# terms

id: MONDO:0013130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any isolated microphthalmia in which the cause of the disease is a mutation in the GDF6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"isolated microphthalmia 4","secondary_identifiers":["UMLS:C2751307","MEDGEN:414346","DOID:0060836","OMIM:613094","MESH:C567757"],"synonyms":[{"name":"GDF6 isolated microphthalmia","type":"exact"},{"name":"MCOP4","type":"exact"},{"name":"isolated microphthalmia caused by mutation in GDF6","type":"exact"},{"name":"isolated microphthalmia type 4","type":"exact"},{"name":"microphthalmia, isolated 4","type":"related"},{"name":"microphthalmia, isolated type 4","type":"exact"}],"termid":"MONDO:0013130","xrefs":{"Monarch":{"xref_id":"0013130"}}}


id: MONDO:0001609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A decrease in the number of mature granulocytes (neutrophils, eosinophils, and basophils) in the peripheral blood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukopenia","termid":"MONDO:0003785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"agranulocytosis","secondary_identifiers":["UMLS:C0001824","ICD9:288.8","NCIT:C2863","ICD10CM:D70","icd11.foundation:1913706366","MEDGEN:7932","MESH:D000380","ICD10WHO:D70","SCTID:417672002","DOID:12987"],"synonyms":[{"name":"Granulocytopenic disorder","type":"exact"},{"name":"Granulopenia","type":"exact"},{"name":"granulocytopenia","type":"exact"}],"termid":"MONDO:0001609","xrefs":{"Monarch":{"xref_id":"0001609"}}}


id: PBO:0049279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G1 to S phase transition 2","termid":"PBO:0049279"}


id: PBO:0075132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNRNP40 pseudogene 1","termid":"PBO:0075132"}


id: PBO:0111826
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tf2-type transposon","termid":"PBO:0111826"}


id: GO:2001229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of response to gamma radiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of response to gamma radiation","termid":"GO:2001228"},{"relation_name":"negatively_regulates","term_name":"response to gamma radiation","termid":"GO:0010332"}],"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 response to gamma radiation","synonyms":[{"name":"negative regulation of response to gamma ray","type":"related"},{"name":"negative regulation of response to gamma-ray photon","type":"related"}],"termid":"GO:2001229"}


id: PBO:0002563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"electron transfer flavoprotein alpha subunit (predicted)","termid":"PBO:0002563"}


id: PBO:0028658
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_anaphase-promoting_complex-dependent_proteasomal_ubiquitin-dependent_protein_catabolic_process","termid":"PBO:0028658"}


id: PBO:0091017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudouridine-5'-phosphatase Pud1","termid":"PBO:0091017"}


id: FYPO:0001274
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 measured in a cell during a cellular response to hypoxia is lower than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"},{"relation_name":"is_a","term_name":"altered protein level during cellular response to hypoxia","termid":"FYPO:0001549"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein level during cellular response to hypoxia","synonyms":[{"name":"decreased protein accumulation during cellular response to hypoxia","type":"related"},{"name":"decreased protein level during cellular response to hypoxia during mitotic cell cycle","type":"related"},{"name":"decreased protein level during cellular response to hypoxia during vegetative growth","type":"exact"},{"name":"decreased protein level during cellular response to hypoxic stress","type":"exact"},{"name":"decreased protein level during cellular response to lowered oxygen tension","type":"exact"},{"name":"reduced protein level during cellular response to hypoxia","type":"exact"}],"termid":"FYPO:0001274"}


id: MONDO:0003468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A synovial sarcoma characterized by the presence of both an epithelial and a spindle cell component.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synovial sarcoma","termid":"MONDO:0010434"}],"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":"biphasic synovial sarcoma","secondary_identifiers":["DOID:5492","MEDGEN:137773","NCIT:C4279","UMLS:C0334507","ICDO:9043/3"],"synonyms":[{"name":"biphasic sarcoma of synovium","type":"exact"},{"name":"biphasic sarcoma of the synovium","type":"exact"},{"name":"synovial sarcoma, biphasic","type":"exact"},{"name":"synovial sarcoma, biphasic (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003468","xrefs":{"Monarch":{"xref_id":"0003468"}}}


id: MONDO:0020597
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An angiokeratoma that is located on the scrotum.","definition_xrefs":["NCIT:C7752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"scrotal hemangioma","termid":"MONDO:0003951"},{"relation_name":"is_a","term_name":"angiokeratoma of Fordyce","termid":"MONDO:0003954"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"angiokeratoma of scrotum","secondary_identifiers":["SCTID:735082004"],"synonyms":[{"name":"angiokeratoma of fordyce","type":"broad"},{"name":"angiokeratoma of scrotum","type":"exact"},{"name":"angiokeratoma of the scrotum","type":"exact"},{"name":"fordyce angiokeratoma","type":"broad"},{"name":"fordyce-type angiokeratoma of scrotum","type":"exact"},{"name":"fordyce-type angiokeratoma of the scrotum","type":"exact"},{"name":"scrotal angiokeratoma","type":"exact"},{"name":"scrotal fordyce-type angiokeratoma","type":"exact"},{"name":"scrotum angiokeratoma","type":"exact"}],"termid":"MONDO:0020597","xrefs":{"Monarch":{"xref_id":"0020597"}}}


id: PATO:0002372
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A viviparous organism that has given birth five or more times.","definition_xrefs":["wiki:http://en.wikipedia.org/wiki/Parity_(biology)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiparous","termid":"PATO:0002369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grand multi[arous","termid":"PATO:0002372"}


id: MONDO:0007459
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":"dilution, pigmentary","secondary_identifiers":["UMLS:C1876214","MESH:C566872","SCTID:23006000","MEDGEN:406294","OMIM:126070"],"synonyms":[{"name":"Albinoidism, oculocutaneous, autosomal dominant","type":"related"},{"name":"albinism, partial","type":"related"},{"name":"dilution, pigmentary","type":"exact"},{"name":"hypomelanotic disorder","type":"related"},{"name":"hypopigmentation","type":"related"}],"termid":"MONDO:0007459","xrefs":{"Monarch":{"xref_id":"0007459"}}}


id: MONDO:0060489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"46,XX testicular disorder of sex development","termid":"MONDO:0100249"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"46,XX sex reversal 4","secondary_identifiers":["DOID:0111764","OMIM:617480","MEDGEN:1373282","UMLS:C4479552"],"synonyms":[{"name":"46, XX sex reversal 4","type":"exact"},{"name":"46,XX SEX reversal 4","type":"related"},{"name":"46,XX Sex reversal, Sry-Negative","type":"related"},{"name":"SRXX4","type":"related"}],"termid":"MONDO:0060489","xrefs":{"Monarch":{"xref_id":"0060489"}}}


id: PBO:0038693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTB pseudogene 4","termid":"PBO:0038693"}


id: GO:0141083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts the host signal transduction pathways leading to the production of reactive oxygen species as part of the host innate immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:27473656","PMID:31375544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cellular process","termid":"GO:0044068"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host defense response","termid":"GO:0052031"}],"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 reactive oxygen species generation","synonyms":[{"name":"inhibition by organism of defense-related host active oxygen species production","type":"exact"}],"termid":"GO:0141083"}


id: PBO:0029728
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_1,3-beta-D-glucan_synthase_activity_during_growth_on_aculeacin_A","termid":"PBO:0029728"}


id: GO:0005945
data:
  {"annotated_genes":["SJAG_00605"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[79614],"is_not":false,"summary":null,"term":"GO:0005945"}]},"cv_name":"cellular_component","definition":"A protein complex that possesses 6-phosphofructokinase activity; homodimeric, homooctameric, and allosteric homotetrameric forms are known.","definition_xrefs":["GOC:vw","ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex, transferring phosphorus-containing groups","termid":"GO:0061695"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00605":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005829","GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"6-phosphofructokinase complex","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0005945","terms_by_termid":{"GO:0005945":null}}


id: GO:0099520
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any ion antiporter activity, occurring in the presynaptic membrane, that is involved in regulation of presynaptic membrane potential.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"monoatomic ion antiporter activity involved in regulation of presynaptic membrane potential","synonyms":[{"name":"ion antiporter activity involved in regulation of pre-synaptic membrane potential","type":"exact"},{"name":"ion antiporter activity involved in regulation of presynaptic membrane potential","type":"exact"}],"termid":"GO:0099520"}


id: GO:1901950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement a dense core granule within a cell.","definition_xrefs":["GOC:kmv","GOC:TermGenie","PMID:23358451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytosolic transport","termid":"GO:0016482"},{"relation_name":"is_a","term_name":"dense core granule localization","termid":"GO:0032253"},{"relation_name":"is_a","term_name":"establishment of vesicle localization","termid":"GO:0051650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"dense core granule transport","synonyms":[{"name":"dense core vesicle transport","type":"exact"}],"termid":"GO:1901950"}


id: PBO:0083353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified gene JJJ1/YNL227C","termid":"PBO:0083353"}


id: PBO:0077241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane and coiled-coil domains 2","termid":"PBO:0077241"}


id: GO:0008520
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: L-ascorbate(out) + Na+(out) = L-ascorbate(in) + Na+(in).","definition_xrefs":["PMID:18094143","GOC:yaf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic acid:sodium symporter activity","termid":"GO:0005343"},{"relation_name":"is_a","term_name":"carbohydrate:monoatomic cation symporter activity","termid":"GO:0005402"},{"relation_name":"is_a","term_name":"monosaccharide transmembrane transporter activity","termid":"GO:0015145"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"L-ascorbate:sodium symporter activity","secondary_identifiers":["RHEA:69883","TC:2.A.40.6.1","GO:0070890"],"synonyms":[{"name":"sodium-dependent L-ascorbate transmembrane transporter activity","type":"related"},{"name":"sodium-dependent L-ascorbic acid transporter","type":"related"}],"termid":"GO:0008520"}


id: GO:0141124
data:
  {"annotated_genes":["SJAG_01885","SJAG_00318","SJAG_03592","SJAG_04503","SJAG_03793","SJAG_00845","SJAG_03342","SJAG_02000","SJAG_02342","SJAG_03361","SJAG_00424","SJAG_04873","SJAG_03453","SJAG_03376","SJAG_00229","SJAG_01386","SJAG_03486","SJAG_04551","SJAG_03631","SJAG_02429","SJAG_02013","SJAG_01114","SJAG_04522","SJAG_02923","SJAG_06622","SJAG_03903","SJAG_03936","SJAG_00082","SJAG_03340","SJAG_00027","SJAG_03185","SJAG_00975","SJAG_03501","SJAG_00296","SJAG_06592","SJAG_03893","SJAG_02520","SJAG_01805","SJAG_02878","SJAG_04329","SJAG_03508","SJAG_01181","SJAG_00117","SJAG_00526","SJAG_02592","SJAG_04776","SJAG_03488","SJAG_04777","SJAG_02514","SJAG_03681","SJAG_02392","SJAG_06270","SJAG_03353","SJAG_01787","SJAG_04462","SJAG_04471","SJAG_04943","SJAG_02486","SJAG_03705","SJAG_03879","SJAG_01345","SJAG_03048","SJAG_04455","SJAG_04668","SJAG_03799","SJAG_04666","SJAG_02135","SJAG_04464","SJAG_03263","SJAG_01464","SJAG_03828","SJAG_04871","SJAG_00169","SJAG_02183","SJAG_01188","SJAG_04597","SJAG_02233","SJAG_00883","SJAG_03753","SJAG_01718","SJAG_05000","SJAG_00990","SJAG_03969","SJAG_02858","SJAG_04825","SJAG_01978","SJAG_00781","SJAG_04468","SJAG_02379","SJAG_00610","SJAG_02232","SJAG_00600","SJAG_03384","SJAG_01790","SJAG_06621","SJAG_02072","SJAG_02945","SJAG_00993","SJAG_01587","SJAG_01199","SJAG_00078","SJAG_03625","SJAG_02169","SJAG_03802"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74816,81345,97612,91873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097720"},{"annotations":[97168,116991,90687,66597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019722"},{"annotations":[115743,117845,116083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061762"},{"annotations":[101667,66244,110557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000196"},{"annotations":[98947,71725,82139,109241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140469"},{"annotations":[105827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007254"},{"annotations":[57351,99486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000165"},{"annotations":[115730,100515],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0106057"},{"annotations":[95345,103330,106597,98948,107165,117944],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903138"},{"annotations":[117945,91141,95467,94527,98950,116688],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903753"},{"annotations":[106690,87660],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0180040"},{"annotations":[74086],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0046580"},{"annotations":[73301],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0035024"},{"annotations":[106785,106652,107095,92932,104587,90192,91209,99101,74667,92403,109741,92318,95132,100795,115505],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0031030"},{"annotations":[101281,59334,93850,105828,71824,74890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0038066"},{"annotations":[65812,88696,92798,95881,96549,105829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071507"},{"annotations":[110558,101671],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0050850"},{"annotations":[117518,69403,87534,90234,91892,88900],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903139"},{"annotations":[108508,108512,112069,108510,94753,108511,108509,111403,108506,108507,117908,116980],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1900745"},{"annotations":[87596,103231,114223,115191,90314],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0062038"},{"annotations":[89466,93285,101913,110100,86980],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0031031"},{"annotations":[104607,110595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031291"},{"annotations":[82213,76486],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0043408"},{"annotations":[71763,76640],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032483"},{"annotations":[104038,112957,89427],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031029"},{"annotations":[77092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007266"},{"annotations":[76055,100464,93898,88705,105939,106696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031028"}]},"cv_name":"biological_process","definition":"An intracellular signaling module that is part of larger signaling pathways that can be initiated either intracellularly or by cell surface receptors. 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id: PBO:0027260
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-S10_phosphorylation","termid":"PBO:0027260"}


id: GO:1903131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a mononuclear cell.","definition_xrefs":["CL:0000842","PMID:24759906","GO_REF:0000086","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte differentiation","termid":"GO:0002521"}],"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":"mononuclear cell differentiation","termid":"GO:1903131"}


id: PBO:0072829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SANT and BTB domain regulator of CSR","termid":"PBO:0072829"}


id: GO:0099589
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the biogenic amine serotonin and transmitting a signal across a membrane by activating some effector activity. Serotonin (5-hydroxytryptamine) is a neurotransmitter and hormone found in vertebrates and invertebrates.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"serotonin receptor activity","termid":"GO:0099589"}


id: PBO:0117187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DRAM1 antisense RNA 1","termid":"PBO:0117187"}


id: GO:0019517
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L- threonine (the L-enantiomer of 2-amino-3-hydroxybutyric acid) to form the compound methylglyoxal, which is subsequently converted to D-lactate.","definition_xrefs":["GOC:bf","GOC:jl","MetaCyc:THRDLCTCAT-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lactate metabolic process","termid":"GO:0006089"},{"relation_name":"is_a","term_name":"L-threonine catabolic process","termid":"GO:0006567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"L-threonine catabolic process to D-lactate","synonyms":[{"name":"L-threonine breakdown to D-lactate","type":"exact"},{"name":"L-threonine catabolic process to (R)-lactate","type":"broad"},{"name":"L-threonine catabolic process to methylglyoxal","type":"exact"},{"name":"L-threonine catabolic process to pyruvate","type":"related"},{"name":"L-threonine catabolism to D-lactate","type":"exact"},{"name":"L-threonine degradation to D-lactate","type":"exact"},{"name":"threonine catabolic process to D-lactate","type":"broad"}],"termid":"GO:0019517"}


id: GO:0035423
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that terminates the activity of the active enzyme MAP kinase in the context of an innate immune response, a defense response mediated by germline encoded components that directly recognize components of potential pathogens.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete inactivation of MAPK activity involved in innate immune response (obsolete GO:0035423)","termid":"GO:0035423"}


id: PBO:0083456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene HAC1/YFL031W; YFL032W is not an essential gene","termid":"PBO:0083456"}


id: MONDO:0012715
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"migraine with or without aura, susceptibility to","termid":"MONDO:0100246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migraine with or without aura, susceptibility to, 12","secondary_identifiers":["MEDGEN:388698","OMIM:611706","UMLS:C2673676"],"synonyms":[{"name":"MGR12","type":"exact"},{"name":"migraine with or without aura, susceptibility to, 12","type":"exact"},{"name":"migraine, with or without aura, susceptibility to, 12","type":"exact"}],"termid":"MONDO:0012715","xrefs":{"Monarch":{"xref_id":"0012715"}}}


id: PBO:0066302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinol binding protein 4","termid":"PBO:0066302"}


id: GO:0048533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized floral cell acquires the specialized features of a sporocyte. Sporocytes are the haploid spores of angiosperms. Once formed, they undergo meiotic divisions to form microspores and megaspores.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"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":"sporocyte differentiation","synonyms":[{"name":"sporocyte development","type":"narrow"},{"name":"sporocyte morphogenesis","type":"related"}],"termid":"GO:0048533"}


id: GO:0102365
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: taxusin + NADPH + O2 + H+ = 2-alpha-hydroxytaxusin + NADP + H2O. Also converts 7beta-hydroxytaxusin to 2alpha,7beta-dihydroxytaxusin.","definition_xrefs":["PMID:15178487","EC:1.14.14.183"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"taxoid 2alpha-hydroxylase activity","synonyms":[{"name":"taxusin 2-alpha-hydroxylase activity","type":"exact"}],"termid":"GO:0102365"}


id: PBO:0089097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, human RNF13 family homolog, unknown biological role","termid":"PBO:0089097"}


id: MONDO:1010580
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial goiter that occurs in golden hamster.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial goiter, non-human animal","termid":"MONDO:1010053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial goiter, golden hamster","secondary_identifiers":["OMIA:000424-10036"],"termid":"MONDO:1010580","xrefs":{"Monarch":{"xref_id":"1010580"}}}


id: GO:0045876
data:
  {"annotated_genes":["SJAG_00823"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106963],"is_not":false,"summary":null,"term":"GO:0045876"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of sister chromatid cohesion.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sister chromatid cohesion","termid":"GO:0007063"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"is_a","term_name":"positive regulation of chromosome organization","termid":"GO:2001252"},{"relation_name":"positively_regulates","term_name":"sister chromatid cohesion","termid":"GO:0007062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00823":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"positive regulation of sister chromatid cohesion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of sister chromatid cohesion","type":"narrow"},{"name":"stimulation of sister chromatid cohesion","type":"narrow"},{"name":"up regulation of sister chromatid cohesion","type":"exact"},{"name":"up-regulation of sister chromatid cohesion","type":"exact"},{"name":"upregulation of sister chromatid cohesion","type":"exact"}],"termid":"GO:0045876","terms_by_termid":{"GO:0045876":null}}


id: PBO:0058642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6771","termid":"PBO:0058642"}


id: PBO:0070786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 16","termid":"PBO:0070786"}


id: PR:O94428
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug168 gene.","definition_xrefs":["UniProtKB:O94428","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":"meiotically up-regulated gene 168 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC660.09","synonyms":[{"name":"Spom972h-mug168","type":"exact"}],"termid":"PR:O94428"}


id: PBO:0059665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 31","termid":"PBO:0059665"}


id: PBO:0046780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EYA transcriptional coactivator and phosphatase 1","termid":"PBO:0046780"}


id: MONDO:0003990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive malignant tumor that arises from the breast. It is characterized by the presence of spindle-shaped myoepithelial cells. Mitoses are present. Rarely, local recurrences and distant metastases have been reported.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast myoepithelial tumor","termid":"MONDO:0002483"},{"relation_name":"is_a","term_name":"malignant myoepithelioma","termid":"MONDO:0003158"},{"relation_name":"is_a","term_name":"invasive breast carcinoma","termid":"MONDO:0006256"}],"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":"malignant breast myoepithelioma","secondary_identifiers":["DOID:6776","MEDGEN:309375","NCIT:C40395","UMLS:C1518167"],"synonyms":[{"name":"breast malignant myoepithelioma","type":"exact"},{"name":"breast myoepithelial carcinoma","type":"exact"},{"name":"malignant breast myoepithelioma","type":"exact"}],"termid":"MONDO:0003990","xrefs":{"Monarch":{"xref_id":"0003990"}}}


id: MONDO:0044885
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign adipose tissue neoplasm of the tonsils.","definition_xrefs":["NCIT:C5989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"},{"relation_name":"is_a","term_name":"benign neoplasm of tonsil","termid":"MONDO:0021513"}],"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":"tonsillar lipoma","secondary_identifiers":["MEDGEN:234431","UMLS:C1336764"],"synonyms":[{"name":"lipoma of the tonsil","type":"exact"},{"name":"lipoma of tonsil","type":"exact"},{"name":"tonsil lipoma","type":"exact"},{"name":"tonsillar lipoma","type":"exact"}],"termid":"MONDO:0044885","xrefs":{"Monarch":{"xref_id":"0044885"}}}


id: GO:0075103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism modulates the frequency, rate or extent of calcium or calmodulin-mediated signal transduction in the symbiont. 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 modulation by host of symbiont calcium or calmodulin-mediated signal transduction (obsolete GO:0075103)","synonyms":[{"name":"modulation by host of symbiont Ca++ or calmodulin-mediated signal transduction","type":"exact"}],"termid":"GO:0075103"}


id: GO:2000871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of progesterone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of female gonad development","termid":"GO:2000195"},{"relation_name":"is_a","term_name":"negative regulation of steroid hormone secretion","termid":"GO:2000832"},{"relation_name":"is_a","term_name":"regulation of progesterone secretion","termid":"GO:2000870"},{"relation_name":"negatively_regulates","term_name":"progesterone secretion","termid":"GO:0042701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of progesterone secretion","termid":"GO:2000871"}


id: PBO:0047484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferredoxin 1","termid":"PBO:0047484"}


id: PBO:0054655
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 2060","termid":"PBO:0054655"}


id: PBO:0062473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily G member 1","termid":"PBO:0062473"}


id: PBO:0072175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S16 pseudogene 2","termid":"PBO:0072175"}


id: PBO:0078020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 10","termid":"PBO:0078020"}


id: PBO:0061838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opioid growth factor receptor like 1","termid":"PBO:0061838"}


id: PBO:0003715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein Pop3","termid":"PBO:0003715"}


id: MOD:01956
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to (3R)-3-hydroxy-L-arginine.","definition_xrefs":["PubMed:786730","RESID:AA0601","PubMed:23103944","PubMed:10094780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroxylated arginine","termid":"MOD:00682"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(3R)-3-hydroxy-L-arginine","synonyms":[{"name":"(2S,3R)-2-amino-5-[(diaminomethylidene)amino]-3-hydroxypentanoic acid","type":"exact"},{"name":"(3R)-3-hydroxy-L-arginine","type":"exact"},{"name":"2-amino-5-(carbamimidamido)-3-hydroxypentanoic acid [tautomer]","type":"exact"},{"name":"2-amino-5-[(aminoiminomethyl)amino]-3-hydroxypentanoic acid [tautomer]","type":"exact"},{"name":"2-amino-5-guanidino-3-hydroxypentanoic acid","type":"exact"},{"name":"C(beta)-hydroxyarginine","type":"exact"},{"name":"MOD_RES (3R)-3-hydroxyarginine","type":"exact"},{"name":"beta-hydroxyarginine","type":"exact"}],"termid":"MOD:01956"}


id: GO:0072711
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 hydroxyurea stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hydroxyurea","termid":"GO:0072710"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"}],"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 hydroxyurea","synonyms":[{"name":"cellular response to HU","type":"exact"}],"termid":"GO:0072711"}


id: PBO:0003008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER unfolded protein response protein (predicted)","termid":"PBO:0003008"}


id: FYPO:0005497
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription from a promoter that contains one or more CRE elements does not occur.","definition_xrefs":["PMID:26108447","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished transcription from RNA polymerase II promoter","termid":"FYPO:0003796"},{"relation_name":"is_a","term_name":"decreased transcription from CRE promoter","termid":"FYPO:0005496"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"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:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000294","FYPO:0001985"],"is_obsolete":false,"name":"abolished transcription from CRE promoter","synonyms":[{"name":"abolished transcription from CRE promoter during mitotic cell cycle","type":"related"},{"name":"abolished transcription from CRE promoter during vegetative growth","type":"exact"},{"name":"expression of CRE target genes abolished","type":"related"},{"name":"transcription from CRE promoter abolished","type":"exact"}],"termid":"FYPO:0005497"}


id: PBO:0043324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC like kinase 2","termid":"PBO:0043324"}


id: MONDO:0015343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Secondary acute transverse myelitis (ATM) is characterized by focal inflammation within the spinal cord due to a known cause, usually an inflammatory disease.","definition_xrefs":["Orphanet:139420"],"gene_count":0,"genotype_count":0,"name":"obsolete secondary acute transverse myelitis (obsolete MONDO:0015343)","synonyms":[{"name":"disease-associated transverse myelitis","type":"exact"}],"termid":"MONDO:0015343","xrefs":{"Monarch":{"xref_id":"0015343"}}}


id: GO:0034788
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,3-dihydroxy-2'-carboxybiphenyl + O2 = 2-hydroxy-6-oxo-6-(2-carboxyphenyl)-hexa-2,4-dienoate + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,3-dihydroxy-2'-carboxybiphenyl 1,2-dioxygenase activity (obsolete GO:0034788)","termid":"GO:0034788"}


id: GO:0050201
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-fucose + ATP = beta-L-fucose 1-phosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.52","RHEA:13241"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016301"],"is_obsolete":false,"name":"fucokinase activity","secondary_identifiers":["Reactome:R-HSA-6787540","KEGG_REACTION:R03161","MetaCyc:FUCOKINASE-RXN"],"synonyms":[{"name":"ATP:6-deoxy-L-galactose 1-phosphotransferase activity","type":"related"},{"name":"ATP:beta-L-fucose 1-phosphotransferase activity","type":"related"},{"name":"L-fucokinase activity","type":"related"},{"name":"L-fucose kinase activity","type":"related"},{"name":"fucokinase (phosphorylating) activity","type":"related"},{"name":"fucose kinase activity","type":"related"}],"termid":"GO:0050201"}


