# terms

id: GO:0036522
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the normal localization of a protein to the host phagosome. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:PARL","GOC:bf","PMID:25063865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cellular process","termid":"GO:0044068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host protein localization to phagocytic vesicle","synonyms":[{"name":"disruption of host protein localisation to phagosome","type":"exact"},{"name":"inhibition of host protein localisation to phagosome","type":"exact"},{"name":"negative regulation by symbiont of host protein localization to phagocytic vesicle","type":"exact"},{"name":"suppression of host protein localisation to phagosome","type":"exact"}],"termid":"GO:0036522"}


id: GO:0072291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of epithelial cells within a renal tubule that contributes to metanephric distal tubule morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration involved in distal tubule morphogenesis","termid":"GO:0072157"},{"relation_name":"is_a","term_name":"epithelial cell migration involved in metanephric nephron tubule morphogenesis","termid":"GO:0072290"},{"relation_name":"part_of","term_name":"metanephric distal tubule morphogenesis","termid":"GO:0072287"}],"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 metanephric distal tubule morphogenesis","termid":"GO:0072291"}


id: GO:0044467
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of glial cell line-derived neurotrophic factor from a cell. Glial cell-derived neurotrophic factor (GDNF) is a small protein that potently promotes the survival of many types of neurons, notably dopaminergic and motor neurons.","definition_xrefs":["PMID:17505307","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"glial cell-derived neurotrophic factor production","synonyms":[{"name":"GDNF production","type":"exact"},{"name":"glial cell line-derived neurotrophic factor production","type":"related"},{"name":"glial cell-derived neurotrophic factor secretion","type":"narrow"}],"termid":"GO:0044467"}


id: PR:P04910
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H2A.2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PMID:15226425","PMID:19965387","PMID:21516229","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A.2","termid":"PR:000027545"},{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"},{"relation_name":"is_a","term_name":"core histone (Schizosaccharomyces pombe)","termid":"PR:000041293"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H2A-beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19G12.06c","secondary_identifiers":["PR:000027546","UniProtKB:P04910"],"synonyms":[{"name":"SPAC19G12.06C","type":"related"},{"name":"Spom972h-HTA2","type":"exact"}],"termid":"PR:P04910"}


id: FYPO:0000508
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of nuclear export is decreased. Nuclear export is the directed movement of any substance out of the nucleus; export of all substances or a specific substance may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased intracellular transport","termid":"FYPO:0000464"},{"relation_name":"is_a","term_name":"abnormal nuclear export","termid":"FYPO:0000506"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased nuclear export","synonyms":[{"name":"decreased nuclear export during mitotic cell cycle","type":"related"},{"name":"decreased nuclear export during vegetative growth","type":"exact"},{"name":"nuclear export: decreased","type":"related"},{"name":"reduced nuclear export","type":"exact"}],"termid":"FYPO:0000508"}


id: FYPO:0007256
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the meiotic spindle pole body is begins earlier than normal during prophase of the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:22438582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to meiotic spindle pole body","termid":"FYPO:0002771"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0000054","FYPO:0005447"],"is_obsolete":false,"name":"premature protein localization to meiotic spindle pole body during prophase I","synonyms":[{"name":"advanced protein localization to meiotic spindle pole body during prophase I","type":"exact"},{"name":"premature protein localisation to meiotic spindle pole body during prophase I","type":"exact"},{"name":"premature protein localization to meiotic SPB during prophase I","type":"exact"},{"name":"premature protein localization to meiotic spindle pole body during prophase of first meiotic nuclear division","type":"exact"},{"name":"premature protein localization to spindle pole body during meiotic prophase I","type":"exact"}],"termid":"FYPO:0007256"}


id: GO:0060849
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 contributes to the commitment of a venous endothelial cell to a lymphatic endothelial cell.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sdb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription involved in lymphatic endothelial cell fate commitment (obsolete GO:0060849)","termid":"GO:0060849"}


id: PBO:0091119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane chaperone for multipass membrane proteins, PAT complex subunit (asterix), Pat10","termid":"PBO:0091119"}


id: MONDO:1012392
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal encephalopathy with seizures, non-human animal","termid":"MONDO:1011880"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neonatal encephalopathy with seizures, dog","secondary_identifiers":["OMIA:001471-9615"],"termid":"MONDO:1012392","xrefs":{"Monarch":{"xref_id":"1012392"}}}


id: PBO:0000294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L16 (predicted)","termid":"PBO:0000294"}


id: GO:0018589
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: dibutyltin + O2 + 2 H+ + 2 e- = H2O + beta-hydroxybutylbutyltin.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete di-n-butyltin dioxygenase activity (obsolete GO:0018589)","synonyms":[{"name":"DBT dioxygenase activity","type":"exact"}],"termid":"GO:0018589"}


id: PBO:0075317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"superoxide dismutase 1","termid":"PBO:0075317"}


id: PBO:0031116
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mutator","termid":"PBO:0031116"}


id: GO:0009290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of DNA into a cell that contributes to the process of transformation, the uptake of foreign genetic material into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA transport","termid":"GO:0051027"},{"relation_name":"is_a","term_name":"import into cell","termid":"GO:0098657"},{"relation_name":"part_of","term_name":"DNA-mediated transformation","termid":"GO:0009294"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"DNA import into cell involved in transformation","synonyms":[{"name":"DNA import into cell","type":"broad"},{"name":"DNA transport into cell during transformation","type":"related"},{"name":"cellular DNA import during transformation","type":"related"},{"name":"cellular DNA uptake","type":"broad"}],"termid":"GO:0009290"}


id: PBO:0073971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 22 member 20, pseudogene","termid":"PBO:0073971"}


id: PBO:0058664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6792","termid":"PBO:0058664"}


id: GO:0106034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The transfer of an assembled [2Fe-2S] cluster from a scaffold protein to an acceptor protein that contributes to the attainment of the full functional capacity of a protein.","definition_xrefs":["PMID:23615440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein maturation by iron-sulfur cluster transfer","termid":"GO:0097428"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"protein maturation by [2Fe-2S] cluster transfer","termid":"GO:0106034"}


id: GO:0102253
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: neoagarobiose + H2O = 3,6-anhydro-alpha-L-galactopyranose + beta-D-galactoside.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete neoagarobiose 1,3-alpha-3,6-anhydro-L-galactosidase activity (obsolete GO:0102253)","termid":"GO:0102253"}


id: MONDO:1011088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal dysplasia that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal dysplasia, non-human animal","termid":"MONDO:1010268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal dysplasia, domestic cat","secondary_identifiers":["OMIA:001135-9685"],"termid":"MONDO:1011088","xrefs":{"Monarch":{"xref_id":"1011088"}}}


id: PBO:0003343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAG family molecular chaperone regulator Bag102 (predicted)","termid":"PBO:0003343"}


id: MONDO:0004821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder that affects the nasopharynx. Representative examples include nasopharyngitis, angiofibroma, and carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"upper respiratory tract disorder","termid":"MONDO:0004867"},{"relation_name":"is_a","term_name":"disorder of pharynx","termid":"MONDO:0020592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nasopharyngeal disorder","secondary_identifiers":["MEDGEN:45007","DOID:9561","SCTID:123952009","MESH:D009302","NCIT:C35723","UMLS:C0027438"],"synonyms":[{"name":"disease of nasopharynx","type":"exact"},{"name":"disease or disorder of nasopharynx","type":"exact"},{"name":"disorder of nasopharynx","type":"exact"},{"name":"disorder of postnasal space","type":"related"},{"name":"nasopharyngeal disorder","type":"exact"},{"name":"nasopharynx disease","type":"exact"},{"name":"nasopharynx disease or disorder","type":"exact"}],"termid":"MONDO:0004821","xrefs":{"Monarch":{"xref_id":"0004821"}}}


id: PBO:0045150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal heavy chain 8","termid":"PBO:0045150"}


id: GO:0042672
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a retinal cone cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photoreceptor cell fate specification","termid":"GO:0043704"},{"relation_name":"part_of","term_name":"retinal cone cell fate commitment","termid":"GO:0046551"}],"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":"retinal cone cell fate specification","termid":"GO:0042672"}


id: GO:0043136
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + sn-glycerol 3-phosphate = glycerol + phosphate.","definition_xrefs":["RHEA:66372"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016788","GO:0003824"],"is_obsolete":false,"name":"glycerol-3-phosphatase activity","secondary_identifiers":["Reactome:R-HSA-8955794","MetaCyc:GLYCEROL-1-PHOSPHATASE-RXN"],"termid":"GO:0043136"}


id: PBO:0066188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 11","termid":"PBO:0066188"}


id: GO:0035562
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the frequency, rate or extent of chromatin binding. Chromatin binding is the selective interaction with chromatin, the network of fibers of DNA, protein, and sometimes RNA, that make up the chromosomes of the eukaryotic nucleus during interphase.","definition_xrefs":["PMID:20404130","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromatin binding","termid":"GO:0035561"},{"relation_name":"is_a","term_name":"negative regulation of binding","termid":"GO:0051100"}],"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 chromatin binding","termid":"GO:0035562"}


id: GO:0007482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the haltere over time, from its formation to the mature structure. The haltere is the club-shaped 'balancers' found on each side of the metathorax among the true flies (Diptera). They are the much-modified hind wings.","definition_xrefs":["GOC:jid","PMID:32659004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc-derived appendage development","termid":"GO:0048737"},{"relation_name":"part_of","term_name":"haltere disc development","termid":"GO:0035216"}],"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":"haltere development","termid":"GO:0007482"}


id: GO:0045010
data:
  {"annotated_genes":["SJAG_04100","SJAG_01732","SJAG_02245","SJAG_02228","SJAG_03455","SJAG_04624","SJAG_04479","SJAG_01964","SJAG_02075","SJAG_01268","SJAG_03086","SJAG_01384"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88575],"is_not":false,"summary":null,"term":"GO:0045010"},{"annotations":[104326,98034,98877,87363,102489,101922,89884,99055,97112,106321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034314"},{"annotations":[90082],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0034316"}]},"cv_name":"biological_process","definition":"The initial step in the formation of an actin filament, in which actin monomers combine to form a new filament. Nucleation is slow relative to the subsequent addition of more monomers to extend the filament.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament organization","termid":"GO:0007015"}],"gene_count":12,"genes_by_uniquename":{"SJAG_01268":null,"SJAG_01384":null,"SJAG_01732":null,"SJAG_01964":null,"SJAG_02075":null,"SJAG_02228":null,"SJAG_02245":null,"SJAG_03086":null,"SJAG_03455":null,"SJAG_04100":null,"SJAG_04479":null,"SJAG_04624":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"actin nucleation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"actin filament nucleation","type":"exact"}],"termid":"GO:0045010","terms_by_termid":{"GO:0034314":null,"GO:0034316":null,"GO:0045010":null}}


id: MONDO:0000680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An agnosia that is the loss of the ability to recognize objects by touch based on its texture, size and weight.","definition_xrefs":["DOID:0060150"],"direct_ancestors":[{"relation_name":"is_a","term_name":"agnosia","termid":"MONDO:0005638"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"astereognosia","secondary_identifiers":["HP:0010527","icd11.foundation:756147896","MEDGEN:65881","UMLS:C0234505"],"synonyms":[{"name":"astereognosia","type":"exact"},{"name":"astereognosia (disease)","type":"exact"},{"name":"somatosensory agnosia","type":"exact"}],"termid":"MONDO:0000680","xrefs":{"Monarch":{"xref_id":"0000680"}}}


id: MONDO:0008839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxia-microcephaly-cataract syndrome","secondary_identifiers":["MESH:C563086","OMIM:208870","UMLS:C0796056","MEDGEN:167098"],"synonyms":[{"name":"AMC syndrome","type":"related"},{"name":"ataxia-microcephaly-cataract syndrome","type":"exact"}],"termid":"MONDO:0008839","xrefs":{"Monarch":{"xref_id":"0008839"}}}


id: MONDO:0001379
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the ureteral orifice.","direct_ancestors":[{"relation_name":"is_a","term_name":"bladder dome cancer","termid":"MONDO:0001380"},{"relation_name":"is_a","term_name":"ureter cancer","termid":"MONDO:0008627"}],"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":"ureteric orifice cancer","secondary_identifiers":["DOID:11818","SCTID:188245008","MEDGEN:102280","ICD9:188.6","UMLS:C0153614"],"synonyms":[{"name":"cancer of ureteral orifice","type":"exact"},{"name":"malignant neoplasm of ureteral orifice","type":"exact"},{"name":"malignant neoplasm of ureteric orifice of urinary bladder","type":"exact"},{"name":"malignant tumor of ureteric orifice","type":"exact"},{"name":"malignant tumour of ureteric orifice","type":"exact"},{"name":"malignant ureteral orifice neoplasm","type":"exact"},{"name":"orifice of the ureter","type":"exact"},{"name":"ureteral orifice cancer","type":"exact"}],"termid":"MONDO:0001379","xrefs":{"Monarch":{"xref_id":"0001379"}}}


id: PBO:0054120
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 1486","termid":"PBO:0054120"}


id: PBO:0049743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemoglobin subunit gamma 1","termid":"PBO:0049743"}


id: MONDO:0021200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of disease that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare disease (obsolete MONDO:0021200)","secondary_identifiers":["NCIT:C4873","MESH:D035583"],"synonyms":[{"name":"rare disease","type":"exact"},{"name":"rare disease or disorder","type":"exact"},{"name":"rare diseases","type":"exact"},{"name":"rare disorder","type":"exact"}],"termid":"MONDO:0021200","xrefs":{"Monarch":{"xref_id":"0021200"}}}


id: GO:0050954
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive a sensory mechanical stimulus, convert it to a molecular signal, and recognize and characterize the signal. This is a neurological process.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception","termid":"GO:0007600"}],"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":"sensory perception of mechanical stimulus","synonyms":[{"name":"chemi-mechanical coupling","type":"related"},{"name":"mechanosensory perception","type":"exact"},{"name":"perception of mechanical stimulus","type":"exact"}],"termid":"GO:0050954"}


id: GO:0033644
data:
  {"annotated_genes":["SJAG_02392"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[118605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0085039"}]},"cv_name":"cellular_component","definition":"Double layer of lipid molecules as it encloses host cells, and, in eukaryotes, many organelles; may be a single or double lipid bilayer; also includes associated proteins. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell part","termid":"GO:0033643"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02392":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell membrane","references_by_uniquename":{"PMID:30726171":null},"termid":"GO:0033644","terms_by_termid":{"GO:0085039":null}}


id: MONDO:0006098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lobular neoplasia characterized by lobular epithelial proliferation that does not completely fill the lobular unit of the breast.","definition_xrefs":["NCIT:C4730"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system cancer","termid":"MONDO:0000653"},{"relation_name":"is_a","term_name":"lobular neoplasia","termid":"MONDO:0002486"},{"relation_name":"is_a","term_name":"hyperplasia","termid":"MONDO:0005043"}],"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":"atypical lobular breast hyperplasia","secondary_identifiers":["SCTID:450697004","EFO:1000100","UMLS:C1368920","ICD9:610.8","MEDGEN:277968"],"synonyms":[{"name":"ALH","type":"exact"},{"name":"atypical breast lobular hyperplasia","type":"exact"},{"name":"atypical lobular breast hyperplasia","type":"exact"},{"name":"atypical lobular hyperplasia","type":"exact"},{"name":"atypical lobular hyperplasia of breast","type":"exact"},{"name":"atypical lobular hyperplasia of the breast","type":"exact"}],"termid":"MONDO:0006098","xrefs":{"Monarch":{"xref_id":"0006098"}}}


id: GO:0043453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an alkyne, any acyclic branched or unbranched hydrocarbon (compound composed only of carbon and hydrogen) having a carbon-carbon triple bond and the general formula CnH2n-2.","definition_xrefs":["GOC:jl","GOC:krc","Wikipedia:Alkyne"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkyne metabolic process","termid":"GO:0043452"},{"relation_name":"is_a","term_name":"acetylenic compound biosynthetic process","termid":"GO:0120247"},{"relation_name":"is_a","term_name":"hydrocarbon biosynthetic process","termid":"GO:0120251"}],"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":"alkyne biosynthetic process","synonyms":[{"name":"alkyne anabolism","type":"exact"},{"name":"alkyne biosynthesis","type":"exact"},{"name":"alkyne formation","type":"exact"},{"name":"alkyne synthesis","type":"exact"}],"termid":"GO:0043453"}


id: PR:P41390
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An amidophosphoribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11907:SF0","PRO:DNx","OMA:SCHPO02227"],"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":"amidophosphoribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.08c","secondary_identifiers":["UniProtKB:P41390"],"synonyms":[{"name":"ATase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PPAT","type":"exact"},{"name":"glutamine phosphoribosylpyrophosphate amidotransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P41390"}


id: PBO:0041985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC28A antisense RNA 1","termid":"PBO:0041985"}


id: PBO:0000372
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"constitutive","termid":"PBO:0000372"}


id: GO:0010132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dhurrin, a cyanogenic glucoside which functions as a plant defense compound.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyanogenic glycoside biosynthetic process","termid":"GO:0019756"},{"relation_name":"is_a","term_name":"beta-glucoside biosynthetic process","termid":"GO:1901806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"dhurrin biosynthetic process","secondary_identifiers":["MetaCyc:PWY-861"],"synonyms":[{"name":"dhurrin anabolism","type":"exact"},{"name":"dhurrin biosynthesis","type":"exact"},{"name":"dhurrin formation","type":"exact"},{"name":"dhurrin synthesis","type":"exact"}],"termid":"GO:0010132"}


id: PBO:0028516
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_oxidation_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0028516"}


id: GO:0000241
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase which follows diplotene during prophase I of meiosis, the separation of homologous chromosomes is complete and crossing over has occurred.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiosis I cell cycle phase","termid":"GO:0098764"},{"relation_name":"part_of","term_name":"meiotic prophase I","termid":"GO:0007128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007128"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007128","GO:0008150"],"is_obsolete":false,"name":"diakinesis","secondary_identifiers":["Wikipedia:Diakinesis","Wikipedia:Meiosis#Diakinesis"],"termid":"GO:0000241"}


id: GO:0030150
data:
  {"annotated_genes":["SJAG_04336","SJAG_03502","SJAG_01615","SJAG_03358","SJAG_02917","SJAG_04014","SJAG_03515","SJAG_01879","SJAG_00564","SJAG_04432","SJAG_04996","SJAG_04218","SJAG_05259","SJAG_01442","SJAG_00373","SJAG_01597","SJAG_02077","SJAG_03560","SJAG_01684","SJAG_01120","SJAG_03415"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87543,88746,90102,93716,96079,98437,98620,98734,99504,101878,102458,104349,105336,106668,106725,106747,109030,110941,114363,115914,116377],"is_not":false,"summary":null,"term":"GO:0030150"}]},"cv_name":"biological_process","definition":"The import of proteins across the outer and inner mitochondrial membranes into the matrix. Unfolded proteins enter the mitochondrial matrix with a chaperone protein; the information required to target the precursor protein from the cytosol to the mitochondrial matrix is contained within its N-terminal matrix-targeting sequence. Translocation of precursors to the matrix occurs at the rare sites where the outer and inner membranes are close together.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transmembrane import into intracellular organelle","termid":"GO:0044743"},{"relation_name":"is_a","term_name":"establishment of protein localization to mitochondrion","termid":"GO:0072655"},{"relation_name":"is_a","term_name":"import into the mitochondrion","termid":"GO:0170036"},{"relation_name":"part_of","term_name":"protein targeting to mitochondrion","termid":"GO:0006626"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00373":null,"SJAG_00564":null,"SJAG_01120":null,"SJAG_01442":null,"SJAG_01597":null,"SJAG_01615":null,"SJAG_01684":null,"SJAG_01879":null,"SJAG_02077":null,"SJAG_02917":null,"SJAG_03358":null,"SJAG_03415":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03560":null,"SJAG_04014":null,"SJAG_04218":null,"SJAG_04336":null,"SJAG_04432":null,"SJAG_04996":null,"SJAG_05259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0006605"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0055085","GO:0006605"],"is_obsolete":false,"name":"protein import into mitochondrial matrix","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial matrix protein import","type":"exact"},{"name":"mitochondrial translocation","type":"broad"},{"name":"protein transport into mitochondrial matrix","type":"exact"}],"termid":"GO:0030150","terms_by_termid":{"GO:0030150":null}}


id: PBO:0035922
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-K4_acetylation_during_vegetative_growth","termid":"PBO:0035922"}


id: MONDO:0015065
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the ileum.","definition_xrefs":["NCIT:C135092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine neuroendocrine tumor, well differentiated, low or intermediate grade","termid":"MONDO:0002995"},{"relation_name":"is_a","term_name":"ileal neoplasm","termid":"MONDO:0006801"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"ileal neuroendocrine tumor, well differentiated, low or intermediate grade","secondary_identifiers":["MEDGEN:1611292","GARD:19753","UMLS:C4525628","Orphanet:100078"],"synonyms":[{"name":"ileal neuroendocrine neoplasm","type":"exact"},{"name":"ileal neuroendocrine tumor","type":"related"},{"name":"ileal neuroendocrine tumour","type":"related"}],"termid":"MONDO:0015065","xrefs":{"Monarch":{"xref_id":"0015065"}}}


id: GO:0001971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the activation of the membrane attack complex components of the complement cascade.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of activation of membrane attack complex","termid":"GO:0001969"},{"relation_name":"is_a","term_name":"negative regulation of complement activation","termid":"GO:0045916"},{"relation_name":"negatively_regulates","term_name":"activation of membrane attack complex","termid":"GO:0001905"}],"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 activation of membrane attack complex","synonyms":[{"name":"down regulation of activation of membrane attack complex","type":"exact"},{"name":"down-regulation of activation of membrane attack complex","type":"exact"},{"name":"downregulation of activation of membrane attack complex","type":"exact"},{"name":"inhibition of activation of membrane attack complex","type":"narrow"},{"name":"negative regulation of MAC assembly","type":"exact"},{"name":"negative regulation of MAC formation","type":"exact"},{"name":"negative regulation of activation of MAC","type":"exact"},{"name":"negative regulation of activation of TCC","type":"narrow"},{"name":"negative regulation of activation of terminal complement complex","type":"narrow"},{"name":"negative regulation of activation of the terminal complement cascade","type":"narrow"},{"name":"negative regulation of membrane attack complex assembly","type":"exact"},{"name":"negative regulation of membrane attack complex formation","type":"exact"}],"termid":"GO:0001971"}


id: GO:0051898
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of phosphatidylinositol 3-kinase/protein kinase B signal transduction.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction","termid":"GO:0051896"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"phosphatidylinositol 3-kinase/protein kinase B signal transduction","termid":"GO:0043491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction","synonyms":[{"name":"down regulation of protein kinase B signaling cascade","type":"related"},{"name":"down-regulation of protein kinase B signaling cascade","type":"related"},{"name":"downregulation of protein kinase B signaling cascade","type":"related"},{"name":"inhibition of protein kinase B signaling cascade","type":"narrow"},{"name":"negative regulation of AKT signaling cascade","type":"related"},{"name":"negative regulation of AKT signalling cascade","type":"related"},{"name":"negative regulation of PI3K-PKB/Akt pathway","type":"exact"},{"name":"negative regulation of PI3K/Akt signal transduction","type":"exact"},{"name":"negative regulation of PI3K/PKB signal transduction","type":"exact"},{"name":"negative regulation of PKB signaling cascade","type":"related"},{"name":"negative regulation of PKB signalling cascade","type":"related"},{"name":"negative regulation of phosphatidylinositol 3-kinase signaling/protein kinase B signal transduction","type":"exact"},{"name":"negative regulation of protein kinase B signaling","type":"related"},{"name":"negative regulation of protein kinase B signaling cascade","type":"related"},{"name":"negative regulation of protein kinase B signalling cascade","type":"related"}],"termid":"GO:0051898"}


id: PBO:0077882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin polymerization promoting protein family member 2","termid":"PBO:0077882"}


id: GO:0044187
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small lytic vacuole that has cell cycle-independent morphology and is found in most host animal cells and that contains a variety of hydrolases, most of which have their maximal activities in the pH range 5-6. The contained enzymes display latency if properly isolated. About 40 different lysosomal hydrolases are known and host cell lysosomes have a great variety of morphologies and functions.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host intracellular membrane-bounded organelle","termid":"GO:0033648"},{"relation_name":"is_a","term_name":"host cell cytoplasm part","termid":"GO:0033655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell lysosome","termid":"GO:0044187"}


id: PBO:0041336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3 open reading frame 18","termid":"PBO:0041336"}


