# terms

id: PBO:0087170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II largest subunit B220; part of central core; phosphorylation of C-terminal heptapeptide repeat domain regulates association with transcription and splicing factors; similar to bacterial beta-prime","termid":"PBO:0087170"}


id: GO:0045138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the adult male tail tip is generated and organized. In some species of rhabitid nematodes, the male tail tip undergoes a morphological change such that the most posterior hypodermal cells in the tail (hyp8-11 in C. elegans) fuse and retract anteriorly, changing the shape of the tail from a pointed, tapered cone, or spike, to a rounded, blunt dome.","definition_xrefs":["PMID:21408209","PMID:7409314","GOC:kmv","PMID:16806150","PMID:18050419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male anatomical structure morphogenesis","termid":"GO:0090598"}],"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":"nematode male tail tip morphogenesis","synonyms":[{"name":"male tail morphogenesis","type":"broad"},{"name":"male tail tip morphogenesis","type":"related"},{"name":"tail tip morphogenesis","type":"related"}],"termid":"GO:0045138"}


id: PBO:0112000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,2-mannosyltransferase Omh5","termid":"PBO:0112000"}


id: PBO:0079458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminal uridylyl transferase 7","termid":"PBO:0079458"}


id: GO:0009510
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A tightly wound cylinder of membrane that is located within the plasmodesmal pore and runs the length of the plasmodesma. The desmotubule likely provides a rigid stability to plasmodesmata and confers a fixed diameter and pore size to the plasmodesmal canal, and is linked to the endoplasmic reticulum in each of the adjacent cell.","definition_xrefs":["PMID:29880547"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"endoplasmic reticulum","termid":"GO:0005783"},{"relation_name":"part_of","term_name":"plasma membrane","termid":"GO:0005886"},{"relation_name":"part_of","term_name":"plasmodesma","termid":"GO:0009506"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0005886","GO:0005737","GO:0005575","GO:0005783"],"is_obsolete":false,"name":"plasmodesmatal desmotubule","secondary_identifiers":["GO:0009572"],"synonyms":[{"name":"desmotubule central rod","type":"related"}],"termid":"GO:0009510"}


id: MONDO:0012126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Avascular necrosis of femoral head (ANFH) is a severely disabling disease characterized by progressive groin pain, a limping gait, leg length discrepancy, collapse of the subchondral bone, limitation of hip function and eventual degeneration of the hip joint requiring total hip arthroplasty.","definition_xrefs":["Orphanet:86820"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete type 2 collagen-related bone disorder (obsolete MONDO:0019686)","termid":"MONDO:0019686"},{"relation_name":"is_a","term_name":"primary avascular necrosis","termid":"MONDO:0018379"},{"relation_name":"is_a","term_name":"osteonecrosis of genetic origin","termid":"MONDO:0018383"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial avascular necrosis of femoral head","secondary_identifiers":["NCIT:C35480","SCTID:715657008","UMLS:C4275066","icd11.foundation:1216860745","OMIMPS:608805","GARD:10914","MESH:D005271","NANDO:1200373","MEDGEN:909851"],"synonyms":[{"name":"ANFH","type":"related"},{"name":"ANFH1","type":"related"},{"name":"aseptic Necrosis of femoral head","type":"exact"},{"name":"aseptic Necrosis of head of femur","type":"exact"},{"name":"avascular NECROSIS of femoral head, primary","type":"related"},{"name":"avascular NECROSIS of femoral head, primary, 1","type":"related"},{"name":"avascular Necrosis of femoral head, primary, 1","type":"related"},{"name":"familial avascular necrosis of the femoral head","type":"related"},{"name":"familial osteonecrosis of the femoral head","type":"exact"},{"name":"femoral head, aseptic Necrosis of","type":"related"},{"name":"femoral head, avascular Necrosis of","type":"related"},{"name":"ischaemic Necrosis of femoral head","type":"related"},{"name":"ischemic Necrosis of femoral head","type":"related"},{"name":"osteonecrosis of femoral head","type":"related"},{"name":"primary avascular necrosis of the femoral head","type":"related"}],"termid":"MONDO:0012126","xrefs":{"Monarch":{"xref_id":"0012126"}}}


id: MONDO:0009994
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rapidly growing malignant mesenchymal neoplasm. It is characterized by the presence of round cells with myoblastic differentiation and a fibrovascular stroma resembling an alveolar growth pattern. The tumor usually presents in the extremities.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhabdomyosarcoma","termid":"MONDO:0005212"}],"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":"alveolar rhabdomyosarcoma","secondary_identifiers":["icd11.foundation:1742058067","GARD:4701","HP:0006779","ONCOTREE:ARMS","OMIM:268220","DOID:4051","MEDGEN:61651","Orphanet:99756","UMLS:C0206655","ICD9:171.9","EFO:0000248","NCIT:C3749","SCTID:404053004","ICDO:8920/3","MESH:D018232","MedDRA:10065867"],"synonyms":[{"name":"ARMS","type":"exact"},{"name":"RMS2","type":"related"},{"name":"alveolar childhood rhabdomyosarcoma","type":"exact"},{"name":"alveolar rhabdomyosarcoma","type":"exact"},{"name":"alveolar rhabdomyosarcoma (disease)","type":"exact"},{"name":"alveolar rhabdomyosarcoma (morphologic abnormality)","type":"exact"},{"name":"arms","type":"exact"},{"name":"monomorphous round cell rhabdomyosarcoma","type":"exact"},{"name":"paediatric alveolar rhabdomyosarcoma","type":"exact"},{"name":"pediatric alveolar rhabdomyosarcoma","type":"exact"},{"name":"rhabdomyosarcoma 2","type":"related"},{"name":"rhabdomyosarcoma 2, alveolar, somatic mutation","type":"exact"},{"name":"rhabdomyosarcoma alveolar","type":"related"},{"name":"rhabdomyosarcoma type 2","type":"exact"},{"name":"rhabdomyosarcoma, alveolar","type":"related"},{"name":"rhabdomyosarcoma, alveolar, somatic mutation","type":"exact"}],"termid":"MONDO:0009994","xrefs":{"Monarch":{"xref_id":"0009994"}}}


id: PBO:0034630
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_nuclear_envelope_during_G0_to_G1_transition","termid":"PBO:0034630"}


id: PR:P36584
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl302 gene.","definition_xrefs":["UniProtKB:P36584","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L3-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB8E5.06c","synonyms":[{"name":"Spom972h-rpl302","type":"exact"}],"termid":"PR:P36584"}


id: MOD:00242
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-(ADP-ribosyl)-L-serine.","definition_xrefs":["Unimod:213#S","PubMed:3141412","RESID:AA0237","PubMed:15842200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosine diphosphoribosyl (ADP-ribosyl) modified residue","termid":"MOD:00752"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(ADP-ribosyl)-L-serine","synonyms":[{"name":"(S)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]oxy)-propanoic acid","type":"exact"},{"name":"ADP Ribose addition","type":"related"},{"name":"ADP-Ribosyl","type":"related"},{"name":"MOD_RES ADP-ribosylserine","type":"exact"},{"name":"O-(ADP-ribosyl)-L-serine","type":"exact"},{"name":"O3-(ADP-ribosyl)-L-serine","type":"exact"},{"name":"O3-[alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)]-L-serine","type":"exact"},{"name":"O3-alpha-D-ribofuranosyl-L-serine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)","type":"exact"},{"name":"OADPRibSer","type":"exact"}],"termid":"MOD:00242"}