id: PBO:0066761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 59","termid":"PBO:0066761"}


id: MONDO:0009739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infantile neuroaxonal dystrophy (obsolete MONDO:0009739)","secondary_identifiers":["NANDO:2200887"],"termid":"MONDO:0009739","xrefs":{"Monarch":{"xref_id":"0009739"}}}


id: PBO:0000621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar amino acid efflux transporter Atg22","termid":"PBO:0000621"}


id: PBO:0003813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Nop6 (predicted)","termid":"PBO:0003813"}


id: PBO:0065587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prothymosin alpha pseudogene 3","termid":"PBO:0065587"}


id: MONDO:0016144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"sarcoglycanopathy","termid":"MONDO:0016140"},{"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 delta-sarcoglycan","secondary_identifiers":["GARD:20393","Orphanet:207070","UMLS:C5680806","MEDGEN:1826098"],"synonyms":[{"name":"delta-sarcoglycanopathy","type":"exact"}],"termid":"MONDO:0016144","xrefs":{"Monarch":{"xref_id":"0016144"}}}


id: PBO:0113239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear decapping endonuclease; targets mRNAs with unmethylated 7-methylguanosine cap structures and 5'-triphosphates; binds to and stabilizes the exoribonuclease Rat1p; required for pre-rRNA processing; involved in an early step of decapping non-canonical nicotinamide adenine dinucleotide (NAD) capped nuclear mRNAs (NAD-RNAs), part of ncRNA surveillance; relocalizes to the cytosol in response to hypoxia; homologous to human DOM3Z","termid":"PBO:0113239"}


id: GO:1903515
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of calcium ion from cytosol to endoplasmic reticulum.","definition_xrefs":["GOC:rl","GOC:BHF","GO_REF:0000078","GOC:mtg_cardiac_conduct_nov11","GOC:TermGenie","PMID:16402920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytosol to endoplasmic reticulum transport","termid":"GO:0046967"},{"relation_name":"is_a","term_name":"calcium ion transmembrane transport","termid":"GO:0070588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"calcium ion transport from cytosol to endoplasmic reticulum","termid":"GO:1903515"}


id: GO:1904359
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of spore germination.","definition_xrefs":["GOC:TermGenie","PMID:14718564","GO_REF:0000058","PMID:8798577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"spore germination","termid":"GO:0009847"}],"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 spore germination","secondary_identifiers":["GO:0075006"],"synonyms":[{"name":"modulation of spore germination on or near host","type":"narrow"}],"termid":"GO:1904359"}


id: PBO:0089120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane sodium ion/proton antiporter Sod22","termid":"PBO:0089120"}


id: MONDO:0012944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tibial aplasia-ectrodactyly syndrome","termid":"MONDO:0018050"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"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":"chromosome 17P13.3, telomeric, duplication syndrome","secondary_identifiers":["OMIM:612576","GARD:15572","MEDGEN:390813","MESH:C567245","UMLS:C2675492"],"synonyms":[{"name":"chromosome 17P13.3, telomeric, duplication syndrome","type":"exact"},{"name":"split-hand/foot malformation with long bone deficiency 3","type":"related"}],"termid":"MONDO:0012944","xrefs":{"Monarch":{"xref_id":"0012944"}}}


id: PBO:0031135
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_translation_in_response_to_osmotic_stress","termid":"PBO:0031135"}


id: PBO:0054671
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 2077","termid":"PBO:0054671"}


id: PBO:0083893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FG-nucleoporin component of central core of the nuclear pore complex; contributes directly to nucleocytoplasmic transport and maintenance of the nuclear pore complex (NPC) permeability barrier and is involved in gene tethering at the nuclear periphery; NUP100 has a paralog, NUP116, that arose from the whole genome duplication","termid":"PBO:0083893"}


id: PBO:0073141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC22 homolog B4, pseudogene","termid":"PBO:0073141"}


id: PBO:0005814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F0-ATPase delta subunit (predicted)","termid":"PBO:0005814"}


id: PBO:0087876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional regulator; involved in activation of the GAL genes in response to galactose; forms a complex with Gal80p to relieve Gal80p inhibition of Gal4p; binds galactose and ATP but does not have galactokinase activity; GAL3 has a paralog, GAL1, that arose from the whole genome duplication","termid":"PBO:0087876"}


id: MONDO:0001341
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dysgammaglobulinemia characterized by low or undetectable serum levels of immunoglobulin class A (IgA). It is the most common primary antibody deficiency. It may be inherited or the reversible sequela of infection or certain drugs. It may be caused by decreased or inefficient class-switching from progenitor B cells without any corresponding decreases in the other isotypes. Though affected persons may be asymptomatic, low levels of IgA will reduce the immune system's ability to combat infection where IgA is normally secreted, at mucosal surfaces. Selective IgA deficiency is seen in greater proportion among patients with autoimmune disorders.","definition_xrefs":["NCIT:C26964"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"B cell deficiency","termid":"MONDO:0002211"},{"relation_name":"is_a","term_name":"dysgammaglobulinemia","termid":"MONDO:0001342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"selective IgA deficiency disease","secondary_identifiers":["SCTID:29260007","DOID:0060025","EFO:1001929","MESH:D017098","MEDGEN:883982","Orphanet:69127","DOID:11701","UMLS:C4049006","NANDO:1200347","NANDO:2200720"],"synonyms":[{"name":"IgA deficiencies","type":"related"},{"name":"IgA deficiency","type":"exact"},{"name":"SIgAD","type":"exact"},{"name":"deficiencies, IgA","type":"related"},{"name":"deficiency, IgA","type":"related"},{"name":"gamma-A-globulin deficiency","type":"exact"},{"name":"immunoglobulin A deficiency","type":"exact"},{"name":"immunoglobulin alpha deficiency","type":"related"},{"name":"selective IgA immunodeficiency","type":"exact"},{"name":"selective immunoglobulin A deficiency","type":"exact"}],"termid":"MONDO:0001341","xrefs":{"Monarch":{"xref_id":"0001341"}}}


id: PBO:0031375
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_microtubules","termid":"PBO:0031375"}


id: GO:0052787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The breakdown of large alpha-linked polysaccharides by hydrolysis of (1->4)-alpha-D-glucosidic linkages to yield maltopentaose.","definition_xrefs":["PMID:9406414","GOC:mengo_curators","PMID:7511484"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide catabolic process","termid":"GO:0000272"}],"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:0005975","GO:0008150"],"is_obsolete":false,"name":"alpha-linked polysaccharide catabolism to maltopentaose","synonyms":[{"name":"alpha-amylase-mediated polysaccharide catabolism, producing maltopentaose","type":"exact"},{"name":"maltopentaose-forming alpha-amylase activity","type":"related"}],"termid":"GO:0052787"}


id: PR:O13803
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A coiled-coil domain-containing protein 82 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00825"],"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 C17H9.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.06c","secondary_identifiers":["UniProtKB:O13803"],"synonyms":[{"name":"Spom972h-CCDC82","type":"exact"}],"termid":"PR:O13803"}


id: MONDO:0010848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 5 (SCA5) is a rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.","definition_xrefs":["Orphanet:98766"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type III","termid":"MONDO:0019793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0000426","MONDO:0002039"],"is_obsolete":false,"name":"spinocerebellar ataxia type 5","secondary_identifiers":["OMIM:600224","icd11.foundation:78905851","MEDGEN:155705","SCTID:719302009","GARD:4953","UMLS:C0752123","DOID:0050882"],"synonyms":[{"name":"SCA5","type":"exact"},{"name":"spinocerebellar ataxia 5","type":"related"},{"name":"spinocerebellar ataxia type 5","type":"exact"}],"termid":"MONDO:0010848","xrefs":{"Monarch":{"xref_id":"0010848"}}}


id: MONDO:1010872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any mucopolysaccharidosis that occurs in cats due to a mutation in the GUSB gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis or mucopolysaccharidosis-like disorder, non-human animal","termid":"MONDO:1012581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucopolysaccharidosis, GUSB-related, domestic cat","secondary_identifiers":["OMIA:000667-9685"],"synonyms":[{"name":"mucopolysaccharidosis VII, domestic cat","type":"related"}],"termid":"MONDO:1010872","xrefs":{"Monarch":{"xref_id":"1010872"}}}


id: GO:0003279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a cardiac septum over time, from its initial formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"cardiac chamber development","termid":"GO:0003205"}],"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 septum development","synonyms":[{"name":"heart septum development","type":"exact"}],"termid":"GO:0003279"}


id: MONDO:0007779
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal dominant form of Opitz G/BBB syndrome.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant Opitz G/BBB syndrome (obsolete MONDO:0007779)","secondary_identifiers":["Orphanet:306588","OMIM:145410"],"synonyms":[{"name":"ADOS","type":"exact"},{"name":"BBB syndrome","type":"related"},{"name":"G syndrome","type":"related"},{"name":"GBBB syndrome","type":"related"},{"name":"GBBB2","type":"related"},{"name":"Opitz Bbbg syndrome","type":"related"},{"name":"Opitz G/BBB syndrome, autosomal dominant","type":"exact"},{"name":"Opitz GBBB syndrome, autosomal dominant","type":"related"},{"name":"Opitz GBBB syndrome, type 2","type":"related"},{"name":"Opitz GBBB syndrome, type II","type":"related"},{"name":"Opitz oculogenitolaryngeal syndrome, type 2","type":"related"},{"name":"Opitz-Frias syndrome","type":"related"},{"name":"Opitz-G syndrome, type 2","type":"related"},{"name":"autosomal dominant Opitz BBB/G syndrome","type":"exact"},{"name":"autosomal dominant Opitz syndrome","type":"exact"},{"name":"chromosome 22Q11.2 deletion syndrome, Opitz phenotype","type":"related"},{"name":"hypertelorism with esophageal Abnormality and hypospadias","type":"related"},{"name":"hypertelorism-hypospadias syndrome","type":"related"},{"name":"hypospadias-dysphagia syndrome","type":"related"},{"name":"telecanthus with associated abnormalities","type":"related"},{"name":"telecanthus-hypospadias syndrome","type":"related"}],"termid":"MONDO:0007779","xrefs":{"Monarch":{"xref_id":"0007779"}}}


id: _global:causally_upstream_of,_negative_effect
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"p is causally upstream of, negative effect q iff p is casually upstream of q, and the execution of p decreases the execution of q.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_upstream_of","termid":"_global:causally_upstream_of"},{"relation_name":"is_a","term_name":"causally_upstream_of_or_within,_negative_effect","termid":"_global:causally_upstream_of_or_within,_negative_effect"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causally_upstream_of,_negative_effect","secondary_identifiers":["RO:0002305"],"termid":"_global:causally_upstream_of,_negative_effect"}


id: MONDO:0018048
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heparin-induced thrombocytopenia (HIT) is a drug-induced, immune-mediated prothrombotic disorder associated with thrombocytopenia and venous and/or arterial thrombosis.","definition_xrefs":["Orphanet:3325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thrombotic disease","termid":"MONDO:0000831"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heparin-induced thrombocytopenia","secondary_identifiers":["NANDO:2200648","UMLS:C0272285","HP:0011874","MedDRA:10062506","ICD9:289.84","icd11.foundation:1143142333","SCTID:73397007","GARD:2650","MEDGEN:124423"],"synonyms":[{"name":"HAT","type":"exact"},{"name":"HIT","type":"exact"},{"name":"heparin-associated thrombocytopenia","type":"exact"},{"name":"heparin-induced thrombocytopenia","type":"exact"},{"name":"heparin-induced thrombocytopenia (disease)","type":"exact"},{"name":"heparin-induced thrombocytopenia type 2","type":"exact"}],"termid":"MONDO:0018048","xrefs":{"Monarch":{"xref_id":"0018048"}}}


id: PBO:0056389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPK activated protein kinase 5","termid":"PBO:0056389"}


id: PBO:0048009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FERM domain containing 7","termid":"PBO:0048009"}


id: FYECO:0000319
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which brefeldin A (BFA) was added to the medium or assay buffer.","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":"+ BFA","synonyms":[{"name":"+ brefeldin A","type":"exact"}],"termid":"FYECO:0000319"}


id: PBO:0111382
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pentameric","termid":"PBO:0111382"}


id: GO:2000963
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellooligosaccharide catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"is_a","term_name":"regulation of cellooligosaccharide metabolic process","termid":"GO:2000960"},{"relation_name":"regulates","term_name":"cellooligosaccharide catabolic process","termid":"GO:2000903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of cellooligosaccharide catabolic process","synonyms":[{"name":"regulation of cellooligosaccharide catabolism","type":"exact"}],"termid":"GO:2000963"}


id: PBO:0029224
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_homologous_chromosome_pairing","termid":"PBO:0029224"}


id: GO:0000825
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,5-tetrakisphosphate + ATP = 1D-myo-inositol 1,3,4,5,6-pentakisphosphate + ADP + H+.","definition_xrefs":["MetaCyc:RXN-7184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate kinase activity","termid":"GO:0051765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"inositol-1,3,4,5-tetrakisphosphate 6-kinase activity","secondary_identifiers":["KEGG_REACTION:R10953","Reactome:R-HSA-1855206"],"synonyms":[{"name":"1D-myo-inositol-tetrakisphosphate 6-kinase activity","type":"broad"},{"name":"inositol 1,3,4,5-tetrakisphosphate 6-kinase activity","type":"exact"},{"name":"inositol tetrakisphosphate 6-kinase activity","type":"broad"}],"termid":"GO:0000825"}


id: FYPO:0003690
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which a cell population does not grow in a medium containing glycerol and ethanol as the carbon sources.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cell population growth on glycerol/ethanol carbon source","termid":"FYPO:0000442"},{"relation_name":"is_a","term_name":"abolished vegetative cell population growth","termid":"FYPO:0001575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000139","FYPO:0000003","FYPO:0002060","FYPO:0005447","FYPO:0001985","FYPO:0002057"],"is_obsolete":false,"name":"abolished cell population growth on glycerol/ethanol carbon source","synonyms":[{"name":"abolished growth on glycerol/ethanol carbon source","type":"broad"},{"name":"abolished vegetative cell population growth on glycerol/ethanol carbon source","type":"exact"},{"name":"cell population growth on glycerol/ethanol carbon source abolished","type":"exact"}],"termid":"FYPO:0003690"}


id: PBO:0001685
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter contains DRE element","termid":"PBO:0001685"}


id: MONDO:0021017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by dysfunction of synapses.","definition_xrefs":["Wikipedia:Synaptopathy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptopathy","termid":"MONDO:0021017","xrefs":{"Monarch":{"xref_id":"0021017"}}}


id: PR:O74558
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mob2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74558"],"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":"maintenance of ploidy protein mob2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC970.04c","synonyms":[{"name":"Spom972h-mob2","type":"exact"}],"termid":"PR:O74558"}


id: PBO:0004677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-amino-6-(5-phosphoribosylamino) uracil reductase (predicted)","termid":"PBO:0004677"}


id: PBO:0075870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family pseudogene 10","termid":"PBO:0075870"}


id: PATO:0000441
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a single process inhering in a bearer by virtue of the bearer's marked by tedious repetition.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"occurrence","termid":"PATO:0000057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"repetitive","termid":"PATO:0000441"}


id: GO:0004631
data:
  {"annotated_genes":["SJAG_01474"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76067],"is_not":false,"summary":null,"term":"GO:0004631"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-5-phosphomevalonate + ATP = (R)-5-diphosphomevalonate + ADP + H+.","definition_xrefs":["EC:2.7.4.2","RHEA:16341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01474":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016301"],"is_obsolete":false,"name":"phosphomevalonate kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R03245","MetaCyc:PHOSPHOMEVALONATE-KINASE-RXN","Reactome:R-HSA-191422"],"synonyms":[{"name":"5-phosphomevalonate kinase activity","type":"related"},{"name":"ATP:(R)-5-phosphomevalonate phosphotransferase activity","type":"related"},{"name":"ATP:5-phosphomevalonate phosphotransferase activity","type":"related"},{"name":"mevalonate phosphate kinase activity","type":"related"},{"name":"mevalonate-5-phosphate kinase activity","type":"related"},{"name":"mevalonic acid phosphate kinase activity","type":"related"}],"termid":"GO:0004631","terms_by_termid":{"GO:0004631":null}}


id: PBO:0050892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immediate early response 3 interacting protein 1","termid":"PBO:0050892"}


id: PBO:0085404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane protein of unknown function; involved in the proteolytic activation of Rim101p in response to alkaline pH; interacts with Rim21p and Dfg16p to form a pH-sensing complex in the Rim101 pathway and is required to maintain Rim21p levels; has similarity to A. nidulans PalI;","termid":"PBO:0085404"}


id: PBO:0042592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CMT1A duplicated region transcript 5","termid":"PBO:0042592"}


id: PBO:0052464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF transcription factor 11","termid":"PBO:0052464"}


id: PBO:0002703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF2 alpha kinase Hri1","termid":"PBO:0002703"}


id: MONDO:0000537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gastrointestinal carcinoma (obsolete MONDO:0000537)","synonyms":[{"name":"obsolete gastrointestinal carcinoma (disease)","type":"exact"}],"termid":"MONDO:0000537","xrefs":{"Monarch":{"xref_id":"0000537"}}}


id: PBO:0081539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 451","termid":"PBO:0081539"}


id: PR:O94642
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tRNA-specific adenosine deaminase 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DAN","PANTHER:PTHR11079:SF9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-specific adenosine deaminase subunit tad2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.10","secondary_identifiers":["UniProtKB:O94642"],"synonyms":[{"name":"SPBC16D10.10","type":"related"},{"name":"Spom972h-ADAT2","type":"exact"},{"name":"tRNA-specific adenosine-34 deaminase subunit tad2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94642"}


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: GO:0061341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via effectors other than beta-catenin and contributing to the progression of the heart over time.","definition_xrefs":["GOC:dph","PMID:16860783","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Wnt signaling pathway involved in heart development","termid":"GO:0003306"},{"relation_name":"is_a","term_name":"non-canonical Wnt signaling pathway","termid":"GO:0035567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"non-canonical Wnt signaling pathway involved in heart development","synonyms":[{"name":"non-canonical Wnt receptor signaling pathway involved in heart development","type":"exact"},{"name":"non-canonical Wnt receptor signalling pathway involved in heart development","type":"exact"},{"name":"non-canonical Wnt-activated signaling pathway involved in heart development","type":"exact"}],"termid":"GO:0061341"}


id: GO:0008589
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smoothened signaling.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"smoothened signaling pathway","termid":"GO:0007224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of smoothened signaling pathway","secondary_identifiers":["GO:0043109","GO:0007226"],"synonyms":[{"name":"regulation of hedgehog signaling pathway","type":"exact"},{"name":"regulation of hh signaling pathway","type":"exact"},{"name":"regulation of smoothened activity","type":"related"},{"name":"regulation of smoothened by patched","type":"related"},{"name":"regulation of smoothened receptor activity by patched","type":"related"},{"name":"regulation of smoothened signalling pathway","type":"exact"}],"termid":"GO:0008589"}


id: PBO:0067942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 244","termid":"PBO:0067942"}


id: PBO:0088079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin (Ub) chain assembly factor (E4); forms branched Ub chains on substrates destined for degradation, catalyzing K48-linked multi-monoubiquitination of K29-linked Ub chains assembled by the Ub-ligase Ufd4p; involved in the Ub-fusion degradation pathway, OLE membrane fluidity pathway, stress response survival and the ERAD pathway for misfolded proteins, where it promotes ubiquitination and transfer of ERAD substrates to Rad23p; U-box family member; homologous to human Ufd2a and Ufd2b","termid":"PBO:0088079"}


id: PBO:0050553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human papillomavirus (type 18) integration site 2","termid":"PBO:0050553"}


id: FYPO:0003425
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another does not occur during a cellular response to rapamycin. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction","termid":"FYPO:0000705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0000702","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein-protein interaction during cellular response to rapamycin","synonyms":[{"name":"abolished protein binding during cellular response to rapamycin","type":"exact"},{"name":"protein-protein interaction abolished during cellular response to rapamycin","type":"exact"}],"termid":"FYPO:0003425"}


id: MONDO:0009093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatoleukodystrophy is characterized by the association of a progressive leukodystrophy marked by generalized mental and motor impairment with the presence of thickened and wrinkled skin. It has been described in a Japanese brother and sister born to healthy parents. Both patients died in early childhood.","definition_xrefs":["Orphanet:1659"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"dermatoleukodystrophy","secondary_identifiers":["MEDGEN:387794","SCTID:733044009","UMLS:C1857314","GARD:1813","MESH:C538220","OMIM:221790"],"synonyms":[{"name":"Dermatoleukodystrophy","type":"exact"}],"termid":"MONDO:0009093","xrefs":{"Monarch":{"xref_id":"0009093"}}}


id: GO:0061580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a colonic epithelial cell from one site to another, often during the development of a multicellular organism.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal epithelial cell migration","termid":"GO:0061582"}],"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":"colon epithelial cell migration","termid":"GO:0061580"}


id: MONDO:0019060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, intermediate, or malignant neoplasm involving the bone or articular cartilage.","definition_xrefs":["NCIT:C9343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"},{"relation_name":"is_a","term_name":"connective tissue neoplasm","termid":"MONDO:0021581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone neoplasm","secondary_identifiers":["Orphanet:68411","ONCOTREE:BONE","GARD:18892","MEDGEN:488993","UMLS:C2732838","EFO:0003820","ICD10CM:C40-C41"],"synonyms":[{"name":"bone neoplasm","type":"exact"},{"name":"bone neoplasms","type":"exact"},{"name":"bone tissue neoplasm","type":"exact"},{"name":"bone tissue tumor","type":"exact"},{"name":"bone tissue tumour","type":"exact"},{"name":"bone tumor","type":"exact"},{"name":"bone tumors","type":"exact"},{"name":"bone tumour","type":"exact"},{"name":"bone tumours","type":"exact"},{"name":"neoplasm of bone","type":"exact"},{"name":"neoplasm of bone tissue","type":"exact"},{"name":"neoplasm of the bone","type":"exact"},{"name":"osseous neoplasm","type":"exact"},{"name":"osseous tumor","type":"exact"},{"name":"osseous tumour","type":"exact"},{"name":"primary bone cancer","type":"related"},{"name":"primary malignant neoplasm of bone","type":"related"},{"name":"rare bone tumor","type":"related"},{"name":"rare bone tumour","type":"related"},{"name":"tumor of bone","type":"exact"},{"name":"tumor of bone tissue","type":"exact"},{"name":"tumor of the bone","type":"exact"},{"name":"tumour of bone","type":"exact"},{"name":"tumour of bone tissue","type":"exact"},{"name":"tumour of the bone","type":"exact"}],"termid":"MONDO:0019060","xrefs":{"Monarch":{"xref_id":"0019060"}}}


id: GO:1902646
data:
  {"annotated_genes":["SJAG_03170","SJAG_02613","SJAG_00053"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59709,89875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[117141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902648"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate biosynthetic process.","definition_xrefs":["GOC:di","GO_REF:0000058","GOC:TermGenie","PMID:22562153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phosphatidylinositol biosynthetic process","termid":"GO:0010511"},{"relation_name":"regulates","term_name":"1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate biosynthetic process","termid":"GO:1902635"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_02613":null,"SJAG_03170":null},"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 biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate anabolism","type":"exact"},{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate biosynthesis","type":"exact"},{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate formation","type":"exact"},{"name":"regulation of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate synthesis","type":"exact"}],"termid":"GO:1902646","terms_by_termid":{"GO:1902647":null,"GO:1902648":null}}


id: MONDO:0019894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-distal monosomy 7p (obsolete MONDO:0019894)","secondary_identifiers":["Orphanet:96136"],"synonyms":[{"name":"non-distal deletion 7p","type":"exact"},{"name":"non-distal monosomy type 7p","type":"exact"},{"name":"non-telomeric monosomy 7p","type":"exact"}],"termid":"MONDO:0019894","xrefs":{"Monarch":{"xref_id":"0019894"}}}


id: GO:0034466
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a chromaffin granule.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule lumen","termid":"GO:0034774"},{"relation_name":"part_of","term_name":"chromaffin granule","termid":"GO:0042583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"chromaffin granule lumen","termid":"GO:0034466"}


id: MONDO:0006744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An accumulation of endolymph in the inner ear (labyrinth) leading to buildup of pressure and distortion of intralabyrinthine structures, such as cochlea and semicircular canals. It is characterized by sensorineural hearing loss; tinnitus; and sometimes vertigo.","definition_xrefs":["MESH:D018159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral vertigo","termid":"MONDO:0004900"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endolymphatic hydrops","secondary_identifiers":["MEDGEN:60183","SCTID:27621000119100","UMLS:C0206586","EFO:1000918","ICD9:386.8","MedDRA:10049934","DOID:9848"],"synonyms":[{"name":"labyrinthine hydrops","type":"exact"}],"termid":"MONDO:0006744","xrefs":{"Monarch":{"xref_id":"0006744"}}}


id: PBO:0030655
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_amiloride","termid":"PBO:0030655"}


id: PR:Q9P382
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nup82 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P382"],"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":"nucleoporin nup82 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC13A2.02","synonyms":[{"name":"Spom972h-nup82","type":"exact"},{"name":"nuclear pore protein nup82 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P382"}


id: GO:0044840
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A lysosome-related organelle contained within the intestinal cells of the nematode C. elegans. Gut granules are acidified, birefringent, autofluorescent, and contain the vacuolar H+-ATPase. They also serve as sites of cellular zinc storage.","definition_xrefs":["GOC:kmv","PMID:22916203","PMID:24204312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle","termid":"GO:0031410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"gut granule","termid":"GO:0044840"}