id: PBO:0002759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor, Elf1 family (predicted)","termid":"PBO:0002759"}


id: MONDO:0010375
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked intellectual disability-epilepsy syndrome","termid":"MONDO:0016160"},{"relation_name":"is_a","term_name":"hereditary hyperekplexia","termid":"MONDO:0021022"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"},{"relation_name":"is_a","term_name":"X-linked complex neurodevelopmental disorder","termid":"MONDO:0100148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 8","secondary_identifiers":["Orphanet:163985","OMIM:300607","DOID:0080215","UMLS:C1845102","GARD:17010","MEDGEN:375581","MESH:C564474"],"synonyms":[{"name":"DEE8","type":"exact"},{"name":"EIEE8","type":"exact"},{"name":"developmental and epileptic encephalopathy 8","type":"exact"},{"name":"early infantile epileptic encephalopathy 8","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 8","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 8","type":"exact"},{"name":"hyperekplexia and epilepsy","type":"related"},{"name":"hyperekplexia-epilepsy syndrome","type":"exact"}],"termid":"MONDO:0010375","xrefs":{"Monarch":{"xref_id":"0010375"}}}


id: PBO:0113440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sterol-binding protein located at plasma membrane-ER contact sites; role in retrograde transport of sterols from plasma membrane to ER, which is inhibited via phosphorylation by TORC2-dependent protein kinase Ypk1p; contains two StART-like domains that bind sterols and a GRAM domain; co-localizes to puncta in the cortical ER with Sip3p; one of six StART-like domain-containing proteins in yeast that may be involved in sterol transfer between intracellular membranes; conserved across eukaryotes","termid":"PBO:0113440"}


id: PATO:0001511
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A disfunctional quality held by the bearer when the latter is unable to perform a regular function(s).","definition_xrefs":["PATC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functionality","termid":"PATO:0001509"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-functional","secondary_identifiers":["PATO:0001640"],"synonyms":[{"name":"defective","type":"related"},{"name":"disfunctional","type":"exact"},{"name":"failure","type":"related"},{"name":"functional failure","type":"exact"}],"termid":"PATO:0001511"}


id: PBO:0035695
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-involved_in_or_involved_in_regulation_of","termid":"PBO:0035695"}


id: MONDO:8000015
data:
  {"annotated_genes":["SJAG_03077"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85049],"is_not":false,"summary":null,"term":"MONDO:8000015"}]},"cv_name":"mondo","definition":"Any 46,XY complete gonadal dysgenesis in which the cause of the disease is a mutation in the DHX37 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene","OMIM:273250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY complete gonadal dysgenesis","termid":"MONDO:0010765"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03077":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"46,XY sex reversal 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:78602","MedDRA:10002641","ICD9:752.89","SCTID:53599007","MESH:C537770","UMLS:C0266427","GARD:16552","Orphanet:983"],"synonyms":[{"name":"46, XY sex reversal 11","type":"exact"},{"name":"ETRS","type":"exact"},{"name":"SRXY11","type":"exact"},{"name":"TRS","type":"exact"},{"name":"XY gonadal agenesis syndrome","type":"related"},{"name":"anorchia, familial","type":"related"},{"name":"embryonic testicular regression syndrome","type":"exact"},{"name":"testicular regression syndrome","type":"exact"},{"name":"testicular regression, embryonic","type":"related"},{"name":"vanishing testes syndrome","type":"exact"},{"name":"vanishing testis syndrome","type":"exact"}],"termid":"MONDO:8000015","terms_by_termid":{"MONDO:8000015":null},"xrefs":{"Monarch":{"xref_id":"8000015"}}}


id: PBO:0059759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 33","termid":"PBO:0059759"}


id: PBO:0066481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"refilin B","termid":"PBO:0066481"}


id: PBO:0077890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein p63 regulated 1 like pseudogene 1","termid":"PBO:0077890"}


id: PBO:0058800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7706","termid":"PBO:0058800"}


id: GO:0034180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of toll-like receptor 13 signaling pathway.","definition_xrefs":["GOC:add","PMID:16551253","PMID:17328678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of toll-like receptor 13 signaling pathway","termid":"GO:0034179"},{"relation_name":"is_a","term_name":"negative regulation of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039532"},{"relation_name":"negatively_regulates","term_name":"toll-like receptor 13 signaling pathway","termid":"GO:0034178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of toll-like receptor 13 signaling pathway","synonyms":[{"name":"negative regulation of TLR13 signaling pathway","type":"exact"},{"name":"negative regulation of toll-like receptor 13 signalling pathway","type":"exact"}],"termid":"GO:0034180"}


id: PATO:0000532
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000532 micronutrient sensitivity value (obsolete PATO:0000532)","termid":"PATO:0000532"}


id: PBO:0017723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorismate mutase Aro7 (predicted)","termid":"PBO:0017723"}


id: MONDO:0014417
data:
  {"annotated_genes":["SJAG_02885","SJAG_01356"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85516,85517],"is_not":false,"summary":null,"term":"MONDO:0014417"}]},"cv_name":"mondo","definition":"Spinocerebellar ataxia type 38 (SCA38) is a subtype of autosomal dominant cerebellar ataxia type 3 characterized by the adult-onset (average age: 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplopia and axonal neuropathy.","definition_xrefs":["Orphanet:423296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of phospholipids, sphingolipids and fatty acids biosynthesis","termid":"MONDO:0018117"},{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type III","termid":"MONDO:0019793"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0002039","MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"spinocerebellar ataxia type 38","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:12369","UMLS:C4518337","DOID:0050985","SCTID:734021001","MEDGEN:1379865","OMIM:615957"],"synonyms":[{"name":"SCA38","type":"exact"},{"name":"spinocerebellar ataxia 38","type":"related"},{"name":"spinocerebellar ataxia type 38","type":"exact"}],"termid":"MONDO:0014417","terms_by_termid":{"MONDO:0014417":null},"xrefs":{"Monarch":{"xref_id":"0014417"}}}


id: GO:0033745
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-methionine + thioredoxin disulfide + H2O = L-methionine (R)-S-oxide + thioredoxin.","definition_xrefs":["EC:1.8.4.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"L-methionine-(R)-S-oxide reductase activity","secondary_identifiers":["MetaCyc:1.8.4.14-RXN","RHEA:21260"],"synonyms":[{"name":"FRMsr","type":"related"},{"name":"L-methionine:thioredoxin-disulfide S-oxidoreductase [L-methionine (R)-S-oxide-forming] activity","type":"related"},{"name":"free met-R-(o) reductase activity","type":"related"},{"name":"free-methionine (R)-S-oxide reductase activity","type":"related"},{"name":"methionine-R-sulfoxide reductase activity","type":"related"}],"termid":"GO:0033745"}


id: MONDO:0018981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neonatal epilepsy syndrome characterized by seizures without specific underlying etiology, occurring during the first days of life in infants with an otherwise normal neurological state and no family history of neonatal convulsions. The most commonly partial and clonic seizures usually last for one to three minutes. Repeated seizures may lead to status epilepticus lasting up to 20 hours. Overall, remission rates are high and neurological outcome is favorable.","definition_xrefs":["Orphanet:64545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal epilepsy syndrome","termid":"MONDO:0020070"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"benign idiopathic neonatal seizures","secondary_identifiers":["MEDGEN:140738","UMLS:C0393693","icd11.foundation:1131336245","GARD:18860"],"synonyms":[{"name":"BINS","type":"exact"},{"name":"benign nonfamilial neonatal seizures","type":"exact"}],"termid":"MONDO:0018981","xrefs":{"Monarch":{"xref_id":"0018981"}}}


id: PBO:0085876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; identified by gene-trapping, microarray-based expression analysis, and genome-wide homology searching","termid":"PBO:0085876"}


id: PBO:0081051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCHC-type containing 9","termid":"PBO:0081051"}


id: GO:1905297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neural crest cell fate specification.","definition_xrefs":["GOC:rl","GO_REF:0000058","PMID:15073157","GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell fate specification","termid":"GO:0042660"},{"relation_name":"is_a","term_name":"positive regulation of neural crest formation","termid":"GO:0090300"},{"relation_name":"is_a","term_name":"positive regulation of neural crest cell differentiation","termid":"GO:1905294"},{"relation_name":"is_a","term_name":"regulation of neural crest cell fate specification","termid":"GO:1905295"},{"relation_name":"positively_regulates","term_name":"neural crest cell fate specification","termid":"GO:0014036"}],"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 neural crest cell fate specification","synonyms":[{"name":"activation of neural crest cell fate specification","type":"narrow"},{"name":"up regulation of neural crest cell fate specification","type":"exact"},{"name":"up-regulation of neural crest cell fate specification","type":"exact"},{"name":"upregulation of neural crest cell fate specification","type":"exact"}],"termid":"GO:1905297"}


id: PBO:0072329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 15","termid":"PBO:0072329"}


id: GO:0160106
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosine(9) in tRNA + S-adenosyl-L-methionine = H+ + N(1)-methyladenosine(9) in tRNA + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.218"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA (adenine) methyltransferase activity","termid":"GO:0016426"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0140101","GO:0016740","GO:0016741","GO:0140098","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"tRNA (adenine(9)-N1)-methyltransferase activity","secondary_identifiers":["RHEA:43148","Reactome:R-HSA-6787594"],"synonyms":[{"name":"tRNA (adenine(9)-N(1))-methyltransferase activity","type":"exact"},{"name":"tRNA m(1)A(9)-methyltransferase","type":"exact"},{"name":"tRNA(m(1)G(9)/m(1)A(9))-methyltransferase","type":"exact"}],"termid":"GO:0160106"}


id: MONDO:0021153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic and acquired (obsolete MONDO:0021153)","synonyms":[{"name":"somatic genetic","type":"related"}],"termid":"MONDO:0021153","xrefs":{"Monarch":{"xref_id":"0021153"}}}


id: GO:0036078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of tubulin heterodimers from the minus end of a microtubule.","definition_xrefs":["PMID:17452528","GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule depolymerization","termid":"GO:0007019"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0000226","GO:0008150"],"is_obsolete":false,"name":"minus-end specific microtubule depolymerization","termid":"GO:0036078"}


id: PBO:0039457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 9","termid":"PBO:0039457"}


id: PBO:0088660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit alpha 7, Pre10","termid":"PBO:0088660"}


id: PBO:0029040
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_non-ionic_osmotic_stress","termid":"PBO:0029040"}


id: PBO:0047476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyl diphosphate synthase pseudogene 3","termid":"PBO:0047476"}


id: GO:0031025
data:
  {"annotated_genes":["SJAG_03052"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101506],"is_not":false,"summary":null,"term":"GO:0031025"}]},"cv_name":"biological_process","definition":"The process in which the equatorial microtubule organizing center is disassembled at the end of mitosis.","definition_xrefs":["PMID:15068790","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component disassembly","termid":"GO:0022411"},{"relation_name":"is_a","term_name":"microtubule organizing center organization","termid":"GO:0031023"},{"relation_name":"is_a","term_name":"equatorial microtubule organization","termid":"GO:0031121"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03052":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000226","GO:0008150","GO:0007010"],"is_obsolete":false,"name":"equatorial microtubule organizing center disassembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"equatorial microtubule organising center disassembly","type":"exact"}],"termid":"GO:0031025","terms_by_termid":{"GO:0031025":null}}


id: PBO:0040868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bcl2 modifying factor","termid":"PBO:0040868"}


id: PATO:0002197
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality that describes the power of an atom to attract electrons to itself .","definition_xrefs":["PATOC:JH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular quality","termid":"PATO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"electronegativity","termid":"PATO:0002197"}


id: PBO:0111834
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"jmjN domain","termid":"PBO:0111834"}


id: PBO:0056718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meprin A subunit alpha","termid":"PBO:0056718"}


id: GO:0003906
data:
  {"annotated_genes":["SJAG_02298","SJAG_03665","SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[109107,116894],"is_not":false,"summary":null,"term":"GO:0003906"},{"annotations":[95344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140078"}]},"cv_name":"molecular_function","definition":"Catalysis of the cleavage of the C-O-P bond in the AP site created when DNA glycosylase removes a damaged base, involved in the DNA base excision repair pathway (BER).","definition_xrefs":["Wikipedia:AP_endonuclease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02298":null,"SJAG_03665":null,"SJAG_03724":null},"genotype_count":0,"interesting_parent_details":[{"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:0003674","GO:0140097","GO:0003824"],"is_obsolete":false,"name":"DNA-(apurinic or apyrimidinic site) endonuclease activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5649725","Reactome:R-HSA-110375","Reactome:R-HSA-5649711"],"synonyms":[{"name":"AP deoxyendoribonuclease activity","type":"exact"},{"name":"UV endonuclease","type":"broad"},{"name":"abasic deoxyendoribonuclease activity","type":"exact"},{"name":"apurinic deoxyendoribonuclease activity","type":"exact"},{"name":"apurinic/apyrimidinic endodeoxyribonuclease activity","type":"exact"},{"name":"apyrimidinic deoxyendoribonuclease activity","type":"exact"},{"name":"deoxyribonuclease (apurinic or apyrimidinic) activity","type":"exact"},{"name":"endonuclease VIII activity","type":"related"}],"termid":"GO:0003906","terms_by_termid":{"GO:0003906":null,"GO:0140078":null}}


id: MONDO:0001520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by the recurrent failure to resist the impulse to steal items of little intrinsic value; the individual experiences a rising subjective sense of tension before the theft and a sense of gratification or relief during the theft.","definition_xrefs":["NCIT:C94333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impulse control disorder","termid":"MONDO:0001162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kleptomania","secondary_identifiers":["ICD10CM:F63.2","DOID:12400","SCTID:69361009","UMLS:C0022734","icd11.foundation:804604349","MEDGEN:5974","ICD9:312.32"],"synonyms":[{"name":"kleptomania","type":"exact"},{"name":"pathological stealing","type":"exact"}],"termid":"MONDO:0001520","xrefs":{"Monarch":{"xref_id":"0001520"}}}


id: MONDO:0015276
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete prostate cancer (obsolete MONDO:0015276)","termid":"MONDO:0015276","xrefs":{"Monarch":{"xref_id":"0015276"}}}


id: PBO:0004185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase delta catalytic subunit Cdc6","termid":"PBO:0004185"}


id: GO:0031529
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 ruffle, a projection at the leading edge of a crawling cell.","definition_xrefs":["PMID:10036235","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection organization","termid":"GO:0120036"}],"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":"ruffle organization","synonyms":[{"name":"ruffle organisation","type":"exact"},{"name":"ruffle organization and biogenesis","type":"related"}],"termid":"GO:0031529"}


id: PATO:0001843
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An acidity which is relatively low.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"acidity","termid":"PATO:0001842"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased acidity","synonyms":[{"name":"low acidity","type":"exact"}],"termid":"PATO:0001843"}


id: PBO:0079606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2F pseudogene 3","termid":"PBO:0079606"}


id: MONDO:0100078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A severe medical condition which is estimated to appear in 9-18% of hypertensive patients, in which treatment with 3 or more antihypertensive drugs including diuretics are ineffective.","definition_xrefs":["PMID:26935512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertensive disorder","termid":"MONDO:0005044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"resistant hypertension","secondary_identifiers":["MEDGEN:1663781","UMLS:C0745130"],"synonyms":[{"name":"drug resistant hypertension","type":"exact"}],"termid":"MONDO:0100078","xrefs":{"Monarch":{"xref_id":"0100078"}}}


id: PBO:0110049
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial MICOS interactor required for Cristae morphology","termid":"PBO:0110049"}


id: MONDO:0001943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Malaria resulting from infection by Plasmodium malariae.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malaria","termid":"MONDO:0005136"}],"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":"Plasmodium malariae malaria","secondary_identifiers":["ICD9:084.2","SCTID:27618009","UMLS:C0024536","NCIT:C34799","ICD10CM:B52","MEDGEN:44259","DOID:14324"],"synonyms":[{"name":"malaria by Plasmodium malariae","type":"exact"},{"name":"quartan malaria","type":"exact"}],"termid":"MONDO:0001943","xrefs":{"Monarch":{"xref_id":"0001943"}}}


id: FYPO:0005121
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA transcribed from early meiotic genes measured in a cell is lower than normal during the meiotic cell cycle. Early meiotic genes are normally transcribed during pre-meiotic S phase and recombination.","definition_xrefs":["PomBase:al","PMID:17927811","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during meiotic cell cycle","termid":"FYPO:0004630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased level of early meiotic gene mRNA during meiotic cell cycle","synonyms":[{"name":"decreased level of early meiosis gene mRNA during meiotic cell cycle","type":"exact"},{"name":"decreased level of early meiotic gene RNA during meiotic cell cycle","type":"exact"},{"name":"decreased level of early meiotic gene transcripts during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0005121"}


id: GO:0047117
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: acyl-[acyl-carrier protein] + NADP+ = trans-D2-enoyl-[acyl-carrier protein] + NADPH + H+.","definition_xrefs":["EC:1.3.1.39","MetaCyc:1.3.1.39-RXN"],"gene_count":0,"genotype_count":0,"name":"obsolete enoyl-[acyl-carrier-protein] reductase (NADPH, A-specific) activity (obsolete GO:0047117)","synonyms":[{"name":"acyl-acyl-carrier-protein:NADP+ oxidoreductase (A-specific)","type":"related"},{"name":"enoyl-ACP reductase (NADPH, A-specific) activity","type":"exact"},{"name":"enoyl-ACp reductase activity","type":"related"},{"name":"enoyl-[acyl-carrier protein] reductase (NADPH, A-specific) activity","type":"exact"},{"name":"enoyl-acyl carrier protein (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"related"},{"name":"enoyl-acyl-carrier-protein reductase (NADPH, A-specific)","type":"related"}],"termid":"GO:0047117"}


id: MONDO:0800466
data:
  {"annotated_genes":["SJAG_04978"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011301"}]},"cv_name":"mondo","definition":"Any endocrine system disorder in which the cause of the disease is inactivation of the GNAS gene. Phenotypes include pseudohypoparathyroidism Ia, Ib, and Ic (PHP-Ia, -Ib, -Ic), pseudopseudohypoparathyroidism (PPHP), progressive osseous heteroplasia (POH), and osteoma cutis (OC).","definition_xrefs":["PMID:29072892"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04978":null},"genotype_count":0,"is_obsolete":false,"name":"disorder of GNAS inactivation","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0800466","terms_by_termid":{"MONDO:0011301":null},"xrefs":{"Monarch":{"xref_id":"0800466"}}}


id: PBO:0051728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrator complex subunit 1","termid":"PBO:0051728"}


id: PBO:0029658
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_deadenylation-independent_decapping_of_nuclear-transcribed_mRNA","termid":"PBO:0029658"}


id: MONDO:0003266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of neoplasms which arise from the ependymal lining of the cerebral ventricles and from the remnants of the central canal of the spinal cord. Ependymal tumors occur predominantly in children and young adults with varied morphological features and biological behavior. There are 4 types: ependymoma, anaplastic ependymoma, myxopapillary ependymoma and subependymoma. (WHO)","definition_xrefs":["NCIT:C6770"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glioma","termid":"MONDO:0021042"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ependymal tumor","secondary_identifiers":["GARD:16527","MEDGEN:232459","UMLS:C1333407","ONCOTREE:EPMT","EFO:1000027","Orphanet:301"],"synonyms":[{"name":"ependymal neoplasm","type":"exact"},{"name":"ependymal tumor","type":"exact"},{"name":"ependymal tumors","type":"exact"},{"name":"ependymal tumours","type":"exact"},{"name":"ependymomal tumor","type":"related"},{"name":"ependymomal tumour","type":"related"}],"termid":"MONDO:0003266","xrefs":{"Monarch":{"xref_id":"0003266"}}}


id: MONDO:0014522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0004736"],"is_obsolete":false,"name":"retinal dystrophy and obesity","secondary_identifiers":["OMIM:616188","MEDGEN:863861","UMLS:C4015424"],"synonyms":[{"name":"RDOB","type":"related"},{"name":"retinal dystrophy and obesity","type":"exact"}],"termid":"MONDO:0014522","xrefs":{"Monarch":{"xref_id":"0014522"}}}


id: PBO:0002117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumerate reductase (predicted)","termid":"PBO:0002117"}


id: GO:1902641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate catabolic process.","definition_xrefs":["GO_REF:0000058","PMID:22562153","GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipid catabolic process","termid":"GO:0060696"},{"relation_name":"regulates","term_name":"1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate catabolic process","termid":"GO:1902634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate catabolic process","synonyms":[{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate breakdown","type":"exact"},{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate catabolism","type":"exact"},{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate degradation","type":"exact"}],"termid":"GO:1902641"}


id: MONDO:0001186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by persistent or recurrent episodes of feeling detached from one's self (either one's body or one's mental processes), although the sufferer remains aware that this is only a feeling and does not represent reality.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dissociative disorder","termid":"MONDO:0001160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"depersonalization disorder","secondary_identifiers":["NCIT:C94331","SCTID:70764005","UMLS:C0683416","ICD9:300.6","DOID:11038","MEDGEN:151919"],"synonyms":[{"name":"neurotic derealization","type":"exact"}],"termid":"MONDO:0001186","xrefs":{"Monarch":{"xref_id":"0001186"}}}


id: GO:0009338
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An enzyme complex that catalyzes exonucleolytic cleavage (in the presence of ATP) in either 5' to 3' or 3' to 5' direction to yield 5'-phosphooligonucleotides. Exodeoxyribonuclease V shows a preference for double-stranded DNA and possesses DNA-dependent ATPase activity. It acts endonucleolytically on single-stranded circular DNA.","definition_xrefs":["PMID:1618858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"exodeoxyribonuclease V complex","termid":"GO:0009338"}


id: PBO:0089940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"random septum position protein, DNAJ domain protein Rsp1","termid":"PBO:0089940"}


id: SO:0001894
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature ablation whereby the deleted region includes a regulatory region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_ablation","termid":"SO:0001879"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulatory_region_ablation","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"VEP:regulatory_region_ablation","type":"exact"},{"name":"regulatory region ablation","type":"exact"}],"termid":"SO:0001894"}


id: PBO:0071550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 15","termid":"PBO:0071550"}


id: GO:2001227
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to quercitrin.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"flavonoid binding","termid":"GO:0097243"},{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"}],"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":"quercitrin binding","termid":"GO:2001227"}


id: FYPO:0002130
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, does not occur during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation during vegetative growth","termid":"FYPO:0002033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein phosphorylation during cellular response to heat","synonyms":[{"name":"abolished protein phosphorylation during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"abolished protein phosphorylation during cellular response to heat during vegetative growth","type":"exact"},{"name":"abolished protein phosphorylation during cellular response to heat shock","type":"narrow"},{"name":"protein phosphorylation abolished during cellular response to heat","type":"exact"}],"termid":"FYPO:0002130"}


id: GO:0046835
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of introducing a phosphate group into a carbohydrate, any organic compound based on the general formula Cx(H2O)y.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate metabolic process","termid":"GO:0005975"},{"relation_name":"is_a","term_name":"phosphorylation","termid":"GO:0016310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"carbohydrate phosphorylation","termid":"GO:0046835"}


id: PBO:0067971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 273","termid":"PBO:0067971"}


id: MONDO:0016153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of TRIM32","secondary_identifiers":["MEDGEN:1843261","Orphanet:207107","UMLS:C5680829","GARD:20400"],"termid":"MONDO:0016153","xrefs":{"Monarch":{"xref_id":"0016153"}}}


id: MONDO:0009759
data:
  {"annotated_genes":["SJAG_04699","SJAG_01082"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86006,86007],"is_not":false,"summary":null,"term":"MONDO:0009759"}]},"cv_name":"mondo","definition":"Any mosaic variegated aneuploidy syndrome in which the cause of the disease is a mutation in the BUB1B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mosaic variegated aneuploidy syndrome","termid":"MONDO:0000141"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01082":null,"SJAG_04699":null},"genotype_count":0,"is_obsolete":false,"name":"mosaic variegated aneuploidy syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:257300","DOID:0080141","MEDGEN:338026","UMLS:C1850343"],"synonyms":[{"name":"BUB1B mosaic variegated aneuploidy syndrome","type":"exact"},{"name":"MOSAIC variegated aneuploidy syndrome 1","type":"related"},{"name":"MVA syndrome","type":"related"},{"name":"MVA1","type":"related"},{"name":"Mosaic variegated aneuploidy syndrome type 1","type":"exact"},{"name":"mosaic variegated aneuploidy syndrome 1","type":"exact"},{"name":"mosaic variegated aneuploidy syndrome caused by mutation in BUB1B","type":"exact"},{"name":"mosaic variegated aneuploidy syndrome type 1","type":"exact"}],"termid":"MONDO:0009759","terms_by_termid":{"MONDO:0009759":null},"xrefs":{"Monarch":{"xref_id":"0009759"}}}


