# terms

id: GO:0047718
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: indan-1-ol + NAD(P)+ = indanone + NAD(P)H + H+.","definition_xrefs":["EC:1.1.1.112","MetaCyc:INDANOL-DEHYDROGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"indanol dehydrogenase activity","synonyms":[{"name":"indan-1-ol:NAD(P)+ 1-oxidoreductase activity","type":"related"}],"termid":"GO:0047718"}


id: MONDO:0021170
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete amyotonia congenita (obsolete MONDO:0021170)","synonyms":[{"name":"Oppenheim disease","type":"related"},{"name":"Oppenheim's disease","type":"related"},{"name":"amyotonia congenita","type":"related"}],"termid":"MONDO:0021170","xrefs":{"Monarch":{"xref_id":"0021170"}}}


id: PBO:0079848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unc-50 inner nuclear membrane RNA binding protein","termid":"PBO:0079848"}


id: PBO:0040722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL10 antisense RNA 1","termid":"PBO:0040722"}


id: PBO:0070912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 20","termid":"PBO:0070912"}


id: PBO:0041523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 16 open reading frame 78","termid":"PBO:0041523"}


id: PBO:0005054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin family protein Urm1 (predicted)","termid":"PBO:0005054"}


id: GO:0052081
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts a salicylic acid-mediated signal transduction pathway in its host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:35698792","GOC:mtg_pamgo_17jul06"],"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 salicylic acid-mediated signal transduction pathway","secondary_identifiers":["GO:0052445"],"synonyms":[{"name":"modulation by organism of defense-related salicylic acid-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of defense-related host salicylic acid-mediated signal transduction pathway","type":"exact"},{"name":"modulation of defense-related host SA-mediated signal transduction pathway by organism","type":"exact"},{"name":"perturbation of defense-related host salicylic acid-mediated signal transduction pathway","type":"exact"}],"termid":"GO:0052081"}


id: PBO:0088596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor Moc3","termid":"PBO:0088596"}


id: PBO:0044276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine ligand 17","termid":"PBO:0044276"}


id: MONDO:0012624
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder leading to a deficiency of complex I of the respiratory chain and is characterized by neurological dysfunction, hepatic failure and cardiomyopathy.","definition_xrefs":["Orphanet:99901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of fatty acid oxidation and ketogenesis","termid":"MONDO:0017713"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"acyl-CoA dehydrogenase 9 deficiency","secondary_identifiers":["SCTID:725046003","MEDGEN:1648400","OMIM:611126","MESH:C567006","UMLS:C4747517","GARD:12986","DOID:0112072"],"synonyms":[{"name":"ACAD9 deficiency","type":"exact"},{"name":"acyl-CoA dehydrogenase 9 deficiency","type":"exact"},{"name":"mitochondrial complex I deficiency due to ACAD9 deficiency","type":"exact"},{"name":"mitochondrial complex I deficiency, nuclear type 20","type":"exact"}],"termid":"MONDO:0012624","xrefs":{"Monarch":{"xref_id":"0012624"}}}


id: FYPO:0008035
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 chromatin containing the histone H3 variant CenH3 (also called CENP-A; Cnp1 in S. pombe) are assembled in the pericentromeric heterochromatin. CENP-A-containing nucleosomes are normally assembled into chromatin at the centromeres, encompassing the central core and centromeric inner repeat regions.","direct_ancestors":[{"relation_name":"is_a","term_name":"ectopic CENP-A containing chromatin assembly","termid":"FYPO:0005887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000641","FYPO:0001985"],"is_obsolete":false,"name":"ectopic CENP-A containing chromatin assembly at pericentromeric heterochromatin","synonyms":[{"name":"CENP-A containing nucleosome speading into pericentromeric heterochromatin","type":"exact"},{"name":"ectopic CENP-A containing nucleosome assembly at pericentromeric heterochromatin","type":"exact"}],"termid":"FYPO:0008035"}


id: PBO:0039842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP11A divergent transcript","termid":"PBO:0039842"}


id: PBO:0117435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase inhibitor 2A regulated lncRNA","termid":"PBO:0117435"}


id: GO:0001302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process associated with progression of the cell from its inception to the end of its lifespan that occurs as the cell continues cycles of growth and division.","definition_xrefs":["PMID:12044934","GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete replicative cell aging (obsolete GO:0001302)","synonyms":[{"name":"replicative cell ageing","type":"exact"}],"termid":"GO:0001302"}


id: PBO:0031089
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_manganese_depletion","termid":"PBO:0031089"}


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


id: PBO:0049682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxyacylglutathione hydrolase","termid":"PBO:0049682"}


id: GO:0051289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a protein homotetramer, a macromolecular structure consisting of four noncovalently associated identical subunits.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein homooligomerization","termid":"GO:0051260"},{"relation_name":"is_a","term_name":"protein tetramerization","termid":"GO:0051262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"protein homotetramerization","synonyms":[{"name":"protein homotetramer assembly","type":"exact"},{"name":"protein homotetramer biosynthesis","type":"exact"},{"name":"protein homotetramer biosynthetic process","type":"exact"},{"name":"protein homotetramer formation","type":"exact"}],"termid":"GO:0051289"}


id: GO:0016420
data:
  {"annotated_genes":["SJAG_03972","SJAG_04107"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[60265,71956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004314"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a malonyl (HOOC-CH2-CO-) group to an acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03972":null,"SJAG_04107":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"malonyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null},"termid":"GO:0016420","terms_by_termid":{"GO:0004314":null}}


id: PBO:0074114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 29 member 4 pseudogene 2","termid":"PBO:0074114"}


id: PBO:0072809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 4B","termid":"PBO:0072809"}


id: FYPO:0006591
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 DNA damage measured in a cell during S phase of the mitotic cell cycle is greater than normal. The number, extent, or both of damage sites may be increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased DNA damage during vegetative growth","termid":"FYPO:0003547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased DNA damage during mitotic S phase","synonyms":[{"name":"increased DNA damage during S phase during vegetative growth","type":"exact"},{"name":"increased DNA damage during S phase of mitotic cell cycle","type":"exact"},{"name":"increased number of DNA lesions during mitotic S phase","type":"related"}],"termid":"FYPO:0006591"}


id: PBO:0087398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Stress inducible cytoplasmic thioredoxin peroxidase; cooperates with Tsa1p in the removal of reactive oxygen, nitrogen and sulfur species using thioredoxin as hydrogen donor; deletion enhances the mutator phenotype of tsa1 mutants; protein abundance increases in response to DNA replication stress; TSA2 has a paralog, TSA1, that arose from the whole genome duplication","termid":"PBO:0087398"}


id: PBO:0086107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for assembly of the cytochrome bc(1) complex; acts as a chaperone for Rip1p and facilitates its insertion into the complex at a late stage of assembly; localized to the mitochondrial matrix; null mutant exhibits a respiratory growth defect and reduced mitochondrial zinc levels, which is characteristic of mutations affecting bc(1) complex assembly; member of the LYR protein family; human LYRM7 is a functional ortholog","termid":"PBO:0086107"}


id: GO:0052047
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with a second organism mediated by a substance secreted by the first organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiotic process mediated by secreted substance (obsolete GO:0052047)","synonyms":[{"name":"interaction with other organism via secreted substance during symbiotic interaction","type":"related"},{"name":"interaction with other organism via secreted substance involved in symbiotic interaction","type":"related"}],"termid":"GO:0052047"}


id: MONDO:0000729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital ptosis (obsolete MONDO:0000729)","termid":"MONDO:0000729","xrefs":{"Monarch":{"xref_id":"0000729"}}}


id: PBO:0016911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific protein Mug94","termid":"PBO:0016911"}


id: GO:0047916
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-6-deoxy-D-talose + NAD(P)+ = GDP-4-dehydro-6-deoxy-D-talose + NAD(P)H + H+.","definition_xrefs":["MetaCyc:GDP-6-DEOXY-D-TALOSE-4-DEHYDROGENASE-RXN","EC:1.1.1.135"],"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":"GDP-6-deoxy-D-talose 4-dehydrogenase activity","synonyms":[{"name":"GDP-6-deoxy-D-talose:NAD(P)+ 4-oxidoreductase activity","type":"related"},{"name":"guanosine diphospho-6-deoxy-D-talose dehydrogenase activity","type":"related"}],"termid":"GO:0047916"}


id: GO:1904667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ubiquitin protein ligase activity.","definition_xrefs":["GOC:TermGenie","GOC:dph","PMID:26216882","GOC:tb","GO_REF:0000059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ubiquitin-protein transferase activity","termid":"GO:0051444"},{"relation_name":"is_a","term_name":"regulation of ubiquitin protein ligase activity","termid":"GO:1904666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"negative regulation of ubiquitin protein ligase activity","secondary_identifiers":["GO:0060564","GO:1904190"],"synonyms":[{"name":"down regulation of E3","type":"related"},{"name":"down regulation of protein ubiquitination activity","type":"exact"},{"name":"down regulation of ubiquitin ligase activity","type":"exact"},{"name":"down regulation of ubiquitin protein ligase activity","type":"exact"},{"name":"down-regulation of E3","type":"related"},{"name":"down-regulation of protein ubiquitination activity","type":"exact"},{"name":"down-regulation of ubiquitin ligase activity","type":"exact"},{"name":"down-regulation of ubiquitin protein ligase activity","type":"exact"},{"name":"downregulation of E3","type":"related"},{"name":"downregulation of protein ubiquitination activity","type":"exact"},{"name":"downregulation of ubiquitin ligase activity","type":"exact"},{"name":"downregulation of ubiquitin protein ligase activity","type":"exact"},{"name":"inhibition of E3","type":"related"},{"name":"inhibition of protein ubiquitination activity","type":"narrow"},{"name":"inhibition of ubiquitin ligase activity","type":"narrow"},{"name":"inhibition of ubiquitin protein ligase activity","type":"narrow"},{"name":"negative regulation of APC activity during mitotic cell cycle","type":"related"},{"name":"negative regulation of APC-Cdc20 complex activity","type":"narrow"},{"name":"negative regulation of APC-fizzy related complex activity","type":"narrow"},{"name":"negative regulation of APC/C activity during mitotic cell cycle","type":"related"},{"name":"negative regulation of E3","type":"related"},{"name":"negative regulation of anaphase-promoting complex activity during mitotic cell cycle","type":"related"},{"name":"negative regulation of cyclosome activity during mitotic cell cycle","type":"related"},{"name":"negative regulation of mitotic anaphase-promoting complex activity","type":"related"},{"name":"negative regulation of protein ubiquitination activity","type":"exact"},{"name":"negative regulation of ubiquitin ligase activity","type":"exact"}],"termid":"GO:1904667"}


id: GO:0044301
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The axon of inferior olive neuron that projects to the cerebellar cortex, largely via the inferior cerebellar peduncle. They range in diameter from 1-3 um and are myelinated until they enter the granule cell layer. They give off collaterals to the deep cerebellar nuclei. They synapse extensively with the dendrites of Purkinje cells in the molecular layer, where each fiber branches repeatedly to climb along the Purkinje cell dendritic tree. Each Purkinje cell is innervated by only a single climbing fiber.","definition_xrefs":["NIF_Subcellular:nlx_subcell_20090203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon","termid":"GO:0030424"}],"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":"climbing fiber","synonyms":[{"name":"climbing fibre","type":"exact"}],"termid":"GO:0044301"}


id: GO:0000201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a MAP kinase to the nucleus that occurs in the context of cell wall organization or biogenesis.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK import into nucleus involved in cell wall organization or biogenesis (obsolete GO:0000201)","synonyms":[{"name":"MAPK import into nucleus involved in cell wall biogenesis","type":"narrow"},{"name":"MAPK import into nucleus involved in cell wall integrity","type":"exact"},{"name":"cell wall biogenesis, MAPK import into nucleus","type":"exact"},{"name":"cell wall biogenesis, nuclear translocation of MAPK","type":"narrow"},{"name":"nuclear translocation of MAPK involved in cell wall biogenesis","type":"narrow"},{"name":"nuclear translocation of MAPK involved in cell wall integrity","type":"narrow"}],"termid":"GO:0000201"}


id: GO:0005755
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrogen-transporting ATP synthase, coupling factor CF(0) (obsolete GO:0005755)","synonyms":[{"name":"hydrogen-transporting ATP synthase, coupling factor CF(0)","type":"exact"}],"termid":"GO:0005755"}


id: MONDO:0023194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete frints de Smet Fabry Fryns syndrome (obsolete MONDO:0023194)","termid":"MONDO:0023194","xrefs":{"Monarch":{"xref_id":"0023194"}}}


id: PBO:0060951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFIL3 like basic leucine zipper","termid":"PBO:0060951"}


id: GO:0075221
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of zoospore encystment on host. 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":"negative regulation of spore encystment on host","termid":"GO:0075217"},{"relation_name":"is_a","term_name":"modulation of zoospore encystment on host","termid":"GO:0075219"},{"relation_name":"negatively_regulates","term_name":"zoospore encystment on host","termid":"GO:0075218"}],"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 zoospore encystment on host","termid":"GO:0075221"}


id: GO:0080131
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a hydroxyjasmonate + 3'-phosphoadenosine-5'-phosphosulfate = a hydroxyjasmonate sulfate + adenosine-3',5'-diphosphate.","definition_xrefs":["EC:2.8.2.39","PMID:12637544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfotransferase activity","termid":"GO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016782","GO:0003674"],"is_obsolete":false,"name":"hydroxyjasmonate sulfotransferase activity","secondary_identifiers":["MetaCyc:RXN-10451"],"synonyms":[{"name":"11-OHJA sulfotransferase activity","type":"narrow"},{"name":"11-hydroxyjasmonate sulfotransferase activity","type":"narrow"},{"name":"11-hydroxyjasmonic acid sulfotransferase activity","type":"narrow"},{"name":"12-OHJA sulfotransferase activity","type":"narrow"},{"name":"12-hydroxyjasmonate sulfotransferase activity","type":"narrow"},{"name":"12-hydroxyjasmonic acid sulfotransferase activity","type":"narrow"},{"name":"OHJA sulfotransferase activity","type":"exact"},{"name":"hydroxyjasmonic acid sulfotransferase activity","type":"exact"}],"termid":"GO:0080131"}


id: PBO:0004692
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.5.4.25","termid":"PBO:0004692"}


id: GO:0052399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The activation by an organism of programmed cell death in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by organism of symbiont programmed cell death (obsolete GO:0052399)","synonyms":[{"name":"activation by organism of symbiont programmed cell death","type":"exact"},{"name":"induction by organism of symbiont programmed cell death","type":"exact"}],"termid":"GO:0052399"}


id: PBO:0031551
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_peptidase_activity","termid":"PBO:0031551"}


id: PATO:0002438
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's being located or placed beneath the skin.","definition_xrefs":["thefreedictionary:thefreedictionary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subdermal","synonyms":[{"name":"subcutaneous","type":"exact"}],"termid":"PATO:0002438"}


id: MONDO:0009727
data:
  {"annotated_genes":["SJAG_02463","SJAG_01941"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88553,88554],"is_not":false,"summary":null,"term":"MONDO:0009727"}]},"cv_name":"mondo","definition":"A lethal perinatal bone dysplasia characterized by limb shortening, normal sized skull with cleft palate, hitchhiker thumbs, distinctive facial dysmorphism and radiographic skeletal features, caused by mutations in the diastrophic dysplasia sulfate transporter gene.","definition_xrefs":["Orphanet:56304"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"mineral metabolism disease","termid":"MONDO:0000226"},{"relation_name":"is_a","term_name":"atelosteogenesis","termid":"MONDO:0000389"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"SLC26A2-related skeletal dysplasia","termid":"MONDO:0100592"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01941":null,"SJAG_02463":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005497"],"is_obsolete":false,"name":"atelosteogenesis type II","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:8329","ICD10CM:Q77.5","ICD9:756.9","MEDGEN:338072","SCTID:254055004","MESH:C535395","UMLS:C1850554","OMIM:256050"],"synonyms":[{"name":"AO2","type":"exact"},{"name":"AOII","type":"exact"},{"name":"De 50A Chapelle dysplasia","type":"related"},{"name":"De la Chapelle dysplasia","type":"related"},{"name":"atelosteogenesis II","type":"related"},{"name":"atelosteogenesis type 2","type":"exact"},{"name":"atelosteogenesis type II","type":"exact"},{"name":"atelosteogenesis, type 2","type":"related"},{"name":"atelosteogenesis, type II","type":"related"},{"name":"neonatal osseous dysplasia 1","type":"related"},{"name":"neonatal osseous dysplasia type 1","type":"exact"}],"termid":"MONDO:0009727","terms_by_termid":{"MONDO:0009727":null},"xrefs":{"Monarch":{"xref_id":"0009727"}}}


id: PBO:0042643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain Y-linked 18 pseudogene","termid":"PBO:0042643"}


id: GO:0007191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An adenylate cyclase-activating G protein-coupled receptor signaling pathway initiated by dopamine binding to its receptor, and ending with the regulation of a downstream cellular process.","definition_xrefs":["GOC:signaling","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0007189"},{"relation_name":"is_a","term_name":"G protein-coupled dopamine receptor signaling pathway","termid":"GO:0007212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"adenylate cyclase-activating dopamine receptor signaling pathway","synonyms":[{"name":"activation of adenylate cyclase activity by dopamine receptor signaling pathway","type":"related"},{"name":"activation of adenylate cyclase activity by dopamine receptor signalling pathway","type":"related"},{"name":"dopamine receptor, adenylate cyclase activating pathway","type":"exact"},{"name":"dopamine receptor, adenylyl cyclase activating pathway","type":"exact"}],"termid":"GO:0007191"}


id: PBO:0062852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otoferlin","termid":"PBO:0062852"}


id: GO:0009772
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A photosynthetic electron transport chain in which electrons move from the primary electron acceptor (Quinone, Q) through a chain of electron transport molecules in the thylakoid membrane until they reach the ultimate electron acceptor of Photosystem II, which is plastocyanin (PC). The electron is then passed to the P700 chlorophyll a molecules of the reaction centre of photosystem I.","definition_xrefs":["ISBN:0816017360","ISBN:0716731363","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photosynthetic electron transport chain","termid":"GO:0009767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006091"],"is_obsolete":false,"name":"photosynthetic electron transport in photosystem II","termid":"GO:0009772"}


id: GO:0014897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The enlargement or overgrowth of all or part of an organ due to an increase in size of muscle cells without cell division. In the case of striated muscle, this happens due to the additional synthesis of sarcomeric proteins and assembly of myofibrils.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle hypertrophy","termid":"GO:0014896"}],"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":"striated muscle hypertrophy","termid":"GO:0014897"}


id: MONDO:0002852
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare sarcoma that arises from the mediastinum. Examples include liposarcoma, leiomyosarcoma, and angiosarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"},{"relation_name":"is_a","term_name":"mediastinal soft tissue cancer","termid":"MONDO:0037743"}],"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":"mediastinum sarcoma","secondary_identifiers":["DOID:4050","MEDGEN:233687","NCIT:C6606","UMLS:C1334678"],"synonyms":[{"name":"mediastinal sarcoma","type":"exact"},{"name":"mediastinum sarcoma","type":"exact"},{"name":"sarcoma of mediastinum","type":"exact"},{"name":"sarcoma of the mediastinum","type":"exact"}],"termid":"MONDO:0002852","xrefs":{"Monarch":{"xref_id":"0002852"}}}


id: FYPO:0003551
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which an RNA catabolic process is abnormal.","definition_xrefs":["GO:0006401","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA metabolic process","termid":"FYPO:0004851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000294","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal RNA catabolic process","synonyms":[{"name":"abnormal RNA breakdown","type":"exact"},{"name":"abnormal RNA catabolism","type":"exact"},{"name":"abnormal RNA degradation","type":"exact"}],"termid":"FYPO:0003551"}


id: PBO:0080814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-ray repair cross complementing 6 pseudogene 4","termid":"PBO:0080814"}


id: MONDO:0012117
data:
  {"annotated_genes":["SJAG_00334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88253],"is_not":false,"summary":null,"term":"MONDO:0012117"},{"annotations":[89062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009890"}]},"cv_name":"mondo","definition":"A form of congenital disorders of N-linked glycosylation characterized by progressive microcephaly, hypotonia, developmental delay, drug-resistant infantile epilepsy, and hepatomegaly. Additional features that may be observed include failure to thrive, pericardial effusion, renal cysts, skeletal dysplasia, facial dysmorphism (frontal bossing, hypertelorism, depressed nasal bridge, low-seated ears, large mouth) and hydrops fetalis. The disease is caused by loss-of-function mutations in the gene ALG9 (11q23).","definition_xrefs":["Orphanet:79328"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type I","termid":"MONDO:0005500"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00334":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"ALG9-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C2931006","MEDGEN:443955","MESH:C535750","OMIM:608776","SCTID:720978005","DOID:0080564","GARD:9839"],"synonyms":[{"name":"ALG9-CDG","type":"exact"},{"name":"ALG9-CDG (CDG-IL)","type":"related"},{"name":"ALG9-congenital disorder of glycosylation","type":"exact"},{"name":"CDG 1L","type":"related"},{"name":"CDG IL","type":"related"},{"name":"CDG syndrome type IL","type":"exact"},{"name":"CDG-IL","type":"exact"},{"name":"CDG1L","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type 1L","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IL","type":"related"},{"name":"congenital disorder of glycosylation type 1L","type":"exact"},{"name":"congenital disorder of glycosylation type IL","type":"related"},{"name":"congenital disorder of glycosylation, type IL","type":"related"},{"name":"mannosyltransferase 7-9 deficiency","type":"exact"}],"termid":"MONDO:0012117","terms_by_termid":{"MONDO:0009890":null,"MONDO:0012117":null},"xrefs":{"Monarch":{"xref_id":"0012117"}}}


id: GO:1904662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of sensory perception of bitter taste.","definition_xrefs":["GOC:mr","GO_REF:0000058","GOC:TermGenie","PMID:1716172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nervous system process","termid":"GO:0031646"},{"relation_name":"is_a","term_name":"regulation of sensory perception of bitter taste","termid":"GO:1904660"},{"relation_name":"positively_regulates","term_name":"sensory perception of bitter taste","termid":"GO:0050913"}],"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 sensory perception of bitter taste","synonyms":[{"name":"activation of bitter taste perception","type":"narrow"},{"name":"activation of sensory perception of bitter taste","type":"narrow"},{"name":"positive regulation of bitter taste perception","type":"exact"},{"name":"up regulation of bitter taste perception","type":"exact"},{"name":"up regulation of sensory perception of bitter taste","type":"exact"},{"name":"up-regulation of bitter taste perception","type":"exact"},{"name":"up-regulation of sensory perception of bitter taste","type":"exact"},{"name":"upregulation of bitter taste perception","type":"exact"},{"name":"upregulation of sensory perception of bitter taste","type":"exact"}],"termid":"GO:1904662"}


id: MONDO:0000970
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, mesenchymal neoplasm that arises from the breast. It is surrounded by a thin capsule and composed of mature adipose tissue cells. Atypia is absent.","definition_xrefs":["NCIT:C4647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast lipoma","secondary_identifiers":["DOID:10199","UMLS:C0349565","ICD9:214.1","SCTID:276891009","MEDGEN:138103"],"synonyms":[{"name":"breast lipoma","type":"exact"},{"name":"lipoma of breast","type":"exact"},{"name":"lipoma of the breast","type":"exact"}],"termid":"MONDO:0000970","xrefs":{"Monarch":{"xref_id":"0000970"}}}


id: GO:0042181
data:
  {"annotated_genes":["SJAG_01866","SJAG_00459","SJAG_01043","SJAG_01672","SJAG_01865","SJAG_01668","SJAG_04000","SJAG_00721","SJAG_00933","SJAG_04568","SJAG_04642","SJAG_06603","SJAG_01820"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91013],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904775"},{"annotations":[74179,80964,80590,76024,89519,74747,75620,64712,75889,121370,121371,78397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006744"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ketones, a class of organic compounds that contain the carbonyl group, CO, and in which the carbonyl group is bonded only to carbon atoms. The general formula for a ketone is RCOR, where R and R are alkyl or aryl groups.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"small molecule biosynthetic process","termid":"GO:0044283"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00459":null,"SJAG_00721":null,"SJAG_00933":null,"SJAG_01043":null,"SJAG_01668":null,"SJAG_01672":null,"SJAG_01820":null,"SJAG_01865":null,"SJAG_01866":null,"SJAG_04000":null,"SJAG_04568":null,"SJAG_04642":null,"SJAG_06603":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ketone biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"PMID:29191091":null},"synonyms":[{"name":"ketone anabolism","type":"exact"},{"name":"ketone biosynthesis","type":"exact"},{"name":"ketone formation","type":"exact"},{"name":"ketone synthesis","type":"exact"}],"termid":"GO:0042181","terms_by_termid":{"GO:0006744":null,"GO:1904775":null}}


id: MONDO:0033926
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare hypothalamic or pituitary disease (obsolete MONDO:0015889)","termid":"MONDO:0015889"},{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"anorexia nervosa","termid":"MONDO:0005351"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prepubertal anorexia nervosa","secondary_identifiers":["MEDGEN:1799990","GARD:22191","Orphanet:525738","UMLS:C5568567"],"termid":"MONDO:0033926","xrefs":{"Monarch":{"xref_id":"0033926"}}}


id: PBO:0082893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cyclin-dependent kinase inhibitor; activated by environmental stress; interacts with and inhibits the Cdc28p/Cln2p, G1/S phase cyclin-dependent kinase complex but not S-phase, or M-phase complexes; overexpression blocks cells in G1 phase and stabilizes the Cdc28p inhibitor Sic1p, while disruption accelerates the G1/S phase transition; phosphorylated during S phase in a Cdc28p-dependent manner; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and to the nucleus","termid":"PBO:0082893"}


id: PBO:0062996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidyl arginine deiminase 2","termid":"PBO:0062996"}


id: PBO:0068812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 49, pseudogene","termid":"PBO:0068812"}


id: MONDO:0003760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that arises from the ovary and occurs in children.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood germ cell tumor","termid":"MONDO:0003751"},{"relation_name":"is_a","term_name":"ovarian germ cell tumor","termid":"MONDO:0011366"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pediatric ovarian germ cell tumor","secondary_identifiers":["MEDGEN:162990","NCIT:C8588","UMLS:C0796664","DOID:6084"],"synonyms":[{"name":"childhood ovarian germ cell neoplasm","type":"exact"},{"name":"childhood ovarian germ cell tumor","type":"exact"},{"name":"childhood ovarian germ cell tumour","type":"exact"},{"name":"ovarian germ cell tumor","type":"broad"},{"name":"ovarian germ cell tumor of childhood","type":"exact"},{"name":"ovarian germ cell tumour","type":"broad"},{"name":"ovarian germ cell tumour of childhood","type":"exact"},{"name":"paediatric ovarian germ cell neoplasm","type":"exact"},{"name":"pediatric ovarian germ cell neoplasm","type":"exact"},{"name":"pediatric ovarian germ cell tumor","type":"exact"}],"termid":"MONDO:0003760","xrefs":{"Monarch":{"xref_id":"0003760"}}}


id: PBO:0046420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPH receptor A5","termid":"PBO:0046420"}


id: PR:O94700
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An endothelial differentiation-related factor 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02913","PANTHER:PTHR10245:SF1"],"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":"multiprotein-bridging factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.17","secondary_identifiers":["UniProtKB:O94700"],"synonyms":[{"name":"Spom972h-EDF1","type":"exact"}],"termid":"PR:O94700"}


id: GO:0048573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change from the vegetative to the reproductive phase as a result of detection of, or exposure to, a period of light or dark of a given length. The length of the period of light or dark required to initiate the change is set relative to a particular duration known as the 'critical day length'. The critical day length varies between species.","definition_xrefs":["ISBN:0697037754","ISBN:0709408862","GOC:pj","GOC:jid","ISBN:0582015952"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photoperiodism","termid":"GO:0009648"},{"relation_name":"part_of","term_name":"vegetative to reproductive phase transition of meristem","termid":"GO:0010228"}],"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":"photoperiodism, flowering","synonyms":[{"name":"photoperiodic control of flowering time","type":"exact"},{"name":"photoperiodic control of inflorescence development","type":"exact"},{"name":"response to day length, flowering","type":"exact"},{"name":"response to night length, flowering","type":"exact"},{"name":"response to photoperiod, flowering","type":"exact"}],"termid":"GO:0048573"}


id: GO:0045844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of striated muscle development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of striated muscle tissue development","termid":"GO:0016202"},{"relation_name":"is_a","term_name":"positive regulation of muscle organ development","termid":"GO:0048636"},{"relation_name":"is_a","term_name":"positive regulation of muscle tissue development","termid":"GO:1901863"},{"relation_name":"positively_regulates","term_name":"striated muscle tissue development","termid":"GO:0014706"}],"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 striated muscle tissue development","synonyms":[{"name":"activation of striated muscle development","type":"narrow"},{"name":"stimulation of striated muscle development","type":"narrow"},{"name":"up regulation of striated muscle development","type":"exact"},{"name":"up-regulation of striated muscle development","type":"exact"},{"name":"upregulation of striated muscle development","type":"exact"}],"termid":"GO:0045844"}


id: GO:2000341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of chemokine (C-X-C motif) ligand 2 production.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"regulates","term_name":"chemokine (C-X-C motif) ligand 2 production","termid":"GO:0072567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of chemokine (C-X-C motif) ligand 2 production","secondary_identifiers":["GO:0035926","GO:1904207"],"synonyms":[{"name":"chemokine (C-C motif) ligand 2 secretion","type":"narrow"},{"name":"regulation of CCL2 secretion","type":"narrow"},{"name":"regulation of CXCL2 production","type":"exact"},{"name":"regulation of MIP-2 production","type":"exact"},{"name":"regulation of MIP2 production","type":"exact"},{"name":"regulation of SCYB2 production","type":"exact"},{"name":"regulation of chemokine (C-C motif) ligand 2 secretion","type":"narrow"}],"termid":"GO:2000341"}


id: PBO:0042794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 192","termid":"PBO:0042794"}


id: MONDO:0060624
data:
  {"annotated_genes":["SJAG_03915"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86898],"is_not":false,"summary":null,"term":"MONDO:0060624"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03915":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1621102","OMIM:617807","UMLS:C4540498"],"synonyms":[{"name":"NDAGSCW","type":"related"},{"name":"neurodevelopmental disorder with ataxic GAIT, absent speech, and decreased cortical WHITE matter","type":"related"}],"termid":"MONDO:0060624","terms_by_termid":{"MONDO:0060624":null},"xrefs":{"Monarch":{"xref_id":"0060624"}}}


id: PBO:0116765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAV2 divergent transcript","termid":"PBO:0116765"}


id: PBO:0087592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the ASTRA complex, involved in chromatin remodeling; subunit of the telomere cap complex DNA-binding protein specific to single-stranded yeast telomeric DNA repeats, required for telomere length regulation and telomere position effect; involved in the stability or biogenesis of PIKKs such as TORC1","termid":"PBO:0087592"}


id: PBO:0050156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 12","termid":"PBO:0050156"}


id: GO:0061705
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sucrose, to yield fructose-6-phosphate through both glucose and fructose intermediates.","definition_xrefs":["PMID:15012287","GOC:dph","MetaCyc:PWY-621","GOC:glycolysis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sucrose catabolic process","termid":"GO:0005987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"sucrose catabolic process to fructose-6-phosphate through glucose and fructose","termid":"GO:0061705"}


id: MONDO:0021368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the major salivary gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tumor of salivary gland","termid":"MONDO:0021357"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplasm of major salivary gland","secondary_identifiers":["NCIT:C4407","SCTID:126787005","UMLS:C0345599","MEDGEN:83383"],"synonyms":[{"name":"major salivary gland neoplasm","type":"exact"},{"name":"major salivary gland neoplasm (disease)","type":"exact"},{"name":"major salivary gland tumor","type":"exact"},{"name":"major salivary gland tumour","type":"exact"},{"name":"neoplasm of major salivary gland","type":"exact"},{"name":"neoplasm of the Major salivary gland","type":"exact"},{"name":"tumor of Major salivary gland","type":"exact"},{"name":"tumor of major salivary gland","type":"exact"},{"name":"tumor of the Major salivary gland","type":"exact"},{"name":"tumour of Major salivary gland","type":"exact"},{"name":"tumour of major salivary gland","type":"exact"},{"name":"tumour of the Major salivary gland","type":"exact"}],"termid":"MONDO:0021368","xrefs":{"Monarch":{"xref_id":"0021368"}}}


id: GO:1990254
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a keratin filament, an intermediate filament composed of acidic and basic keratins (types I and II), typically expressed in epithelial cells.","definition_xrefs":["GOC:krc","PMID:6170061"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament binding","termid":"GO:0019215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"keratin filament binding","termid":"GO:1990254"}


id: GO:0010164
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 cesium stimulus.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to metal ion","termid":"GO:0010038"}],"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 cesium ion","synonyms":[{"name":"response to cesium","type":"exact"}],"termid":"GO:0010164"}


id: PATO:0001896
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structure quality inhering in a bearer by virtue of the bearer's lacking of a three dimensional space surrounded by one or more anatomical structures and containing one or more anatomical substances.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure, cavities","termid":"PATO:0002014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unlumenized","termid":"PATO:0001896"}


id: FYPO:0007872
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 bulk plasma membrane flow from the cell poles to lateral regions does not occur.","definition_xrefs":["PomBase:mah","PMID:34533984"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal plasma membrane organization","termid":"FYPO:0000813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abolished plasma membrane flow from cell pole to lateral region","synonyms":[{"name":"abolished bulk plasma membrane flow from cell pole to lateral region","type":"exact"},{"name":"abolished plasma membrane flow from cell pole to lateral region during mitotic cell cycle","type":"related"},{"name":"abolished plasma membrane flow from cell pole to lateral region during vegetative growth","type":"exact"},{"name":"plasma membrane flow from cell pole to lateral region abolished","type":"exact"}],"termid":"FYPO:0007872"}


id: GO:0102346
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (R)-3-hydroxycerotoyl-CoA(4-) = trans-2-hexacosenoyl-CoA(4-) + H2O.","definition_xrefs":["GOC:pz","EC:4.2.1.134"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-hydroxy-cerotoyl-CoA dehydratase activity (obsolete GO:0102346)","termid":"GO:0102346"}


id: PBO:0000167
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.1.2.11","termid":"PBO:0000167"}


id: PBO:0062172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily K member 15","termid":"PBO:0062172"}


id: FYPO:0006799
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which nuclear MIS12/MIND complex binding by a gene product (usually a protein) in a mutant does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah","PMID:29180432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction","termid":"FYPO:0000705"},{"relation_name":"is_a","term_name":"abnormal protein complex binding","termid":"FYPO:0003591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000702","FYPO:0000652"],"is_obsolete":false,"name":"abolished nuclear MIS12/MIND complex binding","synonyms":[{"name":"abolished nuclear MIS12/MIND complex binding during mitotic cell cycle","type":"related"},{"name":"abolished nuclear MIS12/MIND complex binding during vegetative growth","type":"exact"},{"name":"nuclear MIS12/MIND complex binding abolished","type":"exact"}],"termid":"FYPO:0006799"}


id: MONDO:0013490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"megalencephalic leukoencephalopathy with subcortical cysts","termid":"MONDO:0011391"}],"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":"megalencephalic leukoencephalopathy with subcortical cysts 2A","secondary_identifiers":["UMLS:C3151355","OMIM:613925","MEDGEN:462705","GARD:15728","DOID:0080318"],"synonyms":[{"name":"MLC2A","type":"related"},{"name":"megalencephalic leukoencephalopathy with subcortical cysts 2A","type":"exact"},{"name":"megalencephalic leukoencephalopathy with subcortical cysts type 2A","type":"exact"}],"termid":"MONDO:0013490","xrefs":{"Monarch":{"xref_id":"0013490"}}}


id: PBO:0055304
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 2731","termid":"PBO:0055304"}


id: GO:0140966
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of heterochromatin into a heterochromatin domain, enriched in histone H3 methylated on lysine 9 (H3K9me), by a process mediated by a Piwi-associated RNA (piRNA).","definition_xrefs":["PMID:23329111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulatory ncRNA-mediated heterochromatin formation","termid":"GO:0031048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006325"],"is_obsolete":false,"name":"piRNA-mediated heterochromatin formation","synonyms":[{"name":"piRNA-directed heterochromatin formation","type":"exact"},{"name":"piwiRNA-directed heterochromatin formation","type":"exact"}],"termid":"GO:0140966"}


id: GO:1905829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of prostaglandin catabolic process.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:12432938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid catabolic process","termid":"GO:0050995"},{"relation_name":"is_a","term_name":"regulation of prostaglandin catabolic process","termid":"GO:1905828"},{"relation_name":"negatively_regulates","term_name":"prostaglandin catabolic process","termid":"GO:1905344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of prostaglandin catabolic process","synonyms":[{"name":"down regulation of prostaglandin breakdown","type":"exact"},{"name":"down regulation of prostaglandin catabolic process","type":"exact"},{"name":"down regulation of prostaglandin catabolism","type":"exact"},{"name":"down regulation of prostaglandin degradation","type":"exact"},{"name":"down-regulation of prostaglandin breakdown","type":"exact"},{"name":"down-regulation of prostaglandin catabolic process","type":"exact"},{"name":"down-regulation of prostaglandin catabolism","type":"exact"},{"name":"down-regulation of prostaglandin degradation","type":"exact"},{"name":"downregulation of prostaglandin breakdown","type":"exact"},{"name":"downregulation of prostaglandin catabolic process","type":"exact"},{"name":"downregulation of prostaglandin catabolism","type":"exact"},{"name":"downregulation of prostaglandin degradation","type":"exact"},{"name":"inhibition of prostaglandin breakdown","type":"narrow"},{"name":"inhibition of prostaglandin catabolic process","type":"narrow"},{"name":"inhibition of prostaglandin catabolism","type":"narrow"},{"name":"inhibition of prostaglandin degradation","type":"narrow"},{"name":"negative regulation of prostaglandin breakdown","type":"exact"},{"name":"negative regulation of prostaglandin catabolism","type":"exact"},{"name":"negative regulation of prostaglandin degradation","type":"exact"}],"termid":"GO:1905829"}