id: FYPO:0000534
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 spindle pole body localization is abnormal. Spindle pole body localization is the process in which a whole spindle pole body is transported to, or maintained in, a specific location.","definition_xrefs":["GO:0070631","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"abnormal mitotic spindle pole body localization","synonyms":[{"name":"abnormal mitotic SPB localization","type":"exact"},{"name":"abnormal mitotic spindle pole body localisation","type":"exact"},{"name":"abnormal position of mitotic spindle pole body","type":"related"},{"name":"abnormal spindle pole body localization during mitotic cell cycle","type":"related"},{"name":"abnormal spindle pole body localization during vegetative growth","type":"exact"},{"name":"position of spindle pole body: abnormal","type":"related"}],"termid":"FYPO:0000534"}


id: MONDO:0056818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon carcinoma that arises from the skin. It is characterized by the presence of malignant glandular and malignant squamous cellular components.","definition_xrefs":["NCIT:C54250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin squamous cell carcinoma","termid":"MONDO:0002529"},{"relation_name":"is_a","term_name":"adenosquamous carcinoma","termid":"MONDO:0006074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"skin adenosquamous carcinoma","secondary_identifiers":["UMLS:C1710103","MEDGEN:313707"],"synonyms":[{"name":"skin adenosquamous cancer","type":"exact"},{"name":"skin adenosquamous carcinoma","type":"exact"}],"termid":"MONDO:0056818","xrefs":{"Monarch":{"xref_id":"0056818"}}}


id: GO:1990312
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type-II cohesin domain of a protein. Type-II cohesin domain is the binding partner of type-II dockerin domain.","definition_xrefs":["PMID:24080387","GOC:mengo_curators","PMID:23195689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"type-II cohesin domain binding","termid":"GO:1990312"}


id: FYPO:0003258
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of proline into the cell occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased amino acid import during vegetative growth","termid":"FYPO:0003169"},{"relation_name":"is_a","term_name":"abnormal proline import","termid":"FYPO:0003256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased proline import","synonyms":[{"name":"increased L-proline import","type":"narrow"},{"name":"increased L-proline import across plasma membrane","type":"exact"},{"name":"increased proline import during mitotic cell cycle","type":"related"},{"name":"increased proline import during vegetative growth","type":"exact"},{"name":"increased proline import into cell","type":"exact"},{"name":"increased proline uptake","type":"exact"}],"termid":"FYPO:0003258"}


id: GO:0033470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of gibberellin 12, (1R,2S,3S,4R,8S,9S,12R)-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid 1meta,4a-dimethyl-8-methylidene-4aalpha,4bbeta-gibbane-1alpha,10beta-dicarboxylic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gibberellin biosynthetic process","termid":"GO:0009686"},{"relation_name":"is_a","term_name":"gibberellin 12 metabolic process","termid":"GO:0033469"},{"relation_name":"is_a","term_name":"dicarboxylic acid biosynthetic process","termid":"GO:0043650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"gibberellin 12 biosynthetic process","secondary_identifiers":["MetaCyc:PWY-5034"],"synonyms":[{"name":"GA12 biosynthetic process","type":"exact"},{"name":"gibberellin 12 anabolism","type":"exact"},{"name":"gibberellin 12 biosynthesis","type":"exact"},{"name":"gibberellin 12 formation","type":"exact"},{"name":"gibberellin 12 synthesis","type":"exact"},{"name":"gibberellin A12 biosynthetic process","type":"exact"}],"termid":"GO:0033470"}


id: FYPO:0002026
data:
  {"alleles_by_uniquename":{"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118936],"is_not":false,"summary":null,"term":"FYPO:0002026"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell forms an actomyosin contractile ring that is perpendicular to the long axis of the cell, but is not located at the midpoint of the long axis.","definition_xrefs":["PMID:8834798","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized actomyosin contractile ring","termid":"FYPO:0001369"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02392":null},"genotype_count":1,"genotypes_by_uniquename":{"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000032","FYPO:0000631","FYPO:0001985","FYPO:0000138","FYPO:0004803","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"actomyosin contractile ring displaced from midpoint","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_02392"],"single_locus_genotype_uniquenames":["pom1delta"],"synonyms":[{"name":"actomyosin contractile ring displaced from cell center","type":"exact"},{"name":"actomyosin contractile ring displaced from cell centre","type":"exact"},{"name":"actomyosin contractile ring displaced from cell midpoint","type":"exact"},{"name":"actomyosin contractile ring displaced from midpoint during mitotic cell cycle","type":"related"},{"name":"actomyosin contractile ring displaced from midpoint during vegetative growth","type":"exact"},{"name":"cytokinetic contractile ring displaced from midpoint","type":"exact"}],"termid":"FYPO:0002026","terms_by_termid":{"FYECO:0000162":null,"FYPO:0002026":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:0009625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from an insect.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to other organism","termid":"GO:0051707"}],"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 insect","secondary_identifiers":["GO:0043019"],"synonyms":[{"name":"response to insects","type":"exact"}],"termid":"GO:0009625"}


id: PBO:0078529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 22","termid":"PBO:0078529"}


id: PBO:0048926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin B1","termid":"PBO:0048926"}


id: PBO:0084599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a discrete protein; YKL199C was originally annotated as an independent ORF, but as a result of a sequence change, it was merged with an adjacent ORF into a single reading frame, designated YKL198C","termid":"PBO:0084599"}


id: FYPO:0000974
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the cellular response to zinc ions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to chemical stimulus during vegetative growth","termid":"FYPO:0001318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000298"],"is_obsolete":false,"name":"normal cellular response to zinc ion","synonyms":[{"name":"normal cellular response to zinc","type":"exact"},{"name":"normal cellular response to zinc ion during mitotic cell cycle","type":"related"},{"name":"normal cellular response to zinc ion during vegetative growth","type":"exact"}],"termid":"FYPO:0000974"}


id: MONDO:0003766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer involving a dorsal plus ventral thalamus.","definition_xrefs":["MONDO:patterns/cancer"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diencephalic cancer","termid":"MONDO:0002786"},{"relation_name":"is_a","term_name":"thalamic disorder","termid":"MONDO:0003081"}],"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":"thalamic cancer","secondary_identifiers":["DOID:6098","icd11.foundation:610018988","MEDGEN:83429","NCIT:C4576","SCTID:188287005","UMLS:C0346902"],"synonyms":[{"name":"cancer of dorsal plus ventral thalamus","type":"exact"},{"name":"dorsal plus ventral thalamus cancer","type":"exact"},{"name":"malignant dorsal plus ventral thalamus neoplasm","type":"exact"},{"name":"malignant neoplasm of dorsal plus ventral thalamus","type":"exact"},{"name":"malignant neoplasm of thalamus","type":"exact"},{"name":"malignant neoplasm of the thalamus","type":"exact"},{"name":"malignant thalamic neoplasm","type":"exact"},{"name":"malignant thalamic neoplasms","type":"exact"},{"name":"malignant thalamic tumor","type":"exact"},{"name":"malignant thalamic tumors","type":"exact"},{"name":"malignant thalamic tumour","type":"exact"},{"name":"malignant thalamic tumours","type":"exact"},{"name":"malignant thalamus neoplasm","type":"exact"},{"name":"malignant thalamus neoplasms","type":"exact"},{"name":"malignant thalamus tumor","type":"exact"},{"name":"malignant thalamus tumors","type":"exact"},{"name":"malignant thalamus tumour","type":"exact"},{"name":"malignant thalamus tumours","type":"exact"},{"name":"malignant tumor of thalamus","type":"exact"},{"name":"malignant tumor of the thalamus","type":"exact"},{"name":"malignant tumour of thalamus","type":"exact"},{"name":"malignant tumour of the thalamus","type":"exact"},{"name":"thalamic neoplasm","type":"related"},{"name":"tumor of thalamus","type":"exact"},{"name":"tumour of thalamus","type":"exact"}],"termid":"MONDO:0003766","xrefs":{"Monarch":{"xref_id":"0003766"}}}


id: PBO:0063183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PBX3 divergent transcript","termid":"PBO:0063183"}


id: PBO:0050054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class I, U (pseudogene)","termid":"PBO:0050054"}


id: MONDO:0001734
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary disease characterized by seizures, intellectual disability, developmental delay, and skin and ocular lesions. First signs usually occur during infancy or childhood but in rare cases may not occur until 2nd or 3rd decade.","definition_xrefs":["NCIT:C3424"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited nervous system cancer-predisposing syndrome (obsolete MONDO:0016756)","termid":"MONDO:0016756"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited renal cancer-predisposing syndrome (obsolete MONDO:0017891)","termid":"MONDO:0017891"},{"relation_name":"excluded_subClassOf","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"neurocutaneous syndrome","termid":"MONDO:0042983"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"tuberous sclerosis","secondary_identifiers":["NANDO:1200607","OMIMPS:191100","GARD:7830","icd11.foundation:1903085809","MEDGEN:22518","Orphanet:805","DOID:13515","ICD9:759.5","NANDO:2200826","SCTID:7199000","UMLS:C0041341","MESH:D014402","MedDRA:10045138","NORD:1802"],"synonyms":[{"name":"Bourneville disease","type":"exact"},{"name":"Bourneville syndrome","type":"exact"},{"name":"Bourneville's disease","type":"exact"},{"name":"Bourneville's syndrome","type":"exact"},{"name":"TSC","type":"exact"},{"name":"adenoma sebaceum","type":"related"},{"name":"adenoma sebaceum syndrome","type":"related"},{"name":"cerebral sclerosis","type":"exact"},{"name":"epiloia","type":"exact"},{"name":"tuberose sclerosis","type":"exact"},{"name":"tuberous sclerosis","type":"exact"},{"name":"tuberous sclerosis complex","type":"exact"},{"name":"tuberous sclerosis syndrome","type":"exact"}],"termid":"MONDO:0001734","xrefs":{"Monarch":{"xref_id":"0001734"}}}


id: FYPO:0001491
data:
  {"alleles_by_uniquename":{"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_01794:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01794","name":"scd2delta","uniquename":"SJAG_01794:allele-1"},"SJAG_02013:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02013","name":"pyp1delta","uniquename":"SJAG_02013:allele-1"},"SJAG_02819:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02819","name":"efc25delta","uniquename":"SJAG_02819:allele-1"},"SJAG_03048:allele-1":{"allele_type":"amino_acid_mutation","description":"G146D","gene_uniquename":"SJAG_03048","name":"cdc2-1w","uniquename":"SJAG_03048:allele-1"},"SJAG_03453:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03453","name":"ras1delta","uniquename":"SJAG_03453:allele-1"},"SJAG_03581:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03581","name":"gef1delta","uniquename":"SJAG_03581:allele-1"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04280:allele-3":{"allele_type":"amino_acid_mutation","description":"G788E","gene_uniquename":"SJAG_04280","name":"wee1-G788E","uniquename":"SJAG_04280:allele-3"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119163,119162,119002,119166],"is_not":false,"rel_names":["is_a","has_part"],"summary":null,"term":"FYPO:0000648"},{"annotations":[118767,118741,118735,118730],"is_not":false,"rel_names":["has_part","is_a"],"summary":null,"term":"FYPO:0002380"},{"annotations":[119165,119171,119164],"is_not":false,"rel_names":["is_a","has_part"],"summary":null,"term":"FYPO:0001877"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a vegetatively growing cell is viable.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable cell","termid":"FYPO:0000124"},{"relation_name":"is_a","term_name":"cellular physical quality phenotype during vegetative growth","termid":"FYPO:0001321"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_01794":null,"SJAG_02013":null,"SJAG_02819":null,"SJAG_03048":null,"SJAG_03453":null,"SJAG_03581":null,"SJAG_04280":null},"genotype_count":9,"genotypes_by_uniquename":{"cdc2-1w-G146D-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc2-1w(G146D aa)","display_uniquename":"cdc2-1w-G146D-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03048:allele-1","expression":"Not assayed or wild type"}]}]},"efc25delta":{"display_name":"efc25delta","display_uniquename":"efc25delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02819:allele-1","expression":"Null"}]}]},"gef1delta":{"display_name":"gef1delta","display_uniquename":"gef1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03581:allele-1","expression":"Null"}]}]},"pyp1delta":{"display_name":"pyp1delta","display_uniquename":"pyp1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02013:allele-1","expression":"Null"}]}]},"ras1delta":{"display_name":"ras1delta","display_uniquename":"ras1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03453:allele-1","expression":"Null"}]}]},"scd1delta":{"display_name":"scd1delta","display_uniquename":"scd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00514:allele-1","expression":"Null"}]}]},"scd2delta":{"display_name":"scd2delta","display_uniquename":"scd2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01794:allele-1","expression":"Null"}]}]},"wee1-G788E-G788E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-G788E(aa)","display_uniquename":"wee1-G788E-G788E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-3","expression":"Not assayed or wild type"}]}]},"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-as8(T582G aa)","display_uniquename":"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"viable vegetative cell","references_by_uniquename":{"PMID:29566183":null,"PMID:30664646":null,"PMID:31150379":null},"single_locus_annotated_genes":["SJAG_04280","SJAG_03048","SJAG_02013","SJAG_02819","SJAG_03581","SJAG_03453","SJAG_00514","SJAG_01794"],"single_locus_genotype_uniquenames":["pyp1delta","gef1delta","scd1delta","wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","wee1-G788E-G788E-amino_acid_mutation-expression-not_assayed_or_wild_type","efc25delta","ras1delta","scd2delta","cdc2-1w-G146D-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"viable cell during vegetative growth","type":"exact"},{"name":"viable vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001491","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000006":null,"FYECO:0000137":null,"FYECO:0000338":null,"FYPO:0000648":null,"FYPO:0001877":null,"FYPO:0002380":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: FYPO:0007440
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 directed movement of sterols within cells is abnormal.","definition_xrefs":["PomBase:mah","GO:0032366"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal intracellular sterol transport","synonyms":[{"name":"abnormal intracellular sterol transport during mitotic cell cycle","type":"related"},{"name":"abnormal intracellular sterol transport during vegetative growth","type":"exact"}],"termid":"FYPO:0007440"}


id: GO:0038001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The transfer of information from one cell to another, where the signal travels from the signal-producing cell to the receiving cell by passive diffusion or bulk flow in intercellular fluid. The signaling cell and the receiving cell are usually in the vicinity of each other.","definition_xrefs":["ISBN:3527303782","GOC:mtg_signaling_feb11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling","termid":"GO:0007267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"paracrine signaling","synonyms":[{"name":"paracrine signalling","type":"exact"}],"termid":"GO:0038001"}


id: GO:0000304
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 singlet oxygen stimulus. Singlet oxygen is a dioxygen (O2) molecule in which two 2p electrons have similar spin. Singlet oxygen is more highly reactive than the form in which these electrons are of opposite spin, and it is produced in mutant chloroplasts lacking carotenoids and by leukocytes during metabolic burst.","definition_xrefs":["ISBN:0198506732","GOC:krc","ISBN:0124325653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to reactive oxygen species","termid":"GO:0000302"}],"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 singlet oxygen","termid":"GO:0000304"}


id: GO:0002772
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to an inhibitory C-type lectin receptor capable of inhibiting an immune effector process contributing to an immune response.","definition_xrefs":["ISBN:0781735149","PMID:15771571","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune response-inhibiting cell surface receptor signaling pathway","termid":"GO:0002767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"inhibitory C-type lectin receptor signaling pathway","synonyms":[{"name":"Ly49 inhibitory receptor signaling pathway","type":"related"},{"name":"inhibitory C-type lectin receptor signalling pathway","type":"exact"}],"termid":"GO:0002772"}


id: GO:0000751
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle regulatory process in which the mitotic cell cycle is halted during G1 as a result of a pheromone stimulus. An example of this process is found in Saccharomyces cerevisiae.","definition_xrefs":["GOC:clt","GOC:mah","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mitotic cell cycle","termid":"GO:0045930"},{"relation_name":"part_of","term_name":"response to pheromone triggering conjugation with cellular fusion","termid":"GO:0000749"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"mitotic cell cycle G1 arrest in response to pheromone","secondary_identifiers":["GO:0030571"],"synonyms":[{"name":"cell cycle arrest in response to pheromone","type":"broad"}],"termid":"GO:0000751"}


id: MONDO:0018793
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"temporomandibular joint disorder","termid":"MONDO:0005473"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary condylar hyperplasia","secondary_identifiers":["UMLS:C5568570","Orphanet:477781","MEDGEN:1799993","GARD:21966"],"synonyms":[{"name":"type 1 condylar hyperplasia","type":"exact"}],"termid":"MONDO:0018793","xrefs":{"Monarch":{"xref_id":"0018793"}}}


id: PBO:0050332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 34","termid":"PBO:0050332"}


id: PBO:0078446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor gamma joining P1","termid":"PBO:0078446"}


id: PBO:0069924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1216, pseudogene","termid":"PBO:0069924"}


id: PBO:0064522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit C","termid":"PBO:0064522"}


id: PBO:0027225
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-bent_vegetative_cell","termid":"PBO:0027225"}


id: GO:0035515
data:
  {"annotated_genes":["SJAG_00892"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990984"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from one or more nucleosides within a RNA molecule involving the oxidation (i.e. electron loss) of one or more atoms.","definition_xrefs":["PMID:12594517","PMID:16482161","PMID:18775698"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"},{"relation_name":"is_a","term_name":"demethylase activity","termid":"GO:0032451"},{"relation_name":"is_a","term_name":"catalytic activity, acting on RNA","termid":"GO:0140098"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00892":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0140098","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"oxidative RNA demethylase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8857692"],"synonyms":[{"name":"2-oxoglutarate-dependent RNA demethylase","type":"exact"}],"termid":"GO:0035515","terms_by_termid":{"GO:1990984":null}}


id: PBO:0001697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar calcium transporting P-type ATPase P2 type, Pmc1","termid":"PBO:0001697"}


id: GO:0039597
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any viral process that activates or increases the frequency, rate or extent of host endoribonuclease activity.","definition_xrefs":["PMID:22174690"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by virus of host endoribonuclease activity (obsolete GO:0039597)","synonyms":[{"name":"viral induction of host RNAse activity","type":"exact"}],"termid":"GO:0039597"}


id: PBO:0012268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carboxylate transporter (predicted)","termid":"PBO:0012268"}


id: GO:0019286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glycine betaine from other compounds, including glycine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycine metabolic process","termid":"GO:0006544"},{"relation_name":"is_a","term_name":"glycine betaine biosynthetic process","termid":"GO:0031456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glycine betaine biosynthetic process from glycine","secondary_identifiers":["MetaCyc:P541-PWY"],"synonyms":[{"name":"N-trimethylglycine biosynthesis from glycine","type":"exact"},{"name":"N-trimethylglycine biosynthetic process from glycine","type":"exact"},{"name":"glycine betaine anabolism from glycine","type":"exact"},{"name":"glycine betaine formation from glycine","type":"exact"},{"name":"glycine betaine synthesis from glycine","type":"exact"}],"termid":"GO:0019286"}


id: PBO:0076695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A N-terminal and central domain containing 2","termid":"PBO:0076695"}


id: PBO:0087147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-dependent ATPase; involved in pre-rRNA processing at sites A0, A1, and A2, and in control of cell cycle progression; contains two upstream open reading frames (uORFs) in 5' untranslated region which regulate translation","termid":"PBO:0087147"}


id: MONDO:0003451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete laryngeal neuroendocrine tumor (obsolete MONDO:0003451)","termid":"MONDO:0003451","xrefs":{"Monarch":{"xref_id":"0003451"}}}


id: PBO:0088824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lem2-Nur1 complex subunit Nur1","termid":"PBO:0088824"}


id: GO:0039019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the pronephric nephron over time, from its formation to the mature structure. A pronephric nephron is the functional unit of the pronephros.","definition_xrefs":["XAO:00002785","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron development","termid":"GO:0072006"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pronephric nephron development","termid":"GO:0039019"}


id: MONDO:1012225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive myopathy, non-human animal","termid":"MONDO:1011793"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive myopathy, pig","secondary_identifiers":["OMIA:000829-9823"],"termid":"MONDO:1012225","xrefs":{"Monarch":{"xref_id":"1012225"}}}


id: MONDO:1011944
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":"multiple exostoses, non-human animal","secondary_identifiers":["OMIA:000354"],"termid":"MONDO:1011944","xrefs":{"Monarch":{"xref_id":"1011944"}}}


id: PR:C6Y4B8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC22F3.15 gene.","definition_xrefs":["UniProtKB:C6Y4B8","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 C22F3.15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22F3.15","synonyms":[{"name":"Spom972h-SPAC22F3.15","type":"exact"}],"termid":"PR:C6Y4B8"}


id: MONDO:0012979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the RSPH9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 12","secondary_identifiers":["DOID:0110601","GARD:15575","MEDGEN:436379","OMIM:612650","UMLS:C2675228","MESH:C567211"],"synonyms":[{"name":"CILD12","type":"exact"},{"name":"RSPH9 primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 12","type":"related"},{"name":"ciliary dyskinesia, primary, 12, without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 12","type":"exact"},{"name":"primary ciliary dyskinesia 12 without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in RSPH9","type":"exact"},{"name":"primary ciliary dyskinesia type 12","type":"exact"}],"termid":"MONDO:0012979","xrefs":{"Monarch":{"xref_id":"0012979"}}}


id: GO:0089709
data:
  {"annotated_genes":["SJAG_03256","SJAG_03400"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0089708"},{"annotations":[103362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090513"}]},"cv_name":"biological_process","definition":"The directed movement of L-histidine across a membrane.","definition_xrefs":["PMID:21307582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"aromatic amino acid transport","termid":"GO:0015801"},{"relation_name":"is_a","term_name":"azole transmembrane transport","termid":"GO:0045117"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03256":null,"SJAG_03400":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:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"L-histidine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0089709","terms_by_termid":{"GO:0089708":null,"GO:0090513":null}}


id: PBO:0055528
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 2963","termid":"PBO:0055528"}


id: PBO:0113533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar membrane protein; required for efflux of amino acids during autophagic body breakdown in vacuole; targeted to vacuole via AP-3 pathway; null mutation causes gradual loss of viability during starvation","termid":"PBO:0113533"}


id: GO:1903752
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of intrinsic apoptotic signaling pathway in response to hydrogen peroxide.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18681888"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of hydrogen peroxide-mediated programmed cell death","termid":"GO:1901300"},{"relation_name":"is_a","term_name":"positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway","termid":"GO:1902177"},{"relation_name":"is_a","term_name":"regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","termid":"GO:1903750"},{"relation_name":"positively_regulates","term_name":"intrinsic apoptotic signaling pathway in response to hydrogen peroxide","termid":"GO:0036481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","synonyms":[{"name":"activation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"activation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"narrow"},{"name":"activation of intrinsic apoptotic signaling pathway in response to H2O2","type":"narrow"},{"name":"activation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"narrow"},{"name":"positive regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"positive regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"positive regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"up regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"up regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"up regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"up regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"exact"},{"name":"up-regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"up-regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"up-regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"up-regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"exact"},{"name":"upregulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"upregulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"upregulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"upregulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"exact"}],"termid":"GO:1903752"}


id: MONDO:0800268
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial atrioventricular septal defect","termid":"MONDO:0020290"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrioventricular septal defect, susceptibility to, 1","secondary_identifiers":["MEDGEN:342900","UMLS:C1853513"],"synonyms":[{"name":"AVC defect","type":"related"},{"name":"AVSD","type":"related"},{"name":"AVSD1","type":"exact"},{"name":"atrioventricular canal defect","type":"related"},{"name":"atrioventricular septal defect","type":"related"},{"name":"endocardial cushion defect","type":"related"}],"termid":"MONDO:0800268","xrefs":{"Monarch":{"xref_id":"0800268"}}}


id: PR:Q1MTQ0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- brl1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q1MTQ0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E3 ubiquitin-protein ligase brl1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1919.15","synonyms":[{"name":"BRE1-like protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RING finger protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-brl1","type":"exact"}],"termid":"PR:Q1MTQ0"}


id: PBO:0089263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dubious, SPNCRNA.800  syntenic position","termid":"PBO:0089263"}


id: GO:0002628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of proteolysis associated with antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proteolysis involved in protein catabolic process","termid":"GO:1903050"},{"relation_name":"regulates","term_name":"proteolysis associated with antigen processing and presentation","termid":"GO:0002496"}],"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 proteolysis associated with antigen processing and presentation","termid":"GO:0002628"}


id: GO:0099500
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Fusion of the membrane of a vesicle with the plasma membrane, thereby releasing its contents into the extracellular space.","definition_xrefs":["PMID:18618940","GOC:aruk","ISBN:0071120009","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion","termid":"GO:0006906"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0061024","GO:0016192"],"is_obsolete":false,"name":"vesicle fusion to plasma membrane","termid":"GO:0099500"}


id: MONDO:0957456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dermatomyositis","termid":"MONDO:0016367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005336"],"is_obsolete":false,"name":"classical dermatomyositis","secondary_identifiers":["UMLS:C5816707","MEDGEN:1843411","Orphanet:645613"],"termid":"MONDO:0957456","xrefs":{"Monarch":{"xref_id":"0957456"}}}


id: PBO:0056995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 34b","termid":"PBO:0056995"}


id: FYPO:0004153
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype that reflects increased occurrence of flocculation when the population is in stationary phase. Flocculation is the non-sexual aggregation of single cells.","definition_xrefs":["PMID:15047724","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased flocculation","termid":"FYPO:0000155"}],"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:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased flocculation in stationary phase","termid":"FYPO:0004153"}


id: PBO:0055428
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 2858","termid":"PBO:0055428"}


id: PBO:0054632
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 2037","termid":"PBO:0054632"}


id: GO:0099019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which localization of a protein is maintained at the growing cell tip.","definition_xrefs":["GOC:vw","PMID:24146635","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of protein localization at cell tip","termid":"GO:0099017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"maintenance of protein localization at growing cell tip","synonyms":[{"name":"maintenance of protein location at growing cell tip","type":"exact"}],"termid":"GO:0099019"}


id: RO:0000081
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"a relation between a role and an independent continuant (the bearer), in which the role specifically depends on the bearer for its existence","direct_ancestors":[{"relation_name":"is_a","term_name":"inheres_in","termid":"RO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"role_of","termid":"RO:0000081"}