id: GO:1903112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of single-strand break repair via homologous recombination.","definition_xrefs":["GOC:bhm","PMID:24339919","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA recombination","termid":"GO:0045911"},{"relation_name":"is_a","term_name":"regulation of single-strand break repair via homologous recombination","termid":"GO:1903110"},{"relation_name":"is_a","term_name":"positive regulation of single strand break repair","termid":"GO:1903518"},{"relation_name":"positively_regulates","term_name":"single-strand break repair via homologous recombination","termid":"GO:1990396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"positively_regulates","termid":"GO:0006310"},{"rel_name":"positively_regulates","termid":"GO:0006281"}],"interesting_parent_ids":["GO:0006259","GO:0006281","GO:0008150","GO:0006310"],"is_obsolete":false,"name":"positive regulation of single-strand break repair via homologous recombination","synonyms":[{"name":"activation of single-strand break repair via homologous recombination","type":"narrow"},{"name":"up regulation of single-strand break repair via homologous recombination","type":"exact"},{"name":"up-regulation of single-strand break repair via homologous recombination","type":"exact"},{"name":"upregulation of single-strand break repair via homologous recombination","type":"exact"}],"termid":"GO:1903112"}


id: GO:0047723
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + IMP = D-ribose 5-phosphate + hypoxanthine.","definition_xrefs":["RHEA:20469","EC:3.2.2.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing N-glycosyl compounds","termid":"GO:0016799"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"inosinate nucleosidase activity","secondary_identifiers":["MetaCyc:INOSINATE-NUCLEOSIDASE-RXN","KEGG_REACTION:R01128"],"synonyms":[{"name":"5'-inosinate phosphoribohydrolase activity","type":"related"}],"termid":"GO:0047723"}


id: PBO:0047793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box F2","termid":"PBO:0047793"}


id: GO:0015926
data:
  {"annotated_genes":["SJAG_02076","SJAG_02131","SJAG_02478","SJAG_05001","SJAG_03824","SJAG_02192","SJAG_02590","SJAG_01888","SJAG_01017","SJAG_03444","SJAG_02718","SJAG_00667","SJAG_03646","SJAG_02446","SJAG_03295","SJAG_02649","SJAG_03280","SJAG_01171","SJAG_04301","SJAG_04363"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89808,93417],"is_not":false,"summary":null,"term":"GO:0015926"},{"annotations":[100784,100785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004558"},{"annotations":[86839,86840,95307,95306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090599"},{"annotations":[114759,86666,107549],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008422"},{"annotations":[86595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106407"},{"annotations":[98980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004573"},{"annotations":[102480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004339"},{"annotations":[88303,110460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051118"},{"annotations":[93223,99337,94299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042973"},{"annotations":[101134,101135,107226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046557"},{"annotations":[87493,107227,101137,94300,101136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004338"},{"annotations":[115259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004575"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of glucosyl compounds, substances containing a group derived from a cyclic form of glucose or a glucose derivative.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00667":null,"SJAG_01017":null,"SJAG_01171":null,"SJAG_01888":null,"SJAG_02076":null,"SJAG_02131":null,"SJAG_02192":null,"SJAG_02446":null,"SJAG_02478":null,"SJAG_02590":null,"SJAG_02649":null,"SJAG_02718":null,"SJAG_03280":null,"SJAG_03295":null,"SJAG_03444":null,"SJAG_03646":null,"SJAG_03824":null,"SJAG_04301":null,"SJAG_04363":null,"SJAG_05001":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:0003674"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003824","GO:0016798","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"glucosidase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0015926","terms_by_termid":{"GO:0004338":null,"GO:0004339":null,"GO:0004558":null,"GO:0004573":null,"GO:0004575":null,"GO:0008422":null,"GO:0015926":null,"GO:0042973":null,"GO:0046557":null,"GO:0051118":null,"GO:0090599":null,"GO:0106407":null}}


id: MONDO:0012146
data:
  {"annotated_genes":["SJAG_02572"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85528],"is_not":false,"summary":null,"term":"MONDO:0012146"}]},"cv_name":"mondo","definition":"Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemophagocytic lymphohistiocytosis","termid":"MONDO:0015541"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02572":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"familial hemophagocytic lymphohistiocytosis 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:332383","MESH:C537251","DOID:0110923","OMIM:608898","UMLS:C1837174","NANDO:2200729","GARD:9928"],"synonyms":[{"name":"FHL3","type":"exact"},{"name":"HLH3","type":"exact"},{"name":"HPLH3","type":"exact"},{"name":"Hlh3","type":"related"},{"name":"Hplh3","type":"related"},{"name":"UNC13D genetic hemophagocytic lymphohistiocytosis","type":"exact"},{"name":"familial hemophagocytic lymphohistiocytosis type 3","type":"exact"},{"name":"genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D","type":"exact"},{"name":"hemophagocytic lymphohistiocytosis, familial, 3","type":"related"},{"name":"hemophagocytic lymphohistiocytosis, familial, type 3","type":"exact"}],"termid":"MONDO:0012146","terms_by_termid":{"MONDO:0012146":null},"xrefs":{"Monarch":{"xref_id":"0012146"}}}


id: PBO:0028845
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_Mmi1_focus","termid":"PBO:0028845"}


id: PBO:0035936
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_dimethylation_at_centromere_inner_repeat_during_vegetative_growth","termid":"PBO:0035936"}


id: GO:0043718
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-(hydroxymethyl)glutarate + NAD+ = 2-formylglutarate + H+ + NADH.","definition_xrefs":["RHEA:15505","EC:1.1.1.291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"2-hydroxymethylglutarate dehydrogenase activity","secondary_identifiers":["MetaCyc:1.1.1.291-RXN","KEGG_REACTION:R07985","Wikipedia:2-hydroxymethylglutarate_dehydrogenase"],"synonyms":[{"name":"(S)-2-hydroxymethylglutarate:NAD+ oxidoreductase activity","type":"related"},{"name":"HgD","type":"exact"}],"termid":"GO:0043718"}


id: PBO:0049026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 6","termid":"PBO:0049026"}


id: PBO:0039853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP19-SLIT1 readthrough (NMD candidate)","termid":"PBO:0039853"}


id: GO:0046029
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-mannitol + NAD+ = D-mannose + H+ + NADH.","definition_xrefs":["RHEA:15029"],"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"},{"relation_name":"is_a","term_name":"hexitol dehydrogenase activity","termid":"GO:0031320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"mannitol dehydrogenase activity","secondary_identifiers":["EC:1.1.1.255","KEGG_REACTION:R07135","MetaCyc:1.1.1.255-RXN"],"synonyms":[{"name":"MTD activity","type":"related"},{"name":"NAD-dependent mannitol dehydrogenase activity","type":"broad"},{"name":"mannitol:NAD+ 1-oxidoreductase activity","type":"related"}],"termid":"GO:0046029"}


id: PBO:0001206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RWD domain","termid":"PBO:0001206"}


id: PBO:0004527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linear element associated protein Hop1","termid":"PBO:0004527"}


id: PBO:0030383
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-slow_vegetative_cell_population_growth","termid":"PBO:0030383"}


id: MONDO:0008442
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spastic paraplegia-neuropathy-poikiloderma syndrome is a complex form of hereditary spastic paraplegia characterized by spastic paraplegia, demyelinating peripheral sensorimotor neuropathy, poikiloderma (manifesting with loss of eyebrows and eyelashes in childhood in addition to delicate, smooth, and wasted skin) and distal amyotrophy (presenting after puberty). There have been no further descriptions in the literature since 1992.","definition_xrefs":["Orphanet:2821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant complex spastic paraplegia","termid":"MONDO:0015087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"spastic paraplegia-neuropathy-poikiloderma syndrome","secondary_identifiers":["OMIM:182815","MEDGEN:355814","MESH:C536870","GARD:4921","UMLS:C1866851"],"synonyms":[{"name":"Antinolo-Nieto-Borrego syndrome","type":"exact"},{"name":"familial spastic paraplegia with neuropathy and poikiloderma","type":"related"},{"name":"spastic paraplegia neuropathy poikiloderma","type":"related"},{"name":"spastic paraplegia with neuropathy and poikiloderma","type":"related"}],"termid":"MONDO:0008442","xrefs":{"Monarch":{"xref_id":"0008442"}}}


id: MONDO:0013900
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alternating hemiplegia of childhood","termid":"MONDO:0016241"},{"relation_name":"is_a","term_name":"ATP1A3-associated neurological disorder","termid":"MONDO:0700002"}],"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 of childhood 2","secondary_identifiers":["MEDGEN:766702","UMLS:C3553788","OMIM:614820","GARD:15845"],"synonyms":[{"name":"AHC2","type":"related"},{"name":"ATP1A3 alternating hemiplegia of childhood","type":"exact"},{"name":"alternating hemiplegia of childhood 2","type":"exact"},{"name":"alternating hemiplegia of childhood caused by mutation in ATP1A3","type":"exact"},{"name":"alternating hemiplegia of childhood type 2","type":"exact"}],"termid":"MONDO:0013900","xrefs":{"Monarch":{"xref_id":"0013900"}}}


id: PBO:0051577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17 receptor A","termid":"PBO:0051577"}


id: GO:0042712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Male behaviors associated with the care and rearing offspring.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parental behavior","termid":"GO:0060746"}],"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":"paternal behavior","synonyms":[{"name":"paternal behaviour","type":"exact"}],"termid":"GO:0042712"}


id: MONDO:0008219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pemphigus is a group of chronic autoimmune skin diseases characterized by blister formations on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterized, of which pemphigus vulgaris is the most frequent (75%).","definition_xrefs":["Orphanet:704"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pemphigus","termid":"MONDO:0006594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"pemphigus vulgaris","secondary_identifiers":["UMLS:C0030809","MEDGEN:10621","NANDO:1200229","ICD10CM:L10.0","GARD:7355","MESH:C536645","icd11.foundation:278358681","MedDRA:10052802","DOID:0060851","NCIT:C34910","SCTID:49420001","OMIM:169610","EFO:0004719"],"synonyms":[{"name":"familial pemphigus vulgaris","type":"exact"},{"name":"pemphigus vulgaris, familial","type":"related"}],"termid":"MONDO:0008219","xrefs":{"Monarch":{"xref_id":"0008219"}}}


id: PBO:0057670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1261","termid":"PBO:0057670"}


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: MONDO:0022559
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A central nervous system vasculitis that has a benign course, with acute onset of neurologic symptoms, usually in the form of severe headache and/or a focal neurologic event.","definition_xrefs":["PMID:17043471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system vasculitis","termid":"MONDO:0003346"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign angiitis of the central nervous system","secondary_identifiers":["GARD:8704"],"synonyms":[{"name":"BACNS","type":"related"}],"termid":"MONDO:0022559","xrefs":{"Monarch":{"xref_id":"0022559"}}}


id: PBO:0085775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein lysine methyltransferase; monomethylates Lys-46 of the ribosomal large subunit Rpl1a/Rpl1b; member of the seven beta-strand methyltransferase superfamily; orthologs only found among fungal species","termid":"PBO:0085775"}


id: GO:0070041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + rRNA = S-adenosyl-L-homocysteine + rRNA containing C5-methyluridine.","definition_xrefs":["GOC:mah","GOC:imk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-methyltransferase activity","termid":"GO:0008169"},{"relation_name":"is_a","term_name":"rRNA (uridine) methyltransferase activity","termid":"GO:0016436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016741","GO:0003824","GO:0003674","GO:0016740","GO:0140098"],"is_obsolete":false,"name":"rRNA (uridine-C5-)-methyltransferase activity","termid":"GO:0070041"}


id: SO:0000433
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A polymeric tract, such as poly(dA), within a non_LTR_retrotransposon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_region","termid":"SO:0000657"},{"relation_name":"is_a","term_name":"repeat_component","termid":"SO:0000840"},{"relation_name":"part_of","term_name":"non_LTR_retrotransposon","termid":"SO:0000189"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non_LTR_retrotransposon_polymeric_tract","synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:non_ltr_retrotransposon_polymeric_tract","type":"exact"},{"name":"non LTR retrotransposon polymeric tract","type":"exact"}],"termid":"SO:0000433"}


id: PR:P87231
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A crossover junction endonuclease MUS81 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04324","PANTHER:PTHR13451:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crossover junction endonuclease mus81 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4G3.05c","secondary_identifiers":["UniProtKB:P87231"],"synonyms":[{"name":"Spom972h-MUS81","type":"exact"}],"termid":"PR:P87231"}


id: PBO:0049283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase alpha 2","termid":"PBO:0049283"}


id: MOD:00988
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a hydrogen atom of an L-tyrosine residue with a bromine atom.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brominated residue","termid":"MOD:00754"},{"relation_name":"is_a","term_name":"halogenated tyrosine","termid":"MOD:00985"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brominated tyrosine","synonyms":[{"name":"BrTyr","type":"exact"}],"termid":"MOD:00988"}


id: PR:P87128
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A eukaryotic translation initiation factor 3 subunit J that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21681:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit J (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A12.13c","secondary_identifiers":["UniProtKB:P87128"],"synonyms":[{"name":"Spom972h-EIF3J","type":"exact"},{"name":"eIF-3 30 kDa (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF3j (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eukaryotic translation initiation factor 3 30 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87128"}


id: PBO:0058908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 12126","termid":"PBO:0058908"}


id: GO:0050869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of B cell activation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of B cell activation","termid":"GO:0050864"},{"relation_name":"is_a","term_name":"negative regulation of lymphocyte activation","termid":"GO:0051250"},{"relation_name":"negatively_regulates","term_name":"B cell activation","termid":"GO:0042113"}],"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 B cell activation","synonyms":[{"name":"down regulation of B cell activation","type":"exact"},{"name":"down-regulation of B cell activation","type":"exact"},{"name":"downregulation of B cell activation","type":"exact"},{"name":"inhibition of B cell activation","type":"narrow"},{"name":"negative regulation of B lymphocyte activation","type":"exact"},{"name":"negative regulation of B-cell activation","type":"exact"},{"name":"negative regulation of B-lymphocyte activation","type":"exact"}],"termid":"GO:0050869"}


id: GO:0008167
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete sigma virus replication (obsolete GO:0008167)","synonyms":[{"name":"sigma virus replication","type":"exact"}],"termid":"GO:0008167"}


id: MONDO:0000233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spotted fever that has material basis in Rickettsia japonica, which is transmitted by ticks (Dermacentor taiwanensis and Haemaphysalis flava). The infection has symptom fever, has symptom eschars, has symptom regional adenopathy, and has symptom rash on extremities.","definition_xrefs":["DOID:0050050"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spotted fever","termid":"MONDO:0001195"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Japanese spotted fever","secondary_identifiers":["UMLS:C2108396","MEDGEN:1371298"],"synonyms":[{"name":"Japanese spotted fever","type":"exact"},{"name":"Japanese spotted fevers","type":"related"},{"name":"Rickettsia japonica spotted fever","type":"exact"},{"name":"fever, Japanese spotted","type":"related"},{"name":"fevers, Japanese spotted","type":"related"},{"name":"oriental spotted fever","type":"related"},{"name":"spotted fever, Japanese","type":"related"}],"termid":"MONDO:0000233","xrefs":{"Monarch":{"xref_id":"0000233"}}}


id: MONDO:0008597
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A trichorhinophalangeal syndrome caused by mutations in TRPS1 characterized by the presence of severe brachydactyly, due to short metacarpals, and severe short stature.","definition_xrefs":["PMID:4025405"],"gene_count":0,"genotype_count":0,"name":"obsolete trichorhinophalangeal syndrome, type III (obsolete MONDO:0008597)","secondary_identifiers":["UMLS:C1860823","MEDGEN:349899","MESH:C566033","GARD:7802","DOID:0080376","NORD:1789","OMIM:190351"],"synonyms":[{"name":"Sugio-Kajii syndrome","type":"related"},{"name":"TRPS 3","type":"exact"},{"name":"TRPS3","type":"exact"},{"name":"Trichorhinophalangeal Syndrome Type III","type":"exact"},{"name":"trichorhinophalangeal syndrome type 3","type":"exact"},{"name":"trichorhinophalangeal syndrome, type 3","type":"exact"},{"name":"trichorhinophalangeal syndrome, type III","type":"exact"}],"termid":"MONDO:0008597","xrefs":{"Monarch":{"xref_id":"0008597"}}}


id: PBO:0056339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase 21","termid":"PBO:0056339"}


id: GO:1903843
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 an arsenite ion stimulus.","definition_xrefs":["GOC:mr","GO_REF:0000071","PMID:12106899","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to arsenic-containing substance","termid":"GO:0071243"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to arsenite ion","termid":"GO:1903842"}],"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 arsenite ion","termid":"GO:1903843"}


id: GO:0030235
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and modulates the activity of nitric oxide synthase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme regulator activity","termid":"GO:0030234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0030234","GO:0003674"],"is_obsolete":false,"name":"nitric-oxide synthase regulator activity","secondary_identifiers":["Reactome:R-HSA-202144","Reactome:R-HSA-202129"],"synonyms":[{"name":"nitric oxide synthase regulator activity","type":"exact"}],"termid":"GO:0030235"}


id: PBO:0043648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COP9 signalosome subunit 7B","termid":"PBO:0043648"}


id: GO:0160089
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A protein adaptor that recognizes and binds an RNA molecule modified by N(7)-methylguanine (m7G), a modification present at internal sites of mRNAs and some non-coding RNAs.","definition_xrefs":["PMID:37379838"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-RNA adaptor activity","termid":"GO:0140517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0030674"],"is_obsolete":false,"name":"internal N(7)-methylguanine-containing RNA reader activity","termid":"GO:0160089"}


id: PBO:0054910
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 2324","termid":"PBO:0054910"}


id: GO:0030600
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: feruloyl-polysaccharide + H2O = ferulate + polysaccharide.","definition_xrefs":["EC:3.1.1.73"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"feruloyl esterase activity","secondary_identifiers":["MetaCyc:3.1.1.73-RXN"],"synonyms":[{"name":"4-hydroxy-3-methoxycinnamoyl-sugar hydrolase activity","type":"related"},{"name":"FAE-I","type":"related"},{"name":"FAE-II","type":"related"},{"name":"FAE-III","type":"related"},{"name":"FAEA","type":"related"},{"name":"cinnAE","type":"related"},{"name":"cinnamoyl ester hydrolase activity","type":"exact"},{"name":"ferulic acid esterase activity","type":"related"},{"name":"hemicellulase accessory","type":"related"},{"name":"hydroxycinnamoyl esterase activity","type":"related"}],"termid":"GO:0030600"}


id: MONDO:1011965
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":"disproportionate short-limbed chondrodysplasia, non-human animal","secondary_identifiers":["OMIA:001886"],"termid":"MONDO:1011965","xrefs":{"Monarch":{"xref_id":"1011965"}}}


id: PR:Q9UUA5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC409.19c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUA5"],"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":"metaxin-like protein C409.19c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC409.19c","synonyms":[{"name":"Spom972h-SPBC409.19c","type":"exact"}],"termid":"PR:Q9UUA5"}


id: PBO:0051640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IMP U3 small nucleolar ribonucleoprotein 4","termid":"PBO:0051640"}


id: MONDO:0018251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A group of inborn errors of glycogen metabolism that is clinically and genetically heterogeneous. This group comprises GSD due to liver phosphorylase kinase (PhK) deficiency, GSD due to muscle PhK deficiency and GSD due to liver and muscle PhK deficiency.","definition_xrefs":["Orphanet:370"],"gene_count":0,"genotype_count":0,"name":"obsolete glycogen storage disease due to phosphorylase kinase deficiency (obsolete MONDO:0018251)","secondary_identifiers":["DOID:0050594","NANDO:1201020","NCIT:C122662","MESH:C580130","NANDO:2200544","SCTID:235908005"],"synonyms":[{"name":"GSD IX","type":"exact"},{"name":"GSD due to phosphorylase kinase deficiency","type":"exact"},{"name":"GSD type 9","type":"exact"},{"name":"GSD type IX","type":"exact"},{"name":"GSDIX","type":"exact"},{"name":"glycogen storage disease IX","type":"exact"},{"name":"glycogen storage disease due to PhK deficiency","type":"exact"},{"name":"glycogen storage disease type 9","type":"exact"},{"name":"glycogen storage disease type IX","type":"exact"},{"name":"glycogenosis due to phosphorylase kinase deficiency","type":"exact"},{"name":"glycogenosis type 9","type":"exact"},{"name":"glycogenosis type IX","type":"exact"},{"name":"gycogenosis due to PhK deficiency","type":"exact"},{"name":"phosphorylase kinase deficiency","type":"exact"}],"termid":"MONDO:0018251","xrefs":{"Monarch":{"xref_id":"0018251"}}}


id: GO:1900696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of N',N'',N'''-triacetylfusarinine C biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of secondary metabolite biosynthetic process","termid":"GO:1900377"},{"relation_name":"is_a","term_name":"regulation of N',N'',N'''-triacetylfusarinine C biosynthetic process","termid":"GO:1900695"},{"relation_name":"negatively_regulates","term_name":"N',N'',N'''-triacetylfusarinine C biosynthetic process","termid":"GO:1900551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"negative regulation of N',N'',N'''-triacetylfusarinine C biosynthetic process","synonyms":[{"name":"down regulation of N',N'',N'''-triacetylfusarinine C anabolism","type":"exact"},{"name":"down regulation of N',N'',N'''-triacetylfusarinine C biosynthesis","type":"exact"},{"name":"down regulation of N',N'',N'''-triacetylfusarinine C biosynthetic process","type":"exact"},{"name":"down regulation of N',N'',N'''-triacetylfusarinine C formation","type":"exact"},{"name":"down regulation of N',N'',N'''-triacetylfusarinine C synthesis","type":"exact"},{"name":"down-regulation of N',N'',N'''-triacetylfusarinine C anabolism","type":"exact"},{"name":"down-regulation of N',N'',N'''-triacetylfusarinine C biosynthesis","type":"exact"},{"name":"down-regulation of N',N'',N'''-triacetylfusarinine C biosynthetic process","type":"exact"},{"name":"down-regulation of N',N'',N'''-triacetylfusarinine C formation","type":"exact"},{"name":"down-regulation of N',N'',N'''-triacetylfusarinine C synthesis","type":"exact"},{"name":"downregulation of N',N'',N'''-triacetylfusarinine C anabolism","type":"exact"},{"name":"downregulation of N',N'',N'''-triacetylfusarinine C biosynthesis","type":"exact"},{"name":"downregulation of N',N'',N'''-triacetylfusarinine C biosynthetic process","type":"exact"},{"name":"downregulation of N',N'',N'''-triacetylfusarinine C formation","type":"exact"},{"name":"downregulation of N',N'',N'''-triacetylfusarinine C synthesis","type":"exact"},{"name":"inhibition of N',N'',N'''-triacetylfusarinine C anabolism","type":"exact"},{"name":"inhibition of N',N'',N'''-triacetylfusarinine C biosynthesis","type":"exact"},{"name":"inhibition of N',N'',N'''-triacetylfusarinine C biosynthetic process","type":"narrow"},{"name":"inhibition of N',N'',N'''-triacetylfusarinine C formation","type":"exact"},{"name":"inhibition of N',N'',N'''-triacetylfusarinine C synthesis","type":"exact"},{"name":"negative regulation of N',N'',N'''-triacetylfusarinine C anabolism","type":"exact"},{"name":"negative regulation of N',N'',N'''-triacetylfusarinine C biosynthesis","type":"exact"},{"name":"negative regulation of N',N'',N'''-triacetylfusarinine C formation","type":"exact"},{"name":"negative regulation of N',N'',N'''-triacetylfusarinine C synthesis","type":"exact"}],"termid":"GO:1900696"}


id: GO:1990012
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytoplasmic inclusion body found in some lateral geniculate neurons and composed of sheets of tubules (25 nm in diameter) separated by dense material (about 75 nm wide), which together with the tubules whorl give a structure resembling a fingerprint.","definition_xrefs":["NIF_Subcellular:nlx_151681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laminated body","termid":"GO:1990011"}],"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":"complex laminated body","synonyms":[{"name":"CLB","type":"related"}],"termid":"GO:1990012"}


id: PBO:0087156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA helicase in the DEAH-box family; functions in both RNA polymerase I and polymerase II transcript metabolism; catalyzes removal of U2, U5, and U6 snRNPs from the postsplicing lariat-intron ribonucleoprotein complex; required for efficient biogenesis of both small- and large-subunit rRNAs; acts with Sqs1p to promote 20S to 18S rRNA processing catalyzed by endonuclease Nob1p","termid":"PBO:0087156"}