id: GO:1900636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of heptadecane.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkane biosynthetic process","termid":"GO:0043447"},{"relation_name":"is_a","term_name":"heptadecane metabolic process","termid":"GO:1900635"}],"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":"heptadecane biosynthetic process","synonyms":[{"name":"heptadecane anabolism","type":"exact"},{"name":"heptadecane biosynthesis","type":"exact"},{"name":"heptadecane formation","type":"exact"},{"name":"heptadecane synthesis","type":"exact"}],"termid":"GO:1900636"}


id: GO:0009348
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A homotrimeric protein complex that catalyzes the transfer of a carbamoyl group to ornithine, forming citrulline.","definition_xrefs":["GOC:mah","EC:2.1.3.3"],"gene_count":0,"genotype_count":0,"name":"obsolete ornithine carbamoyltransferase complex (obsolete GO:0009348)","termid":"GO:0009348"}


id: PBO:0049259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"goosecoid homeobox","termid":"PBO:0049259"}


id: PBO:0004152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sad1-UNC-like protein involved protein folding in the ER (predicted)","termid":"PBO:0004152"}


id: PBO:0038986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenoceptor alpha 2C","termid":"PBO:0038986"}


id: MONDO:0004336
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infiltrating adenocarcinoma arising from the rectum. It is characterized by the presence of malignant glandular cells with prominent intracytoplasmic mucin. These cells constitute more than 50% of the malignant cellular population.","definition_xrefs":["NCIT:C9168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectum adenocarcinoma","termid":"MONDO:0002169"},{"relation_name":"is_a","term_name":"colorectal signet ring cell carcinoma","termid":"MONDO:0044336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"rectal signet ring cell adenocarcinoma","secondary_identifiers":["UMLS:C0279654","MEDGEN:124641","DOID:7707"],"synonyms":[{"name":"rectal signet Ring cell adenocarcinoma","type":"exact"},{"name":"rectum signet ring adenocarcinoma","type":"related"},{"name":"rectum signet ring cell carcinoma","type":"exact"},{"name":"signet Ring adenocarcinoma of rectum","type":"exact"},{"name":"signet Ring adenocarcinoma of the rectum","type":"exact"},{"name":"signet Ring cell adenocarcinoma of rectum","type":"exact"},{"name":"signet Ring cell adenocarcinoma of the rectum","type":"exact"}],"termid":"MONDO:0004336","xrefs":{"Monarch":{"xref_id":"0004336"}}}


id: PBO:0110976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily B member 6 (LAN blood group)","termid":"PBO:0110976"}


id: GO:0034717
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains Gemin6, Gemin7, and unrip (STRAP), and can bind to snRNAs; may play a role in snRNP assembly.","definition_xrefs":["GOC:mah","PMID:17640873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Gemin6-Gemin7-unrip complex","termid":"GO:0034717"}


id: GO:1900039
data:
  {"annotated_genes":["SJAG_03345","SJAG_01585"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88739,115890],"is_not":false,"summary":null,"term":"GO:1900039"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cellular response to hypoxia.","definition_xrefs":["GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of cellular response to hypoxia","termid":"GO:1900037"},{"relation_name":"positively_regulates","term_name":"cellular response to hypoxia","termid":"GO:0071456"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01585":null,"SJAG_03345":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cellular response to hypoxia","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of cellular response to hypoxia","type":"related"},{"name":"activation of cellular response to hypoxic stress","type":"exact"},{"name":"activation of cellular response to lowered oxygen tension","type":"exact"},{"name":"positive regulation of cellular response to hypoxic stress","type":"exact"},{"name":"positive regulation of cellular response to lowered oxygen tension","type":"exact"},{"name":"up regulation of cellular response to hypoxia","type":"related"},{"name":"up regulation of cellular response to hypoxic stress","type":"exact"},{"name":"up regulation of cellular response to lowered oxygen tension","type":"exact"},{"name":"up-regulation of cellular response to hypoxia","type":"related"},{"name":"up-regulation of cellular response to hypoxic stress","type":"exact"},{"name":"up-regulation of cellular response to lowered oxygen tension","type":"exact"},{"name":"upregulation of cellular response to hypoxia","type":"related"},{"name":"upregulation of cellular response to hypoxic stress","type":"exact"},{"name":"upregulation of cellular response to lowered oxygen tension","type":"exact"}],"termid":"GO:1900039","terms_by_termid":{"GO:1900039":null}}


id: MONDO:0009808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A small, benign, bone-forming neoplasm that can arise from any bone but more frequently affects the long bones. The central portion of the neoplasm (nidus) contains differentiated osteoblasts which produce osteoid and sometimes bone. The lesion is usually surrounded by hypervascular sclerotic bone and has limited growth potential. Clinical signs and symptoms include pain and localized tenderness, at the site of the lesion. The pain may be intense but in the majority of cases it is completely alleviated by non-steroidal anti-inflammatory drugs. Prognosis is excellent and recurrences are rare.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone benign neoplasm","termid":"MONDO:0000631"},{"relation_name":"is_a","term_name":"benign osteogenic neoplasm","termid":"MONDO:0045052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoid osteoma","secondary_identifiers":["NCIT:C3297","HP:0030433","MESH:D010017","OMIM:259550","SCTID:302859004","MEDGEN:18221","ICDO:9191/0","UMLS:C0029441"],"synonyms":[{"name":"osteoid osteoma","type":"exact"},{"name":"osteoid osteoma (disease)","type":"exact"}],"termid":"MONDO:0009808","xrefs":{"Monarch":{"xref_id":"0009808"}}}


id: PBO:0053561
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 571","termid":"PBO:0053561"}


id: GO:0045276
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A part of the respiratory chain located in the plasma membrane, containing about 10 polypeptide subunits including four redox centers: cytochrome b/b6, cytochrome c1 and an 2Fe-2S cluster. Catalyzes the oxidation of ubiquinol by oxidized cytochrome c1. Examples of this component are found in bacterial species.","definition_xrefs":["ISBN:0198547684","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete plasma membrane respiratory chain complex III (obsolete GO:0045276)","synonyms":[{"name":"plasma membrane coenzyme Q-cytochrome c oxidoreductase complex","type":"exact"},{"name":"plasma membrane coenzyme Q-cytochrome c reductase complex","type":"exact"},{"name":"plasma membrane cytochrome bc1 complex","type":"exact"},{"name":"plasma membrane ubiquinol-cytochrome-c reductase complex","type":"exact"},{"name":"respiratory chain complex III","type":"broad"},{"name":"ubiquinol-cytochrome c oxidoreductase complex","type":"broad"},{"name":"ubiquinol-cytochrome-c reductase complex","type":"broad"}],"termid":"GO:0045276"}


id: PBO:0075809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"single stranded DNA binding protein 2","termid":"PBO:0075809"}


id: PBO:0016889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific protein Mug121","termid":"PBO:0016889"}


id: PBO:0114533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-H4 chaperone (ATP-dependent) Abo2","termid":"PBO:0114533"}


id: GO:1900564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving chanoclavine-I.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary alcohol metabolic process","termid":"GO:0034308"},{"relation_name":"is_a","term_name":"ergot alkaloid metabolic process","termid":"GO:0035836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"chanoclavine-I metabolic process","synonyms":[{"name":"chanoclavine-I metabolism","type":"exact"}],"termid":"GO:1900564"}