id: GO:0061971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which bones are generated and organized as a result of the conversion of another structural tissue into bone.","definition_xrefs":["PMID:29852585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone morphogenesis","termid":"GO:0060349"}],"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":"replacement bone morphogenesis","termid":"GO:0061971"}


id: MONDO:0005799
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of humans or animals with hookworms other than those caused by the genus Ancylostoma or Necator, for which the specific terms ancylostomiasis and necatoriasis are available.","definition_xrefs":["MESH:D006725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infectious disease","termid":"MONDO:0005550"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hookworm infectious disease","secondary_identifiers":["EFO:0007314"],"synonyms":[{"name":"Bunostomiases","type":"related"},{"name":"Bunostomiasis","type":"related"},{"name":"hookworm infection","type":"related"},{"name":"infection, hookworm","type":"related"},{"name":"infections, hookworm","type":"related"}],"termid":"MONDO:0005799","xrefs":{"Monarch":{"xref_id":"0005799"}}}


id: PBO:0039124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AIFM1 pseudogene 1","termid":"PBO:0039124"}


id: PBO:0082805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of U2 snRNP complex; disruption causes reduced U2 snRNP levels; physically interacts with Msl1p; putative homolog of human U2A' snRNP protein","termid":"PBO:0082805"}


id: PBO:0038283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genotype_comment","termid":"PBO:0038283"}


id: PBO:0047627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOXO induced long non-coding RNA 1","termid":"PBO:0047627"}


id: GO:0050461
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3,4-dihydroxypyridine + O-acetyl-L-serine = 3-(3,4-dihydroxypyridinium-1-yl)-L-alanine + acetate.","definition_xrefs":["RHEA:12693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"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:0016765"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016765","GO:0016740"],"is_obsolete":false,"name":"L-mimosine synthase activity","secondary_identifiers":["EC:2.5.1.52","KEGG_REACTION:R04091","MetaCyc:RXN-7461"],"synonyms":[{"name":"3-O-acetyl-L-serine:3,4-dihydroxypyridine 1-(2-amino-2-carboxyethyl)transferase activity","type":"related"},{"name":"O(3)-acetyl-L-serine acetate-lyase (adding 3,4-dihydroxypyridin-1-yl) activity","type":"related"},{"name":"O3-acetyl-L-serine acetate-lyase (adding 3,4-dihydroxypyridin-1-yl)","type":"related"},{"name":"O3-acetyl-L-serine:3,4-dihydroxypyridine 1-(2-amino-2-carboxyethyl)transferase activity","type":"related"}],"termid":"GO:0050461"}


id: PBO:0081434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 285D, pseudogene","termid":"PBO:0081434"}


id: FYPO:0007273
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 cortical endoplasmic reticulum (ER) remodeling occurs to a greater extent than normal. Cortical ER remodeling is the dynamic spatial rearrangement of ER tubules near the cell cortex.","definition_xrefs":["PomBase:mah","PMID:32023460"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cortical endoplasmic reticulum organization","termid":"FYPO:0007571"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased cortical endoplasmic reticulum remodeling","synonyms":[{"name":"increased cortical ER remodeling","type":"exact"},{"name":"increased cortical endoplasmic reticulum remodeling during mitotic cell cycle","type":"related"},{"name":"increased cortical endoplasmic reticulum remodeling during vegetative growth","type":"exact"}],"termid":"FYPO:0007273"}


id: GO:0039593
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a virus interferes with the host cell completing the M phase of the cell cycle.","definition_xrefs":["VZ:877"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cell cycle progression","termid":"GO:0044071"}],"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 exit from mitosis","synonyms":[{"name":"inhibition of host mitotic exit by virus","type":"exact"},{"name":"perturbation by virus of host exit from mitosis","type":"narrow"},{"name":"suppression by virus of host exit from mitosis","type":"related"}],"termid":"GO:0039593"}


id: MONDO:0021653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mucinosis","termid":"MONDO:0002523"}],"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":"cutaneous focal mucinosis","secondary_identifiers":["UMLS:C0406659","MEDGEN:590585","SCTID:110981005","ICD9:701.8"],"synonyms":[{"name":"focal mucinoses","type":"related"},{"name":"focal mucinosis","type":"related"}],"termid":"MONDO:0021653","xrefs":{"Monarch":{"xref_id":"0021653"}}}


id: GO:0007253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The selective interaction of the transcription factor NF-kappaB with specific molecules in the cytoplasm, thereby inhibiting its translocation into the nucleus.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cytoplasmic sequestering of NF-kappaB (obsolete GO:0007253)","synonyms":[{"name":"cytoplasmic NF-kappaB retention","type":"exact"},{"name":"cytoplasmic NF-kappaB sequestration","type":"exact"},{"name":"cytoplasmic NF-kappaB storage","type":"exact"},{"name":"cytoplasmic retention of NF-kappaB","type":"exact"},{"name":"cytoplasmic sequestration of NF-kappaB","type":"exact"},{"name":"cytoplasmic storage of NF-kappaB","type":"exact"},{"name":"maintenance of NF-kappaB location in cytoplasm","type":"exact"}],"termid":"GO:0007253"}


id: PBO:0053605
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 638","termid":"PBO:0053605"}


id: GO:0043726
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-amino-6-(5-phospho-D-ribitylamino)uracil + H2O = 5-amino-6-(D-ribitylamino)uracil + phosphate.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787","GO:0016788"],"is_obsolete":false,"name":"5-amino-6-(5-phosphoribitylamino)uracil phosphatase activity","secondary_identifiers":["MetaCyc:RIBOPHOSPHAT-RXN","RHEA:25197","GO:0019173","EC:3.1.3.104"],"synonyms":[{"name":"pyrimidine phosphatase activity","type":"exact"}],"termid":"GO:0043726"}


id: MONDO:0015037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lissencephaly with cerebellar hypoplasia type D (LCHd) is a form of lissencephaly with cerebellar hypoplasia characterized by pronounced microcephaly (at least B1 3 SD), intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres.","definition_xrefs":["Orphanet:100014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly with cerebellar hypoplasia","termid":"MONDO:0019450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"lissencephaly with cerebellar hypoplasia type D","secondary_identifiers":["icd11.foundation:1633599738","UMLS:C4274991","MEDGEN:895252","SCTID:715821000","GARD:19734"],"termid":"MONDO:0015037","xrefs":{"Monarch":{"xref_id":"0015037"}}}


id: GO:0047955
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + glycerol = AH(2) + glycerone.","definition_xrefs":["RHEA:17493","EC:1.1.99.22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH-OH group of donors","termid":"GO:0016614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"glycerol dehydrogenase (acceptor) activity","secondary_identifiers":["KEGG_REACTION:R01045","MetaCyc:GLYCEROL-DEHYDROGENASE-ACCEPTOR-RXN"],"synonyms":[{"name":"glycerol:(acceptor) 1-oxidoreductase activity","type":"related"},{"name":"glycerol:acceptor 1-oxidoreductase activity","type":"related"}],"termid":"GO:0047955"}


id: PBO:0062362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily V member 1","termid":"PBO:0062362"}


id: PBO:0040147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asialoglycoprotein receptor 2","termid":"PBO:0040147"}


id: FYPO:0005984
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 the dye Congo Red. Cells stop growing (and may die) at a concentration of Congo Red that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0000003","FYPO:0005447","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to Congo Red","synonyms":[{"name":"hypersensitive to Congo Red","type":"exact"},{"name":"sensitive to Congo Red during mitotic cell cycle","type":"related"},{"name":"sensitive to Congo Red during vegetative growth","type":"exact"}],"termid":"FYPO:0005984"}


id: SO:0000097
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene from nucleomorph sequence.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"nucleomorphic_sequence","termid":"SO:0000739"},{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleomorph_gene","synonyms":[{"name":"nucleomorph gene","type":"exact"}],"termid":"SO:0000097"}


id: MONDO:0009600
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":"metaphyseal dysplasia, anetoderma, and optic atrophy","secondary_identifiers":["MEDGEN:381576","UMLS:C1855174","MESH:C565395","OMIM:250450"],"synonyms":[{"name":"metaphyseal dysplasia, anetoderma, and optic atrophy","type":"exact"}],"termid":"MONDO:0009600","xrefs":{"Monarch":{"xref_id":"0009600"}}}


id: PBO:0113418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein that associates with polysomes; may be involved in regulating mRNA translation; involved in the copper-dependent mineralization of copper sulfide complexes on cell surface in cells cultured in copper salts; role in preventing L-A mycovirus pathogenesis; SLF1 has a paralog, SRO9, that arose from the whole genome duplication; protein abundance increases in response to DNA replication stress","termid":"PBO:0113418"}


id: PBO:0047460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fc receptor like 1","termid":"PBO:0047460"}


id: GO:0070517
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex containing three of the five subunits of eukaryotic replication factor C, those corresponding to human p40, p38, and p37.","definition_xrefs":["PMID:9228079","PMID:8692848","PMID:9582326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear DNA replication factor C complex","termid":"GO:0043599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005694","GO:0005634"],"is_obsolete":false,"name":"DNA replication factor C core complex","synonyms":[{"name":"RFC core complex","type":"exact"}],"termid":"GO:0070517"}


id: MOD:00053
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to N-acetyl-L-glutamic acid.","definition_xrefs":["PubMed:6725286","ChEBI:17533","RESID:AA0044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"},{"relation_name":"is_a","term_name":"alpha-amino acetylated residue","termid":"MOD:01458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408"],"is_obsolete":false,"name":"N-acetyl-L-glutamic acid","synonyms":[{"name":"(2S)-2-(acetamido)pentanedioic acid","type":"exact"},{"name":"2-(acetylamino)pentanedioic acid","type":"exact"},{"name":"2-(acetylazanyl)pentanedioic acid","type":"exact"},{"name":"AcGlu","type":"exact"},{"name":"MOD_RES N-acetylglutamate","type":"exact"},{"name":"N-acetyl-L-glutamic acid","type":"exact"},{"name":"N-acetylated L-glutamic acid","type":"exact"},{"name":"acetylglutamic acid","type":"exact"}],"termid":"MOD:00053"}


id: PBO:0075862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family pseudogene 1","termid":"PBO:0075862"}


id: PBO:0041981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 25","termid":"PBO:0041981"}


id: PBO:0084431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAL-activator protein; encoded within the complex locus MAL2; required for maltose and isomaltose utilization","termid":"PBO:0084431"}


id: GO:0015918
data:
  {"annotated_genes":["SJAG_03718","SJAG_00261","SJAG_01722","SJAG_01329","SJAG_02323","SJAG_00355","SJAG_01407","SJAG_01590","SJAG_02375","SJAG_03247"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111314,118203,113291,93316,110144,104511,96090,108256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120011"},{"annotations":[73695,78768,62949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032366"}]},"cv_name":"biological_process","definition":"The directed movement of sterols into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Sterols are steroids with one or more hydroxyl groups and a hydrocarbon side-chain in the molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"},{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00261":null,"SJAG_00355":null,"SJAG_01329":null,"SJAG_01407":null,"SJAG_01590":null,"SJAG_01722":null,"SJAG_02323":null,"SJAG_02375":null,"SJAG_03247":null,"SJAG_03718":null},"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:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"sterol transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015918","terms_by_termid":{"GO:0032366":null,"GO:0120011":null}}


id: MONDO:0016729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of central nervous system neoplasms with a variable amount of neuronal and, less consistently, glial differentiation. They occur at a low frequency and usually carry a favorable prognosis. Representative examples include dysplastic cerebellar gangliocytoma, desmoplastic infantile ganglioglioma, desmoplastic infantile astrocytoma, and dysembryoplastic neuroepithelial tumor. (Adapted from WHO)","definition_xrefs":["NCIT:C4747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroepithelial neoplasm","termid":"MONDO:0021193"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mixed neuronal-glial tumor","secondary_identifiers":["icd11.foundation:1792897751","GARD:20728","MEDGEN:105377","Orphanet:251934","UMLS:C0474844"],"synonyms":[{"name":"neuronal and Glio-neuronal neoplasm","type":"exact"},{"name":"neuronal and Glio-neuronal tumor","type":"exact"},{"name":"neuronal and Glio-neuronal tumour","type":"exact"},{"name":"neuronal and mixed neuronal-glial tumor","type":"exact"},{"name":"neuronal and mixed neuronal-glial tumors","type":"exact"},{"name":"neuronal and mixed neuronal-glial tumour","type":"exact"},{"name":"neuronal and mixed neuronal-glial tumours","type":"exact"}],"termid":"MONDO:0016729","xrefs":{"Monarch":{"xref_id":"0016729"}}}


id: MONDO:0006685
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ischemia) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ischemic attack, transient; brain infarction; brain edema; coma; and other conditions.","definition_xrefs":["MESH:D020925"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"brain ischemia","termid":"MONDO:0005299"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain hypoxia - ischemia","secondary_identifiers":["MEDGEN:199862","UMLS:C0752308"],"termid":"MONDO:0006685","xrefs":{"Monarch":{"xref_id":"0006685"}}}


id: PBO:0027782
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_threonine_phosphorylation","termid":"PBO:0027782"}


id: PBO:0000445
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.7.6","termid":"PBO:0000445"}


id: MONDO:0010941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nocturnal enuresis where the child has been dry for at least 6 months but enuresis has recurred.","direct_ancestors":[{"relation_name":"is_a","term_name":"nocturnal enuresis","termid":"MONDO:0000022"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nocturnal enuresis, 2","secondary_identifiers":["MEDGEN:331473","OMIM:600808","MESH:C563439","UMLS:C1833268"],"synonyms":[{"name":"ENUR2","type":"related"},{"name":"enuresis, nocturnal, 2","type":"related"}],"termid":"MONDO:0010941","xrefs":{"Monarch":{"xref_id":"0010941"}}}


id: PBO:0017858
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrolysis rate of dextrin to glucose is 7.6 (uM min-1 ml-2)","termid":"PBO:0017858"}


id: MONDO:0007597
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":"factor VIII and Factor IX, combined deficiency of","secondary_identifiers":["OMIM:134510","MEDGEN:341994","MESH:C565024","UMLS:C1851376"],"synonyms":[{"name":"F8F9D","type":"related"},{"name":"factor 8 and Factor IX, combined deficiency of","type":"related"},{"name":"factor VIII and Factor IX, combined deficiency of","type":"exact"},{"name":"factor VIII and factor IX, combined deficiency OF","type":"related"},{"name":"familial multiple coagulation Factor deficiency 2","type":"related"}],"termid":"MONDO:0007597","xrefs":{"Monarch":{"xref_id":"0007597"}}}


id: PBO:0029039
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_glycerol_level","termid":"PBO:0029039"}


id: GO:0004369
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sn-glycerol 3-phosphate + O2 = glycerone phosphate + H2O2.","definition_xrefs":["RHEA:18369","EC:1.1.3.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"glycerol-3-phosphate oxidase activity","secondary_identifiers":["KEGG_REACTION:R00846","MetaCyc:GLYCEROL-3-PHOSPHATE-OXIDASE-RXN"],"synonyms":[{"name":"L-alpha-glycerol-3-phosphate oxidase activity","type":"related"},{"name":"L-alpha-glycerophosphate oxidase activity","type":"related"},{"name":"alpha-glycerophosphate oxidase activity","type":"related"},{"name":"glycerol phosphate oxidase activity","type":"related"},{"name":"glycerol-1-phosphate oxidase activity","type":"related"},{"name":"sn-glycerol-3-phosphate:oxygen 2-oxidoreductase activity","type":"related"}],"termid":"GO:0004369"}


id: MONDO:0010045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. This syndrome is characterized by slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit. It has been reported in five patients, among which there were two sets of identical twins. The significance of the relationship between the twinning process and the condition is not clear. The mode of inheritance is unknown but single-gene transmission seems likely.","definition_xrefs":["Orphanet:2823"],"gene_count":0,"genotype_count":0,"name":"obsolete paraplegia-brachydactyly-cone-shaped epiphysis syndrome (obsolete MONDO:0010045)","secondary_identifiers":["MESH:C537938","OMIM:270710"],"synonyms":[{"name":"FITZSIMMONS-Guilbert syndrome","type":"related"},{"name":"Fitzsimmons syndrome","type":"related"},{"name":"Fitzsimmons-Guilbert syndrome","type":"exact"},{"name":"moved to 270550, 190350, and 616944","type":"related"},{"name":"spastic paraplegia associated with brachydactyly type E","type":"related"}],"termid":"MONDO:0010045","xrefs":{"Monarch":{"xref_id":"0010045"}}}


id: PBO:0043338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLN8 transmembrane ER and ERGIC protein","termid":"PBO:0043338"}


id: MONDO:0008020
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":"multiple exostoses with spastic tetraparesis","secondary_identifiers":["OMIM:158345","UMLS:C1834724","MESH:C563566","MEDGEN:371889"],"synonyms":[{"name":"Hamann Zanki schimrigk syndrome","type":"related"},{"name":"multiple exostoses with spastic tetraparesis","type":"exact"},{"name":"spasticity multiple exostoses","type":"related"}],"termid":"MONDO:0008020","xrefs":{"Monarch":{"xref_id":"0008020"}}}


id: MONDO:0971008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyloid neuropathy","termid":"MONDO:0007100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0021179","MONDO:0005244","MONDO:0005066"],"is_obsolete":false,"name":"amyloidosis, hereditary systemic 3","secondary_identifiers":["UMLS:C4551500","OMIM:620657","MEDGEN:1635231"],"termid":"MONDO:0971008","xrefs":{"Monarch":{"xref_id":"0971008"}}}


id: MONDO:0016844
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterized by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features.","definition_xrefs":["Orphanet:261318"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial trisomy of chromosome 20","termid":"MONDO:0016938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy 20p","secondary_identifiers":["ICD9:758.5","SCTID:111311004","MEDGEN:418939","UMLS:C2930888","MESH:C535371","GARD:5333"],"synonyms":[{"name":"20p duplication","type":"related"},{"name":"20p trisomy","type":"related"},{"name":"Duplication 20p","type":"related"},{"name":"Duplication of 20p","type":"exact"},{"name":"chromosome 20p duplication","type":"related"},{"name":"dup(20p)","type":"exact"},{"name":"partial duplication of chromosome 20p","type":"exact"},{"name":"partial duplication of the short arm of chromosome 20","type":"exact"},{"name":"partial trisomy 20p","type":"related"},{"name":"partial trisomy of chromosome 20p","type":"exact"},{"name":"partial trisomy of the short arm of chromosome 20","type":"exact"},{"name":"trisomy 20p","type":"exact"},{"name":"trisomy type 20p","type":"exact"}],"termid":"MONDO:0016844","xrefs":{"Monarch":{"xref_id":"0016844"}}}


id: GO:0001832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An increase in size of a blastocyst due to expansion of the blastocoelic cavity cell shape changes and cell proliferation.","definition_xrefs":["ISBN:0198542771","GOC:dph","ISBN:0124020607"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental growth","termid":"GO:0048589"},{"relation_name":"part_of","term_name":"blastocyst development","termid":"GO:0001824"}],"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":"blastocyst growth","synonyms":[{"name":"blastula growth","type":"related"}],"termid":"GO:0001832"}


id: MONDO:0858939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A high grade glioma that is characterized by the absence of histone H3, IDH1, and IDH2 mutations.","definition_xrefs":["DOID:0081277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pediatric high-grade glioma","termid":"MONDO:1010030"}],"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":"diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype","secondary_identifiers":["NCIT:C185467","UMLS:C5669918","MEDGEN:1808288"],"termid":"MONDO:0858939","xrefs":{"Monarch":{"xref_id":"0858939"}}}


id: MONDO:0013055
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":"Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features","secondary_identifiers":["MEDGEN:1680314","OMIM:612948","MESH:C548086","UMLS:C5193232"],"synonyms":[{"name":"Stargardt macular degeneration absent or hypoplastic corpus callosum intellectual disability and dysmorphic features","type":"related"},{"name":"Stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features","type":"related"},{"name":"Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features","type":"exact"},{"name":"Stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic features","type":"exact"}],"termid":"MONDO:0013055","xrefs":{"Monarch":{"xref_id":"0013055"}}}


id: PBO:0054898
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 2312","termid":"PBO:0054898"}


id: PBO:0036130
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_trimethylation_at_centromere_inner_repeat_during_vegetative_growth","termid":"PBO:0036130"}


id: GO:0006786
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of heme c, a derivative of heme found in cytochromes c, b4, and f.","definition_xrefs":["PubChem_Compound:122208","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme biosynthetic process","termid":"GO:0006783"},{"relation_name":"is_a","term_name":"heme C metabolic process","termid":"GO:0046162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"heme C biosynthetic process","synonyms":[{"name":"haem C biosynthesis","type":"exact"},{"name":"haem C biosynthetic process","type":"exact"},{"name":"heme C anabolism","type":"exact"},{"name":"heme C biosynthesis","type":"exact"},{"name":"heme C formation","type":"exact"},{"name":"heme C synthesis","type":"exact"}],"termid":"GO:0006786"}


id: MONDO:0012184
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pierson syndrome is characterized by the association of congenital nephrotic syndrome and ocular anomalies with microcoria.","definition_xrefs":["Orphanet:2670"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"LAMB2-related infantile-onset nephrotic syndrome","termid":"MONDO:0013621"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"Pierson syndrome","secondary_identifiers":["NCIT:C128145","NANDO:2200117","DOID:0060852","SCTID:723449004","OMIM:609049","GARD:9420","UMLS:C1836876","MESH:C537185","icd11.foundation:555082533","MEDGEN:373199"],"synonyms":[{"name":"Pierson syndrome","type":"exact"},{"name":"microcoria - congenital nephrosis","type":"related"},{"name":"microcoria - congenital nephrotic syndrome","type":"related"},{"name":"microcoria-congenital nephrosis syndrome","type":"exact"},{"name":"microcoria-congenital nephrotic syndrome","type":"related"}],"termid":"MONDO:0012184","xrefs":{"Monarch":{"xref_id":"0012184"}}}


id: PR:O94662
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC651.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94662"],"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 C651.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC651.04","synonyms":[{"name":"Spom972h-SPBC651.04","type":"exact"}],"termid":"PR:O94662"}


id: PBO:0087914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor involved in regulating arginine-responsive genes; acts with Arg81p and Arg82p","termid":"PBO:0087914"}


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: PBO:0056529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoma cell adhesion molecule","termid":"PBO:0056529"}


id: MONDO:1011730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 4 deficiency, non-human animal","secondary_identifiers":["OMIA:001626"],"synonyms":[{"name":"C4 deficiency, non-human animal","type":"exact"}],"termid":"MONDO:1011730","xrefs":{"Monarch":{"xref_id":"1011730"}}}


id: GO:0007032
data:
  {"annotated_genes":["SJAG_01448","SJAG_01571","SJAG_03005","SJAG_02100","SJAG_04966","SJAG_01772"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76880,78284,81597,81860,104561],"is_not":false,"summary":null,"term":"GO:0007032"},{"annotations":[76099],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034496"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of endosomes.","definition_xrefs":["GOC:dph","GOC:jl","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle organization","termid":"GO:0016050"},{"relation_name":"part_of","term_name":"endomembrane system organization","termid":"GO:0010256"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01448":null,"SJAG_01571":null,"SJAG_01772":null,"SJAG_02100":null,"SJAG_03005":null,"SJAG_04966":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"endosome organization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"endosome organisation","type":"exact"},{"name":"endosome organization and biogenesis","type":"related"}],"termid":"GO:0007032","terms_by_termid":{"GO:0007032":null,"GO:0034496":null}}


id: FYPO:0003136
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain more plasma membrane than normal. Excess plasma membrane may appear as bubble-like structures inside the cell, and may be concentrated in the mating projection during conjugation.","definition_xrefs":["PomBase:mah","PMID:19627505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal plasma membrane during vegetative growth","termid":"FYPO:0003278"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"excess plasma membrane present","synonyms":[{"name":"excess mating projection membrane present","type":"narrow"},{"name":"excess plasma membrane present during mitotic cell cycle","type":"related"},{"name":"excess plasma membrane present during vegetative growth","type":"exact"},{"name":"increased invagination of the plasma membrane","type":"narrow"},{"name":"internal membrane bubbles present","type":"related"}],"termid":"FYPO:0003136"}


id: MONDO:0015172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. This syndrome is characterized by the association of severe congenital colitis with sensorineural deafness.","definition_xrefs":["Orphanet:103912"],"gene_count":0,"genotype_count":0,"name":"obsolete epithelio-exfoliative colitis-deafness syndrome (obsolete MONDO:0015172)","termid":"MONDO:0015172","xrefs":{"Monarch":{"xref_id":"0015172"}}}


id: PBO:0080921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YWHAQ pseudogene","termid":"PBO:0080921"}


id: GO:0019842
data:
  {"annotated_genes":["SJAG_02305","SJAG_04145","SJAG_03362","SJAG_04031","SJAG_03312","SJAG_04149","SJAG_00495","SJAG_03306","SJAG_02791","SJAG_03961","SJAG_04842","SJAG_05230","SJAG_00432","SJAG_00830","SJAG_03861","SJAG_02205","SJAG_04988","SJAG_04178","SJAG_03671","SJAG_00714","SJAG_00673","SJAG_00582","SJAG_02972","SJAG_03743","SJAG_00706","SJAG_04678","SJAG_03434","SJAG_00097","SJAG_02464","SJAG_03102","SJAG_03055","SJAG_03985","SJAG_02734","SJAG_01766","SJAG_01019","SJAG_00869","SJAG_00186","SJAG_03914","SJAG_00937"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[65946,59532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031177"},{"annotations":[75933,80182,69437,70192,76179,66309,64393,67674,81377,66541,112394,69389,60579,62318,68896,58041,66781,75090,73829,65633,70398,67715,58392,74213,81090,66726,67445,71622,72265,57199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030170"},{"annotations":[68484],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030975"},{"annotations":[65507,74993,62423,58816,59263,57571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030976"}]},"cv_name":"molecular_function","definition":"Binding to a vitamin, one of a number of unrelated organic substances that occur in many foods in small amounts and that are necessary in trace amounts for the normal metabolic functioning of the body.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_00186":null,"SJAG_00432":null,"SJAG_00495":null,"SJAG_00582":null,"SJAG_00673":null,"SJAG_00706":null,"SJAG_00714":null,"SJAG_00830":null,"SJAG_00869":null,"SJAG_00937":null,"SJAG_01019":null,"SJAG_01766":null,"SJAG_02205":null,"SJAG_02305":null,"SJAG_02464":null,"SJAG_02734":null,"SJAG_02791":null,"SJAG_02972":null,"SJAG_03055":null,"SJAG_03102":null,"SJAG_03306":null,"SJAG_03312":null,"SJAG_03362":null,"SJAG_03434":null,"SJAG_03671":null,"SJAG_03743":null,"SJAG_03861":null,"SJAG_03914":null,"SJAG_03961":null,"SJAG_03985":null,"SJAG_04031":null,"SJAG_04145":null,"SJAG_04149":null,"SJAG_04178":null,"SJAG_04678":null,"SJAG_04842":null,"SJAG_04988":null,"SJAG_05230":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"vitamin binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0019842","terms_by_termid":{"GO:0030170":null,"GO:0030975":null,"GO:0030976":null,"GO:0031177":null}}


id: SO:0001082
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Incompatibility in the sequence due to some experimental problem.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"remark","termid":"SO:0000700"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide_sequencing_information","secondary_identifiers":["BS:00125"],"synonyms":[{"name":"sequencing_information","type":"exact"}],"termid":"SO:0001082"}


id: PBO:0064287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"placenta expressed transcript 1","termid":"PBO:0064287"}


id: PBO:0000037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase interaction types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interacts_genetically","termid":"PBO:0000037"}


id: FYPO:0004672
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is inviable, is elongated, and contains a nucleus that is broken into small fragments.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"fragmented nucleus during vegetative growth","termid":"FYPO:0001919"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000005","FYPO:0002403","FYPO:0001985","FYPO:0001320","FYPO:0000004"],"is_obsolete":false,"name":"inviable elongated vegetative cell with fragmented nucleus","synonyms":[{"name":"elongated inviable cell with fragmented nucleus","type":"exact"},{"name":"inviable elongated cell with fragmented nucleus during vegetative growth","type":"exact"},{"name":"inviable elongated vegetative cell with fragmented DNA","type":"related"},{"name":"inviable elongated vegetative cell with fragmented nucleus during mitotic cell cycle","type":"related"},{"name":"lethal; elongated vegetative cell with fragmented nucleus","type":"exact"}],"termid":"FYPO:0004672"}


id: MONDO:0005958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sex cord-stromal tumor (obsolete MONDO:0005958)","termid":"MONDO:0005958","xrefs":{"Monarch":{"xref_id":"0005958"}}}


id: MONDO:0001652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma (disease) that involves the scrotum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"scrotum neoplasm","termid":"MONDO:0003319"},{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scrotum melanoma","secondary_identifiers":["MEDGEN:233100","NCIT:C7361","UMLS:C1331544","DOID:13160"],"synonyms":[{"name":"melanoma (disease) of scrotum","type":"exact"},{"name":"melanoma of scrotum","type":"exact"},{"name":"melanoma of the scrotum","type":"exact"},{"name":"scrotal melanoma","type":"exact"},{"name":"scrotum melanoma (disease)","type":"exact"}],"termid":"MONDO:0001652","xrefs":{"Monarch":{"xref_id":"0001652"}}}


id: PBO:0054020
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 1350","termid":"PBO:0054020"}


id: PBO:0018021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-U ortholog Mis17","termid":"PBO:0018021"}


id: MONDO:0008878
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bone dysplasia lethal Holmgren type (BDLH) is a lethal bone dysplasia characterized at birth by low birth weight, a rhizomelic dwarfism, bent femora and short chest producing asphyxia. It was described in three siblings from healthy, non-consanguineous parents of Finnish and in four siblings from non-consanguineous parents of French origin with no family history of dwarfism. The initial cases could have been diagnosed as Desbuquois syndrome, or a recessive Larsen syndrome. There has been no further description of BDLH in the literature since 1988.","definition_xrefs":["Orphanet:1842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"}],"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":"bone dysplasia, lethal Holmgren type","secondary_identifiers":["SCTID:732249002","MEDGEN:347872","OMIM:211120","GARD:922","UMLS:C1859407","MESH:C565896"],"synonyms":[{"name":"autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type","type":"exact"},{"name":"bone dysplasia lethal Holmgren type","type":"related"},{"name":"bone dysplasia, lethal, Holmgren type","type":"related"}],"termid":"MONDO:0008878","xrefs":{"Monarch":{"xref_id":"0008878"}}}


id: PBO:0034553
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transcription_from_CRE_promoter","termid":"PBO:0034553"}


id: GO:0043759
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + 2-methylbutanoate + CoA = AMP + diphosphate + 2-methylbutanoyl-CoA.","definition_xrefs":["RHEA:46180"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short-chain fatty acid-CoA ligase activity","termid":"GO:0031955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"2-methylbutanoate-CoA ligase activity","synonyms":[{"name":"branched chain acyl CoA synthetase (ADP-forming) activity","type":"exact"},{"name":"branched chain acyl-CoA synthetase (ADP-forming) activity","type":"exact"},{"name":"branched-chain acyl CoA synthetase (ADP-forming) activity","type":"exact"},{"name":"branched-chain acyl-CoA synthetase (ADP-forming) activity","type":"related"}],"termid":"GO:0043759"}


id: PBO:0005116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choline transmembrane transporter family protein (predicted)","termid":"PBO:0005116"}


id: MONDO:0015155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spotted fever rickettsiosis (obsolete MONDO:0015155)","termid":"MONDO:0015155","xrefs":{"Monarch":{"xref_id":"0015155"}}}


id: SO:0000173
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A conserved GC-rich region located upstream of the start point of eukaryotic transcription units which may occur in multiple copies or in either orientation; consensus=GGGCGG.","direct_ancestors":[{"relation_name":"is_a","term_name":"promoter_element","termid":"SO:0001659"},{"relation_name":"part_of","term_name":"RNApol_II_promoter","termid":"SO:0000170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GC_rich_promoter_region","synonyms":[{"name":"GC rich promoter region","type":"exact"},{"name":"GC-rich region","type":"exact"},{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:GC_rich_promoter_region","type":"exact"}],"termid":"SO:0000173"}


id: PBO:0109134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CRIPTO pseudogene 7","termid":"PBO:0109134"}


id: PR:P32747
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A dihydroorotate dehydrogenase (quinone), mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11938:SF7","PRO:DNx","OMA:SCHPO00561"],"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":"dihydroorotate dehydrogenase (quinone), mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A10.12c","secondary_identifiers":["UniProtKB:P32747"],"synonyms":[{"name":"DHOD (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DHODase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DHOdehase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-DHODH","type":"exact"},{"name":"dihydroorotate oxidase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P32747"}


id: PBO:0004926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetra spanning protein 1, Tts1","termid":"PBO:0004926"}


id: FYPO:0008243
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the nucleus is abnormal during sporulation.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear morphology during meiotic cell cycle","termid":"FYPO:0008242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002403","FYPO:0000002"],"is_obsolete":false,"name":"abnormal nuclear morphology during sporulation","termid":"FYPO:0008243"}


id: PBO:0072046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 16","termid":"PBO:0072046"}


id: PBO:0054134
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 1500","termid":"PBO:0054134"}


id: GO:0002368
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that contributes to cytokine production by a B cell.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production involved in immune response","termid":"GO:0002367"},{"relation_name":"is_a","term_name":"B cell mediated immunity","termid":"GO:0019724"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"B cell cytokine production","synonyms":[{"name":"B lymphocyte cytokine production","type":"exact"},{"name":"B-cell cytokine production","type":"exact"},{"name":"B-lymphocyte cytokine production","type":"exact"}],"termid":"GO:0002368"}


id: GO:1901144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of insulin.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete insulin biosynthetic process (obsolete GO:1901144)","synonyms":[{"name":"insulin anabolism","type":"exact"},{"name":"insulin biosynthesis","type":"exact"},{"name":"insulin biosynthetic process","type":"exact"},{"name":"insulin formation","type":"exact"},{"name":"insulin synthesis","type":"exact"}],"termid":"GO:1901144"}


id: PBO:0071590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 7","termid":"PBO:0071590"}


id: PBO:0016534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HECT-type ubiquitin-protein ligase E3 Pub2","termid":"PBO:0016534"}


id: PBO:0076172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1C member 3","termid":"PBO:0076172"}


id: MONDO:0044282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. The Vel blood group system is defined by the presence of the Vel antigen on red blood cells. Vel is a high frequency antigen that shows variable strength, ranging from strong to weak. The rare Vel-negative blood type is inherited as an autosomal recessive trait and is typically unveiled when Vel-negative individuals develop anti-Vel antibodies after transfusion or pregnancy; Vel alloantibodies are never 'naturally occurring.' Individuals with anti-Vel antibodies may develop severe acute hemolytic transfusion reactions when transfused with Vel-positive blood. Individuals negative for the Vel antigen are rare and are required for the safe transfusion of patients with antibodies to Vel (summary by {3:Daniels, 2002}; {5:Storry et al., 2013}; {2:Cvejic et al., 2013}; {1:Ballif et al., 2013}).","definition_xrefs":["OMIM:615264"],"gene_count":0,"genotype_count":0,"name":"obsolete blood group, vel system (obsolete MONDO:0044282)","synonyms":[{"name":"VEL","type":"related"},{"name":"Vel-null phenotype","type":"related"},{"name":"blood group, VEL system","type":"related"},{"name":"blood group, Vel system","type":"exact"}],"termid":"MONDO:0044282","xrefs":{"Monarch":{"xref_id":"0044282"}}}


id: PBO:0075264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 18 pseudogene 17","termid":"PBO:0075264"}


id: SO:1000119
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000119 sequence_variant_causing_inactive_ligand_binding_site (obsolete SO:1000119)","synonyms":[{"name":"mutation causing inactive ligand binding site","type":"related"},{"name":"sequence variant causing inactive ligand binding site","type":"exact"}],"termid":"SO:1000119"}


id: PBO:0117417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zDHHC palmitoyltransferase 12","termid":"PBO:0117417"}


id: SO:0000040
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A clone of a DNA region of a genome.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"genomic_DNA","termid":"SO:0000991"},{"relation_name":"is_a","term_name":"clone","termid":"SO:0000151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genomic_clone","synonyms":[{"name":"genomic clone","type":"exact"}],"termid":"SO:0000040"}


id: GO:0052184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of the levels of hormones or growth regulators in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont hormone or growth regulator levels (obsolete GO:0052184)","synonyms":[{"name":"modulation by organism of symbiont hormone or growth regulator levels","type":"exact"}],"termid":"GO:0052184"}


id: GO:0002665
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of T cell tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of tolerance induction","termid":"GO:0002644"},{"relation_name":"is_a","term_name":"regulation of T cell tolerance induction","termid":"GO:0002664"},{"relation_name":"negatively_regulates","term_name":"T cell tolerance induction","termid":"GO:0002517"}],"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 T cell tolerance induction","synonyms":[{"name":"down regulation of T cell tolerance induction","type":"exact"},{"name":"down-regulation of T cell tolerance induction","type":"exact"},{"name":"downregulation of T cell tolerance induction","type":"exact"},{"name":"inhibition of T cell tolerance induction","type":"narrow"},{"name":"negative regulation of T lymphocyte tolerance induction","type":"exact"},{"name":"negative regulation of T-cell tolerance induction","type":"exact"},{"name":"negative regulation of T-lymphocyte tolerance induction","type":"exact"}],"termid":"GO:0002665"}


id: PBO:0051652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 1 pseudogene 7","termid":"PBO:0051652"}


id: PBO:0108625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein Cox1102/ mitochondrial ribosome assembly protein Rsm2202, fusion protein","termid":"PBO:0108625"}


id: GO:0071405
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 methanol stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to methanol","termid":"GO:0033986"},{"relation_name":"is_a","term_name":"cellular response to alcohol","termid":"GO:0097306"}],"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 methanol","termid":"GO:0071405"}


id: PBO:0081477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 354A","termid":"PBO:0081477"}


id: PBO:0050328
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 30","termid":"PBO:0050328"}


id: PR:Q9Y7M5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 39S ribosomal protein L15, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03015","PANTHER:PTHR12934:SF1","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":"54S ribosomal protein L10, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC9B6.06","secondary_identifiers":["UniProtKB:Q9Y7M5"],"synonyms":[{"name":"Spom972h-MRPL15","type":"exact"}],"termid":"PR:Q9Y7M5"}


id: GO:0061290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes that contribute to the progression of the metanephric kidney over time. In this pathway, the activated receptor signals via downstream effectors that result in the inhibition of beta-catenin phosphorylation, thereby preventing degradation of beta-catenin. Stabilized beta-catenin can then accumulate and travel to the nucleus to trigger changes in transcription of target genes.","definition_xrefs":["GOC:mtg_kidney_jan10"],"gene_count":0,"genotype_count":0,"name":"obsolete canonical Wnt signaling pathway involved in metanephric kidney development (obsolete GO:0061290)","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in metanephric kidney development","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in metanephric kidney development","type":"exact"},{"name":"canonical Wnt-activated signaling pathway involved in metanephric kidney development","type":"exact"}],"termid":"GO:0061290"}


id: MONDO:0001919
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"degeneration of macula and posterior pole","termid":"MONDO:0002175"}],"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":"cystoid macular retinal degeneration","secondary_identifiers":["MEDGEN:472900","UMLS:C0154850","DOID:14245","ICD9:362.53","SCTID:14046000"],"synonyms":[{"name":"cystoid macular degeneration of retina","type":"exact"}],"termid":"MONDO:0001919","xrefs":{"Monarch":{"xref_id":"0001919"}}}


id: PBO:0073665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal induced proliferation associated 1 like 1","termid":"PBO:0073665"}


id: MONDO:0013153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inflammatory bowel disease in which the cause of the disease is a mutation in the IL10RA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"IL10-related early-onset inflammatory bowel disease","termid":"MONDO:0016542"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"inflammatory bowel disease 28","secondary_identifiers":["MEDGEN:442630","NCIT:C164676","OMIM:613148","MESH:C567728","DOID:0110899","NANDO:2200447","GARD:18343","UMLS:C2751053"],"synonyms":[{"name":"IBD28","type":"exact"},{"name":"IL10RA inflammatory bowel disease","type":"exact"},{"name":"early onset autosomal recessive inflammatory bowel disease 28","type":"exact"},{"name":"inflammatory bowel disease 28","type":"exact"},{"name":"inflammatory bowel disease 28, autosomal recessive","type":"exact"},{"name":"inflammatory bowel disease 28, early onset, autosomal recessive","type":"exact"},{"name":"inflammatory bowel disease caused by mutation in IL10RA","type":"exact"},{"name":"inflammatory bowel disease type 28","type":"exact"},{"name":"inflammatory bowel disease, early-onset, autosomal recessive","type":"exact"}],"termid":"MONDO:0013153","xrefs":{"Monarch":{"xref_id":"0013153"}}}


id: PBO:0047604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile histidine triad diadenosine triphosphatase","termid":"PBO:0047604"}


id: PBO:0056900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIER family member 2","termid":"PBO:0056900"}


id: MONDO:0017217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Visceral calciphylaxis is a rare, life-threatening, non-inflammatory vasculopathy disorder characterized by diffuse precipitation of calcium in viscera (mainly in the heart or lungs, but also in the stomach or kidneys) leading to fibrosis and thrombosis, which eventually cause necrotic ulcerations of the tissue. Patients may present with dyspnea, cough and respiratory failure or acute heart block and subsequent sudden cardiac death, depending on the affected organ. The disease mainly affects patients on dialysis or patients having undergone renal transplantation.","definition_xrefs":["Orphanet:280068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calciphylaxis","termid":"MONDO:0017215"}],"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":"visceral calciphylaxis","secondary_identifiers":["MEDGEN:1664968","UMLS:C4749793","GARD:21071"],"termid":"MONDO:0017217","xrefs":{"Monarch":{"xref_id":"0017217"}}}