id: PR:C6Y4C7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cox14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4C7"],"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 membrane protein C757.15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC757.15","synonyms":[{"name":"Spom972h-cox14","type":"exact"}],"termid":"PR:C6Y4C7"}


id: PBO:0000178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S3a","termid":"PBO:0000178"}


id: GO:0018943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving organotin, an organic compound containing a tin atom.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organometal metabolic process","termid":"GO:0018942"}],"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":"organotin metabolic process","synonyms":[{"name":"organotin metabolism","type":"exact"}],"termid":"GO:0018943"}


id: MONDO:0000104
data:
  {"annotated_genes":["SJAG_01007"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84320],"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:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"anemia, hypochromic microcytic with iron overload","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C567144","OMIMPS:206100","UMLS:C2673913","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:0034053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a symbiont modulates the frequency, rate or extent of defense-related programmed cell death in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiont-mediated perturbation of host defense-related programmed cell death (obsolete GO:0034053)","synonyms":[{"name":"modulation by symbiont of host HR","type":"narrow"},{"name":"modulation by symbiont of host defense-related PCD","type":"exact"},{"name":"modulation by symbiont of host defense-related programmed cell death","type":"exact"},{"name":"modulation by symbiont of host hypersensitive response","type":"narrow"},{"name":"modulation by symbiont of plant HR","type":"narrow"},{"name":"modulation by symbiont of plant hypersensitive response","type":"narrow"}],"termid":"GO:0034053"}


id: MONDO:0018342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Joubert syndrome with Jeune asphyxiating thoracic dystrophy (JATD) is an extremely rare genetic bone disorder characterized by the classic features of Joubert syndrome (i.e. malformation of the brainstem causing ataxia, hypotonia,cognitive impairment, and abnormal eyemovements), associated with the skeletal anomalies found in JATD including short-rib dysplasia and narrow thorax causing respiratory failure, short limbs, and metaphyseal changes.","definition_xrefs":["Orphanet:397715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome and related disorders","termid":"MONDO:0015369"},{"relation_name":"is_a","term_name":"short rib-polydactyly syndrome","termid":"MONDO:0015461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Joubert syndrome with Jeune asphyxiating thoracic dystrophy","secondary_identifiers":["SCTID:733418003","GARD:17637","UMLS:C4518774","MEDGEN:1371401"],"synonyms":[{"name":"JBTS with JATD","type":"exact"},{"name":"Joubert syndrome with JATD","type":"exact"}],"termid":"MONDO:0018342","xrefs":{"Monarch":{"xref_id":"0018342"}}}


id: PBO:0053996
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 1318","termid":"PBO:0053996"}


id: GO:1900001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of anthocyanin catabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of anthocyanin metabolic process","termid":"GO:0031538"},{"relation_name":"is_a","term_name":"regulation of anthocyanin catabolic process","termid":"GO:1900000"},{"relation_name":"negatively_regulates","term_name":"anthocyanin-containing compound catabolic process","termid":"GO:0046284"}],"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 anthocyanin catabolic process","synonyms":[{"name":"down regulation of anthocyanin breakdown","type":"exact"},{"name":"down regulation of anthocyanin catabolic process","type":"related"},{"name":"down regulation of anthocyanin catabolism","type":"exact"},{"name":"down regulation of anthocyanin degradation","type":"exact"},{"name":"negative regulation of anthocyanin breakdown","type":"exact"},{"name":"negative regulation of anthocyanin catabolism","type":"exact"},{"name":"negative regulation of anthocyanin degradation","type":"exact"}],"termid":"GO:1900001"}


id: MONDO:0004309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The occurrence of several sarcomas in different anatomic locations.","definition_xrefs":["NCIT:C4243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"}],"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":"sarcomatosis","secondary_identifiers":["DOID:7615","ICDO:8800/9","MEDGEN:83152","UMLS:C0334451"],"synonyms":[{"name":"sarcomatosis","type":"exact"},{"name":"sarcomatosis (morphologic abnormality)","type":"exact"},{"name":"sarcomatosis NOS (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004309","xrefs":{"Monarch":{"xref_id":"0004309"}}}


id: SO:0001221
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing an epigenetic process where a gene is inactivated by histone modification.","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"silenced","termid":"SO:0000893"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silenced_by_histone_modification","synonyms":[{"name":"silenced by histone modification","type":"exact"}],"termid":"SO:0001221"}


id: PR:Q10189
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo12 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10189"],"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":"mitosis-specific protein spo12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3F10.15c","synonyms":[{"name":"Spom972h-spo12","type":"exact"}],"termid":"PR:Q10189"}


id: GO:1905884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of triglyceride transport.","definition_xrefs":["GO_REF:0000058","PMID:25849533","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of acylglycerol transport","termid":"GO:1901507"},{"relation_name":"is_a","term_name":"regulation of triglyceride transport","termid":"GO:1905883"},{"relation_name":"negatively_regulates","term_name":"triglyceride transport","termid":"GO:0034197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of triglyceride transport","synonyms":[{"name":"down regulation of triacylglycerol transport","type":"exact"},{"name":"down regulation of triglyceride transport","type":"exact"},{"name":"down-regulation of triacylglycerol transport","type":"exact"},{"name":"down-regulation of triglyceride transport","type":"exact"},{"name":"downregulation of triacylglycerol transport","type":"exact"},{"name":"downregulation of triglyceride transport","type":"exact"},{"name":"inhibition of triacylglycerol transport","type":"narrow"},{"name":"inhibition of triglyceride transport","type":"narrow"},{"name":"negative regulation of triacylglycerol transport","type":"exact"}],"termid":"GO:1905884"}


id: GO:1901069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of guanosine-containing compounds (guanosines).","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleoside catabolic process","termid":"GO:0046130"},{"relation_name":"is_a","term_name":"guanosine-containing compound metabolic process","termid":"GO:1901068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"guanosine-containing compound catabolic process","synonyms":[{"name":"guanosine-containing compound breakdown","type":"exact"},{"name":"guanosine-containing compound catabolism","type":"exact"},{"name":"guanosine-containing compound degradation","type":"exact"},{"name":"guanosines breakdown","type":"exact"},{"name":"guanosines catabolic process","type":"exact"},{"name":"guanosines catabolism","type":"exact"},{"name":"guanosines degradation","type":"exact"}],"termid":"GO:1901069"}


id: PBO:0070967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18 pseudogene 5","termid":"PBO:0070967"}


id: PR:Q09840
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- aah2 gene.","definition_xrefs":["UniProtKB:Q09840","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":"alpha-amylase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23D3.14c","synonyms":[{"name":"1,4-alpha-D-glucan glucanohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-aah2","type":"exact"}],"termid":"PR:Q09840"}


id: PBO:0003582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein","termid":"PBO:0003582"}


id: PBO:0074319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD family member 9","termid":"PBO:0074319"}


id: MONDO:0011769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial aortic dissection (obsolete MONDO:0011769)","termid":"MONDO:0011769","xrefs":{"Monarch":{"xref_id":"0011769"}}}


id: PR:Q10191
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein LTV1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01197","PANTHER:PTHR21531:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein LTV1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3F10.17","secondary_identifiers":["UniProtKB:Q10191"],"synonyms":[{"name":"Spom972h-LTV1","type":"exact"}],"termid":"PR:Q10191"}


id: PBO:0043139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 7","termid":"PBO:0043139"}


id: GO:1990154
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of the pentameric maltose transporter complex bound to two enzyme IIA (EIIA) molecules. EIIA is a component of the glucose-specific phosphotransferase system that inhibits maltose transport from the periplasm to the cytoplasm. When EIIA-bound, the maltose transporter remains in the open, inward-facing conformation, which prevents binding of maltose-loaded maltose binding protein (MBP) to the transporter.","definition_xrefs":["GOC:bhm","GOC:bf","PMID:23770568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-binding cassette (ABC) transporter complex","termid":"GO:0043190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"enzyme IIA-maltose transporter complex","synonyms":[{"name":"EIIA(Glc)-MalFGK2 complex","type":"exact"},{"name":"EIIA(Glc)-maltose transporter complex","type":"exact"},{"name":"maltose transporter inhibitor complex","type":"related"}],"termid":"GO:1990154"}


id: MONDO:0006353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papilloma that arises from the ciliated respiratory mucosa that lines the paranasal sinuses. It is classified as inverted papilloma and oncocytic papilloma.","definition_xrefs":["NCIT:C6835"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system benign neoplasm","termid":"MONDO:0000382"},{"relation_name":"is_a","term_name":"bone benign neoplasm","termid":"MONDO:0000631"},{"relation_name":"is_a","term_name":"sensory organ benign neoplasm","termid":"MONDO:0000633"},{"relation_name":"is_a","term_name":"paranasal sinus neoplasm","termid":"MONDO:0005289"},{"relation_name":"is_a","term_name":"glandular papilloma","termid":"MONDO:0021078"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paranasal sinus Schneiderian papilloma","secondary_identifiers":["MEDGEN:235462","UMLS:C1335343"],"synonyms":[{"name":"Schneiderian papilloma of accessory sinus","type":"related"},{"name":"Schneiderian papilloma of paranasal sinus","type":"related"},{"name":"Schneiderian papilloma of the accessory sinus","type":"related"},{"name":"Schneiderian papilloma of the paranasal sinus","type":"related"},{"name":"accessory sinus Schneiderian papilloma","type":"related"},{"name":"paranasal sinus Schneiderian papilloma","type":"exact"}],"termid":"MONDO:0006353","xrefs":{"Monarch":{"xref_id":"0006353"}}}


id: PBO:0086664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; identified by expression profiling and mass spectrometry","termid":"PBO:0086664"}


id: GO:0047950
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 glutathione + O2 = glutathione disulfide + H2O2.","definition_xrefs":["EC:1.8.3.3","RHEA:24112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor","termid":"GO:0016670"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"glutathione oxidase activity","secondary_identifiers":["KEGG_REACTION:R00120","MetaCyc:GLUTATHIONE-OXIDASE-RXN"],"synonyms":[{"name":"glutathione:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0047950"}


id: PBO:0049518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.J histone","termid":"PBO:0049518"}


id: FYPO:0002410
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, cell shape is altered, and cell size remains normal, and in which vacuoles are more visible (usually by microscopy) than normal.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"has_part","term_name":"vacuolated","termid":"FYPO:0001581"},{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"inviable vegetative cell, abnormal cell shape, normal cell size","termid":"FYPO:0001511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0001985","FYPO:0000004","FYPO:0000257"],"is_obsolete":false,"name":"inviable vacuolated vegetative cell, abnormal cell shape, normal cell size","synonyms":[{"name":"inviable vacuolated vegetative cell with abnormal cell shape and normal cell size","type":"related"},{"name":"inviable vacuolated vegetative cell, abnormal cell shape, normal cell length","type":"narrow"},{"name":"inviable vacuolated vegetative cell, abnormal cell shape, normal cell size during mitotic cell cycle","type":"related"},{"name":"inviable vegetative misshapen vacuolated cell","type":"related"},{"name":"inviable, vacuolated, abnormal cell shape, normal cell size during vegetative growth","type":"exact"},{"name":"lethal; vacuolated vegetative cell, abnormal cell shape, normal cell size","type":"exact"}],"termid":"FYPO:0002410"}


id: PBO:0005533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cu metalloregulatory transcription factor Cuf2 (predicted)","termid":"PBO:0005533"}


id: GO:0000743
data:
  {"annotated_genes":["SJAG_01613","SJAG_02286","SJAG_02045","SJAG_00113","SJAG_00140"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[86973,90592,94403,96772,98429],"is_not":false,"summary":null,"term":"GO:0000743"}]},"cv_name":"biological_process","definition":"The microtubule-based movement of nuclei towards one another as a prelude to karyogamy in organisms undergoing conjugation with cellular fusion.","definition_xrefs":["GOC:clt","GOC:vw","PMID:16380440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear migration along microtubule","termid":"GO:0030473"},{"relation_name":"part_of","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00113":null,"SJAG_00140":null,"SJAG_01613":null,"SJAG_02045":null,"SJAG_02286":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000747","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"nuclear migration involved in conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0006946"],"synonyms":[{"name":"nuclear congression","type":"exact"},{"name":"nuclear migration during conjugation with cellular fusion","type":"related"}],"termid":"GO:0000743","terms_by_termid":{"GO:0000743":null}}


id: GO:0032999
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of an Fc-alpha R alpha chain and an Fc-epsilon RI gamma chain dimer with or without additional signaling components. The complex functions primarily as an activating receptor for IgA.","definition_xrefs":["GOC:add","PMID:12524384","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fc receptor complex","termid":"GO:0032997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"Fc-alpha receptor I complex","synonyms":[{"name":"FcaRI complex","type":"exact"},{"name":"IgA receptor complex","type":"broad"},{"name":"immunoglobulin A receptor complex","type":"broad"}],"termid":"GO:0032999"}


id: GO:0044126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont regulates the increase in its size or mass within the cells or tissues of the host organism. This may (but not necessarily) include a filamentous growth form, and also can include secretion of proteases and lipases to break down. The host is defined as the larger of the organisms involved in the symbiotic interaction.","definition_xrefs":["GOC:jl","GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of growth of symbiont in host (obsolete GO:0044126)","termid":"GO:0044126"}


id: PBO:0061660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 35","termid":"PBO:0061660"}


id: GO:0004174
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a ubiquinone + reduced [electron-transfer flavoprotein] = a ubiquinol + H+ + oxidized [electron-transfer flavoprotein].","definition_xrefs":["RHEA:24052"],"direct_ancestors":[{"relation_name":"is_a","term_name":"electron transfer activity","termid":"GO:0009055"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor","termid":"GO:0016649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"electron-transferring-flavoprotein dehydrogenase activity","secondary_identifiers":["Reactome:R-HSA-169270","MetaCyc:RXN66-550","EC:1.5.5.1"],"synonyms":[{"name":"ETF dehydrogenase activity","type":"related"},{"name":"ETF-QO activity","type":"related"},{"name":"ETF-ubiquinone oxidoreductase activity","type":"related"},{"name":"ETF:ubiquinone oxidoreductase activity","type":"related"},{"name":"electron transfer flavoprotein Q oxidoreductase activity","type":"related"},{"name":"electron transfer flavoprotein dehydrogenase activity","type":"related"},{"name":"electron transfer flavoprotein reductase activity","type":"related"},{"name":"electron transfer flavoprotein-ubiquinone oxidoreductase activity","type":"related"},{"name":"electron-transferring-flavoprotein:ubiquinone oxidoreductase activity","type":"related"}],"termid":"GO:0004174"}


id: PBO:0081374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 213","termid":"PBO:0081374"}


id: PBO:0079520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosinase like (pseudogene)","termid":"PBO:0079520"}


id: GO:0015768
data:
  {"annotated_genes":["SJAG_03960"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"}]},"cv_name":"biological_process","definition":"The directed movement of maltose into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Maltose is the disaccharide 4-O-alpha-D-glucopyranosyl-D-glucopyranose, an intermediate in the catabolism of glycogen and starch.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide transport","termid":"GO:0015766"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"maltose transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0015768","terms_by_termid":{"GO:0106081":null}}


id: GO:0030460
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:elh"],"gene_count":0,"genotype_count":0,"name":"obsolete nuclear translocation of MAPK (mating sensu Fungi) (obsolete GO:0030460)","synonyms":[{"name":"nuclear translocation of MAPK (mating sensu Fungi)","type":"exact"}],"termid":"GO:0030460"}


id: PBO:0085191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ORF with sequence and positional similarity to the MAL64 gene; the MAL64 gene is thought to be a nonfunctional copy of MAL63; encoded within the complex locus MAL3 in some strains of S. cerevisiae, but not in S288C","termid":"PBO:0085191"}


id: PBO:0027922
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_cell-cell_contact_point_during_conjugation","termid":"PBO:0027922"}


id: PBO:0048505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDF5 antisense RNA 1","termid":"PBO:0048505"}


id: PBO:0031095
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-formation_of_azygotic_ascus_upon_sporulation_(obsolete_FYPO:0000279)","termid":"PBO:0031095"}


id: MONDO:0019599
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Primary lipodystrophies represent a heterogeneous group of very rare diseases characterized by a generalized or localized loss of body fat (lipoatrophy).","definition_xrefs":["Orphanet:90970"],"gene_count":0,"genotype_count":0,"name":"obsolete primary lipodystrophy (obsolete MONDO:0019599)","termid":"MONDO:0019599","xrefs":{"Monarch":{"xref_id":"0019599"}}}


id: PBO:0081579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 506","termid":"PBO:0081579"}


id: MONDO:0022646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiofacial syndrome short limbs","termid":"MONDO:0022646","xrefs":{"Monarch":{"xref_id":"0022646"}}}


id: FYPO:0000343
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the concentration of hydrogen sulfide released into the growth medium by cells is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased concentration of substance in growth medium","termid":"FYPO:0000800"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001155"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001155"],"is_obsolete":false,"name":"increased concentration of hydrogen sulfide in growth medium","synonyms":[{"name":"increased concentration of H2S in growth medium","type":"exact"},{"name":"increased hydrogen sulfide biosynthesis","type":"related"}],"termid":"FYPO:0000343"}


id: MONDO:0007100
data:
  {"annotated_genes":["SJAG_04300"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86441],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971004"}]},"cv_name":"mondo","definition":"A rare genetic systemic disease characterized by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement.","definition_xrefs":["Orphanet:271861"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary amyloidosis","termid":"MONDO:0018634"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04300":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"familial amyloid neuropathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:277.39","OMIMPS:105210","GARD:21017","NCIT:C84554","DOID:0050761","ICD10EXP:G63.3*","DOID:0050638","EFO:0004129","MESH:C567782","NANDO:1200214","UMLS:C0206245","icd11.foundation:807065795","SCTID:42295001","MEDGEN:104815","NANDO:1201060","ICD10EXP:E85.1+"],"synonyms":[{"name":"ATTRv amyloidosis","type":"exact"},{"name":"Corino de Andrade's disease","type":"exact"},{"name":"TTR amyloidosis","type":"exact"},{"name":"amyloid neuropathies, familial","type":"exact"},{"name":"amyloidosis, hereditary, transthyretin-related","type":"exact"},{"name":"familial TTR-related amyloidosis","type":"exact"},{"name":"familial amyloid neuropathy","type":"exact"},{"name":"familial amyloid polyneuropathy","type":"exact"},{"name":"familial transthyretin amyloidosis","type":"exact"},{"name":"familial transthyretin-related amyloidosis","type":"exact"},{"name":"hATTR","type":"exact"},{"name":"hereditary TTR amyloid polyneuropathy","type":"exact"},{"name":"hereditary TTR amyloidosis","type":"exact"},{"name":"hereditary amyloidosis, transthyretin-related","type":"related"},{"name":"hereditary transthyretin amyloid polyneuropathy","type":"exact"},{"name":"paramyloidosis","type":"exact"},{"name":"transthyretin-related hereditary amyloidosis","type":"exact"}],"termid":"MONDO:0007100","terms_by_termid":{"MONDO:0971004":null},"xrefs":{"Monarch":{"xref_id":"0007100"}}}


id: MONDO:0012122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Moyamoya disease","termid":"MONDO:0016820"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"moyamoya disease 3","secondary_identifiers":["OMIM:608796","GARD:15442","MEDGEN:373326","MESH:C536993","UMLS:C1837418"],"synonyms":[{"name":"MYMY3","type":"exact"},{"name":"Moyamoya disease 3","type":"related"}],"termid":"MONDO:0012122","xrefs":{"Monarch":{"xref_id":"0012122"}}}


id: PBO:0090961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine-uridine preferring nucleoside hydrolase","termid":"PBO:0090961"}


id: GO:0006718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of juvenile hormones, the three sesquiterpenoid derivatives that function to maintain the larval state of insects at molting and that may be required for other processes, e.g. oogenesis.","definition_xrefs":["ISBN:0198547684","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile hormone metabolic process","termid":"GO:0006716"},{"relation_name":"is_a","term_name":"sesquiterpenoid biosynthetic process","termid":"GO:0016106"},{"relation_name":"is_a","term_name":"hormone biosynthetic process","termid":"GO:0042446"}],"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":"juvenile hormone biosynthetic process","synonyms":[{"name":"juvenile hormone anabolism","type":"exact"},{"name":"juvenile hormone biosynthesis","type":"exact"},{"name":"juvenile hormone formation","type":"exact"},{"name":"juvenile hormone synthesis","type":"exact"}],"termid":"GO:0006718"}


id: PBO:0052290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain containing 1","termid":"PBO:0052290"}


id: PBO:0044324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 4","termid":"PBO:0044324"}


id: PBO:0001246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protein Mdm31 (predicted)","termid":"PBO:0001246"}


id: PBO:0080450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VSIG10L antisense RNA 1","termid":"PBO:0080450"}


id: PBO:0081557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 479","termid":"PBO:0081557"}


id: PBO:0004707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin activating enzyme E1","termid":"PBO:0004707"}


id: MONDO:0015976
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hyper-IgM syndrome without susceptibility to opportunistic infections (obsolete MONDO:0015976)","secondary_identifiers":["Orphanet:183666"],"synonyms":[{"name":"HIGM without susceptibility to opportunistic infections","type":"exact"}],"termid":"MONDO:0015976","xrefs":{"Monarch":{"xref_id":"0015976"}}}


id: FYPO:0007859
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the nucleus divides into two or more fragments, each enclosed by nuclear envelope and containing a DNA mass, in a cell that does not form a mitotic spindle or undergo cytokinesis. In these cells, the nucleus does not elongate into a dumbbell shape, but instead the nuclear envelope takes on a ruffled aspect and then eventually pinches into two nuclear masses.","definition_xrefs":["PMID:20967237","PomBase:jh","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitosis","termid":"FYPO:0000337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000337","FYPO:0000631","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"nuclear division in absence of mitotic spindle","synonyms":[{"name":"nuclear division in absence of mitotic spindle during mitotic cell cycle","type":"related"},{"name":"nuclear division in absence of mitotic spindle during vegetative growth","type":"exact"},{"name":"nuclear fission","type":"exact"},{"name":"nuclear fission in absence of mitotic spindle","type":"exact"},{"name":"rel syn DNA segregation in absence of mitotic spindle","type":"related"}],"termid":"FYPO:0007859"}


id: GO:0102043
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: isopentenyl phosphate(2-) + ATP(4-) = isopentenyl diphosphate(3-) + ADP(3-).","definition_xrefs":["RHEA:33963","GOC:pz","PMID:19928876"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"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:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"isopentenyl phosphate kinase activity","secondary_identifiers":["MetaCyc:RXN-10068","EC:2.7.4.26"],"termid":"GO:0102043"}


id: GO:0018839
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-4-(2-(3-hydroxy)-thionaphthenyl)-2-oxo-3-butenoate = trans-4-(2-(3-hydroxy)-thionaphthenyl)-2-oxo-3-butenoate.","definition_xrefs":["UM-BBD_reactionID:r0163"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-4-[2-(3-hydroxy)-thionaphthenyl]-2-oxo-3-butenoate isomerase activity (obsolete GO:0018839)","termid":"GO:0018839"}


id: PBO:0041213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1D nuclear receptor corepressor pseudogene 1","termid":"PBO:0041213"}


id: PBO:0108894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 7","termid":"PBO:0108894"}


id: GO:0060379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a cardiac myoblast. A cardiac myoblast is a precursor cell that has been committed to a cardiac muscle cell fate but retains the ability to divide and proliferate throughout life.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardioblast differentiation","termid":"GO:0010002"},{"relation_name":"is_a","term_name":"myoblast differentiation","termid":"GO:0045445"}],"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":"cardiac muscle cell myoblast differentiation","synonyms":[{"name":"cardiac myoblast differentiation","type":"related"},{"name":"myocardial precursor cell differentiation","type":"exact"}],"termid":"GO:0060379"}


id: _global:capable_of_regulating
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"Holds between c and p if and only if c is capable of some activity a, and a regulates p.","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_agent_in_process","termid":"_global:causal_agent_in_process"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capable_of_regulating","secondary_identifiers":["RO:0002596"],"termid":"_global:capable_of_regulating"}


id: SO:0000063
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An interchromosomal transposition whereby a translocation in which one of the four broken ends loses a segment before re-joining.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interchromosomal_transposition","termid":"SO:1000155"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deficient_interchromosomal_transposition","synonyms":[{"name":"deficient interchromosomal transposition","type":"exact"}],"termid":"SO:0000063"}