id: MONDO:0011529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.","definition_xrefs":["Orphanet:98768"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type I","termid":"MONDO:0019792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"spinocerebellar ataxia type 13","secondary_identifiers":["GARD:9611","MEDGEN:344297","SCTID:719209002","UMLS:C1854488","OMIM:605259","DOID:0050963","icd11.foundation:1191033828","MESH:C537195"],"synonyms":[{"name":"SCA13","type":"exact"},{"name":"autosomal dominant cerebellar ataxia with intellectual disability","type":"related"},{"name":"autosomal dominant cerebellar ataxia with mental retardation","type":"related"},{"name":"cerebellar ataxia, autosomal dominant with intellectual disability","type":"related"},{"name":"cerebellar ataxia, autosomal dominant with mental retardation","type":"related"},{"name":"spinocerebellar ataxia 13","type":"related"},{"name":"spinocerebellar ataxia type 13","type":"exact"}],"termid":"MONDO:0011529","xrefs":{"Monarch":{"xref_id":"0011529"}}}


id: PBO:0058293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4667","termid":"PBO:0058293"}


id: PBO:0069484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 751, pseudogene","termid":"PBO:0069484"}


id: GO:1904162
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any 5'-3' exodeoxyribonuclease activity that is involved in UV-damage excision repair.","definition_xrefs":["GO_REF:0000061","GOC:TermGenie","PMID:10704216"],"gene_count":0,"genotype_count":0,"name":"obsolete 5'-3' exodeoxyribonuclease activity involved in UV-damage excision repair (obsolete GO:1904162)","synonyms":[{"name":"5'-3' exodeoxyribonuclease activity involved in AER","type":"related"},{"name":"5'-3' exodeoxyribonuclease activity involved in UV-damaged DNA endonuclease-dependent excision repair","type":"exact"},{"name":"5'-3' exodeoxyribonuclease activity involved in UVDE-dependent excision repair","type":"exact"},{"name":"5'-3' exodeoxyribonuclease activity involved in UVER","type":"exact"},{"name":"5'-3' exodeoxyribonuclease activity involved in alternative excision repair","type":"related"}],"termid":"GO:1904162"}


id: GO:0102251
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 10'-apo-beta-carotenal + O2 = 13-apo-beta-carotenone + 4-methylocta-2,4,6-trienedial.","definition_xrefs":["EC:1.13.11.70","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"all-trans-beta-apo-10'-carotenal cleavage oxygenase activity","secondary_identifiers":["RHEA:26401","MetaCyc:RXN-12393"],"termid":"GO:0102251"}


id: GO:0044192
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the host cell mitochondrial envelope. It is highly folded to form cristae.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell mitochondrial membrane","termid":"GO:0044191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell mitochondrial inner membrane","termid":"GO:0044192"}


id: PBO:0074210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 41 member 3","termid":"PBO:0074210"}


id: PBO:0089459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 snRNP-associated protein, WD repeat protein Sap130","termid":"PBO:0089459"}


id: PBO:0051037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGF like family receptor 1","termid":"PBO:0051037"}


id: PBO:0071312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 35","termid":"PBO:0071312"}


id: PBO:0071696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL38 pseudogene 2","termid":"PBO:0071696"}


id: GO:1902996
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neurofibrillary tangle assembly.","definition_xrefs":["GO_REF:0000058","GOC:sjp","PMID:15897157","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inclusion body assembly","termid":"GO:0090083"},{"relation_name":"regulates","term_name":"neurofibrillary tangle assembly","termid":"GO:1902988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of neurofibrillary tangle assembly","synonyms":[{"name":"regulation of flame-shaped neurofibrillary tangle assembly","type":"narrow"},{"name":"regulation of flame-shaped neurofibrillary tangle formation","type":"narrow"},{"name":"regulation of neurofibrillary tangle formation","type":"exact"},{"name":"regulation of star-shaped neurofibrillary tangle assembly","type":"narrow"},{"name":"regulation of star-shaped neurofibrillary tangle formation","type":"narrow"}],"termid":"GO:1902996"}


id: PBO:0110158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exon junction complex subunit Sap18","termid":"PBO:0110158"}


id: PBO:0089377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor, pinin ortholog Pnn1","termid":"PBO:0089377"}


id: GO:0015731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of 3-hydroxyphenyl propanoate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"3-hydroxyphenyl propanoate transport","synonyms":[{"name":"3-hydroxyphenyl propionate transport","type":"exact"}],"termid":"GO:0015731"}


id: MONDO:1010709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trimethylaminuria (fishy taint) that occurs in mallard.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"trimethylaminuria (fishy taint), non-human animal","termid":"MONDO:1010104"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trimethylaminuria (fishy taint), mallard","secondary_identifiers":["OMIA:001360-8839"],"termid":"MONDO:1010709","xrefs":{"Monarch":{"xref_id":"1010709"}}}


id: PBO:0061105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family CARD domain containing 3","termid":"PBO:0061105"}


id: PBO:0040503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aurora kinase C","termid":"PBO:0040503"}


id: PATO:0000960
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000960 absolute opacity (obsolete PATO:0000960)","termid":"PATO:0000960"}


id: FYPO:0000946
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is shaped in the form of a spheroid, and has a normal volume.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"spheroid vegetative cell","termid":"FYPO:0000021"},{"relation_name":"has_part","term_name":"normal volume vegetative cell","termid":"FYPO:0000926"},{"relation_name":"is_a","term_name":"spheroid vegetative cell","termid":"FYPO:0000021"},{"relation_name":"is_a","term_name":"normal volume vegetative cell","termid":"FYPO:0000926"},{"relation_name":"is_a","term_name":"vegetative cell, abnormal cell shape, normal cell size","termid":"FYPO:0001121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000005","FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"normal volume spheroid vegetative cell","synonyms":[{"name":"normal volume rounded vegetative cell","type":"exact"},{"name":"normal volume spheroid cell during vegetative growth","type":"exact"},{"name":"normal volume spheroid vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000946"}


id: PBO:0002985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homologous Pmf1 factor 1, implicated in isoleucine biosynthesis (predicted)","termid":"PBO:0002985"}


id: PBO:0086421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative GTPase peripheral to the mitochondrial inner membrane; essential for respiratory competence, likely functions in assembly of the large ribosomal subunit, has homologs in plants and animals","termid":"PBO:0086421"}


id: GO:1990108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A protein deubiquitination process in which a linear polymer of ubiquitin, formed by the amino-terminal methionine (M1) of one ubiquitin molecule and by the carboxy-terminal glycine (G76) of the next, is removed from a protein.","definition_xrefs":["PMID:23708998"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein deubiquitination","termid":"GO:0016579"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein linear deubiquitination","termid":"GO:1990108"}


id: MONDO:0022464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete anophthalmia microcephaly hypogonadism (obsolete MONDO:0022464)","termid":"MONDO:0022464","xrefs":{"Monarch":{"xref_id":"0022464"}}}


id: PBO:0040173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASNS pseudogene 4","termid":"PBO:0040173"}


id: PBO:0061462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative regulator of antiviral response","termid":"PBO:0061462"}