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


id: GO:0052546
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving pectin, a polymer containing a backbone of alpha-1,4-linked D-galacturonic acid residues, as part of the organization and biogenesis of the cell wall.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pectin metabolic process","termid":"GO:0045488"},{"relation_name":"part_of","term_name":"plant-type cell wall organization","termid":"GO:0009664"}],"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:0005975","GO:0008150","GO:0071554"],"is_obsolete":false,"name":"cell wall pectin metabolic process","synonyms":[{"name":"cell wall pectin metabolism","type":"exact"},{"name":"cellulose and pectin-containing cell wall pectin metabolic process","type":"exact"},{"name":"pectin metabolism during cell wall biogenesis","type":"exact"},{"name":"plant-type cell wall pectin metabolic process","type":"exact"}],"termid":"GO:0052546"}


id: MONDO:0020487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pontiac fever (PF) is a mild form of legionellosis manifesting with flu-like symptoms such as nausea, myalgia, fever, cough and headache but without pneumonia.","definition_xrefs":["Orphanet:99748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"legionellosis","termid":"MONDO:0005823"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pontiac fever","secondary_identifiers":["icd11.foundation:1670562980","NCIT:C128335","MedDRA:10054161","DOID:0050150","ICD9:041.89","SCTID:240447002","UMLS:C0343528","MEDGEN:575661","GARD:13588"],"termid":"MONDO:0020487","xrefs":{"Monarch":{"xref_id":"0020487"}}}


id: PBO:0044145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 11","termid":"PBO:0044145"}


id: MONDO:0003105
data:
  {"annotated_genes":["SJAG_00997","SJAG_04885"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89126,89127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013872"}]},"cv_name":"mondo","definition":"A disease involving the prostate gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00997":null,"SJAG_04885":null},"genotype_count":0,"is_obsolete":false,"name":"prostate disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0009602","DOID:47","NCIT:C26865","MEDGEN:10964","ICD9:602.8","UMLS:C0033575","MESH:D011469","SCTID:30281009","ICD9:602.9"],"synonyms":[{"name":"disease of prostate gland","type":"exact"},{"name":"disease or disorder of prostate gland","type":"exact"},{"name":"disorder of prostate gland","type":"exact"},{"name":"prostate disease","type":"exact"},{"name":"prostate disorder","type":"exact"},{"name":"prostate gland disease","type":"exact"},{"name":"prostate gland disease or disorder","type":"exact"}],"termid":"MONDO:0003105","terms_by_termid":{"MONDO:0013872":null},"xrefs":{"Monarch":{"xref_id":"0003105"}}}


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":["EC:1.14.14.183","PMID:15178487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"taxoid 2alpha-hydroxylase activity","synonyms":[{"name":"taxusin 2-alpha-hydroxylase activity","type":"exact"}],"termid":"GO:0102365"}


id: PBO:0041546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 18 putative open reading frame 15","termid":"PBO:0041546"}


id: GO:0046331
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Signaling between cells of equivalent developmental potential that results in these cells adopting different developmental fates. An example is the suppression by cells with a particular fate of the adoption of the same fate by surrounding cells.","definition_xrefs":["GOC:bf","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling involved in cell fate commitment","termid":"GO:0045168"}],"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":"lateral inhibition","termid":"GO:0046331"}


id: PBO:0041504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 13 open reading frame 42","termid":"PBO:0041504"}


id: MONDO:0018401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete female infertility due to an anomaly of ovarian function (obsolete MONDO:0018401)","secondary_identifiers":["Orphanet:399853"],"termid":"MONDO:0018401","xrefs":{"Monarch":{"xref_id":"0018401"}}}


id: GO:0034160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of toll-like receptor 8 signaling pathway.","definition_xrefs":["GOC:add","PMID:17328678","PMID:16551253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of toll-like receptor 8 signaling pathway","termid":"GO:0034159"},{"relation_name":"is_a","term_name":"negative regulation of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039532"},{"relation_name":"negatively_regulates","term_name":"toll-like receptor 8 signaling pathway","termid":"GO:0034158"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of toll-like receptor 8 signaling pathway","synonyms":[{"name":"negative regulation of TLR8 signaling pathway","type":"exact"},{"name":"negative regulation of toll-like receptor 8 signalling pathway","type":"exact"}],"termid":"GO:0034160"}


id: MONDO:0020690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"adult infiltrating astrocytic neoplasm","termid":"MONDO:0004320"},{"relation_name":"is_a","term_name":"glioblastoma","termid":"MONDO:0018177"}],"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":"adult glioblastoma","secondary_identifiers":["NANDO:2200087","NCIT:C9094","MEDGEN:124527","UMLS:C0278878"],"synonyms":[{"name":"adult glioblastoma","type":"exact"},{"name":"adult glioblastoma multiforme","type":"exact"},{"name":"glioblastoma","type":"broad"},{"name":"grade IV adult astrocytic neoplasm","type":"exact"},{"name":"grade IV adult astrocytic tumor","type":"exact"},{"name":"grade IV adult astrocytic tumour","type":"exact"}],"termid":"MONDO:0020690","xrefs":{"Monarch":{"xref_id":"0020690"}}}


id: FYPO:0002741
data:
  {"alleles_by_uniquename":{"SJAG_04883:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04883","name":"ptp4delta","uniquename":"SJAG_04883:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001007"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a cell executes a mitotic cell cycle process normally (i.e. indistinguishably from wild type). A mitotic cell cycle process is any of the processes that form part of the mitotic cell cycle, and thereby ensures successive accurate and complete genome replication and chromosome segregation.","definition_xrefs":["GO:1903047","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle","termid":"FYPO:0000411"},{"relation_name":"is_a","term_name":"normal cell cycle process","termid":"FYPO:0006915"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04883":null},"genotype_count":1,"genotypes_by_uniquename":{"ptp4delta":{"display_name":"ptp4delta","display_uniquename":"ptp4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04883:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal mitotic cell cycle process","references_by_uniquename":{"PMID:36695178":null},"single_locus_annotated_genes":["SJAG_04883"],"single_locus_genotype_uniquenames":["ptp4delta"],"termid":"FYPO:0002741","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0001007":null}}


id: MONDO:0001581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tolosa-hunt syndrome (obsolete MONDO:0001581)","termid":"MONDO:0001581","xrefs":{"Monarch":{"xref_id":"0001581"}}}


id: PBO:0073749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC2A4 regulator","termid":"PBO:0073749"}


id: PR:Q09751
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A lactoylglutathione lyase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR10374: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":"lactoylglutathione lyase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12C2.12c","secondary_identifiers":["UniProtKB:Q09751"],"synonyms":[{"name":"Aldoketomutase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Glx I (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Methylglyoxalase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"S-D-lactoylglutathione methylglyoxal lyase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBC12C2.12c","type":"related"},{"name":"Spom972h-GLO1","type":"exact"},{"name":"glyoxalase I (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ketone-aldehyde mutase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09751"}


id: GO:0005295
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: neutral L-amino acid(out) + Na+(out) = neutral L-amino acid(in) + Na+(in).","definition_xrefs":["TC:2.A.23.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:sodium symporter activity","termid":"GO:0005283"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"neutral L-amino acid:sodium symporter activity","secondary_identifiers":["GO:0005282"],"synonyms":[{"name":"neutral amino acid-sodium cotransporter","type":"broad"},{"name":"neutral amino acid:sodium symporter activity","type":"exact"},{"name":"sodium/neutral amino acid transporter","type":"broad"}],"termid":"GO:0005295"}


id: PR:O43079
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An AP-1 complex subunit beta-1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02550","PRO:DNx","PANTHER:PTHR11134: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":"AP-1 complex subunit beta-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC947.02","secondary_identifiers":["UniProtKB:O43079"],"synonyms":[{"name":"Spom972h-AP1B1","type":"exact"},{"name":"beta(1)-adaptin (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"beta-1-adaptin (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"clathrin assembly protein complex 1 beta-1 large chain (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"clathrin assembly protein large beta-1 chain (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43079"}


id: FYPO:0004181
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the region of contact between two cells undergoing conjugation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:24514900","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization","termid":"FYPO:0003627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to cell-cell contact point during mating","synonyms":[{"name":"normal protein localisation to cell-cell contact point during mating","type":"exact"},{"name":"normal protein localization to cell-cell contact point during conjugation","type":"exact"}],"termid":"FYPO:0004181"}