id: PBO:0114475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tandem fusion lysine methyltransferase/ citidine deaminase involved in riboflavin biosynthesis","termid":"PBO:0114475"}


id: PBO:0065248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 20A","termid":"PBO:0065248"}


id: MONDO:0018751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary otorhinolaryngologic disease","secondary_identifiers":["UMLS:C5681130","Orphanet:466084","GARD:21935","MEDGEN:1842579"],"synonyms":[{"name":"genetic otorhinolaryngologic disease","type":"exact"}],"termid":"MONDO:0018751","xrefs":{"Monarch":{"xref_id":"0018751"}}}


id: PBO:0050080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group AT-hook 1","termid":"PBO:0050080"}


id: MONDO:0014694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive spondylocostal dysostosis in which the cause of the disease is a mutation in the RIPPLY2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive spondylocostal dysostosis","termid":"MONDO:0010180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0024322","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"spondylocostal dysostosis 6, autosomal recessive","secondary_identifiers":["MEDGEN:899713","DOID:0112360","GARD:12807","UMLS:C4225279","OMIM:616566"],"synonyms":[{"name":"RIPPLY2 autosomal recessive spondylocostal dysostosis","type":"exact"},{"name":"SCDO6","type":"related"},{"name":"autosomal recessive spondylocostal dysostosis caused by mutation in RIPPLY2","type":"exact"},{"name":"spondylocostal dysostosis 6","type":"related"},{"name":"spondylocostal dysostosis 6, autosomal recessive","type":"exact"}],"termid":"MONDO:0014694","xrefs":{"Monarch":{"xref_id":"0014694"}}}


id: MONDO:0002752
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma that arises from the ovary. It is the most common type of ovarian carcinoma. It includes the serous adenocarcinoma, mucinous adenocarcinoma, clear cell adenocarcinoma, and endometrioid adenocarcinoma.","definition_xrefs":["NCIT:C7700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"ovarian carcinoma","termid":"MONDO:0005140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian adenocarcinoma","secondary_identifiers":["EFO:0006460","Orphanet:213504","UMLS:C0948216","GARD:20466","DOID:3713","MedDRA:10051938","MEDGEN:181757"],"synonyms":[{"name":"adenocarcinoma of ovary","type":"exact"},{"name":"adenocarcinoma of the ovary","type":"exact"},{"name":"ovarian adenocarcinoma","type":"exact"},{"name":"ovary adenocarcinoma","type":"exact"}],"termid":"MONDO:0002752","xrefs":{"Monarch":{"xref_id":"0002752"}}}


id: PBO:0054602
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 2006","termid":"PBO:0054602"}


id: PBO:0070863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L14 pseudogene 1","termid":"PBO:0070863"}


id: PBO:0086944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Receptor for a factor pheromone; couples to MAP kinase cascade to mediate pheromone response; transcribed in alpha cells and required for mating by alpha cells, ligand bound receptors endocytosed and recycled to the plasma membrane; GPCR","termid":"PBO:0086944"}


id: GO:1905782
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of phosphatidylserine exposure on apoptotic cell surface.","definition_xrefs":["GOC:kmv","PMID:17401362","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of phospholipid translocation","termid":"GO:0061092"},{"relation_name":"is_a","term_name":"regulation of phosphatidylserine exposure on apoptotic cell surface","termid":"GO:1905780"},{"relation_name":"positively_regulates","term_name":"phosphatidylserine exposure on apoptotic cell surface","termid":"GO:0070782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0061024"],"is_obsolete":false,"name":"positive regulation of phosphatidylserine exposure on apoptotic cell surface","synonyms":[{"name":"activation of externalization of phosphatidylserine","type":"narrow"},{"name":"activation of phosphatidylserine exposure on apoptotic cell surface","type":"narrow"},{"name":"positive regulation of externalization of phosphatidylserine","type":"exact"},{"name":"up regulation of externalization of phosphatidylserine","type":"exact"},{"name":"up regulation of phosphatidylserine exposure on apoptotic cell surface","type":"exact"},{"name":"up-regulation of externalization of phosphatidylserine","type":"exact"},{"name":"up-regulation of phosphatidylserine exposure on apoptotic cell surface","type":"exact"},{"name":"upregulation of externalization of phosphatidylserine","type":"exact"},{"name":"upregulation of phosphatidylserine exposure on apoptotic cell surface","type":"exact"}],"termid":"GO:1905782"}


id: PBO:0080174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"voltage dependent anion channel 1 pseudogene 9","termid":"PBO:0080174"}


id: PBO:0029519
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_morphology_viable_vegetative_cell_population_(obsolete_FYPO:0002195)","termid":"PBO:0029519"}


id: PBO:0077611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMSB4X pseudogene 2","termid":"PBO:0077611"}


id: PBO:0059954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 40","termid":"PBO:0059954"}


id: PBO:0042563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase like 5","termid":"PBO:0042563"}


id: MONDO:0014879
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete patent ductus arteriosus 3 (obsolete MONDO:0014879)","termid":"MONDO:0014879","xrefs":{"Monarch":{"xref_id":"0014879"}}}


id: GO:0048806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the genitalia over time, from its formation to the mature structure.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"},{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"},{"relation_name":"part_of","term_name":"sex differentiation","termid":"GO:0007548"}],"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":"genitalia development","synonyms":[{"name":"genital development","type":"exact"}],"termid":"GO:0048806"}


id: PBO:0064650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPFIA1 pseudogene 1","termid":"PBO:0064650"}


id: PBO:0036288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-acylglycerol-3-phosphate O-acyltransferase Vps66 (predicted)","termid":"PBO:0036288"}


id: PBO:0089871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine decarboxylase T subunit","termid":"PBO:0089871"}


id: PR:O13938
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC23H3.04 gene.","definition_xrefs":["UniProtKB:O13938","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":"UPF0658 Golgi apparatus membrane protein C23H3.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23H3.04","synonyms":[{"name":"Spom972h-SPAC23H3.04","type":"exact"}],"termid":"PR:O13938"}


id: MONDO:0001705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"idiopathic aplastic anemia","termid":"MONDO:0012197"},{"relation_name":"is_a","term_name":"anemia","termid":"MONDO:0002280"}],"gene_count":0,"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":"pure red-cell aplasia","secondary_identifiers":["MESH:D012010","NORD:1636","NCIT:C34974","NANDO:2100177","GARD:7504","ICD9:284.81","DOID:1340","MEDGEN:11154","SCTID:50715003","UMLS:C0034902"],"synonyms":[{"name":"PRCA","type":"exact"},{"name":"Pure Red Cell Aplasia, Acquired","type":"exact"},{"name":"primary red cell aplasia","type":"exact"},{"name":"pure red cell aplasia","type":"exact"},{"name":"red cell hypoplasia","type":"exact"}],"termid":"MONDO:0001705","xrefs":{"Monarch":{"xref_id":"0001705"}}}


id: GO:0030558
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Specifies the site of pseudouridylation in an RNA molecule by base pairing with a short sequence around the target residue.","definition_xrefs":["PMID:12457565","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA modification guide activity","termid":"GO:0030555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003723","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"RNA pseudouridylation guide activity","termid":"GO:0030558"}


id: PBO:0031449
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_pre-replicative_complex_assembly","termid":"PBO:0031449"}


id: _global:has_negative_regulatory_component_activity
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A relationship that holds between a GO molecular function and a component of that molecular function that negatively regulates the activity of the whole.  More formally, A 'has regulatory component activity' B iff :A and B are GO molecular functions (GO_0003674), A has_component B and A is negatively regulated by B.","direct_ancestors":[{"relation_name":"is_a","term_name":"has_regulatory_component_activity","termid":"_global:has_regulatory_component_activity"},{"relation_name":"is_a","term_name":"negatively_regulated_by","termid":"_global:negatively_regulated_by"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_negative_regulatory_component_activity","secondary_identifiers":["RO:0002014"],"termid":"_global:has_negative_regulatory_component_activity"}


id: PBO:0114111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"REX family exonuclease, implicated in rDNA metabolism or ribosome biogenesis, potential human ISG20L2 ortholog","termid":"PBO:0114111"}


id: PBO:0059382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S21 pseudogene 7","termid":"PBO:0059382"}


id: GO:0048623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a seed germinates before being shed from the parent plant.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"seed germination","termid":"GO:0009845"}],"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":"seed germination on parent plant","synonyms":[{"name":"non-vegetative vivipary","type":"broad"},{"name":"pre-harvest sprouting","type":"exact"},{"name":"vivipary","type":"broad"}],"termid":"GO:0048623"}


id: PBO:0071541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 6","termid":"PBO:0071541"}


id: GO:0007083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The cell cycle process in which chromosome structure is altered from the condensed form taken on during mitosis to the relaxed disperse form held in resting cells.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete mitotic chromosome decondensation (obsolete GO:0007083)","termid":"GO:0007083"}


id: PBO:0064611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 5 homeobox 1B","termid":"PBO:0064611"}


id: PBO:0080199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VENT homeobox pseudogene 7","termid":"PBO:0080199"}


id: MOD:00717
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to a methylated phenylalanine, such as N-methyl-L-phenylalanine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated phenylalanine","synonyms":[{"name":"MePhe","type":"exact"}],"termid":"MOD:00717"}


id: FYECO:0000376
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in defined medium containing pyruvate, salts and water. May be supplemented with a set of amino acids as per the auxotrophic requirements of the strain.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate MM","synonyms":[{"name":"pyruvate minimal medium","type":"exact"}],"termid":"FYECO:0000376"}


id: PBO:0029803
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-short_actin_cables","termid":"PBO:0029803"}


id: PBO:0028789
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_heterochromatin_assembly_at_centromere_outer_repeat","termid":"PBO:0028789"}


id: MONDO:1011899
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olivopontocerebellar degeneration, non-human animal","secondary_identifiers":["OMIA:002454"],"termid":"MONDO:1011899","xrefs":{"Monarch":{"xref_id":"1011899"}}}


id: PBO:0053725
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 939","termid":"PBO:0053725"}


id: PBO:0036112
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-K4_acetylation_during_vegetative_growth","termid":"PBO:0036112"}


id: PBO:0073385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET domain containing 1B, histone lysine methyltransferase","termid":"PBO:0073385"}


id: PBO:0031139
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_actomyosin_contractile_ring_myosin_filament_organization","termid":"PBO:0031139"}


id: GO:0048383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesectoderm over time, from its formation to the mature structure. In animal embryos, mesectoderm development processes give rise to both mesoderm and ectoderm tissues.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"},{"relation_name":"part_of","term_name":"ectoderm development","termid":"GO:0007398"},{"relation_name":"part_of","term_name":"mesoderm development","termid":"GO:0007498"}],"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":"mesectoderm development","termid":"GO:0048383"}


id: GO:0106120
data:
  {"annotated_genes":["SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of a sterol biosynthetic process.","definition_xrefs":["PMID:16459310","GOC:BHF_miRNA","GOC:rph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of steroid biosynthetic process","termid":"GO:0010893"},{"relation_name":"is_a","term_name":"regulation of sterol biosynthetic process","termid":"GO:0106118"},{"relation_name":"positively_regulates","term_name":"sterol biosynthetic process","termid":"GO:0016126"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of sterol biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106120","terms_by_termid":{"GO:0070452":null}}


id: GO:0010657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A form of programmed cell death induced by external or internal signals that trigger the activity of proteolytic caspases, whose actions dismantle a muscle cell and result in its death. A muscle cell is a mature contractile cell, commonly known as a myocyte, that forms one of three kinds of muscle.","definition_xrefs":["GOC:mtg_apoptosis","GOC:dph","GOC:tb","CL:0000187"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"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":"muscle cell apoptotic process","synonyms":[{"name":"muscle cell apoptosis","type":"narrow"}],"termid":"GO:0010657"}


id: GO:1990170
data:
  {"annotated_genes":["SJAG_04516","SJAG_01344","SJAG_02599","SJAG_01351","SJAG_00988","SJAG_03497"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96517,107991,117821,72607,96555,92781],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098849"}]},"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 a cadmium ion stimulus.","definition_xrefs":["GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cadmium ion","termid":"GO:0046686"},{"relation_name":"is_a","term_name":"stress response to metal ion","termid":"GO:0097501"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00988":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_02599":null,"SJAG_03497":null,"SJAG_04516":null},"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 cadmium ion","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"response to cadmium ion stress","type":"exact"},{"name":"response to cadmium toxicity","type":"related"},{"name":"stress response to cadmium","type":"broad"}],"termid":"GO:1990170","terms_by_termid":{"GO:0098849":null}}


id: FYPO:0005551
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 localization of a protein to the cleavage furrow is decreased.","definition_xrefs":["PMID:27082518","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to cell division site","termid":"FYPO:0002869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to cleavage furrow","synonyms":[{"name":"decreased protein localisation to cleavage furrow","type":"exact"},{"name":"decreased protein localization to cleavage furrow during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to cleavage furrow during vegetative growth","type":"exact"},{"name":"reduced protein localization to cleavage furrow","type":"exact"}],"termid":"FYPO:0005551"}


id: PBO:0003512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR6 family, implicated in cell cycle","termid":"PBO:0003512"}


id: GO:0086069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that mediates interactions between a bundle of His cell and its surroundings that contributes to the process of the bundle of His cell communicating with a Purkinje myocyte in cardiac conduction. Encompasses interactions such as signaling or attachment between one cell and another cell, between a cell and an extracellular matrix, or between a cell and any other aspect of its environment.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell communication involved in cardiac conduction","termid":"GO:0086065"}],"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":"bundle of His cell to Purkinje myocyte communication","synonyms":[{"name":"atrioventricular junction myocyte to bundle branch myocyte","type":"narrow"},{"name":"bundle branch myocyte to Purkinje myocyte communication","type":"narrow"},{"name":"bundle of His cardiac muscle cell to Purkinje myocyte communication","type":"exact"},{"name":"bundle of His myocyte to atrioventricular junction myocyte","type":"narrow"},{"name":"ventricular conduction system cell to cell communication","type":"exact"}],"termid":"GO:0086069"}


id: PBO:0060854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEK2 pseudogene 2","termid":"PBO:0060854"}


id: MONDO:0008546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Thanatophoric dysplasia type 1 (TD1) is a form of TD characterized by short, bowed femurs, micromelia, narrow thorax, and brachydactyly.","definition_xrefs":["Orphanet:1860"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"severe achondroplasia-developmental delay-acanthosis nigricans syndrome","termid":"MONDO:0014658"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"thanatophoric dysplasia","termid":"MONDO:0017042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005497"],"is_obsolete":false,"name":"thanatophoric dysplasia type 1","secondary_identifiers":["OMIM:187600","OMIM:270230","NANDO:1200875","UMLS:C1868678","NCIT:C98583","GARD:9295","MEDGEN:358383"],"synonyms":[{"name":"PLSD San Diego type","type":"related"},{"name":"Platyspondylic lethal skeletal dysplasia, San Diego type","type":"related"},{"name":"TD1","type":"exact"},{"name":"lethal short-limbed Platyspondylic dwarfism, San Diego type","type":"related"},{"name":"thanatophoric dwarfism","type":"related"},{"name":"thanatophoric dwarfism 1","type":"related"},{"name":"thanatophoric dwarfism type 1","type":"exact"},{"name":"thanatophoric dysplasia","type":"related"},{"name":"thanatophoric dysplasia type I","type":"related"},{"name":"thanatophoric dysplasia, type 1","type":"exact"},{"name":"thanatophoric dysplasia, type I","type":"related"},{"name":"type 1 thanatophoric dysplasia","type":"exact"}],"termid":"MONDO:0008546","xrefs":{"Monarch":{"xref_id":"0008546"}}}


id: PBO:0061144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NME/NM23 family member 7","termid":"PBO:0061144"}


id: PBO:0085724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in the HOG (high osmolarity glycerol) pathway; negatively regulates Hog1p by recruitment of phosphatase Ptc1p to the Pbs2p-Hog1p complex; interacts with Bck1p and down regulates the cell wall integrity pathway; found in the nucleus and cytoplasm; contains an SH3 domain and a Ptc1p binding domain (PBM)","termid":"PBO:0085724"}


id: MONDO:0003428
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the brain.","definition_xrefs":["NCIT:C7739"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracranial hemangioma","termid":"MONDO:0002328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain hemangioma","secondary_identifiers":["MEDGEN:116075","DOID:5393","UMLS:C0238814"],"synonyms":[{"name":"brain angioma","type":"exact"},{"name":"brain hemangioma","type":"exact"}],"termid":"MONDO:0003428","xrefs":{"Monarch":{"xref_id":"0003428"}}}


id: PBO:0041729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAMK2G antisense RNA 1","termid":"PBO:0041729"}


id: PBO:0047101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAM151B divergent transcript","termid":"PBO:0047101"}


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:14512630","PMID:22814176"],"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:0050587
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: chloride + O2 = chlorite.","definition_xrefs":["RHEA:21404","EC:1.13.11.49"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"chlorite O2-lyase activity","secondary_identifiers":["KEGG_REACTION:R05721","GO:0030065","MetaCyc:1.13.11.49-RXN","UM-BBD_reactionID:r0982"],"synonyms":[{"name":"chloride:oxygen oxidoreductase activity","type":"related"},{"name":"chlorite dismutase activity","type":"related"}],"termid":"GO:0050587"}


id: PBO:0054761
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 2173","termid":"PBO:0054761"}


id: MONDO:0013234
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypokalemic periodic paralysis","termid":"MONDO:0008223"},{"relation_name":"is_a","term_name":"SCN4A-related channelopathy","termid":"MONDO:0800468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hypokalemic periodic paralysis, type 2","secondary_identifiers":["OMIM:613345","UMLS:C2750061","GARD:15649","MEDGEN:413748","MESH:C567635"],"synonyms":[{"name":"HOKPP2","type":"related"},{"name":"hypokalemic periodic paralysis, type 2","type":"exact"}],"termid":"MONDO:0013234","xrefs":{"Monarch":{"xref_id":"0013234"}}}


id: GO:0052163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a symbiont modulates the frequency, rate or extent of the production of nitric oxide as part of the innate immune response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiont defense to host-produced nitric oxide (obsolete GO:0052163)","synonyms":[{"name":"defense response to host innate immune response nitric oxide production","type":"narrow"},{"name":"evasion or tolerance by organism of host NO","type":"exact"},{"name":"evasion or tolerance by organism of host nitric oxide","type":"exact"},{"name":"evasion or tolerance by organism of host-produced NO","type":"exact"},{"name":"evasion or tolerance by organism of host-produced nitric oxide","type":"exact"},{"name":"evasion or tolerance by organism of nitric oxide produced by other organism involved in symbiotic interaction","type":"broad"},{"name":"evasion or tolerance by symbiont of host-produced nitric oxide","type":"exact"},{"name":"evasion or tolerance of NO produced by host in response to organism","type":"exact"},{"name":"evasion or tolerance of nitric oxide produced by host in response to organism","type":"exact"},{"name":"modulation by organism of defense-related host NO production","type":"exact"},{"name":"modulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of defense-related host nitric oxide production","type":"related"},{"name":"response to defense-related host nitric oxide production","type":"related"},{"name":"response to defense-related nitric oxide production by other organism involved in symbiotic interaction","type":"broad"}],"termid":"GO:0052163"}


id: GO:1990590
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Transcription factor complex consisting of ATF1 and ATF4 subunits that is capable of binding to cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3') of the GRP78 (HSPA5) promoter. Involved in the ER stress response pathway.","definition_xrefs":["GOC:bhm","PMID:12871976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"ATF1-ATF4 transcription factor complex","termid":"GO:1990590"}


id: PBO:0076514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 15 pseudogene","termid":"PBO:0076514"}


id: GO:0006561
data:
  {"annotated_genes":["SJAG_00660","SJAG_00495","SJAG_03457","SJAG_00120"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79649,90349,65687,68786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0055129"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of proline (pyrrolidine-2-carboxylic acid), a chiral, cyclic, nonessential alpha-amino acid found in peptide linkage in proteins.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proline metabolic process","termid":"GO:0006560"},{"relation_name":"is_a","term_name":"glutamine family amino acid biosynthetic process","termid":"GO:0009084"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00120":null,"SJAG_00495":null,"SJAG_00660":null,"SJAG_03457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"proline biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"proline anabolism","type":"exact"},{"name":"proline biosynthesis","type":"exact"},{"name":"proline formation","type":"exact"},{"name":"proline synthesis","type":"exact"}],"termid":"GO:0006561","terms_by_termid":{"GO:0055129":null}}


id: GO:0018040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a C-terminal peptidyl-glutamic acid amide by hydrolysis and oxidation of an interior Glu-Gly peptide in a secreted protein.","definition_xrefs":["RESID:AA0087"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal peptidyl-glutamic acid amidation (obsolete GO:0018040)","termid":"GO:0018040"}


id: MONDO:0018520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare epithelial tumor of pancreas (obsolete MONDO:0018520)","secondary_identifiers":["Orphanet:424033"],"synonyms":[{"name":"rare pancreatic epithelial tumor","type":"exact"}],"termid":"MONDO:0018520","xrefs":{"Monarch":{"xref_id":"0018520"}}}


id: PBO:0116708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily H member 1 pseudogene (gene/pseudogene)","termid":"PBO:0116708"}


id: PBO:0113417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein involved in asymmetric localization of ASH1 mRNA; represses translation of ASH1 mRNA, an effect reversed by Yck1p-dependent phosphoryation; regulates telomere position effect and length; similarity to hnRNP-K; increases mRNA stability by binding (CNN)n repeat elements","termid":"PBO:0113417"}


id: MONDO:0957281
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nemaline myopathy","termid":"MONDO:0018958"}],"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":"nemaline myopathy 5B, autosomal recessive, childhood-onset","secondary_identifiers":["MEDGEN:1841181","UMLS:C5830545","OMIM:620386","DOID:0081374"],"termid":"MONDO:0957281","xrefs":{"Monarch":{"xref_id":"0957281"}}}


id: PBO:0111344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small subunit processome, U3 snoRNA associated protein Dip2","termid":"PBO:0111344"}


id: GO:0070316
data:
  {"annotated_genes":["SJAG_03689","SJAG_03356","SJAG_02621"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99073,115584,117710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070317"}]},"cv_name":"biological_process","definition":"A cell cycle process that modulates the rate or extent of the transition from the G0 quiescent state to the G1 phase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"regulates","term_name":"G0 to G1 transition","termid":"GO:0045023"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03356":null,"SJAG_03689":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of G0 to G1 transition","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070316","terms_by_termid":{"GO:0070317":null}}


id: GO:0050280
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-5-O-methyl-myo-inositol + NAD+ = 2D-5-O-methyl-2,3,5/4,6-pentahydroxycyclohexanone + H+ + NADH.","definition_xrefs":["EC:1.1.1.143","RHEA:11300"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"sequoyitol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R03497","MetaCyc:SEQUOYITOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"5-O-methyl-myo-inositol:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0050280"}


id: PBO:0111773
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-DNL","termid":"PBO:0111773"}


id: GO:0052244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism within a second organism towards a lower level of a physical stimulus involved in energy generation, such as light, oxygen, and oxidizable substrates, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative energy taxis in other organism involved in symbiotic interaction (obsolete GO:0052244)","synonyms":[{"name":"negative energy taxis in other organism during symbiotic interaction","type":"related"},{"name":"negative energy taxis within other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052244"}


id: GO:0008409
data:
  {"annotated_genes":["SJAG_03734","SJAG_03994","SJAG_04410","SJAG_01648","SJAG_03276","SJAG_04587","SJAG_05280","SJAG_01173","SJAG_01832","SJAG_02275"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80247],"is_not":false,"summary":null,"term":"GO:0008409"},{"annotations":[87850,73038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035312"},{"annotations":[75260,79681,71747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004534"},{"annotations":[78809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033699"},{"annotations":[107312,96631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051908"},{"annotations":[74408,96633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045145"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within nucleic acids by removing nucleotide residues from the 5' end.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exonuclease activity","termid":"GO:0004527"}],"gene_count":10,"genes_by_uniquename":{"SJAG_01173":null,"SJAG_01648":null,"SJAG_01832":null,"SJAG_02275":null,"SJAG_03276":null,"SJAG_03734":null,"SJAG_03994":null,"SJAG_04410":null,"SJAG_04587":null,"SJAG_05280":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0016787","GO:0004527","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"5'-3' exonuclease activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5358599","Reactome:R-HSA-5358619"],"termid":"GO:0008409","terms_by_termid":{"GO:0004534":null,"GO:0008409":null,"GO:0033699":null,"GO:0035312":null,"GO:0045145":null,"GO:0051908":null}}


id: GO:1901571
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a fatty acid derivative into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"fatty acid derivative transport","termid":"GO:1901571"}


id: GO:0044616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism induces paralysis in another organism via the action of a venom. Paralysis is the loss of the ability to voluntarily control muscles. This can occur by blocking nerve signals at the neuromuscular junction or by directly interfering with muscle contraction.","definition_xrefs":["PMID:28422078","PMID:36668869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of nervous system process","termid":"GO:0140136"}],"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":"venom-mediated paralysis","synonyms":[{"name":"envenomation resulting in paralysis in another organism","type":"exact"},{"name":"modulation of relaxation of muscle in another organism","type":"related"},{"name":"modulation of relaxation of muscle in other organism","type":"exact"},{"name":"regulation of relaxation of muscle in other organism","type":"exact"}],"termid":"GO:0044616"}


id: PBO:0076374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGF-beta activated kinase 1 (MAP3K7) binding protein 2","termid":"PBO:0076374"}


id: SO:0000464
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non-functional descendant of an exon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudogenic_region","termid":"SO:0000462"},{"relation_name":"non_functional_homolog_of","term_name":"exon","termid":"SO:0000147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decayed_exon","synonyms":[{"name":"decayed exon","type":"exact"}],"termid":"SO:0000464"}


id: PBO:0040299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP2B2 intronic transcript 1","termid":"PBO:0040299"}