id: GO:0016798
data:
  {"annotated_genes":["SJAG_03444","SJAG_00096","SJAG_02718","SJAG_04327","SJAG_03280","SJAG_03295","SJAG_00667","SJAG_04850","SJAG_00310","SJAG_01858","SJAG_02179","SJAG_02528","SJAG_04301","SJAG_02711","SJAG_00485","SJAG_03824","SJAG_02435","SJAG_01029","SJAG_05001","SJAG_03032","SJAG_01017","SJAG_04789","SJAG_02799","SJAG_04363","SJAG_01883","SJAG_04851","SJAG_02478","SJAG_04927","SJAG_04859","SJAG_01974","SJAG_05257","SJAG_02192","SJAG_01171","SJAG_03646","SJAG_04238","SJAG_02261","SJAG_01971","SJAG_01119","SJAG_02649","SJAG_02076","SJAG_02131","SJAG_01888","SJAG_02590","SJAG_00957","SJAG_02949","SJAG_01781","SJAG_04864","SJAG_05272","SJAG_02446","SJAG_00620","SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[115600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070694"},{"annotations":[95633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[94353,95634,73627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"},{"annotations":[101077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003905"},{"annotations":[111005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004555"},{"annotations":[101098,101099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004558"},{"annotations":[94324,117284,103503,117836,113491,94701,93535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004556"},{"annotations":[99846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004557"},{"annotations":[87102,95598,87101,95597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090599"},{"annotations":[87782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004559"},{"annotations":[115621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004564"},{"annotations":[107884,115122,86928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008422"},{"annotations":[101012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004568"},{"annotations":[101079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052820"},{"annotations":[74067,101080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008725"},{"annotations":[74065,101081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043916"},{"annotations":[93508,99646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052861"},{"annotations":[86857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106407"},{"annotations":[99286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004573"},{"annotations":[102805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004339"},{"annotations":[88572,110808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051118"},{"annotations":[99647,93509,94588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042973"},{"annotations":[101449,101450,107558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046557"},{"annotations":[87757,101451,94589,101452,107559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004338"},{"annotations":[90080,93703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015926"},{"annotations":[106184,88170,97742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004553"},{"annotations":[101758,96422,101747,118272,101759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008496"},{"annotations":[95197,66284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004571"},{"annotations":[90137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070635"},{"annotations":[90138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070636"},{"annotations":[95637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008534"},{"annotations":[95638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000703"},{"annotations":[111665,90139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008477"},{"annotations":[94356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000701"},{"annotations":[98091,98090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106432"},{"annotations":[115622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004575"},{"annotations":[113396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004844"},{"annotations":[90140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045437"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any glycosyl bond.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity","termid":"GO:0016787"}],"gene_count":51,"genes_by_uniquename":{"SJAG_00096":null,"SJAG_00310":null,"SJAG_00485":null,"SJAG_00620":null,"SJAG_00667":null,"SJAG_00957":null,"SJAG_01017":null,"SJAG_01029":null,"SJAG_01119":null,"SJAG_01171":null,"SJAG_01781":null,"SJAG_01858":null,"SJAG_01883":null,"SJAG_01888":null,"SJAG_01971":null,"SJAG_01974":null,"SJAG_02076":null,"SJAG_02131":null,"SJAG_02179":null,"SJAG_02192":null,"SJAG_02261":null,"SJAG_02435":null,"SJAG_02446":null,"SJAG_02478":null,"SJAG_02528":null,"SJAG_02590":null,"SJAG_02649":null,"SJAG_02711":null,"SJAG_02718":null,"SJAG_02799":null,"SJAG_02949":null,"SJAG_03032":null,"SJAG_03280":null,"SJAG_03295":null,"SJAG_03444":null,"SJAG_03646":null,"SJAG_03724":null,"SJAG_03824":null,"SJAG_04238":null,"SJAG_04301":null,"SJAG_04327":null,"SJAG_04363":null,"SJAG_04789":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04859":null,"SJAG_04864":null,"SJAG_04927":null,"SJAG_05001":null,"SJAG_05257":null,"SJAG_05272":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"hydrolase activity, acting on glycosyl bonds","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1793176","Reactome:R-HSA-2065233","EC:3.2.-.-"],"synonyms":[{"name":"N-glycosylase","type":"narrow"},{"name":"glycosidase activity","type":"exact"},{"name":"glycosylase","type":"narrow"}],"termid":"GO:0016798","terms_by_termid":{"GO:0000701":null,"GO:0000703":null,"GO:0003905":null,"GO:0004338":null,"GO:0004339":null,"GO:0004553":null,"GO:0004555":null,"GO:0004556":null,"GO:0004557":null,"GO:0004558":null,"GO:0004559":null,"GO:0004564":null,"GO:0004568":null,"GO:0004571":null,"GO:0004573":null,"GO:0004575":null,"GO:0004844":null,"GO:0008422":null,"GO:0008477":null,"GO:0008496":null,"GO:0008534":null,"GO:0008725":null,"GO:0015926":null,"GO:0034039":null,"GO:0034042":null,"GO:0034043":null,"GO:0042973":null,"GO:0043916":null,"GO:0045437":null,"GO:0046557":null,"GO:0051118":null,"GO:0052820":null,"GO:0052861":null,"GO:0070635":null,"GO:0070636":null,"GO:0070694":null,"GO:0090599":null,"GO:0106407":null,"GO:0106432":null}}


id: MONDO:1012035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiomyopathy and woolly haircoat syndrome, non-human animal","termid":"MONDO:1011641"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiomyopathy and woolly haircoat syndrome, cattle","secondary_identifiers":["OMIA:000161-9913"],"termid":"MONDO:1012035","xrefs":{"Monarch":{"xref_id":"1012035"}}}


id: MONDO:0012886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory bowel disease that has material basis in variation in the chromosome region 17q21.2.","definition_xrefs":["PMID:18438405","DOID:0110905"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"inflammatory bowel disease 22","secondary_identifiers":["OMIM:612380","MEDGEN:382862","MESH:C567327","UMLS:C2676485"],"synonyms":[{"name":"IBD22","type":"exact"},{"name":"inflammatory bowel disease 22","type":"exact"},{"name":"inflammatory bowel disease type 22","type":"exact"}],"termid":"MONDO:0012886","xrefs":{"Monarch":{"xref_id":"0012886"}}}


id: MONDO:0006906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pigmented villonodular synovitis (obsolete MONDO:0006906)","termid":"MONDO:0006906","xrefs":{"Monarch":{"xref_id":"0006906"}}}


id: GO:0002675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of an acute inflammatory response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of acute inflammatory response","termid":"GO:0002673"},{"relation_name":"is_a","term_name":"positive regulation of inflammatory response","termid":"GO:0050729"},{"relation_name":"positively_regulates","term_name":"acute inflammatory response","termid":"GO:0002526"}],"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 acute inflammatory response","synonyms":[{"name":"activation of acute inflammatory response","type":"narrow"},{"name":"stimulation of acute inflammatory response","type":"narrow"},{"name":"up regulation of acute inflammatory response","type":"exact"},{"name":"up-regulation of acute inflammatory response","type":"exact"},{"name":"upregulation of acute inflammatory response","type":"exact"}],"termid":"GO:0002675"}


id: GO:2000808
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synaptic vesicle clustering.","definition_xrefs":["PMID:21513708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle clustering","termid":"GO:2000807"},{"relation_name":"negatively_regulates","term_name":"synaptic vesicle clustering","termid":"GO:0097091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of synaptic vesicle clustering","termid":"GO:2000808"}


id: PBO:0067441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 563, pseudogene","termid":"PBO:0067441"}