id: GO:0005829
data:
  {"annotated_genes":["SJAG_03752","SJAG_02889","SJAG_00004","SJAG_00476","SJAG_00611","SJAG_04369","SJAG_03519","SJAG_04894","SJAG_03919","SJAG_00126","SJAG_02891","SJAG_02686","SJAG_03629","SJAG_02518","SJAG_01618","SJAG_03224","SJAG_02369","SJAG_04539","SJAG_01383","SJAG_03632","SJAG_04653","SJAG_03214","SJAG_00067","SJAG_03726","SJAG_00892","SJAG_02805","SJAG_01379","SJAG_03544","SJAG_04407","SJAG_04843","SJAG_03856","SJAG_01027","SJAG_04966","SJAG_02912","SJAG_03119","SJAG_04476","SJAG_05351","SJAG_00691","SJAG_03069","SJAG_04658","SJAG_02992","SJAG_04871","SJAG_01794","SJAG_04859","SJAG_00633","SJAG_03682","SJAG_00971","SJAG_03862","SJAG_00223","SJAG_02281","SJAG_02038","SJAG_04002","SJAG_04477","SJAG_02378","SJAG_02520","SJAG_02370","SJAG_00577","SJAG_03407","SJAG_04107","SJAG_01047","SJAG_03534","SJAG_04824","SJAG_03209","SJAG_00843","SJAG_03131","SJAG_02292","SJAG_01397","SJAG_04710","SJAG_02033","SJAG_04682","SJAG_00980","SJAG_03087","SJAG_01521","SJAG_03892","SJAG_03082","SJAG_02505","SJAG_02918","SJAG_02997","SJAG_02745","SJAG_02812","SJAG_00512","SJAG_00289","SJAG_01240","SJAG_00827","SJAG_00958","SJAG_00521","SJAG_01371","SJAG_02444","SJAG_02022","SJAG_04166","SJAG_02270","SJAG_02509","SJAG_05260","SJAG_02576","SJAG_01805","SJAG_04932","SJAG_02436","SJAG_01673","SJAG_04030","SJAG_03034","SJAG_03181","SJAG_02203","SJAG_00172","SJAG_05332","SJAG_01783","SJAG_04091","SJAG_04772","SJAG_03582","SJAG_03597","SJAG_01637","SJAG_05185","SJAG_00609","SJAG_00881","SJAG_01501","SJAG_00526","SJAG_01824","SJAG_00325","SJAG_01740","SJAG_04649","SJAG_04083","SJAG_04688","SJAG_00567","SJAG_03533","SJAG_03845","SJAG_01944","SJAG_00585","SJAG_05290","SJAG_01698","SJAG_03137","SJAG_04818","SJAG_00397","SJAG_06634","SJAG_01440","SJAG_05303","SJAG_04974","SJAG_05184","SJAG_01582","SJAG_01385","SJAG_00178","SJAG_02608","SJAG_01149","SJAG_03262","SJAG_04920","SJAG_00869","SJAG_00041","SJAG_03215","SJAG_03507","SJAG_00685","SJAG_02840","SJAG_00129","SJAG_04486","SJAG_04290","SJAG_02738","SJAG_02245","SJAG_02283","SJAG_03354","SJAG_00662","SJAG_04106","SJAG_02237","SJAG_03325","SJAG_00967","SJAG_00104","SJAG_03802","SJAG_04944","SJAG_04021","SJAG_01787","SJAG_03035","SJAG_00228","SJAG_00902","SJAG_04579","SJAG_00987","SJAG_00811","SJAG_05343","SJAG_01311","SJAG_02401","SJAG_02950","SJAG_03377","SJAG_04384","SJAG_03756","SJAG_03915","SJAG_03883","SJAG_01556","SJAG_04156","SJAG_00382","SJAG_05004","SJAG_02798","SJAG_01159","SJAG_02705","SJAG_02044","SJAG_01704","SJAG_05018","SJAG_00592","SJAG_05179","SJAG_01869","SJAG_04022","SJAG_00331","SJAG_00806","SJAG_04660","SJAG_02832","SJAG_02243","SJAG_00954","SJAG_01151","SJAG_01161","SJAG_03362","SJAG_02450","SJAG_02020","SJAG_00137","SJAG_00757","SJAG_04350","SJAG_03051","SJAG_02760","SJAG_03036","SJAG_03794","SJAG_04344","SJAG_04266","SJAG_04860","SJAG_01825","SJAG_03277","SJAG_02294","SJAG_02016","SJAG_00605","SJAG_02004","SJAG_05266","SJAG_04092","SJAG_02531","SJAG_03037","SJAG_02589","SJAG_02336","SJAG_03551","SJAG_04299","SJAG_00859","SJAG_04390","SJAG_03463","SJAG_02405","SJAG_01954","SJAG_05193","SJAG_02098","SJAG_01519","SJAG_01864","SJAG_07011","SJAG_04031","SJAG_05216","SJAG_01287","SJAG_03730","SJAG_01759","SJAG_04089","SJAG_02400","SJAG_02214","SJAG_02193","SJAG_01810","SJAG_02645","SJAG_00117","SJAG_02121","SJAG_02789","SJAG_00546","SJAG_01656","SJAG_01453","SJAG_02692","SJAG_02713","SJAG_00298","SJAG_04261","SJAG_03356","SJAG_03646","SJAG_03540","SJAG_04013","SJAG_00670","SJAG_00822","SJAG_03375","SJAG_03963","SJAG_00963","SJAG_01979","SJAG_03688","SJAG_03631","SJAG_02740","SJAG_02321","SJAG_06612","SJAG_02522","SJAG_03882","SJAG_02764","SJAG_02814","SJAG_03581","SJAG_04213","SJAG_03144","SJAG_02329","SJAG_00143","SJAG_02923","SJAG_04704","SJAG_01030","SJAG_04866","SJAG_00039","SJAG_00738","SJAG_00629","SJAG_03659","SJAG_04936","SJAG_01359","SJAG_00272","SJAG_01850","SJAG_01342","SJAG_00599","SJAG_04232","SJAG_00206","SJAG_02453","SJAG_03879","SJAG_03839","SJAG_00045","SJAG_05032","SJAG_02610","SJAG_02275","SJAG_01995","SJAG_00355","SJAG_03049","SJAG_04590","SJAG_04283","SJAG_03102","SJAG_01788","SJAG_03074","SJAG_02314","SJAG_00248","SJAG_02182","SJAG_01844","SJAG_00379","SJAG_01622","SJAG_00252","SJAG_04354","SJAG_02852","SJAG_02420","SJAG_01203","SJAG_00596","SJAG_01199","SJAG_05333","SJAG_04921","SJAG_00049","SJAG_02256","SJAG_03788","SJAG_02313","SJAG_01926","SJAG_00432","SJAG_00678","SJAG_01339","SJAG_04576","SJAG_02169","SJAG_03669","SJAG_03504","SJAG_01708","SJAG_01765","SJAG_04268","SJAG_00093","SJAG_01760","SJAG_00682","SJAG_04699","SJAG_00584","SJAG_04227","SJAG_02604","SJAG_04950","SJAG_01703","SJAG_00465","SJAG_04901","SJAG_04928","SJAG_01248","SJAG_00449","SJAG_03835","SJAG_00903","SJAG_03498","SJAG_04306","SJAG_02611","SJAG_03663","SJAG_00720","SJAG_03357","SJAG_00378","SJAG_04465","SJAG_05252","SJAG_00166","SJAG_03457","SJAG_00161","SJAG_01898","SJAG_04085","SJAG_02553","SJAG_04338","SJAG_00839","SJAG_03383","SJAG_01551","SJAG_03932","SJAG_03312","SJAG_04551","SJAG_03884","SJAG_01487","SJAG_05208","SJAG_02572","SJAG_02801","SJAG_00663","SJAG_00100","SJAG_03482","SJAG_01146","SJAG_03500","SJAG_01588","SJAG_00857","SJAG_01617","SJAG_01370","SJAG_05276","SJAG_02796","SJAG_01277","SJAG_00296","SJAG_03164","SJAG_02811","SJAG_00395","SJAG_03888","SJAG_04848","SJAG_02887","SJAG_02414","SJAG_03486","SJAG_00820","SJAG_02081","SJAG_01715","SJAG_00580","SJAG_02491","SJAG_02542","SJAG_04051","SJAG_00150","SJAG_04342","SJAG_03857","SJAG_02672","SJAG_04077","SJAG_04182","SJAG_01042","SJAG_03272","SJAG_03455","SJAG_00119","SJAG_04674","SJAG_00448","SJAG_01645","SJAG_00690","SJAG_04159","SJAG_01467","SJAG_04891","SJAG_03986","SJAG_01026","SJAG_03626","SJAG_03789","SJAG_00885","SJAG_02708","SJAG_04842","SJAG_01852","SJAG_03852","SJAG_02015","SJAG_02376","SJAG_01528","SJAG_02482","SJAG_03197","SJAG_01443","SJAG_04079","SJAG_01444","SJAG_04181","SJAG_03761","SJAG_02549","SJAG_04981","SJAG_01279","SJAG_00376","SJAG_02474","SJAG_00978","SJAG_04249","SJAG_03479","SJAG_03089","SJAG_01136","SJAG_04988","SJAG_02854","SJAG_02905","SJAG_00435","SJAG_01529","SJAG_05312","SJAG_06588","SJAG_04470","SJAG_01789","SJAG_01128","SJAG_01139","SJAG_00463","SJAG_02696","SJAG_04177","SJAG_02756","SJAG_02902","SJAG_03662","SJAG_03422","SJAG_00918","SJAG_00692","SJAG_04003","SJAG_02673","SJAG_02715","SJAG_02181","SJAG_01137","SJAG_00244","SJAG_01482","SJAG_00894","SJAG_02679","SJAG_02477","SJAG_00443","SJAG_00032","SJAG_04383","SJAG_04397","SJAG_01664","SJAG_03624","SJAG_02461","SJAG_01776","SJAG_00461","SJAG_01942","SJAG_02864","SJAG_00696","SJAG_03549","SJAG_00586","SJAG_00471","SJAG_02234","SJAG_05694","SJAG_02766","SJAG_01162","SJAG_03210","SJAG_00482","SJAG_04429","SJAG_03708","SJAG_04849","SJAG_05243","SJAG_01070","SJAG_00207","SJAG_01775","SJAG_02585","SJAG_02702","SJAG_00579","SJAG_01458","SJAG_01018","SJAG_02640","SJAG_05007","SJAG_04036","SJAG_03476","SJAG_00038","SJAG_04157","SJAG_01885","SJAG_03697","SJAG_00072","SJAG_03537","SJAG_01341","SJAG_02287","SJAG_04074","SJAG_04027","SJAG_01833","SJAG_02995","SJAG_00808","SJAG_02959","SJAG_02687","SJAG_04114","SJAG_04304","SJAG_02349","SJAG_03231","SJAG_01721","SJAG_04709","SJAG_03541","SJAG_03784","SJAG_01427","SJAG_02172","SJAG_00975","SJAG_03849","SJAG_01432","SJAG_01317","SJAG_01744","SJAG_03453","SJAG_03668","SJAG_04827","SJAG_02786","SJAG_06284","SJAG_00095","SJAG_04312","SJAG_01270","SJAG_02224","SJAG_03254","SJAG_02790","SJAG_01917","SJAG_02512","SJAG_00541","SJAG_00203","SJAG_02266","SJAG_01598","SJAG_03374","SJAG_02456","SJAG_00326","SJAG_00578","SJAG_03854","SJAG_01472","SJAG_04453","SJAG_01163","SJAG_03431","SJAG_00948","SJAG_03527","SJAG_02170","SJAG_00144","SJAG_03996","SJAG_03107","SJAG_03690","SJAG_04334","SJAG_05413","SJAG_02791","SJAG_03245","SJAG_01366","SJAG_01081","SJAG_02342","SJAG_03291","SJAG_03998","SJAG_02057","SJAG_01461","SJAG_02093","SJAG_03605","SJAG_03703","SJAG_00560","SJAG_03618","SJAG_04628","SJAG_00707","SJAG_05314","SJAG_02265","SJAG_01522","SJAG_01900","SJAG_01325","SJAG_01384","SJAG_02688","SJAG_02594","SJAG_02671","SJAG_04890","SJAG_02503","SJAG_04456","SJAG_04518","SJAG_03811","SJAG_04474","SJAG_04865","SJAG_04303","SJAG_00293","SJAG_00059","SJAG_01797","SJAG_01562","SJAG_00423","SJAG_02177","SJAG_04754","SJAG_00505","SJAG_04487","SJAG_02075","SJAG_01992","SJAG_03275","SJAG_03193","SJAG_04534","SJAG_01497","SJAG_00832","SJAG_02390","SJAG_02851","SJAG_01372","SJAG_03167","SJAG_02184","SJAG_00509","SJAG_03704","SJAG_04337","SJAG_04917","SJAG_02765","SJAG_04144","SJAG_02471","SJAG_01496","SJAG_02661","SJAG_01658","SJAG_03568","SJAG_03712","SJAG_01949","SJAG_02734","SJAG_07017","SJAG_04291","SJAG_06440","SJAG_03142","SJAG_00908","SJAG_04948","SJAG_03219","SJAG_01737","SJAG_01181","SJAG_01625","SJAG_04020","SJAG_01488","SJAG_00937","SJAG_05223","SJAG_00850","SJAG_02138","SJAG_04663","SJAG_03617","SJAG_04176","SJAG_00615","SJAG_02058","SJAG_04452","SJAG_05256","SJAG_01314","SJAG_04449","SJAG_04150","SJAG_02198","SJAG_01166","SJAG_04242","SJAG_02211","SJAG_02146","SJAG_04285","SJAG_04229","SJAG_00237","SJAG_03501","SJAG_03326","SJAG_00483","SJAG_00468","SJAG_04784","SJAG_01772","SJAG_03367","SJAG_04072","SJAG_00656","SJAG_04153","SJAG_00128","SJAG_04846","SJAG_03528","SJAG_04454","SJAG_02720","SJAG_00356","SJAG_01644","SJAG_00491","SJAG_03983","SJAG_01762","SJAG_02101","SJAG_00439","SJAG_02619","SJAG_03485","SJAG_01362","SJAG_04693","SJAG_04460","SJAG_00243","SJAG_00758","SJAG_01226","SJAG_04501","SJAG_03889","SJAG_00988","SJAG_01083","SJAG_01918","SJAG_05926","SJAG_02145","SJAG_00823","SJAG_04611","SJAG_02508","SJAG_01826","SJAG_00474","SJAG_03234","SJAG_02462","SJAG_04100","SJAG_03815","SJAG_01361","SJAG_03588","SJAG_03891","SJAG_00290","SJAG_02600","SJAG_03771","SJAG_00917","SJAG_00390","SJAG_01908","SJAG_03805","SJAG_02736","SJAG_03665","SJAG_02335","SJAG_02151","SJAG_01510","SJAG_01261","SJAG_06309","SJAG_02415","SJAG_03859","SJAG_01351","SJAG_00871","SJAG_02186","SJAG_02627","SJAG_01630","SJAG_00436","SJAG_03017","SJAG_00173","SJAG_02000","SJAG_02194","SJAG_01621","SJAG_01629","SJAG_04968","SJAG_02024","SJAG_02179","SJAG_01075","SJAG_02419","SJAG_16457","SJAG_05019","SJAG_02718","SJAG_03936","SJAG_03681","SJAG_00749","SJAG_01786","SJAG_00791","SJAG_05228","SJAG_03793","SJAG_02868","SJAG_03781","SJAG_00422","SJAG_00534","SJAG_00221","SJAG_04978","SJAG_02366","SJAG_04999","SJAG_02013","SJAG_04368","SJAG_01194","SJAG_04998","SJAG_04781","SJAG_04764","SJAG_04359","SJAG_02546","SJAG_05248","SJAG_02176","SJAG_04473","SJAG_02723","SJAG_03278","SJAG_03470","SJAG_04324","SJAG_02973","SJAG_04149","SJAG_00352","SJAG_01675","SJAG_02106","SJAG_04744","SJAG_00242","SJAG_03128","SJAG_02240","SJAG_00027","SJAG_02374","SJAG_01063","SJAG_04837","SJAG_00430","SJAG_02681","SJAG_02289","SJAG_01365","SJAG_02367","SJAG_01039","SJAG_00718","SJAG_04172","SJAG_01022","SJAG_03141","SJAG_03009","SJAG_02282","SJAG_00837","SJAG_02803","SJAG_01534","SJAG_03229","SJAG_00624","SJAG_00645","SJAG_02197","SJAG_04168","SJAG_02300","SJAG_01540","SJAG_00113","SJAG_04190","SJAG_04033","SJAG_04567","SJAG_04455","SJAG_01312","SJAG_01791","SJAG_03575","SJAG_04128","SJAG_02768","SJAG_01679","SJAG_04388","SJAG_02911","SJAG_04408","SJAG_02857","SJAG_06576","SJAG_00063","SJAG_02510","SJAG_04536","SJAG_03990","SJAG_04540","SJAG_01720","SJAG_00743","SJAG_01114","SJAG_02524","SJAG_03425","SJAG_03937","SJAG_00225","SJAG_03494","SJAG_00858","SJAG_03950","SJAG_01655","SJAG_00527","SJAG_04385","SJAG_01291","SJAG_04320","SJAG_04060","SJAG_03070","SJAG_00563","SJAG_04565","SJAG_02309","SJAG_02426","SJAG_03041","SJAG_04711","SJAG_02551","SJAG_01222","SJAG_02041","SJAG_00309","SJAG_02956","SJAG_02833","SJAG_03352","SJAG_04776","SJAG_03285","SJAG_03022","SJAG_01231","SJAG_00518","SJAG_00464","SJAG_02069","SJAG_01216","SJAG_03005","SJAG_04656","SJAG_01360","SJAG_03717","SJAG_00118","SJAG_05205","SJAG_00982","SJAG_00229","SJAG_03714","SJAG_02206","SJAG_00856","SJAG_01817","SJAG_02375","SJAG_04086","SJAG_01499","SJAG_02178","SJAG_02741","SJAG_00653","SJAG_03548","SJAG_03335","SJAG_04874","SJAG_03782","SJAG_00853","SJAG_02285","SJAG_01292","SJAG_01088","SJAG_01367","SJAG_02490","SJAG_02813","SJAG_03113","SJAG_00913","SJAG_02998","SJAG_03732","SJAG_00762","SJAG_04431","SJAG_01087","SJAG_02878","SJAG_03094","SJAG_00550","SJAG_00704","SJAG_03283","SJAG_01298","SJAG_02569","SJAG_03828","SJAG_01184","SJAG_02747","SJAG_01676","SJAG_00384","SJAG_04214","SJAG_05003","SJAG_02297","SJAG_02630","SJAG_04466","SJAG_01207","SJAG_00712","SJAG_03130","SJAG_04655","SJAG_00419","SJAG_00033","SJAG_04845","SJAG_01651","SJAG_02648","SJAG_03411","SJAG_01375","SJAG_04973","SJAG_00942","SJAG_03601","SJAG_01024","SJAG_03634","SJAG_01492","SJAG_04844","SJAG_04234","SJAG_02728","SJAG_04061","SJAG_05337","SJAG_00409","SJAG_04160","SJAG_02704","SJAG_03346","SJAG_04007","SJAG_00523","SJAG_00840","SJAG_03562","SJAG_04953","SJAG_03614","SJAG_04326","SJAG_00600","SJAG_01197","SJAG_04762","SJAG_02802","SJAG_04062","SJAG_02886","SJAG_00251","SJAG_03151","SJAG_04211","SJAG_01358","SJAG_02481","SJAG_04650","SJAG_04220","SJAG_04264","SJAG_01694","SJAG_00179","SJAG_03045","SJAG_03743","SJAG_05214","SJAG_00990","SJAG_01516","SJAG_01220","SJAG_01830","SJAG_03276","SJAG_03893","SJAG_04987","SJAG_04123","SJAG_01055","SJAG_02647","SJAG_03798","SJAG_02870","SJAG_03263","SJAG_01048","SJAG_01667","SJAG_00191","SJAG_00287","SJAG_03706","SJAG_04282","SJAG_04618","SJAG_01229","SJAG_03592","SJAG_00507","SJAG_04183","SJAG_03775","SJAG_03127","SJAG_00107","SJAG_04728","SJAG_02876","SJAG_05010","SJAG_04747","SJAG_01255","SJAG_04946","SJAG_03751","SJAG_02135","SJAG_00724","SJAG_00504","SJAG_03153","SJAG_04751","SJAG_01308","SJAG_03323","SJAG_01827","SJAG_03886","SJAG_04379","SJAG_00053","SJAG_03021","SJAG_01134","SJAG_00381","SJAG_01545","SJAG_04863","SJAG_04858","SJAG_02271","SJAG_02251","SJAG_01150","SJAG_00467","SJAG_01436","SJAG_02165","SJAG_02339","SJAG_04879","SJAG_02498","SJAG_03090","SJAG_01126","SJAG_00120","SJAG_01608","SJAG_00925","SJAG_02731","SJAG_01696","SJAG_04481","SJAG_04436","SJAG_01665","SJAG_02730","SJAG_03147","SJAG_01818","SJAG_04943","SJAG_04352","SJAG_04907","SJAG_02380","SJAG_03072","SJAG_00135","SJAG_01596","SJAG_02858","SJAG_00503","SJAG_00280","SJAG_03434","SJAG_03818","SJAG_04880","SJAG_03096","SJAG_00910","SJAG_01154","SJAG_02470","SJAG_02269","SJAG_01404","SJAG_01245","SJAG_05024","SJAG_04735","SJAG_00486","SJAG_02116","SJAG_04651","SJAG_01074","SJAG_03191","SJAG_00189","SJAG_03921","SJAG_02479","SJAG_00940","SJAG_02752","SJAG_03684","SJAG_04025","SJAG_02871","SJAG_02442","SJAG_02347","SJAG_01121","SJAG_04896","SJAG_00306","SJAG_00786","SJAG_02770","SJAG_02755","SJAG_00956","SJAG_04815","SJAG_02180","SJAG_03063","SJAG_04192","SJAG_00765","SJAG_03043","SJAG_05222","SJAG_05331","SJAG_03174","SJAG_02290","SJAG_04012","SJAG_01611","SJAG_02312","SJAG_04054","SJAG_00955","SJAG_04015","SJAG_04554","SJAG_00694","SJAG_01302","SJAG_01449","SJAG_03122","SJAG_02609","SJAG_00052","SJAG_01568","SJAG_01218","SJAG_00964","SJAG_03012","SJAG_01064","SJAG_01198","SJAG_02034","SJAG_01175","SJAG_03753","SJAG_03872","SJAG_01328","SJAG_01974","SJAG_04084","SJAG_01014","SJAG_04633","SJAG_04912","SJAG_02467","SJAG_01919","SJAG_02725","SJAG_04457","SJAG_00321","SJAG_00733","SJAG_02951","SJAG_02904","SJAG_01251","SJAG_04607","SJAG_03029","SJAG_04400","SJAG_05245","SJAG_03185","SJAG_03603","SJAG_01434","SJAG_04563","SJAG_04634","SJAG_05978","SJAG_00637","SJAG_04964","SJAG_00524","SJAG_04011","SJAG_02625","SJAG_01587","SJAG_00092","SJAG_01566","SJAG_02921","SJAG_00366","SJAG_01418","SJAG_02583","SJAG_01809","SJAG_04756","SJAG_03227","SJAG_04088","SJAG_04082","SJAG_00301","SJAG_03288","SJAG_03488","SJAG_04817","SJAG_03166","SJAG_04814","SJAG_01693","SJAG_04980","SJAG_01132","SJAG_00800","SJAG_05225","SJAG_02592","SJAG_04204","SJAG_01609","SJAG_04516","SJAG_02320","SJAG_00316","SJAG_02926","SJAG_02441","SJAG_03718","SJAG_04774","SJAG_00764","SJAG_03067","SJAG_03558","SJAG_04297","SJAG_01663","SJAG_00320","SJAG_03158","SJAG_01840","SJAG_02166","SJAG_02017","SJAG_04475","SJAG_00931","SJAG_00748","SJAG_01185","SJAG_04307","SJAG_04404","SJAG_04612","SJAG_00234","SJAG_00972","SJAG_02425","SJAG_03409","SJAG_02009","SJAG_04700","SJAG_04121","SJAG_03723","SJAG_01548","SJAG_04347","SJAG_02561","SJAG_04097","SJAG_05230","SJAG_00815","SJAG_02063","SJAG_04499","SJAG_04548","SJAG_00317","SJAG_02763","SJAG_02515","SJAG_04414","SJAG_00938","SJAG_04191","SJAG_02066","SJAG_01938","SJAG_02517","SJAG_01415","SJAG_00224","SJAG_01320","SJAG_02618","SJAG_04070","SJAG_04573","SJAG_01561","SJAG_03720","SJAG_02595","SJAG_04496","SJAG_03371","SJAG_01079","SJAG_03623","SJAG_04480","SJAG_03472","SJAG_05192","SJAG_02750","SJAG_03554","SJAG_01512","SJAG_00069","SJAG_04760","SJAG_03760","SJAG_04355","SJAG_05008","SJAG_04343","SJAG_03955","SJAG_03589","SJAG_03150","SJAG_04201","SJAG_00190","SJAG_02874","SJAG_04274","SJAG_00037","SJAG_01438","SJAG_03438","SJAG_01650","SJAG_02808","SJAG_01901","SJAG_02659","SJAG_03901","SJAG_00457","SJAG_04125","SJAG_06270","SJAG_06355","SJAG_02506","SJAG_00401","SJAG_03571","SJAG_00661","SJAG_04109","SJAG_01768","SJAG_02040","SJAG_00181","SJAG_04112","SJAG_00591","SJAG_02749","SJAG_03095","SJAG_05023","SJAG_02866","SJAG_00702","SJAG_04935","SJAG_04300","SJAG_00544","SJAG_02575","SJAG_02030","SJAG_01742","SJAG_01590","SJAG_01632","SJAG_03570","SJAG_01233","SJAG_04287","SJAG_03722","SJAG_00327","SJAG_00359","SJAG_03924","SJAG_01252","SJAG_02783","SJAG_02788","SJAG_07013","SJAG_02769","SJAG_03132","SJAG_00314","SJAG_00184","SJAG_00226","SJAG_03545","SJAG_01182","SJAG_04990","SJAG_00726","SJAG_03345","SJAG_02434","SJAG_04292","SJAG_04069","SJAG_01697","SJAG_05261","SJAG_00364","SJAG_01666","SJAG_02994","SJAG_00531","SJAG_01799","SJAG_01346","SJAG_04461","SJAG_02267","SJAG_03136","SJAG_02202","SJAG_02746","SJAG_03159","SJAG_03958","SJAG_04043","SJAG_05316","SJAG_02748","SJAG_00532","SJAG_03487","SJAG_03658","SJAG_00768","SJAG_03350","SJAG_02091","SJAG_02621","SJAG_00084","SJAG_03865","SJAG_01605","SJAG_00821","SJAG_01641","SJAG_03298","SJAG_03250","SJAG_01610","SJAG_01274","SJAG_01012","SJAG_01500","SJAG_03384","SJAG_02869","SJAG_00377","SJAG_03124","SJAG_03855","SJAG_00186","SJAG_01801","SJAG_03523","SJAG_01186","SJAG_00333","SJAG_01072","SJAG_04256","SJAG_02733","SJAG_00044","SJAG_06622","SJAG_03791","SJAG_00040","SJAG_00508","SJAG_01870","SJAG_03677","SJAG_00668","SJAG_03529","SJAG_01606","SJAG_03182","SJAG_03106","SJAG_03686","SJAG_03237","SJAG_02978","SJAG_03013","SJAG_04029","SJAG_02230","SJAG_02695","SJAG_04520","SJAG_02048","SJAG_02233","SJAG_04969","SJAG_01135","SJAG_02226","SJAG_04970","SJAG_02288","SJAG_04841","SJAG_04163","SJAG_02485","SJAG_03320","SJAG_01910","SJAG_04009","SJAG_03959","SJAG_03085","SJAG_03762","SJAG_02043","SJAG_00644","SJAG_03620","SJAG_03799","SJAG_03267","SJAG_01202","SJAG_01575","SJAG_02352","SJAG_01364","SJAG_03881","SJAG_04657","SJAG_02277","SJAG_04549","SJAG_02655","SJAG_00245","SJAG_01228","SJAG_00479","SJAG_00246","SJAG_02218","SJAG_05000","SJAG_01053","SJAG_01283","SJAG_04652","SJAG_00706","SJAG_02591","SJAG_02828","SJAG_01565","SJAG_03977","SJAG_02253","SJAG_04878","SJAG_00991","SJAG_01127","SJAG_01235","SJAG_01544","SJAG_00202","SJAG_02497","SJAG_05329","SJAG_05283","SJAG_02422","SJAG_04187","SJAG_04609","SJAG_04629","SJAG_01746","SJAG_05197","SJAG_04235","SJAG_03525","SJAG_02295","SJAG_04066","SJAG_01635","SJAG_02424","SJAG_05011","SJAG_03876","SJAG_02386","SJAG_04877","SJAG_03424","SJAG_04175","SJAG_04403","SJAG_04273","SJAG_00537","SJAG_01858","SJAG_02154","SJAG_04371","SJAG_03108","SJAG_03660","SJAG_02822","SJAG_01841","SJAG_01515","SJAG_01266","SJAG_02597","SJAG_03140","SJAG_01886","SJAG_02164","SJAG_00572","SJAG_16460","SJAG_01209","SJAG_04491","SJAG_04044","SJAG_05206","SJAG_02207","SJAG_04765","SJAG_04335","SJAG_00220","SJAG_03258","SJAG_02035","SJAG_00353","SJAG_02896","SJAG_04309","SJAG_01447","SJAG_04131","SJAG_00413","SJAG_02945","SJAG_02988","SJAG_04380","SJAG_03475","SJAG_02774","SJAG_00400","SJAG_04758","SJAG_03081","SJAG_00947","SJAG_01543","SJAG_04169","SJAG_02026","SJAG_04825","SJAG_04626","SJAG_02235","SJAG_01480","SJAG_03293","SJAG_01533","SJAG_04129","SJAG_01781","SJAG_02357","SJAG_00125","SJAG_03241","SJAG_01859","SJAG_01477","SJAG_01714","SJAG_02189","SJAG_01580","SJAG_01535","SJAG_03689","SJAG_03126","SJAG_01690","SJAG_02493","SJAG_03403","SJAG_00514","SJAG_01914","SJAG_04147","SJAG_01646","SJAG_00686","SJAG_04595","SJAG_05232","SJAG_02225","SJAG_00993","SJAG_05021","SJAG_02573","SJAG_03907","SJAG_00642","SJAG_00573","SJAG_00719","SJAG_02210","SJAG_01061","SJAG_04861","SJAG_01581","SJAG_03454","SJAG_00147","SJAG_00269","SJAG_04746","SJAG_00739","SJAG_03673","SJAG_00957","SJAG_00440","SJAG_00803","SJAG_02879","SJAG_00091","SJAG_05009","SJAG_02570","SJAG_02047","SJAG_00043","SJAG_04484","SJAG_01986","SJAG_00571","SJAG_03313","SJAG_02280","SJAG_02535","SJAG_00485","SJAG_00574","SJAG_04219","SJAG_02358","SJAG_04271","SJAG_02174","SJAG_04938","SJAG_01624","SJAG_05029","SJAG_01943","SJAG_02845","SJAG_03786","SJAG_01259","SJAG_02408","SJAG_00729","SJAG_05015","SJAG_03495","SJAG_03364","SJAG_01408","SJAG_01599","SJAG_01016","SJAG_00343","SJAG_04577","SJAG_02304","SJAG_04126","SJAG_04897","SJAG_00854","SJAG_03666","SJAG_04463","SJAG_01474","SJAG_00921","SJAG_02601","SJAG_03821","SJAG_04198","SJAG_02663","SJAG_03133","SJAG_04118","SJAG_00035","SJAG_04535","SJAG_04559","SJAG_00102","SJAG_01722","SJAG_02061","SJAG_02582","SJAG_00270","SJAG_01457","SJAG_02499","SJAG_00214","SJAG_02843","SJAG_02890","SJAG_03758","SJAG_00414","SJAG_02191","SJAG_00489","SJAG_00450","SJAG_05253","SJAG_00374","SJAG_01997","SJAG_01489","SJAG_03561","SJAG_01118","SJAG_05030","SJAG_04602","SJAG_02540","SJAG_07014","SJAG_04170","SJAG_00795","SJAG_02428","SJAG_00256","SJAG_04286","SJAG_03532","SJAG_00756","SJAG_01851","SJAG_02307","SJAG_03949","SJAG_00916","SJAG_04263","SJAG_04248","SJAG_00986","SJAG_02327","SJAG_00594","SJAG_00995","SJAG_03404","SJAG_02819","SJAG_04130","SJAG_03423","SJAG_04399","SJAG_03643","SJAG_02502","SJAG_00736","SJAG_04783","SJAG_02337","SJAG_01310","SJAG_01812","SJAG_00350","SJAG_03580","SJAG_01382","SJAG_04375","SJAG_02465","SJAG_01172","SJAG_03019","SJAG_04410","SJAG_01475","SJAG_00983","SJAG_03433","SJAG_04148","SJAG_04275","SJAG_04631","SJAG_02850","SJAG_00365","SJAG_04902","SJAG_03692","SJAG_01386","SJAG_01748","SJAG_02393","SJAG_01187","SJAG_02215","SJAG_03373","SJAG_04434","SJAG_01411","SJAG_01466","SJAG_04482","SJAG_02699","SJAG_00805","SJAG_02065","SJAG_00103","SJAG_03233","SJAG_03693","SJAG_01142","SJAG_03010","SJAG_03678","SJAG_03868","SJAG_04870","SJAG_01628","SJAG_04617","SJAG_03556","SJAG_01131","SJAG_01659","SJAG_00689","SJAG_03225","SJAG_03630","SJAG_01784","SJAG_01354","SJAG_02895","SJAG_00845","SJAG_00455","SJAG_04381","SJAG_04581","SJAG_02799","SJAG_02972","SJAG_01686","SJAG_05195","SJAG_02605","SJAG_03694","SJAG_01531","SJAG_04372","SJAG_04927","SJAG_02984","SJAG_00890","SJAG_04847","SJAG_01576","SJAG_01733","SJAG_01020","SJAG_00778","SJAG_00728","SJAG_01213","SJAG_04188","SJAG_05211","SJAG_00188","SJAG_02439","SJAG_03934","SJAG_03847","SJAG_02885","SJAG_04638","SJAG_01481","SJAG_01430","SJAG_03246","SJAG_00501","SJAG_00447","SJAG_02171","SJAG_03257","SJAG_02541","SJAG_01620","SJAG_06636","SJAG_02042","SJAG_03321","SJAG_03248","SJAG_03361","SJAG_00141","SJAG_02082","SJAG_00424","SJAG_03204","SJAG_02315","SJAG_00114","SJAG_00960","SJAG_02239","SJAG_04042","SJAG_00074","SJAG_00529","SJAG_03499","SJAG_05027","SJAG_03086","SJAG_02785","SJAG_03638","SJAG_00683","SJAG_04713","SJAG_03211","SJAG_04587","SJAG_03014","SJAG_01117","SJAG_04055","SJAG_00777","SJAG_04472","SJAG_04417","SJAG_00632","SJAG_04580","SJAG_01313","SJAG_00155","SJAG_02213","SJAG_03026","SJAG_02387","SJAG_04161","SJAG_03306","SJAG_01822","SJAG_01238","SJAG_01003","SJAG_03469","SJAG_03055","SJAG_01502","SJAG_02726","SJAG_04174","SJAG_03266","SJAG_01508","SJAG_04357","SJAG_00115","SJAG_03653","SJAG_03473","SJAG_05287","SJAG_01214","SJAG_05014","SJAG_04179","SJAG_00480","SJAG_04531","SJAG_04741","SJAG_00162","SJAG_00941","SJAG_00533","SJAG_00898","SJAG_03432","SJAG_02562","SJAG_00176","SJAG_04681","SJAG_03186","SJAG_01352","SJAG_03062","SJAG_02279","SJAG_04771","SJAG_04960","SJAG_03655","SJAG_02046","SJAG_00106","SJAG_03508","SJAG_00809","SJAG_00324","SJAG_01734","SJAG_01387","SJAG_03627","SJAG_01267","SJAG_01301","SJAG_04458","SJAG_02148","SJAG_01808","SJAG_03179","SJAG_00441","SJAG_01680","SJAG_04253","SJAG_04289","SJAG_02682","SJAG_03380","SJAG_00134","SJAG_00145","SJAG_01089","SJAG_03863","SJAG_01389","SJAG_02684","SJAG_05198","SJAG_04666","SJAG_03376","SJAG_02817","SJAG_01191","SJAG_00878","SJAG_03679","SJAG_04425","SJAG_05346","SJAG_00427","SJAG_00969","SJAG_00801","SJAG_03309","SJAG_01897","SJAG_01269","SJAG_01322","SJAG_04311","SJAG_02323","SJAG_04724","SJAG_00472","SJAG_03408","SJAG_04963","SJAG_02010","SJAG_00490","SJAG_07000","SJAG_00167","SJAG_03696","SJAG_02697","SJAG_02664","SJAG_04459","SJAG_02954","SJAG_01010","SJAG_02753","SJAG_02894","SJAG_00674","SJAG_04505","SJAG_00487","SJAG_02797","SJAG_04972","SJAG_00338","SJAG_04541","SJAG_00169","SJAG_02404","SJAG_05304","SJAG_00164","SJAG_01425","SJAG_00807","SJAG_04467","SJAG_01002","SJAG_02580","SJAG_02593","SJAG_03964","SJAG_00341","SJAG_05334","SJAG_03825","SJAG_04427","SJAG_03098","SJAG_00874","SJAG_04672","SJAG_01662","SJAG_03238","SJAG_01268","SJAG_01167","SJAG_00249","SJAG_03319","SJAG_05277","SJAG_04155","SJAG_00112","SJAG_01937","SJAG_05240","SJAG_04366","SJAG_03243","SJAG_00281","SJAG_00864","SJAG_00989","SJAG_04212","SJAG_03279","SJAG_03547","SJAG_01702","SJAG_01774","SJAG_00498","SJAG_02231","SJAG_01455","SJAG_03842","SJAG_00660","SJAG_04394","SJAG_04627","SJAG_02596","SJAG_02863","SJAG_00742","SJAG_00614","SJAG_03733","SJAG_01338","SJAG_02005","SJAG_04726","SJAG_03838","SJAG_04495","SJAG_00208","SJAG_06592","SJAG_03228","SJAG_00065","SJAG_01987","SJAG_00230","SJAG_00561","SJAG_06599","SJAG_04197","SJAG_04977","SJAG_00798","SJAG_01376","SJAG_02700","SJAG_01874","SJAG_02689","SJAG_01122","SJAG_00495","SJAG_01631","SJAG_03188","SJAG_00968","SJAG_00796","SJAG_04519","SJAG_01296","SJAG_00766","SJAG_01958","SJAG_04202","SJAG_00283","SJAG_02547","SJAG_03922","SJAG_04695","SJAG_04544","SJAG_00219","SJAG_02107","SJAG_03810","SJAG_04332","SJAG_03903","SJAG_02558","SJAG_03896","SJAG_03189","SJAG_02364","SJAG_01547","SJAG_02070","SJAG_04665","SJAG_01652","SJAG_04511","SJAG_03091","SJAG_03230","SJAG_04521","SJAG_04276","SJAG_03616","SJAG_02771","SJAG_03890","SJAG_03398","SJAG_01284","SJAG_00581","SJAG_02340","SJAG_02268","SJAG_04763","SJAG_04023","SJAG_00746","SJAG_00888","SJAG_04939","SJAG_04233","SJAG_00814","SJAG_01153","SJAG_01148","SJAG_05033","SJAG_04586","SJAG_02667","SJAG_04108","SJAG_01428","SJAG_04270","SJAG_04360","SJAG_06621","SJAG_01853","SJAG_01710","SJAG_00337","SJAG_03340","SJAG_03002","SJAG_02794","SJAG_02712","SJAG_01058","SJAG_03172","SJAG_00779","SJAG_01054","SJAG_04032","SJAG_01955","SJAG_05210","SJAG_02379","SJAG_00622","SJAG_03264","SJAG_01193","SJAG_02938","SJAG_01000","SJAG_00036","SJAG_00034","SJAG_02421","SJAG_03576","SJAG_03797","SJAG_00466","SJAG_03336","SJAG_04778","SJAG_04888","SJAG_01333","SJAG_00788","SJAG_04478","SJAG_03349","SJAG_01884","SJAG_02096","SJAG_03651","SJAG_01479","SJAG_02486","SJAG_01335","SJAG_03971","SJAG_01643","SJAG_01293","SJAG_00420","SJAG_04679","SJAG_01839","SJAG_00469","SJAG_03492","SJAG_02861","SJAG_01558","SJAG_03223","SJAG_04093","SJAG_02012"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[57188,57882,58085,58612,59278,59323,59348,59430,59696,59738,59776,59784,59829,59895,60358,60523,60772,60948,61883,62044,62137,62202,62475,62733,62833,63416,64614,64955,64989,65372,65554,66049,66559,66575,67012,67143,67226,67376,67480,67597,67605,67721,67767,68629,69129,69934,70426,70574,70608,70938,71552,71584,71597,71656,71697,71715,71732,71739,71769,71780,71798,71812,71878,71944,71951,72021,72056,72122,72173,72201,72272,72295,72312,72345,72393,72498,72506,72567,72653,72712,72720,72731,72754,72801,72842,72916,72952,72978,73075,73188,73239,73277,73321,73357,73384,73439,73450,73487,73570,73573,73595,73604,73655,73662,73680,73771,73781,73800,73865,73874,73890,73944,73967,73984,74071,74081,74186,74262,74290,74311,74321,74329,74364,74449,74475,74496,74531,74603,74743,74773,74786,74813,74819,74832,74838,74907,75003,75052,75059,75072,75083,75102,75114,75132,75149,75358,75422,75456,75462,75465,75527,75546,75601,75637,75685,75724,75743,75798,75814,75878,75940,76014,76033,76037,76065,76088,76147,76212,76232,76310,76378,76388,76396,76406,76450,76470,76559,76639,76644,76647,76677,76686,76754,76766,76775,76789,76827,76864,76911,76937,76980,76993,77027,77044,77058,77085,77110,77119,77156,77264,77287,77320,77374,77440,77468,77529,77559,77564,77613,77696,77712,77719,77725,77737,77862,77897,77907,77976,78004,78047,78162,78165,78187,78259,78330,78336,78355,78366,78389,78498,78550,78561,78704,78754,78841,78851,78858,78865,78930,78934,79001,79004,79063,79089,79099,79166,79168,79207,79259,79363,79406,79476,79580,79598,79623,79647,79657,79731,79765,79776,79907,79912,79920,79923,79951,80007,80026,80101,80154,80227,80277,80290,80305,80342,80371,80383,80402,80414,80428,80500,80522,80528,80557,80561,80568,80603,80632,80638,80671,80698,80774,80799,80807,80828,80847,80849,80866,80875,80883,80977,80986,80988,80998,81017,81058,81130,81139,81151,81225,81258,81273,81317,81324,81328,81362,81401,81412,81417,81462,81482,81656,81683,81697,81725,81729,81871,81954,81964,82053,82071,82120,82159,82206,82239,82246,89185,89208,89232,89241,89264,89269,89272,89283,89316,89324,89334,89410,89441,89449,89459,89464,89522,89538,89543,89551,89574,89593,89598,89607,89616,89657,89724,89752,89774,89782,89800,89807,89818,89856,89882,89940,89985,90003,90013,90039,90050,90052,90104,90109,90113,90121,90132,90150,90162,90169,90171,90176,90199,90219,90233,90262,90294,90330,90345,90372,90381,90388,90394,90400,90414,90434,90440,90469,90503,90522,90541,90545,90586,90592,90597,90614,90619,90626,90649,90657,90669,90687,90696,90708,90728,90735,90780,90784,90878,90976,91030,91055,91122,91127,91143,91165,91205,91215,91235,91245,91284,91294,91307,91326,91350,91365,91368,91393,91408,91432,91460,91467,91472,91493,91501,91519,91537,91563,91573,91602,91609,91616,91622,91647,91658,91681,91707,91715,91719,91723,91741,91748,91759,91770,91840,91899,91912,91989,91992,92008,92022,92033,92074,92101,92122,92132,92151,92157,92181,92212,92224,92230,92251,92256,92265,92281,92375,92411,92426,92432,92446,92454,92468,92486,92495,92516,92533,92540,92569,92576,92589,92630,92652,92666,92689,92700,92765,92803,92814,92828,92894,92899,92904,92908,92930,92966,92990,93037,93045,93065,93081,93087,93116,93151,93157,93187,93235,93259,93268,93279,93285,93288,93301,93308,93320,93330,93356,93378,93384,93398,93410,93414,93450,93453,93499,93508,93543,93565,93589,93607,93612,93650,93673,93707,93758,93769,93793,93807,93818,93832,93835,93842,93854,93864,93919,93923,93937,93944,93950,93971,94007,94023,94036,94041,94044,94049,94054,94058,94066,94100,94132,94170,94180,94190,94201,94282,94297,94302,94305,94311,94341,94349,94356,94364,94437,94476,94501,94506,94512,94529,94533,94604,94642,94650,94678,94688,94709,94717,94726,94749,94756,94773,94795,94810,94818,94832,94848,94863,94872,94930,94961,94962,94973,95013,95055,95078,95090,95098,95100,95133,95145,95155,95162,95186,95189,95199,95220,95227,95233,95237,95244,95289,95302,95313,95323,95326,95332,95343,95374,95383,95425,95465,95483,95492,95532,95546,95560,95592,95596,95628,95669,95745,95777,95801,95837,95849,95886,95916,95934,95947,95953,95961,95975,95994,96000,96008,96013,96024,96030,96068,96081,96096,96115,96131,96135,96143,96156,96177,96191,96201,96208,96244,96282,96301,96348,96365,96376,96393,96421,96428,96441,96449,96474,96513,96536,96544,96548,96554,96609,96642,96670,96682,96693,96758,96778,96805,96826,96844,96848,96853,96858,96884,96891,96902,96907,96926,96934,96946,96996,97009,97014,97033,97049,97056,97089,97095,97111,97127,97158,97204,97214,97226,97247,97273,97279,97287,97298,97305,97323,97348,97354,97389,97394,97401,97423,97430,97447,97450,97470,97484,97494,97500,97516,97548,97576,97593,97610,97616,97645,97652,97734,97763,97769,97789,97801,97804,97810,97815,97821,97831,97897,97903,97909,97919,97925,97941,97956,97965,97994,98067,98079,98093,98099,98133,98140,98172,98177,98183,98192,98197,98245,98255,98278,98312,98335,98351,98357,98376,98383,98391,98402,98409,98445,98454,98461,98479,98538,98573,98596,98619,98625,98668,98680,98691,98733,98781,98807,98814,98819,98823,98843,98857,98874,98898,98910,98933,98935,98966,98973,98980,99002,99008,99012,99019,99052,99072,99080,99107,99140,99173,99232,99267,99344,99379,99385,99386,99387,99388,99389,99433,99448,99456,99492,99552,99569,99577,99583,99601,99609,99615,99628,99659,99670,99690,99701,99713,99715,99720,99729,99765,99782,99810,99816,99822,99839,99908,99939,99978,100018,100024,100057,100106,100111,100115,100125,100138,100152,100156,100176,100184,100185,100186,100187,100188,100215,100224,100249,100312,100333,100336,100344,100395,100414,100457,100458,100563,100598,100611,100672,100685,100689,100710,100717,100723,100730,100760,100767,100785,100802,100864,100874,100890,100896,100911,101012,101022,101063,101140,101146,101164,101208,101214,101218,101224,101254,101258,101270,101308,101360,101365,101375,101402,101427,101435,101456,101472,101485,101521,101542,101551,101560,101574,101590,101631,101649,101693,101742,101803,101812,101822,101851,101872,101951,101957,101965,101980,101987,101995,102042,102050,102057,102086,102098,102107,102117,102123,102136,102151,102184,102194,102208,102228,102237,102278,102304,102334,102399,102404,102420,102433,102450,102454,102456,102462,102496,102505,102516,102528,102548,102558,102569,102581,102584,102604,102609,102612,102619,102627,102688,102715,102727,102732,102751,102757,102782,102788,102809,102824,102829,102841,102846,102857,102882,102893,102914,102944,102949,102994,103001,103034,103038,103049,103072,103095,103111,103123,103127,103136,103144,103151,103169,103198,103208,103282,103317,103343,103413,103426,103441,103480,103481,103531,103578,103649,103660,103667,103676,103679,103688,103698,103729,103752,103763,103773,103780,103813,103822,103854,103873,103950,103970,103991,103992,104001,104013,104035,104092,104107,104120,104154,104199,104223,104237,104309,104317,104339,104354,104437,104452,104462,104471,104476,104481,104485,104537,104547,104566,104576,104586,104606,104623,104633,104646,104684,104691,104724,104768,104774,104789,104841,104846,104865,104888,104962,104987,104998,105030,105060,105076,105113,105136,105169,105187,105211,105234,105244,105247,105261,105270,105275,105324,105370,105398,105409,105430,105463,105479,105496,105512,105515,105520,105526,105558,105584,105614,105619,105637,105655,105702,105722,105726,105767,105780,105785,105841,105850,105856,105863,105869,105934,105941,105958,105970,106023,106038,106044,106051,106121,106161,106176,106211,106217,106224,106231,106248,106254,106304,106322,106338,106359,106415,106450,106463,106476,106482,106486,106503,106514,106540,106588,106613,106623,106629,106640,106642,106646,106657,106671,106684,106698,106718,106731,106740,106750,106753,106761,106810,106830,106849,106860,106884,106889,106934,106942,106947,106962,106971,106976,106978,106990,106993,107031,107040,107048,107073,107080,107089,107095,107113,107135,107149,107164,107167,107173,107191,107198,107221,107247,107254,107270,107285,107293,107313,107329,107336,107360,107403,107421,107429,107438,107452,107462,107485,107487,107520,107530,107537,107542,107630,107637,107662,107672,107688,107701,107707,107727,107751,107811,107837,107845,107855,107894,107949,107967,107991,108007,108037,108048,108054,108063,108074,108079,108104,108165,108167,108174,108208,108222,108262,108281,108293,108329,108339,108347,108365,108370,108388,108405,108411,108419,108453,108462,108463,108495,108527,108530,108539,108570,108595,108607,108625,108667,108689,108700,108713,108718,108723,108745,108750,108759,108766,108771,108781,108794,108826,108851,108863,108885,108898,108933,108940,108944,108965,108988,108997,109032,109048,109054,109062,109082,109135,109144,109216,109231,109240,109295,109335,109355,109404,109416,109418,109430,109441,109446,109467,109475,109505,109530,109533,109556,109568,109585,109606,109694,109735,109793,109799,109811,109889,109939,109979,109982,109991,110003,110039,110063,110111,110122,110210,110233,110275,110295,110318,110377,110391,110418,110427,110434,110439,110461,110467,110486,110510,110536,110547,110573,110618,110633,110655,110660,110690,110698,110719,110739,110746,110771,110777,110808,110819,110923,110934,110956,110963,110968,111021,111043,111062,111084,111092,111102,111103,111149,111164,111196,111210,111254,111294,111299,111328,111333,111335,111337,111338,111413,111429,111442,111450,111468,111474,111512,111523,111529,111545,111564,111569,111586,111594,111647,111657,111669,111686,111693,111702,111727,111734,111765,111772,111819,111832,111879,111888,111923,111949,111950,111983,112000,112011,112054,112083,112091,112102,112107,112111,112118,112124,112127,112156,112183,112192,112213,112225,112270,112291,112314,112341,112344,112365,112370,112375,112386,112417,112458,112466,112471,112487,112492,112519,112528,112568,112573,112587,112612,112623,112628,112633,112648,112665,112671,112747,112771,112801,112809,112821,112832,112833,112838,112872,112880,112899,112902,112913,112934,112968,112981,112987,113009,113026,113052,113077,113080,113085,113111,113115,113122,113188,113203,113211,113222,113225,113255,113274,113296,113322,113331,113362,113409,113414,113422,113433,113446,113471,113477,113482,113491,113497,113505,113524,113554,113596,113606,113616,113636,113649,113671,113733,113742,113757,113779,113785,113790,113800,113860,113874,113892,113914,113940,113974,114037,114043,114054,114090,114102,114135,114139,114182,114194,114201,114237,114253,114257,114282,114320,114331,114344,114361,114389,114396,114420,114433,114438,114531,114604,114610,114620,114639,114645,114664,114686,114706,114730,114793,114815,114884,114888,114948,114956,114991,115000,115029,115055,115090,115094,115121,115152,115186,115211,115243,115293,115315,115325,115416,115429,115433,115445,115451,115492,115499,115520,115532,115548,115605,115613,115647,115662,115684,115767,115782,115786,115796,115802,115817,115822,115841,115920,115944,115970,115976,115981,115986,116031,116040,116050,116086,116093,116119,116141,116190,116225,116235,116245,116253,116304,116331,116335,116344,116388,116396,116418,116483,116543,116554,116565,116577,116600,116607,116619,116624,116639,116644,116652,116668,116684,116700,116739,116745,116753,116783,116790,116794,116799,116820,116825,116830,116845,116848,116894,116906,116931,116938,116959,116969,116976,116998,117020,117043,117082,117100,117109,117116,117133,117163,117179,117223,117230,117240,117242,117283,117306,117316,117323,117343,117353,117360,117362,117371,117378,117392,117400,117412,117420,117435,117460,117492,117503,117523,117530,117536,117554,117559,117597,117616,117626,117640,117653,117665,117685,117706,117711,117718,117723,117742,117753,117765,117777,117782,117807,117815,117819,117860,117877,117893,117947,117959,118007,118024,118031,118038,118050,118063,118069,118072,118082,118094,118108,118120,118130,118134,118171,118176,118212,118229,118243,118292,118311,118315,118344,118350,118355,118360,118378,118417,118426,118433,118439,118463,118477,118482,118506,118587,118608,118618,118624,118631,118706,118727,118747,118769,118807,118810,118879,118887,118895,118900,118907,118909,118940,118974,118983,118994,119005,119038,119067,119075,119077,119082,119119,119126,119156,119160,119168,119215,119258,119275,119279,119290,119308,119324,119331,119348,119376,119391,119409,119431,119443,119473,119494,119502,119532,119552,119560,119602,119608,119682,119729,119753,119789,119791,119826,119835,119860,119879,119915,119933,119962,119970,119982,119994,120014,120022,120031,120058,120064,120073,120085,120176,120182,120211,120217,120223,120287,120293,120305,120322,120361,120370,120381,120390,120437,120479,120480,120481,120497,120514,120521,120553,120581,120610,120618,120626,120654,120660,120680,120682,120735,120751,120831,120842,120876,120901,120924,120930,120956,120965,121003,121011,121501],"is_not":false,"summary":null,"term":"GO:0005829"},{"annotations":[79611],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005945"},{"annotations":[79930,71547,77941,74419,79836,75364,78564,81588],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005832"},{"annotations":[119417,72059,72070,76680,77137,73512,118868,79358,78181,71932,73881,75295,80855,81606,114161,73793,79823,72053,73029,75362,81999,75238,73961,77961,74672,79938,81849,74207,82178,58341,75820,78591,80225,98948,99031,73857,96766,69163,89887,78154,78924,96765,74972,77170,76017,79901,75093,114162,73478,76487,72852,73034,71895,77540,75562,64919,116456,75811,79185,92852,80935,101041,75982,116501,77179,76523,76415,78616,78237,80173,107567,107568,72922,116500,78759,73645,92851,75807,73847,76009,76127,71558,80222],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022625"},{"annotations":[109829],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022626"},{"annotations":[81680,73678,101670,59126,79011,115396,71571,80433,78929,77000,70372,71717,107346,79411,72940,81895,81898,103448,75209,76243,101671,76222,115398,116174,76280,75389,76951,107345,72872,75921,80260,72926,103449,72694,76394,76995,101929,76475,72170,80144,77747,80539,108635,74997,75143,75509,76284,78433,76320,74521,78421,96615,76503,80904,77699,107320,93438,75628,116173,75488],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022627"},{"annotations":[79307,107780],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002144"},{"annotations":[65658,93533,96817,120563],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090730"},{"annotations":[108806,65061,105007,95028,94800,115845,111630],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099128"},{"annotations":[72139,71581,78769],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000015"},{"annotations":[109184,78234],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005971"},{"annotations":[81298,117075],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0072380"},{"annotations":[81709,71849,74923],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033596"}]},"cv_name":"cellular_component","definition":"The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.","definition_xrefs":["GOC:jl","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":2115,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00032":null,"SJAG_00033":null,"SJAG_00034":null,"SJAG_00035":null,"SJAG_00036":null,"SJAG_00037":null,"SJAG_00038":null,"SJAG_00039":null,"SJAG_00040":null,"SJAG_00041":null,"SJAG_00043":null,"SJAG_00044":null,"SJAG_00045":null,"SJAG_00049":null,"SJAG_00052":null,"SJAG_00053":null,"SJAG_00059":null,"SJAG_00063":null,"SJAG_00065":null,"SJAG_00067":null,"SJAG_00069":null,"SJAG_00072":null,"SJAG_00074":null,"SJAG_00084":null,"SJAG_00091":null,"SJAG_00092":null,"SJAG_00093":null,"SJAG_00095":null,"SJAG_00100":null,"SJAG_00102":null,"SJAG_00103":null,"SJAG_00104":null,"SJAG_00106":null,"SJAG_00107":null,"SJAG_00112":null,"SJAG_00113":null,"SJAG_00114":null,"SJAG_00115":null,"SJAG_00117":null,"SJAG_00118":null,"SJAG_00119":null,"SJAG_00120":null,"SJAG_00125":null,"SJAG_00126":null,"SJAG_00128":null,"SJAG_00129":null,"SJAG_00134":null,"SJAG_00135":null,"SJAG_00137":null,"SJAG_00141":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00145":null,"SJAG_00147":null,"SJAG_00150":null,"SJAG_00155":null,"SJAG_00161":null,"SJAG_00162":null,"SJAG_00164":null,"SJAG_00166":null,"SJAG_00167":null,"SJAG_00169":null,"SJAG_00172":null,"SJAG_00173":null,"SJAG_00176":null,"SJAG_00178":null,"SJAG_00179":null,"SJAG_00181":null,"SJAG_00184":null,"SJAG_00186":null,"SJAG_00188":null,"SJAG_00189":null,"SJAG_00190":null,"SJAG_00191":null,"SJAG_00202":null,"SJAG_00203":null,"SJAG_00206":null,"SJAG_00207":null,"SJAG_00208":null,"SJAG_00214":null,"SJAG_00219":null,"SJAG_00220":null,"SJAG_00221":null,"SJAG_00223":null,"SJAG_00224":null,"SJAG_00225":null,"SJAG_00226":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00230":null,"SJAG_00234":null,"SJAG_00237":null,"SJAG_00242":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00245":null,"SJAG_00246":null,"SJAG_00248":null,"SJAG_00249":null,"SJAG_00251":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00269":null,"SJAG_00270":null,"SJAG_00272":null,"SJAG_00280":null,"SJAG_00281":null,"SJAG_00283":null,"SJAG_00287":null,"SJAG_00289":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00298":null,"SJAG_00301":null,"SJAG_00306":null,"SJAG_00309":null,"SJAG_00314":null,"SJAG_00316":null,"SJAG_00317":null,"SJAG_00320":null,"SJAG_00321":null,"SJAG_00324":null,"SJAG_00325":null,"SJAG_00326":null,"SJAG_00327":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00337":null,"SJAG_00338":null,"SJAG_00341":null,"SJAG_00343":null,"SJAG_00350":null,"SJAG_00352":null,"SJAG_00353":null,"SJAG_00355":null,"SJAG_00356":null,"SJAG_00359":null,"SJAG_00364":null,"SJAG_00365":null,"SJAG_00366":null,"SJAG_00374":null,"SJAG_00376":null,"SJAG_00377":null,"SJAG_00378":null,"SJAG_00379":null,"SJAG_00381":null,"SJAG_00382":null,"SJAG_00384":null,"SJAG_00390":null,"SJAG_00395":null,"SJAG_00397":null,"SJAG_00400":null,"SJAG_00401":null,"SJAG_00409":null,"SJAG_00413":null,"SJAG_00414":null,"SJAG_00419":null,"SJAG_00420":null,"SJAG_00422":null,"SJAG_00423":null,"SJAG_00424":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00432":null,"SJAG_00435":null,"SJAG_00436":null,"SJAG_00439":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00448":null,"SJAG_00449":null,"SJAG_00450":null,"SJAG_00455":null,"SJAG_00457":null,"SJAG_00461":null,"SJAG_00463":null,"SJAG_00464":null,"SJAG_00465":null,"SJAG_00466":null,"SJAG_00467":null,"SJAG_00468":null,"SJAG_00469":null,"SJAG_00471":null,"SJAG_00472":null,"SJAG_00474":null,"SJAG_00476":null,"SJAG_00479":null,"SJAG_00480":null,"SJAG_00482":null,"SJAG_00483":null,"SJAG_00485":null,"SJAG_00486":null,"SJAG_00487":null,"SJAG_00489":null,"SJAG_00490":null,"SJAG_00491":null,"SJAG_00495":null,"SJAG_00498":null,"SJAG_00501":null,"SJAG_00503":null,"SJAG_00504":null,"SJAG_00505":null,"SJAG_00507":null,"SJAG_00508":null,"SJAG_00509":null,"SJAG_00512":null,"SJAG_00514":null,"SJAG_00518":null,"SJAG_00521":null,"SJAG_00523":null,"SJAG_00524":null,"SJAG_00526":null,"SJAG_00527":null,"SJAG_00529":null,"SJAG_00531":null,"SJAG_00532":null,"SJAG_00533":null,"SJAG_00534":null,"SJAG_00537":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00546":null,"SJAG_00550":null,"SJAG_00560":null,"SJAG_00561":null,"SJAG_00563":null,"SJAG_00567":null,"SJAG_00571":null,"SJAG_00572":null,"SJAG_00573":null,"SJAG_00574":null,"SJAG_00577":null,"SJAG_00578":null,"SJAG_00579":null,"SJAG_00580":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00585":null,"SJAG_00586":null,"SJAG_00591":null,"SJAG_00592":null,"SJAG_00594":null,"SJAG_00596":null,"SJAG_00599":null,"SJAG_00600":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00611":null,"SJAG_00614":null,"SJAG_00615":null,"SJAG_00622":null,"SJAG_00624":null,"SJAG_00629":null,"SJAG_00632":null,"SJAG_00633":null,"SJAG_00637":null,"SJAG_00642":null,"SJAG_00644":null,"SJAG_00645":null,"SJAG_00653":null,"SJAG_00656":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00668":null,"SJAG_00670":null,"SJAG_00674":null,"SJAG_00678":null,"SJAG_00682":null,"SJAG_00683":null,"SJAG_00685":null,"SJAG_00686":null,"SJAG_00689":null,"SJAG_00690":null,"SJAG_00691":null,"SJAG_00692":null,"SJAG_00694":null,"SJAG_00696":null,"SJAG_00702":null,"SJAG_00704":null,"SJAG_00706":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00718":null,"SJAG_00719":null,"SJAG_00720":null,"SJAG_00724":null,"SJAG_00726":null,"SJAG_00728":null,"SJAG_00729":null,"SJAG_00733":null,"SJAG_00736":null,"SJAG_00738":null,"SJAG_00739":null,"SJAG_00742":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00758":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00765":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00777":null,"SJAG_00778":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00788":null,"SJAG_00791":null,"SJAG_00795":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00800":null,"SJAG_00801":null,"SJAG_00803":null,"SJAG_00805":null,"SJAG_00806":null,"SJAG_00807":null,"SJAG_00808":null,"SJAG_00809":null,"SJAG_00811":null,"SJAG_00814":null,"SJAG_00815":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00822":null,"SJAG_00823":null,"SJAG_00827":null,"SJAG_00832":null,"SJAG_00837":null,"SJAG_00839":null,"SJAG_00840":null,"SJAG_00843":null,"SJAG_00845":null,"SJAG_00850":null,"SJAG_00853":null,"SJAG_00854":null,"SJAG_00856":null,"SJAG_00857":null,"SJAG_00858":null,"SJAG_00859":null,"SJAG_00864":null,"SJAG_00869":null,"SJAG_00871":null,"SJAG_00874":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00885":null,"SJAG_00888":null,"SJAG_00890":null,"SJAG_00892":null,"SJAG_00894":null,"SJAG_00898":null,"SJAG_00902":null,"SJAG_00903":null,"SJAG_00908":null,"SJAG_00910":null,"SJAG_00913":null,"SJAG_00916":null,"SJAG_00917":null,"SJAG_00918":null,"SJAG_00921":null,"SJAG_00925":null,"SJAG_00931":null,"SJAG_00937":null,"SJAG_00938":null,"SJAG_00940":null,"SJAG_00941":null,"SJAG_00942":null,"SJAG_00947":null,"SJAG_00948":null,"SJAG_00954":null,"SJAG_00955":null,"SJAG_00956":null,"SJAG_00957":null,"SJAG_00958":null,"SJAG_00960":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00967":null,"SJAG_00968":null,"SJAG_00969":null,"SJAG_00971":null,"SJAG_00972":null,"SJAG_00975":null,"SJAG_00978":null,"SJAG_00980":null,"SJAG_00982":null,"SJAG_00983":null,"SJAG_00986":null,"SJAG_00987":null,"SJAG_00988":null,"SJAG_00989":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01003":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01014":null,"SJAG_01016":null,"SJAG_01018":null,"SJAG_01020":null,"SJAG_01022":null,"SJAG_01024":null,"SJAG_01026":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01042":null,"SJAG_01047":null,"SJAG_01048":null,"SJAG_01053":null,"SJAG_01054":null,"SJAG_01055":null,"SJAG_01058":null,"SJAG_01061":null,"SJAG_01063":null,"SJAG_01064":null,"SJAG_01070":null,"SJAG_01072":null,"SJAG_01074":null,"SJAG_01075":null,"SJAG_01079":null,"SJAG_01081":null,"SJAG_01083":null,"SJAG_01087":null,"SJAG_01088":null,"SJAG_01089":null,"SJAG_01114":null,"SJAG_01117":null,"SJAG_01118":null,"SJAG_01121":null,"SJAG_01122":null,"SJAG_01126":null,"SJAG_01127":null,"SJAG_01128":null,"SJAG_01131":null,"SJAG_01132":null,"SJAG_01134":null,"SJAG_01135":null,"SJAG_01136":null,"SJAG_01137":null,"SJAG_01139":null,"SJAG_01142":null,"SJAG_01146":null,"SJAG_01148":null,"SJAG_01149":null,"SJAG_01150":null,"SJAG_01151":null,"SJAG_01153":null,"SJAG_01154":null,"SJAG_01159":null,"SJAG_01161":null,"SJAG_01162":null,"SJAG_01163":null,"SJAG_01166":null,"SJAG_01167":null,"SJAG_01172":null,"SJAG_01175":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01184":null,"SJAG_01185":null,"SJAG_01186":null,"SJAG_01187":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01194":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01199":null,"SJAG_01202":null,"SJAG_01203":null,"SJAG_01207":null,"SJAG_01209":null,"SJAG_01213":null,"SJAG_01214":null,"SJAG_01216":null,"SJAG_01218":null,"SJAG_01220":null,"SJAG_01222":null,"SJAG_01226":null,"SJAG_01228":null,"SJAG_01229":null,"SJAG_01231":null,"SJAG_01233":null,"SJAG_01235":null,"SJAG_01238":null,"SJAG_01240":null,"SJAG_01245":null,"SJAG_01248":null,"SJAG_01251":null,"SJAG_01252":null,"SJAG_01255":null,"SJAG_01259":null,"SJAG_01261":null,"SJAG_01266":null,"SJAG_01267":null,"SJAG_01268":null,"SJAG_01269":null,"SJAG_01270":null,"SJAG_01274":null,"SJAG_01277":null,"SJAG_01279":null,"SJAG_01283":null,"SJAG_01284":null,"SJAG_01287":null,"SJAG_01291":null,"SJAG_01292":null,"SJAG_01293":null,"SJAG_01296":null,"SJAG_01298":null,"SJAG_01301":null,"SJAG_01302":null,"SJAG_01308":null,"SJAG_01310":null,"SJAG_01311":null,"SJAG_01312":null,"SJAG_01313":null,"SJAG_01314":null,"SJAG_01317":null,"SJAG_01320":null,"SJAG_01322":null,"SJAG_01325":null,"SJAG_01328":null,"SJAG_01333":null,"SJAG_01335":null,"SJAG_01338":null,"SJAG_01339":null,"SJAG_01341":null,"SJAG_01342":null,"SJAG_01346":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01359":null,"SJAG_01360":null,"SJAG_01361":null,"SJAG_01362":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01367":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01372":null,"SJAG_01375":null,"SJAG_01376":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01383":null,"SJAG_01384":null,"SJAG_01385":null,"SJAG_01386":null,"SJAG_01387":null,"SJAG_01389":null,"SJAG_01397":null,"SJAG_01404":null,"SJAG_01408":null,"SJAG_01411":null,"SJAG_01415":null,"SJAG_01418":null,"SJAG_01425":null,"SJAG_01427":null,"SJAG_01428":null,"SJAG_01430":null,"SJAG_01432":null,"SJAG_01434":null,"SJAG_01436":null,"SJAG_01438":null,"SJAG_01440":null,"SJAG_01443":null,"SJAG_01444":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01453":null,"SJAG_01455":null,"SJAG_01457":null,"SJAG_01458":null,"SJAG_01461":null,"SJAG_01466":null,"SJAG_01467":null,"SJAG_01472":null,"SJAG_01474":null,"SJAG_01475":null,"SJAG_01477":null,"SJAG_01479":null,"SJAG_01480":null,"SJAG_01481":null,"SJAG_01482":null,"SJAG_01487":null,"SJAG_01488":null,"SJAG_01489":null,"SJAG_01492":null,"SJAG_01496":null,"SJAG_01497":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01501":null,"SJAG_01502":null,"SJAG_01508":null,"SJAG_01510":null,"SJAG_01512":null,"SJAG_01515":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01521":null,"SJAG_01522":null,"SJAG_01528":null,"SJAG_01529":null,"SJAG_01531":null,"SJAG_01533":null,"SJAG_01534":null,"SJAG_01535":null,"SJAG_01540":null,"SJAG_01543":null,"SJAG_01544":null,"SJAG_01545":null,"SJAG_01547":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01556":null,"SJAG_01558":null,"SJAG_01561":null,"SJAG_01562":null,"SJAG_01565":null,"SJAG_01566":null,"SJAG_01568":null,"SJAG_01575":null,"SJAG_01576":null,"SJAG_01580":null,"SJAG_01581":null,"SJAG_01582":null,"SJAG_01587":null,"SJAG_01588":null,"SJAG_01590":null,"SJAG_01596":null,"SJAG_01598":null,"SJAG_01599":null,"SJAG_01605":null,"SJAG_01606":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01617":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01621":null,"SJAG_01622":null,"SJAG_01624":null,"SJAG_01625":null,"SJAG_01628":null,"SJAG_01629":null,"SJAG_01630":null,"SJAG_01631":null,"SJAG_01632":null,"SJAG_01635":null,"SJAG_01637":null,"SJAG_01641":null,"SJAG_01643":null,"SJAG_01644":null,"SJAG_01645":null,"SJAG_01646":null,"SJAG_01650":null,"SJAG_01651":null,"SJAG_01652":null,"SJAG_01655":null,"SJAG_01656":null,"SJAG_01658":null,"SJAG_01659":null,"SJAG_01662":null,"SJAG_01663":null,"SJAG_01664":null,"SJAG_01665":null,"SJAG_01666":null,"SJAG_01667":null,"SJAG_01673":null,"SJAG_01675":null,"SJAG_01676":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01686":null,"SJAG_01690":null,"SJAG_01693":null,"SJAG_01694":null,"SJAG_01696":null,"SJAG_01697":null,"SJAG_01698":null,"SJAG_01702":null,"SJAG_01703":null,"SJAG_01704":null,"SJAG_01708":null,"SJAG_01710":null,"SJAG_01714":null,"SJAG_01715":null,"SJAG_01720":null,"SJAG_01721":null,"SJAG_01722":null,"SJAG_01733":null,"SJAG_01734":null,"SJAG_01737":null,"SJAG_01740":null,"SJAG_01742":null,"SJAG_01744":null,"SJAG_01746":null,"SJAG_01748":null,"SJAG_01759":null,"SJAG_01760":null,"SJAG_01762":null,"SJAG_01765":null,"SJAG_01768":null,"SJAG_01772":null,"SJAG_01774":null,"SJAG_01775":null,"SJAG_01776":null,"SJAG_01781":null,"SJAG_01783":null,"SJAG_01784":null,"SJAG_01786":null,"SJAG_01787":null,"SJAG_01788":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01794":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01801":null,"SJAG_01805":null,"SJAG_01808":null,"SJAG_01809":null,"SJAG_01810":null,"SJAG_01812":null,"SJAG_01817":null,"SJAG_01818":null,"SJAG_01822":null,"SJAG_01824":null,"SJAG_01825":null,"SJAG_01826":null,"SJAG_01827":null,"SJAG_01830":null,"SJAG_01833":null,"SJAG_01839":null,"SJAG_01840":null,"SJAG_01841":null,"SJAG_01844":null,"SJAG_01850":null,"SJAG_01851":null,"SJAG_01852":null,"SJAG_01853":null,"SJAG_01858":null,"SJAG_01859":null,"SJAG_01864":null,"SJAG_01869":null,"SJAG_01870":null,"SJAG_01874":null,"SJAG_01884":null,"SJAG_01885":null,"SJAG_01886":null,"SJAG_01897":null,"SJAG_01898":null,"SJAG_01900":null,"SJAG_01901":null,"SJAG_01908":null,"SJAG_01910":null,"SJAG_01914":null,"SJAG_01917":null,"SJAG_01918":null,"SJAG_01919":null,"SJAG_01926":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01943":null,"SJAG_01944":null,"SJAG_01949":null,"SJAG_01954":null,"SJAG_01955":null,"SJAG_01958":null,"SJAG_01974":null,"SJAG_01979":null,"SJAG_01986":null,"SJAG_01987":null,"SJAG_01992":null,"SJAG_01995":null,"SJAG_01997":null,"SJAG_02000":null,"SJAG_02004":null,"SJAG_02005":null,"SJAG_02009":null,"SJAG_02010":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02015":null,"SJAG_02016":null,"SJAG_02017":null,"SJAG_02020":null,"SJAG_02022":null,"SJAG_02024":null,"SJAG_02026":null,"SJAG_02030":null,"SJAG_02033":null,"SJAG_02034":null,"SJAG_02035":null,"SJAG_02038":null,"SJAG_02040":null,"SJAG_02041":null,"SJAG_02042":null,"SJAG_02043":null,"SJAG_02044":null,"SJAG_02046":null,"SJAG_02047":null,"SJAG_02048":null,"SJAG_02057":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02063":null,"SJAG_02065":null,"SJAG_02066":null,"SJAG_02069":null,"SJAG_02070":null,"SJAG_02075":null,"SJAG_02081":null,"SJAG_02082":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02096":null,"SJAG_02098":null,"SJAG_02101":null,"SJAG_02106":null,"SJAG_02107":null,"SJAG_02116":null,"SJAG_02121":null,"SJAG_02135":null,"SJAG_02138":null,"SJAG_02145":null,"SJAG_02146":null,"SJAG_02148":null,"SJAG_02151":null,"SJAG_02154":null,"SJAG_02164":null,"SJAG_02165":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02170":null,"SJAG_02171":null,"SJAG_02172":null,"SJAG_02174":null,"SJAG_02176":null,"SJAG_02177":null,"SJAG_02178":null,"SJAG_02179":null,"SJAG_02180":null,"SJAG_02181":null,"SJAG_02182":null,"SJAG_02184":null,"SJAG_02186":null,"SJAG_02189":null,"SJAG_02191":null,"SJAG_02193":null,"SJAG_02194":null,"SJAG_02197":null,"SJAG_02198":null,"SJAG_02202":null,"SJAG_02203":null,"SJAG_02206":null,"SJAG_02207":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02213":null,"SJAG_02214":null,"SJAG_02215":null,"SJAG_02218":null,"SJAG_02224":null,"SJAG_02225":null,"SJAG_02226":null,"SJAG_02230":null,"SJAG_02231":null,"SJAG_02233":null,"SJAG_02234":null,"SJAG_02235":null,"SJAG_02237":null,"SJAG_02239":null,"SJAG_02240":null,"SJAG_02243":null,"SJAG_02245":null,"SJAG_02251":null,"SJAG_02253":null,"SJAG_02256":null,"SJAG_02265":null,"SJAG_02266":null,"SJAG_02267":null,"SJAG_02268":null,"SJAG_02269":null,"SJAG_02270":null,"SJAG_02271":null,"SJAG_02275":null,"SJAG_02277":null,"SJAG_02279":null,"SJAG_02280":null,"SJAG_02281":null,"SJAG_02282":null,"SJAG_02283":null,"SJAG_02285":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02289":null,"SJAG_02290":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02300":null,"SJAG_02304":null,"SJAG_02307":null,"SJAG_02309":null,"SJAG_02312":null,"SJAG_02313":null,"SJAG_02314":null,"SJAG_02315":null,"SJAG_02320":null,"SJAG_02321":null,"SJAG_02323":null,"SJAG_02327":null,"SJAG_02329":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02337":null,"SJAG_02339":null,"SJAG_02340":null,"SJAG_02342":null,"SJAG_02347":null,"SJAG_02349":null,"SJAG_02352":null,"SJAG_02357":null,"SJAG_02358":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02367":null,"SJAG_02369":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02375":null,"SJAG_02376":null,"SJAG_02378":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02386":null,"SJAG_02387":null,"SJAG_02390":null,"SJAG_02393":null,"SJAG_02400":null,"SJAG_02401":null,"SJAG_02404":null,"SJAG_02405":null,"SJAG_02408":null,"SJAG_02414":null,"SJAG_02415":null,"SJAG_02419":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02422":null,"SJAG_02424":null,"SJAG_02425":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02434":null,"SJAG_02436":null,"SJAG_02439":null,"SJAG_02441":null,"SJAG_02442":null,"SJAG_02444":null,"SJAG_02450":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02461":null,"SJAG_02462":null,"SJAG_02465":null,"SJAG_02467":null,"SJAG_02470":null,"SJAG_02471":null,"SJAG_02474":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02481":null,"SJAG_02482":null,"SJAG_02485":null,"SJAG_02486":null,"SJAG_02490":null,"SJAG_02491":null,"SJAG_02493":null,"SJAG_02497":null,"SJAG_02498":null,"SJAG_02499":null,"SJAG_02502":null,"SJAG_02503":null,"SJAG_02505":null,"SJAG_02506":null,"SJAG_02508":null,"SJAG_02509":null,"SJAG_02510":null,"SJAG_02512":null,"SJAG_02515":null,"SJAG_02517":null,"SJAG_02518":null,"SJAG_02520":null,"SJAG_02522":null,"SJAG_02524":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02540":null,"SJAG_02541":null,"SJAG_02542":null,"SJAG_02546":null,"SJAG_02547":null,"SJAG_02549":null,"SJAG_02551":null,"SJAG_02553":null,"SJAG_02558":null,"SJAG_02561":null,"SJAG_02562":null,"SJAG_02569":null,"SJAG_02570":null,"SJAG_02572":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02583":null,"SJAG_02585":null,"SJAG_02589":null,"SJAG_02591":null,"SJAG_02592":null,"SJAG_02593":null,"SJAG_02594":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02597":null,"SJAG_02600":null,"SJAG_02601":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02608":null,"SJAG_02609":null,"SJAG_02610":null,"SJAG_02611":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02621":null,"SJAG_02625":null,"SJAG_02627":null,"SJAG_02630":null,"SJAG_02640":null,"SJAG_02645":null,"SJAG_02647":null,"SJAG_02648":null,"SJAG_02655":null,"SJAG_02659":null,"SJAG_02661":null,"SJAG_02663":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02671":null,"SJAG_02672":null,"SJAG_02673":null,"SJAG_02679":null,"SJAG_02681":null,"SJAG_02682":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02687":null,"SJAG_02688":null,"SJAG_02689":null,"SJAG_02692":null,"SJAG_02695":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02699":null,"SJAG_02700":null,"SJAG_02702":null,"SJAG_02704":null,"SJAG_02705":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02715":null,"SJAG_02718":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02726":null,"SJAG_02728":null,"SJAG_02730":null,"SJAG_02731":null,"SJAG_02733":null,"SJAG_02734":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02740":null,"SJAG_02741":null,"SJAG_02745":null,"SJAG_02746":null,"SJAG_02747":null,"SJAG_02748":null,"SJAG_02749":null,"SJAG_02750":null,"SJAG_02752":null,"SJAG_02753":null,"SJAG_02755":null,"SJAG_02756":null,"SJAG_02760":null,"SJAG_02763":null,"SJAG_02764":null,"SJAG_02765":null,"SJAG_02766":null,"SJAG_02768":null,"SJAG_02769":null,"SJAG_02770":null,"SJAG_02771":null,"SJAG_02774":null,"SJAG_02783":null,"SJAG_02785":null,"SJAG_02786":null,"SJAG_02788":null,"SJAG_02789":null,"SJAG_02790":null,"SJAG_02791":null,"SJAG_02794":null,"SJAG_02796":null,"SJAG_02797":null,"SJAG_02798":null,"SJAG_02799":null,"SJAG_02801":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02805":null,"SJAG_02808":null,"SJAG_02811":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02814":null,"SJAG_02817":null,"SJAG_02819":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_02832":null,"SJAG_02833":null,"SJAG_02840":null,"SJAG_02843":null,"SJAG_02845":null,"SJAG_02850":null,"SJAG_02851":null,"SJAG_02852":null,"SJAG_02854":null,"SJAG_02857":null,"SJAG_02858":null,"SJAG_02861":null,"SJAG_02863":null,"SJAG_02864":null,"SJAG_02866":null,"SJAG_02868":null,"SJAG_02869":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02874":null,"SJAG_02876":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02885":null,"SJAG_02886":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02895":null,"SJAG_02896":null,"SJAG_02902":null,"SJAG_02904":null,"SJAG_02905":null,"SJAG_02911":null,"SJAG_02912":null,"SJAG_02918":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02938":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_02956":null,"SJAG_02959":null,"SJAG_02972":null,"SJAG_02973":null,"SJAG_02978":null,"SJAG_02984":null,"SJAG_02988":null,"SJAG_02992":null,"SJAG_02994":null,"SJAG_02995":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03009":null,"SJAG_03010":null,"SJAG_03012":null,"SJAG_03013":null,"SJAG_03014":null,"SJAG_03017":null,"SJAG_03019":null,"SJAG_03021":null,"SJAG_03022":null,"SJAG_03026":null,"SJAG_03029":null,"SJAG_03034":null,"SJAG_03035":null,"SJAG_03036":null,"SJAG_03037":null,"SJAG_03041":null,"SJAG_03043":null,"SJAG_03045":null,"SJAG_03049":null,"SJAG_03051":null,"SJAG_03055":null,"SJAG_03062":null,"SJAG_03063":null,"SJAG_03067":null,"SJAG_03069":null,"SJAG_03070":null,"SJAG_03072":null,"SJAG_03074":null,"SJAG_03081":null,"SJAG_03082":null,"SJAG_03085":null,"SJAG_03086":null,"SJAG_03087":null,"SJAG_03089":null,"SJAG_03090":null,"SJAG_03091":null,"SJAG_03094":null,"SJAG_03095":null,"SJAG_03096":null,"SJAG_03098":null,"SJAG_03102":null,"SJAG_03106":null,"SJAG_03107":null,"SJAG_03108":null,"SJAG_03113":null,"SJAG_03119":null,"SJAG_03122":null,"SJAG_03124":null,"SJAG_03126":null,"SJAG_03127":null,"SJAG_03128":null,"SJAG_03130":null,"SJAG_03131":null,"SJAG_03132":null,"SJAG_03133":null,"SJAG_03136":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03141":null,"SJAG_03142":null,"SJAG_03144":null,"SJAG_03147":null,"SJAG_03150":null,"SJAG_03151":null,"SJAG_03153":null,"SJAG_03158":null,"SJAG_03159":null,"SJAG_03164":null,"SJAG_03166":null,"SJAG_03167":null,"SJAG_03172":null,"SJAG_03174":null,"SJAG_03179":null,"SJAG_03181":null,"SJAG_03182":null,"SJAG_03185":null,"SJAG_03186":null,"SJAG_03188":null,"SJAG_03189":null,"SJAG_03191":null,"SJAG_03193":null,"SJAG_03197":null,"SJAG_03204":null,"SJAG_03209":null,"SJAG_03210":null,"SJAG_03211":null,"SJAG_03214":null,"SJAG_03215":null,"SJAG_03219":null,"SJAG_03223":null,"SJAG_03224":null,"SJAG_03225":null,"SJAG_03227":null,"SJAG_03228":null,"SJAG_03229":null,"SJAG_03230":null,"SJAG_03231":null,"SJAG_03233":null,"SJAG_03234":null,"SJAG_03237":null,"SJAG_03238":null,"SJAG_03241":null,"SJAG_03243":null,"SJAG_03245":null,"SJAG_03246":null,"SJAG_03248":null,"SJAG_03250":null,"SJAG_03254":null,"SJAG_03257":null,"SJAG_03258":null,"SJAG_03262":null,"SJAG_03263":null,"SJAG_03264":null,"SJAG_03266":null,"SJAG_03267":null,"SJAG_03272":null,"SJAG_03275":null,"SJAG_03276":null,"SJAG_03277":null,"SJAG_03278":null,"SJAG_03279":null,"SJAG_03283":null,"SJAG_03285":null,"SJAG_03288":null,"SJAG_03291":null,"SJAG_03293":null,"SJAG_03298":null,"SJAG_03306":null,"SJAG_03309":null,"SJAG_03312":null,"SJAG_03313":null,"SJAG_03319":null,"SJAG_03320":null,"SJAG_03321":null,"SJAG_03323":null,"SJAG_03325":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03336":null,"SJAG_03340":null,"SJAG_03345":null,"SJAG_03346":null,"SJAG_03349":null,"SJAG_03350":null,"SJAG_03352":null,"SJAG_03354":null,"SJAG_03356":null,"SJAG_03357":null,"SJAG_03361":null,"SJAG_03362":null,"SJAG_03364":null,"SJAG_03367":null,"SJAG_03371":null,"SJAG_03373":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03376":null,"SJAG_03377":null,"SJAG_03380":null,"SJAG_03383":null,"SJAG_03384":null,"SJAG_03398":null,"SJAG_03403":null,"SJAG_03404":null,"SJAG_03407":null,"SJAG_03408":null,"SJAG_03409":null,"SJAG_03411":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03431":null,"SJAG_03432":null,"SJAG_03433":null,"SJAG_03434":null,"SJAG_03438":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03455":null,"SJAG_03457":null,"SJAG_03463":null,"SJAG_03469":null,"SJAG_03470":null,"SJAG_03472":null,"SJAG_03473":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03482":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03487":null,"SJAG_03488":null,"SJAG_03492":null,"SJAG_03494":null,"SJAG_03495":null,"SJAG_03498":null,"SJAG_03499":null,"SJAG_03500":null,"SJAG_03501":null,"SJAG_03504":null,"SJAG_03507":null,"SJAG_03508":null,"SJAG_03519":null,"SJAG_03523":null,"SJAG_03525":null,"SJAG_03527":null,"SJAG_03528":null,"SJAG_03529":null,"SJAG_03532":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03537":null,"SJAG_03540":null,"SJAG_03541":null,"SJAG_03544":null,"SJAG_03545":null,"SJAG_03547":null,"SJAG_03548":null,"SJAG_03549":null,"SJAG_03551":null,"SJAG_03554":null,"SJAG_03556":null,"SJAG_03558":null,"SJAG_03561":null,"SJAG_03562":null,"SJAG_03568":null,"SJAG_03570":null,"SJAG_03571":null,"SJAG_03575":null,"SJAG_03576":null,"SJAG_03580":null,"SJAG_03581":null,"SJAG_03582":null,"SJAG_03588":null,"SJAG_03589":null,"SJAG_03592":null,"SJAG_03597":null,"SJAG_03601":null,"SJAG_03603":null,"SJAG_03605":null,"SJAG_03614":null,"SJAG_03616":null,"SJAG_03617":null,"SJAG_03618":null,"SJAG_03620":null,"SJAG_03623":null,"SJAG_03624":null,"SJAG_03626":null,"SJAG_03627":null,"SJAG_03629":null,"SJAG_03630":null,"SJAG_03631":null,"SJAG_03632":null,"SJAG_03634":null,"SJAG_03638":null,"SJAG_03643":null,"SJAG_03646":null,"SJAG_03651":null,"SJAG_03653":null,"SJAG_03655":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03662":null,"SJAG_03663":null,"SJAG_03665":null,"SJAG_03666":null,"SJAG_03668":null,"SJAG_03669":null,"SJAG_03673":null,"SJAG_03677":null,"SJAG_03678":null,"SJAG_03679":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03686":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03690":null,"SJAG_03692":null,"SJAG_03693":null,"SJAG_03694":null,"SJAG_03696":null,"SJAG_03697":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03706":null,"SJAG_03708":null,"SJAG_03712":null,"SJAG_03714":null,"SJAG_03717":null,"SJAG_03718":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03723":null,"SJAG_03726":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03733":null,"SJAG_03743":null,"SJAG_03751":null,"SJAG_03752":null,"SJAG_03753":null,"SJAG_03756":null,"SJAG_03758":null,"SJAG_03760":null,"SJAG_03761":null,"SJAG_03762":null,"SJAG_03771":null,"SJAG_03775":null,"SJAG_03781":null,"SJAG_03782":null,"SJAG_03784":null,"SJAG_03786":null,"SJAG_03788":null,"SJAG_03789":null,"SJAG_03791":null,"SJAG_03793":null,"SJAG_03794":null,"SJAG_03797":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03805":null,"SJAG_03810":null,"SJAG_03811":null,"SJAG_03815":null,"SJAG_03818":null,"SJAG_03821":null,"SJAG_03825":null,"SJAG_03828":null,"SJAG_03835":null,"SJAG_03838":null,"SJAG_03839":null,"SJAG_03842":null,"SJAG_03845":null,"SJAG_03847":null,"SJAG_03849":null,"SJAG_03852":null,"SJAG_03854":null,"SJAG_03855":null,"SJAG_03856":null,"SJAG_03857":null,"SJAG_03859":null,"SJAG_03862":null,"SJAG_03863":null,"SJAG_03865":null,"SJAG_03868":null,"SJAG_03872":null,"SJAG_03876":null,"SJAG_03879":null,"SJAG_03881":null,"SJAG_03882":null,"SJAG_03883":null,"SJAG_03884":null,"SJAG_03886":null,"SJAG_03888":null,"SJAG_03889":null,"SJAG_03890":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03901":null,"SJAG_03903":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03919":null,"SJAG_03921":null,"SJAG_03922":null,"SJAG_03924":null,"SJAG_03932":null,"SJAG_03934":null,"SJAG_03936":null,"SJAG_03937":null,"SJAG_03949":null,"SJAG_03950":null,"SJAG_03955":null,"SJAG_03958":null,"SJAG_03959":null,"SJAG_03963":null,"SJAG_03964":null,"SJAG_03971":null,"SJAG_03977":null,"SJAG_03983":null,"SJAG_03986":null,"SJAG_03990":null,"SJAG_03996":null,"SJAG_03998":null,"SJAG_04002":null,"SJAG_04003":null,"SJAG_04007":null,"SJAG_04009":null,"SJAG_04011":null,"SJAG_04012":null,"SJAG_04013":null,"SJAG_04015":null,"SJAG_04020":null,"SJAG_04021":null,"SJAG_04022":null,"SJAG_04023":null,"SJAG_04025":null,"SJAG_04027":null,"SJAG_04029":null,"SJAG_04030":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04033":null,"SJAG_04036":null,"SJAG_04042":null,"SJAG_04043":null,"SJAG_04044":null,"SJAG_04051":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04060":null,"SJAG_04061":null,"SJAG_04062":null,"SJAG_04066":null,"SJAG_04069":null,"SJAG_04070":null,"SJAG_04072":null,"SJAG_04074":null,"SJAG_04077":null,"SJAG_04079":null,"SJAG_04082":null,"SJAG_04083":null,"SJAG_04084":null,"SJAG_04085":null,"SJAG_04086":null,"SJAG_04088":null,"SJAG_04089":null,"SJAG_04091":null,"SJAG_04092":null,"SJAG_04093":null,"SJAG_04097":null,"SJAG_04100":null,"SJAG_04106":null,"SJAG_04107":null,"SJAG_04108":null,"SJAG_04109":null,"SJAG_04112":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04123":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04128":null,"SJAG_04129":null,"SJAG_04130":null,"SJAG_04131":null,"SJAG_04144":null,"SJAG_04147":null,"SJAG_04148":null,"SJAG_04149":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04155":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04159":null,"SJAG_04160":null,"SJAG_04161":null,"SJAG_04163":null,"SJAG_04166":null,"SJAG_04168":null,"SJAG_04169":null,"SJAG_04170":null,"SJAG_04172":null,"SJAG_04174":null,"SJAG_04175":null,"SJAG_04176":null,"SJAG_04177":null,"SJAG_04179":null,"SJAG_04181":null,"SJAG_04182":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04188":null,"SJAG_04190":null,"SJAG_04191":null,"SJAG_04192":null,"SJAG_04197":null,"SJAG_04198":null,"SJAG_04201":null,"SJAG_04202":null,"SJAG_04204":null,"SJAG_04211":null,"SJAG_04212":null,"SJAG_04213":null,"SJAG_04214":null,"SJAG_04219":null,"SJAG_04220":null,"SJAG_04227":null,"SJAG_04229":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04234":null,"SJAG_04235":null,"SJAG_04242":null,"SJAG_04248":null,"SJAG_04249":null,"SJAG_04253":null,"SJAG_04256":null,"SJAG_04261":null,"SJAG_04263":null,"SJAG_04264":null,"SJAG_04266":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04271":null,"SJAG_04273":null,"SJAG_04274":null,"SJAG_04275":null,"SJAG_04276":null,"SJAG_04282":null,"SJAG_04283":null,"SJAG_04285":null,"SJAG_04286":null,"SJAG_04287":null,"SJAG_04289":null,"SJAG_04290":null,"SJAG_04291":null,"SJAG_04292":null,"SJAG_04297":null,"SJAG_04299":null,"SJAG_04300":null,"SJAG_04303":null,"SJAG_04304":null,"SJAG_04306":null,"SJAG_04307":null,"SJAG_04309":null,"SJAG_04311":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04324":null,"SJAG_04326":null,"SJAG_04332":null,"SJAG_04334":null,"SJAG_04335":null,"SJAG_04337":null,"SJAG_04338":null,"SJAG_04342":null,"SJAG_04343":null,"SJAG_04344":null,"SJAG_04347":null,"SJAG_04350":null,"SJAG_04352":null,"SJAG_04354":null,"SJAG_04355":null,"SJAG_04357":null,"SJAG_04359":null,"SJAG_04360":null,"SJAG_04366":null,"SJAG_04368":null,"SJAG_04369":null,"SJAG_04371":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04379":null,"SJAG_04380":null,"SJAG_04381":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04385":null,"SJAG_04388":null,"SJAG_04390":null,"SJAG_04394":null,"SJAG_04397":null,"SJAG_04399":null,"SJAG_04400":null,"SJAG_04403":null,"SJAG_04404":null,"SJAG_04407":null,"SJAG_04408":null,"SJAG_04410":null,"SJAG_04414":null,"SJAG_04417":null,"SJAG_04425":null,"SJAG_04427":null,"SJAG_04429":null,"SJAG_04431":null,"SJAG_04434":null,"SJAG_04436":null,"SJAG_04449":null,"SJAG_04452":null,"SJAG_04453":null,"SJAG_04454":null,"SJAG_04455":null,"SJAG_04456":null,"SJAG_04457":null,"SJAG_04458":null,"SJAG_04459":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04463":null,"SJAG_04465":null,"SJAG_04466":null,"SJAG_04467":null,"SJAG_04470":null,"SJAG_04472":null,"SJAG_04473":null,"SJAG_04474":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04477":null,"SJAG_04478":null,"SJAG_04480":null,"SJAG_04481":null,"SJAG_04482":null,"SJAG_04484":null,"SJAG_04486":null,"SJAG_04487":null,"SJAG_04491":null,"SJAG_04495":null,"SJAG_04496":null,"SJAG_04499":null,"SJAG_04501":null,"SJAG_04505":null,"SJAG_04511":null,"SJAG_04516":null,"SJAG_04518":null,"SJAG_04519":null,"SJAG_04520":null,"SJAG_04521":null,"SJAG_04531":null,"SJAG_04534":null,"SJAG_04535":null,"SJAG_04536":null,"SJAG_04539":null,"SJAG_04540":null,"SJAG_04541":null,"SJAG_04544":null,"SJAG_04548":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04554":null,"SJAG_04559":null,"SJAG_04563":null,"SJAG_04565":null,"SJAG_04567":null,"SJAG_04573":null,"SJAG_04576":null,"SJAG_04577":null,"SJAG_04579":null,"SJAG_04580":null,"SJAG_04581":null,"SJAG_04586":null,"SJAG_04587":null,"SJAG_04590":null,"SJAG_04595":null,"SJAG_04602":null,"SJAG_04607":null,"SJAG_04609":null,"SJAG_04611":null,"SJAG_04612":null,"SJAG_04617":null,"SJAG_04618":null,"SJAG_04626":null,"SJAG_04627":null,"SJAG_04628":null,"SJAG_04629":null,"SJAG_04631":null,"SJAG_04633":null,"SJAG_04634":null,"SJAG_04638":null,"SJAG_04649":null,"SJAG_04650":null,"SJAG_04651":null,"SJAG_04652":null,"SJAG_04653":null,"SJAG_04655":null,"SJAG_04656":null,"SJAG_04657":null,"SJAG_04658":null,"SJAG_04660":null,"SJAG_04663":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04672":null,"SJAG_04674":null,"SJAG_04679":null,"SJAG_04681":null,"SJAG_04682":null,"SJAG_04688":null,"SJAG_04693":null,"SJAG_04695":null,"SJAG_04699":null,"SJAG_04700":null,"SJAG_04704":null,"SJAG_04709":null,"SJAG_04710":null,"SJAG_04711":null,"SJAG_04713":null,"SJAG_04724":null,"SJAG_04726":null,"SJAG_04728":null,"SJAG_04735":null,"SJAG_04741":null,"SJAG_04744":null,"SJAG_04746":null,"SJAG_04747":null,"SJAG_04751":null,"SJAG_04754":null,"SJAG_04756":null,"SJAG_04758":null,"SJAG_04760":null,"SJAG_04762":null,"SJAG_04763":null,"SJAG_04764":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04772":null,"SJAG_04774":null,"SJAG_04776":null,"SJAG_04778":null,"SJAG_04781":null,"SJAG_04783":null,"SJAG_04784":null,"SJAG_04814":null,"SJAG_04815":null,"SJAG_04817":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04827":null,"SJAG_04837":null,"SJAG_04841":null,"SJAG_04842":null,"SJAG_04843":null,"SJAG_04844":null,"SJAG_04845":null,"SJAG_04846":null,"SJAG_04847":null,"SJAG_04848":null,"SJAG_04849":null,"SJAG_04858":null,"SJAG_04859":null,"SJAG_04860":null,"SJAG_04861":null,"SJAG_04863":null,"SJAG_04865":null,"SJAG_04866":null,"SJAG_04870":null,"SJAG_04871":null,"SJAG_04874":null,"SJAG_04877":null,"SJAG_04878":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04888":null,"SJAG_04890":null,"SJAG_04891":null,"SJAG_04894":null,"SJAG_04896":null,"SJAG_04897":null,"SJAG_04901":null,"SJAG_04902":null,"SJAG_04907":null,"SJAG_04912":null,"SJAG_04917":null,"SJAG_04920":null,"SJAG_04921":null,"SJAG_04927":null,"SJAG_04928":null,"SJAG_04932":null,"SJAG_04935":null,"SJAG_04936":null,"SJAG_04938":null,"SJAG_04939":null,"SJAG_04943":null,"SJAG_04944":null,"SJAG_04946":null,"SJAG_04948":null,"SJAG_04950":null,"SJAG_04953":null,"SJAG_04960":null,"SJAG_04963":null,"SJAG_04964":null,"SJAG_04966":null,"SJAG_04968":null,"SJAG_04969":null,"SJAG_04970":null,"SJAG_04972":null,"SJAG_04973":null,"SJAG_04974":null,"SJAG_04977":null,"SJAG_04978":null,"SJAG_04980":null,"SJAG_04981":null,"SJAG_04987":null,"SJAG_04988":null,"SJAG_04990":null,"SJAG_04998":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05004":null,"SJAG_05007":null,"SJAG_05008":null,"SJAG_05009":null,"SJAG_05010":null,"SJAG_05011":null,"SJAG_05014":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05021":null,"SJAG_05023":null,"SJAG_05024":null,"SJAG_05027":null,"SJAG_05029":null,"SJAG_05030":null,"SJAG_05032":null,"SJAG_05033":null,"SJAG_05179":null,"SJAG_05184":null,"SJAG_05185":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05195":null,"SJAG_05197":null,"SJAG_05198":null,"SJAG_05205":null,"SJAG_05206":null,"SJAG_05208":null,"SJAG_05210":null,"SJAG_05211":null,"SJAG_05214":null,"SJAG_05216":null,"SJAG_05222":null,"SJAG_05223":null,"SJAG_05225":null,"SJAG_05228":null,"SJAG_05230":null,"SJAG_05232":null,"SJAG_05240":null,"SJAG_05243":null,"SJAG_05245":null,"SJAG_05248":null,"SJAG_05252":null,"SJAG_05253":null,"SJAG_05256":null,"SJAG_05260":null,"SJAG_05261":null,"SJAG_05266":null,"SJAG_05276":null,"SJAG_05277":null,"SJAG_05283":null,"SJAG_05287":null,"SJAG_05290":null,"SJAG_05303":null,"SJAG_05304":null,"SJAG_05312":null,"SJAG_05314":null,"SJAG_05316":null,"SJAG_05329":null,"SJAG_05331":null,"SJAG_05332":null,"SJAG_05333":null,"SJAG_05334":null,"SJAG_05337":null,"SJAG_05343":null,"SJAG_05346":null,"SJAG_05351":null,"SJAG_05413":null,"SJAG_05694":null,"SJAG_05926":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_06284":null,"SJAG_06309":null,"SJAG_06355":null,"SJAG_06440":null,"SJAG_06576":null,"SJAG_06588":null,"SJAG_06592":null,"SJAG_06599":null,"SJAG_06612":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06634":null,"SJAG_06636":null,"SJAG_07000":null,"SJAG_07011":null,"SJAG_07013":null,"SJAG_07014":null,"SJAG_07017":null,"SJAG_16457":null,"SJAG_16460":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cytosol","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:31956022":null},"secondary_identifiers":["Wikipedia:Cytosol","NIF_Subcellular:sao101633890"],"termid":"GO:0005829","terms_by_termid":{"GO:0000015":null,"GO:0002144":null,"GO:0005829":null,"GO:0005832":null,"GO:0005945":null,"GO:0005971":null,"GO:0022625":null,"GO:0022626":null,"GO:0022627":null,"GO:0033596":null,"GO:0072380":null,"GO:0090730":null,"GO:0099128":null}}