id: FYPO:0003484
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 mitotic spindle midzone does not occur. The mitotic spindle midzone is the area in the center of the mitotic spindle where the spindle microtubules from opposite poles overlap.","definition_xrefs":["GO:1990023","PomBase:mah","GO:1902967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to mitotic spindle","termid":"FYPO:0003186"},{"relation_name":"is_a","term_name":"abnormal protein localization to mitotic spindle midzone","termid":"FYPO:0004883"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to mitotic spindle midzone","synonyms":[{"name":"abolished protein localization to mitotic spindle midzone during mitotic cell cycle","type":"related"},{"name":"protein absent from mitotic spindle midzone","type":"related"},{"name":"protein localisation to mitotic spindle midzone abolished","type":"exact"},{"name":"protein localization to mitotic spindle midzone abolished","type":"exact"},{"name":"protein localization to spindle midzone abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0003484"}


id: SO:0001455
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A relatively rare amino acid encoded by the codon UGA in some contexts, whereas UGA is a termination codon in other contexts.","definition_xrefs":["PMID:23275319"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenocysteine","synonyms":[{"name":"Sec","type":"exact"},{"name":"U","type":"exact"}],"termid":"SO:0001455"}


id: MONDO:0001972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.","definition_xrefs":["DOID:14456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brucellosis","termid":"MONDO:0005683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Brucella melitensis brucellosis","secondary_identifiers":["MEDGEN:549869","ICD9:023.0","UMLS:C0302362","SCTID:427999003"],"termid":"MONDO:0001972","xrefs":{"Monarch":{"xref_id":"0001972"}}}


id: GO:0085032
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts an NF-kappaB-mediated signaling cascade in its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host signal transduction pathway","termid":"GO:0052027"}],"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 NF-kappaB cascade","synonyms":[{"name":"modulation by symbiont of host I-kappaB kinase/NF-kappaB cascade","type":"related"},{"name":"modulation by symbiont of host NF-kappaB-mediated signal transduction pathway","type":"exact"},{"name":"perturbation of host I-kappaB kinase/NF-kappaB cascade","type":"exact"},{"name":"perturbation of host canonical NF-kappaB cascade","type":"related"},{"name":"symbiont-mediated perturbation of host canonical NF-kappaB cascade","type":"related"}],"termid":"GO:0085032"}


id: MONDO:0002503
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An astrocytic tumor occurring during adulthood. Representative examples include diffuse astrocytoma, anaplastic astrocytoma, and glioblastoma.","definition_xrefs":["NCIT:C7049"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astrocytic tumor","termid":"MONDO:0021636"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adult astrocytic tumor","secondary_identifiers":["MEDGEN:272290","UMLS:C1332183","DOID:3076"],"synonyms":[{"name":"adult astrocytic neoplasm","type":"exact"},{"name":"adult astrocytic tumor","type":"exact"},{"name":"adult astrocytoma","type":"exact"},{"name":"astrocytic tumor","type":"broad"},{"name":"astrocytic tumour","type":"broad"}],"termid":"MONDO:0002503","xrefs":{"Monarch":{"xref_id":"0002503"}}}


id: PBO:0041864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 9","termid":"PBO:0041864"}


id: PBO:0080239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 2","termid":"PBO:0080239"}


id: MONDO:0004351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that arises within the eye. Signs and symptoms include decreased vision, uveitis, and vitreous floaters.","definition_xrefs":["NCIT:C9184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye lymphoma","termid":"MONDO:0004034"},{"relation_name":"is_a","term_name":"primary organ-specific lymphoma","termid":"MONDO:0017207"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"intraocular lymphoma","secondary_identifiers":["Orphanet:279904","ICD9:200.50","GARD:21063","MEDGEN:79344","SCTID:420788006","UMLS:C0281658","MONDO:0017206","DOID:775","MESH:D064090"],"synonyms":[{"name":"PIOL","type":"exact"},{"name":"intraocular lymphoma","type":"exact"},{"name":"primary intraocular lymphoma","type":"exact"},{"name":"primary intraocular non-Hodgkin's lymphoma","type":"exact"}],"termid":"MONDO:0004351","xrefs":{"Monarch":{"xref_id":"0004351"}}}


id: PBO:0043977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSAG family member 3","termid":"PBO:0043977"}


id: GO:0098023
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The basal end of the virus tail, which is used by the virus to attach to the host cell.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"virion component","termid":"GO:0044423"},{"relation_name":"part_of","term_name":"virus tail","termid":"GO:0098015"}],"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":"virus tail, tip","synonyms":[{"name":"bacteriophage tail tip","type":"narrow"}],"termid":"GO:0098023"}


id: PBO:0038448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanyl-tRNA synthetase 1","termid":"PBO:0038448"}


id: GO:0009377
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the ATP-dependent hydrolysis of peptide bonds in substrates including E. coli SulA and misfolded proteins.","definition_xrefs":["GOC:mah","PMID:10368141"],"gene_count":0,"genotype_count":0,"name":"obsolete HslUV protease activity (obsolete GO:0009377)","synonyms":[{"name":"HslUV protease activity","type":"exact"}],"termid":"GO:0009377"}


id: PBO:0066656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIO kinase 3 pseudogene 1","termid":"PBO:0066656"}


id: PBO:0071136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22","termid":"PBO:0071136"}


id: PBO:0071111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 113","termid":"PBO:0071111"}


id: PBO:0081124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFHX2 antisense RNA 1","termid":"PBO:0081124"}


id: GO:0042602
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: reduced riboflavin + NADP+ = riboflavin + NADPH + 2 H+.","definition_xrefs":["RHEA:19377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"riboflavin reductase [NAD(P)H] activity","termid":"GO:0052875"}],"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":"riboflavin reductase (NADPH) activity","secondary_identifiers":["MetaCyc:NADPH-DEHYDROGENASE-FLAVIN-RXN","EC:1.5.1.30","KEGG_REACTION:R05707"],"synonyms":[{"name":"FMN reductase (NADPH) activity","type":"related"},{"name":"NADPH dehydrogenase (riboflavin) activity","type":"related"},{"name":"NADPH-FMN reductase activity","type":"related"},{"name":"NADPH-dependent FMN reductase activity","type":"related"},{"name":"NADPH-riboflavin oxidoreductase activity","type":"exact"},{"name":"NADPH-riboflavin reductase activity","type":"related"},{"name":"NADPH-specific FMN reductase activity","type":"related"},{"name":"NADPH:riboflavin oxidoreductase activity","type":"related"},{"name":"flavin reductase activity","type":"related"},{"name":"reduced-riboflavin:NADP+ oxidoreductase activity","type":"related"},{"name":"riboflavin mononucleotide (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"related"},{"name":"riboflavin mononucleotide reductase activity","type":"broad"},{"name":"riboflavine mononucleotide reductase activity","type":"broad"}],"termid":"GO:0042602"}


id: PBO:0082201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha 1,2-mannosyltransferase; involved in glycosyl phosphatidyl inositol (GPI) biosynthesis; required for addition of the fourth, side branching mannose to the GPI core structure","termid":"PBO:0082201"}


id: GO:0046354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mannan, the main hemicellulose of soft (coniferous) wood, made up of D-mannose, D-glucose and D-galactose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannan metabolic process","termid":"GO:0010412"},{"relation_name":"is_a","term_name":"cell wall polysaccharide biosynthetic process","termid":"GO:0070592"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0071554"],"is_obsolete":false,"name":"mannan biosynthetic process","synonyms":[{"name":"mannan anabolism","type":"exact"},{"name":"mannan biosynthesis","type":"exact"},{"name":"mannan formation","type":"exact"},{"name":"mannan synthesis","type":"exact"}],"termid":"GO:0046354"}


id: MONDO:0011041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ectodermal dysplasia with natal teeth, Turnpenny type is characterized by hypo- or oligodontia and acanthosis nigricans. It has been described in four generations of one family. Onset generally occurs during adolescence. Some patients were born with multiple teeth. Hair anomalies (sparse body and scalp hair) were also reported. Inheritance is autosomal dominant.","definition_xrefs":["Orphanet:69083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ectodermal dysplasia with natal teeth, Turnpenny type","secondary_identifiers":["MESH:C563347","OMIM:601345","UMLS:C1832444","SCTID:715576000","MEDGEN:371331","GARD:10526","icd11.foundation:612149960"],"synonyms":[{"name":"ectodermal dysplasia with natal teeth Turnpenny type","type":"related"},{"name":"ectodermal dysplasia with natal teeth, Turnpenny type","type":"exact"},{"name":"ectodermal dysplasia, hair/Tooth type","type":"related"}],"termid":"MONDO:0011041","xrefs":{"Monarch":{"xref_id":"0011041"}}}


id: GO:1904848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell chemotaxis to fibroblast growth factor.","definition_xrefs":["GO_REF:0000058","GOC:BHF_miRNA","GOC:rph","PMID:23233752","GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell migration","termid":"GO:0030336"},{"relation_name":"is_a","term_name":"negative regulation of chemotaxis","termid":"GO:0050922"},{"relation_name":"is_a","term_name":"negative regulation of cellular response to growth factor stimulus","termid":"GO:0090288"},{"relation_name":"is_a","term_name":"regulation of cell chemotaxis to fibroblast growth factor","termid":"GO:1904847"},{"relation_name":"negatively_regulates","term_name":"cell chemotaxis to fibroblast growth factor","termid":"GO:0035766"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of cell chemotaxis to fibroblast growth factor","synonyms":[{"name":"down regulation of cell chemotaxis to fibroblast growth factor","type":"exact"},{"name":"down-regulation of cell chemotaxis to fibroblast growth factor","type":"exact"},{"name":"downregulation of cell chemotaxis to fibroblast growth factor","type":"exact"},{"name":"inhibition of cell chemotaxis to fibroblast growth factor","type":"narrow"}],"termid":"GO:1904848"}


id: PR:P30776
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A double-strand-break repair protein rad21 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR12585:SF5"],"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":"cohesin subunit rad21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC338.17c","secondary_identifiers":["UniProtKB:P30776"],"synonyms":[{"name":"SCC1 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPCC338.17c","type":"related"},{"name":"Spom972h-RAD21","type":"exact"},{"name":"double-strand-break repair protein rad21 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P30776"}


id: PBO:0108568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo-type fold protein, zf-MYND type zinc finger protein, Mub1-Rad6-Ubr2 ubiquitin ligase complex Mub1","termid":"PBO:0108568"}


id: PBO:0091356
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Target Of Sbf, after S. cerevisiae","termid":"PBO:0091356"}


id: MOD:00366
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-sulfo-L-serine.","definition_xrefs":["RESID:AA0361","Unimod:40#S","PubMed:14752058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfated residue","termid":"MOD:00695"},{"relation_name":"is_a","term_name":"residues isobaric at 166.98-167.00 Da","termid":"MOD:00771"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-sulfo-L-serine","synonyms":[{"name":"(2S)-2-amino-3-(sulfooxy)propanoic acid","type":"exact"},{"name":"2-amino-3-hydroxypropanoic acid 3-sulfate","type":"exact"},{"name":"MOD_RES Sulfoserine","type":"exact"},{"name":"O-Sulfonation","type":"related"},{"name":"O-sulfo-L-serine","type":"exact"},{"name":"O3-sulfonoserine","type":"exact"},{"name":"O3-sulfoserine","type":"exact"},{"name":"Sulfo","type":"related"},{"name":"serine sulfate ester","type":"exact"}],"termid":"MOD:00366"}


id: MONDO:0013510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial melanoma","termid":"MONDO:0018961"},{"relation_name":"excluded_subClassOf","term_name":"susceptibility to familial cutaneous melanoma","termid":"MONDO:0024462"},{"relation_name":"is_a","term_name":"susceptibility to familial cutaneous melanoma","termid":"MONDO:0024462"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoma, cutaneous malignant, susceptibility to, 6","secondary_identifiers":["OMIM:613972","MEDGEN:462767","UMLS:C3151417"],"synonyms":[{"name":"CMM6","type":"related"},{"name":"melanoma, cutaneous malignant, 6","type":"exact"},{"name":"melanoma, cutaneous malignant, susceptibility to, 6","type":"exact"},{"name":"melanoma, cutaneous malignant, susceptibility to, type 6","type":"exact"},{"name":"susceptibility to cutaneous malignant melanoma 6","type":"related"}],"termid":"MONDO:0013510","xrefs":{"Monarch":{"xref_id":"0013510"}}}


id: PR:Q09150
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A WD repeat-containing protein 61 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03420","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":"meiotic recombination protein rec14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC32F12.02","secondary_identifiers":["UniProtKB:Q09150"],"synonyms":[{"name":"Spom972h-WDR61","type":"exact"}],"termid":"PR:Q09150"}


id: PBO:0071068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 70","termid":"PBO:0071068"}


id: MONDO:0018175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Combined deficiency of factor V and factor VIII is an inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms.","definition_xrefs":["Orphanet:35909"],"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":"combined deficiency of factor V and factor VIII","secondary_identifiers":["icd11.foundation:184219764","GARD:16639","MEDGEN:384006","NANDO:2200686","SCTID:715559004","UMLS:C1856883"],"synonyms":[{"name":"F5F8D","type":"exact"},{"name":"FV and FVIII combined deficiency","type":"exact"},{"name":"combined deficiency of factor V and factor type VIII","type":"exact"},{"name":"familial multiple coagulation factor deficiency","type":"exact"}],"termid":"MONDO:0018175","xrefs":{"Monarch":{"xref_id":"0018175"}}}


id: PBO:0054622
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 2027","termid":"PBO:0054622"}


id: GO:0021636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the trigeminal nerve is generated and organized. The trigeminal nerve is composed of three large branches. They are the ophthalmic (V1, sensory), maxillary (V2, sensory) and mandibular (V3, motor and sensory) branches. The sensory ophthalmic branch travels through the superior orbital fissure and passes through the orbit to reach the skin of the forehead and top of the head. The maxillary nerve contains sensory branches that reach the pterygopalatine fossa via the inferior orbital fissure (face, cheek and upper teeth) and pterygopalatine canal (soft and hard palate, nasal cavity and pharynx). The motor part of the mandibular branch is distributed to the muscles of mastication, the mylohyoid muscle and the anterior belly of the digastric. The mandibular nerve also innervates the tensor veli palatini and tensor tympani muscles. The sensory part of the mandibular nerve is composed of branches that carry general sensory information from the mucous membranes of the mouth and cheek, anterior two-thirds of the tongue, lower teeth, skin of the lower jaw, side of the head and scalp and meninges of the anterior and middle cranial fossae.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:dph","GOC:jid","GOC:cls","ISBN:0838580343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve morphogenesis","termid":"GO:0021602"},{"relation_name":"part_of","term_name":"trigeminal nerve development","termid":"GO:0021559"}],"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":"trigeminal nerve morphogenesis","synonyms":[{"name":"CN V morphogenesis","type":"related"}],"termid":"GO:0021636"}


id: GO:0016866
data:
  {"annotated_genes":["SJAG_00518","SJAG_00319","SJAG_00134","SJAG_02783","SJAG_02978","SJAG_04065","SJAG_01209","SJAG_00978","SJAG_03572","SJAG_00088","SJAG_03360","SJAG_00624","SJAG_03723","SJAG_02009","SJAG_04754","SJAG_01172"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67800],"is_not":false,"summary":null,"term":"GO:0016866"},{"annotations":[76733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004106"},{"annotations":[75725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000250"},{"annotations":[112076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160153"},{"annotations":[72752,73689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004610"},{"annotations":[78370,115443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004614"},{"annotations":[74193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004619"},{"annotations":[80982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004615"},{"annotations":[75198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008973"},{"annotations":[105781,94854,113898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106032"},{"annotations":[90681,94151,113899],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106029"},{"annotations":[105782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160150"},{"annotations":[102021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160148"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a functional group from one position to another within a single molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isomerase activity","termid":"GO:0016853"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00088":null,"SJAG_00134":null,"SJAG_00319":null,"SJAG_00518":null,"SJAG_00624":null,"SJAG_00978":null,"SJAG_01172":null,"SJAG_01209":null,"SJAG_02009":null,"SJAG_02783":null,"SJAG_02978":null,"SJAG_03360":null,"SJAG_03572":null,"SJAG_03723":null,"SJAG_04065":null,"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"intramolecular transferase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:5.4.-.-"],"synonyms":[{"name":"intramolecular transferase activity, transferring other groups","type":"narrow"},{"name":"mutase activity","type":"exact"}],"termid":"GO:0016866","terms_by_termid":{"GO:0000250":null,"GO:0004106":null,"GO:0004610":null,"GO:0004614":null,"GO:0004615":null,"GO:0004619":null,"GO:0008973":null,"GO:0016866":null,"GO:0106029":null,"GO:0106032":null,"GO:0160148":null,"GO:0160150":null,"GO:0160153":null}}


id: PBO:0070931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 39","termid":"PBO:0070931"}


id: PBO:0003734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L51 (predicted)","termid":"PBO:0003734"}


id: GO:0061407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a hydrogen peroxide (H2O2) stimulus.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to hydrogen peroxide (obsolete GO:0061407)","termid":"GO:0061407"}


id: GO:0001792
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a J-chain-containing polymeric immunoglobulin of the IgA or IgM isotypes via the Fc region, and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:add","GOC:signaling","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin receptor activity","termid":"GO:0019763"}],"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":"polymeric immunoglobulin receptor activity","termid":"GO:0001792"}


id: PBO:0027049
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_ionizing_radiation_during_mitotic_G1_phase","termid":"PBO:0027049"}


id: FYPO:0006312
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of DNA-3'-diphospho-5'-guanosine diphosphatase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal DNA-3'-diphospho-5'-guanosine diphosphatase activity","termid":"FYPO:0006310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000661","FYPO:0000707","FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"decreased DNA-3'-diphospho-5'-guanosine diphosphatase activity","synonyms":[{"name":"reduced DNA-3'-diphospho-5'-guanosine diphosphatase activity","type":"exact"}],"termid":"FYPO:0006312"}


id: SO:0000429
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The U3 segment of the three-prime long terminal repeat.","direct_ancestors":[{"relation_name":"is_a","term_name":"U3_LTR_region","termid":"SO:0000424"},{"relation_name":"is_a","term_name":"five_prime_LTR_component","termid":"SO:0000850"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3_five_prime_LTR_region","synonyms":[{"name":"U3 5' long term repeat region","type":"exact"},{"name":"U3 five prime LTR region","type":"exact"}],"termid":"SO:0000429"}


id: PBO:0116991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPN2 antisense RNA 1","termid":"PBO:0116991"}


id: PBO:0049316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase theta 4","termid":"PBO:0049316"}


id: MONDO:0003280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital locomotor ataxia of lambs, thought to be associated with copper deficiency. It is characterized clinically by progressive incoordination of the hind limbs and pathologically by disruption of neuron and myelin development in the central nervous system. It is caused by a deficiency of metabolizable copper in the ewe during the last half of her pregnancy. (Dorland, 28th ed; Stedman, 26th ed)","definition_xrefs":["MESH:D013540"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sheep disease","termid":"MONDO:0024985"},{"relation_name":"is_a","term_name":"nutritional deficiency disease, non-human animal","termid":"MONDO:0700103"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"swayback","secondary_identifiers":["DOID:5112","SCTID:61960001"],"synonyms":[{"name":"swayback of sheep","type":"exact"}],"termid":"MONDO:0003280","xrefs":{"Monarch":{"xref_id":"0003280"}}}


id: MONDO:0001018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lymphoblastic leukemia (obsolete MONDO:0001018)","termid":"MONDO:0001018","xrefs":{"Monarch":{"xref_id":"0001018"}}}


id: GO:1901478
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of amitrole from one side of a membrane to the other.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"azole transmembrane transporter activity","termid":"GO:1901474"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"aminotriazole transmembrane transporter activity","secondary_identifiers":["GO:0015241"],"synonyms":[{"name":"aminotriazole transporter activity","type":"broad"}],"termid":"GO:1901478"}


id: PATO:0001004
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001004 absolute alternation value (obsolete PATO:0001004)","termid":"PATO:0001004"}


id: GO:0021853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of GABAergic interneuron precursors from the subpallium to the cerebral cortex.","definition_xrefs":["GOC:jid","GOC:cls","GO_REF:0000021","GOC:dgh","GOC:dph","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interneuron migration from the subpallium to the cortex","termid":"GO:0021830"},{"relation_name":"is_a","term_name":"interneuron migration","termid":"GO:1904936"},{"relation_name":"part_of","term_name":"cerebral cortex GABAergic interneuron development","termid":"GO:0021894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebral cortex GABAergic interneuron migration","termid":"GO:0021853"}


id: MONDO:0014001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.","definition_xrefs":["DOID:0110837","PMID:22718019"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Usher syndrome type 1","termid":"MONDO:0010168"}],"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":"Usher syndrome type 1K","secondary_identifiers":["OMIM:614990","GARD:15890","UMLS:C3539124","MEDGEN:761332","ICD10CM:H35.5"],"synonyms":[{"name":"USH1K","type":"exact"},{"name":"USHER syndrome, type IK","type":"related"},{"name":"Usher syndrome type IK","type":"exact"}],"termid":"MONDO:0014001","xrefs":{"Monarch":{"xref_id":"0014001"}}}


id: PR:Q9US01
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC664.13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9US01"],"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 C664.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC664.13","synonyms":[{"name":"Spom972h-SPAC664.13","type":"exact"}],"termid":"PR:Q9US01"}


id: GO:0014031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a mesenchymal cell over time, from initial commitment of the cell to its specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:ef","GOC:dh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"mesenchymal cell differentiation","termid":"GO:0048762"}],"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":"mesenchymal cell development","termid":"GO:0014031"}


id: PBO:0052274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 5B","termid":"PBO:0052274"}


id: MONDO:0040872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of primary polydipsia not caused by underlying psychiatric symptoms.","definition_xrefs":["Wikipedia:Primary_polydipsia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary polydipsia","termid":"MONDO:0040870"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-psychogenic polydipsia","synonyms":[{"name":"idiopathic polydipsia","type":"narrow"}],"termid":"MONDO:0040872","xrefs":{"Monarch":{"xref_id":"0040872"}}}


id: MONDO:1010493
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ventricular septal defect that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular septal defect, non-human animal","termid":"MONDO:1010022"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventricular septal defect, cattle","secondary_identifiers":["OMIA:001041-9913"],"termid":"MONDO:1010493","xrefs":{"Monarch":{"xref_id":"1010493"}}}


id: GO:0046253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of toluene, a volatile monoaromatic hydrocarbon found in crude petroleum and petroleum products, in the absence of oxygen.","definition_xrefs":["GOC:ai","PMID:8573493"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaerobic toluene metabolic process","termid":"GO:0018971"},{"relation_name":"is_a","term_name":"toluene biosynthetic process","termid":"GO:0046252"}],"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":"anaerobic toluene biosynthetic process","synonyms":[{"name":"anaerobic toluene anabolism","type":"exact"},{"name":"anaerobic toluene biosynthesis","type":"exact"},{"name":"anaerobic toluene formation","type":"exact"},{"name":"anaerobic toluene synthesis","type":"exact"}],"termid":"GO:0046253"}


id: MONDO:1010446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dilated cardiomyopathy that occurs in sea otter.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dilated cardiomyopathy, non-human animal","termid":"MONDO:1010011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilated cardiomyopathy, sea otter","secondary_identifiers":["OMIA:000162-34882"],"termid":"MONDO:1010446","xrefs":{"Monarch":{"xref_id":"1010446"}}}


id: PR:Q10236
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ribonuclease H2 subunit A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10954:SF7","OMA:SCHPO00931","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":"ribonuclease H2 subunit A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4G9.02","secondary_identifiers":["UniProtKB:Q10236"],"synonyms":[{"name":"RNase H2 subunit A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNase HI large subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RNASEH2A","type":"exact"},{"name":"ribonuclease HI large subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ribonuclease HI subunit A (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10236"}


id: MONDO:0006782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Blood-filled uterus.","definition_xrefs":["MESH:D006409"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine disorder","termid":"MONDO:0002654"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemometra","secondary_identifiers":["SCTID:38280009","ICD10CM:N85.7","DOID:9958","ICD9:621.4","UMLS:C0018948","MEDGEN:6776"],"synonyms":[{"name":"hematometra","type":"exact"}],"termid":"MONDO:0006782","xrefs":{"Monarch":{"xref_id":"0006782"}}}


id: PBO:0051362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 3-15","termid":"PBO:0051362"}


id: GO:0035299
data:
  {"annotated_genes":["SJAG_01148"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76547],"is_not":false,"summary":null,"term":"GO:0035299"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,5,6-pentakisphosphate + ATP = 1D-myo-inositol hexakisphosphate + ADP + H+.","definition_xrefs":["RHEA:20313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol pentakisphosphate kinase activity","termid":"GO:0120517"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01148":null},"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:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"inositol-1,3,4,5,6-pentakisphosphate 2-kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:2.7.1.158","KEGG_REACTION:R05202","Reactome:R-HSA-1855176","Reactome:R-HSA-1855179","MetaCyc:RXN-7163"],"synonyms":[{"name":"IP5 2-kinase activity","type":"related"},{"name":"Ins(1,3,4,5,6)P5 2-kinase activity","type":"related"},{"name":"inositol hexakisphosphate synthase","type":"related"},{"name":"inositol pentakisphosphate 2-kinase activity","type":"exact"},{"name":"inositol polyphosphate kinase activity","type":"related"},{"name":"inositol-pentakisphosphate 2-kinase activity","type":"related"}],"termid":"GO:0035299","terms_by_termid":{"GO:0035299":null}}