id: GO:0002748
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 pattern recognition receptor (PRR).","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation initiated by receptor mediated uptake of antigen","termid":"GO:0002745"}],"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 pattern recognition receptor mediated uptake of antigen","synonyms":[{"name":"antigen processing and presentation initiated by PAMP receptor mediated uptake of antigen","type":"exact"},{"name":"antigen processing and presentation initiated by PRR mediated uptake of antigen","type":"exact"}],"termid":"GO:0002748"}


id: PR:O36033
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tetratricopeptide repeat protein 27 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02024"],"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":"TPR repeat-containing protein C19B12.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19B12.01","secondary_identifiers":["UniProtKB:O36033"],"synonyms":[{"name":"Spom972h-TTC27","type":"exact"}],"termid":"PR:O36033"}


id: PBO:0075000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-11","termid":"PBO:0075000"}


id: PBO:0080283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 46 pseudogene","termid":"PBO:0080283"}


id: SO:0001042
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The nucleotide sequence of a virus that infects bacteria.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral_sequence","termid":"SO:0001041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phage_sequence","secondary_identifiers":["http://en.wikipedia.org/wiki/Bacteriophage"],"synonyms":[{"name":"bacteriophage","type":"exact"},{"name":"phage","type":"exact"},{"name":"phage sequence","type":"exact"}],"termid":"SO:0001042"}


id: PBO:0089598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphomethylpyrimidine kinase Thi201","termid":"PBO:0089598"}


id: GO:0038109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of stem cell factor to the tyrosine kinase receptor KIT on the surface of a target cell, and ending with regulation of a downstream cellular process, e.g. transcription. Stem cell factor (KIT ligand) binding to the receptor Kit mediates receptor dimerization, activation of its intrinsic tyrosine kinase activity and autophosphorylation. The activated receptor then phosphorylates various substrates, thereby activating distinct signaling cascades within the cell that trigger a change in state or activity of the cell.","definition_xrefs":["GOC:signaling","GOC:nhn","PMID:16129412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor protein tyrosine kinase signaling pathway","termid":"GO:0007169"},{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to stem cell factor stimulus","termid":"GO:0036216"}],"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":"Kit signaling pathway","synonyms":[{"name":"Kit signalling pathway","type":"exact"},{"name":"SCF signaling pathway","type":"exact"},{"name":"stem cell factor receptor signaling pathway","type":"exact"},{"name":"stem cell factor signaling pathway","type":"exact"}],"termid":"GO:0038109"}


id: GO:0010607
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the aggregation, arrangement and bonding together of proteins and RNA molecules to form a cytoplasmic mRNA processing body.","definition_xrefs":["GOC:tb","GOC:krc","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytoplasmic mRNA processing body assembly","termid":"GO:0010603"},{"relation_name":"is_a","term_name":"negative regulation of organelle assembly","termid":"GO:1902116"},{"relation_name":"negatively_regulates","term_name":"P-body assembly","termid":"GO:0033962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cytoplasmic mRNA processing body assembly","termid":"GO:0010607"}


id: PBO:0042576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDKN2B antisense RNA 1","termid":"PBO:0042576"}


id: PBO:0039349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy and beclin 1 regulator 1","termid":"PBO:0039349"}


id: PBO:0082847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Copper-binding protein of the mitochondrial intermembrane space; evolutionarily conserved; may be involved in delivering copper from the matrix to the cytochrome c oxidase complex; contains a twin CX9C motif","termid":"PBO:0082847"}


id: PATO:0005016
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being enclosed on all sides by another entity.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surrounded by","synonyms":[{"name":"enclosed by","type":"exact"}],"termid":"PATO:0005016"}


id: PBO:0015267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation regulator/ ubiquitin-protein ligase (predicted)","termid":"PBO:0015267"}


id: MONDO:0014198
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any mitochondrial DNA depletion syndrome in which the cause of the disease is a mutation in the FBXL4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial DNA depletion syndrome, encephalomyopathic form","termid":"MONDO:0016796"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial DNA depletion syndrome 13","secondary_identifiers":["MEDGEN:815922","SCTID:765403009","Orphanet:369897","UMLS:C3809592","DOID:0080131","NCIT:C172095","OMIM:615471","GARD:13298"],"synonyms":[{"name":"BXL4-related early-onset mitochondrial encephalopathy","type":"related"},{"name":"FBXL4 deficiency","type":"related"},{"name":"FBXL4 mitochondrial DNA depletion syndrome","type":"exact"},{"name":"FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome","type":"related"},{"name":"MTDPS13","type":"related"},{"name":"encephalomyopathic mitochondrial DNA depletion syndrome-13","type":"related"},{"name":"mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)","type":"related"},{"name":"mitochondrial DNA depletion syndrome caused by mutation in FBXL4","type":"exact"},{"name":"mitochondrial DNA depletion syndrome type 13","type":"exact"},{"name":"mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies","type":"related"},{"name":"mtDNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies","type":"exact"}],"termid":"MONDO:0014198","xrefs":{"Monarch":{"xref_id":"0014198"}}}


id: PBO:0072701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RUVBL1 antisense RNA 1","termid":"PBO:0072701"}


id: MONDO:0004642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the tonsillar pillar.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"oropharynx cancer","termid":"MONDO:0004608"},{"relation_name":"is_a","term_name":"musculoskeletal system cancer","termid":"MONDO:0000637"},{"relation_name":"is_a","term_name":"muscle tissue disorder","termid":"MONDO:0003939"},{"relation_name":"is_a","term_name":"tonsil cancer","termid":"MONDO:0006998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"tonsillar pillar cancer","secondary_identifiers":["ICD10CM:C09.1","UMLS:C0153385","ICD9:146.2","DOID:8688","MEDGEN:509270","SCTID:187675005"],"synonyms":[{"name":"malignant neoplasm of tonsillar pillar","type":"exact"},{"name":"malignant neoplasm of tonsillar pillars, posterior","type":"exact"},{"name":"malignant tumor of tonsillar pillar","type":"exact"},{"name":"malignant tumour of tonsillar pillar","type":"exact"}],"termid":"MONDO:0004642","xrefs":{"Monarch":{"xref_id":"0004642"}}}


id: PBO:0071301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 24","termid":"PBO:0071301"}


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


id: FYPO:0003078
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the autophosphorylation of one or more specific proteins, or of specific protein sites, does not occur during a cellular response to DNA damage. Protein autophosphorylation is the phosphorylation by a protein of one or more of its own amino acid residues, or residues on an identical protein.","definition_xrefs":["GO:0031952","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation during cellular response to DNA damage","termid":"FYPO:0002898"},{"relation_name":"is_a","term_name":"abolished protein autophosphorylation during vegetative growth","termid":"FYPO:0003020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"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:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0002274"],"is_obsolete":false,"name":"abolished protein autophosphorylation during cellular response to DNA damage","synonyms":[{"name":"abolished protein autophosphorylation during cellular response to DNA damage during mitotic cell cycle","type":"related"},{"name":"abolished protein autophosphorylation during cellular response to DNA damage during vegetative growth","type":"exact"},{"name":"protein autophosphorylation abolished during cellular response to DNA damage during vegetative growth","type":"exact"}],"termid":"FYPO:0003078"}