id: MONDO:0000839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any abnormality, anatomical or biochemical, evident at birth or during the neonatal period.","definition_xrefs":["NCIT:C2849"],"gene_count":0,"genotype_count":0,"name":"obsolete congenital abnormality (obsolete MONDO:0000839)","secondary_identifiers":["DOID:0080015","MESH:D000013","ICD9:759.89","ICD9:759.9","NANDO:1200957","SCTID:276654001"],"synonyms":[{"name":"CM - congenital malformation","type":"related"},{"name":"SCONG","type":"exact"},{"name":"birth defect","type":"exact"},{"name":"congenital Abnormality","type":"exact"},{"name":"congenital abnormality","type":"exact"},{"name":"congenital anatomic Abnormality","type":"exact"},{"name":"congenital anatomical Abnormality","type":"exact"},{"name":"congenital anomalies of fetus","type":"exact"},{"name":"congenital anomaly","type":"exact"},{"name":"congenital anomaly or birth defect","type":"exact"},{"name":"congenital defect","type":"exact"},{"name":"congenital defect/deformity","type":"exact"},{"name":"congenital deformity","type":"exact"},{"name":"congenital malformation","type":"exact"},{"name":"defect/deformity, Congenital","type":"exact"},{"name":"defect/deformity, congenital","type":"exact"},{"name":"deformity/defect, Congenital","type":"exact"},{"name":"fetal developmental abnormality","type":"related"},{"name":"fetal malformation","type":"related"},{"name":"physical disorder","type":"exact"}],"termid":"MONDO:0000839","xrefs":{"Monarch":{"xref_id":"0000839"}}}