id: PBO:0085691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in regulation of phospholipid metabolism; one of 6 proteins (Ist2p, Scs2p, Scs22p, Tcb1p, Tcb2p, Tcb3p) that connect the ER and plasma membrane (PM); regulates PM PI4P levels by controlling access of the Sac1p phosphatase to its substrate, PI4P; human VAP homolog; similar to D. melanogaster inturned protein; SWAT-GFP and mCherry fusion proteins localize to the cytosol; SCS22 has a paralog, SCS2, that arose from the whole genome duplication","termid":"PBO:0085691"}


id: MOD:00326
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to L-pyrrolysine (not known as a natural, post-translational modification process).","definition_xrefs":["PubMed:11435424","PubMed:12029131","PubMed:12029132","PubMed:15314242","PubMed:16096277","RESID:AA0321#LYS","Unimod:435#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"L-pyrrolysine residue","termid":"MOD:01187"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-pyrrolysine (Lys)","synonyms":[{"name":"(2S)-2-amino-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]aminohexanoic acid","type":"exact"},{"name":"2-azanyl-6-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-ylcarbonyl]azanylhexanoic acid","type":"exact"},{"name":"L-pyrrolysine","type":"exact"},{"name":"N6-(4-methyl-1,2-didehydropyrrolidine-5-carboxyl)-L-lysine","type":"exact"},{"name":"N6-(4-methyl-delta-1-pyrroline-5-carboxyl)-L-lysine","type":"exact"},{"name":"N6-([(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrol-2-yl]carbonyl)-L-lysine","type":"exact"},{"name":"NON_STD Pyrrolysine","type":"exact"},{"name":"Pyl(Lys)","type":"exact"},{"name":"monomethylamine methyltransferase cofactor lysine adduct","type":"exact"}],"termid":"MOD:00326"}


id: MONDO:0100080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cardioectodermal syndromes are those in which phenotypic manifestations occur in the heart, skin, and/or hair. Variation in the genes of interest may occur in both an autosomal dominant inheritance pattern, or in an autosomal recessive inheritance pattern which may result in an earlier and/or more severe phenotypic presentation.","definition_xrefs":["PMID:27933191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardioectodermal syndrome","synonyms":[{"name":"cardio-ectodermal syndrome","type":"exact"}],"termid":"MONDO:0100080","xrefs":{"Monarch":{"xref_id":"0100080"}}}


id: GO:0005508
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 copper/cadmium binding (obsolete GO:0005508)","synonyms":[{"name":"copper/cadmium binding","type":"exact"}],"termid":"GO:0005508"}


id: PBO:0031146
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_polysaccharide_level","termid":"PBO:0031146"}


id: PBO:0071496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34","termid":"PBO:0071496"}


id: PBO:0018133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase, translational elongation factor eEF1 (predicted)","termid":"PBO:0018133"}


id: PBO:0091697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane spermidine transmembrane transporter Mfs3","termid":"PBO:0091697"}


id: PBO:0070540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 6","termid":"PBO:0070540"}


id: GO:0039589
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the activity of the host TAP complex, a heterodimer composed of the subunits TAP1 and TAP2 (transporter associated with antigen presentation). The TAP complex functions in the transport of antigenic peptides from the cytosol to the lumen of the endoplasmic reticulum, where they are loaded onto the MHC class I. By inhibiting the TAP complex, the virus prevents viral particles being presented at the cell surface, and thus evades the host immune response.","definition_xrefs":["PMID:16691491","UniProtKB-KW:KW-1107","VZ:817"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host TAP complex (obsolete GO:0039589)","synonyms":[{"name":"inhibition of host TAP by virus","type":"exact"}],"termid":"GO:0039589"}


id: FYPO:0001449
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 trehalose measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal cellular trehalose level","synonyms":[{"name":"normal cellular trehalose accumulation","type":"related"},{"name":"normal cellular trehalose level during mitotic cell cycle","type":"related"},{"name":"normal cellular trehalose level during vegetative growth","type":"exact"}],"termid":"FYPO:0001449"}


id: GO:0048290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The switching of activated B cells from IgM biosynthesis to biosynthesis of an IgA isotype, accomplished through a recombination process involving an intrachromosomal deletion between switch regions that reside 5' of the IgM and one of the IgA constant region gene segments in the immunoglobulin heavy chain locus.","definition_xrefs":["ISBN:0781735149","PMID:2113175","PMID:12370374","PMID:9186655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotype switching","termid":"GO:0045190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006259","GO:0006310"],"is_obsolete":false,"name":"isotype switching to IgA isotypes","synonyms":[{"name":"class switching to IgA isotypes","type":"exact"},{"name":"isotype switch recombination to IgA isotypes","type":"exact"}],"termid":"GO:0048290"}


id: MOD:01235
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label - alkaline phosphatase to dephosphorylate","definition_xrefs":["PubMed:11467524","PubMed:15549660","Unimod:258#T"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(18)O monosubstituted residue","termid":"MOD:00581"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(18)O monosubstituted L-threonine","synonyms":[{"name":"Label:18O(1)","type":"related"},{"name":"O18 Labeling","type":"related"}],"termid":"MOD:01235"}


id: GO:0016679
data:
  {"annotated_genes":["SJAG_01490","SJAG_02646","SJAG_MIT03","SJAG_07006","SJAG_00601","SJAG_00755","SJAG_03490"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[116816,107120,103667,118179,112534,117289,103254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008121"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a diphenol or related substance acts as a hydrogen or electron donor and reduces a hydrogen or electron acceptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00601":null,"SJAG_00755":null,"SJAG_01490":null,"SJAG_02646":null,"SJAG_03490":null,"SJAG_07006":null,"SJAG_MIT03":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on diphenols and related substances as donors","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:1.10.-.-"],"synonyms":[{"name":"oxidoreductase activity, acting on diphenols and related substances as donors, other acceptors","type":"narrow"}],"termid":"GO:0016679","terms_by_termid":{"GO:0008121":null}}


id: PBO:0064172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group VI","termid":"PBO:0064172"}


id: GO:0006535
data:
  {"annotated_genes":["SJAG_00582","SJAG_00283","SJAG_04305","SJAG_01880"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94689,96084,101075,108608],"is_not":false,"summary":null,"term":"GO:0006535"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cysteine from other compounds, including serine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-serine metabolic process","termid":"GO:0006563"},{"relation_name":"is_a","term_name":"cysteine biosynthetic process","termid":"GO:0019344"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00283":null,"SJAG_00582":null,"SJAG_01880":null,"SJAG_04305":null},"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:0006790"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"cysteine biosynthetic process from serine","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:CYSTSYN-PWY"],"synonyms":[{"name":"cysteine anabolism from serine","type":"exact"},{"name":"cysteine formation from serine","type":"exact"},{"name":"cysteine synthesis from serine","type":"exact"}],"termid":"GO:0006535","terms_by_termid":{"GO:0006535":null}}


id: PBO:0004298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FANCM-MHF complex subunit Mhf1","termid":"PBO:0004298"}


id: PBO:0085872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; HVG1 has a paralog, VRG4, that arose from the whole genome duplication","termid":"PBO:0085872"}


id: PBO:0063213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCCA antisense RNA 1","termid":"PBO:0063213"}


id: MOD:00950
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decomposed carboxymethylated methionine","termid":"MOD:00950"}


id: GO:1904787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of asymmetric protein localization involved in cell fate determination.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:17476329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein localization","termid":"GO:1903829"},{"relation_name":"is_a","term_name":"regulation of asymmetric protein localization involved in cell fate determination","termid":"GO:1904785"},{"relation_name":"positively_regulates","term_name":"asymmetric protein localization involved in cell fate determination","termid":"GO:0045167"}],"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 asymmetric protein localization involved in cell fate determination","synonyms":[{"name":"activation of asymmetric protein localisation involved in cell fate determination","type":"narrow"},{"name":"activation of asymmetric protein localization involved in cell fate commitment","type":"narrow"},{"name":"activation of asymmetric protein localization involved in cell fate determination","type":"narrow"},{"name":"activation of asymmetric protein localization resulting in cell fate commitment","type":"narrow"},{"name":"activation of cell fate commitment, asymmetric protein localization","type":"narrow"},{"name":"positive regulation of asymmetric protein localisation involved in cell fate determination","type":"exact"},{"name":"positive regulation of asymmetric protein localization involved in cell fate commitment","type":"exact"},{"name":"positive regulation of asymmetric protein localization resulting in cell fate commitment","type":"exact"},{"name":"positive regulation of cell fate commitment, asymmetric protein localization","type":"exact"},{"name":"up regulation of asymmetric protein localisation involved in cell fate determination","type":"exact"},{"name":"up regulation of asymmetric protein localization involved in cell fate commitment","type":"exact"},{"name":"up regulation of asymmetric protein localization involved in cell fate determination","type":"exact"},{"name":"up regulation of asymmetric protein localization resulting in cell fate commitment","type":"exact"},{"name":"up regulation of cell fate commitment, asymmetric protein localization","type":"exact"},{"name":"up-regulation of asymmetric protein localisation involved in cell fate determination","type":"exact"},{"name":"up-regulation of asymmetric protein localization involved in cell fate commitment","type":"exact"},{"name":"up-regulation of asymmetric protein localization involved in cell fate determination","type":"exact"},{"name":"up-regulation of asymmetric protein localization resulting in cell fate commitment","type":"exact"},{"name":"up-regulation of cell fate commitment, asymmetric protein localization","type":"exact"},{"name":"upregulation of asymmetric protein localisation involved in cell fate determination","type":"exact"},{"name":"upregulation of asymmetric protein localization involved in cell fate commitment","type":"exact"},{"name":"upregulation of asymmetric protein localization involved in cell fate determination","type":"exact"},{"name":"upregulation of asymmetric protein localization resulting in cell fate commitment","type":"exact"},{"name":"upregulation of cell fate commitment, asymmetric protein localization","type":"exact"}],"termid":"GO:1904787"}


id: MONDO:1010445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dilated cardiomyopathy that occurs in golden hamster.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dilated cardiomyopathy, non-human animal","termid":"MONDO:1010011"},{"relation_name":"is_a","term_name":"cardiomyopathy, golden hamster","termid":"MONDO:1010437"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilated cardiomyopathy, golden hamster","secondary_identifiers":["OMIA:000162-10036"],"termid":"MONDO:1010445","xrefs":{"Monarch":{"xref_id":"1010445"}}}


id: PBO:0042784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 128","termid":"PBO:0042784"}


id: GO:0047574
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-acetamidobutanoyl-CoA + H2O = 4-aminobutanoyl-CoA + acetate.","definition_xrefs":["EC:3.5.1.51","RHEA:22928"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0019213","GO:0016810","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"4-acetamidobutyryl-CoA deacetylase activity","secondary_identifiers":["MetaCyc:4-ACETAMIDOBUTYRYL-COA-DEACETYLASE-RXN","KEGG_REACTION:R04056"],"synonyms":[{"name":"4-acetamidobutanoyl-CoA amidohydrolase activity","type":"related"},{"name":"aminobutyryl-CoA thiolesterase activity","type":"related"},{"name":"deacetylase-thiolesterase activity","type":"related"}],"termid":"GO:0047574"}


id: GO:0006564
data:
  {"annotated_genes":["SJAG_02313","SJAG_04449","SJAG_02791","SJAG_04964"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91418,99450,109289,116043],"is_not":false,"summary":null,"term":"GO:0006564"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-serine, the L-enantiomer of serine, i.e. (2S)-2-amino-3-hydroxypropanoic acid.","definition_xrefs":["GOC:ai","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-serine metabolic process","termid":"GO:0006563"},{"relation_name":"is_a","term_name":"serine family amino acid biosynthetic process","termid":"GO:0009070"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02313":null,"SJAG_02791":null,"SJAG_04449":null,"SJAG_04964":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"L-serine biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:SERSYN-PWY"],"synonyms":[{"name":"L-serine anabolism","type":"exact"},{"name":"L-serine biosynthesis","type":"exact"},{"name":"L-serine formation","type":"exact"},{"name":"L-serine synthesis","type":"exact"}],"termid":"GO:0006564","terms_by_termid":{"GO:0006564":null}}


id: PBO:0040153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASH2L pseudogene 2","termid":"PBO:0040153"}


id: PBO:0002936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cis-prenyltransferase (predicted)","termid":"PBO:0002936"}


id: GO:0033769
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: 2-dimethylallyl-(6aS,11aS)-3,6a,9-trihydroxypterocarpan + NADPH + H+ + O2 = glyceollin II or glyceollin III + NADP+ + 2 H2O, and 4-dimethylallyl-(6aS,11aS)-3,6a,9-trihydroxypterocarpan + NADPH + H+ + O2 = glyceollin I + NADP+ + 2 H2O.","definition_xrefs":["EC:1.14.14.135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"glyceollin synthase activity","synonyms":[{"name":"dimethylallyl-3,6a,9-trihydroxypterocarpan cyclase activity","type":"exact"}],"termid":"GO:0033769"}


id: MONDO:0016009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fetal trimethadione syndrome is a drug-related embryofetopathy that can occur when an embryo/fetus is exposed to trimethadione and that is characterized by pre- and post-natal growth retardation, intellectual deficit, developmental and speech delay, craniofacial anomalies (with some similarities to those seen in fetal valproate syndrome), and less commonly, cleft palate, malformations of the heart, urogenital system and limbs. Trimethadione is an antiepileptic drug that has been removed from the market in Europe and is no longer used much in other countries due to teratogenicity and potential side effects.","definition_xrefs":["Orphanet:1913"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxic or drug-related embryofetopathy","termid":"MONDO:0016677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fetal trimethadione syndrome","secondary_identifiers":["ICD9:759.89","GARD:18750","MEDGEN:120538","icd11.foundation:1743242235","MESH:C537798","SCTID:66351003","UMLS:C0265373"],"termid":"MONDO:0016009","xrefs":{"Monarch":{"xref_id":"0016009"}}}


id: MONDO:0010292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"FHL1-related myopathy","termid":"MONDO:0800462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"Uruguay Faciocardiomusculoskeletal syndrome","secondary_identifiers":["DOID:0112148","UMLS:C1846010","OMIM:300280","MEDGEN:335320","MESH:C564544"],"synonyms":[{"name":"FCMSU","type":"related"},{"name":"Fcms","type":"related"},{"name":"URUGUAY FACIOCARDIOMUSCULOSKELETAL syndrome","type":"related"},{"name":"Uruguay Faciocardiomusculoskeletal syndrome","type":"exact"},{"name":"faciocardiomusculoskeletal syndrome, Uruguay type","type":"related"},{"name":"uruguay faciocardiomusculoskeletal syndrome, X-linked recessive","type":"exact"}],"termid":"MONDO:0010292","xrefs":{"Monarch":{"xref_id":"0010292"}}}


id: GO:0055007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cardiac muscle precursor cell acquires specialized features of a cardiac muscle cell. Cardiac muscle cells are striated muscle cells that are responsible for heart contraction.","definition_xrefs":["GOC:mtg_heart","GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiocyte differentiation","termid":"GO:0035051"},{"relation_name":"is_a","term_name":"striated muscle cell differentiation","termid":"GO:0051146"},{"relation_name":"part_of","term_name":"cardiac muscle tissue development","termid":"GO:0048738"}],"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":"cardiac muscle cell differentiation","synonyms":[{"name":"cardiomyocyte differentiation","type":"exact"},{"name":"heart muscle cell differentiation","type":"related"}],"termid":"GO:0055007"}


id: MONDO:0002175
data:
  {"annotated_genes":["SJAG_00737","SJAG_01356","SJAG_02885","SJAG_03258"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86512,86511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012419"},{"annotations":[85327,85328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010819"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"macular degeneration","termid":"MONDO:0003004"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00737":null,"SJAG_01356":null,"SJAG_02885":null,"SJAG_03258":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"degeneration of macula and posterior pole","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:2007","MEDGEN:573150","SCTID:267611002","ICD10CM:H35.3","ICD9:362.5","UMLS:C0339436"],"synonyms":[{"name":"degeneration of macula and posterior pole of retina","type":"exact"},{"name":"degeneration of macula or posterior pole","type":"exact"}],"termid":"MONDO:0002175","terms_by_termid":{"MONDO:0010819":null,"MONDO:0012419":null},"xrefs":{"Monarch":{"xref_id":"0002175"}}}


id: GO:0052208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the structure or function of a second organism, mediated by a substance secreted by a type IV secretion system in the first organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete modification of morphology or physiology of other organism via substance secreted by type IV secretion system involved in symbiotic interaction (obsolete GO:0052208)","synonyms":[{"name":"modification of morphology or physiology of other organism via substance secreted by type IV secretion system during symbiotic interaction","type":"related"}],"termid":"GO:0052208"}


id: PBO:0034318
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-receives_input_from","termid":"PBO:0034318"}


id: PR:Q9P6K5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dml1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6K5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein dml1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC30C2.06c","synonyms":[{"name":"Spom972h-dml1","type":"exact"}],"termid":"PR:Q9P6K5"}


id: MONDO:1012342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"renal cysts, non-human animal","termid":"MONDO:1011913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal cysts, pig","secondary_identifiers":["OMIA:001257-9823"],"termid":"MONDO:1012342","xrefs":{"Monarch":{"xref_id":"1012342"}}}


id: GO:0006567
data:
  {"annotated_genes":["SJAG_02450","SJAG_00830"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76762,93404],"is_not":false,"summary":null,"term":"GO:0006567"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of threonine (2-amino-3-hydroxybutyric acid), a polar, uncharged, essential amino acid found in peptide linkage in proteins.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"threonine metabolic process","termid":"GO:0006566"},{"relation_name":"is_a","term_name":"aspartate family amino acid catabolic process","termid":"GO:0009068"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00830":null,"SJAG_02450":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0044248","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"threonine catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["UM-BBD_pathwayID:met","MetaCyc:THREOCAT-PWY"],"synonyms":[{"name":"threonine breakdown","type":"exact"},{"name":"threonine catabolism","type":"exact"},{"name":"threonine degradation","type":"exact"}],"termid":"GO:0006567","terms_by_termid":{"GO:0006567":null}}


id: PBO:0031194
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_camptothecin","termid":"PBO:0031194"}


id: PBO:0057076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 155","termid":"PBO:0057076"}


id: PBO:0059327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S2","termid":"PBO:0059327"}


id: FYPO:0007800
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the endoplasmic reticulum is abolished, and some of the protein is present at the cell surface instead.","definition_xrefs":["PMID:33536395","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0003777"},{"relation_name":"is_a","term_name":"protein mislocalized to cell surface during vegetative growth","termid":"FYPO:0007799"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to endoplasmic reticulum, with protein mislocalized to cell surface","synonyms":[{"name":"abolished luminal ER protein retention","type":"exact"},{"name":"abolished protein localization to ER, with protein mislocalized to cell surface","type":"exact"},{"name":"abolished protein localization to endoplasmic reticulum, with protein mislocalized to cell surface during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to endoplasmic reticulum, with protein mislocalized to cell surface during vegetative growth","type":"exact"}],"termid":"FYPO:0007800"}


id: GO:0052752
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: reduced coenzyme F420 + CoB-S-S-CoM = coenzyme F420 + CoM-SH + CoB-SH.","definition_xrefs":["GOC:mengo_curators","PMID:9914308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors","termid":"GO:0016667"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"reduced coenzyme F420:heterodisulfide oxidoreductase activity","synonyms":[{"name":"F420-dependent heterodisulfide oxidoreductase activity","type":"exact"},{"name":"F420H2:heterodisulfide oxidoreductase activity","type":"exact"},{"name":"coenzyme F420-dependent heterodisulfide oxidoreductase activity","type":"exact"}],"termid":"GO:0052752"}


id: GO:0071402
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 lipoprotein particle stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stimulus","termid":"GO:0051716"}],"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 lipoprotein particle stimulus","termid":"GO:0071402"}


id: PBO:0001831
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternative transcripts, alternative polyadenylation","termid":"PBO:0001831"}


id: PBO:0057410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548l","termid":"PBO:0057410"}


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: FYPO:0001226
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 a cell is inviable, and contains a single nucleus and an asymmetrically located septum. The septum divides the cell into two compartments, one of which contains the nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"mislocalized septum during vegetative growth","termid":"FYPO:0000339"},{"relation_name":"is_a","term_name":"inviable mononucleate monoseptate vegetative cell with anucleate compartment","termid":"FYPO:0002303"},{"relation_name":"is_a","term_name":"mononucleate vegetative cell with mislocalized septum and anucleate compartment","termid":"FYPO:0007652"}],"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:0000631"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000337","FYPO:0000032","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000004","FYPO:0000002","FYPO:0000631","FYPO:0000641"],"is_obsolete":false,"name":"inviable mononucleate vegetative cell with mislocalized septum and anucleate compartment","synonyms":[{"name":"inviable mononucleate cell with mislocalized septum during vegetative growth","type":"exact"},{"name":"inviable mononucleate monoseptate vegetative cell with mislocalized septum","type":"exact"},{"name":"inviable mononucleate vegetative cell with abnormal septum location","type":"exact"},{"name":"inviable mononucleate vegetative cell with abnormal septum position","type":"exact"},{"name":"inviable mononucleate vegetative cell with asymmetric septum","type":"exact"},{"name":"inviable mononucleate vegetative cell with asymmetrically located septum","type":"exact"},{"name":"inviable mononucleate vegetative cell with mislocalised septum","type":"exact"},{"name":"inviable mononucleate vegetative cell with mislocalized septum","type":"exact"},{"name":"inviable mononucleate vegetative cell with mislocalized septum during mitotic cell cycle","type":"related"},{"name":"inviable mononucleate vegetative cell with misplaced septum","type":"exact"},{"name":"inviable mononucleate vegetative cell with single mislocalized septum","type":"exact"},{"name":"lethal; mononucleate vegetative cell with mislocalized septum","type":"exact"}],"termid":"FYPO:0001226"}


id: MONDO:0700083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which (part or full) chromosome 21 has been exchange with another chromosome, resulting in the presence of a third copy of (part or full) chromosome 21 genetic material. A reciprocal translocation is a chromosome abnormality caused by exchange of parts between non-homologous chromosomes.","definition_xrefs":["PMID:134161","PMID:29956287"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translocation Down syndrome","termid":"MONDO:0700128"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reciprocal translocation down syndrome","termid":"MONDO:0700083","xrefs":{"Monarch":{"xref_id":"0700083"}}}


id: GO:0062129
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any constituent part of a chitin-based noncellular, hardened, or membranous extracellular matrix secreted from the apical surface of an epithelial sheet.","definition_xrefs":["PMID:23955854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix","termid":"GO:0031012"}],"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":"chitin-based extracellular matrix","synonyms":[{"name":"chitin-based ECM","type":"exact"}],"termid":"GO:0062129"}


id: PR:Q9UT94
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A HemK methyltransferase family member 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR18895:SF8","PRO:DNx","OMA:SCHPO01624"],"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":"eRF1 methyltransferase catalytic subunit mtq2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC323.05c","secondary_identifiers":["UniProtKB:Q9UT94"],"synonyms":[{"name":"N(5)-glutamine methyltransferase catalytic subunit mtq2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-N6AMT1","type":"exact"},{"name":"eRF1 MTase catalytic subunit mtq2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT94"}


id: RO:0002589
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"p results in catabolism of c if and only if p is a catabolic process, and the execution of p results in c being broken into smaller parts with energy being released.","direct_ancestors":[{"relation_name":"is_a","term_name":"results_in_breakdown_of","termid":"RO:0002586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_catabolism_of","termid":"RO:0002589"}


id: PBO:0064903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP3CB antisense RNA 1 (head to head)","termid":"PBO:0064903"}


id: FYPO:0005708
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the interphase microtubule organizing center (iMTOC) is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cytoskeleton during vegetative growth","termid":"FYPO:0003184"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000138","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to iMTOC","synonyms":[{"name":"normal protein localisation to iMTOC","type":"exact"},{"name":"normal protein localization to iMTOC during mitotic cell cycle","type":"related"},{"name":"normal protein localization to iMTOC during vegetative growth","type":"exact"},{"name":"normal protein localization to interphase microtubule organizing center","type":"exact"}],"termid":"FYPO:0005708"}


id: PBO:0074037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 22","termid":"PBO:0074037"}


id: GO:0070429
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of the nucleotide-binding oligomerization domain containing 1 (NOD1) pathway.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","termid":"GO:0070425"},{"relation_name":"is_a","term_name":"regulation of nucleotide-binding oligomerization domain containing 1 signaling pathway","termid":"GO:0070428"},{"relation_name":"negatively_regulates","term_name":"nucleotide-binding oligomerization domain containing 1 signaling pathway","termid":"GO:0070427"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of nucleotide-binding oligomerization domain containing 1 signaling pathway","synonyms":[{"name":"negative regulation of NOD1 signaling pathway","type":"exact"},{"name":"negative regulation of nucleotide-binding oligomerization domain containing 1 signalling pathway","type":"exact"}],"termid":"GO:0070429"}