id: MONDO:0007057
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic osteolysis syndrome characterized by acroosteolysis of distal phalanges and generalized osteoporosis, associated with additional ossification anomalies, craniofacial dysmorphism, dental anomalies and a wide range of other characteristics.","definition_xrefs":["Orphanet:955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"disappearing bone disease","termid":"MONDO:0003157"},{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"relation_name":"is_a","term_name":"acroosteolysis","termid":"MONDO:0007056"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Acroosteolysis dominant type","secondary_identifiers":["DOID:2736","ICD9:756.59","MEDGEN:182961","NORD:1214","MESH:C537586","OMIM:102500","UMLS:C0917715","MESH:C531695","SCTID:63122002","MESH:C535663","GARD:508","NCIT:C84745"],"synonyms":[{"name":"Arthrodentoosteodysplasia","type":"exact"},{"name":"Cheney syndrome","type":"exact"},{"name":"HJCYS","type":"related"},{"name":"Hajdu Cheney Syndrome","type":"exact"},{"name":"Hajdu-Cheney syndrome","type":"exact"},{"name":"acrodentoosteodysplasia","type":"exact"},{"name":"acroosteolysis with osteoporosis and changes in skull and mandible","type":"exact"},{"name":"serpentine fibula polycystic kidney syndrome","type":"exact"},{"name":"serpentine fibula-polycystic kidney syndrome","type":"exact"},{"name":"serpentine fibula-polycystic kidneys syndrome","type":"exact"}],"termid":"MONDO:0007057","xrefs":{"Monarch":{"xref_id":"0007057"}}}


id: PBO:0055087
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 2505","termid":"PBO:0055087"}


id: PBO:0058314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4687","termid":"PBO:0058314"}


id: GO:1903409
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of reactive oxygen species, any molecules or ions formed by the incomplete one-electron reduction of oxygen.","definition_xrefs":["GO_REF:0000068","GOC:bf","GOC:PARL","PMID:24252804","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"reactive oxygen species metabolic process","termid":"GO:0072593"}],"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":"reactive oxygen species biosynthetic process","synonyms":[{"name":"ROS formation","type":"related"},{"name":"ROS generation","type":"related"},{"name":"reactive oxygen species anabolism","type":"exact"},{"name":"reactive oxygen species biosynthesis","type":"exact"},{"name":"reactive oxygen species formation","type":"exact"},{"name":"reactive oxygen species generation","type":"related"},{"name":"reactive oxygen species synthesis","type":"exact"}],"termid":"GO:1903409"}


id: PBO:0051355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2/OR2-7D (pseudogene)","termid":"PBO:0051355"}


id: MONDO:1011100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nephropathy characterized by renal tubular necrosis with extensive oxalate crystal deposition that occurs in dogs due to a mutation in the AGXT gene.","definition_xrefs":["PMID:22486513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"nephropathy, dog","termid":"MONDO:1012186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary hyperoxaluria, AGXT-related, dog","secondary_identifiers":["OMIA:001672-9615"],"synonyms":[{"name":"primary hyperoxaluria type I (Oxalosis I), dog","type":"related"}],"termid":"MONDO:1011100","xrefs":{"Monarch":{"xref_id":"1011100"}}}


id: MONDO:0014735
data:
  {"annotated_genes":["SJAG_03345"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85437],"is_not":false,"summary":null,"term":"MONDO:0014735"}]},"cv_name":"mondo","definition":"Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the VCP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03345":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 2Y","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C168974","OMIM:616687","Orphanet:435387","UMLS:C5569026","GARD:17714","DOID:0110168","MEDGEN:1800449"],"synonyms":[{"name":"CMT2 due to VCP mutation","type":"exact"},{"name":"CMT2Y","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2 caused by mutation in VCP","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Y","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2Y","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2y","type":"exact"},{"name":"Charcot-Marie-Tooth disease, type 2Y","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy type 2Y","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 2Y","type":"related"},{"name":"VCP Charcot-Marie-Tooth disease type 2","type":"exact"},{"name":"autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation","type":"exact"},{"name":"autosomal dominant Charcot-Marie-Tooth disease type 2Y","type":"related"},{"name":"autosomal dominant axonal Charcot-Marie-Tooth type 2Y","type":"exact"}],"termid":"MONDO:0014735","terms_by_termid":{"MONDO:0014735":null},"xrefs":{"Monarch":{"xref_id":"0014735"}}}


id: MONDO:0021834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by frontal bossing, cloudy corneae, low nasal ridge, and micrognathia, hypoplastic thorax, and rhizomelic micromelia.","definition_xrefs":["PMID:8989469"],"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":"Akaba Hayasaka syndrome","secondary_identifiers":["MESH:C535609","UMLS:C2930948","MEDGEN:443940"],"synonyms":[{"name":"frontal bossing, cloudy corneae, low nasal ridge, and micrognathia, hypoplastic thorax, and rhizomelic micromelia","type":"related"}],"termid":"MONDO:0021834","xrefs":{"Monarch":{"xref_id":"0021834"}}}


id: GO:0032075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of nuclease activity, the hydrolysis of ester linkages within nucleic acids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nucleobase-containing compound metabolic process","termid":"GO:0045935"},{"relation_name":"is_a","term_name":"positive regulation of hydrolase activity","termid":"GO:0051345"}],"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 nuclease activity","synonyms":[{"name":"activation of nuclease activity","type":"narrow"},{"name":"nuclease activator","type":"related"},{"name":"stimulation of nuclease activity","type":"narrow"},{"name":"up regulation of nuclease activity","type":"exact"},{"name":"up-regulation of nuclease activity","type":"exact"},{"name":"upregulation of nuclease activity","type":"exact"}],"termid":"GO:0032075"}


id: PBO:0077359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 98","termid":"PBO:0077359"}


id: SO:0001775
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant in the genetic material inherited from the mother.","direct_ancestors":[{"relation_name":"is_a","term_name":"variant_origin","termid":"SO:0001762"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternal_variant","synonyms":[{"name":"maternal variant","type":"exact"}],"termid":"SO:0001775"}


id: MONDO:0020634
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant meningioma with aggressive clinical course. It recurs in approximately 50-78% of the cases. This category includes the anaplastic (malignant) meningioma, papillary meningioma, and rhabdoid meningioma.","definition_xrefs":["NCIT:C38938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grade III meningioma","secondary_identifiers":["UMLS:C0280801","MEDGEN:79186"],"synonyms":[{"name":"WHO grade III meningioma","type":"exact"},{"name":"grade 3 meningioma","type":"exact"},{"name":"grade III meningioma","type":"exact"},{"name":"meningioma, malignant","type":"exact"}],"termid":"MONDO:0020634","xrefs":{"Monarch":{"xref_id":"0020634"}}}


id: MONDO:0022981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"die Smulders droog van dijk syndrome","termid":"MONDO:0022981","xrefs":{"Monarch":{"xref_id":"0022981"}}}


id: GO:0060576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a columnar/cuboidal epithelial cell of the intestine over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell development","termid":"GO:0002066"},{"relation_name":"part_of","term_name":"intestinal epithelial cell differentiation","termid":"GO:0060575"}],"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":"intestinal epithelial cell development","termid":"GO:0060576"}


id: PBO:0002980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid permease (predicted)","termid":"PBO:0002980"}