id: RO:HOM0000019
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Historical homology that involves two members sharing no other homologs in the lineages considered.","definition_xrefs":["BGEE:curator"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in_historical_homology_relationship_with","termid":"RO:HOM0000007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_1_to_1_homology_relationship_with","synonyms":[{"name":"1 to 1 homologous to","type":"exact"},{"name":"1:1 homology","type":"exact"},{"name":"one-to-one homology","type":"exact"}],"termid":"RO:HOM0000019"}


id: GO:0032153
data:
  {"annotated_genes":["SJAG_05978","SJAG_03010","SJAG_00018","SJAG_02431","SJAG_03011","SJAG_01350","SJAG_03486","SJAG_00333","SJAG_02576","SJAG_01720","SJAG_03602","SJAG_04460","SJAG_02075","SJAG_00800","SJAG_01718","SJAG_02761","SJAG_00845","SJAG_05290","SJAG_03688","SJAG_00805","SJAG_02916","SJAG_00445","SJAG_02729","SJAG_03681","SJAG_01196","SJAG_04637","SJAG_05264","SJAG_03753","SJAG_01889","SJAG_03353","SJAG_04917","SJAG_01686","SJAG_00236","SJAG_01118","SJAG_02241","SJAG_05232","SJAG_03331","SJAG_02602","SJAG_02712","SJAG_01855","SJAG_04595","SJAG_04479","SJAG_03835","SJAG_01964","SJAG_04706","SJAG_05210","SJAG_03119","SJAG_01794","SJAG_02684","SJAG_03655","SJAG_04044","SJAG_03074","SJAG_00264","SJAG_03704","SJAG_04771","SJAG_00118","SJAG_01978","SJAG_01319","SJAG_01448","SJAG_00268","SJAG_04074","SJAG_03936","SJAG_00663","SJAG_02581","SJAG_01738","SJAG_01822","SJAG_01255","SJAG_03793","SJAG_00666","SJAG_00652","SJAG_00072","SJAG_00442","SJAG_02333","SJAG_00101","SJAG_03407","SJAG_03086","SJAG_04421","SJAG_00856","SJAG_00521","SJAG_04258","SJAG_04609","SJAG_01631","SJAG_00669","SJAG_01732","SJAG_03703","SJAG_03986","SJAG_02104","SJAG_07018","SJAG_01665","SJAG_01003","SJAG_00661","SJAG_01456","SJAG_04655","SJAG_04050","SJAG_03891","SJAG_01943","SJAG_03005","SJAG_04462","SJAG_04960","SJAG_02727","SJAG_03146","SJAG_02797","SJAG_00575","SJAG_00063","SJAG_00587","SJAG_03432","SJAG_04375","SJAG_03374","SJAG_01799","SJAG_01703","SJAG_02392","SJAG_04280","SJAG_05205","SJAG_04597","SJAG_01817","SJAG_01268","SJAG_03172","SJAG_01697","SJAG_04621","SJAG_01146","SJAG_03429","SJAG_03705","SJAG_02065","SJAG_02422","SJAG_04012","SJAG_03606","SJAG_03708","SJAG_05004","SJAG_01459","SJAG_02733","SJAG_01247","SJAG_03246","SJAG_04931","SJAG_02222","SJAG_02760","SJAG_03564","SJAG_02278","SJAG_01835","SJAG_02700","SJAG_03088","SJAG_01453","SJAG_04001","SJAG_04457","SJAG_03795","SJAG_04051","SJAG_01769","SJAG_00028","SJAG_01171","SJAG_01894","SJAG_00424","SJAG_01993","SJAG_00589","SJAG_01925","SJAG_01215","SJAG_04781","SJAG_04620","SJAG_02957","SJAG_01754","SJAG_02848","SJAG_02657","SJAG_04167","SJAG_00229","SJAG_05001","SJAG_02169","SJAG_02730","SJAG_00082","SJAG_00472","SJAG_04724","SJAG_01774","SJAG_02737","SJAG_03754","SJAG_04776","SJAG_01290","SJAG_05179","SJAG_03643","SJAG_03600","SJAG_02753","SJAG_04982","SJAG_01956","SJAG_03536","SJAG_02320","SJAG_02132","SJAG_03052","SJAG_03748","SJAG_01071","SJAG_01353","SJAG_03637","SJAG_02508","SJAG_04069","SJAG_03338","SJAG_01189","SJAG_01460","SJAG_02968","SJAG_04666","SJAG_02277","SJAG_04566","SJAG_02114","SJAG_02058","SJAG_04703","SJAG_04828","SJAG_01571","SJAG_00514","SJAG_04470","SJAG_00331","SJAG_04690","SJAG_02609","SJAG_02152","SJAG_03915","SJAG_04268","SJAG_03453","SJAG_04287","SJAG_01277","SJAG_00030","SJAG_03123","SJAG_04624","SJAG_00850","SJAG_01317","SJAG_01898","SJAG_03158","SJAG_03810","SJAG_00152","SJAG_04522","SJAG_00279","SJAG_02022","SJAG_03126","SJAG_05198","SJAG_04062","SJAG_01181","SJAG_04591","SJAG_01901","SJAG_02902","SJAG_03596","SJAG_01167","SJAG_00216","SJAG_03379","SJAG_01756","SJAG_01095","SJAG_01281","SJAG_03145","SJAG_01143","SJAG_02322","SJAG_04461","SJAG_03625","SJAG_01360","SJAG_02186","SJAG_01848","SJAG_04901","SJAG_03380","SJAG_02572","SJAG_03264","SJAG_04058","SJAG_00546","SJAG_00280","SJAG_00162","SJAG_04668","SJAG_02215","SJAG_03073","SJAG_00700","SJAG_00289","SJAG_05285","SJAG_03025","SJAG_00750","SJAG_04077","SJAG_00667","SJAG_03229","SJAG_02716","SJAG_04322","SJAG_00910","SJAG_03887","SJAG_00938","SJAG_00551","SJAG_01888","SJAG_00773","SJAG_03731","SJAG_04829","SJAG_03746","SJAG_01590","SJAG_02550","SJAG_00104","SJAG_04551","SJAG_02943","SJAG_03131","SJAG_00137","SJAG_00317","SJAG_04935","SJAG_00318","SJAG_02645","SJAG_04787","SJAG_01658","SJAG_00807","SJAG_01288","SJAG_03631","SJAG_00724","SJAG_02511","SJAG_05315","SJAG_03537","SJAG_02886","SJAG_02864","SJAG_02004","SJAG_02366","SJAG_02228","SJAG_02166","SJAG_01863","SJAG_04013","SJAG_03760","SJAG_04455","SJAG_01373","SJAG_01114","SJAG_03581","SJAG_00185","SJAG_02202","SJAG_02266","SJAG_00245","SJAG_00610","SJAG_02062","SJAG_03375","SJAG_04315","SJAG_04509","SJAG_04486","SJAG_01135","SJAG_01787","SJAG_00692","SJAG_02838","SJAG_02368","SJAG_04887","SJAG_04498","SJAG_02566","SJAG_00228","SJAG_01384","SJAG_04673","SJAG_03938","SJAG_04765","SJAG_01983","SJAG_02831","SJAG_00916","SJAG_02379","SJAG_00677","SJAG_00993","SJAG_00743","SJAG_02412","SJAG_04358","SJAG_01770","SJAG_05185","SJAG_02444"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[59415,66903,67183,67793,70168,77223,80877,89258,89864,89946,90048,90066,90432,90596,91153,91187,91252,91430,91526,91645,92031,92164,92289,92290,92291,92292,92293,92294,92295,92296,92297,92785,92897,92963,92987,93091,93306,93427,93471,93588,93680,93942,93949,94021,94106,94168,94546,94870,95310,95337,95490,95683,95716,95974,96067,96228,96242,96803,96851,97556,97814,98132,98170,98191,98277,98340,98444,98562,98666,98806,98894,99423,100101,100245,100684,100693,100708,100783,101162,101465,101558,102018,102056,102275,102331,102494,102807,102839,103244,103316,103366,103643,103811,104033,104118,104338,104508,104621,104637,104659,104908,105208,105350,105362,105408,105424,105613,105636,106527,106557,106638,106738,107078,107535,107552,107836,108279,108404,108409,108593,108599,108615,108769,108778,108938,109031,109086,109110,109151,109994,110120,110231,110274,110304,110551,110581,110697,110737,111318,111464,111472,112116,112126,112640,112815,112878,113008,113216,113387,113430,113454,113614,113634,113891,113909,113973,114101,114126,114435,114444,114965,115178,115209,115414,115630,115633,115742,115800,116128,116143,116296,116809,116893,116904,116930,117042,117271,117304,117623,118037,118048,118060,118170,118461,118715,118816,118906,119003,119492,119510,119715,119988,120006,120334,120335,120434,120533,120551,120579,120594,120734,120755,120795,120873,120984],"is_not":false,"summary":null,"term":"GO:0032153"},{"annotations":[121110,121113,121111,121114,121247,121495,121112],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005826"},{"annotations":[105383,100296,100872,117982],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110115"},{"annotations":[117791,108964,94232,108024,101638,89688,91679],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032154"},{"annotations":[93112,89799],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090689"},{"annotations":[90278,95576,92541,103833,104538,95400,73393,118546,89335,112055,92667,119894,91553,94233,92570,98734,105387,103834,102072,90087,96429,106576,94101,94252,97517,116015,108200,112935,113323,101620,69383,92590,115044,108025,71881,89317,102818,116353,119880],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000935"},{"annotations":[95201,121235,121228,121496,121233,121226],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990753"},{"annotations":[104215,101966,103320,102870,111546,112529,110786,114731,102254,118923,119177,108371],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000923"},{"annotations":[100770,94254,73938,107262,89961,90280,99789,101196,70352,104963,112472,57493,112752,119881,104558,63071,96431,112711,97229,109539,75710,107062,120884,101783,99595,66290,115014,94378,89336],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031097"},{"annotations":[109890,99691,105819,103662,120646,58192,102847,119862,101997,114743],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036391"},{"annotations":[90772,95703,94425,108125,119019,119863,107096,102585,90083,94160,99898,103152,98184,92543],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071341"},{"annotations":[116355,102243,102564,114309,94236,94426,98866],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032178"},{"annotations":[94379,121626,78083,121234,121232,107271,103153,121236,96432,121229,91147,120845,117880,95666,89695,117796,108818,121227,76703,92545,91636,100158,112713,103160,119629],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110085"},{"annotations":[111003,102587,102421,119865,107063],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120106"},{"annotations":[96252,102820,115327,105595,119883,96797,98186,112754,99068,119866,97705,92592,90085,91809,114268,111004,108127],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120105"},{"annotations":[111005,110069,80000,58191,94162,99521,102000,119021,108968,99900,105821,81556,58723,118927,102849],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120104"},{"annotations":[58657,65186,102034,117799],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000936"},{"annotations":[96358,102003,107937,117951],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032169"}]},"cv_name":"cellular_component","definition":"The eventual plane of cell division (also known as cell cleavage or cytokinesis) in a dividing cell. In Eukaryotes, the cleavage apparatus, composed of septin structures and the actomyosin contractile ring, forms along this plane, and the mitotic, or meiotic, spindle is aligned perpendicular to the division plane. In bacteria, the cell division site is generally located at mid-cell and is the site at which the cytoskeletal structure, the Z-ring, assembles.","definition_xrefs":["GOC:krc","GOC:ns","PMID:15380095","PMID:12101122","GOC:bf","PMID:18165305","GOC:imk","PMID:16983191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":344,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00028":null,"SJAG_00030":null,"SJAG_00063":null,"SJAG_00072":null,"SJAG_00082":null,"SJAG_00101":null,"SJAG_00104":null,"SJAG_00118":null,"SJAG_00137":null,"SJAG_00152":null,"SJAG_00162":null,"SJAG_00185":null,"SJAG_00216":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00236":null,"SJAG_00245":null,"SJAG_00264":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00280":null,"SJAG_00289":null,"SJAG_00317":null,"SJAG_00318":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00424":null,"SJAG_00442":null,"SJAG_00445":null,"SJAG_00472":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00546":null,"SJAG_00551":null,"SJAG_00575":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00610":null,"SJAG_00652":null,"SJAG_00661":null,"SJAG_00663":null,"SJAG_00666":null,"SJAG_00667":null,"SJAG_00669":null,"SJAG_00677":null,"SJAG_00692":null,"SJAG_00700":null,"SJAG_00724":null,"SJAG_00743":null,"SJAG_00750":null,"SJAG_00773":null,"SJAG_00800":null,"SJAG_00805":null,"SJAG_00807":null,"SJAG_00845":null,"SJAG_00850":null,"SJAG_00856":null,"SJAG_00910":null,"SJAG_00916":null,"SJAG_00938":null,"SJAG_00993":null,"SJAG_01003":null,"SJAG_01071":null,"SJAG_01095":null,"SJAG_01114":null,"SJAG_01118":null,"SJAG_01135":null,"SJAG_01143":null,"SJAG_01146":null,"SJAG_01167":null,"SJAG_01171":null,"SJAG_01181":null,"SJAG_01189":null,"SJAG_01196":null,"SJAG_01215":null,"SJAG_01247":null,"SJAG_01255":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01281":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01317":null,"SJAG_01319":null,"SJAG_01350":null,"SJAG_01353":null,"SJAG_01360":null,"SJAG_01373":null,"SJAG_01384":null,"SJAG_01448":null,"SJAG_01453":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01460":null,"SJAG_01571":null,"SJAG_01590":null,"SJAG_01631":null,"SJAG_01658":null,"SJAG_01665":null,"SJAG_01686":null,"SJAG_01697":null,"SJAG_01703":null,"SJAG_01718":null,"SJAG_01720":null,"SJAG_01732":null,"SJAG_01738":null,"SJAG_01754":null,"SJAG_01756":null,"SJAG_01769":null,"SJAG_01770":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01794":null,"SJAG_01799":null,"SJAG_01817":null,"SJAG_01822":null,"SJAG_01835":null,"SJAG_01848":null,"SJAG_01855":null,"SJAG_01863":null,"SJAG_01888":null,"SJAG_01889":null,"SJAG_01894":null,"SJAG_01898":null,"SJAG_01901":null,"SJAG_01925":null,"SJAG_01943":null,"SJAG_01956":null,"SJAG_01964":null,"SJAG_01978":null,"SJAG_01983":null,"SJAG_01993":null,"SJAG_02004":null,"SJAG_02022":null,"SJAG_02058":null,"SJAG_02062":null,"SJAG_02065":null,"SJAG_02075":null,"SJAG_02104":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02152":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02202":null,"SJAG_02215":null,"SJAG_02222":null,"SJAG_02228":null,"SJAG_02241":null,"SJAG_02266":null,"SJAG_02277":null,"SJAG_02278":null,"SJAG_02320":null,"SJAG_02322":null,"SJAG_02333":null,"SJAG_02366":null,"SJAG_02368":null,"SJAG_02379":null,"SJAG_02392":null,"SJAG_02412":null,"SJAG_02422":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02508":null,"SJAG_02511":null,"SJAG_02550":null,"SJAG_02566":null,"SJAG_02572":null,"SJAG_02576":null,"SJAG_02581":null,"SJAG_02602":null,"SJAG_02609":null,"SJAG_02645":null,"SJAG_02657":null,"SJAG_02684":null,"SJAG_02700":null,"SJAG_02712":null,"SJAG_02716":null,"SJAG_02727":null,"SJAG_02729":null,"SJAG_02730":null,"SJAG_02733":null,"SJAG_02737":null,"SJAG_02753":null,"SJAG_02760":null,"SJAG_02761":null,"SJAG_02797":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02848":null,"SJAG_02864":null,"SJAG_02886":null,"SJAG_02902":null,"SJAG_02916":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02968":null,"SJAG_03005":null,"SJAG_03010":null,"SJAG_03011":null,"SJAG_03025":null,"SJAG_03052":null,"SJAG_03073":null,"SJAG_03074":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03119":null,"SJAG_03123":null,"SJAG_03126":null,"SJAG_03131":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03158":null,"SJAG_03172":null,"SJAG_03229":null,"SJAG_03246":null,"SJAG_03264":null,"SJAG_03331":null,"SJAG_03338":null,"SJAG_03353":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03407":null,"SJAG_03429":null,"SJAG_03432":null,"SJAG_03453":null,"SJAG_03486":null,"SJAG_03536":null,"SJAG_03537":null,"SJAG_03564":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03600":null,"SJAG_03602":null,"SJAG_03606":null,"SJAG_03625":null,"SJAG_03631":null,"SJAG_03637":null,"SJAG_03643":null,"SJAG_03655":null,"SJAG_03681":null,"SJAG_03688":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03705":null,"SJAG_03708":null,"SJAG_03731":null,"SJAG_03746":null,"SJAG_03748":null,"SJAG_03753":null,"SJAG_03754":null,"SJAG_03760":null,"SJAG_03793":null,"SJAG_03795":null,"SJAG_03810":null,"SJAG_03835":null,"SJAG_03887":null,"SJAG_03891":null,"SJAG_03915":null,"SJAG_03936":null,"SJAG_03938":null,"SJAG_03986":null,"SJAG_04001":null,"SJAG_04012":null,"SJAG_04013":null,"SJAG_04044":null,"SJAG_04050":null,"SJAG_04051":null,"SJAG_04058":null,"SJAG_04062":null,"SJAG_04069":null,"SJAG_04074":null,"SJAG_04077":null,"SJAG_04167":null,"SJAG_04258":null,"SJAG_04268":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04315":null,"SJAG_04322":null,"SJAG_04358":null,"SJAG_04375":null,"SJAG_04421":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04462":null,"SJAG_04470":null,"SJAG_04479":null,"SJAG_04486":null,"SJAG_04498":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04551":null,"SJAG_04566":null,"SJAG_04591":null,"SJAG_04595":null,"SJAG_04597":null,"SJAG_04609":null,"SJAG_04620":null,"SJAG_04621":null,"SJAG_04624":null,"SJAG_04637":null,"SJAG_04655":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04673":null,"SJAG_04690":null,"SJAG_04703":null,"SJAG_04706":null,"SJAG_04724":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04776":null,"SJAG_04781":null,"SJAG_04787":null,"SJAG_04828":null,"SJAG_04829":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04917":null,"SJAG_04931":null,"SJAG_04935":null,"SJAG_04960":null,"SJAG_04982":null,"SJAG_05001":null,"SJAG_05004":null,"SJAG_05179":null,"SJAG_05185":null,"SJAG_05198":null,"SJAG_05205":null,"SJAG_05210":null,"SJAG_05232":null,"SJAG_05264":null,"SJAG_05285":null,"SJAG_05290":null,"SJAG_05315":null,"SJAG_05978":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cell division site","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:25866389":null,"PMID:27059155":null,"PMID:27734801":null,"PMID:28655757":null,"PMID:36148799":null},"synonyms":[{"name":"cell division plane","type":"exact"}],"termid":"GO:0032153","terms_by_termid":{"GO:0000085":null,"GO:0000923":null,"GO:0000935":null,"GO:0000936":null,"GO:0005826":null,"GO:0031097":null,"GO:0032153":null,"GO:0032154":null,"GO:0032169":null,"GO:0032178":null,"GO:0036391":null,"GO:0051325":null,"GO:0051329":null,"GO:0071341":null,"GO:0090689":null,"GO:0110085":null,"GO:0110115":null,"GO:0120104":null,"GO:0120105":null,"GO:0120106":null,"GO:1990753":null}}


id: MONDO:0015912
data:
  {"annotated_genes":["SJAG_03703","SJAG_02431"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88170,88171],"is_not":false,"summary":null,"term":"MONDO:0015912"}]},"cv_name":"mondo","definition":"An inherited giant platelet disorder with a complex phenotype characterized by congenital thrombocytopenia and possible subsequent manifestations of sensorineural hearing loss, presenile cataracts, elevation of liver enzymes, and/or progressive nephropathy often leading to end-stage renal disease (ESRD). Epstein syndrome, Fechtner syndrome, May-Hegglin anomaly and Sebastian syndrome, previously described as distinct disorders, represent some of the different clinical presentations of MYH9-RD.","definition_xrefs":["Orphanet:182050"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"syndromic constitutional thrombocytopenia","termid":"MONDO:0018795"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C131646","ICD9:582.89","MEDGEN:1704278","Orphanet:1984","SCTID:234485006","ICD9:759.89","SCTID:236422008","DOID:0060651","EFO:0009646","MESH:C537831","OMIM:153640","OMIM:605249","Orphanet:807","SCTID:234484005","OMIM:155100","SCTID:712922002","UMLS:C5200934","NCIT:C158788","Orphanet:1019","ICD9:287.33","Orphanet:850","OMIM:600208","GARD:180"],"synonyms":[{"name":"Alport syndrome with macrothrombocytopenia","type":"related"},{"name":"Alport syndrome with macrothrombocytopenia, formerly","type":"related"},{"name":"Brodie Chole griffin syndrome","type":"related"},{"name":"Brodie Chole gryphon syndrome","type":"related"},{"name":"Dohle leukocyte inclusions with giant platelets","type":"related"},{"name":"Epstein syndrome","type":"exact"},{"name":"FTNS","type":"related"},{"name":"Fechtner syndrome","type":"exact"},{"name":"MHA","type":"related"},{"name":"MYH-9 related disease","type":"exact"},{"name":"MYH9 related disorders","type":"related"},{"name":"MYH9 related thrombocytopenia","type":"related"},{"name":"MYH9-RD","type":"exact"},{"name":"MYH9-related disease","type":"exact"},{"name":"MYH9-related disorder","type":"exact"},{"name":"MYH9-related syndrome","type":"exact"},{"name":"MYH9-related syndromic thrombocytopenia","type":"exact"},{"name":"May-Hegglin anomaly","type":"exact"},{"name":"May-Hegglin thrombocytopenia","type":"related"},{"name":"SBS","type":"related"},{"name":"Sebastian platelet syndrome","type":"exact"},{"name":"Sebastian syndrome","type":"exact"},{"name":"bleeding disorder, Platelet-type, 6","type":"related"},{"name":"giant platelet syndrome with thrombocytopenia","type":"exact"},{"name":"macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss","type":"exact"},{"name":"macrothrombocytopenia and progressive sensorineural deafness","type":"exact"},{"name":"macrothrombocytopenia progressive deafness","type":"related"},{"name":"macrothrombocytopenia with dispersed leukocytic inclusions","type":"related"},{"name":"macrothrombocytopenia with leukocyte inclusions","type":"related"},{"name":"macrothrombocytopenia, nephritis, and deafness","type":"related"},{"name":"macrothrombocytopenia, nephritis, deafness, and leukocyte inclusions","type":"related"},{"name":"matins","type":"related"}],"termid":"MONDO:0015912","terms_by_termid":{"MONDO:0015912":null},"xrefs":{"Monarch":{"xref_id":"0015912"}}}


id: MONDO:0004460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A thyroid gland adenoma composed of microfollicular structures.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"follicular thyroid adenoma","termid":"MONDO:0005032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid gland fetal adenoma","secondary_identifiers":["DOID:8102","UMLS:C0334328","NCIT:C4160","ICDO:8333/0","MEDGEN:137743"],"synonyms":[{"name":"foetal adenoma","type":"related"},{"name":"microfollicular adenoma","type":"exact"},{"name":"microfollicular adenoma (morphologic abnormality)","type":"exact"},{"name":"thyroid fetal adenoma","type":"exact"},{"name":"thyroid foetal adenoma","type":"exact"},{"name":"thyroid gland microfollicular adenoma","type":"exact"}],"termid":"MONDO:0004460","xrefs":{"Monarch":{"xref_id":"0004460"}}}


id: PBO:0078492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 11-1","termid":"PBO:0078492"}


id: PBO:0049494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 1","termid":"PBO:0049494"}


id: PBO:0057308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 516b-1","termid":"PBO:0057308"}


id: MONDO:0004912
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete muscular dystrophy (obsolete MONDO:0004912)","termid":"MONDO:0004912","xrefs":{"Monarch":{"xref_id":"0004912"}}}


id: PBO:0070955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18a pseudogene 10","termid":"PBO:0070955"}


id: GO:0039508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the frequency, rate or extent of the functional activity of a host receptor.","definition_xrefs":["GOC:sp","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host receptor activity (obsolete GO:0039508)","synonyms":[{"name":"down-regulation by virus of host receptor activity","type":"exact"},{"name":"downregulation by virus of host receptor activity","type":"exact"},{"name":"inhibition by virus of host receptor activity","type":"narrow"},{"name":"negative regulation by virus of host receptor activity","type":"exact"},{"name":"suppression by virus of host receptor function","type":"exact"},{"name":"viral inhibition of host receptor","type":"exact"}],"termid":"GO:0039508"}


id: GO:0002261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of lymphocytes such that the total number of lymphocytes within the mucosal tissue of an organism is stable over time in the absence of an outside stimulus.","definition_xrefs":["PMID:15609020","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte homeostasis","termid":"GO:0002260"}],"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":"mucosal lymphocyte homeostasis","termid":"GO:0002261"}


id: MONDO:0012644
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Jeune syndrome in which the cause of the disease is a mutation in the IFT80 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"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":"asphyxiating thoracic dystrophy 2","secondary_identifiers":["MESH:C566982","OMIM:611263","MEDGEN:370804","DOID:0110086","UMLS:C1970005","GARD:15511"],"synonyms":[{"name":"ATD2","type":"exact"},{"name":"IFT80 Jeune syndrome","type":"exact"},{"name":"Jeune syndrome caused by mutation in IFT80","type":"exact"},{"name":"SRTD2","type":"exact"},{"name":"asphyxiating thoracic dystrophy 2","type":"exact"},{"name":"asphyxiating thoracic dystrophy type 2","type":"exact"},{"name":"short-rib thoracic dysplasia 2 with or without polydactyly","type":"exact"}],"termid":"MONDO:0012644","xrefs":{"Monarch":{"xref_id":"0012644"}}}


id: FYPO:0003465
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of alpha,alpha-trehalase activity is lower than normal during a cellular response to salt stress.","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 alpha,alpha-trehalase activity","termid":"FYPO:0001479"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0000652","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"decreased alpha,alpha-trehalase activity during cellular response to salt stress","synonyms":[{"name":"decreased neutral trehalase activity during cellular response to salt stress","type":"exact"},{"name":"decreased trehalase activity during cellular response to salt stress","type":"broad"},{"name":"reduced alpha,alpha-trehalase activity during cellular response to v","type":"exact"}],"termid":"FYPO:0003465"}


id: PBO:0059310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L51 pseudogene 1","termid":"PBO:0059310"}


id: GO:0004086
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of a reaction that results in the formation of carbamoyl phosphate.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete carbamoyl-phosphate synthase activity (obsolete GO:0004086)","synonyms":[{"name":"carbamoyl phosphate synthase activity","type":"exact"},{"name":"carbamoyl-phosphate synthase activity","type":"exact"}],"termid":"GO:0004086"}


id: PBO:0015252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3/phosphatidylinositol(3)-phosphate binding protein (predicted)","termid":"PBO:0015252"}


id: PBO:0064023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 57","termid":"PBO:0064023"}


id: PBO:0035767
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H2A_phosphorylation_at_rDNA_during_vegetative_growth","termid":"PBO:0035767"}


id: PBO:0028353
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_CTD_phosphatase_activity","termid":"PBO:0028353"}


id: MONDO:0018566
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short stature-advanced bone age-early-onset osteoarthritis syndrome","secondary_identifiers":["Orphanet:435804","UMLS:C5681177","MEDGEN:1811782","GARD:17717"],"termid":"MONDO:0018566","xrefs":{"Monarch":{"xref_id":"0018566"}}}


id: MONDO:0021090
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive breast carcinoma characterized by the presence of cytoplasmic neutral lipids in the vast majority of the malignant cells.","definition_xrefs":["NCIT:C40365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid-rich carcinoma","termid":"MONDO:0003570"},{"relation_name":"is_a","term_name":"bilateral breast carcinoma","termid":"MONDO:0003982"}],"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":"lipid-rich breast carcinoma","secondary_identifiers":["DOID:7076","UMLS:C1517894","MEDGEN:274685"],"synonyms":[{"name":"breast lipid-rich carcinoma","type":"exact"},{"name":"lipid secreting breast carcinoma","type":"related"},{"name":"lipid-rich breast carcinoma","type":"exact"}],"termid":"MONDO:0021090","xrefs":{"Monarch":{"xref_id":"0021090"}}}


id: PBO:0005061
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.12","termid":"PBO:0005061"}