id: GO:0032043
data:
  {"annotated_genes":["SJAG_01948"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89843],"is_not":false,"summary":null,"term":"GO:0032043"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of mitochondrial DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA catabolic process","termid":"GO:0006308"},{"relation_name":"is_a","term_name":"mitochondrial DNA metabolic process","termid":"GO:0032042"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01948":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0007005","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"mitochondrial DNA catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial DNA breakdown","type":"exact"},{"name":"mitochondrial DNA catabolism","type":"exact"},{"name":"mitochondrial DNA degradation","type":"exact"},{"name":"mtDNA breakdown","type":"exact"},{"name":"mtDNA catabolic process","type":"exact"},{"name":"mtDNA catabolism","type":"exact"},{"name":"mtDNA degradation","type":"exact"}],"termid":"GO:0032043","terms_by_termid":{"GO:0032043":null}}


id: FYPO:0009062
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 cells show decreased sensitivity to X-rays.","direct_ancestors":[{"relation_name":"is_a","term_name":"resistance to ionizing radiation during vegetative growth","termid":"FYPO:0002312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"resistance to X-rays during vegetative growth","synonyms":[{"name":"increased vegetative cell population growth during cellular response to X rays","type":"exact"},{"name":"increased vegetative cell population growth during cellular response to X-rays","type":"exact"},{"name":"resistant to X rays during vegetative growth","type":"exact"},{"name":"resistant to X-rays during vegetative growth","type":"exact"}],"termid":"FYPO:0009062"}


id: MONDO:0700262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any type 1 interferonopathies in which the cause of the disease is a variation in the IFIH1 gene. Individuals with variants in IFIH1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and singleton-Merten syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFIH1-related type 1 interferonopathy","termid":"MONDO:0700262","xrefs":{"Monarch":{"xref_id":"0700262"}}}


id: PATO:0001862
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A fertility quality inhering in a bearer by virtue of the bearer's disposition to make its offspring sterile.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fertility","termid":"PATO:0000274"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lack of fertility in offspring","synonyms":[{"name":"grandchildless","type":"related"}],"termid":"PATO:0001862"}


id: FYPO:0001034
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 tunicamycin than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002682","FYPO:0001985","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"resistance to tunicamycin","synonyms":[{"name":"resistance to tunicamycin during mitotic cell cycle","type":"related"},{"name":"resistance to tunicamycin during vegetative growth","type":"exact"},{"name":"resistant to TM","type":"exact"},{"name":"resistant to tunicamycin","type":"exact"}],"termid":"FYPO:0001034"}


id: PBO:0078281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 14-1","termid":"PBO:0078281"}


id: GO:0072281
data:
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id: PBO:0060027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 15","termid":"PBO:0060027"}


id: PBO:0075403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small regulatory polypeptide of amino acid response","termid":"PBO:0075403"}


id: PR:Q09172
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein phosphatase 1N that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04857","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 phosphatase 2C homolog 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1223.11","secondary_identifiers":["UniProtKB:Q09172"],"synonyms":[{"name":"PP2C-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PPM1N","type":"exact"}],"termid":"PR:Q09172"}


id: PBO:0078505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tribbles pseudokinase 2","termid":"PBO:0078505"}


id: MONDO:0000015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic deficiency of any early component of the classical pathway (C1q, C1r/s, C2, C4, and C3) that is associated with autoimmune diseases due to the failure of clearance of immune complexes (IC) and apoptotic materials, and the impairment of normal humoral response.","definition_xrefs":["PMID:22773339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complement deficiency","termid":"MONDO:0003832"}],"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":"classic complement early component deficiency","secondary_identifiers":["GARD:9526","SCTID:363009005","MEDGEN:226929","UMLS:C1285186","ICD9:279.8"],"synonyms":[{"name":"genetic deficiency of early component of the classical complement pathway","type":"exact"}],"termid":"MONDO:0000015","xrefs":{"Monarch":{"xref_id":"0000015"}}}


id: GO:0044078
data:
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id: GO:0060090
data:
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id: PBO:0078840
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon TGG) 3-4","termid":"PBO:0078840"}


id: PBO:0056541
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCF.2 cell line derived transforming sequence like","termid":"PBO:0056541"}


id: MONDO:1011885
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"episodic falling, non-human animal","secondary_identifiers":["OMIA:001592"],"termid":"MONDO:1011885","xrefs":{"Monarch":{"xref_id":"1011885"}}}


id: PBO:0078178
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta joining 2-2P (non-functional)","termid":"PBO:0078178"}


id: GO:0072059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cortical collecting duct over time, from its formation to the mature structure. The cortical collecting duct is the portion of the collecting duct that resides in the renal cortex.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"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":"cortical collecting duct development","termid":"GO:0072059"}


id: MONDO:0100547
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system.","definition_xrefs":["PMID:32341133"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"}],"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":"cardiogenetic disease","synonyms":[{"name":"hereditary heart disease","type":"exact"}],"termid":"MONDO:0100547","xrefs":{"Monarch":{"xref_id":"0100547"}}}


id: PBO:0076137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUCLA2 pseudogene 2","termid":"PBO:0076137"}


id: PBO:0003354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lsk1 associated cyclin","termid":"PBO:0003354"}


id: GO:0102569
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: FR-900098 + 2-oxoglutarate(2-) + O2 = FR-33289 + succinate(2-) + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete FR-33289 synthase activity (obsolete GO:0102569)","termid":"GO:0102569"}


id: PBO:0067584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 743, pseudogene","termid":"PBO:0067584"}


id: MONDO:0003720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually aggressive malignant neoplasm arising from the kidney. It is characterized by the presence of spindle-shaped fibroblasts and collagenous stroma formation in a herringbone growth pattern.","definition_xrefs":["NCIT:C7726"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney sarcoma","termid":"MONDO:0002930"},{"relation_name":"is_a","term_name":"fibrosarcoma","termid":"MONDO:0005164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"kidney fibrosarcoma","secondary_identifiers":["DOID:5982","MEDGEN:116050","UMLS:C0238208"],"synonyms":[{"name":"fibrosarcoma of kidney","type":"exact"},{"name":"fibrosarcoma of the kidney","type":"exact"},{"name":"kidney fibrosarcoma","type":"exact"},{"name":"kidney fibrosarcoma (disease)","type":"exact"},{"name":"renal fibrosarcoma","type":"exact"}],"termid":"MONDO:0003720","xrefs":{"Monarch":{"xref_id":"0003720"}}}


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: MONDO:0001483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Crimean-Congo hemorrhagic fever (obsolete MONDO:0001483)","termid":"MONDO:0001483","xrefs":{"Monarch":{"xref_id":"0001483"}}}


id: PBO:0076361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SZRD1 pseudogene 1","termid":"PBO:0076361"}


id: GO:1905854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of heparan sulfate binding.","definition_xrefs":["PMID:7683668","GOC:bc","GO_REF:0000059","GOC:aruk","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of heparan sulfate binding (obsolete GO:1905854)","synonyms":[{"name":"down regulation of heparan sulfate binding","type":"exact"},{"name":"down-regulation of heparan sulfate binding","type":"exact"},{"name":"downregulation of heparan sulfate binding","type":"exact"},{"name":"inhibition of heparan sulfate binding","type":"narrow"}],"termid":"GO:1905854"}


id: PBO:0074038
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 23","termid":"PBO:0074038"}


id: PR:O94511
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A very-long-chain enoyl-CoA reductase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02643"],"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":"enoyl reductase C646.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC646.07c","secondary_identifiers":["UniProtKB:O94511"],"synonyms":[{"name":"Spom972h-TECR","type":"exact"}],"termid":"PR:O94511"}


id: GO:0008115
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + O2 + sarcosine = formaldehyde + glycine + H2O2.","definition_xrefs":["EC:1.5.3.1","RHEA:13313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor","termid":"GO:0016647"}],"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":"sarcosine oxidase activity","secondary_identifiers":["MetaCyc:SARCOX-RXN","KEGG_REACTION:R00610"],"synonyms":[{"name":"sarcosine:oxygen oxidoreductase (demethylating)","type":"related"}],"termid":"GO:0008115"}


id: PBO:0000783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-glucosidase (predicted)","termid":"PBO:0000783"}


id: PBO:0070881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 13","termid":"PBO:0070881"}


id: GO:0004986
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Combining with an opioid to initiate a change in cell activity, with the pharmacological characteristics of delta-opioid receptors, including the activity of enkephalins as ligands.","definition_xrefs":["IUPHAR_RECEPTOR:317","PMID:10471416"],"gene_count":0,"genotype_count":0,"name":"obsolete delta-opioid receptor activity (obsolete GO:0004986)","secondary_identifiers":["Wikipedia:Delta_Opioid_receptor"],"synonyms":[{"name":"delta-opioid receptor activity","type":"exact"}],"termid":"GO:0004986"}


id: MONDO:0011515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete papillary renal cell carcinoma (obsolete MONDO:0011515)","termid":"MONDO:0011515","xrefs":{"Monarch":{"xref_id":"0011515"}}}


id: PBO:0050092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 1","termid":"PBO:0050092"}


id: GO:0009718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of anthocyanins, any member of a group of intensely colored soluble glycosides of anthocyanidins.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavonoid biosynthetic process","termid":"GO:0009813"},{"relation_name":"is_a","term_name":"pigment biosynthetic process","termid":"GO:0046148"},{"relation_name":"is_a","term_name":"anthocyanin-containing compound metabolic process","termid":"GO:0046283"}],"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":"anthocyanin-containing compound biosynthetic process","synonyms":[{"name":"anthocyanin anabolism","type":"exact"},{"name":"anthocyanin biosynthesis","type":"exact"},{"name":"anthocyanin biosynthetic process","type":"exact"},{"name":"anthocyanin formation","type":"exact"},{"name":"anthocyanin synthesis","type":"exact"}],"termid":"GO:0009718"}


id: RO:0002509
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"s 'determined by part of' w if and only if there exists some f such that (1) s 'determined by' f and (2) f part_of w, or f=w.","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"},{"relation_name":"is_a","term_name":"causal_relation_between_material_entities","termid":"RO:0002506"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"determined_by_part_of","termid":"RO:0002509"}


id: PBO:0031293
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_cell_cycle_checkpoint_phenotype","termid":"PBO:0031293"}


id: FYPO:0002985
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to methyl methanesulfonate is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased RNA level during cellular response to methyl methanesulfonate","synonyms":[{"name":"increased RNA accumulation during cellular response to methyl methanesulfonate","type":"related"},{"name":"increased RNA level during cellular response to MMS","type":"exact"},{"name":"increased RNA level during cellular response to methyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"increased RNA level during cellular response to methyl methanesulfonate during vegetative growth","type":"exact"},{"name":"increased RNA level during cellular response to methyl methanesulphonate","type":"exact"},{"name":"increased mRNA level during cellular response to methyl methanesulfonate","type":"narrow"},{"name":"increased transcript level during cellular response to methyl methanesulfonate","type":"exact"}],"termid":"FYPO:0002985"}


id: PBO:0062057
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 W member 4 pseudogene","termid":"PBO:0062057"}


id: PBO:0068916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 159, pseudogene","termid":"PBO:0068916"}


id: GO:0008820
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosylcobinamide phosphate + GTP + 2 H+ = adenosylcobinamide-GDP + diphosphate.","definition_xrefs":["RHEA:22712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanylyltransferase activity","termid":"GO:0070568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016779","GO:0003824"],"is_obsolete":false,"name":"cobinamide phosphate guanylyltransferase activity","secondary_identifiers":["EC:2.7.7.62","GO:0043753","MetaCyc:COBINPGUANYLYLTRANS-RXN","KEGG_REACTION:R05222"],"synonyms":[{"name":"AdoCbi kinase/AdoCbi-phosphate guanylyltransferase","type":"broad"},{"name":"CobU","type":"related"},{"name":"GTP:adenosylcobinamide-phosphate guanylyltransferase activity","type":"exact"},{"name":"GTP:cobinamide phosphate guanylyltransferase activity","type":"exact"},{"name":"adenosylcobinamide kinase/adenosylcobinamide-phosphate guanylyltransferase","type":"broad"},{"name":"adenosylcobinamide-phosphate guanylyltransferase activity","type":"exact"}],"termid":"GO:0008820"}


id: GO:0160103
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: guanosine(26)/guanosine(27) in tRNA + 4 S-adenosyl-L-methionine = 4 H+ + N(2)-dimethylguanosine(26)/N(2)-dimethylguanosine(27) in tRNA + 4 S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"tRNA (guanine) methyltransferase activity","termid":"GO:0016423"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0140098","GO:0003674","GO:0140101","GO:0003824","GO:0016741","GO:0016740"],"is_obsolete":false,"name":"tRNA (guanine(26)-N2/guanine(27)-N2)-dimethyltransferase activity","secondary_identifiers":["RHEA:43136"],"synonyms":[{"name":"tRNA (guanine(26)-N(2)/guanine(27)-N(2))-dimethyltransferase activity","type":"exact"},{"name":"tRNA (guanosine(26)-N(2)/guanosine(27)-N(2))-dimethyltransferase activity","type":"exact"}],"termid":"GO:0160103"}


id: SO:0001027
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A genotype is a variant genome, complete or incomplete.","definition_xrefs":["SO:immuno_workshop"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variant_collection","termid":"SO:0001507"},{"relation_name":"variant_of","term_name":"genome","termid":"SO:0001026"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genotype","secondary_identifiers":["http://en.wikipedia.org/wiki/Genotype"],"termid":"SO:0001027"}


id: MONDO:0037735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the sebaceous gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"},{"relation_name":"is_a","term_name":"sebaceous gland neoplasm","termid":"MONDO:0006963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"sebaceous gland cancer","secondary_identifiers":["NCIT:C8409","UMLS:C1382026","MEDGEN:235134"],"synonyms":[{"name":"cancer of sebaceous gland","type":"exact"},{"name":"malignant neoplasm of sebaceous gland","type":"exact"},{"name":"malignant neoplasm of the sebaceous gland","type":"exact"},{"name":"malignant sebaceous gland neoplasm","type":"exact"},{"name":"malignant sebaceous gland tumor","type":"exact"},{"name":"malignant sebaceous gland tumour","type":"exact"},{"name":"malignant sebaceous neoplasm","type":"exact"},{"name":"malignant sebaceous tumor","type":"exact"},{"name":"malignant sebaceous tumour","type":"exact"},{"name":"malignant tumor of sebaceous gland","type":"exact"},{"name":"malignant tumor of the sebaceous gland","type":"exact"},{"name":"malignant tumour of sebaceous gland","type":"exact"},{"name":"malignant tumour of the sebaceous gland","type":"exact"}],"termid":"MONDO:0037735","xrefs":{"Monarch":{"xref_id":"0037735"}}}


id: MONDO:0016040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Harlequin syndrome (HSD) is an autonomic disorder occurring at any age and characterized by unilateral flushing and sweating, involving the face and sometimes arm and chest, in condition of thermal, exercise or emotional stress without sympathetic ocular manifestations. However, tonic pupils, parasympathetic oculomotor lesion and pre- or postganglionic sudomotor sympathetic deficit can rarely occur.","definition_xrefs":["Orphanet:199282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autonomic nervous system disorder","termid":"MONDO:0001292"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"harlequin syndrome","secondary_identifiers":["SCTID:14070001000004105","GARD:8610","MESH:C535634","UMLS:C2029348","MEDGEN:384475","ICD9:705.89"],"synonyms":[{"name":"progressive isolated segmental anhidrosis","type":"exact"},{"name":"sudden onset of unilateral flushing and sweating","type":"related"},{"name":"unilateral loss of facial flushing and sweating with contralateral anhidrosis","type":"related"}],"termid":"MONDO:0016040","xrefs":{"Monarch":{"xref_id":"0016040"}}}


id: MONDO:0003501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the skin of the external ear.","definition_xrefs":["NCIT:C6083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external ear carcinoma","termid":"MONDO:0002944"},{"relation_name":"is_a","term_name":"head and neck squamous cell carcinoma","termid":"MONDO:0010150"}],"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":"external ear squamous cell carcinoma","secondary_identifiers":["DOID:5538","UMLS:C1333494","MEDGEN:232478"],"synonyms":[{"name":"epidermoid carcinoma of external Ear","type":"exact"},{"name":"epidermoid carcinoma of the external Ear","type":"exact"},{"name":"epidermoid carcinoma of the external ear","type":"exact"},{"name":"external Ear epidermoid carcinoma","type":"exact"},{"name":"external Ear squamous cell carcinoma","type":"exact"},{"name":"external ear squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of external Ear","type":"exact"},{"name":"squamous cell carcinoma of external ear","type":"related"},{"name":"squamous cell carcinoma of the external Ear","type":"exact"}],"termid":"MONDO:0003501","xrefs":{"Monarch":{"xref_id":"0003501"}}}


id: GO:0021704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the locus ceruleus is generated and organized. In mice, the locus ceruleus is a dense cluster of neurons within the dorsorostral pons. This nucleus is the major location of neurons that release norepinephrine throughout the brain, and is responsible for physiological responses to stress and panic.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:cls","GOC:dph","GO_REF:0000021","ISBN:0838580343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"pons morphogenesis","termid":"GO:0021583"},{"relation_name":"part_of","term_name":"locus ceruleus development","termid":"GO:0021703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"locus ceruleus morphogenesis","termid":"GO:0021704"}


id: PBO:0069825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1111, pseudogene","termid":"PBO:0069825"}


id: MONDO:0030052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disease with punctate palmoplantar keratoderma as a major feature (obsolete MONDO:0030052)","termid":"MONDO:0030052","xrefs":{"Monarch":{"xref_id":"0030052"}}}


id: PBO:0038400
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-relation_between_physical_entity_and_a_process_or_stage","termid":"PBO:0038400"}


id: MONDO:1010994
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Olivopontocerebellar atrophy that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"olivopontocerebellar atrophy, non-human animal","termid":"MONDO:1010234"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olivopontocerebellar atrophy, domestic cat","secondary_identifiers":["OMIA:000740-9685"],"termid":"MONDO:1010994","xrefs":{"Monarch":{"xref_id":"1010994"}}}


id: PR:P78847
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nuclear pore complex protein Nup205 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04901"],"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":"nucleoporin nup186 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC290.03c","secondary_identifiers":["UniProtKB:P78847"],"synonyms":[{"name":"Spom972h-NUP205","type":"exact"},{"name":"nuclear pore protein nup186 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P78847"}


id: GO:0001076
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to an RNA polymerase II transcription factor, which may be a single protein or a complex, in order to modulate transcription. A protein binding transcription factor may or may not also interact with the template nucleic acid (either DNA or RNA) as well.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor activity, RNA polymerase II transcription factor binding (obsolete GO:0001076)","synonyms":[{"name":"RNA polymerase II transcription factor binding transcription factor activity","type":"exact"}],"termid":"GO:0001076"}


id: PBO:0047281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FA complementation group E","termid":"PBO:0047281"}


id: PR:O14200
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pxa1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14200"],"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":"PXA domain protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5D6.07c","synonyms":[{"name":"Spom972h-pxa1","type":"exact"}],"termid":"PR:O14200"}


id: PBO:0001886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DASH complex subunit Dam1","termid":"PBO:0001886"}


id: PBO:0073255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 7","termid":"PBO:0073255"}


id: PBO:0004602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin protease cofactor Glp1 (predicted)","termid":"PBO:0004602"}


id: PBO:0068444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 18, pseudogene","termid":"PBO:0068444"}


id: MONDO:0015441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 7 syndrome is a rare chromosomal anomaly syndrome, with highly variable phenotype, principally characterized by growth failure, short stature, intellectual disability, dermatological abnormalities (nevus flammeus, dark pigmented nevi, café-au-lait spots), microcephaly and facial dysmorphism (incl. facial asymmetry, small ears, abnormal palpebral fissures, ptosis, epicanthic folds, hyper/hypotelorism). Additional reported features include convulsions, cleft lip and palate, clinodactyly, kyphoscoliosis and genital anomalies (i.e. cryptorchidism, hypospadias, micropenis).","definition_xrefs":["Orphanet:1449"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 7 disorder","termid":"MONDO:0700014"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 7","secondary_identifiers":["SCTID:765489006","UMLS:C2931622","GARD:1345","MESH:C537813","MEDGEN:419454","NCIT:C121986"],"synonyms":[{"name":"R7","type":"related"},{"name":"Ring 7","type":"related"},{"name":"Ring chromosome 7 syndrome","type":"related"},{"name":"Ring chromosome type 7","type":"exact"},{"name":"chromosome 7 ring","type":"related"},{"name":"rose cluster 7","type":"exact"}],"termid":"MONDO:0015441","xrefs":{"Monarch":{"xref_id":"0015441"}}}


id: PBO:0004599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine carboxyl methyltransferase Ppm1 (predicted)","termid":"PBO:0004599"}


id: GO:0043651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving linoleic acid, an unsaturated omega-6 fatty acid that has the molecular formula C18H32O2.","definition_xrefs":["Wikipedia:Linoleic_Acid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid metabolic process","termid":"GO:0001676"},{"relation_name":"is_a","term_name":"unsaturated fatty acid metabolic process","termid":"GO:0033559"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"linoleic acid metabolic process","secondary_identifiers":["Wikipedia:Linoleic_acid","Reactome:R-HSA-2046105"],"synonyms":[{"name":"linoleic acid metabolism","type":"exact"}],"termid":"GO:0043651"}


id: MONDO:0019424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability-acromegaly-hyperactivity syndrome is characterized by severe intellectual deficit, acromegaly and hyperactivity. The syndrome has been described in two half-brothers. Dysarthria, aggressive behavior, a characteristic facies (an acromegalic and triangular face with a long nose) and macroorchidism were also present. The mother displayed moderate intellectual deficit and milder facial anomalies. Central nervous system anomalies were identified in the two boys: subarachnoid cysts and hyperdensity in the pontine region.","definition_xrefs":["Orphanet:85327"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability-acromegaly-hyperactivity syndrome","secondary_identifiers":["MEDGEN:930076","UMLS:C4304407","GARD:19060"],"termid":"MONDO:0019424","xrefs":{"Monarch":{"xref_id":"0019424"}}}


id: GO:0097704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any response to oscillatory fluid shear stress that occurs at the level of a cell.","definition_xrefs":["PMID:21768538","GOC:BHF","GOC:BHF_miRNA","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to fluid shear stress","termid":"GO:0071498"},{"relation_name":"is_a","term_name":"response to oscillatory fluid shear stress","termid":"GO:0097702"}],"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 oscillatory fluid shear stress","termid":"GO:0097704"}


id: PBO:0077756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of outer mitochondrial membrane 20","termid":"PBO:0077756"}


id: PR:Q9UUI7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC22F8.05 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUI7"],"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,alpha-trehalose-phosphate synthase [UDP-forming] 100 kDa subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22F8.05","synonyms":[{"name":"Spom972h-SPAC22F8.05","type":"exact"},{"name":"UDP-glucose-glucosephosphate glucosyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"trehalose-6-phosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUI7"}


id: PBO:0039692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloid P component, serum","termid":"PBO:0039692"}


id: MONDO:0003251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tumor that usually presents with small nodules or small sessile polyps, predominantly in the distal esophagus. Histologically, it is composed of sheets of oval to polygonal cells with a small central nucleus and abundant granular cytoplasm. This is usually a benign tumor. (WHO, 2000) -- 2003","definition_xrefs":["NCIT:C5700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"granular cell tumor","termid":"MONDO:0006235"},{"relation_name":"is_a","term_name":"neoplasm of esophagus","termid":"MONDO:0021355"}],"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":"esophageal granular cell tumor","secondary_identifiers":["UMLS:C1333448","DOID:5040","MEDGEN:234228"],"synonyms":[{"name":"esophageal granular cell myoblastoma","type":"exact"},{"name":"esophageal granular cell neoplasm","type":"exact"},{"name":"esophageal granular cell tumor","type":"exact"},{"name":"esophagus granular cell tumor","type":"exact"},{"name":"granular cell esophageal tumor","type":"exact"},{"name":"granular cell esophageal tumour","type":"exact"},{"name":"granular cell esophagus myoblastoma","type":"exact"},{"name":"granular cell esophagus neoplasm","type":"exact"},{"name":"granular cell esophagus tumor","type":"exact"},{"name":"granular cell myoblastoma of esophagus","type":"exact"},{"name":"granular cell myoblastoma of oesophagus","type":"exact"},{"name":"granular cell myoblastoma of the esophagus","type":"exact"},{"name":"granular cell myoblastoma of the oesophagus","type":"exact"},{"name":"granular cell neoplasm of esophagus","type":"exact"},{"name":"granular cell neoplasm of oesophagus","type":"exact"},{"name":"granular cell neoplasm of the esophagus","type":"exact"},{"name":"granular cell neoplasm of the oesophagus","type":"exact"},{"name":"granular cell oesophagus myoblastoma","type":"exact"},{"name":"granular cell oesophagus neoplasm","type":"exact"},{"name":"granular cell oesophagus tumour","type":"exact"},{"name":"granular cell tumor of esophagus","type":"exact"},{"name":"granular cell tumor of the esophagus","type":"exact"},{"name":"granular cell tumour of oesophagus","type":"exact"},{"name":"granular cell tumour of the oesophagus","type":"exact"},{"name":"malignant granular cell esophageal tumor","type":"related"},{"name":"malignant granular cell esophageal tumour","type":"related"},{"name":"oesophagus granular cell tumour","type":"exact"}],"termid":"MONDO:0003251","xrefs":{"Monarch":{"xref_id":"0003251"}}}


id: PBO:0062207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily AC member 2","termid":"PBO:0062207"}


id: PR:Q10481
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial import inner membrane translocase subunit Tim13 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01858","PANTHER:PTHR19338: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":"mitochondrial import inner membrane translocase subunit tim13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17C9.09c","secondary_identifiers":["UniProtKB:Q10481"],"synonyms":[{"name":"Spom972h-TIMM13","type":"exact"}],"termid":"PR:Q10481"}


id: FYPO:0002865
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 polypeptone. Cells stop growing (and may die) at a concentration of polypeptone that allows wild type cells to grow. Polypeptone is a mixture of peptones made up of equal parts of pancreatic digest of casein and peptic digest of animal used in media.","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:0002683","FYPO:0005447","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to polypeptone","synonyms":[{"name":"hypersensitive to polypeptone","type":"exact"},{"name":"sensitive to polypeptone during mitotic cell cycle","type":"related"},{"name":"sensitive to polypeptone during vegetative growth","type":"exact"}],"termid":"FYPO:0002865"}