id: FYPO:0004400
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 the protein kinase inhibitor KT5823.","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:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0002058","FYPO:0000003","FYPO:0002057","FYPO:0000139","FYPO:0000257"],"is_obsolete":false,"name":"normal growth on KT5823","synonyms":[{"name":"normal cell population growth in presence of KT5823","type":"exact"},{"name":"normal cell population growth on KT5823","type":"exact"},{"name":"normal cellular response to KT5823","type":"related"},{"name":"normal vegetative cell population growth on KT5823","type":"exact"}],"termid":"FYPO:0004400"}


id: GO:0031810
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a H4 histamine receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled histamine receptor binding","termid":"GO:0031806"}],"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:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"H4 histamine receptor binding","synonyms":[{"name":"H4 histamine receptor ligand","type":"narrow"}],"termid":"GO:0031810"}


id: PBO:0067437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 558, pseudogene","termid":"PBO:0067437"}


id: MONDO:0019448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Benign adult familial myoclonic epilepsy (BAFME) is an inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia.","definition_xrefs":["Orphanet:86814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epilepsy, familial adult myoclonic","termid":"MONDO:0000160"},{"relation_name":"is_a","term_name":"adolescent-onset epilepsy syndrome","termid":"MONDO:0020073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"benign adult familial myoclonic epilepsy","secondary_identifiers":["UMLS:C4273988","MEDGEN:908684","icd11.foundation:1036649329","SCTID:717225001","NANDO:1200956","GARD:16758"],"synonyms":[{"name":"ADCME","type":"exact"},{"name":"BAFME","type":"exact"},{"name":"FAME","type":"exact"},{"name":"FCMTE","type":"exact"},{"name":"autosomal dominant cortical myoclonus and epilepsy","type":"exact"},{"name":"benign adult familial myoclonus epilepsy","type":"exact"},{"name":"familial adult myoclonic epilepsy","type":"exact"},{"name":"familial cortical myoclonic tremor and epilepsy","type":"exact"}],"termid":"MONDO:0019448","xrefs":{"Monarch":{"xref_id":"0019448"}}}


id: MONDO:0006250
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the ileum. 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:C4935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestinal neuroendocrine tumor G1","termid":"MONDO:0000540"},{"relation_name":"is_a","term_name":"colon neuroendocrine tumor G1","termid":"MONDO:0006155"},{"relation_name":"is_a","term_name":"ileal neuroendocrine tumor, well differentiated, low or intermediate grade","termid":"MONDO:0015065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"ileal neuroendocrine tumor G1","secondary_identifiers":["MONDO:0021536","MEDGEN:155426","SCTID:425318003","EFO:1000300","UMLS:C0745216","ICD9:209.03"],"synonyms":[{"name":"carcinoid tumor of ileum","type":"exact"},{"name":"carcinoid tumor of the ileum","type":"exact"},{"name":"carcinoid tumour of ileum","type":"exact"},{"name":"carcinoid tumour of the ileum","type":"exact"},{"name":"grade 1 neuroendocrine neoplasm of ileum","type":"exact"},{"name":"ileal NET G1","type":"exact"},{"name":"ileal carcinoid tumor","type":"exact"},{"name":"ileal carcinoid tumour","type":"exact"},{"name":"ileal neuroendocrine tumor G1","type":"exact"},{"name":"ileum NET G1","type":"exact"},{"name":"ileum carcinoid tumor","type":"exact"},{"name":"ileum carcinoid tumor (disease)","type":"exact"},{"name":"ileum carcinoid tumour","type":"exact"},{"name":"ileum carcinoid tumour (disease)","type":"exact"},{"name":"ileum neuroendocrine neoplasm G1","type":"exact"},{"name":"ileum neuroendocrine tumor, well differentiated, low grade","type":"exact"}],"termid":"MONDO:0006250","xrefs":{"Monarch":{"xref_id":"0006250"}}}


id: PBO:0087058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L28; homologous to mammalian ribosomal protein L27A and bacterial L15; may have peptidyl transferase activity; can mutate to cycloheximide resistance","termid":"PBO:0087058"}


id: PBO:0047814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box N3","termid":"PBO:0047814"}


id: FYPO:0002064
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a 3'-5'-exoribonuclease activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal 3'-5'-exoribonuclease activity","termid":"FYPO:0002063"},{"relation_name":"is_a","term_name":"abolished ribonuclease activity","termid":"FYPO:0006301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0000654","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"abolished 3'-5'-exoribonuclease activity","synonyms":[{"name":"3'-5'-exoribonuclease activity abolished","type":"exact"}],"termid":"FYPO:0002064"}


id: SO:0000727
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A regulatory region where transcription factor binding sites are clustered to regulate various aspects of transcription activities. (CRMs can be located a few kb to hundreds of kb upstream of the core promoter, in the coding sequence, within introns, or in the untranslated regions (UTR) sequences, and even on a different chromosome). A single gene can be regulated by multiple CRMs to give precise control of its spatial and temporal expression. CRMs function as nodes in large, intertwined regulatory network. CRM DNA accessibility is subject to regulation by dbTFs and transcription co-TFs.","definition_xrefs":["PMID:19660565","SO:SG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptional_cis_regulatory_region","termid":"SO:0001055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cis_regulatory_module","synonyms":[{"name":"CRM","type":"exact"},{"name":"TF module","type":"exact"},{"name":"cis regulatory module","type":"exact"},{"name":"transcription factor module","type":"exact"}],"termid":"SO:0000727"}


id: GO:1904289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mitotic DNA damage checkpoint.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:16549501","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle","termid":"GO:0007346"},{"relation_name":"is_a","term_name":"regulation of DNA damage checkpoint","termid":"GO:2000001"},{"relation_name":"regulates","term_name":"mitotic DNA damage checkpoint signaling","termid":"GO:0044773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of mitotic DNA damage checkpoint","termid":"GO:1904289"}


id: FYPO:0003671
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ATP binding by a gene product (usually a protein) in a mutant is abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"},{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abnormal ATP binding","termid":"FYPO:0003671"}


id: GO:0018727
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-phenanthrol + X-SO3(-) = HX + 2-phenanthrylsulfate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-phenanthrol sulfotransferase activity (obsolete GO:0018727)","synonyms":[{"name":"2-phenanthrol sulphotransferase activity","type":"exact"}],"termid":"GO:0018727"}


id: GO:1902472
data:
  {"annotated_genes":["SJAG_03309","SJAG_02392","SJAG_02380","SJAG_00845","SJAG_02838","SJAG_01787","SJAG_00256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87326,100885,110867],"is_not":false,"summary":null,"term":"GO:1902472"},{"annotations":[110256,118761,103204,90250,95342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903617"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mitotic cytokinesis, division site positioning.","definition_xrefs":["PMID:9852154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cytokinetic process","termid":"GO:1903436"},{"relation_name":"is_a","term_name":"regulation of cytokinesis, site selection","termid":"GO:2000073"},{"relation_name":"regulates","term_name":"mitotic cytokinesis, division site positioning","termid":"GO:1902408"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00256":null,"SJAG_00845":null,"SJAG_01787":null,"SJAG_02380":null,"SJAG_02392":null,"SJAG_02838":null,"SJAG_03309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000281"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0000281","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of mitotic cytokinesis, division site positioning","references_by_uniquename":{"GO_REF:0000107":null,"PMID:25866389":null},"synonyms":[{"name":"regulation of mitotic cytokinesis, site selection","type":"exact"}],"termid":"GO:1902472","terms_by_termid":{"GO:1902472":null,"GO:1903617":null}}