id: FYPO:0000336
data:
  {"alleles_by_uniquename":{"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592: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_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[121551],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[121130,121442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[121240],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[121497,121208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[121552],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which any process of cellular component assembly at the cellular level is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component organization","termid":"FYPO:0000335"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01143":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_04280":null,"SJAG_04522":null},"genotype_count":6,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04280","SJAG_02392","SJAG_01143","SJAG_04522"],"name":"abnormal cellular component assembly","references_by_uniquename":{"PMID:25866389":null,"PMID:27059155":null,"PMID:30664646":null,"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_02592","SJAG_04522","SJAG_02392","SJAG_01143"],"single_locus_genotype_uniquenames":["mid1delta","sty1delta","rga4delta","pom1delta"],"synonyms":[{"name":"abnormal cellular component assembly at cellular level","type":"exact"}],"termid":"FYPO:0000336","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000248":null,"FYECO:0000338":null,"FYPO:0000729":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0002998":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:1900061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of transcription from RNA polymerase II promoter that is involved in calcium-mediated signaling.","definition_xrefs":["GOC:TermGenie","PMID:9407035","PMID:9407036"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in calcium-mediated signaling (obsolete GO:1900061)","synonyms":[{"name":"activation of global transcription from RNA polymerase II promoter of calcium ion signaling","type":"related"},{"name":"activation of global transcription from RNA polymerase II promoter of calcium signaling","type":"related"},{"name":"activation of global transcription from RNA polymerase II promoter of calcium signalling","type":"related"},{"name":"activation of global transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"activation of global transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"related"},{"name":"activation of transcription from RNA polymerase II promoter of calcium ion signaling","type":"narrow"},{"name":"activation of transcription from RNA polymerase II promoter of calcium signaling","type":"narrow"},{"name":"activation of transcription from RNA polymerase II promoter of calcium signalling","type":"narrow"},{"name":"activation of transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"narrow"},{"name":"activation of transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"narrow"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of calcium ion signaling","type":"related"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of calcium signaling","type":"related"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of calcium signalling","type":"related"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of calcium ion signaling","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of calcium signaling","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of calcium signalling","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of calcium-mediated signaling","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of calcium-mediated signalling","type":"related"},{"name":"positive regulation of transcription from Pol II promoter of calcium ion signaling","type":"exact"},{"name":"positive regulation of transcription from Pol II promoter of calcium signaling","type":"exact"},{"name":"positive regulation of transcription from Pol II promoter of calcium signalling","type":"exact"},{"name":"positive regulation of transcription from Pol II promoter of calcium-mediated signaling","type":"related"},{"name":"positive regulation of transcription from Pol II promoter of calcium-mediated signalling","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter involved in calcium-mediated signaling","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter of calcium ion signaling","type":"related"},{"name":"positive regulation of transcription from RNA polymerase II promoter of calcium signaling","type":"related"},{"name":"positive regulation of transcription from RNA polymerase II promoter of calcium signalling","type":"related"},{"name":"positive regulation of transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"positive regulation of transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter of calcium ion signaling","type":"narrow"},{"name":"stimulation of global transcription from RNA polymerase II promoter of calcium signaling","type":"narrow"},{"name":"stimulation of global transcription from RNA polymerase II promoter of calcium signalling","type":"narrow"},{"name":"stimulation of global transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"narrow"},{"name":"stimulation of transcription from RNA polymerase II promoter of calcium ion signaling","type":"exact"},{"name":"stimulation of transcription from RNA polymerase II promoter of calcium signaling","type":"exact"},{"name":"stimulation of transcription from RNA polymerase II promoter of calcium signalling","type":"exact"},{"name":"stimulation of transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"stimulation of transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"exact"},{"name":"up regulation of global transcription from RNA polymerase II promoter of calcium ion signaling","type":"related"},{"name":"up regulation of global transcription from RNA polymerase II promoter of calcium signaling","type":"related"},{"name":"up regulation of global transcription from RNA polymerase II promoter of calcium signalling","type":"related"},{"name":"up regulation of global transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"up regulation of global transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"related"},{"name":"up regulation of transcription from RNA polymerase II promoter of calcium ion signaling","type":"exact"},{"name":"up regulation of transcription from RNA polymerase II promoter of calcium signaling","type":"exact"},{"name":"up regulation of transcription from RNA polymerase II promoter of calcium signalling","type":"exact"},{"name":"up regulation of transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"up regulation of transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"exact"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of calcium ion signaling","type":"related"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of calcium signaling","type":"related"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of calcium signalling","type":"related"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"related"},{"name":"up-regulation of transcription from RNA polymerase II promoter of calcium ion signaling","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase II promoter of calcium signaling","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase II promoter of calcium signalling","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"up-regulation of transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"exact"},{"name":"upregulation of global transcription from RNA polymerase II promoter of calcium ion signaling","type":"related"},{"name":"upregulation of global transcription from RNA polymerase II promoter of calcium signaling","type":"related"},{"name":"upregulation of global transcription from RNA polymerase II promoter of calcium signalling","type":"related"},{"name":"upregulation of global transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"upregulation of global transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"related"},{"name":"upregulation of transcription from RNA polymerase II promoter of calcium ion signaling","type":"exact"},{"name":"upregulation of transcription from RNA polymerase II promoter of calcium signaling","type":"exact"},{"name":"upregulation of transcription from RNA polymerase II promoter of calcium signalling","type":"exact"},{"name":"upregulation of transcription from RNA polymerase II promoter of calcium-mediated signaling","type":"related"},{"name":"upregulation of transcription from RNA polymerase II promoter of calcium-mediated signalling","type":"exact"}],"termid":"GO:1900061"}


id: PBO:0063162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paired box 7","termid":"PBO:0063162"}


id: GO:0034711
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an inhibin monomer, any of the polypeptides that combine to form activin and inhibin dimers.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"inhibin binding","secondary_identifiers":["GO:0048187","GO:0048186","GO:0034712"],"synonyms":[{"name":"inhibin alpha binding","type":"narrow"},{"name":"inhibin beta-A binding","type":"narrow"},{"name":"inhibin beta-B binding","type":"narrow"},{"name":"inhibin monomer binding","type":"exact"}],"termid":"GO:0034711"}


id: PBO:0031390
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_lysine","termid":"PBO:0031390"}


id: GO:0071201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A voltage-gated potassium channel complex that contains the peptidase-related protein DPP6 associated with the channel via interaction with the Kv alpha subunit 4.3.","definition_xrefs":["PMID:15911355","PMID:12575952"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Kv4.3-DPP6 channel complex","secondary_identifiers":["CORUM:599"],"synonyms":[{"name":"Kv4.3-DPPX channel complex","type":"exact"}],"termid":"GO:0071201"}


id: GO:1901872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ecgonone methyl ester.","definition_xrefs":["PMID:22665766","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tropane alkaloid biosynthetic process","termid":"GO:0009710"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"ecgonone methyl ester metabolic process","termid":"GO:1901870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ecgonone methyl ester biosynthetic process","synonyms":[{"name":"ecgonone methyl ester anabolism","type":"exact"},{"name":"ecgonone methyl ester biosynthesis","type":"exact"},{"name":"ecgonone methyl ester formation","type":"exact"},{"name":"ecgonone methyl ester synthesis","type":"exact"}],"termid":"GO:1901872"}


id: GO:0050400
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + xylitol = ADP + 2 H+ + xylitol 5-phosphate.","definition_xrefs":["EC:2.7.1.122","RHEA:20209"],"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:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"xylitol kinase activity","secondary_identifiers":["KEGG_REACTION:R02136","MetaCyc:XYLITOL-KINASE-RXN"],"synonyms":[{"name":"ATP:xylitol 5-phosphotransferase activity","type":"related"},{"name":"xylitol phosphotransferase activity","type":"related"}],"termid":"GO:0050400"}


id: PBO:0055907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 31","termid":"PBO:0055907"}


id: PBO:0065766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptide YY 3 (pseudogene)","termid":"PBO:0065766"}


id: GO:0046332
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a SMAD signaling protein.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"SMAD binding","termid":"GO:0046332"}


id: PR:Q9C0Y4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- agl1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0Y4"],"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-glucosidase Agl1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB24D3.10c","synonyms":[{"name":"SPAPB24D3.10c","type":"related"},{"name":"Spom972h-agl1","type":"exact"},{"name":"agl","type":"related"},{"name":"maltase (Schizosaccharomyces pombe 972h-)","type":"broad"}],"termid":"PR:Q9C0Y4"}


id: GO:0141179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont avoids the effects of recognition by a host  antimicrobial peptide by altering molecules on the symbiont surface. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:11401964","PMID:25537831","PMID:22966934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated evasion of recognition by host innate immune effector","termid":"GO:0141177"}],"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 evasion of recognition by host antimicrobial peptide","termid":"GO:0141179"}


id: PBO:0026769
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_cell_surface","termid":"PBO:0026769"}


id: PBO:0062813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxysterol binding protein like 9 pseudogene 4","termid":"PBO:0062813"}


id: GO:0009918
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 5-dehydroepisterol = 24-methylenecholesterol.","definition_xrefs":["ISBN:0943088399"],"gene_count":0,"genotype_count":0,"name":"obsolete sterol delta7 reductase activity (obsolete GO:0009918)","synonyms":[{"name":"sterol delta-7 reductase activity","type":"exact"}],"termid":"GO:0009918"}


id: PBO:0018160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOG/XMAP14 family protein Alp14","termid":"PBO:0018160"}


id: GO:1990824
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that depends on magnesium in order for one or more of its components to remain a part of the complex.","definition_xrefs":["PMID:10220587"],"gene_count":0,"genotype_count":0,"name":"obsolete magnesium-dependent protein complex (obsolete GO:1990824)","termid":"GO:1990824"}


id: MONDO:0100589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital disorder of glycosylation in which the cause of the disease is a mutation in ALG10.","definition_xrefs":["PMID:33798445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"ALG10-congenital disorder of glycosylation","synonyms":[{"name":"ALG10-CDG","type":"exact"},{"name":"ALG10-congenital disorder of glycosylation","type":"exact"}],"termid":"MONDO:0100589","xrefs":{"Monarch":{"xref_id":"0100589"}}}


id: GO:0030806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of chemical reactions and pathways resulting in the breakdown of cyclic nucleotides.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cyclic nucleotide catabolic process (obsolete GO:0030806)","synonyms":[{"name":"down regulation of cyclic nucleotide catabolic process","type":"exact"},{"name":"down-regulation of cyclic nucleotide catabolic process","type":"exact"},{"name":"downregulation of cyclic nucleotide catabolic process","type":"exact"},{"name":"inhibition of cyclic nucleotide catabolic process","type":"narrow"},{"name":"negative regulation of cyclic nucleotide breakdown","type":"exact"},{"name":"negative regulation of cyclic nucleotide catabolism","type":"exact"},{"name":"negative regulation of cyclic nucleotide degradation","type":"exact"}],"termid":"GO:0030806"}


id: GO:0140841
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + RNA polymerase II large subunit CTD heptapeptide repeat (YSPTSPS) = UDP + RNA polymerase II large subunit CTD heptapeptide repeat 3-O-(N-acetyl-D-glucosaminyl)-L-serine.","definition_xrefs":["PMID:22605332"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein O-acetylglucosaminyltransferase activity","termid":"GO:0097363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0140096","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"RNA polymerase II C-terminal domain O-GlcNAc transferase activity","termid":"GO:0140841"}


id: PBO:0085401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane protein involved in protoprophyrin and heme transport; roles in the uptake of protoprophyrin IX and the efflux of heme; expression is induced under both low-heme and low-oxygen conditions; member of the fungal lipid-translocating exporter (LTE) family of proteins","termid":"PBO:0085401"}


id: PR:G2TRQ8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tam9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRQ8"],"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":"54S ribosomal protein L36, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1711.18","synonyms":[{"name":"Spom972h-tam9","type":"exact"},{"name":"transcripts altered in meiosis protein 9 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:G2TRQ8"}


id: PBO:0090204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOG/XMAP215 microtubule plus end tracking polymerase Alp14","termid":"PBO:0090204"}


id: PATO:0001009
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001009 relative latency value (obsolete PATO:0001009)","termid":"PATO:0001009"}


id: PBO:0042149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine ligand 8","termid":"PBO:0042149"}


id: GO:0047081
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: O2 + NADPH + H+ + 3-hydroxy-2-methylpyridine-5-carboxylate = NADP+ + 2-(acetamidomethylene)succinate.","definition_xrefs":["MetaCyc:1.14.12.4-RXN","EC:1.14.13.242"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","termid":"GO:0016708"}],"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":"3-hydroxy-2-methylpyridinecarboxylate dioxygenase activity","secondary_identifiers":["RHEA:10864"],"synonyms":[{"name":"2-methyl-3-hydroxypyridine 5-carboxylic acid dioxygenase activity","type":"related"},{"name":"3-hydroxy-2-methylpyridine-5-carboxylate,NADPH:oxygen oxidoreductase (decyclizing)","type":"related"},{"name":"3-hydroxy-3-methylpyridinecarboxylate dioxygenase activity","type":"related"},{"name":"methylhydroxypyridine carboxylate dioxygenase activity","type":"related"},{"name":"methylhydroxypyridinecarboxylate oxidase activity","type":"related"}],"termid":"GO:0047081"}


id: FYPO:0004402
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 JM216 (also called satraplatin). Cells stop growing (and may die) at a concentration of JM216 that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0002683","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to JM216","synonyms":[{"name":"hypersensitive to JM216","type":"exact"},{"name":"sensitive to JM216 during mitotic cell cycle","type":"related"},{"name":"sensitive to JM216 during vegetative growth","type":"exact"},{"name":"sensitive to satraplatin","type":"exact"}],"termid":"FYPO:0004402"}


id: PBO:0041019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BPI fold containing family B member 2","termid":"PBO:0041019"}


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:0055057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process resulting in the physical partitioning and separation of a neuroblast into daughter cells. A neuroblast is any cell that will divide and give rise to a neuron.","definition_xrefs":["PMID:11163136","PMID:11250167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell division","termid":"GO:0051301"},{"relation_name":"part_of","term_name":"neuroblast proliferation","termid":"GO:0007405"}],"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":"neuroblast division","synonyms":[{"name":"neuroblast cell division","type":"exact"}],"termid":"GO:0055057"}


id: PBO:0076112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin 18","termid":"PBO:0076112"}


id: PBO:0043827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleavage and polyadenylation specific factor 1","termid":"PBO:0043827"}


id: PBO:0077622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymosin beta 15A","termid":"PBO:0077622"}


id: GO:0000426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Degradation of a peroxisome by microautophagy.","definition_xrefs":["GOC:autophagy","GOC:pad","PMID:15350980","PMID:16973210","PMID:12914914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microautophagy","termid":"GO:0016237"},{"relation_name":"is_a","term_name":"autophagy of peroxisome","termid":"GO:0030242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"micropexophagy","termid":"GO:0000426"}


id: internal:systematic
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"systematic","termid":"internal:systematic"}


id: PBO:0083748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the TIM23 complex; tethers the import motor and regulatory factors (PAM complex) to the translocation channel (Tim23p-Tim17p core complex); TIM23 complex is short for the translocase of the inner mitochondrial membrane","termid":"PBO:0083748"}


id: PBO:0048954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GOT2 pseudogene 5","termid":"PBO:0048954"}


id: MONDO:1011794
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":"spastic lameness, non-human animal","secondary_identifiers":["OMIA:000926"],"termid":"MONDO:1011794","xrefs":{"Monarch":{"xref_id":"1011794"}}}


id: PBO:0030563
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_phenylalanine_level","termid":"PBO:0030563"}


id: PBO:0082572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chitin deacetylase; together with Cda2p involved in the biosynthesis ascospore wall component, chitosan; required for proper rigidity of the ascospore wall","termid":"PBO:0082572"}


id: PR:O94614
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- chr4 gene.","definition_xrefs":["UniProtKB:O94614","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":"chitin synthase regulatory factor 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1289.01c","synonyms":[{"name":"Chs four homolog 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-chr4","type":"exact"}],"termid":"PR:O94614"}


id: GO:0009849
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of indoleacetic acid, independent of tryptophan.","definition_xrefs":["GOC:lr","PMID:10375566","GOC:go_curators","GOC:lm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indoleacetic acid biosynthetic process","termid":"GO:0009684"}],"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":"tryptophan-independent indoleacetic acid biosynthetic process","synonyms":[{"name":"indoleacetic acid biosynthesis, tryptophan-independent","type":"exact"},{"name":"indoleacetic acid biosynthetic process, tryptophan-independent","type":"exact"},{"name":"tryptophan-independent IAA biosynthetic process","type":"exact"},{"name":"tryptophan-independent indoleacetic acid anabolism","type":"exact"},{"name":"tryptophan-independent indoleacetic acid biosynthesis","type":"exact"},{"name":"tryptophan-independent indoleacetic acid formation","type":"exact"},{"name":"tryptophan-independent indoleacetic acid synthesis","type":"exact"}],"termid":"GO:0009849"}


id: MONDO:0100087
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A degenerative disease of the brain that causes gradual loss of memory, judgment, and the ability to function socially. About 25% of all Alzheimer disease is familial (more than 2 people in a family have AD). When Alzheimer disease begins before 60 or 65 years of age (early-onset AD) about 60% of the cases are familial (also known as Early-onset familial AD). These cases appear to be inherited in an autosomal dominant manner.","definition_xrefs":["GARD:0000632"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alzheimer disease","termid":"MONDO:0004975"},{"relation_name":"is_a","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"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:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"familial Alzheimer disease","secondary_identifiers":["UMLS:C0276496","MEDGEN:82914"],"synonyms":[{"name":"Alzheimer disease, familial","type":"exact"},{"name":"FAD","type":"exact"},{"name":"GARD:0000632","type":"exact"}],"termid":"MONDO:0100087","xrefs":{"Monarch":{"xref_id":"0100087"}}}


id: MONDO:0002350
data:
  {"annotated_genes":["SJAG_04013","SJAG_00093","SJAG_04000","SJAG_04621","SJAG_03182","SJAG_00471","SJAG_01374","SJAG_04017","SJAG_01185","SJAG_03986","SJAG_00864","SJAG_03361","SJAG_04148","SJAG_00933"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[86913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[87717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014752"},{"annotations":[87641,87642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014817"},{"annotations":[87640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014818"},{"annotations":[88201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032580"},{"annotations":[88202,88203],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032581"},{"annotations":[88199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032582"},{"annotations":[87727,87726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026726"},{"annotations":[86830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014099"},{"annotations":[87646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrotic syndrome","termid":"MONDO:0005377"},{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00471":null,"SJAG_00864":null,"SJAG_00933":null,"SJAG_01185":null,"SJAG_01374":null,"SJAG_03182":null,"SJAG_03361":null,"SJAG_03986":null,"SJAG_04000":null,"SJAG_04013":null,"SJAG_04017":null,"SJAG_04148":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"familial nephrotic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3501848","DOID:2590","NCIT:C35337","OMIMPS:256300","MEDGEN:502251","SCTID:48796009","icd11.foundation:1524476844"],"synonyms":[{"name":"congenital nephrotic syndrome","type":"exact"},{"name":"hereditary nephrotic syndrome","type":"exact"}],"termid":"MONDO:0002350","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013836":null,"MONDO:0014099":null,"MONDO:0014257":null,"MONDO:0014752":null,"MONDO:0014817":null,"MONDO:0014818":null,"MONDO:0026726":null,"MONDO:0032580":null,"MONDO:0032581":null,"MONDO:0032582":null},"xrefs":{"Monarch":{"xref_id":"0002350"}}}


id: PBO:0111745
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C2H2 type","termid":"PBO:0111745"}


id: MONDO:0002981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A small round cell tumor with neural differentiation arising from the bone. It may be associated with pain.","definition_xrefs":["NCIT:C8776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone cancer","termid":"MONDO:0002129"},{"relation_name":"is_a","term_name":"peripheral primitive neuroectodermal tumor","termid":"MONDO:0018271"},{"relation_name":"is_a","term_name":"Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone","termid":"MONDO:0021123"}],"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":"peripheral primitive neuroectodermal tumor of bone","secondary_identifiers":["DOID:4388","UMLS:C0855009","MEDGEN:163179"],"synonyms":[{"name":"bone peripheral neuroepithelioma","type":"exact"},{"name":"bone tissue peripheral primitive neuroectodermal tumor","type":"exact"},{"name":"bone tissue peripheral primitive neuroectodermal tumour","type":"exact"},{"name":"osseous peripheral neuroepithelioma","type":"exact"},{"name":"peripheral neuroectodermal tumor of bone","type":"exact"},{"name":"peripheral neuroectodermal tumor of the bone","type":"exact"},{"name":"peripheral neuroectodermal tumour of bone","type":"exact"},{"name":"peripheral neuroectodermal tumour of the bone","type":"exact"},{"name":"peripheral neuroepithelioma of bone","type":"exact"},{"name":"peripheral neuroepithelioma of the bone","type":"exact"},{"name":"peripheral primitive neuroectodermal tumor of bone","type":"exact"},{"name":"peripheral primitive neuroectodermal tumor of bone tissue","type":"exact"},{"name":"peripheral primitive neuroectodermal tumour of bone tissue","type":"exact"}],"termid":"MONDO:0002981","xrefs":{"Monarch":{"xref_id":"0002981"}}}


id: GO:0061838
data:
  {"annotated_genes":["SJAG_02465","SJAG_05321","SJAG_02513","SJAG_00935"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[92603,110083,114141,119430],"is_not":false,"summary":null,"term":"GO:0061838"}]},"cv_name":"cellular_component","definition":"A histone-variant containing protein complex which forms a centromere specific nucleosome-like structure, involved in centromeric chromatin organization.","definition_xrefs":["PMID:22304909","PMID:22304917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"chromosome, centromeric region","termid":"GO:0000775"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00935":null,"SJAG_02465":null,"SJAG_02513":null,"SJAG_05321":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"CENP-T-W-S-X complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061838","terms_by_termid":{"GO:0061838":null}}


id: GO:0048222
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An extracellular matrix part that consists of cross-linked glycoproteins.","definition_xrefs":["PMID:18508691","PMID:7048321","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"primary cell wall","termid":"GO:0009530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005618"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005618"],"is_obsolete":false,"name":"glycoprotein network","secondary_identifiers":["Wikipedia:Extensin"],"synonyms":[{"name":"extensin","type":"exact"}],"termid":"GO:0048222"}


id: MOD:00846
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"stub","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"levuglandinyl (prostaglandin H2) adduct","termid":"MOD:00846"}


id: PBO:0035909
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_acetylation_at_centromere_during_vegetative_growth","termid":"PBO:0035909"}


id: PBO:0091268
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homomeric(1)","termid":"PBO:0091268"}


id: GO:0098823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The amidinylation of peptidyl-cysteine to form peptidyl-S-amidino-L-cysteine.","definition_xrefs":["RESID:AA0335"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-cysteine modification to S-amindino-L-cysteine (obsolete GO:0098823)","termid":"GO:0098823"}


id: PBO:0054984
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 2398","termid":"PBO:0054984"}


id: MONDO:0012260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in variation in the region 19q13.","definition_xrefs":["PMID:15671291","DOID:0110261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset nuclear cataract","termid":"MONDO:0020376"}],"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":"cataract 35","secondary_identifiers":["MESH:C563728","OMIM:609376","UMLS:C1836272","MEDGEN:373050","GARD:9492"],"synonyms":[{"name":"CATCN1","type":"exact"},{"name":"CTRCT35","type":"exact"},{"name":"autosomal recessive congenital nuclear cataract 1","type":"exact"},{"name":"cataract 35","type":"exact"},{"name":"cataract 35, congenital nuclear","type":"exact"},{"name":"cataract type 35","type":"exact"},{"name":"cataract, congenital nuclear, autosomal recessive 1","type":"related"}],"termid":"MONDO:0012260","xrefs":{"Monarch":{"xref_id":"0012260"}}}


id: GO:0050825
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to ice, water reduced to the solid state by cold temperature. It is a white or transparent colorless substance, crystalline, brittle, and viscoidal.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"ice binding","synonyms":[{"name":"ice crystal binding","type":"exact"},{"name":"ice nucleation inhibitor activity","type":"related"}],"termid":"GO:0050825"}


id: MONDO:1012395
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"rupture of the cranial cruciate ligament, non-human animal","termid":"MONDO:1011960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rupture of the cranial cruciate ligament, dog","secondary_identifiers":["OMIA:001474-9615"],"termid":"MONDO:1012395","xrefs":{"Monarch":{"xref_id":"1012395"}}}


id: GO:0042398
data:
  {"annotated_genes":["SJAG_03275","SJAG_02599","SJAG_00988","SJAG_03856","SJAG_00106","SJAG_03679","SJAG_05200","SJAG_01198","SJAG_02408","SJAG_00832","SJAG_04481","SJAG_03494","SJAG_01126","SJAG_02225","SJAG_01616","SJAG_01233","SJAG_00529","SJAG_03224","SJAG_01351","SJAG_00815","SJAG_04156"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110287,114380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009257"},{"annotations":[69991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006761"},{"annotations":[105528,113499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052699"},{"annotations":[61191,106705,108009,110288,114381,70621,57105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046656"},{"annotations":[74316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009396"},{"annotations":[110372,80535,57850,79212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006750"},{"annotations":[74122,64005,79439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015940"},{"annotations":[68727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006659"},{"annotations":[72671,105529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903257"},{"annotations":[72811,61193,57104,81582,108010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046654"},{"annotations":[69992,73968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046901"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of compounds derived from amino acids, organic acids containing one or more amino substituents.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_00529":null,"SJAG_00815":null,"SJAG_00832":null,"SJAG_00988":null,"SJAG_01126":null,"SJAG_01198":null,"SJAG_01233":null,"SJAG_01351":null,"SJAG_01616":null,"SJAG_02225":null,"SJAG_02408":null,"SJAG_02599":null,"SJAG_03224":null,"SJAG_03275":null,"SJAG_03494":null,"SJAG_03679":null,"SJAG_03856":null,"SJAG_04156":null,"SJAG_04481":null,"SJAG_05200":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modified amino acid biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"amino acid derivative biosynthetic process","type":"exact"},{"name":"cellular amino acid derivative anabolism","type":"exact"},{"name":"cellular amino acid derivative biosynthesis","type":"exact"},{"name":"cellular amino acid derivative biosynthetic process","type":"exact"},{"name":"cellular amino acid derivative formation","type":"exact"},{"name":"cellular amino acid derivative synthesis","type":"exact"},{"name":"cellular modified amino acid anabolism","type":"exact"},{"name":"cellular modified amino acid biosynthesis","type":"exact"},{"name":"cellular modified amino acid formation","type":"exact"},{"name":"cellular modified amino acid synthesis","type":"exact"}],"termid":"GO:0042398","terms_by_termid":{"GO:0006659":null,"GO:0006750":null,"GO:0006761":null,"GO:0009257":null,"GO:0009396":null,"GO:0015940":null,"GO:0046654":null,"GO:0046656":null,"GO:0046901":null,"GO:0052699":null,"GO:1903257":null}}


id: MONDO:0012135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"restless legs syndrome, susceptibility to","termid":"MONDO:0100170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restless legs syndrome, susceptibility to, 2","secondary_identifiers":["MEDGEN:324722","UMLS:C1837285","OMIM:608831"],"synonyms":[{"name":"RLS2","type":"exact"},{"name":"restless legs syndrome 2","type":"exact"},{"name":"restless legs syndrome, susceptibility to, 2","type":"exact"}],"termid":"MONDO:0012135","xrefs":{"Monarch":{"xref_id":"0012135"}}}


id: MONDO:0022759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 22 is a chromosome disorder in which an extra (third) copy of chromosome 22 is present in every cell of the body where there should normally only be two copies. This condition is commonly found in miscarriages, but only rarely in liveborn infants. Most affected individuals die shortly before or shortly after birth due to severe complications. Common features include an underdeveloped midface (midface hypoplasia)with flat/broad nasal bridge, malformed ears with pits or tags, cleft palate, hypertelorism (wide-spaced eyes), microcephaly and other cranial abnormalities, congenital heart disease, genital abnormalities, and intrauterine growth restriction (IUGR).","definition_xrefs":["GARD:0005335"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 22 disorder","termid":"MONDO:0700026"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy 22","secondary_identifiers":["MEDGEN:82711","MESH:C536799","SCTID:205655003","UMLS:C0265490","GARD:5335"],"synonyms":[{"name":"chromosome 22 trisomy","type":"related"}],"termid":"MONDO:0022759","xrefs":{"Monarch":{"xref_id":"0022759"}}}


id: MONDO:0001762
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tooth erosion, non-bacterial that involves the dentine.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tooth erosion, non-bacterial","termid":"MONDO:0002325"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dentine erosion","secondary_identifiers":["DOID:13629","MEDGEN:1843465","ICD9:521.32","UMLS:C1456162"],"synonyms":[{"name":"dentine tooth erosion, non-bacterial","type":"exact"},{"name":"tooth erosion, non-bacterial of dentine","type":"exact"}],"termid":"MONDO:0001762","xrefs":{"Monarch":{"xref_id":"0001762"}}}


id: PBO:0072050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 20","termid":"PBO:0072050"}


id: FYPO:0004614
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 microtubule polymerization, i.e. the addition of tubulin dimers to the plus end of a microtubule, is abnormal.","definition_xrefs":["GO:0046785","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-containing complex assembly","termid":"FYPO:0000447"},{"relation_name":"is_a","term_name":"abnormal microtubule dynamics during vegetative growth","termid":"FYPO:0000901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000054"],"is_obsolete":false,"name":"abnormal microtubule polymerization during vegetative growth","synonyms":[{"name":"abnormal microtubule growth","type":"exact"},{"name":"abnormal microtubule polymerisation","type":"exact"},{"name":"abnormal microtubule polymerisation during vegetative growth","type":"exact"},{"name":"abnormal microtubule polymerization during mitotic cell cycle","type":"related"},{"name":"abnormal microtubule rescue","type":"related"}],"termid":"FYPO:0004614"}


id: PR:O13783
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A programmed cell death 6-interacting protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar protein-sorting protein bro1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.05c","secondary_identifiers":["UniProtKB:O13783"],"synonyms":[{"name":"BRO domain-containing protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC17G6.05c","type":"related"},{"name":"Spom972h-PDCD6IP","type":"exact"}],"termid":"PR:O13783"}


id: PBO:0063715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PGM5P3 antisense RNA 1","termid":"PBO:0063715"}


id: GO:0017105
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an 11,12-saturated fatty acyl-CoA + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = an (11Z)-delta-11-fatty acyl-CoA + 2 Fe(III)-[cytochrome b5] + 2 H2O.","definition_xrefs":["PMID:15544945","RHEA:25852","PMID:15063718"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA desaturase activity","termid":"GO:0016215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"acyl-CoA 11-(Z)-desaturase activity","secondary_identifiers":["MetaCyc:1.14.99.32-RXN","GO:0050601","EC:1.14.19.5"],"synonyms":[{"name":"Z/E11-desaturase","type":"broad"},{"name":"acyl-CoA D11-desaturase activity","type":"exact"},{"name":"acyl-CoA delta(11)-desaturase activity","type":"exact"},{"name":"acyl-CoA delta11-(Z)-desaturase activity","type":"exact"},{"name":"acyl-CoA delta11-desaturase activity","type":"broad"},{"name":"delta(11) desaturase","type":"broad"},{"name":"delta(11)-fatty-acid desaturase","type":"broad"},{"name":"delta(11)-palmitoyl-CoA desaturase","type":"narrow"},{"name":"fatty acid delta(11)-desaturase","type":"broad"},{"name":"myristoyl-CoA 11-(Z) desaturase activity","type":"narrow"}],"termid":"GO:0017105"}


id: PBO:0030549
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_asparagine_import","termid":"PBO:0030549"}


id: PBO:0029603
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_transporter_activity","termid":"PBO:0029603"}


id: GO:0102616
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin D + NAD(P) = oryzalexin A + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin A synthase activity (obsolete GO:0102616)","termid":"GO:0102616"}


id: PBO:0029535
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_normal_volume_spheroid_vegetative_cell","termid":"PBO:0029535"}


id: FYPO:0007744
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a short spindle assembles during the first meiotic nuclear division, and may begin elongation, but does not elongate normally or completely, and collapses during prophase I. Upon collapse the spindle may break or shrink.","definition_xrefs":["PMID:32723864","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle collapse during meiosis I","termid":"FYPO:0007103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"spindle collapse during meiotic prophase I","synonyms":[{"name":"broken meiotic spindle during prophase I","type":"related"},{"name":"meiotic spindle breakage during prophase I","type":"exact"},{"name":"spindle collapse during prophase I of meiotic cell cycle","type":"related"},{"name":"spindle collapse during prophase of meiosis I","type":"exact"}],"termid":"FYPO:0007744"}


id: PBO:0040437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 8A2 pseudogene 2","termid":"PBO:0040437"}


id: MONDO:0017637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare parkinsonian syndrome due to intoxication (obsolete MONDO:0017637)","secondary_identifiers":["Orphanet:306679"],"termid":"MONDO:0017637","xrefs":{"Monarch":{"xref_id":"0017637"}}}


id: FYPO:0007357
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the cell does not contain a detectable Smp focus.","definition_xrefs":["PomBase:mah","PMID:31811152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"},{"relation_name":"is_a","term_name":"altered level of macromolecular complex","termid":"FYPO:0007316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"Smp focus absent from cell","synonyms":[{"name":"Sme2 focus absent from cell","type":"narrow"},{"name":"Smp dot complex absent from cell","type":"exact"},{"name":"Smp focus absent from cell during meiotic cell cycle","type":"exact"},{"name":"absence of Smp focus","type":"exact"},{"name":"absent Smp focus","type":"exact"}],"termid":"FYPO:0007357"}


id: FYPO:0001568
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 L-glutamate measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular glutamate level","synonyms":[{"name":"increased cellular L-glutamate level","type":"exact"},{"name":"increased cellular glutamate level during mitotic cell cycle","type":"related"},{"name":"increased cellular glutamate level during vegetative growth","type":"exact"},{"name":"increased glutamate accumulation","type":"related"}],"termid":"FYPO:0001568"}


id: GO:0031472
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An organelle found in bacteria consisting of a proteinaceous coat containing enzymes for the degradation of 1,2-propanediol whose purpose is the protection of the rest of the cell from the toxic propionaldehyde product of the enzyme diol dehydratase.","definition_xrefs":["PMID:12923081","GOC:js","PMID:10498708","PMID:11844753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial microcompartment","termid":"GO:0031469"}],"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":"propanediol degradation polyhedral organelle","termid":"GO:0031472"}


id: PBO:0041633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CACNA1C antisense RNA 3","termid":"PBO:0041633"}


id: MONDO:0042976
data:
  {"annotated_genes":["SJAG_04459","SJAG_01199","SJAG_04425","SJAG_04042"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87064,87065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[87673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[88493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"}]},"cv_name":"mondo","definition":"A condition due to deficiency in any member of the vitamin B complex. These B vitamins are water-soluble and must be obtained from the diet because they are easily lost in the urine. Unlike the lipid-soluble vitamins, they cannot be stored in the body fat.","definition_xrefs":["MESH:D014804"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin deficiency disorder","termid":"MONDO:0024298"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01199":null,"SJAG_04042":null,"SJAG_04425":null,"SJAG_04459":null},"genotype_count":0,"is_obsolete":false,"name":"vitamin B deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:22669","SCTID:47903000","NCIT:C35129","UMLS:C0042850"],"synonyms":[{"name":"deficiencies, vitamin B","type":"related"},{"name":"deficiency, vitamin B","type":"related"},{"name":"vitamin B deficiencies","type":"related"}],"termid":"MONDO:0042976","terms_by_termid":{"MONDO:0009354":null,"MONDO:0009609":null,"MONDO:0010184":null},"xrefs":{"Monarch":{"xref_id":"0042976"}}}


id: PBO:0046859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fas associated factor family member 2","termid":"PBO:0046859"}


id: GO:0046168
data:
  {"annotated_genes":["SJAG_01012","SJAG_00409"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63803,70809],"is_not":false,"summary":null,"term":"GO:0046168"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycerol-3-phosphate, a phosphoric monoester of glycerol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerol-3-phosphate metabolic process","termid":"GO:0006072"},{"relation_name":"is_a","term_name":"organophosphate catabolic process","termid":"GO:0046434"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00409":null,"SJAG_01012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glycerol-3-phosphate catabolic process","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"glycerol-3-phosphate breakdown","type":"exact"},{"name":"glycerol-3-phosphate catabolism","type":"exact"},{"name":"glycerol-3-phosphate degradation","type":"exact"}],"termid":"GO:0046168","terms_by_termid":{"GO:0046168":null}}


id: PBO:0090022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unknown protein, may bind replication origins Abp2","termid":"PBO:0090022"}


id: GO:0006184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of GTP, guanosine triphosphate.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete GTP catabolic process (obsolete GO:0006184)","synonyms":[{"name":"GTP breakdown","type":"exact"},{"name":"GTP catabolism","type":"exact"},{"name":"GTP degradation","type":"exact"},{"name":"GTP hydrolysis","type":"narrow"}],"termid":"GO:0006184"}


id: MONDO:0016076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lymphatic filariasis (obsolete MONDO:0016076)","termid":"MONDO:0016076","xrefs":{"Monarch":{"xref_id":"0016076"}}}


id: MOD:00787
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod - label for the active site serine of the serine esterase/protease family also shown to label tyrosine in serum albumin","definition_xrefs":["Unimod:362"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diisopropylphosphoserine","synonyms":[{"name":"Diisopropylphosphate","type":"related"},{"name":"O-Diisopropylphosphorylation","type":"related"}],"termid":"MOD:00787"}


id: MONDO:0045072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormal secretion of hormones in conjunction with neoplastic growth occurring anywhere in the body.","definition_xrefs":["NCIT:C4065"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplastic syndrome","termid":"MONDO:0021058"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectopic hormone secretion syndrome associated with neoplasia","secondary_identifiers":["UMLS:C0851689","MEDGEN:208863"],"synonyms":[{"name":"ectopic hormone secretion syndrome associated with neoplasia","type":"exact"},{"name":"neoplasm associated ectopic hormone secretion syndrome","type":"exact"}],"termid":"MONDO:0045072","xrefs":{"Monarch":{"xref_id":"0045072"}}}


id: MONDO:0016136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cerebellar ataxia with peripheral neuropathy (obsolete MONDO:0016136)","secondary_identifiers":["Orphanet:207028"],"termid":"MONDO:0016136","xrefs":{"Monarch":{"xref_id":"0016136"}}}


id: PBO:0077852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triosephosphate isomerase 1 pseudogene 3","termid":"PBO:0077852"}


id: GO:0046646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of gamma-delta T cell proliferation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell proliferation","termid":"GO:0042129"},{"relation_name":"is_a","term_name":"regulation of gamma-delta T cell activation","termid":"GO:0046643"},{"relation_name":"regulates","term_name":"gamma-delta T cell proliferation","termid":"GO:0046630"}],"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 gamma-delta T cell proliferation","synonyms":[{"name":"regulation of gamma-delta T lymphocyte proliferation","type":"exact"},{"name":"regulation of gamma-delta T-cell proliferation","type":"exact"},{"name":"regulation of gamma-delta T-lymphocyte proliferation","type":"exact"}],"termid":"GO:0046646"}