id: MOD:01213
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to an iodoacetamide derivatized histidine, either 1'- or 3'-(carboxamidolmethyl)histidine.","definition_xrefs":["PubMed:2026710","PubMed:11510821","PubMed:15627961","Unimod:4#H","OMSSA:28","PubMed:12422359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iodoacetamide derivatized residue","termid":"MOD:00397"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iodoacetamide derivatized histidine","synonyms":[{"name":"Carbamidomethyl","type":"related"},{"name":"Iodoacetamide derivative","type":"related"},{"name":"carbamidometylh","type":"exact"}],"termid":"MOD:01213"}


id: GO:1905894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cellular response to tunicamycin.","definition_xrefs":["GOC:TermGenie","GOC:bc","GO_REF:0000058","GOC:aruk","PMID:21803450"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular response to tunicamycin (obsolete GO:1905894)","termid":"GO:1905894"}


id: PBO:0079820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UL16 binding protein 2","termid":"PBO:0079820"}


id: SO:0000571
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that can be transcribed into a microRNA (miRNA).","direct_ancestors":[{"relation_name":"is_a","term_name":"non_protein_coding","termid":"SO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miRNA_encoding","synonyms":[{"name":"miRNA encoding","type":"exact"}],"termid":"SO:0000571"}


id: PBO:0035943
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cytoplasmic_microtubule_nucleation_during_mitotic_interphase","termid":"PBO:0035943"}


id: GO:1900034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to heat.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to heat","termid":"GO:0034605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cellular response to heat","secondary_identifiers":["Reactome:R-HSA-3371453","Reactome:R-HSA-3371571"],"synonyms":[{"name":"regulation of cellular response to heat stress","type":"exact"}],"termid":"GO:1900034"}


id: PBO:0113206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial DNA-binding and packaging factor; mtDNA maintenance factor involved in mitochondrial DNA replication and recombination, regulating mtDNA copy number in opposition to DPI34; HMG1 DNA-binding protein family member containing two HMG-boxes; activity may be regulated by protein kinase A phosphorylation; ABF2 has a paralog, IXR1, that arose from the whole genome duplication; human homolog TFAM can complement yeast abf2 mutant, rescuing the loss-of-mitochondrial DNA phenotype","termid":"PBO:0113206"}


id: MONDO:0100500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"},{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500","xrefs":{"Monarch":{"xref_id":"0100500"}}}


id: PBO:0070899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 7","termid":"PBO:0070899"}


id: PBO:0072063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S11 pseudogene 1","termid":"PBO:0072063"}


id: PBO:0069390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 650, pseudogene","termid":"PBO:0069390"}


id: PBO:0043085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic delta subunit","termid":"PBO:0043085"}


id: MONDO:0021005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature. This includes X-linked, AR and AD forms of Aarskog syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"faciodigitogenital syndrome","secondary_identifiers":["MedDRA:10067148","Orphanet:915","DOID:0111824","GARD:4775"],"synonyms":[{"name":"Aarskog syndrome","type":"narrow"},{"name":"Aarskog-Scott syndrome","type":"narrow"},{"name":"faciogenital dysplasia","type":"related"}],"termid":"MONDO:0021005","xrefs":{"Monarch":{"xref_id":"0021005"}}}


id: PBO:0057781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2861","termid":"PBO:0057781"}


id: PBO:0081002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 40","termid":"PBO:0081002"}


id: MONDO:0014746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066","MONDO:0020022","MONDO:0002320"],"is_obsolete":false,"name":"SLC39A8-CDG","secondary_identifiers":["UMLS:C4225234","Orphanet:468699","GARD:17846","DOID:0070266","MEDGEN:899837","OMIM:616721"],"synonyms":[{"name":"CDG IIn","type":"related"},{"name":"CDG syndrome type IIn","type":"exact"},{"name":"CDG-IIn","type":"exact"},{"name":"CDG2N","type":"exact"},{"name":"SLC39A8 deficiency","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IIn","type":"exact"},{"name":"congenital disorder of glycosylation type 2n","type":"exact"},{"name":"congenital disorder of glycosylation type IIn","type":"exact"},{"name":"congenital disorder of glycosylation, type IIn","type":"exact"}],"termid":"MONDO:0014746","xrefs":{"Monarch":{"xref_id":"0014746"}}}


id: PBO:0039703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aprataxin and PNKP like factor","termid":"PBO:0039703"}


id: PBO:0034634
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromosome_segregation_during_meiosis_I_with_split_kinetochore_and_normal_chromosome_separation","termid":"PBO:0034634"}


id: PBO:0070778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 8","termid":"PBO:0070778"}


id: GO:0102878
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E)-farnesyl diphosphate = (+)-alpha-barbatene + diphosphate.","definition_xrefs":["RHEA:29499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"(+)-alpha-barbatene synthase activity","secondary_identifiers":["EC:4.2.3.69","MetaCyc:RXN-8417"],"termid":"GO:0102878"}


id: PBO:0057264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 489","termid":"PBO:0057264"}


id: MONDO:0003020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete orofaciodigital syndrome (obsolete MONDO:0003020)","termid":"MONDO:0003020","xrefs":{"Monarch":{"xref_id":"0003020"}}}


id: GO:0080120
data:
  {"annotated_genes":["SJAG_00730","SJAG_03396"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71835,76665],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071586"}]},"cv_name":"biological_process","definition":"A series of specific posttranslational modifications to the CAAX box region of CAAX box proteins. CAAX box proteins are eukaryotic proteins that contain a CAAX motif where the C is a cysteine, the two A residues are aliphatic amino acids and the X can be one of several amino acids. The CAAX-box proteins undergo three sequential, enzymatic, post-translational modifications essential to their targeting: First, the proteins are prenylated by one of two prenyltransferases called farnesyltransferase and geranylgeranyltransferase-I. Prenylation results in the covalent attachment of either farnesyl or geranylgeranyl isoprenoid groups to the cysteine in the CAAX box motif. Prenylation is followed by proteolytic removal of the last three amino acids of the protein (AAX). Finally, the newly exposed carboxylate group of the isoprenylcysteine is methylated by an ER-associated prenyl-dependent carboxylmethyltransferase.","definition_xrefs":["PMID:17114793","PMID:18641086","PMID:12039957"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein maturation","termid":"GO:0051604"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00730":null,"SJAG_03396":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"CAAX-box protein maturation","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"CAAX-box protein processing","type":"related"},{"name":"farnesylated protein maturation","type":"related"}],"termid":"GO:0080120","terms_by_termid":{"GO:0071586":null}}


id: PBO:0052541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein related peptidase 14","termid":"PBO:0052541"}


id: FYPO:0008341
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 nucleosome occupancy is lower than normal within the body of a gene. Nucleosome occupancy measures the tendency for DNA in a given region to be packaged into nucleosomes.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased nucleosome occupancy","termid":"FYPO:0004491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000641","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased nucleosome occupancy in gene body","termid":"FYPO:0008341"}


id: PR:P46960
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A geranylgeranyl transferase type-2 subunit beta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00626","PANTHER:PTHR11774:SF5","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":"geranylgeranyl transferase type-2 subunit beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC167.02","secondary_identifiers":["UniProtKB:P46960"],"synonyms":[{"name":"GGTase-II-beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RABGGTB","type":"exact"},{"name":"geranylgeranyl transferase type II subunit beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"type II protein geranyl-geranyltransferase subunit beta (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P46960"}


id: PBO:0078349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 15-1","termid":"PBO:0078349"}


id: PBO:0028787
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_heterochromatin_assembly_at_protein_coding_gene","termid":"PBO:0028787"}


id: FYPO:0002704
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which autophagic vacuole docking is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"part_of","term_name":"normal macroautophagy","termid":"FYPO:0000385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal autophagic vacuole docking","termid":"FYPO:0002704"}


id: MONDO:0012077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the VAPB gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis type 8","secondary_identifiers":["OMIM:608627","GARD:10499","MESH:C563895","DOID:0050752","UMLS:C1837728","MEDGEN:325237"],"synonyms":[{"name":"ALS8","type":"exact"},{"name":"VAPB amyotrophic lateral sclerosis","type":"exact"},{"name":"amyotrophic lateral sclerosis 8","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in VAPB","type":"exact"},{"name":"amyotrophic lateral sclerosis type 8","type":"exact"}],"termid":"MONDO:0012077","xrefs":{"Monarch":{"xref_id":"0012077"}}}


id: PBO:0039729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein C1","termid":"PBO:0039729"}


id: PBO:0080373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-set pre-B cell surrogate light chain 3","termid":"PBO:0080373"}


id: GO:0004058
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-amino acid + H+ = R-H + CO2.","definition_xrefs":["EC:4.1.1.28"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"aromatic-L-amino-acid decarboxylase activity","secondary_identifiers":["Reactome:R-HSA-209924","GO:0016400","MetaCyc:AROMATIC-L-AMINO-ACID-DECARBOXYLASE-RXN","Reactome:R-HSA-209859"],"synonyms":[{"name":"aromatic-L-amino-acid carboxy-lyase activity","type":"related"},{"name":"hydroxytryptophan decarboxylase activity","type":"narrow"},{"name":"tryptophan decarboxylase activity","type":"narrow"},{"name":"5-hydroxytryptophan decarboxylase activity","type":"narrow"},{"name":"DOPA decarboxylase activity","type":"narrow"},{"name":"L-DOPA decarboxylase activity","type":"narrow"},{"name":"aromatic amino acid decarboxylase activity","type":"related"},{"name":"aromatic-L-amino-acid carboxy-lyase (tryptamine-forming)","type":"narrow"}],"termid":"GO:0004058"}


id: GO:0140328
data:
  {"annotated_genes":["SJAG_00669","SJAG_01945","SJAG_01731","SJAG_05209","SJAG_03774","SJAG_02897"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034202"},{"annotations":[97439,93911,99714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090554"},{"annotations":[93913,97441,98990,112089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090556"}]},"cv_name":"molecular_function","definition":"Catalysis of the movement of a lipid from the cytosolic to the exoplasmic leaflet of a membrane, using energy from the hydrolysis of ATP.","definition_xrefs":["Wikipedia:Flippase","PMID:25284293","PMID:20043909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase-coupled intramembrane lipid transporter activity","termid":"GO:0140326"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00669":null,"SJAG_01731":null,"SJAG_01945":null,"SJAG_02897":null,"SJAG_03774":null,"SJAG_05209":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0140303","GO:0003674"],"is_obsolete":false,"name":"floppase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"floppase activity (cytosolic to exoplasmic leaflet)","type":"exact"}],"termid":"GO:0140328","terms_by_termid":{"GO:0034202":null,"GO:0090554":null,"GO:0090556":null}}


id: GO:0019246
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L(+)-lactate from other compounds, including pyruvate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lactate biosynthetic process from pyruvate","termid":"GO:0019244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"L(+)-lactate biosynthetic process from pyruvate","secondary_identifiers":["MetaCyc:PWY-5481"],"synonyms":[{"name":"L(+)-lactate anabolism from pyruvate","type":"exact"},{"name":"L(+)-lactate formation from pyruvate","type":"exact"},{"name":"L(+)-lactate synthesis from pyruvate","type":"exact"},{"name":"S-lactate biosynthetic process from pyruvate","type":"exact"}],"termid":"GO:0019246"}


id: PBO:0051227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-20-1 (pseudogene)","termid":"PBO:0051227"}


id: PBO:0060397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEDD4 binding protein 2 like 1","termid":"PBO:0060397"}


id: MOD:01007
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes an anisyl (methoxyphenyl) group for a hydroxyl group, typically at the 4 or para position.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anisyl modified residue","termid":"MOD:01007"}


id: PBO:0041657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CACNG2 divergent transcript","termid":"PBO:0041657"}


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


id: GO:1900385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of flavonol biosynthetic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of flavonoid biosynthetic process","termid":"GO:0009964"},{"relation_name":"is_a","term_name":"regulation of flavonol biosynthetic process","termid":"GO:1900384"},{"relation_name":"negatively_regulates","term_name":"flavonol biosynthetic process","termid":"GO:0051555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of flavonol biosynthetic process","synonyms":[{"name":"down regulation of flavonol biosynthetic process","type":"exact"},{"name":"down-regulation of flavonol biosynthetic process","type":"exact"},{"name":"downregulation of flavonol biosynthetic process","type":"exact"},{"name":"inhibition of flavonol biosynthetic process","type":"narrow"}],"termid":"GO:1900385"}


id: MONDO:0003580
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete embryonal testis carcinoma (obsolete MONDO:0003580)","termid":"MONDO:0003580","xrefs":{"Monarch":{"xref_id":"0003580"}}}


id: MOD:00351
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a glycine residue to N-glycyl-1-(phosphatidyl)ethanolamine.","definition_xrefs":["PubMed:11100732","RESID:AA0346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified glycine residue","termid":"MOD:00908"},{"relation_name":"is_a","term_name":"lipoconjugated residue","termid":"MOD:01155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"N-glycyl-1-(phosphatidyl)ethanolamine","synonyms":[{"name":"(R)-1-hexadecanoyloxy-2-((Z)-9-octadecenoyloxy)-3-[2-(aminoacetylamino)ethyloxyphospho]propane","type":"exact"},{"name":"LIPID Phosphatidylethanolamine amidated glycine","type":"exact"},{"name":"N-glycyl-1-(phosphatidyl)ethanolamine","type":"exact"},{"name":"N-glycyl-1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine","type":"exact"}],"termid":"MOD:00351"}


id: GO:1902874
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of horizontal cell localization.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:16872597","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"regulation of horizontal cell localization","termid":"GO:1902872"},{"relation_name":"positively_regulates","term_name":"horizontal cell localization","termid":"GO:0035852"}],"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 horizontal cell localization","synonyms":[{"name":"activation of horizontal cell localisation","type":"narrow"},{"name":"activation of horizontal cell localization","type":"narrow"},{"name":"activation of horizontal cell positioning","type":"narrow"},{"name":"activation of laminar positioning of retinal horizontal cell","type":"narrow"},{"name":"activation of retinal horizontal cell positioning","type":"narrow"},{"name":"positive regulation of horizontal cell localisation","type":"exact"},{"name":"positive regulation of horizontal cell positioning","type":"exact"},{"name":"positive regulation of laminar positioning of retinal horizontal cell","type":"exact"},{"name":"positive regulation of retinal horizontal cell positioning","type":"exact"},{"name":"up regulation of horizontal cell localisation","type":"exact"},{"name":"up regulation of horizontal cell localization","type":"exact"},{"name":"up regulation of horizontal cell positioning","type":"exact"},{"name":"up regulation of laminar positioning of retinal horizontal cell","type":"exact"},{"name":"up regulation of retinal horizontal cell positioning","type":"exact"},{"name":"up-regulation of horizontal cell localisation","type":"exact"},{"name":"up-regulation of horizontal cell localization","type":"exact"},{"name":"up-regulation of horizontal cell positioning","type":"exact"},{"name":"up-regulation of laminar positioning of retinal horizontal cell","type":"exact"},{"name":"up-regulation of retinal horizontal cell positioning","type":"exact"},{"name":"upregulation of horizontal cell localisation","type":"exact"},{"name":"upregulation of horizontal cell localization","type":"exact"},{"name":"upregulation of horizontal cell positioning","type":"exact"},{"name":"upregulation of laminar positioning of retinal horizontal cell","type":"exact"},{"name":"upregulation of retinal horizontal cell positioning","type":"exact"}],"termid":"GO:1902874"}


id: PBO:0108939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 18","termid":"PBO:0108939"}


id: GO:0032677
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-8 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-8 production","termid":"GO:0032637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-8 production","secondary_identifiers":["GO:0045414","GO:2000482"],"synonyms":[{"name":"regulation of IL-8 production","type":"exact"},{"name":"regulation of interleukin-8 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-8 secretion","type":"narrow"}],"termid":"GO:0032677"}


id: GO:0061576
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that catalyzes the reaction acyl-CoA + sphingosine = CoA + N-acylsphingosine. In S. cerevisiae it contains three subunits: lag1, lac1 and lip1.","definition_xrefs":["GOC:dph","PMID:15692566"],"direct_ancestors":[{"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:0032991","GO:0005575"],"is_obsolete":false,"name":"acyl-CoA ceramide synthase complex","termid":"GO:0061576"}


id: MONDO:1011979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal dysplasia, non-human animal","secondary_identifiers":["OMIA:000868"],"termid":"MONDO:1011979","xrefs":{"Monarch":{"xref_id":"1011979"}}}


id: PBO:0058774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7108","termid":"PBO:0058774"}


id: GO:0007302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Attachment of the nurse cell nucleus to the plasma membrane.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus localization","termid":"GO:0051647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"nurse cell nucleus anchoring","termid":"GO:0007302"}


id: MONDO:0026141
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic urticaria (obsolete MONDO:0026141)","secondary_identifiers":["Orphanet:182734"],"termid":"MONDO:0026141","xrefs":{"Monarch":{"xref_id":"0026141"}}}


id: GO:0075063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates, maintains or increases the frequency, rate or extent of symbiont invasive hypha formation within host. 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 positive regulation of invasive hypha growth (obsolete GO:0075063)","synonyms":[{"name":"positive regulation of symbiont invasive hypha formation in host","type":"exact"},{"name":"positive regulation of symbiont invasive hypha formation within host","type":"exact"}],"termid":"GO:0075063"}


id: GO:1904749
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to nucleolus.","definition_xrefs":["GOC:TermGenie","PMID:24415760","GO_REF:0000058","GOC:BHF","GOC:nc","GOC:BHF_telomere"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to nucleus","termid":"GO:1900180"},{"relation_name":"regulates","term_name":"protein localization to nucleolus","termid":"GO:1902570"}],"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 protein localization to nucleolus","synonyms":[{"name":"regulation of protein localisation in nucleolus","type":"exact"},{"name":"regulation of protein localisation to nucleolus","type":"exact"},{"name":"regulation of protein localization in nucleolus","type":"exact"}],"termid":"GO:1904749"}


id: PBO:0038940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADH5 pseudogene 4","termid":"PBO:0038940"}


id: MONDO:1011357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Serositis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serositis, non-human animal","termid":"MONDO:1011357","xrefs":{"Monarch":{"xref_id":"1011357"}}}


id: GO:0070601
data:
  {"annotated_genes":["SJAG_01082","SJAG_00229","SJAG_01601","SJAG_00600","SJAG_03681","SJAG_04126","SJAG_03353","SJAG_04259","SJAG_04699","SJAG_03926","SJAG_01805","SJAG_03989","SJAG_03418"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104035,107378,115503,112817,100794,114096,93275,113377,98631,101321],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990813"},{"annotations":[66079,72310,90389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051754"},{"annotations":[90391,98633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071962"}]},"cv_name":"biological_process","definition":"The cell cycle process in which the sister chromatids of a replicated chromosome are joined along the length of the centromeric region of the chromosome.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sister chromatid cohesion","termid":"GO:0007062"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00229":null,"SJAG_00600":null,"SJAG_01082":null,"SJAG_01601":null,"SJAG_01805":null,"SJAG_03353":null,"SJAG_03418":null,"SJAG_03681":null,"SJAG_03926":null,"SJAG_03989":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04699":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"centromeric sister chromatid cohesion","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"sister chromatid cohesion at centromere","type":"exact"}],"termid":"GO:0070601","terms_by_termid":{"GO:0051754":null,"GO:0071962":null,"GO:1990813":null}}


id: PBO:0053049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"La ribonucleoprotein 7, transcriptional regulator","termid":"PBO:0053049"}


id: GO:0042911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the directed movement of acridine (10-azaanthracene), a heterocyclic ring compound found in crude coal-tar anthracene from one side of a membrane to the other.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete acridine transmembrane transporter activity (obsolete GO:0042911)","synonyms":[{"name":"acridine transporter activity","type":"related"}],"termid":"GO:0042911"}


id: PR:O74562
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An exocyst complex component 4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR14146:SF0","OMA:SCHPO04337","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":"exocyst complex component sec8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC970.09","secondary_identifiers":["UniProtKB:O74562"],"synonyms":[{"name":"Spom972h-EXOC4","type":"exact"}],"termid":"PR:O74562"}


id: GO:0034879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,3,6-trihydroxyisonicotinate = 2,3,6-trihydroxypyridine + CO2.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,3,6-trihydroxyisonicotinate decarboxylase activity (obsolete GO:0034879)","termid":"GO:0034879"}


id: PBO:0088155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vesicle membrane protein (v-SNARE) with acyltransferase activity; involved in trafficking to and within the Golgi, endocytic trafficking to the vacuole, and vacuolar fusion; membrane localization due to prenylation at the carboxy-terminus; human homolog YKT6 can complement yeast ykt6 mutant","termid":"PBO:0088155"}


id: GO:0050456
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 L-cysteine + NAD+ = L-cystine + H+ + NADH.","definition_xrefs":["EC:1.8.1.6","RHEA:20597"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"L-cystine reductase (NADH) activity","secondary_identifiers":["KEGG_REACTION:R00892","MetaCyc:CYSTINE-REDUCTASE-NADH-RXN"],"synonyms":[{"name":"L-cysteine:NAD+ oxidoreductase","type":"related"},{"name":"NADH-dependent cystine reductase activity","type":"related"},{"name":"NADH2:L-cystine oxidoreductase","type":"related"},{"name":"NADH:L-cystine oxidoreductase activity","type":"related"},{"name":"cystine reductase (NADH) activity","type":"related"},{"name":"cystine reductase (NADH2)","type":"related"},{"name":"cystine reductase activity","type":"exact"}],"termid":"GO:0050456"}


id: GO:0170008
data:
  {"annotated_genes":["SJAG_02638","SJAG_01746","SJAG_05694"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90800,109459,111743],"is_not":false,"summary":null,"term":"GO:0170008"}]},"cv_name":"molecular_function","definition":"Binds to and increases the activity of mRNA phosphatase.","definition_xrefs":["PMID:22323607"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01746":null,"SJAG_02638":null,"SJAG_05694":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0003674","GO:0140677","GO:0030234","GO:0098772"],"is_obsolete":false,"name":"mRNA phosphatase activator activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0170008","terms_by_termid":{"GO:0170008":null}}


id: PBO:0052054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KAT8 regulatory NSL complex subunit 3","termid":"PBO:0052054"}


id: PBO:0073687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIVA1 apoptosis inducing factor","termid":"PBO:0073687"}


id: GO:0051327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cell cycle phase during which nuclear division occurs, and which is comprises the phases: prophase, metaphase, anaphase and telophase and occurs as part of a meiotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"M phase","termid":"GO:0000279"},{"relation_name":"is_a","term_name":"meiotic cell cycle phase","termid":"GO:0098762"}],"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":"meiotic M phase","synonyms":[{"name":"M phase of meiotic cell cycle","type":"exact"}],"termid":"GO:0051327"}


id: GO:1901263
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of sorocarp spore cell differentiation.","definition_xrefs":["GOC:rjd","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of sorocarp spore cell differentiation","termid":"GO:1901261"},{"relation_name":"positively_regulates","term_name":"sorocarp spore cell differentiation","termid":"GO:0044671"}],"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 sorocarp spore cell differentiation","synonyms":[{"name":"activation of sorocarp spore cell differentiation","type":"narrow"},{"name":"up regulation of sorocarp spore cell differentiation","type":"exact"},{"name":"up-regulation of sorocarp spore cell differentiation","type":"exact"},{"name":"upregulation of sorocarp spore cell differentiation","type":"exact"}],"termid":"GO:1901263"}


id: PBO:0001261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk13 (predicted)","termid":"PBO:0001261"}


id: PBO:0054445
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 1842","termid":"PBO:0054445"}


id: MOD:00128
data:
  {"annotated_genes":["SJAG_00432","SJAG_02972","SJAG_00937","SJAG_02450","SJAG_03671","SJAG_00043","SJAG_05230","SJAG_03914","SJAG_04149","SJAG_03861","SJAG_02205","SJAG_01766"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82266,82278,82297,82382,82423,82462,82465,82478,82501,82525,82527,82549],"is_not":false,"summary":null,"term":"MOD:00128"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-pyridoxal phosphate-L-lysine.","definition_xrefs":["DeltaMass:0","RESID:AA0119","Unimod:46#K","PubMed:1544460"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00043":null,"SJAG_00432":null,"SJAG_00937":null,"SJAG_01766":null,"SJAG_02205":null,"SJAG_02450":null,"SJAG_02972":null,"SJAG_03671":null,"SJAG_03861":null,"SJAG_03914":null,"SJAG_04149":null,"SJAG_05230":null},"genotype_count":0,"is_obsolete":false,"name":"N6-pyridoxal phosphate-L-lysine","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"(2S)-2-amino-6-[([3-hydroxy-2-methyl-5-phosphonooxymethylpyridin-4-yl]methylidene)amino]hexanoic acid","type":"exact"},{"name":"MOD_RES N6-(pyridoxal phosphate)lysine","type":"exact"},{"name":"N6-pyridoxal phosphate-L-lysine","type":"exact"},{"name":"N6PydoxLys","type":"exact"},{"name":"Pyridoxal phosphate","type":"related"},{"name":"Pyridoxal phosphate (Schiff Base formed to lysine)","type":"exact"},{"name":"PyridoxalPhosphate","type":"related"}],"termid":"MOD:00128","terms_by_termid":{"MOD:00128":null}}


id: PR:O74944
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA polymerase kappa that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11076:SF12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase kappa (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC553.07c","secondary_identifiers":["UniProtKB:O74944"],"synonyms":[{"name":"SPCC553.07c","type":"related"},{"name":"Spom972h-POLK","type":"exact"},{"name":"meiotically up-regulated gene 40 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74944"}