id: GO:0042248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The maintenance of an established polarized follicular epithelial sheet.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment or maintenance of polarity of follicular epithelium","termid":"GO:0016334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"maintenance of polarity of follicular epithelium","termid":"GO:0042248"}


id: MONDO:0017481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"amelia of lower limb","termid":"MONDO:0017438"}],"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":"amelia of lower limb, bilateral","secondary_identifiers":["MEDGEN:1775586","Orphanet:295059","UMLS:C2910294","icd11.foundation:1627185647"],"termid":"MONDO:0017481","xrefs":{"Monarch":{"xref_id":"0017481"}}}


id: GO:0061233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesonephric glomerular basement membrane over time, from its formation to the mature structure. The mesonephric glomerular basement membrane is the basal laminal portion of the mesonephric glomerulus which performs the actual filtration.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular basement membrane development","termid":"GO:0032836"},{"relation_name":"part_of","term_name":"mesonephric glomerulus development","termid":"GO:0061224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric glomerular basement membrane development","termid":"GO:0061233"}


id: GO:0047412
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N-(long-chain-acyl)ethanolamine = ethanolamine + a fatty acid.","definition_xrefs":["MetaCyc:3.5.1.60-RXN","EC:3.5.1.60"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016810"],"is_obsolete":false,"name":"N-(long-chain-acyl)ethanolamine deacylase activity","secondary_identifiers":["RHEA:17505"],"synonyms":[{"name":"N-(long-chain-acyl)ethanolamine amidohydrolase activity","type":"exact"},{"name":"N-acylethanolamine amidohydrolase activity","type":"exact"},{"name":"acylethanolamine amidase activity","type":"exact"}],"termid":"GO:0047412"}


id: FYPO:0000880
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the trimethylation of lysine at position 9 of histone H3 in centromeric regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 trimethylation at centromere during vegetative growth","termid":"FYPO:0000864"},{"relation_name":"is_a","term_name":"increased histone H3-K9 trimethylation during vegetative growth","termid":"FYPO:0000879"},{"relation_name":"is_a","term_name":"increased histone H3-K9 methylation at centromere during vegetative growth","termid":"FYPO:0005066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0002494","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H3-K9 trimethylation at centromere during vegetative growth","synonyms":[{"name":"increased centromeric histone H3-K9 trimethylation during vegetative growth","type":"exact"},{"name":"increased histone H3 K9 trimethylation at centromere during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 trimethylation at centromere during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 trimethylation at centromere during vegetative growth","type":"exact"},{"name":"increased histone H3K9me3 at centromere during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 trimethylation at centromere during vegetative growth","type":"exact"}],"termid":"FYPO:0000880"}


id: PBO:0085390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane low glucose sensor, regulates glucose transport; high affinity sensor that contains 12 predicted transmembrane segments and a long C-terminal tail required for induction of hexose transporters; also senses fructose and mannose; SNF3 has a paralog, RGT2, that arose from the whole genome duplication","termid":"PBO:0085390"}


id: PBO:0030208
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_elongated_vegetative_cell","termid":"PBO:0030208"}


id: PATO:0001224
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001224 real number (obsolete PATO:0001224)","termid":"PATO:0001224"}


id: PBO:0085367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphorylated protein of the mitochondrial outer membrane; localizes only to mitochondria of the bud; interacts with Myo2p to mediate mitochondrial distribution to buds; mRNA is targeted to the bud via the transport system involving She2p","termid":"PBO:0085367"}


id: GO:0043323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of natural killer cell degranulation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte degranulation","termid":"GO:0043302"},{"relation_name":"is_a","term_name":"regulation of natural killer cell degranulation","termid":"GO:0043321"},{"relation_name":"is_a","term_name":"positive regulation of natural killer cell mediated cytotoxicity","termid":"GO:0045954"},{"relation_name":"positively_regulates","term_name":"natural killer cell degranulation","termid":"GO:0043320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"positive regulation of natural killer cell degranulation","synonyms":[{"name":"activation of natural killer cell degranulation","type":"narrow"},{"name":"positive regulation of NK cell degranulation","type":"exact"},{"name":"positive regulation of NK cell granule exocytosis","type":"exact"},{"name":"positive regulation of natural killer cell granule exocytosis","type":"exact"},{"name":"stimulation of natural killer cell degranulation","type":"narrow"},{"name":"up regulation of natural killer cell degranulation","type":"exact"},{"name":"up-regulation of natural killer cell degranulation","type":"exact"},{"name":"upregulation of natural killer cell degranulation","type":"exact"}],"termid":"GO:0043323"}


id: GO:0071207
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a conserved stem-loop structure found in histone pre-mRNAs.","definition_xrefs":["PMID:19470752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pre-mRNA binding","termid":"GO:0036002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0003723"],"is_obsolete":false,"name":"histone pre-mRNA stem-loop binding","termid":"GO:0071207"}


id: PBO:0050455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOMER2 pseudogene 1","termid":"PBO:0050455"}


id: PBO:0047867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(2)(q31)","termid":"PBO:0047867"}


id: MONDO:0030423
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type 2v","secondary_identifiers":["OMIM:619493","MEDGEN:1794181","UMLS:C5561971"],"synonyms":[{"name":"CDG2V","type":"exact"}],"termid":"MONDO:0030423","xrefs":{"Monarch":{"xref_id":"0030423"}}}


id: MONDO:0016811
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal tubulopathy - encephalopathy - liver failure describes a spectrum of phenotypes with manifestations similar but milder than those seen in Gracile syndrome and that can be associated with encephalopathy and psychiatric disorders.","definition_xrefs":["Orphanet:254902"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex III deficiency nuclear type 1","termid":"MONDO:0007415"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"renal tubulopathy-encephalopathy-liver failure syndrome","secondary_identifiers":["MEDGEN:900319","UMLS:C4274075","GARD:17231"],"termid":"MONDO:0016811","xrefs":{"Monarch":{"xref_id":"0016811"}}}


id: PBO:0064979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 35, pseudogene","termid":"PBO:0064979"}


id: PBO:0062036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily T member 5","termid":"PBO:0062036"}


id: PBO:0028949
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_cell_tip","termid":"PBO:0028949"}


id: PATO:0000466
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000466 none (obsolete PATO:0000466)","termid":"PATO:0000466"}


id: MONDO:0005596
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant cystic epithelial neoplasm arising from the glandular epithelium. The malignant epithelial cells invade the stroma. The cystic spaces contain serous or mucinous fluid. Representative examples include ovarian and pancreatic cystadenocarcinomas.","definition_xrefs":["NCIT:C2971"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"cystic neoplasm","termid":"MONDO:0021077"}],"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":"cystadenocarcinoma","secondary_identifiers":["EFO:0006387","MESH:D003536","DOID:3111","UMLS:C0010631","ICDO:8440/3","MEDGEN:41385"],"synonyms":[{"name":"cystadenocarcinoma","type":"exact"},{"name":"cystadenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"cystadenocarcinoma NOS (morphologic abnormality)","type":"exact"},{"name":"cystadenocarcinoma, malignant","type":"exact"}],"termid":"MONDO:0005596","xrefs":{"Monarch":{"xref_id":"0005596"}}}


id: MONDO:0032619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 14","secondary_identifiers":["MEDGEN:1648440","OMIM:618236","UMLS:C4748777","DOID:0112094","GARD:16322"],"synonyms":[{"name":"MC1DN14","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14","type":"related"}],"termid":"MONDO:0032619","xrefs":{"Monarch":{"xref_id":"0032619"}}}


id: MONDO:0012378
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary gingival fibromatosis","termid":"MONDO:0016070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibromatosis, gingival, 3","secondary_identifiers":["GARD:9911","MESH:C537928","OMIM:609955","UMLS:C1864960","MEDGEN:351261"],"synonyms":[{"name":"GGF3","type":"related"},{"name":"GINGF3","type":"exact"},{"name":"HGF3","type":"related"},{"name":"fibromatosis gingival, hereditary, 3","type":"related"},{"name":"fibromatosis, gingival, 3","type":"exact"},{"name":"fibromatosis, gingival, hereditary, 3","type":"related"},{"name":"gingival fibromatosis, 3","type":"related"},{"name":"hereditary gingival fibromatosis, 3","type":"related"}],"termid":"MONDO:0012378","xrefs":{"Monarch":{"xref_id":"0012378"}}}


id: PBO:0030202
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_elongated_multiseptate_vegetative_cell","termid":"PBO:0030202"}


id: GO:0150044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of postsynaptic dense core vesicle exocytosis.","definition_xrefs":["PMID:19448629","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of dense core granule exocytosis","termid":"GO:1905413"},{"relation_name":"regulates","term_name":"postsynaptic dense core vesicle exocytosis","termid":"GO:0150038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"regulation of postsynaptic dense core vesicle exocytosis","termid":"GO:0150044"}


id: GO:0010380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of chlorophyll, any compound of magnesium complexed in a porphyrin (tetrapyrrole) ring and which functions as a photosynthetic pigment, from less complex precursors.","definition_xrefs":["PMID:17291312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chlorophyll metabolic process","termid":"GO:0090056"},{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process","termid":"GO:1901463"},{"relation_name":"regulates","term_name":"chlorophyll biosynthetic process","termid":"GO:0015995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"regulation of chlorophyll biosynthetic process","termid":"GO:0010380"}


id: PBO:0068984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 228, pseudogene","termid":"PBO:0068984"}


id: MONDO:0017765
data:
  {"annotated_genes":["SJAG_03371"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859328"}]},"cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of magnesium ion transport.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of mineral absorption and transport","termid":"MONDO:0017761"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03371":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"disorder of magnesium transport","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842842","UMLS:C5681030","Orphanet:309848","GARD:21357"],"synonyms":[{"name":"inborn error of magnesium ion transport","type":"exact"},{"name":"inborn magnesium ion transport disorder","type":"exact"},{"name":"rare inborn error of magnesium ion transport","type":"exact"}],"termid":"MONDO:0017765","terms_by_termid":{"MONDO:0859328":null},"xrefs":{"Monarch":{"xref_id":"0017765"}}}


id: PBO:0050555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Helicobacter pylori responsive 1","termid":"PBO:0050555"}


id: GO:0045228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of polysaccharides in the slime layer, a diffused layer of polysaccharide exterior to the bacterial cell wall.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide biosynthetic process","termid":"GO:0000271"},{"relation_name":"is_a","term_name":"slime layer organization","termid":"GO:0045231"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"slime layer polysaccharide biosynthetic process","synonyms":[{"name":"slime layer polysaccharide anabolism","type":"exact"},{"name":"slime layer polysaccharide biosynthesis","type":"exact"},{"name":"slime layer polysaccharide formation","type":"exact"},{"name":"slime layer polysaccharide synthesis","type":"exact"}],"termid":"GO:0045228"}


id: PBO:0058159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4453 host gene","termid":"PBO:0058159"}


id: GO:0097265
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-HETE + NADP+ = 5-oxo-ETE + NADPH + H+.","definition_xrefs":["PMID:1326548","GOC:mw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"5(S)-hydroxyeicosatetraenoic acid dehydrogenase activity","secondary_identifiers":["Reactome:R-HSA-2161776"],"synonyms":[{"name":"5(S)-HETE dehydrogenase activity","type":"exact"},{"name":"5-HETE dehydrogenase activity","type":"exact"},{"name":"5-hydroxy-eicosatetraenoic acid dehydrogenase activity","type":"exact"}],"termid":"GO:0097265"}


id: MONDO:1011137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in dogs in which the cause of the disease is a mutation in the CCDC39 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia, dog","termid":"MONDO:1012138"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia CCDC39-related, dog","secondary_identifiers":["OMIA:001540-9615"],"termid":"MONDO:1011137","xrefs":{"Monarch":{"xref_id":"1011137"}}}


id: GO:1901953
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of anterograde dense core granule transport.","definition_xrefs":["PMID:23358451","GOC:kmv","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of vesicle transport along microtubule","termid":"GO:1901610"},{"relation_name":"is_a","term_name":"regulation of anterograde dense core granule transport","termid":"GO:1901951"},{"relation_name":"is_a","term_name":"positive regulation of dense core granule transport","termid":"GO:1904811"},{"relation_name":"positively_regulates","term_name":"anterograde neuronal dense core vesicle transport","termid":"GO:1990048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of anterograde dense core granule transport","synonyms":[{"name":"activation of anterograde dense core granule transport","type":"narrow"},{"name":"up regulation of anterograde dense core granule transport","type":"exact"},{"name":"up-regulation of anterograde dense core granule transport","type":"exact"},{"name":"upregulation of anterograde dense core granule transport","type":"exact"}],"termid":"GO:1901953"}


id: GO:0018137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a peptidyl cysteine-peptidyl glycine cross-link by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.","definition_xrefs":["RESID:AA0241"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via glycine thiazolecarboxylic acid (obsolete GO:0018137)","termid":"GO:0018137"}


id: MONDO:0017015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease specific to childhood","termid":"MONDO:0017014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary interstitial lung disease specific to childhood","secondary_identifiers":["GARD:10559","MEDGEN:853969","Orphanet:264665","UMLS:C3161253","icd11.foundation:1408868257"],"synonyms":[{"name":"child","type":"related"},{"name":"children's interstitial lung disease","type":"related"},{"name":"primary ILD specific to childhood","type":"exact"},{"name":"primary interstitial lung disease specific to childhood","type":"exact"}],"termid":"MONDO:0017015","xrefs":{"Monarch":{"xref_id":"0017015"}}}


id: MONDO:0000991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A bundle branch block in which the activation of the left ventricle is delayed.","definition_xrefs":["Wikipedia:Left_bundle_branch_block"],"gene_count":0,"genotype_count":0,"name":"obsolete left bundle branch block (obsolete MONDO:0000991)","secondary_identifiers":["SCTID:4973001","DOID:10272","SCTID:63467002","ICD9:426.2"],"synonyms":[{"name":"left bundle branch [block] or [hemiblock]","type":"related"},{"name":"left bundle branch hemiblock","type":"related"}],"termid":"MONDO:0000991","xrefs":{"Monarch":{"xref_id":"0000991"}}}


id: PBO:0027257
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_phosphorylation_during_mitosis","termid":"PBO:0027257"}


id: PBO:0075654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splA/ryanodine receptor domain and SOCS box containing 3","termid":"PBO:0075654"}


id: GO:0008938
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine(1+) + nicotinate = N-methylnicotinate + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.7","RHEA:20241"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"nicotinate N-methyltransferase activity","secondary_identifiers":["MetaCyc:NICOTINATE-N-METHYLTRANSFERASE-RXN","KEGG_REACTION:R01721"],"synonyms":[{"name":"S-adenosyl-L-methionine:nicotinate N-methyltransferase activity","type":"related"},{"name":"furanocoumarin 8-O-methyltransferase activity","type":"related"}],"termid":"GO:0008938"}


id: FYPO:0002119
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a specified transporter activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transmembrane transporter activity","termid":"FYPO:0002116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0002114"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002114","FYPO:0000652","FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0000707"],"is_obsolete":false,"name":"increased transporter activity","termid":"FYPO:0002119"}


id: MONDO:0021084
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014872"}]},"cv_name":"mondo","definition":"Any impairment to the vision.","definition_xrefs":["NCIT:C35126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perceptual disorders","termid":"MONDO:0024417"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"genotype_count":0,"is_obsolete":false,"name":"vision disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:12103","UMLS:C0042790","MedDRA:10047518","MESH:D014786","SCTID:95677002"],"synonyms":[{"name":"disorder of vision","type":"exact"},{"name":"disorder of visual system","type":"broad"},{"name":"vision disorder","type":"exact"},{"name":"visual Field disorder","type":"related"},{"name":"visual disorder","type":"exact"},{"name":"visual system disorder","type":"broad"}],"termid":"MONDO:0021084","terms_by_termid":{"MONDO:0014872":null},"xrefs":{"Monarch":{"xref_id":"0021084"}}}


id: PBO:0005082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,2-galactosyltransferase Gma12","termid":"PBO:0005082"}


id: PBO:0081373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 212","termid":"PBO:0081373"}


id: MONDO:0024620
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infectious meningitis","termid":"MONDO:0004796"},{"relation_name":"is_a","term_name":"viral infection of central nervous system","termid":"MONDO:0024318"},{"relation_name":"is_a","term_name":"poliovirus infection","termid":"MONDO:0024618"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meningitis caused by poliovirus","secondary_identifiers":["MEDGEN:928803","SCTID:721765009","UMLS:C4303134"],"synonyms":[{"name":"meningitis caused by human poliovirus","type":"exact"},{"name":"polio virus meningitis","type":"related"}],"termid":"MONDO:0024620","xrefs":{"Monarch":{"xref_id":"0024620"}}}


id: MONDO:0007135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"anonychia-onychodystrophy syndrome","termid":"MONDO:0019577"},{"relation_name":"is_a","term_name":"isolated congenital anonychia","termid":"MONDO:0019211"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nonsyndromic congenital nail disorder 6","secondary_identifiers":["DOID:0080084","GARD:15040","OMIM:107000","UMLS:C3275544","MEDGEN:477175"],"synonyms":[{"name":"NDNC6","type":"related"},{"name":"absent nails and dystrophic nails","type":"related"},{"name":"anonychia, partial","type":"related"},{"name":"anonychia/hyponychia and onychodystrophy","type":"related"},{"name":"nail disorder, nonsyndromic congenital, 6","type":"related"},{"name":"nonsyndromic congenital nail disorder type 6","type":"exact"},{"name":"onychodystrophy-anonychia","type":"related"}],"termid":"MONDO:0007135","xrefs":{"Monarch":{"xref_id":"0007135"}}}


id: PBO:0089021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk6","termid":"PBO:0089021"}


id: GO:1905310
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac neural crest cell migration involved in outflow tract morphogenesis.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:17628518","GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"regulates","term_name":"cardiac neural crest cell migration involved in outflow tract morphogenesis","termid":"GO:0003253"}],"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 cardiac neural crest cell migration involved in outflow tract morphogenesis","termid":"GO:1905310"}


id: GO:0015620
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of ferric-enterobactin from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore-iron transmembrane transporter activity","termid":"GO:0015343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ferric-enterobactin transmembrane transporter activity","termid":"GO:0015620"}


id: PBO:0088688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal protein, implicated in vesicle trafficking or lipid metabolism","termid":"PBO:0088688"}


id: GO:0022602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involved in the sexual cycle seen in females, often with physiologic changes in the endometrium that recur at regular intervals during the reproductive years.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive process","termid":"GO:0022414"},{"relation_name":"is_a","term_name":"rhythmic process","termid":"GO:0048511"},{"relation_name":"part_of","term_name":"ovulation cycle","termid":"GO:0042698"}],"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":"ovulation cycle process","synonyms":[{"name":"estrous cycle process","type":"related"},{"name":"menstrual cycle process","type":"related"}],"termid":"GO:0022602"}


id: GO:0008018
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 structural protein of chorion (sensu Drosophila) (obsolete GO:0008018)","synonyms":[{"name":"structural protein of chorion (sensu Drosophila)","type":"exact"}],"termid":"GO:0008018"}


id: PR:O42634
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A meiotic recombination protein DMC1/LIM15 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic recombination protein dmc1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8E11.03c","secondary_identifiers":["UniProtKB:O42634"],"synonyms":[{"name":"Spom972h-DMC1","type":"exact"}],"termid":"PR:O42634"}


id: PBO:0049451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GXYLT1 pseudogene 5","termid":"PBO:0049451"}


id: GO:0036287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an iloperidone stimulus.","definition_xrefs":["GOC:hp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organic cyclic compound","termid":"GO:0014070"},{"relation_name":"is_a","term_name":"response to ether","termid":"GO:0045472"},{"relation_name":"is_a","term_name":"response to monoamine","termid":"GO:0071867"},{"relation_name":"is_a","term_name":"response to ketone","termid":"GO:1901654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to iloperidone","termid":"GO:0036287"}


id: MONDO:0001283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign pathologic process characterized by the transformation of the mesothelium into fallopian tube epithelium. It occurs in the peritoneum and may affect the serosa surface of the uterus and the adnexa. It may be asymptomatic or present as pelvic pain.","definition_xrefs":["NCIT:C40121"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"endometriosis","termid":"MONDO:0005133"},{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endosalpingiosis","secondary_identifiers":["SCTID:55850004","UMLS:C0269106","DOID:11427","MEDGEN:78704"],"synonyms":[{"name":"endosalpingiosis","type":"exact"}],"termid":"MONDO:0001283","xrefs":{"Monarch":{"xref_id":"0001283"}}}


id: PBO:0086636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; YLR287C is not an essential gene","termid":"PBO:0086636"}


id: PBO:0072342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 28","termid":"PBO:0072342"}


id: MONDO:0044250
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tongue curling, folding, or rolling (obsolete MONDO:0044250)","secondary_identifiers":["OMIM:189300"],"synonyms":[{"name":"cloverleaf tongue","type":"related"},{"name":"tongue curling, folding, or rolling","type":"related"},{"name":"trefoil tongue","type":"related"}],"termid":"MONDO:0044250","xrefs":{"Monarch":{"xref_id":"0044250"}}}


id: MONDO:0005243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Cushing syndrome (obsolete MONDO:0005243)","termid":"MONDO:0005243","xrefs":{"Monarch":{"xref_id":"0005243"}}}


id: GO:0030145
data:
  {"annotated_genes":["SJAG_00181","SJAG_02247","SJAG_04407","SJAG_05010","SJAG_03398","SJAG_01254","SJAG_03744","SJAG_01896","SJAG_03303","SJAG_05373"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87457,87711,87763,88192,90761,96547,99040,104918,105072,112340,114795],"is_not":false,"summary":null,"term":"GO:0030145"}]},"cv_name":"molecular_function","definition":"Binding to a manganese ion (Mn).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion binding","termid":"GO:0046914"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_01254":null,"SJAG_01896":null,"SJAG_02247":null,"SJAG_03303":null,"SJAG_03398":null,"SJAG_03744":null,"SJAG_04407":null,"SJAG_05010":null,"SJAG_05373":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0046872","GO:0005488"],"is_obsolete":false,"name":"manganese ion binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Mn binding","type":"exact"},{"name":"manganese binding","type":"exact"}],"termid":"GO:0030145","terms_by_termid":{"GO:0030145":null}}


id: PBO:0054101
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 1460","termid":"PBO:0054101"}


id: GO:0070930
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A protein modification process in which a polypeptide is added to a nascent polypeptide cotranslationally by trans-translation.","definition_xrefs":["GOC:jh2","GOC:mah","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"co-translational protein modification","termid":"GO:0043686"}],"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":"trans-translation-dependent protein tagging","synonyms":[{"name":"co-translational protein tagging","type":"exact"},{"name":"cotranslational protein tagging","type":"exact"},{"name":"protein modification by trans-translation","type":"exact"}],"termid":"GO:0070930"}


id: MONDO:0032877
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures","secondary_identifiers":["OMIM:618709","UMLS:C5231470","MEDGEN:1684757"],"synonyms":[{"name":"NEDBAS","type":"related"},{"name":"NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES","type":"related"},{"name":"neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures","type":"exact"}],"termid":"MONDO:0032877","xrefs":{"Monarch":{"xref_id":"0032877"}}}


id: GO:0005783
data:
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id: MONDO:0008374
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id: PBO:0081941
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id: PBO:0040315
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id: MONDO:0015446
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id: MONDO:0010572
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id: PBO:0034764
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id: MONDO:0032868
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id: FYPO:0006626
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id: MONDO:0014269
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  {"annotated_genes":["SJAG_00894"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84882],"is_not":false,"summary":null,"term":"MONDO:0014269"}]},"cv_name":"mondo","definition":"Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the LYRM4 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_00894":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation deficiency 19","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:397593","MEDGEN:816385","UMLS:C3810055","OMIM:615595","DOID:0111476","GARD:18466"],"synonyms":[{"name":"COXPD19","type":"related"},{"name":"LYRM4 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 19","type":"exact"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in LYRM4","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 19","type":"exact"},{"name":"severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency","type":"exact"}],"termid":"MONDO:0014269","terms_by_termid":{"MONDO:0014269":null},"xrefs":{"Monarch":{"xref_id":"0014269"}}}