id: PBO:0077946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 6-1","termid":"PBO:0077946"}


id: MONDO:0021529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the chest wall.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thoracic benign neoplasm","termid":"MONDO:0000634"},{"relation_name":"is_a","term_name":"neoplasm of chest wall","termid":"MONDO:0021388"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of chest wall","secondary_identifiers":["ICD9:229.8","MEDGEN:195776","NCIT:C8529","UMLS:C0684831","SCTID:92058007"],"synonyms":[{"name":"benign chest wall neoplasm","type":"exact"},{"name":"benign chest wall tumor","type":"exact"},{"name":"benign chest wall tumour","type":"exact"},{"name":"benign neoplasm of the chest wall","type":"exact"},{"name":"benign tumor of chest wall","type":"exact"},{"name":"benign tumor of the chest wall","type":"exact"},{"name":"benign tumour of chest wall","type":"exact"},{"name":"benign tumour of the chest wall","type":"exact"},{"name":"chest wall benign neoplasm","type":"exact"}],"termid":"MONDO:0021529","xrefs":{"Monarch":{"xref_id":"0021529"}}}


id: PBO:0051316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1/OR2-118 (pseudogene)","termid":"PBO:0051316"}


id: FYPO:0003232
data:
  {"alleles_by_uniquename":{"SJAG_02621:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02621","name":"ago1delta","uniquename":"SJAG_02621:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121615,121616],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}],"single_locus_phenotype":[{"annotations":[121608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which methylation of lysine at position 9 of histone H3 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03118":null,"SJAG_03689":null},"genotype_count":3,"genotypes_by_uniquename":{"ago1delta__leo1delta":{"display_name":"ago1delta leo1delta","display_uniquename":"ago1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02621:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]},"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]},"dcr1delta__leo1delta":{"display_name":"dcr1delta leo1delta","display_uniquename":"dcr1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03689","SJAG_02621","SJAG_03118"],"name":"normal histone H3-K9 methylation during vegetative growth","references_by_uniquename":{"PMID:35226668":null},"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"normal histone H3 K9 methylation during vegetative growth","type":"exact"},{"name":"normal histone H3-K9 methylation during mitotic cell cycle","type":"related"},{"name":"normal histone H3K9me during vegetative growth","type":"exact"},{"name":"normal histone lysine H3 K9 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0003232","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0006989":null}}


id: GO:0051435
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a BH4 protein domain, present in Bcl-2 family members. All anti-apoptotic proteins contain BH1 and BH2 domains; some also contain an additional N-terminal BH4 domain, which is almost never seen in pro-apoptotic proteins. Loss of the BH4 domain can diminish or abrogate anti-apoptotic function or even impart outright death-promoting properties to the protein.","definition_xrefs":["PMID:9704409","Prosite:PS01260","Prosite:PS50063","PMID:12133724","InterPro:IPR003093","PMID:11048732","PMID:9020082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BH domain binding","termid":"GO:0051400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"BH4 domain binding","termid":"GO:0051435"}


id: GO:0060726
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate or frequency of coreceptor activity involved in epidermal growth factor receptor signaling pathway.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of coreceptor activity involved in epidermal growth factor receptor signaling pathway (obsolete GO:0060726)","synonyms":[{"name":"regulation of Neu/ErbB-2 receptor activity","type":"narrow"},{"name":"regulation of coreceptor activity involved in epidermal growth factor receptor signalling pathway","type":"exact"}],"termid":"GO:0060726"}


id: MONDO:0000540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small intestine. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.","definition_xrefs":["NCIT:C4638"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine neuroendocrine tumor, well differentiated, low or intermediate grade","termid":"MONDO:0002995"},{"relation_name":"is_a","term_name":"intestinal neuroendocrine tumor G1","termid":"MONDO:0021533"}],"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":"small intestinal neuroendocrine tumor G1","secondary_identifiers":["DOID:0050925","MEDGEN:91150","UMLS:C0349536","SCTID:276818002"],"synonyms":[{"name":"carcinoid tumor of small bowel","type":"exact"},{"name":"carcinoid tumor of small intestine","type":"exact"},{"name":"carcinoid tumor of the small bowel","type":"exact"},{"name":"carcinoid tumor of the small intestine","type":"exact"},{"name":"carcinoid tumour of small bowel","type":"exact"},{"name":"carcinoid tumour of small intestine","type":"exact"},{"name":"carcinoid tumour of the small bowel","type":"exact"},{"name":"carcinoid tumour of the small intestine","type":"exact"},{"name":"grade 1 neuroendocrine neoplasm of small intestine","type":"exact"},{"name":"small bowel carcinoid tumor","type":"exact"},{"name":"small bowel carcinoid tumour","type":"exact"},{"name":"small intestinal NET G1","type":"exact"},{"name":"small intestinal carcinoid tumor","type":"exact"},{"name":"small intestinal carcinoid tumour","type":"exact"},{"name":"small intestinal neuroendocrine tumor G1","type":"exact"},{"name":"small intestine NET G1","type":"exact"},{"name":"small intestine carcinoid neuroendocrine tumor","type":"related"},{"name":"small intestine carcinoid neuroendocrine tumour","type":"related"},{"name":"small intestine carcinoid tumor","type":"exact"},{"name":"small intestine carcinoid tumor (disease)","type":"exact"},{"name":"small intestine carcinoid tumour","type":"exact"},{"name":"small intestine carcinoid tumour (disease)","type":"exact"},{"name":"small intestine neuroendocrine neoplasm G1","type":"exact"},{"name":"small intestine neuroendocrine tumor, well differentiated, low grade","type":"exact"}],"termid":"MONDO:0000540","xrefs":{"Monarch":{"xref_id":"0000540"}}}


id: GO:0009637
data:
  {"annotated_genes":["SJAG_05242","SJAG_02860"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009785"},{"annotations":[121533,121534],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071483"}]},"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 blue light stimulus. Blue light is electromagnetic radiation with a wavelength of between 440 and 500nm.","definition_xrefs":["GOC:ai","GOC:mtg_far_red"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to light stimulus","termid":"GO:0009416"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02860":null,"SJAG_05242":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to blue light","references_by_uniquename":{"GO_REF:0000108":null,"PMID:23873862":null},"synonyms":[{"name":"blue light response","type":"exact"},{"name":"blue-light response","type":"exact"},{"name":"response to blue light stimulus","type":"exact"}],"termid":"GO:0009637","terms_by_termid":{"GO:0009785":null,"GO:0071483":null}}


id: PBO:0070070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 27, pseudogene","termid":"PBO:0070070"}


id: GO:0004919
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-9 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"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":"interleukin-9 receptor activity","synonyms":[{"name":"IL-9 receptor activity","type":"exact"},{"name":"IL-9R","type":"exact"}],"termid":"GO:0004919"}


id: MOD:01386
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-valine residue to 3-hydroxy-L-valine.","definition_xrefs":["ChEBI:141793","PubMed:7328054","RESID:AA0463"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroxylated residue","termid":"MOD:00677"},{"relation_name":"is_a","term_name":"modified L-valine residue","termid":"MOD:00920"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxy-L-valine","synonyms":[{"name":"(2S)-2-amino-3-hydroxy-3-methylbutanoic acid","type":"exact"},{"name":"3-hydroxy-L-valine","type":"exact"},{"name":"3-hydroxyvaline","type":"exact"},{"name":"3HyVal","type":"exact"},{"name":"MOD_RES 3-hydroxyvaline","type":"exact"}],"termid":"MOD:01386"}


id: GO:0046912
data:
  {"annotated_genes":["SJAG_02841","SJAG_04688","SJAG_04499","SJAG_01922"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003852"},{"annotations":[101344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036440"},{"annotations":[78002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004410"},{"annotations":[81912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004421"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an acyl group from one compound (donor) to another (acceptor), with the acyl group being converted into alkyl on transfer.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity","termid":"GO:0016746"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01922":null,"SJAG_02841":null,"SJAG_04499":null,"SJAG_04688":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"acyltransferase activity, acyl groups converted into alkyl on transfer","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:2.3.3.-"],"synonyms":[{"name":"acyltransferase, acyl groups converted into alkyl on transfer","type":"exact"},{"name":"transferase activity, transferring acyl groups, acyl groups converted into alkyl on transfer","type":"exact"}],"termid":"GO:0046912","terms_by_termid":{"GO:0003852":null,"GO:0004410":null,"GO:0004421":null,"GO:0036440":null}}


id: PBO:0052444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kruppel like factor 2 pseudogene 1","termid":"PBO:0052444"}


id: PBO:0056549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCHR2 antisense RNA 1","termid":"PBO:0056549"}


id: GO:0008224
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Inhibits the growth of, or directly kills, Gram-positive bacterial cells.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete Gram-positive antibacterial peptide activity (obsolete GO:0008224)","synonyms":[{"name":"Gram-positive antibacterial peptide activity","type":"exact"}],"termid":"GO:0008224"}


id: GO:0016324
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of the plasma membrane located at the apical end of the cell.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"},{"relation_name":"part_of","term_name":"apical part of cell","termid":"GO:0045177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"apical plasma membrane","termid":"GO:0016324"}


id: PBO:0048789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit alpha i2","termid":"PBO:0048789"}


id: PBO:0032767
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ark1 kinase consensus phosphorylation site is [RK]-X-[ST]","termid":"PBO:0032767"}


id: PBO:0113415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosome biogenesis factor; methyltransferase that methylates residue G1575 of 18S rRNA; required for rRNA processing and nuclear export of 40S ribosomal subunits independently of methylation activity; required for recruitment of Rps2p; functions with DEAH-box RNA helicase Ecm16p; diploid mutant displays random budding pattern; functional homolog of human WBSCR22","termid":"PBO:0113415"}


id: GO:0036013
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outer, i.e. cytoplasm-facing, lipid bilayer of the cyanelle envelope.","definition_xrefs":["GOC:aa"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid outer membrane","termid":"GO:0009527"},{"relation_name":"is_a","term_name":"cyanelle membrane","termid":"GO:0033113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cyanelle outer membrane","termid":"GO:0036013"}


id: GO:1905620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of alpha-(1->3)-fucosyltransferase activity.","definition_xrefs":["GOC:TermGenie","PMID:15364955","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of alpha-(1->3)-fucosyltransferase activity (obsolete GO:1905620)","synonyms":[{"name":"down regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"down regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"down regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"down regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"down-regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"down-regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"down-regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"down-regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"downregulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"downregulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"downregulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"downregulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"inhibition of alpha(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"inhibition of alpha-(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"inhibition of alpha-(1->3)-fucosyltransferase activity","type":"narrow"},{"name":"inhibition of alpha-1,3-fucosyltransferase activity","type":"narrow"},{"name":"negative regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"negative regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"negative regulation of alpha-1,3-fucosyltransferase activity","type":"exact"}],"termid":"GO:1905620"}


id: PBO:0081664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 586","termid":"PBO:0081664"}


id: MONDO:0003725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic disorder characterized by epithelial and/or myoepithelial tissue growth in the breast lobules. It may be associated with apocrine changes or sclerosis.","definition_xrefs":["NCIT:C3484"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast adenosis","secondary_identifiers":["EFO:0006891","DOID:5998","MEDGEN:39336","MESH:D005348","UMLS:C0085750"],"synonyms":[{"name":"adenosis","type":"broad"},{"name":"adenosis - breast","type":"exact"},{"name":"adenosis of breast","type":"exact"},{"name":"adenosis of the breast","type":"exact"},{"name":"breast adenosis","type":"exact"},{"name":"microglandular adenosis","type":"related"}],"termid":"MONDO:0003725","xrefs":{"Monarch":{"xref_id":"0003725"}}}


id: FYPO:0005499
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 occurs to a lower extent than normal during a cellular response to miconazole.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0000294","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased transcription from CRE promoter during cellular response to miconazole","synonyms":[{"name":"decreased transcription from CRE promoter during cellular response to miconazole during mitotic cell cycle","type":"related"},{"name":"decreased transcription from CRE promoter during cellular response to miconazole during vegetative growth","type":"exact"},{"name":"expression of CRE target genes decreased during cellular response to miconazole","type":"related"}],"termid":"FYPO:0005499"}


id: PBO:0058976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloid leukemia factor 2","termid":"PBO:0058976"}


id: GO:0038014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which internalization of an insulin receptor stops, prevents, or reduces the frequency, rate or extent of insulin receptor signal transduction. Internalization of insulin in association with its receptor clears insulin from the circulation and is necessary for subsequent insulin dissociation from the receptor and insulin degradation.","definition_xrefs":["PMID:7821727","GOC:bf","PMID:18492485","PMID:7978876","PMID:9609114","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction by receptor internalization","termid":"GO:0038011"},{"relation_name":"is_a","term_name":"insulin receptor internalization","termid":"GO:0038016"},{"relation_name":"is_a","term_name":"negative regulation of insulin receptor signaling pathway","termid":"GO:0046627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0016192","GO:0051179","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of insulin receptor signaling pathway by insulin receptor internalization","synonyms":[{"name":"agonist-stimulated insulin receptor internalization","type":"broad"},{"name":"negative regulation of insulin receptor signalling pathway by insulin receptor internalization","type":"exact"}],"termid":"GO:0038014"}


id: FYPO:0002238
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 cerulenin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000003","FYPO:0002060","FYPO:0002057","FYPO:0000139","FYPO:0002058"],"is_obsolete":false,"name":"normal growth on cerulenin","synonyms":[{"name":"normal cell population growth in presence of cerulenin","type":"exact"},{"name":"normal cell population growth on cerulenin","type":"exact"},{"name":"normal cellular response to cerulenin","type":"related"},{"name":"normal vegetative cell population growth on cerulenin","type":"exact"}],"termid":"FYPO:0002238"}


id: PBO:0052069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine acetyltransferase 8","termid":"PBO:0052069"}


id: GO:1901699
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 nitrogen compound stimulus.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"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 nitrogen compound","synonyms":[{"name":"cellular response to nitrogen molecular entity","type":"exact"}],"termid":"GO:1901699"}


id: GO:0034822
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: citronellal + NAD+ + OH- = citronellate + NADH + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete citronellal dehydrogenase activity (obsolete GO:0034822)","termid":"GO:0034822"}


id: MONDO:0020577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that arises from the testis or ovary and occurs during childhood.","definition_xrefs":["NCIT:C114801"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood germ cell tumor","termid":"MONDO:0003751"},{"relation_name":"is_a","term_name":"gonadal germ cell tumor","termid":"MONDO:0018202"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood gonadal germ cell tumor","secondary_identifiers":["MEDGEN:859251","UMLS:C3899657"],"synonyms":[{"name":"childhood gonadal germ cell tumor","type":"exact"},{"name":"gonadal germ cell tumor of childhood","type":"exact"},{"name":"gonadal germ cell tumour of childhood","type":"exact"},{"name":"paediatric gonadal germ cell tumour","type":"exact"},{"name":"pediatric gonadal germ cell tumor","type":"exact"}],"termid":"MONDO:0020577","xrefs":{"Monarch":{"xref_id":"0020577"}}}


id: PBO:0061217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein 8 pseudogene 1","termid":"PBO:0061217"}


id: GO:0072354
data:
  {"annotated_genes":["SJAG_00678"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80017],"is_not":false,"summary":null,"term":"GO:0072354"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H3-threonine (position 3) + ATP = histone H3-phosphothreonine (position 3) + ADP. This reaction is the addition of a phosphate group to the threonine residue at position 3 of histone H3.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"},{"relation_name":"is_a","term_name":"histone H3 kinase activity","termid":"GO:0140996"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00678":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"}],"interesting_parent_ids":["GO:0003674","GO:0004672","GO:0016301","GO:0140096","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"histone H3T3 kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"histone H3-T3 kinase activity","type":"exact"},{"name":"histone kinase activity (H3-T3 specific)","type":"exact"},{"name":"histone threonine kinase activity (H3-T3 specific)","type":"exact"},{"name":"histone-threonine kinase activity (H3-T3 specific)","type":"exact"}],"termid":"GO:0072354","terms_by_termid":{"GO:0072354":null}}


id: MONDO:0012422
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing type 1 diabetes mellitus that has material basis in mutation of the locus at chromosome 2q24.3.","definition_xrefs":["DOID:0110756","MONDO:patterns/inherited_susceptibility","PMID:16699517"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","termid":"MONDO:0010255"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus 19","secondary_identifiers":["UMLS:C1857808","MEDGEN:346669","OMIM:610155","MESH:C565715"],"synonyms":[{"name":"IDDM19","type":"exact"},{"name":"diabetes mellitus, insulin-dependent, 19","type":"related"},{"name":"insulin-dependent diabetes mellitus 19","type":"exact"}],"termid":"MONDO:0012422","xrefs":{"Monarch":{"xref_id":"0012422"}}}


id: FYPO:0000725
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 methyl methanesulfonate than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0002682","FYPO:0001985","FYPO:0000139"],"is_obsolete":false,"name":"resistance to methyl methanesulfonate","synonyms":[{"name":"resistance to MMS","type":"exact"},{"name":"resistance to methyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"resistance to methyl methanesulfonate during vegetative growth","type":"exact"},{"name":"resistance to methyl methanesulphonate","type":"exact"},{"name":"resistant to methyl methanesulfonate","type":"exact"}],"termid":"FYPO:0000725"}


id: GO:0061820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A telomere loop disassembly process that results in the disassembly of telomeric D-loops. A telomeric D-loop is a three-stranded DNA displacement loop that forms at the site where the telomeric 3' single-stranded DNA overhang (formed of the repeat sequence TTAGGG in mammals) is tucked back inside the double-stranded component of telomeric DNA molecule, thus forming a t-loop or telomeric-loop and protecting the chromosome terminus.","definition_xrefs":["PMID:10338204","GOC:BHF","PMID:24012755","GOC:BHF_telomere","GOC:nc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomeric loop disassembly","termid":"GO:0090657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0032200","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"telomeric D-loop disassembly","termid":"GO:0061820"}


id: MONDO:1012814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypogonadism characterized by dysfunctional GnRH release leading to low blood testosterone and pituitary hormone levels and impaired testicular function that occurs in cats due to a mutation in the TAC3 gene.","definition_xrefs":["PMID:31615056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadism, non-human animal","termid":"MONDO:1010276"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism, TAC3-related, domestic cat","secondary_identifiers":["OMIA:002219-9685"],"synonyms":[{"name":"testicular hypoplasia and persistent primary dentition, domestic cat","type":"related"}],"termid":"MONDO:1012814","xrefs":{"Monarch":{"xref_id":"1012814"}}}


id: FYPO:0002344
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 phleomycin. Cells stop growing (and may die) at a concentration of phleomycin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to DNA damaging agents","termid":"FYPO:0000266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000003","FYPO:0001985","FYPO:0002683","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to phleomycin","synonyms":[{"name":"hypersensitive to phleomycin","type":"exact"},{"name":"sensitive to phleomycin during mitotic cell cycle","type":"related"},{"name":"sensitive to phleomycin during vegetative growth","type":"exact"}],"termid":"FYPO:0002344"}


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


id: GO:0140425
data:
  {"annotated_genes":["SJAG_00057"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112602],"is_not":false,"summary":null,"term":"GO:0140425"}]},"cv_name":"biological_process","definition":"The directed movement of galactose from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:21621292","PMID:23254763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactose transmembrane transport","termid":"GO:0015757"},{"relation_name":"is_a","term_name":"hexose import across plasma membrane","termid":"GO:0140271"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00057":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"galactose import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140425","terms_by_termid":{"GO:0140425":null}}


id: PBO:0012255
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetratrico peptide repeat","termid":"PBO:0012255"}


id: PBO:0071529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 32","termid":"PBO:0071529"}


id: GO:0140719
data:
  {"annotated_genes":["SJAG_00961","SJAG_03997","SJAG_00142","SJAG_02594","SJAG_03844","SJAG_00058","SJAG_00769","SJAG_02401","SJAG_02416","SJAG_01075","SJAG_04942","SJAG_03543","SJAG_00756","SJAG_01008","SJAG_02725","SJAG_04253","SJAG_02621","SJAG_01601","SJAG_02311","SJAG_03356","SJAG_04061","SJAG_02592","SJAG_00676","SJAG_00302","SJAG_00934","SJAG_04039","SJAG_02846","SJAG_00341","SJAG_00266","SJAG_00087","SJAG_00414","SJAG_01675","SJAG_04141","SJAG_03042","SJAG_04574","SJAG_00335","SJAG_01599","SJAG_04030","SJAG_03689","SJAG_00160","SJAG_03680","SJAG_03128","SJAG_04186","SJAG_02342","SJAG_03982","SJAG_03624","SJAG_01540","SJAG_03193","SJAG_02119","SJAG_02409","SJAG_02778","SJAG_01579","SJAG_03916","SJAG_02576"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115575],"is_not":false,"summary":null,"term":"GO:0140719"},{"annotations":[96194,100127,74168,114593,113233,94667,110098,114592,64581,61226,106096,93911,95286,92036,95926,104681,105995,115264,114072,115964,116401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[93017],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[112297,96220,93018],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[99058,102189],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[101005,93106,120095,119689,94596,113170,105998,96196,114074,114176,109913,106097,95927,115266,73410,98603,115643,115966,101444,117406,120828,119978,117967,61225,110100,113234,97383,112440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[112610,120097,97201,93107,95939,98604,119979,116548,117969,113171,90594,101446,112442,115644,90651,120829,101006,116286,108479,117407,119690,114177],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[96197,114076,61227,93108,120098,92037,60393,113235,115645,120830,112443,115267,105999,93914,100128,95928,110101,74169,114178,115968,79121,98605,119691,101007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[118524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"}]},"cv_name":"biological_process","definition":"The compaction of chromatin into heterochromatin, a conformation that is refractory to transcription. Constitutive heterochromatin cannot be converted back to euchromatin, the transcriptionally-active conformation. In metazoa, this involves the methylation of histone H3K9.","definition_xrefs":["PMID:17936700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heterochromatin formation","termid":"GO:0031507"}],"gene_count":54,"genes_by_uniquename":{"SJAG_00058":null,"SJAG_00087":null,"SJAG_00142":null,"SJAG_00160":null,"SJAG_00266":null,"SJAG_00302":null,"SJAG_00335":null,"SJAG_00341":null,"SJAG_00414":null,"SJAG_00676":null,"SJAG_00756":null,"SJAG_00769":null,"SJAG_00934":null,"SJAG_00961":null,"SJAG_01008":null,"SJAG_01075":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01675":null,"SJAG_02119":null,"SJAG_02311":null,"SJAG_02342":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02416":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02621":null,"SJAG_02725":null,"SJAG_02778":null,"SJAG_02846":null,"SJAG_03042":null,"SJAG_03128":null,"SJAG_03193":null,"SJAG_03356":null,"SJAG_03543":null,"SJAG_03624":null,"SJAG_03680":null,"SJAG_03689":null,"SJAG_03844":null,"SJAG_03916":null,"SJAG_03982":null,"SJAG_03997":null,"SJAG_04030":null,"SJAG_04039":null,"SJAG_04061":null,"SJAG_04141":null,"SJAG_04186":null,"SJAG_04253":null,"SJAG_04574":null,"SJAG_04942":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006325"],"is_obsolete":false,"name":"constitutive heterochromatin formation","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"constitutive heterochromatin assembly","type":"exact"}],"termid":"GO:0140719","terms_by_termid":{"GO:0030466":null,"GO:0031508":null,"GO:0031509":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0140719":null,"GO:0140727":null,"GO:0141005":null}}


id: MONDO:0018839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of schizencephaly that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schizencephaly","termid":"MONDO:0010011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"acquired schizencephaly","secondary_identifiers":["MEDGEN:1825983","GARD:17879","UMLS:C5681246","Orphanet:485275"],"synonyms":[{"name":"acquired schizencephaly","type":"exact"}],"termid":"MONDO:0018839","xrefs":{"Monarch":{"xref_id":"0018839"}}}


id: PBO:0046779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EXTL3 antisense RNA 1","termid":"PBO:0046779"}


id: GO:0075164
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism stops, prevents, or reduces the frequency, rate or extent of its symbiont G-protein beta subunit-mediated signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of G-protein beta subunit-mediated signal transduction in response to host (obsolete GO:0075164)","synonyms":[{"name":"negative regulation of symbiont G-protein beta subunit-mediated signal transduction in response to host","type":"exact"}],"termid":"GO:0075164"}


id: GO:0160022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a substance by a cell or a tissue by discharging a portion of the secreting cell when intracellular components are freed into a lumen through the shedding of whole pieces of the cytoplasm.","definition_xrefs":["PMID:25960390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretion","termid":"GO:0046903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"apocrine secretion","synonyms":[{"name":"secretion by cell decapitation","type":"related"},{"name":"secretion by membrane budding","type":"related"}],"termid":"GO:0160022"}


id: PBO:0091132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial LYR family protein","termid":"PBO:0091132"}


id: MONDO:0020396
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anomaly of the tricuspid valve chordae is a rare, congenital anomaly of the tricuspid subvalvular apparatus characterized by aberrant tendinous chords, which insert at the clear zone of the leaflet instead of its free edge and connect to the endocardium instead of the papillary muscles. Resulting tethering of one or more tricuspid leaflets leads to their impaired mobility and tricuspid regurgitation. Association with other congenital cardiac anomalies has been reported.","definition_xrefs":["Orphanet:99055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital tricuspid malformation","termid":"MONDO:0020289"}],"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":"anomaly of the tricuspid valve chordae","secondary_identifiers":["GARD:19623","MEDGEN:757566","UMLS:C3165162"],"termid":"MONDO:0020396","xrefs":{"Monarch":{"xref_id":"0020396"}}}


id: GO:0004481
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + phospholipid olefinic fatty acid = S-adenosyl-L-homocysteine + phospholipid methylene fatty acid.","definition_xrefs":["EC:2.1.1.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016741","GO:0003674"],"is_obsolete":false,"name":"methylene-fatty-acyl-phospholipid synthase activity","secondary_identifiers":["RHEA:17549","MetaCyc:2.1.1.16-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:unsaturated-phospholipid methyltransferase (methenylating)","type":"related"},{"name":"cyclopropane synthetase activity","type":"broad"},{"name":"unsaturated-phospholipid methyltransferase activity","type":"broad"}],"termid":"GO:0004481"}


id: MONDO:0010377
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"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":"myopia 13, X-linked","secondary_identifiers":["OMIM:300613","UMLS:C1845096","MESH:C564473","MEDGEN:335097"],"synonyms":[{"name":"MYP13","type":"exact"},{"name":"myopia 13","type":"exact"},{"name":"myopia 13, X-linked","type":"exact"}],"termid":"MONDO:0010377","xrefs":{"Monarch":{"xref_id":"0010377"}}}


id: PR:O42939
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A SUMO-activating enzyme subunit 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10953: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":"ubiquitin-activating enzyme E1-like (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16H5.03c","secondary_identifiers":["UniProtKB:O42939"],"synonyms":[{"name":"SPBC16H5.03c","type":"related"},{"name":"Spom972h-UBA2","type":"exact"},{"name":"pmt3-activating enzyme subunit 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42939"}


id: MONDO:0007689
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":"guanylate kinase 3","secondary_identifiers":["OMIM:139290","UMLS:C1841763","MEDGEN:331129"],"synonyms":[{"name":"GUK3","type":"related"},{"name":"guanylate KINASE 3","type":"related"},{"name":"guanylate kinase 3","type":"exact"},{"name":"guanylate kinase type 3","type":"exact"}],"termid":"MONDO:0007689","xrefs":{"Monarch":{"xref_id":"0007689"}}}


id: GO:0006040
data:
  {"annotated_genes":["SJAG_02845","SJAG_00978","SJAG_01443","SJAG_04728","SJAG_00442","SJAG_04868","SJAG_00620","SJAG_00519","SJAG_03723"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80124,112001,73683,75995,72736,76205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006031"},{"annotations":[68421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006032"},{"annotations":[72737,73684,68662,58443,78373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006048"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving any amino sugar, sugars containing an amino group in place of a hydroxyl group.","definition_xrefs":["GOC:jl","ISBN:0192801023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00442":null,"SJAG_00519":null,"SJAG_00620":null,"SJAG_00978":null,"SJAG_01443":null,"SJAG_02845":null,"SJAG_03723":null,"SJAG_04728":null,"SJAG_04868":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"amino sugar metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"amino sugar metabolism","type":"exact"},{"name":"aminosaccharide metabolic process","type":"exact"},{"name":"aminosaccharide metabolism","type":"exact"}],"termid":"GO:0006040","terms_by_termid":{"GO:0006031":null,"GO:0006032":null,"GO:0006048":null}}


id: PBO:0059997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 17","termid":"PBO:0059997"}


id: PBO:0061500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropilin 2","termid":"PBO:0061500"}


id: PBO:0005872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Lysine, mitochondrial","termid":"PBO:0005872"}


id: MONDO:0020406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complete atrioventricular canal","termid":"MONDO:0015273"}],"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":"complete atrioventricular canal-left heart obstruction syndrome","secondary_identifiers":["Orphanet:99066"],"synonyms":[{"name":"CAVC type A","type":"exact"},{"name":"CAVC-left heart obstruction syndrome","type":"exact"},{"name":"complete atrioventricular canal type A","type":"exact"}],"termid":"MONDO:0020406","xrefs":{"Monarch":{"xref_id":"0020406"}}}


id: PBO:0067231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 302, pseudogene","termid":"PBO:0067231"}


id: PBO:0039279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 8, pseudogene","termid":"PBO:0039279"}


id: GO:0071379
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 prostagladin stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to hormone stimulus","termid":"GO:0032870"},{"relation_name":"is_a","term_name":"response to prostaglandin","termid":"GO:0034694"},{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"}],"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 prostaglandin stimulus","termid":"GO:0071379"}


id: PBO:0068872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 112, pseudogene","termid":"PBO:0068872"}


id: PBO:0017947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"supeoxide dismutase, mitochondrial ribosomal protein subunit (predicted)","termid":"PBO:0017947"}


id: PBO:0086102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for actin organization and passage through Start; highly conserved nuclear protein; required for actin cytoskeleton organization; plays a critical role in G1 events; binds Nap1p; involved in 60S ribosome biogenesis","termid":"PBO:0086102"}


id: GO:0008879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-glucose 1-phosphate + dTTP = diphosphate + dTDP-glucose.","definition_xrefs":["RHEA:15225","EC:2.7.7.24"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotidyltransferase activity","termid":"GO:0016779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016779","GO:0003824"],"is_obsolete":false,"name":"glucose-1-phosphate thymidylyltransferase activity","secondary_identifiers":["KEGG_REACTION:R02328","MetaCyc:DTDPGLUCOSEPP-RXN"],"synonyms":[{"name":"TDP-glucose pyrophosphorylase activity","type":"related"},{"name":"dTDP-glucose diphosphorylase activity","type":"related"},{"name":"dTDP-glucose pyrophosphorylase activity","type":"related"},{"name":"dTDP-glucose synthase activity","type":"related"},{"name":"dTTP:alpha-D-glucose-1-phosphate thymidylyltransferase activity","type":"related"},{"name":"glucose 1-phosphate thymidylyltransferase activity","type":"related"},{"name":"thymidine diphosphate glucose pyrophosphorylase activity","type":"related"},{"name":"thymidine diphosphoglucose pyrophosphorylase activity","type":"related"}],"termid":"GO:0008879"}


id: PBO:0061452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor subfamily 4 group A member 3","termid":"PBO:0061452"}


id: MONDO:0044675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRP5-related primary osteoporosis","secondary_identifiers":["GARD:22031","UMLS:C5567241","MEDGEN:1798664","Orphanet:498481"],"termid":"MONDO:0044675","xrefs":{"Monarch":{"xref_id":"0044675"}}}


id: PBO:0000156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate mutase family","termid":"PBO:0000156"}


id: GO:1903619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of transdifferentiation.","definition_xrefs":["PMID:22118091","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of transdifferentiation","termid":"GO:1903618"},{"relation_name":"negatively_regulates","term_name":"transdifferentiation","termid":"GO:0060290"}],"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 transdifferentiation","synonyms":[{"name":"down regulation of transdifferentiation","type":"exact"},{"name":"down-regulation of transdifferentiation","type":"exact"},{"name":"downregulation of transdifferentiation","type":"exact"},{"name":"inhibition of transdifferentiation","type":"narrow"}],"termid":"GO:1903619"}


id: PBO:0091751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal cell surface protein, Kre9/Knh1 family, Knh4","termid":"PBO:0091751"}


id: PATO:0001252
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of grey color and high brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grey","termid":"PATO:0000950"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light grey","termid":"PATO:0001252"}


id: MONDO:0007036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic syndrome featuring connective tissue abnormalities. Clinical signs include brachycephaly, arachnodactyly, receding mandible and joint laxity at the hands and feet.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Achard syndrome","secondary_identifiers":["DOID:6686","UMLS:C1332135","MEDGEN:272277","NCIT:C35809","MESH:C536012","OMIM:100700"],"synonyms":[{"name":"Achard syndrome","type":"exact"},{"name":"arachnodactyly, receding lower jaw and joint laxity of hands/feet","type":"related"}],"termid":"MONDO:0007036","xrefs":{"Monarch":{"xref_id":"0007036"}}}


id: GO:0015771
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of trehalose into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Trehalose is a disaccharide that consists of two molecules of glucose and is isomeric with sucrose.","definition_xrefs":["PMID:17606922","GOC:ai","PMID:20035867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide transport","termid":"GO:0015766"}],"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:0008150","GO:0006810"],"is_obsolete":false,"name":"trehalose transport","termid":"GO:0015771"}


id: GO:0002745
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Antigen processing and presentation which is initiated by uptake of antigen bound to a cell surface receptor.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation","termid":"GO:0019882"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"antigen processing and presentation initiated by receptor mediated uptake of antigen","termid":"GO:0002745"}


id: PBO:0061163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear-encoded mitochondrial tRNA-Leu (TAA) 1-1","termid":"PBO:0061163"}


id: MONDO:1010423
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paroxysmal dyskinesia that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paroxysmal dyskinesia, non-human animal","termid":"MONDO:1010004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paroxysmal dyskinesia, domestic cat","secondary_identifiers":["OMIA:001543-9685"],"termid":"MONDO:1010423","xrefs":{"Monarch":{"xref_id":"1010423"}}}


id: GO:0051419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to nebulin, a large protein (approximately 800kD) that is anchored at the Z-disc by its C-terminal region and spans the length of the thin filament, ending at the edge of the H-zone.","definition_xrefs":["PMID:11699871"],"gene_count":0,"genotype_count":0,"name":"obsolete nebulin binding (obsolete GO:0051419)","synonyms":[{"name":"nebulin binding","type":"exact"}],"termid":"GO:0051419"}


id: MONDO:0800374
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"catecholaminergic polymorphic ventricular tachycardia","termid":"MONDO:0017990"}],"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":"ventricular tachycardia, catecholaminergic polymorphic 6","secondary_identifiers":["MEDGEN:1712279","UMLS:C5394069"],"synonyms":[{"name":"CPVT6","type":"exact"}],"termid":"MONDO:0800374","xrefs":{"Monarch":{"xref_id":"0800374"}}}


id: PBO:0027983
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_small_cell_with_abnormal_septum_morphology","termid":"PBO:0027983"}


id: MONDO:0015675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distomatosis is a group of parasitoses caused by flat worms that live in contact with epitheliums. Clinical classification depends on the organ infected by the adult parasite: liver, lungs, or intestines.","definition_xrefs":["Orphanet:1685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distomatosis","secondary_identifiers":["GARD:1891","ICD9:121.9","ICD9:121.8","MEDGEN:21251","SCTID:26089000","UMLS:C0040820"],"synonyms":[{"name":"distomiasis","type":"exact"},{"name":"fluke infection","type":"exact"}],"termid":"MONDO:0015675","xrefs":{"Monarch":{"xref_id":"0015675"}}}


id: GO:1902282
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a potassium ion by a voltage-gated channel through the plasma membrane of a ventricular cardiomyocyte contributing to the repolarization phase of an action potential. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["PMID:8528244","GOC:BHF","GOC:rl","GOC:mtg_cardiac_conduct_nov11","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization","termid":"GO:0086008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization","synonyms":[{"name":"voltage gated potassium channel activity involved in ventricular cardiac muscle cell action potential","type":"narrow"},{"name":"voltage-dependent potassium channel activity involved in ventricular cardiac muscle cell action potential","type":"exact"},{"name":"voltage-gated potassium ion channel activity involved in ventricular cardiac muscle cell action potential","type":"exact"},{"name":"voltage-sensitive potassium channel involved in ventricular cardiac muscle cell action potential","type":"exact"}],"termid":"GO:1902282"}


id: GO:0060244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of cell proliferation in response to cell density.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"part_of","term_name":"contact inhibition","termid":"GO:0060242"}],"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 proliferation involved in contact inhibition","termid":"GO:0060244"}


id: PBO:0083947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gamma subunit of C-terminal domain kinase I; CTDK-I phosphorylates RNA polymerase II subunit Rpo21p to affect transcription and pre-mRNA 3' end processing, and also phosphorylates ribosomal protein Rps2p to increase translational fidelity; protein abundance increases in response to DNA replication stress","termid":"PBO:0083947"}


id: PBO:0079036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon AAC) 5-1","termid":"PBO:0079036"}


id: PBO:0046014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 2 alpha kinase 1","termid":"PBO:0046014"}


id: PBO:0047183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 201 member A","termid":"PBO:0047183"}


