mental retardation, X-linked, syndromic 32","type":"exact"},{"name":"mental retardation, X-linked, syndromic type 32","type":"exact"}],"termid":"MONDO:0010473","xrefs":{"Monarch":{"xref_id":"0010473"}}}


id: GO:0071290
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 platinum stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to platinum ion","termid":"GO:0070541"},{"relation_name":"is_a","term_name":"cellular response to metal ion","termid":"GO:0071248"}],"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 platinum ion","synonyms":[{"name":"cellular response to platinum","type":"exact"}],"termid":"GO:0071290"}


id: GO:0052876
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2O + methylamine + 2 oxidized [amicyanin] = formaldehyde + 2 H+ + NH4+ + 2 reduced [amicyanin].","definition_xrefs":["RHEA:30207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, with a copper protein as acceptor","termid":"GO:0052877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"methylamine dehydrogenase (amicyanin) activity","secondary_identifiers":["KEGG_REACTION:R00606","UM-BBD_reactionID:r0075","EC:1.4.9.1"],"synonyms":[{"name":"MADH activity","type":"broad"},{"name":"amine dehydrogenase","type":"broad"},{"name":"methylamine dehydrogenase activity","type":"exact"},{"name":"methylamine:amicyanin oxidoreductase (deaminating) activity","type":"exact"},{"name":"primary-amine dehydrogenase","type":"broad"}],"termid":"GO:0052876"}


id: GO:0016243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the size of the autophagosome.","definition_xrefs":["GOC:krc","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component size","termid":"GO:0032535"},{"relation_name":"is_a","term_name":"autophagosome organization","termid":"GO:1905037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"regulation of autophagosome size","synonyms":[{"name":"regulation of autophagic vacuole size","type":"exact"}],"termid":"GO:0016243"}


id: PATO:0001767
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"fertility","termid":"PATO:0000274"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semi-fertile","termid":"PATO:0001767"}


id: GO:0031878
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 somatostatin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatostatin receptor binding","termid":"GO:0031877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"type 1 somatostatin receptor binding","synonyms":[{"name":"type 1 somatostatin receptor ligand","type":"narrow"}],"termid":"GO:0031878"}


id: MONDO:1011887
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":"retinal dysplasia and internal hydrocephalus, non-human animal","secondary_identifiers":["OMIA:001663"],"termid":"MONDO:1011887","xrefs":{"Monarch":{"xref_id":"1011887"}}}


id: PBO:0012838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosomal 3'-to-5' phosphorolytic exoribonuclease Rrp41","termid":"PBO:0012838"}


id: GO:0031802
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 5 metabotropic glutamate receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled glutamate receptor binding","termid":"GO:0035256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 5 metabotropic glutamate receptor binding","synonyms":[{"name":"type 5 metabotropic glutamate receptor ligand","type":"narrow"}],"termid":"GO:0031802"}


id: PBO:0073694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIX homeobox 6","termid":"PBO:0073694"}


id: PBO:0012022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MFS family transmembrane transporter Mfs3","termid":"PBO:0012022"}


id: SO:0001786
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A functional variant whereby the sequence alteration causes a loss of function of one allele of a gene.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_abnormal","termid":"SO:0002218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"loss_of_heterozygosity","synonyms":[{"name":"LOH","type":"exact"},{"name":"loss of heterozygosity","type":"exact"}],"termid":"SO:0001786"}


id: GO:0030197
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Functions as a lubricant for an extracellular matrix, such as a mucous membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix structural constituent","termid":"GO:0005201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0005198","GO:0003674"],"is_obsolete":false,"name":"extracellular matrix constituent, lubricant activity","synonyms":[{"name":"core extracellular matrix","type":"broad"},{"name":"core matrisome","type":"broad"}],"termid":"GO:0030197"}


id: PBO:0079490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin domain containing 11","termid":"PBO:0079490"}


id: PBO:0079006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon CGT) 6-1","termid":"PBO:0079006"}


id: PBO:0072403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 8","termid":"PBO:0072403"}


id: SO:0001683
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence motif is a nucleotide or amino-acid sequence pattern that may have biological significance.","direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_motif","secondary_identifiers":["http://en.wikipedia.org/wiki/Sequence_motif"],"synonyms":[{"name":"sequence motif","type":"related"}],"termid":"SO:0001683"}


id: MONDO:0002923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A uterine corpus sarcoma originating from the endometrial stroma. It is further subdivided into low grade and high grade endometrial stromal sarcoma.","definition_xrefs":["NCIT:C40219"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine corpus sarcoma","termid":"MONDO:0005210"},{"relation_name":"is_a","term_name":"endometrioid stromal sarcoma","termid":"MONDO:0006745"}],"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 endometrial stromal sarcoma","secondary_identifiers":["MEDGEN:275553","UMLS:C1519849","DOID:4227"],"synonyms":[{"name":"body of uterus endometrial stromal sarcoma","type":"exact"},{"name":"body of uterus endometrioid stromal sarcoma","type":"exact"},{"name":"endometrioid stromal sarcoma of body of uterus","type":"exact"},{"name":"uterine corpus endometrial stromal sarcoma","type":"exact"},{"name":"uterine corpus endometrial stromal tumor","type":"exact"},{"name":"uterine corpus endometrial stromal tumour","type":"exact"},{"name":"uterine corpus ess","type":"exact"}],"termid":"MONDO:0002923","xrefs":{"Monarch":{"xref_id":"0002923"}}}


id: GO:0000468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in generating the mature 3'-end of an LSU-rRNA derived from a tricistronic rRNA transcript that contained the Small SubUnit (SSU) rRNA, the 5.8S rRNA, and the Large SubUnit (LSU) rRNA, in that order, from 5' to 3' along the primary transcript.","definition_xrefs":["GOC:krc","PMID:10690410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA 3'-end processing","termid":"GO:0031125"},{"relation_name":"part_of","term_name":"maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","termid":"GO:0000463"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0042254"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0042254","GO:0044085"],"is_obsolete":false,"name":"generation of mature 3'-end of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","synonyms":[{"name":"processing at B2","type":"narrow"}],"termid":"GO:0000468"}