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


id: FYPO:0006273
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the structure of the glycan moiety of a nascent glycoprotein in the endoplasmic reticulum lumen differs from wild type.","definition_xrefs":["PomBase:mah","PMID:27587357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glycoprotein glycan structure","termid":"FYPO:0003290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0003290"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0003290","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"abnormal glycoprotein glycan structure in endoplasmic reticulum lumen","synonyms":[{"name":"abnormal glycoprotein glycan structure in ER lumen","type":"exact"},{"name":"abnormal glycoprotein oligosaccharide structure in endoplasmic reticulum lumen","type":"related"}],"termid":"FYPO:0006273"}


id: GO:0030420
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a naturally transformable bacterium acquires the ability to take up exogenous DNA. This term should be applied only to naturally transformable bacteria, and should not be used in the context of artificially induced bacterial transformation.","definition_xrefs":["ISBN:1555811027","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stimulus","termid":"GO:0051716"},{"relation_name":"part_of","term_name":"DNA-mediated transformation","termid":"GO:0009294"}],"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":"establishment of competence for transformation","termid":"GO:0030420"}


id: PR:A6X982
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC15D4.13c gene.","definition_xrefs":["UniProtKB:A6X982","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 C15D4.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC15D4.13c","synonyms":[{"name":"Spom972h-SPBC15D4.13c","type":"exact"}],"termid":"PR:A6X982"}


id: FYPO:0003426
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA measured in a cell during a cellular response to a pheromone is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level","termid":"FYPO:0000826"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased RNA level during cellular response to pheromone","synonyms":[{"name":"decreased RNA accumulation during cellular response to pheromone","type":"related"},{"name":"decreased transcript level during cellular response to pheromone","type":"exact"},{"name":"reduced RNA level during cellular response to pheromone","type":"exact"}],"termid":"FYPO:0003426"}


id: MONDO:0003940
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that presents as vertebral osteonecrosis typically affecting a thoracic vertebra with compression deformity, intravertebral vacuum cleft, and exaggerated kyphosis weeks to months after a minor traumatic injury.","definition_xrefs":["PMID:23814399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloarthropathy","termid":"MONDO:0005095"},{"relation_name":"is_a","term_name":"osteonecrosis","termid":"MONDO:0005380"},{"relation_name":"is_a","term_name":"vertebral disorder","termid":"MONDO:0045002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"Kummell disease","secondary_identifiers":["MEDGEN:508880","UMLS:C0152088","DOID:6603","ICD10CM:M48.3","ICD9:721.7","SCTID:111232005"],"synonyms":[{"name":"Kummell disease","type":"exact"},{"name":"Kummell's disease","type":"exact"},{"name":"Kummell's spondylitis","type":"exact"},{"name":"avascular necrosis of a vertebral body","type":"exact"},{"name":"bony vertebral centrum osteonecrosis","type":"exact"},{"name":"osteonecrosis of bony vertebral centrum","type":"exact"},{"name":"traumatic spondylopathy","type":"exact"}],"termid":"MONDO:0003940","xrefs":{"Monarch":{"xref_id":"0003940"}}}


id: MONDO:0001080
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of gonococcal cervicitis.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute cervicitis","termid":"MONDO:0001081"},{"relation_name":"is_a","term_name":"gonococcal cervicitis","termid":"MONDO:0021157"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute gonococcal cervicitis","secondary_identifiers":["DOID:10615","MEDGEN:509197","UMLS:C0153195","icd11.foundation:2071927498","ICD9:098.15","SCTID:20943002"],"synonyms":[{"name":"acute gonorrhea of cervix","type":"exact"},{"name":"acute gonorrhoea of cervix","type":"exact"},{"name":"gonococcal cervicitis (acute)","type":"exact"},{"name":"gonococcal cervicitis, acute","type":"exact"}],"termid":"MONDO:0001080","xrefs":{"Monarch":{"xref_id":"0001080"}}}


id: PBO:0090094
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit Rcf2","termid":"PBO:0090094"}


id: PBO:0086911
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative Y' element ATP-dependent helicase","termid":"PBO:0086911"}


id: MONDO:1012452
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal cobalamin (vitamin B12) malabsorption, non-human animal","termid":"MONDO:1011719"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intestinal cobalamin (vitamin B12) malabsorption, domestic cat","secondary_identifiers":["OMIA:001791-9685"],"termid":"MONDO:1012452","xrefs":{"Monarch":{"xref_id":"1012452"}}}


id: FYPO:0007445
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id: GO:0002621
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of non-professional antigen presenting cell antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of antigen processing and presentation","termid":"GO:0002579"},{"relation_name":"is_a","term_name":"regulation of non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002619"},{"relation_name":"positively_regulates","term_name":"non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002473"}],"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 non-professional antigen presenting cell antigen processing and presentation","synonyms":[{"name":"activation of non-professional antigen presenting cell antigen processing and presentation","type":"narrow"},{"name":"stimulation of non-professional antigen presenting cell antigen processing and presentation","type":"narrow"},{"name":"up regulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"},{"name":"up-regulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"},{"name":"upregulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"}],"termid":"GO:0002621"}


id: MONDO:0958297
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sarcoma with BCOR genetic alterations that occurs during childhood.","definition_xrefs":["DOID:0081405"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sarcoma with BCOR genetic alterations","termid":"MONDO:0958159"}],"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":"childhood sarcoma with BCOR genetic alterations","secondary_identifiers":["MEDGEN:1817088","UMLS:C5708183"],"termid":"MONDO:0958297","xrefs":{"Monarch":{"xref_id":"0958297"}}}


id: PBO:0044495
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 51 subfamily A member 1 pseudogene 3","termid":"PBO:0044495"}


id: GO:2000790
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mesenchymal cell proliferation involved in lung development.","definition_xrefs":["PMID:21513708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal cell proliferation","termid":"GO:0010464"},{"relation_name":"regulates","term_name":"mesenchymal cell proliferation involved in lung development","termid":"GO:0060916"}],"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 mesenchymal cell proliferation involved in lung development","termid":"GO:2000790"}


id: GO:0098642
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen trimer that forms networks.","definition_xrefs":["PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collagen trimer","termid":"GO:0005581"},{"relation_name":"part_of","term_name":"collagen network","termid":"GO:0098645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"network-forming collagen trimer","termid":"GO:0098642"}


id: PBO:0072533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 63","termid":"PBO:0072533"}


id: PBO:0029291
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_meiosis","termid":"PBO:0029291"}


id: SO:0001662
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A TATA box core promoter of a gene transcribed by RNA polymerase III.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TATA_box","termid":"SO:0000174"},{"relation_name":"part_of","term_name":"RNApol_III_promoter","termid":"SO:0000171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA_polymerase_III_TATA_box","synonyms":[{"name":"RNA polymerase III TATA box","type":"exact"}],"termid":"SO:0001662"}


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


id: PBO:0003735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic thiouridylase subunit Ctu2","termid":"PBO:0003735"}


id: CHEBI:17858
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione disulfide","termid":"CHEBI:17858"}


id: PR:O74731
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tRNA-dihydrouridine synthase 2-like that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11082:SF4","PRO:DNx","OMA:SCHPO02719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-dihydrouridine(20) synthase [NAD(P)+] (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1709.06","secondary_identifiers":["UniProtKB:O74731"],"synonyms":[{"name":"Spom972h-DUS2","type":"exact"},{"name":"tRNA-dihydrouridine synthase 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74731"}


id: MONDO:0005355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction.","definition_xrefs":["MESH:D023903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coronary stenosis","termid":"MONDO:0006715"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"coronary restenosis","secondary_identifiers":["DOID:4247","MEDGEN:182688","EFO:0004224","UMLS:C0948480"],"termid":"MONDO:0005355","xrefs":{"Monarch":{"xref_id":"0005355"}}}


id: GO:0005035
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an extracellular messenger (called a death ligand), and transmitting the signal from one side of the plasma membrane to the other to initiate apoptotic or necrotic cell death.","definition_xrefs":["PMID:10209153","GOC:BHF","GOC:ecd","GOC:bf","GOC:mtg_apoptosis","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"death receptor activity","synonyms":[{"name":"apoptosis-activating receptor activity","type":"related"}],"termid":"GO:0005035"}


id: SO:0000792
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000792 cloned_cDNA (obsolete SO:0000792)","termid":"SO:0000792"}


id: MONDO:0009951
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":"radiculoneuropathy, fatal neonatal","secondary_identifiers":["MESH:C564857","UMLS:C1849471","MEDGEN:376592","OMIM:266250"],"synonyms":[{"name":"Radiculoneuropathy, fatal neonatal","type":"exact"}],"termid":"MONDO:0009951","xrefs":{"Monarch":{"xref_id":"0009951"}}}


id: PBO:0109656
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae MDI1","termid":"PBO:0109656"}


id: PBO:0065593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prothymosin alpha pseudogene 9","termid":"PBO:0065593"}


id: PBO:0053375
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 301","termid":"PBO:0053375"}


id: SO:0000892
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is positively autoregulated.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"positively_autoregulated","termid":"SO:0000475"},{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"positively_autoregulated_gene","synonyms":[{"name":"positively autoregulated gene","type":"exact"}],"termid":"SO:0000892"}


id: PBO:0029689
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_iron_ion_starvation-induced_proteins","termid":"PBO:0029689"}


id: FYECO:0000226
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which leucine was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ leu","synonyms":[{"name":"leucine added","type":"exact"}],"termid":"FYECO:0000226"}


id: MONDO:0000551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroblastoma that involves the retroperitoneal space.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroblastoma","termid":"MONDO:0005072"},{"relation_name":"is_a","term_name":"retroperitoneal neoplasm","termid":"MONDO:0024645"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retroperitoneal neuroblastoma","secondary_identifiers":["MEDGEN:1843500","UMLS:C2211613","DOID:0050937"],"synonyms":[{"name":"neuroblastoma of retroperitoneal space","type":"exact"},{"name":"retroperitoneal space neuroblastoma","type":"exact"}],"termid":"MONDO:0000551","xrefs":{"Monarch":{"xref_id":"0000551"}}}


id: PBO:0047469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fc receptor like B","termid":"PBO:0047469"}


id: GO:0006004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving fucose, or 6-deoxygalactose, which has two enantiomers, D-fucose and L-fucose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose metabolic process","termid":"GO:0019318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"fucose metabolic process","synonyms":[{"name":"fucose metabolism","type":"exact"}],"termid":"GO:0006004"}


id: MONDO:0018670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fragile X syndrome","termid":"MONDO:0010383"},{"relation_name":"is_a","term_name":"premature ovarian failure 1","termid":"MONDO:0010706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"symptomatic form of fragile X syndrome in female carrier","secondary_identifiers":["MEDGEN:1814467","UMLS:C5681104","GARD:17783","Orphanet:449291"],"termid":"MONDO:0018670","xrefs":{"Monarch":{"xref_id":"0018670"}}}


id: PBO:0054251
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 1634","termid":"PBO:0054251"}


id: PR:Q9P7Z7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cytochrome c oxidase copper chaperone that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR16719:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase copper chaperone (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC26H8.14c","secondary_identifiers":["UniProtKB:Q9P7Z7"],"synonyms":[{"name":"SPBC26H8.14c","type":"related"},{"name":"Spom972h-COX17","type":"exact"}],"termid":"PR:Q9P7Z7"}


id: MONDO:0800446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, isolated constitutional thrombocytopenia disease characterized by impaired platelet aggregation resulting from a defect in thromboxane synthesis or signaling, manifesting with mild to moderate mucocutaneous, gastrointestinal or surgical bleeding (e.g. easy bruising, prolonged epistaxis, excessive bleeding after a tooth extraction).","definition_xrefs":["Orphanet:220443"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"}],"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":"bleeding diathesis due to thromboxane synthesis deficiency","secondary_identifiers":["GARD:17132","icd11.foundation:1676860885","MEDGEN:1678745","UMLS:C5190857"],"termid":"MONDO:0800446","xrefs":{"Monarch":{"xref_id":"0800446"}}}


id: MOD:01362
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-thiophospho-L-serine.","definition_xrefs":["PubMed:11507762","Unimod:260#S","PubMed:12110917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiophosphorylated residue","termid":"MOD:00583"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-thiophospho-L-serine","synonyms":[{"name":"Thiophospho","type":"related"},{"name":"Thiophosphorylation","type":"related"}],"termid":"MOD:01362"}


id: FYECO:0000304
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which tert-butyl hydroperoxide was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ TBHP","synonyms":[{"name":"TBH","type":"exact"},{"name":"tert-butyl hydroperoxide","type":"exact"}],"termid":"FYECO:0000304"}


id: PR:O42851
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC23A1.14c gene.","definition_xrefs":["UniProtKB:O42851","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 trans-sulfuration enzyme C23A1.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.14c","synonyms":[{"name":"Spom972h-SPAC23A1.14c","type":"exact"}],"termid":"PR:O42851"}


id: PBO:0051046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 1-20","termid":"PBO:0051046"}


id: PBO:0069522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 791, pseudogene","termid":"PBO:0069522"}


id: MONDO:0006032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the urinary bladder.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder disorder","termid":"MONDO:0006026"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystitis","secondary_identifiers":["icd11.foundation:1181120673","EFO:1000025","ICD9:595","ICD9:595.9","SCTID:38822007","ICD9:595.89","NCIT:C26738","MEDGEN:8227","UMLS:C0010692","MESH:D003556","DOID:1679"],"synonyms":[{"name":"bladder infection","type":"exact"},{"name":"inflammation of urinary bladder","type":"exact"},{"name":"urinary bladder inflammation","type":"exact"}],"termid":"MONDO:0006032","xrefs":{"Monarch":{"xref_id":"0006032"}}}


id: PATO:0000496
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000496 phase value (obsolete PATO:0000496)","termid":"PATO:0000496"}


id: MONDO:0008866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive form of bifid nose.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bifid nose","termid":"MONDO:0000110"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"bifid nose, autosomal recessive","secondary_identifiers":["OMIM:210400","GARD:15142","UMLS:C3887497","MEDGEN:854359"],"synonyms":[{"name":"Nose, Median cleft of","type":"related"},{"name":"autosomal recessive bifid nose","type":"exact"},{"name":"bifid nose, autosomal recessive","type":"exact"},{"name":"median fissure of Nose","type":"related"}],"termid":"MONDO:0008866","xrefs":{"Monarch":{"xref_id":"0008866"}}}


id: GO:0004205
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete caspase-8 activity (obsolete GO:0004205)","synonyms":[{"name":"caspase-8 activity","type":"exact"}],"termid":"GO:0004205"}


id: MONDO:0030679
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005046"],"is_obsolete":false,"name":"Noonan syndrome 14","secondary_identifiers":["OMIM:619745","MEDGEN:1807988","UMLS:C5676916"],"synonyms":[{"name":"NS14","type":"exact"},{"name":"Noonan syndrome 14","type":"exact"}],"termid":"MONDO:0030679","xrefs":{"Monarch":{"xref_id":"0030679"}}}


id: PBO:0090482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase, Sirtuin family, NAD-dependent Hst4","termid":"PBO:0090482"}


id: PR:Q09822
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdc15 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09822"],"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":"cell division control protein 15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20G8.05c","synonyms":[{"name":"Spom972h-cdc15","type":"exact"}],"termid":"PR:Q09822"}


id: PBO:0079099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 12-1","termid":"PBO:0079099"}


id: RO:HOM0000072
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Biological homology that involves an ectopic structure and the normally positioned structure.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_biological_homology_relationship_with","termid":"RO:HOM0000008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_homeosis_relationship_with","synonyms":[{"name":"heterotopy","type":"related"}],"termid":"RO:HOM0000072"}


id: GO:0015213
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of uridine, uracil riboside, from one side of a membrane to the other.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside transmembrane transporter activity","termid":"GO:0015214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"uridine transmembrane transporter activity","synonyms":[{"name":"uracil/uridine permease activity","type":"narrow"}],"termid":"GO:0015213"}


id: PBO:0041839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer susceptibility 19","termid":"PBO:0041839"}


id: PBO:0018056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorein homolog Vps13a (predicted)","termid":"PBO:0018056"}


id: GO:0051627
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of epinephrine into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of epinephrine uptake","termid":"GO:0051626"},{"relation_name":"negatively_regulates","term_name":"epinephrine uptake","termid":"GO:0051625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of epinephrine uptake","synonyms":[{"name":"down regulation of epinephrine uptake","type":"exact"},{"name":"down-regulation of epinephrine uptake","type":"exact"},{"name":"downregulation of epinephrine uptake","type":"exact"},{"name":"negative regulation of adrenaline uptake","type":"exact"},{"name":"negative regulation of epinephrine import","type":"exact"}],"termid":"GO:0051627"}


id: FYPO:0004180
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein present as aggregates of misfolded protein is greater than normal.","definition_xrefs":["PMID:24936793","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased cellular protein aggregate level","synonyms":[{"name":"increased cellular protein aggregate level during mitotic cell cycle","type":"related"},{"name":"increased cellular protein aggregate level during vegetative growth","type":"exact"}],"termid":"FYPO:0004180"}


id: PBO:0070678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 49","termid":"PBO:0070678"}


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


id: PR:O43048
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC215.01 gene.","definition_xrefs":["UniProtKB:O43048","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":"TBC domain-containing protein C215.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC215.01","synonyms":[{"name":"Spom972h-SPBC215.01","type":"exact"}],"termid":"PR:O43048"}


id: GO:0033923
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->6)-alpha-D-glucosidic linkages in polysaccharides, to remove successive isomaltose units from the non-reducing ends of the chains.","definition_xrefs":["EC:3.2.1.94"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"glucan 1,6-alpha-isomaltosidase activity","secondary_identifiers":["MetaCyc:3.2.1.94-RXN"],"synonyms":[{"name":"1,6-alpha-D-glucan isomaltohydrolase activity","type":"related"},{"name":"G2-dextranase activity","type":"related"},{"name":"exo-isomaltohydrolase activity","type":"related"},{"name":"isomalto-dextranase activity","type":"related"},{"name":"isomaltodextranase activity","type":"related"}],"termid":"GO:0033923"}


id: PBO:0108950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPOPL pseudogene 2","termid":"PBO:0108950"}


id: PBO:0085700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in ribosome biogenesis; forms a nucleolar complex with Mak21p that binds to 90S and 66S pre-ribosomes; forms a nuclear complex with Noc3p that binds to 66S pre-ribosomes; both complexes mediate intranuclear transport of ribosomal precursors; acts as part of a Mak21p-Noc2p-Rrp5p module that associates with nascent pre-rRNA during transcription and has a role in bigenesis of the large ribosomal subunit","termid":"PBO:0085700"}


id: MONDO:0100393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly t(8;16). (A cytogenetic abnormality that involves a translocation between chromosomes 8 and 16.)","definition_xrefs":["NCIT:C175583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, t(8;16)","synonyms":[{"name":"AML, t(8;16)","type":"exact"}],"termid":"MONDO:0100393","xrefs":{"Monarch":{"xref_id":"0100393"}}}


id: PR:O74352
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A bridging integrator 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03271","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":"protein hob1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21D10.12","secondary_identifiers":["UniProtKB:O74352"],"synonyms":[{"name":"Spom972h-BIN2","type":"exact"},{"name":"homolog of Bin1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74352"}


id: GO:0009823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of cytokinins, a class of adenine-derived compounds that can function in plants as plant growth regulators.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokinin metabolic process","termid":"GO:0009690"},{"relation_name":"is_a","term_name":"hormone catabolic process","termid":"GO:0042447"}],"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":"cytokinin catabolic process","synonyms":[{"name":"cytokinin breakdown","type":"exact"},{"name":"cytokinin catabolism","type":"exact"},{"name":"cytokinin degradation","type":"exact"}],"termid":"GO:0009823"}


id: MONDO:0016908
data:
  {"annotated_genes":["SJAG_00112"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 9","termid":"MONDO:0016874"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00112":null},"genotype_count":0,"is_obsolete":false,"name":"partial monosomy of the long arm of chromosome 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20829","icd11.foundation:1051626600","Orphanet:262074","MEDGEN:1826024","UMLS:C5679677"],"synonyms":[{"name":"partial deletion of chromosome 9q","type":"exact"},{"name":"partial deletion of the long arm of chromosome 9","type":"exact"},{"name":"partial monosomy of chromosome 9q","type":"exact"},{"name":"partial monosomy of the long arm of chromosome type 9","type":"exact"}],"termid":"MONDO:0016908","terms_by_termid":{"MONDO:0014848":null},"xrefs":{"Monarch":{"xref_id":"0016908"}}}


id: MONDO:1010886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuronal ceroid lipofuscinosis that occurs in pigs due to a mutation in the TPP1 gene created using gene editing.","definition_xrefs":["OMIA:001472-9823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis, pig","termid":"MONDO:1011577"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal ceroid lipofuscinosis, TPP1-related, pig","synonyms":[{"name":"neuronal ceroid lipofuscinosis, 2, pig","type":"related"}],"termid":"MONDO:1010886","xrefs":{"Monarch":{"xref_id":"1010886"}}}


id: GO:0141031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of the host actin cytoskeleton by actin crosslinking the host actin filaments. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:22814176","PMID:14512630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host actin cytoskeleton","termid":"GO:0141027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host actin cytoskeleton via actin crosslinking","synonyms":[{"name":"perturbation by symbiont of host actin cytoskeleton via actin crosslinking","type":"exact"}],"termid":"GO:0141031"}


id: GO:0072012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a glomerulus vasculature from an initial condition to its mature state. This process begins with the formation of the glomerulus vasculature and ends with the mature structure. The glomerulus vasculature is composed of the tubule structures that carry blood or lymph in the glomerulus.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel development","termid":"GO:0001568"},{"relation_name":"is_a","term_name":"kidney vasculature development","termid":"GO:0061440"},{"relation_name":"part_of","term_name":"glomerulus development","termid":"GO:0032835"}],"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":"glomerulus vasculature development","synonyms":[{"name":"glomerulus capillary development","type":"related"}],"termid":"GO:0072012"}


id: PBO:0044957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase/reductase 4","termid":"PBO:0044957"}


id: PBO:0089450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane pyridoxal family transmembrane transporter","termid":"PBO:0089450"}


id: GO:0004796
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: prostaglandin H(2) = thromboxane A(2).","definition_xrefs":["EC:5.3.99.5","RHEA:17137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity","termid":"GO:0016860"}],"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:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"thromboxane-A synthase activity","secondary_identifiers":["MetaCyc:THROMBOXANE-A-SYNTHASE-RXN","GO:0008400","KEGG_REACTION:R02268","Reactome:R-HSA-5603275","Reactome:R-HSA-76500"],"synonyms":[{"name":"(5Z,13E)-(15S)-9alpha,11alpha-epidioxy-15-hydroxyprosta-5,13-dienoate isomerase activity","type":"related"},{"name":"(5Z,13E)-(15S)-9alpha,11alpha-epidioxy-15-hydroxyprosta-5,13-dienoate thromboxane-A2-isomerase activity","type":"related"},{"name":"cytochrome P450 CYP5","type":"narrow"},{"name":"thromboxane synthase activity","type":"related"},{"name":"thromboxane synthetase activity","type":"related"}],"termid":"GO:0004796"}


id: PBO:0069863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1150, pseudogene","termid":"PBO:0069863"}


id: GO:0060833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of Wnt protein to a frizzled family receptor on the surface of the target cell contributing to the specification of the animal/vegetal axis of an oocyte.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete Wnt signaling pathway involved in animal/vegetal axis specification (obsolete GO:0060833)","synonyms":[{"name":"Wnt receptor signaling pathway involved in animal/vegetal axis specification","type":"exact"},{"name":"Wnt receptor signalling pathway involved in animal/vegetal axis specification","type":"exact"},{"name":"Wnt- activated signaling pathway involved in animal/vegetal axis specification","type":"exact"}],"termid":"GO:0060833"}


id: FYPO:0005919
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 TOP-53. Cells stop growing (and may die) at a concentration of TOP-53 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:0002683","FYPO:0000139","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to TOP-53","synonyms":[{"name":"hypersensitive to TOP-53","type":"exact"},{"name":"sensitive to TOP-53 during mitotic cell cycle","type":"related"},{"name":"sensitive to TOP-53 during vegetative growth","type":"exact"}],"termid":"FYPO:0005919"}