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


id: MONDO:0000161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adrenal hyperplasia (obsolete MONDO:0000161)","synonyms":[{"name":"obsolete adrenal hyperplasia (disease)","type":"exact"}],"termid":"MONDO:0000161","xrefs":{"Monarch":{"xref_id":"0000161"}}}


id: PBO:0044178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catenin beta interacting protein 1","termid":"PBO:0044178"}


id: GO:0048447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the sepal are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ morphogenesis","termid":"GO:0048444"},{"relation_name":"part_of","term_name":"sepal development","termid":"GO:0048442"}],"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":"sepal morphogenesis","secondary_identifiers":["GO:0048422"],"termid":"GO:0048447"}


id: PBO:0030623
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_alpha-glucosidase_activity","termid":"PBO:0030623"}


id: PBO:0059299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L48","termid":"PBO:0059299"}


id: GO:0052807
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: aflatoxin + 1,5-dihydrocoenzyme F420 = aflatoxin with reduced furanocoumarin moiety + coenzyme F420. 1,5-dihydrocoenzyme F420 is also known as reduced coenzyme F420.","definition_xrefs":["PMID:20807200","GOC:mengo_curators"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"aflatoxin reductase (coenzyme F420) activity","synonyms":[{"name":"aflatoxin:coenzyme F420 oxidoreductase activity","type":"exact"},{"name":"aflatoxin:reduced coenzyme F420 reductase activity","type":"exact"},{"name":"coenzyme F420-aflatoxin reductase activity","type":"exact"},{"name":"coenzyme F420-dependent aflatoxin reductase activity","type":"exact"}],"termid":"GO:0052807"}


id: PR:Q9USY8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC16H5.15 gene.","definition_xrefs":["UniProtKB:Q9USY8","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 C16H5.15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16H5.15","synonyms":[{"name":"Spom972h-SPBC16H5.15","type":"exact"}],"termid":"PR:Q9USY8"}


id: PBO:0043471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-NOT transcription complex subunit 8","termid":"PBO:0043471"}


id: MONDO:0017153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Pulmonary arterial hypertension (PAH) associated with HIV infection (PAH-HIV) is a form of PAH characterized by elevated pulmonary arterial resistance leading to right heart failure observed as a complication of HIV infection.","definition_xrefs":["Orphanet:275808"],"gene_count":0,"genotype_count":0,"name":"obsolete pulmonary arterial hypertension associated with HIV infection (obsolete MONDO:0017153)","secondary_identifiers":["ICD9:416.8","SCTID:697904001"],"synonyms":[{"name":"PAH associated with HIV infaction","type":"exact"}],"termid":"MONDO:0017153","xrefs":{"Monarch":{"xref_id":"0017153"}}}


id: PBO:0061071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NKD inhibitor of WNT signaling pathway 2","termid":"PBO:0061071"}


id: PBO:0088418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF4050 family protein, conserved in fungi and plants","termid":"PBO:0088418"}


id: GO:0048095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Establishment of a pattern of pigment in females.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex-specific pigmentation","termid":"GO:0048071"},{"relation_name":"part_of","term_name":"female sex differentiation","termid":"GO:0046660"}],"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":"female pigmentation","termid":"GO:0048095"}


id: MONDO:0004882
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A angioid streaks that involves the optic choroid.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choroidal sclerosis","termid":"MONDO:0004885"},{"relation_name":"is_a","term_name":"angioid streaks","termid":"MONDO:0011782"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005559"],"is_obsolete":false,"name":"angioid streaks of choroid","secondary_identifiers":["ICD9:363.43","DOID:979","UMLS:C0002983","MEDGEN:507444","SCTID:86103006"],"synonyms":[{"name":"angioid streaks of optic choroid","type":"exact"},{"name":"optic choroid angioid streaks","type":"exact"}],"termid":"MONDO:0004882","xrefs":{"Monarch":{"xref_id":"0004882"}}}


id: PR:O94527
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A WD and tetratricopeptide repeats protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03590"],"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":"WD repeat protein iqw1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC609.03","secondary_identifiers":["UniProtKB:O94527"],"synonyms":[{"name":"Spom972h-WDTC1","type":"exact"}],"termid":"PR:O94527"}


id: PR:O60146
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- can1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60146"],"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 transporter C18H10.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18H10.16","synonyms":[{"name":"Spom972h-can1","type":"exact"}],"termid":"PR:O60146"}


id: GO:0048890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the lateral line ganglion over time, from its formation to the mature structure. The lateral line ganglion develops from cranial ectodermal placodes situated between the eye and ear and behind the ear.","definition_xrefs":["ISBN:0125296509","ISBN:0387968377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial ganglion development","termid":"GO:0061550"},{"relation_name":"part_of","term_name":"peripheral nervous system development","termid":"GO:0007422"},{"relation_name":"part_of","term_name":"lateral line system development","termid":"GO:0048925"}],"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":"lateral line ganglion development","synonyms":[{"name":"gLL ganglion development","type":"exact"}],"termid":"GO:0048890"}


id: PBO:0073472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sarcoglycan beta","termid":"PBO:0073472"}


id: GO:0006311
data:
  {"annotated_genes":["SJAG_02267","SJAG_02460"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88756,100066],"is_not":false,"summary":null,"term":"GO:0006311"}]},"cv_name":"biological_process","definition":"The cell cycle process in which genetic information is transferred from one helix to another. It often occurs in association with general genetic recombination events, and is believed to be a straightforward consequence of the mechanisms of general recombination and DNA repair. For example, meiosis might yield three copies of the maternal version of an allele and only one copy of the paternal allele, indicating that one of the two copies of the paternal allele has been changed to a copy of the maternal allele.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene conversion","termid":"GO:0035822"},{"relation_name":"is_a","term_name":"meiosis I cell cycle process","termid":"GO:0061982"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02267":null,"SJAG_02460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006310","GO:0007049","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"meiotic gene conversion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"gene conversion without reciprocal crossover","type":"exact"}],"termid":"GO:0006311","terms_by_termid":{"GO:0006311":null}}


id: PBO:0029595
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_plasma_membrane_during_vegetative_growth","termid":"PBO:0029595"}


id: MONDO:0004330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sarcoma arising from the leptomeninges.","definition_xrefs":["NCIT:C8312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant leptomeningeal tumor","termid":"MONDO:0003762"},{"relation_name":"is_a","term_name":"meningeal sarcoma","termid":"MONDO:0004308"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"leptomeningeal sarcoma","secondary_identifiers":["MEDGEN:235139","DOID:7689","UMLS:C1384416"],"synonyms":[{"name":"leptomeningeal sarcoma","type":"exact"},{"name":"leptomeninges sarcoma","type":"related"},{"name":"leptomeninx sarcoma","type":"exact"},{"name":"sarcoma of leptomeninges","type":"exact"},{"name":"sarcoma of leptomeninx","type":"exact"},{"name":"sarcoma of the leptomeninges","type":"exact"},{"name":"sarcoma, leptomeningeal, malignant","type":"exact"},{"name":"sarcoma, meningeal","type":"exact"}],"termid":"MONDO:0004330","xrefs":{"Monarch":{"xref_id":"0004330"}}}


id: GO:0030005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the maintenance of an internal steady state of divalent or trivalent cations at the level of a cell.","definition_xrefs":["GOC:mah","GOC:ceb"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular di-, tri-valent inorganic cation homeostasis (obsolete GO:0030005)","synonyms":[{"name":"cellular di-, tri-valent inorganic cation homeostasis","type":"exact"}],"termid":"GO:0030005"}


id: PBO:0072796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spalt like transcription factor 4 pseudogene 2","termid":"PBO:0072796"}


id: GO:0051945
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 catecholamine neurotransmitters into a neuron or glial cell.","definition_xrefs":["GOC:ai","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of neurotransmitter uptake","termid":"GO:0051581"},{"relation_name":"is_a","term_name":"regulation of catecholamine uptake involved in synaptic transmission","termid":"GO:0051940"},{"relation_name":"is_a","term_name":"negative regulation of amine transport","termid":"GO:0051953"},{"relation_name":"negatively_regulates","term_name":"catecholamine uptake involved in synaptic transmission","termid":"GO:0051934"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of catecholamine uptake involved in synaptic transmission","synonyms":[{"name":"down regulation of catecholamine uptake during transmission of nerve impulse","type":"exact"},{"name":"down-regulation of catecholamine uptake during transmission of nerve impulse","type":"exact"},{"name":"downregulation of catecholamine uptake during transmission of nerve impulse","type":"exact"},{"name":"inhibition of catecholamine uptake during transmission of nerve impulse","type":"narrow"},{"name":"negative regulation of catecholamine neurotransmitter reuptake","type":"exact"},{"name":"negative regulation of catecholamine neurotransmitter uptake","type":"exact"},{"name":"negative regulation of catecholamine uptake during transmission of nerve impulse","type":"broad"}],"termid":"GO:0051945"}


id: PBO:0074207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 40 member 1","termid":"PBO:0074207"}


id: PBO:0045525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DTWD1 pseudogene 1","termid":"PBO:0045525"}


id: PATO:0000204
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000204 absolute locomotor_activity (obsolete PATO:0000204)","termid":"PATO:0000204"}


id: PBO:0085099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear pore protein; involved in nuclear export of pre-tRNA and in re-export of mature tRNAs after their retrograde import from the cytoplasm; deletion mutation extends replicative lifespan, as does exclusion of Los1p from the nucleus in response to caloric restriction","termid":"PBO:0085099"}


id: GO:0005034
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Sensing extracellular osmolarity to initiate a change in cell activity, and spanning the membrane of the cell.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"},{"relation_name":"is_a","term_name":"molecular sensor activity","termid":"GO:0140299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140299"}],"interesting_parent_ids":["GO:0140299","GO:0098772","GO:0003674","GO:0038023"],"is_obsolete":false,"name":"osmosensor activity","termid":"GO:0005034"}


id: GO:0102719
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: eugenol + S-adenosyl-L-methionine = H+ + O-methyleugenol + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete S-adenosyl-L-methionine:eugenol-O-methyltransferase activity (obsolete GO:0102719)","termid":"GO:0102719"}


id: GO:0042450
data:
  {"annotated_genes":["SJAG_01019","SJAG_01461","SJAG_00392","SJAG_00695","SJAG_04577","SJAG_01592","SJAG_00412","SJAG_00635","SJAG_00636"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72076,80268,97665,102150,106071,110040,110661,111491,118015],"is_not":false,"summary":null,"term":"GO:0042450"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of arginine (2-amino-5-guanidinopentanoic acid) via the intermediate compound ornithine.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-arginine biosynthetic process","termid":"GO:0006526"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00392":null,"SJAG_00412":null,"SJAG_00635":null,"SJAG_00636":null,"SJAG_00695":null,"SJAG_01019":null,"SJAG_01461":null,"SJAG_01592":null,"SJAG_04577":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:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"L-arginine biosynthetic process via ornithine","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"arginine anabolism via ornithine","type":"exact"},{"name":"arginine biosynthesis, acetylated pathway","type":"exact"},{"name":"arginine formation via ornithine","type":"exact"},{"name":"arginine synthesis via ornithine","type":"exact"},{"name":"classical arginine biosynthesis pathway","type":"exact"}],"termid":"GO:0042450","terms_by_termid":{"GO:0042450":null}}


id: MONDO:0006144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An embryonal neoplasm arising from the cervix with morphologic features resembling Wilms tumor of the kidney.","definition_xrefs":["NCIT:C40236"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"cervical carcinosarcoma","termid":"MONDO:0002877"},{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"},{"relation_name":"is_a","term_name":"Wilms tumor","termid":"MONDO:0006058"}],"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":"cervical Wilms tumor","secondary_identifiers":["UMLS:C1516437","DOID:5190","MEDGEN:273129"],"synonyms":[{"name":"cervical Wilms tumor","type":"exact"},{"name":"cervical Wilms' tumor","type":"exact"},{"name":"cervical Wilms' tumour","type":"exact"}],"termid":"MONDO:0006144","xrefs":{"Monarch":{"xref_id":"0006144"}}}


id: GO:0097231
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the controlled self-propelled movement of a cell that results in translocation of the cell from one place to another as a result of a calcium ion stimulus.","definition_xrefs":["PMID:19363786","GOC:pf","PMID:21239624","PMID:8937985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell motility","termid":"GO:0048870"},{"relation_name":"part_of","term_name":"cellular response to calcium ion","termid":"GO:0071277"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell motility in response to calcium ion","synonyms":[{"name":"Ca2+ facilitation of cell motility","type":"exact"},{"name":"calcium ion facilitation of cell motility","type":"exact"}],"termid":"GO:0097231"}


id: MONDO:0019761
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Laryngo-tracheo-esophageal cleft (LC) type 1 is a congenital respiratory tract anomaly characterized by a supraglottic, interarytenoid cleft above the vocal folds with moderate respiratory symptoms.","definition_xrefs":["Orphanet:93938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngotracheoesophageal cleft","termid":"MONDO:0016060"}],"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":"laryngotracheoesophageal cleft type 1","secondary_identifiers":["GARD:19236","MEDGEN:667239","UMLS:C0584823"],"synonyms":[{"name":"LTEC I","type":"exact"},{"name":"LTEC1","type":"exact"},{"name":"laryngo-tracheo-esophageal cleft type 1","type":"exact"}],"termid":"MONDO:0019761","xrefs":{"Monarch":{"xref_id":"0019761"}}}


id: PBO:0001027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Usp (universal stress protein) family protein, implicated in meiotic chromosome segregation","termid":"PBO:0001027"}


id: MONDO:0012124
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sudden infant death with dysgenesis of the testes (SIDDT) syndrome is a lethal condition in infants with dysgenesis of testes.","definition_xrefs":["Orphanet:168593"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sudden infant death-dysgenesis of the testes syndrome","secondary_identifiers":["MESH:C563856","GARD:12382","OMIM:608800","MEDGEN:332428","UMLS:C1837371"],"synonyms":[{"name":"SIDDT","type":"exact"},{"name":"sudden infant death - dysgenesis of the testes","type":"related"},{"name":"sudden infant death with dysgenesis of the testes syndrome","type":"related"}],"termid":"MONDO:0012124","xrefs":{"Monarch":{"xref_id":"0012124"}}}


id: PBO:0029994
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_actomyosin_contractile_ring_disassembly","termid":"PBO:0029994"}


id: PR:Q09735
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cytosol aminopeptidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00229","PRO:DNx","PANTHER:PTHR11963:SF3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminopeptidase C13A11.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13A11.05","secondary_identifiers":["UniProtKB:Q09735"],"synonyms":[{"name":"Spom972h-LAP3","type":"exact"}],"termid":"PR:Q09735"}


id: MONDO:0024238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurodegenerative disease that involves the telencephalon.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"cerebral degeneration","secondary_identifiers":["UMLS:C0154671","MEDGEN:56343","SCTID:418143002","ICD9:331.9"],"synonyms":[{"name":"cerebral degeneration","type":"exact"},{"name":"neurodegenerative disease of telencephalon","type":"exact"},{"name":"telencephalon neurodegenerative disease","type":"exact"}],"termid":"MONDO:0024238","xrefs":{"Monarch":{"xref_id":"0024238"}}}


id: GO:1990297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A renal system process in which amino acids are taken up from the collecting ducts, glomerulus and proximal and distal loops of the nephron. In non-mammalian species, absorption may occur in related structures.","definition_xrefs":["GOC:hjd","PMID:1526373"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal absorption","termid":"GO:0070293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal amino acid absorption","termid":"GO:1990297"}


id: PBO:0081494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF385D antisense RNA 2","termid":"PBO:0081494"}


id: PBO:0049573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B.W histone 1","termid":"PBO:0049573"}


id: MONDO:0019909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 16 is characterized bypostnatal growthdeficiency, intellectual disability, microcephaly, broad flat nasal bridge, down-turned mouth, low-set and dysmorphic (abnormally-shaped) ears and speech delay.To date, less than 10 cases have been reported in the medical literature.","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 16 disorder","termid":"MONDO:0700023"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 16","secondary_identifiers":["SCTID:763406004","GARD:10855","Orphanet:96178","UMLS:C4706449","MEDGEN:1641955"],"synonyms":[{"name":"R16","type":"related"},{"name":"Ring 16","type":"related"},{"name":"Ring chromosome 16 syndrome","type":"related"},{"name":"Ring chromosome type 16","type":"exact"},{"name":"chromosome 16 ring","type":"related"}],"termid":"MONDO:0019909","xrefs":{"Monarch":{"xref_id":"0019909"}}}


id: MONDO:0003137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the glomeruli, in which all glomeruli are affected, resulting in renal failure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephritis","termid":"MONDO:0002462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"diffuse glomerulonephritis","secondary_identifiers":["UMLS:C0859036","NCIT:C35799","MEDGEN:163563","DOID:4781"],"termid":"MONDO:0003137","xrefs":{"Monarch":{"xref_id":"0003137"}}}


id: PBO:0015256
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by hamster Dpagt1","termid":"PBO:0015256"}


id: MONDO:0017323
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypocalcemic rickets is a group of genetic diseases characterized by hypocalcemia and rickets. It comprises hypocalcemic vitamin D dependent rickets (VDDR-I) and hypocalcemic vitamin D resistant rickets (HVDRR).","definition_xrefs":["Orphanet:289103"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rickets","termid":"MONDO:0005520"},{"relation_name":"is_a","term_name":"disorders of vitamin D metabolism","termid":"MONDO:0017322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hypocalcemic rickets","secondary_identifiers":["GARD:21133","SCTID:722947004","UMLS:C4302195","NCIT:C131421","MEDGEN:927864"],"synonyms":[{"name":"Calciopenic rickets","type":"exact"},{"name":"calcium deficiency rickets","type":"exact"}],"termid":"MONDO:0017323","xrefs":{"Monarch":{"xref_id":"0017323"}}}


id: GO:0098777
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Protein secretion through the outer membrane via the mechanism used for the secretion of curli subunits.","definition_xrefs":["PMID:24080089","PMID:19299134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport across the cell outer membrane","termid":"GO:0098776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"protein secretion by the type VIII secretion system","synonyms":[{"name":"T8SS","type":"exact"}],"termid":"GO:0098777"}


id: SO:0002211
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  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A self replicating circular nucleic acid molecule that is distinct from a chromosome in the organism.","definition_xrefs":["PMID:21719542","SBOL:jb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasmid","termid":"SO:0000155"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"circular_plasmid","synonyms":[{"name":"circular plasmid","type":"exact"}],"termid":"SO:0002211"}


id: MONDO:0859151
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id: GO:0060786
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id: PBO:0053127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphocyte cytosolic protein 1","termid":"PBO:0053127"}


id: PBO:0088190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc-finger protein of unknown function; possibly involved in pre-tRNA splicing and in uptake of branched-chain amino acids; STP3 has a paralog, STP4, that arose from the whole genome duplication","termid":"PBO:0088190"}


id: PBO:0027262
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  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sporulation_resulting_in_formation_of_ascus_with_single_large_spore","termid":"PBO:0027262"}


id: PBO:0077214
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane 9 superfamily member 5, pseudogene","termid":"PBO:0077214"}


id: GO:0061369
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of blood vessel morphogenesis in the testicle.","definition_xrefs":["GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of blood vessel morphogenesis","termid":"GO:2000181"}],"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 testicular blood vessel morphogenesis","synonyms":[{"name":"negative regulation of testicular vasculature morphogenesis","type":"broad"}],"termid":"GO:0061369"}


id: GO:0098917
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id: GO:0008380
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id: PBO:0071128
data:
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id: PBO:0065761
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id: PBO:0078312
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id: MONDO:0030718
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id: GO:1900544
data:
  {"annotated_genes":["SJAG_00685"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905857"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of purine nucleotide metabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nucleotide metabolic process","termid":"GO:0045981"},{"relation_name":"is_a","term_name":"regulation of purine nucleotide metabolic process","termid":"GO:1900542"},{"relation_name":"positively_regulates","term_name":"purine nucleotide metabolic process","termid":"GO:0006163"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00685":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0055086"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of purine nucleotide metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of purine metabolic process","type":"narrow"},{"name":"activation of purine metabolism","type":"narrow"},{"name":"activation of purine nucleotide metabolic process","type":"narrow"},{"name":"activation of purine nucleotide metabolism","type":"narrow"},{"name":"positive regulation of purine metabolic process","type":"narrow"},{"name":"positive regulation of purine metabolism","type":"narrow"},{"name":"positive regulation of purine nucleotide metabolism","type":"exact"},{"name":"up regulation of purine metabolic process","type":"narrow"},{"name":"up regulation of purine metabolism","type":"narrow"},{"name":"up regulation of purine nucleotide metabolic process","type":"exact"},{"name":"up regulation of purine nucleotide metabolism","type":"exact"},{"name":"up-regulation of purine metabolic process","type":"narrow"},{"name":"up-regulation of purine metabolism","type":"narrow"},{"name":"up-regulation of purine nucleotide metabolic process","type":"exact"},{"name":"up-regulation of purine nucleotide metabolism","type":"exact"},{"name":"upregulation of purine metabolic process","type":"narrow"},{"name":"upregulation of purine metabolism","type":"narrow"},{"name":"upregulation of purine nucleotide metabolic process","type":"exact"},{"name":"upregulation of purine nucleotide metabolism","type":"exact"}],"termid":"GO:1900544","terms_by_termid":{"GO:1905857":null}}


id: FYPO:0002079
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing calcium ions during a cellular hypotonic response.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal growth on calcium","termid":"FYPO:0001020"},{"relation_name":"is_a","term_name":"normal growth during cellular response to osmotic stress","termid":"FYPO:0001021"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0002058","FYPO:0000257","FYPO:0002060","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on calcium during cellular hypotonic response","synonyms":[{"name":"normal cell population growth in presence of calcium ions during cellular hypotonic response","type":"exact"},{"name":"normal cell population growth on calcium during cellular hypotonic response","type":"exact"},{"name":"normal cell population growth on calcium ion during cellular hypoosmotic response","type":"exact"},{"name":"normal cell population growth on calcium ion during cellular hypotonic response","type":"exact"},{"name":"normal cell population growth on excess calcium during cellular hypotonic response","type":"exact"},{"name":"normal cellular response to calcium ion during cellular hypotonic response","type":"related"},{"name":"normal growth on calcium ion during cellular hypotonic response","type":"exact"},{"name":"normal vegetative cell population growth on calcium ion during cellular hypotonic response","type":"exact"}],"termid":"FYPO:0002079"}


id: PBO:0082753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Sec23p-Sfb3p heterodimer of the COPII vesicle coat; COPII coat is required for cargo selection during vesicle formation in ER to Golgi transport; scaffolding function of Lst1p required to generate vesicles that can accommodate difficult cargo proteins that include large oligomeric assemblies and asymmetrically distributed membrane proteins; with Atg40p acts in autophagy of the ER; homologous to Sec24p and Sfb2p","termid":"PBO:0082753"}


id: GO:0061700
data:
  {"annotated_genes":["SJAG_00209","SJAG_00561","SJAG_02424","SJAG_03907","SJAG_04496"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[77162,87468,87763,88876,106120],"is_not":false,"summary":null,"term":"GO:0061700"}]},"cv_name":"cellular_component","definition":"A multiprotein subcomplex of the GATOR complex that regulates TORC1 signaling by interacting with the Rag GTPase. In human, this complex consists of WDR24, WDR59, MIOS, SEH1L, and SEC13. In S. cerevisiae, this complex is referred to as SEACAT and contains the Sea2p, Sea3p, Sea4p, Seh1p, Sec13p proteins.","definition_xrefs":["GOC:rb","PMID:25934700","GOC:krc","PMID:23723238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"Seh1-associated complex","termid":"GO:0035859"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00209":null,"SJAG_00561":null,"SJAG_02424":null,"SJAG_03907":null,"SJAG_04496":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"GATOR2 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"SEACAT complex","type":"exact"}],"termid":"GO:0061700","terms_by_termid":{"GO:0061700":null}}


id: PBO:0001411
data:
  {"annotation_feature_type":"gene","cv_name":"sequence_feature","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein NES","termid":"PBO:0001411"}


id: GO:0002800
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of antifungal peptide secretion.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antifungal peptide production","termid":"GO:0002788"},{"relation_name":"is_a","term_name":"regulation of antimicrobial peptide secretion","termid":"GO:0002794"},{"relation_name":"regulates","term_name":"antifungal peptide secretion","termid":"GO:0002782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of antifungal peptide secretion","termid":"GO:0002800"}


id: PBO:0030837
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_guanine_import","termid":"PBO:0030837"}


id: PBO:0067847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 149","termid":"PBO:0067847"}


id: MONDO:0008880
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":"Bowen syndrome of multiple malformations","secondary_identifiers":["MESH:C538164","Orphanet:1271","OMIM:211200","MEDGEN:349159","UMLS:C1859404"],"synonyms":[{"name":"Bowen syndrome","type":"exact"},{"name":"Bowen syndrome of multiple malformations","type":"exact"}],"termid":"MONDO:0008880","xrefs":{"Monarch":{"xref_id":"0008880"}}}


id: GO:0015792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which arabitol is transported across a lipid bilayer, from one side of a membrane to the other. Arabitol is the pentitol derived from arabinose or lyxose by reduction of the aldehyde group. The D enantiomer is present in lichens and mushrooms.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyol transmembrane transport","termid":"GO:0015791"},{"relation_name":"is_a","term_name":"carbohydrate transmembrane transport","termid":"GO:0034219"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"arabinitol transmembrane transport","synonyms":[{"name":"arabinitol transport","type":"related"},{"name":"arabitol transport","type":"related"}],"termid":"GO:0015792"}


id: GO:0044557
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which the extent of smooth muscle contraction is reduced. Smooth muscle differs from striated muscle in the much higher actin/myosin ratio, the absence of conspicuous sarcomeres and the ability to contract to a much smaller fraction of its resting length.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"relaxation of muscle","termid":"GO:0090075"}],"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":"relaxation of smooth muscle","synonyms":[{"name":"smooth muscle relaxation","type":"exact"}],"termid":"GO:0044557"}