id: GO:0006538
data:
  {"annotated_genes":["SJAG_03434","SJAG_00937"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78936,90906],"is_not":false,"summary":null,"term":"GO:0006538"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glutamate, the anion of 2-aminopentanedioic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate metabolic process","termid":"GO:0006536"},{"relation_name":"is_a","term_name":"glutamine family amino acid catabolic process","termid":"GO:0009065"},{"relation_name":"is_a","term_name":"dicarboxylic acid catabolic process","termid":"GO:0043649"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00937":null,"SJAG_03434":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044248","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"glutamate catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0019459"],"synonyms":[{"name":"glutamate breakdown","type":"exact"},{"name":"glutamate catabolism","type":"exact"},{"name":"glutamate deamidation","type":"related"},{"name":"glutamate degradation","type":"exact"},{"name":"glutamic acid catabolic process","type":"exact"},{"name":"glutamic acid catabolism","type":"exact"}],"termid":"GO:0006538","terms_by_termid":{"GO:0006538":null}}


id: GO:0097532
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 disturbance in organismal or cellular homeostasis caused by the chemical structure of the anion portion of a dissociated acid (rather than the acid acting as a proton donor). The acid chemical may be in gaseous, liquid or solid form.","definition_xrefs":["GOC:go_curators","GOC:aa","GOC:BHF","PMID:10615049","Wikipedia:Acid","GOC:rl","PMID:19170886"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to acid chemical","termid":"GO:0001101"},{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"}],"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":"stress response to acid chemical","synonyms":[{"name":"response to acid stress","type":"broad"},{"name":"stress response to acid","type":"broad"}],"termid":"GO:0097532"}


id: MONDO:0014132
data:
  {"annotated_genes":["SJAG_02306"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85249],"is_not":false,"summary":null,"term":"MONDO:0014132"}]},"cv_name":"mondo","definition":"Any fatal multiple mitochondrial dysfunctions syndrome in which the cause of the disease is a mutation in the IBA57 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatal multiple mitochondrial dysfunctions syndrome","termid":"MONDO:0017338"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02306":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525","MONDO:0004069"],"is_obsolete":false,"name":"multiple mitochondrial dysfunctions syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17555","DOID:0080135","MEDGEN:815495","OMIM:615330","UMLS:C3809165","Orphanet:363424"],"synonyms":[{"name":"IBA57 deficiency","type":"exact"},{"name":"IBA57 fatal multiple mitochondrial dysfunctions syndrome","type":"exact"},{"name":"MMDS3","type":"related"},{"name":"fatal multiple mitochondrial dysfunctions syndrome caused by mutation in IBA57","type":"exact"},{"name":"multiple mitochondrial dysfunctions syndrome 3","type":"exact"},{"name":"multiple mitochondrial dysfunctions syndrome type 3","type":"exact"}],"termid":"MONDO:0014132","terms_by_termid":{"MONDO:0014132":null},"xrefs":{"Monarch":{"xref_id":"0014132"}}}


id: PBO:0045671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein cytoplasmic 1 intermediate chain 2","termid":"PBO:0045671"}


id: MONDO:0021208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia","termid":"MONDO:0004907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endocrine alopecia","secondary_identifiers":["ICD9:704.09","MEDGEN:507423","SCTID:54539003","UMLS:C0002176"],"termid":"MONDO:0021208","xrefs":{"Monarch":{"xref_id":"0021208"}}}


id: PBO:0077354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 94","termid":"PBO:0077354"}


id: GO:0140473
data:
  {"annotated_genes":["SJAG_01263","SJAG_05226"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105120,116688],"is_not":false,"summary":null,"term":"GO:0140473"}]},"cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together the telomeric region of a chromosome and the inner nuclear membrane by interacting with both the telomere and the nuclear membrane, in order to establish and maintain the telomeric location.","definition_xrefs":["PMID:31635174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-membrane adaptor activity","termid":"GO:0043495"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01263":null,"SJAG_05226":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0030674","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"telomere-nuclear envelope anchor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"nuclear envelope-telomere anchor activity","type":"exact"},{"name":"telomere-nuclear envelope anchoring activity","type":"exact"}],"termid":"GO:0140473","terms_by_termid":{"GO:0140473":null}}


id: GO:0045945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of transcription mediated by RNA polymerase III.","definition_xrefs":["GOC:go_curators","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transcription by RNA polymerase III","termid":"GO:0006359"},{"relation_name":"is_a","term_name":"positive regulation of DNA-templated transcription","termid":"GO:0045893"},{"relation_name":"positively_regulates","term_name":"transcription by RNA polymerase III","termid":"GO:0006383"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006355"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006351","GO:0006355"],"is_obsolete":false,"name":"positive regulation of transcription by RNA polymerase III","synonyms":[{"name":"activation of transcription from RNA polymerase III promoter","type":"narrow"},{"name":"positive regulation of transcription from Pol III promoter","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase III promoter","type":"exact"},{"name":"stimulation of transcription from RNA polymerase III promoter","type":"narrow"},{"name":"up regulation of transcription from RNA polymerase III promoter","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase III promoter","type":"exact"},{"name":"upregulation of transcription from RNA polymerase III promoter","type":"exact"}],"termid":"GO:0045945"}


id: GO:0070650
data:
  {"annotated_genes":["SJAG_00938","SJAG_03011","SJAG_04498","SJAG_02864","SJAG_04621"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061573"},{"annotations":[97223,97488,88535,107289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071520"}]},"cv_name":"biological_process","definition":"Any cellular process that establishes the spatial arrangement of actin filament bundles within the cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament bundle organization","termid":"GO:0061572"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_02864":null,"SJAG_03011":null,"SJAG_04498":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0030036","GO:0007010"],"is_obsolete":false,"name":"actin filament bundle distribution","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070650","terms_by_termid":{"GO:0061573":null,"GO:0071520":null}}


id: PBO:0042462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDCA3 pseudogene 1","termid":"PBO:0042462"}


id: PBO:0071736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 34","termid":"PBO:0071736"}


id: MONDO:0000986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the pleura. It is usually caused by infections. Chest pain while breathing or coughing is the presenting symptom.","definition_xrefs":["NCIT:C26860"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pleural disorder","termid":"MONDO:0002037"},{"relation_name":"is_a","term_name":"serositis","termid":"MONDO:0043786"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleurisy","secondary_identifiers":["icd11.foundation:317852053","ICD9:511.8","EFO:1001825","MESH:D010998","SCTID:196075003","UMLS:C0032231","ICD10CM:R09.1","MEDGEN:10807","DOID:10247"],"synonyms":[{"name":"inflammation of pleura","type":"exact"},{"name":"pleura inflammation","type":"exact"},{"name":"pleuritis","type":"exact"}],"termid":"MONDO:0000986","xrefs":{"Monarch":{"xref_id":"0000986"}}}


id: FYPO:0000768
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 valinomycin 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:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0000139"],"is_obsolete":false,"name":"resistance to valinomycin","synonyms":[{"name":"resistance to valinomycin during mitotic cell cycle","type":"related"},{"name":"resistance to valinomycin during vegetative growth","type":"exact"},{"name":"resistant to valinomycin","type":"exact"}],"termid":"FYPO:0000768"}


id: GO:0036529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of glyoxal from a glycated protein, to form glycolate and a deglycated protein.","definition_xrefs":["GOC:PARL","PMID:25416785","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein deglycation","termid":"GO:0036525"},{"relation_name":"is_a","term_name":"glycolate biosynthetic process","termid":"GO:0046295"},{"relation_name":"is_a","term_name":"glyoxal metabolic process","termid":"GO:1903189"}],"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:0008150","GO:0044281"],"is_obsolete":false,"name":"protein deglycation, glyoxal removal","synonyms":[{"name":"protein deglycation of glyoxal-glycated protein","type":"related"}],"termid":"GO:0036529"}


id: MONDO:0003491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rectum squamous cell carcinoma (obsolete MONDO:0003491)","termid":"MONDO:0003491","xrefs":{"Monarch":{"xref_id":"0003491"}}}


id: PBO:0017969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetolactate synthase regulatory unit Ilv6 (predicted)","termid":"PBO:0017969"}


id: FYPO:0002247
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of glucose binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal monosaccharide binding","termid":"FYPO:0002245"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"decreased glucose binding","synonyms":[{"name":"reduced glucose binding","type":"exact"}],"termid":"FYPO:0002247"}


id: MONDO:0018491
data:
  {"annotated_genes":["SJAG_02791","SJAG_02313"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009736"},{"annotations":[86103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014466"},{"annotations":[86145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011152"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurometabolic disorder due to serine deficiency","termid":"MONDO:0018162"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02313":null,"SJAG_02791":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":"3-phosphoglycerate dehydrogenase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0580190","Orphanet:422519","ICD9:270.7","icd11.foundation:460538363","SCTID:303098002","MEDGEN:663158"],"termid":"MONDO:0018491","terms_by_termid":{"MONDO:0009736":null,"MONDO:0011152":null,"MONDO:0014466":null},"xrefs":{"Monarch":{"xref_id":"0018491"}}}


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


id: MONDO:0018060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital deficiencies of fibrinogen are coagulation disorders characterized by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenemia (complete absence of fibrinogen) and hypofibrinogenemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenemia may be frequently combined (hypodysfibrinogenemia).","definition_xrefs":["Orphanet:335"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"},{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"}],"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":"congenital fibrinogen deficiency","secondary_identifiers":["UMLS:C2062367","MEDGEN:412157","GARD:2320","icd11.foundation:1452989457"],"synonyms":[{"name":"congenital fibrinogen deficiency","type":"exact"},{"name":"fibrinogen deficiency, congenital","type":"related"}],"termid":"MONDO:0018060","xrefs":{"Monarch":{"xref_id":"0018060"}}}


id: PBO:0074993
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 115-4","termid":"PBO:0074993"}


id: MONDO:0850450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute biphenotypic leukemia that is characterized by blasts which carry a translocation between the MLL (KMT2A) gene at 11q23.3 and another gene partner.","definition_xrefs":["DOID:0081037"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute biphenotypic leukemia","termid":"MONDO:0020322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"mixed phenotype acute leukemia with MLL rearranged","termid":"MONDO:0850450","xrefs":{"Monarch":{"xref_id":"0850450"}}}


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


id: PBO:0042385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD300a molecule","termid":"PBO:0042385"}


id: PR:Q09896
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A brain protein 44 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00081","PANTHER:PTHR14154:SF2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyruvate carrier 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.09","secondary_identifiers":["UniProtKB:Q09896"],"synonyms":[{"name":"MPC2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MPC2","type":"exact"}],"termid":"PR:Q09896"}


id: PBO:0073449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted frizzled related protein 4","termid":"PBO:0073449"}


id: GO:0032396
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a MHC class I protein complex to mediate signaling that inhibits activation of a lymphocyte.","definition_xrefs":["PMID:11858820","PMID:9368779","GOC:add","PMID:9597134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MHC class I receptor activity","termid":"GO:0032393"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"inhibitory MHC class I receptor activity","termid":"GO:0032396"}


id: GO:0015399
data:
  {"annotated_genes":["SJAG_00136","SJAG_01817","SJAG_02023","SJAG_02782","SJAG_01355","SJAG_03515","SJAG_01190","SJAG_03406","SJAG_02504","SJAG_03358","SJAG_07007","SJAG_04167","SJAG_03785","SJAG_04277","SJAG_03337","SJAG_02077","SJAG_01490","SJAG_01400","SJAG_01447","SJAG_03490","SJAG_02399","SJAG_02602","SJAG_03415","SJAG_01471","SJAG_02457","SJAG_MIT03","SJAG_MIT04","SJAG_03497","SJAG_00976","SJAG_00212","SJAG_00516","SJAG_01669","SJAG_00601","SJAG_MIT20","SJAG_05213","SJAG_01397","SJAG_01077","SJAG_05629","SJAG_01435","SJAG_03502","SJAG_03866","SJAG_04757","SJAG_01129","SJAG_01597","SJAG_MIT13","SJAG_07006","SJAG_04258","SJAG_05294","SJAG_03560","SJAG_00755","SJAG_02646","SJAG_01344","SJAG_04015","SJAG_03363","SJAG_03850","SJAG_04955","SJAG_01879","SJAG_04152","SJAG_01913","SJAG_00373"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88483],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140481"},{"annotations":[107820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015410"},{"annotations":[106347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015421"},{"annotations":[117330,96249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044604"},{"annotations":[111482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140679"},{"annotations":[100064,100777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140359"},{"annotations":[95268,117079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008559"},{"annotations":[94653,114222,100206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019829"},{"annotations":[117333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042626"},{"annotations":[118175,118202,118203,113791,118174,88432,107437,114592,91151,113360,115953,87411,118153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004129"},{"annotations":[111992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008137"},{"annotations":[100818,107824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005388"},{"annotations":[107014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043682"},{"annotations":[100208,114223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015662"},{"annotations":[107015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140581"},{"annotations":[111485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008556"},{"annotations":[111486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"},{"annotations":[112905,86917,86916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008553"},{"annotations":[111487],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008554"},{"annotations":[94654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140358"},{"annotations":[110943,98738,106750,90104,96081,104351,102461,106729,99507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015450"},{"annotations":[109026,99133,99203,100824,95814,101856,89055,91254,103088,117854,87251,98115,94851,89371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046961"},{"annotations":[103667,103254,112534,116816,117289,118179,107120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008121"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a solute from one side of a membrane to the other, up the solute's concentration gradient, by binding the solute and undergoing a series of conformational changes. Transport works equally well in either direction and is powered by a primary energy source. Primary energy sources known to be coupled to transport are chemical such as ATP hydrolysis, redox energy and photon energy.","definition_xrefs":["GOC:mtg_transport","PMID:31613498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"active transmembrane transporter activity","termid":"GO:0022804"}],"gene_count":60,"genes_by_uniquename":{"SJAG_00136":null,"SJAG_00212":null,"SJAG_00373":null,"SJAG_00516":null,"SJAG_00601":null,"SJAG_00755":null,"SJAG_00976":null,"SJAG_01077":null,"SJAG_01129":null,"SJAG_01190":null,"SJAG_01344":null,"SJAG_01355":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01435":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01490":null,"SJAG_01597":null,"SJAG_01669":null,"SJAG_01817":null,"SJAG_01879":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02077":null,"SJAG_02399":null,"SJAG_02457":null,"SJAG_02504":null,"SJAG_02602":null,"SJAG_02646":null,"SJAG_02782":null,"SJAG_03337":null,"SJAG_03358":null,"SJAG_03363":null,"SJAG_03406":null,"SJAG_03415":null,"SJAG_03490":null,"SJAG_03497":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03560":null,"SJAG_03785":null,"SJAG_03850":null,"SJAG_03866":null,"SJAG_04015":null,"SJAG_04152":null,"SJAG_04167":null,"SJAG_04258":null,"SJAG_04277":null,"SJAG_04757":null,"SJAG_04955":null,"SJAG_05213":null,"SJAG_05294":null,"SJAG_05629":null,"SJAG_07006":null,"SJAG_07007":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT20":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:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"primary active transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:7.-.-.-","TC:3"],"synonyms":[{"name":"primary active transporter","type":"related"}],"termid":"GO:0015399","terms_by_termid":{"GO:0004129":null,"GO:0005388":null,"GO:0008121":null,"GO:0008137":null,"GO:0008553":null,"GO:0008554":null,"GO:0008556":null,"GO:0008559":null,"GO:0008900":null,"GO:0015410":null,"GO:0015421":null,"GO:0015450":null,"GO:0015662":null,"GO:0019829":null,"GO:0042626":null,"GO:0043682":null,"GO:0044604":null,"GO:0046961":null,"GO:0140358":null,"GO:0140359":null,"GO:0140481":null,"GO:0140581":null,"GO:0140679":null}}


id: FYPO:0005764
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 replication fork pausing occurs to a greater extent than normal in regions containing G-quartet (G4) motifs.","definition_xrefs":["PomBase:mah","PMID:27611590","PMID:25471935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased replication fork pausing","termid":"FYPO:0005763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"increased replication fork pausing at G4 motif","synonyms":[{"name":"increased replication fork pausing at G-quadruplex","type":"exact"},{"name":"increased replication fork pausing at G-quartet","type":"exact"},{"name":"increased replication fork pausing at G4 motif during mitotic cell cycle","type":"related"},{"name":"increased replication fork pausing at G4 motif during vegetative growth","type":"exact"}],"termid":"FYPO:0005764"}


id: GO:0071928
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of tyramine binding to a cell surface receptor.","definition_xrefs":["PMID:15355245","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"octopamine or tyramine signaling pathway","termid":"GO:0007211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"tyramine signaling pathway","synonyms":[{"name":"tyramine signalling pathway","type":"exact"}],"termid":"GO:0071928"}


id: PATO:0001385
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A ploidy quality inhering in a bearer by virtue of the bearer's containing a non-integral multiple of the monoploid number, due to extra or missing chromosomes.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Aneuploid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ploidy","termid":"PATO:0001374"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneuploid","termid":"PATO:0001385"}


id: MONDO:0009690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the DOK7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"},{"relation_name":"is_a","term_name":"postsynaptic congenital myasthenic syndrome","termid":"MONDO:0020344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"congenital myasthenic syndrome 10","secondary_identifiers":["OMIM:609456","MESH:C563716","OMIM:254300","SCTID:230687001","ICD9:358.00","GARD:15206","DOID:0110638","UMLS:C1850792","MEDGEN:376880","DOID:0110668"],"synonyms":[{"name":"CMS Ib","type":"related"},{"name":"CMS10","type":"exact"},{"name":"CMS1B","type":"related"},{"name":"Cms Ib","type":"related"},{"name":"Cms Ib, formerly","type":"related"},{"name":"DOK7 congenital myasthenic syndrome","type":"exact"},{"name":"LGM","type":"exact"},{"name":"congenital muscular dystrophy merosin-positive","type":"exact"},{"name":"congenital myasthenic syndrome 10","type":"exact"},{"name":"congenital myasthenic syndrome caused by mutation in DOK7","type":"exact"},{"name":"congenital myasthenic syndrome type 10","type":"exact"},{"name":"congenital myasthenic syndrome type IB","type":"related"},{"name":"congenital myasthenic syndrome type IB, formerly","type":"related"},{"name":"familial limb-girdle myasthenia","type":"exact"},{"name":"muscular dystrophy, congenital, merosin-POSITIVE","type":"related"},{"name":"myasthenia, limb-girdle, familial","type":"related"},{"name":"myasthenia, limb-girdle, familial, formerly","type":"related"},{"name":"myasthenic myopathy","type":"related"},{"name":"myasthenic myopathy, formerly","type":"related"},{"name":"myasthenic syndrome, congenital, 10","type":"related"},{"name":"myasthenic syndrome, congenital, type 10","type":"exact"}],"termid":"MONDO:0009690","xrefs":{"Monarch":{"xref_id":"0009690"}}}


id: PBO:0034446
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_okadaic_acid","termid":"PBO:0034446"}


id: SO:0001735
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 79th residue (a lysine), from the start of the H3 histone protein is methylated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_methylation_site","termid":"SO:0001701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H3K79_methylation_site","synonyms":[{"name":"H3K79 methylation site","type":"exact"}],"termid":"SO:0001735"}


id: PBO:0005282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sim4 and Mal2 associated (4 and 2 associated) protein 4","termid":"PBO:0005282"}


id: MONDO:0023197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frontonasal dysplasia Klippel feil syndrome","termid":"MONDO:0023197","xrefs":{"Monarch":{"xref_id":"0023197"}}}


id: PBO:0012010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein, G-patch domain, PINX1 family (predicted)","termid":"PBO:0012010"}


id: GO:1904634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glomerular visceral epithelial cell apoptotic process.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:23692924"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell apoptotic process","termid":"GO:1904036"},{"relation_name":"is_a","term_name":"regulation of podocyte apoptotic process","termid":"GO:1904633"},{"relation_name":"negatively_regulates","term_name":"podocyte apoptotic process","termid":"GO:1903210"}],"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 podocyte apoptotic process","synonyms":[{"name":"down regulation of glomerular podocyte apoptosis","type":"narrow"},{"name":"down regulation of glomerular podocyte apoptotic process","type":"exact"},{"name":"down regulation of glomerular visceral epithelial cell apoptosis","type":"narrow"},{"name":"down regulation of glomerular visceral epithelial cell apoptotic process","type":"exact"},{"name":"down regulation of podocyte apoptosis","type":"narrow"},{"name":"down regulation of podocyte apoptotic process","type":"exact"},{"name":"down-regulation of glomerular podocyte apoptosis","type":"narrow"},{"name":"down-regulation of glomerular podocyte apoptotic process","type":"exact"},{"name":"down-regulation of glomerular visceral epithelial cell apoptosis","type":"narrow"},{"name":"down-regulation of glomerular visceral epithelial cell apoptotic process","type":"exact"},{"name":"down-regulation of podocyte apoptosis","type":"narrow"},{"name":"down-regulation of podocyte apoptotic process","type":"exact"},{"name":"downregulation of glomerular podocyte apoptosis","type":"narrow"},{"name":"downregulation of glomerular podocyte apoptotic process","type":"exact"},{"name":"downregulation of glomerular visceral epithelial cell apoptosis","type":"narrow"},{"name":"downregulation of glomerular visceral epithelial cell apoptotic process","type":"exact"},{"name":"downregulation of podocyte apoptosis","type":"narrow"},{"name":"downregulation of podocyte apoptotic process","type":"exact"},{"name":"inhibition of glomerular podocyte apoptosis","type":"narrow"},{"name":"inhibition of glomerular podocyte apoptotic process","type":"narrow"},{"name":"inhibition of glomerular visceral epithelial cell apoptosis","type":"narrow"},{"name":"inhibition of glomerular visceral epithelial cell apoptotic process","type":"narrow"},{"name":"inhibition of podocyte apoptosis","type":"narrow"},{"name":"inhibition of podocyte apoptotic process","type":"narrow"},{"name":"negative regulation of glomerular podocyte apoptosis","type":"narrow"},{"name":"negative regulation of glomerular podocyte apoptotic process","type":"exact"},{"name":"negative regulation of glomerular visceral epithelial cell apoptosis","type":"narrow"},{"name":"negative regulation of glomerular visceral epithelial cell apoptotic process","type":"exact"},{"name":"negative regulation of podocyte apoptosis","type":"exact"}],"termid":"GO:1904634"}


id: PBO:0113538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar membrane zinc transporter; transports zinc from storage in vacuole to cytoplasm when needed; transcription induced under conditions of zinc deficiency; targeted to vacuole via AP-3 pathway","termid":"PBO:0113538"}


id: GO:0043451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of an alkene, any acyclic branched or unbranched hydrocarbon having one carbon-carbon double bond and the general formula CnH2n.","definition_xrefs":["Wikipedia:Alkene","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkene metabolic process","termid":"GO:0043449"},{"relation_name":"is_a","term_name":"hydrocarbon catabolic process","termid":"GO:0120253"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"}],"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":"alkene catabolic process","synonyms":[{"name":"alkene breakdown","type":"exact"},{"name":"alkene catabolism","type":"exact"},{"name":"alkene degradation","type":"exact"}],"termid":"GO:0043451"}


id: PBO:0114495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that regulates peroxisome populations; interacts with Pex11p, Pex25p, and Pex27p to control both constitutive peroxisome division and peroxisome morphology and abundance during peroxisome proliferation; mediates contacts between mitochondria and peroxisomes that stimulate transport of citrate, converted from acetyl-CoA, from peroxisomes to mitochondria; peroxisomal integral membrane protein that is enriched at peroxisomal-mitochondrial (PerMit) contact sites","termid":"PBO:0114495"}


id: GO:0006590
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of either of the compounds secreted by the thyroid gland, mainly thyroxine and triiodothyronine. This is achieved by the iodination and joining of tyrosine molecules to form the precursor thyroglobin, proteolysis of this precursor gives rise to the thyroid hormones.","definition_xrefs":["GOC:jl","ISBN:0716720094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid hormone metabolic process","termid":"GO:0042403"}],"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":"thyroid hormone generation","termid":"GO:0006590"}


id: MONDO:0000491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A ischemia that involves the limb.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ischemic disease","termid":"MONDO:0005053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"limb ischemia","secondary_identifiers":["DOID:0050852","SCTID:21631000119105","UMLS:C2945695","MEDGEN:754513"],"synonyms":[{"name":"ischaemic disease of limb","type":"exact"},{"name":"ischemic disease of limb","type":"exact"},{"name":"limb ischaemic disease","type":"exact"},{"name":"limb ischemia","type":"exact"},{"name":"limb ischemic disease","type":"exact"}],"termid":"MONDO:0000491","xrefs":{"Monarch":{"xref_id":"0000491"}}}


id: PBO:0056505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP3K12 binding inhibitory protein 1","termid":"PBO:0056505"}


id: MONDO:0957230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte/zygote/embryo maturation arrest 18","secondary_identifiers":["MEDGEN:1841077","OMIM:620332","UMLS:C5830441"],"termid":"MONDO:0957230","xrefs":{"Monarch":{"xref_id":"0957230"}}}