id: GO:0033870
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phosphoadenylyl sulfate + a thiol = adenosine 3',5'-bisphosphate + an S-alkyl thiosulfate.","definition_xrefs":["EC:2.8.2.16"],"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:0016782"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016782","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"thiol sulfotransferase activity","secondary_identifiers":["MetaCyc:THIOL-SULFOTRANSFERASE-RXN","RHEA:14637"],"synonyms":[{"name":"3'-phosphoadenylyl-sulfate:thiol S-sulfotransferase activity","type":"related"},{"name":"PAPS sulfotransferase activity","type":"broad"},{"name":"adenosine 3'-phosphate 5'-sulphatophosphate sulfotransferase activity","type":"related"}],"termid":"GO:0033870"}


id: PBO:0060953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear factor kappa B subunit 1","termid":"PBO:0060953"}


id: GO:1904313
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 methamphetamine hydrochloride stimulus.","definition_xrefs":["GOC:TermGenie","PMID:22174933","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to amine","termid":"GO:0014075"}],"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 methamphetamine hydrochloride","synonyms":[{"name":"response to methamphetamine HCL","type":"exact"}],"termid":"GO:1904313"}


id: GO:0043778
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cobalt-precorrin 8 = cobyrinate.","definition_xrefs":["MetaCyc:RXN-8768"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular acyltransferase activity","termid":"GO:0016867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"cobalt-precorrin-8 methylmutase activity","secondary_identifiers":["RHEA:16209","EC:5.4.99.60"],"synonyms":[{"name":"cobalt-precorrin 8 methylmutase activity","type":"exact"},{"name":"cobalt-precorrin 8X methylmutase activity","type":"exact"},{"name":"cobalt-precorrin-8X methylmutase activity","type":"exact"}],"termid":"GO:0043778"}


id: PBO:0046403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythrocyte membrane protein band 4.2","termid":"PBO:0046403"}


id: PBO:0067137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 185, pseudogene","termid":"PBO:0067137"}


id: PBO:0027594
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_tyrosine_phosphorylation_during_cellular_response_to_UV","termid":"PBO:0027594"}


id: PBO:0034248
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_syntenic_orthology_relationship_with","termid":"PBO:0034248"}


id: PBO:0060934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear factor of activated T cells 3","termid":"PBO:0060934"}


id: MONDO:0009074
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome is characterized by Dandy-Walker malformation, severe intellectual deficit, macrocephaly, brachytelephalangy, facial dysmorphism and severe myopia. Three cases have been described. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:1970"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0020022"],"is_obsolete":false,"name":"facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome","secondary_identifiers":["GARD:2222","UMLS:C1857352","MEDGEN:341752","MESH:C535985","OMIM:220219"],"synonyms":[{"name":"Dandy-Walker malformation with intellectual disability, macrocephaly, myopia, and BRACHYTELEPHALANGY","type":"related"},{"name":"Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and BRACHYTELEPHALANGY","type":"related"}],"termid":"MONDO:0009074","xrefs":{"Monarch":{"xref_id":"0009074"}}}


id: GO:0048731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an organismal system over time, from its formation to the mature structure. A system is a regularly interacting or interdependent group of organs or tissues that work together to carry out a given biological process.","definition_xrefs":["GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"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":"system development","termid":"GO:0048731"}


id: MONDO:0044279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bone mineral density quantitative trait locus 15 (obsolete MONDO:0044279)","secondary_identifiers":["OMIM:613418"],"synonyms":[{"name":"BMND15","type":"related"},{"name":"bone mineral density QTL 15","type":"exact"},{"name":"bone mineral density quantitative trait locus 15","type":"related"},{"name":"compression fracture, susceptibility to","type":"related"},{"name":"metaphyseal fracture, susceptibility to","type":"related"},{"name":"osteoporosis, susceptibility to","type":"related"}],"termid":"MONDO:0044279","xrefs":{"Monarch":{"xref_id":"0044279"}}}


id: GO:1990320
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(XXI) chains; type XXI collagen triple helices found in the extracellular matrix component of blood vessel walls and in the cytoplasm of cultured human aortic smooth muscle.","definition_xrefs":["GOC:bhm","PMID:17876790"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FACIT collagen trimer","termid":"GO:0005593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"collagen type XXI trimer","termid":"GO:1990320"}


id: PBO:0053366
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 278","termid":"PBO:0053366"}


id: PBO:0078334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon CTC) 1-6","termid":"PBO:0078334"}


id: GO:0007285
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phase of growth and gene expression that male germ cells undergo as they enter the spermatocyte stage. The cells grow in volume and transcribe most of the gene products needed for the morphological events that follow meiosis.","definition_xrefs":["GOC:jid","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"developmental cell growth","termid":"GO:0048588"},{"relation_name":"part_of","term_name":"spermatogenesis","termid":"GO:0007283"}],"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":"primary spermatocyte growth","termid":"GO:0007285"}


id: PBO:0089582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DYRK family cell polarity protein kinase Pom1","termid":"PBO:0089582"}


id: PBO:0088480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial LYR family protein Cup1/Lyr1","termid":"PBO:0088480"}


id: PATO:0000984
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A porosity quality inhering in a bearer by virtue of the bearer's being capable of admitting the passage of gas or liquid through pores or interstices.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porosity","termid":"PATO:0000973"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"porous","termid":"PATO:0000984"}


id: GO:0103048
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2 S-adenosyl-L-methionine + an adenine37 in tRNA = S-adenosyl-L-homocysteine + L-methionine + 5'-deoxyadenosine + a 2-methyladenine37 in tRNA.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA m2A37 methyltransferase activity (obsolete GO:0103048)","termid":"GO:0103048"}


id: PBO:0064099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi like RNA-mediated gene silencing 1","termid":"PBO:0064099"}


id: MONDO:0021045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant neoplasm characterized by the presence of an epithelial and a fibrous component. Representative examples are fibroadenoma and phyllodes tumor.","definition_xrefs":["NCIT:C3743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mixed neoplasm","termid":"MONDO:0021043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroepithelial neoplasm","secondary_identifiers":["UMLS:C0206649","EFO:0007271","MEDGEN:104908","MESH:D018225"],"synonyms":[{"name":"fibroepithelial neoplasm","type":"exact"},{"name":"fibroepithelial tumor","type":"exact"},{"name":"fibroepithelial tumour","type":"exact"}],"termid":"MONDO:0021045","xrefs":{"Monarch":{"xref_id":"0021045"}}}


id: MONDO:0009011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete constriction rings syndrome (obsolete MONDO:0009011)","termid":"MONDO:0009011","xrefs":{"Monarch":{"xref_id":"0009011"}}}


id: PBO:0084033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi PI4K effector, PtdIns4P sensor, and retention receptor; interacts with glycosyltransferases, and in the PtdIns4P-bound state mediates retention of these enzymes in the Golgi; PtdIns4P sensor that limits PI4K signaling and regulates lipid homeostasis, interacting with the catalytic domain of Sac1p, the major PtdIns4P phosphatase, directing dephosphosphorylation of the Golgi pool of PtdIns4P; tetramerization required for function; contributes to telomere function; ortholog of human GOLPH3","termid":"PBO:0084033"}


id: GO:0061294
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Signaling at short range between cells of the ureteric bud terminus and the kidney mesenchyme that positively regulates the formation of the mesonephric renal vesicle.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesonephros development","termid":"GO:0061217"},{"relation_name":"is_a","term_name":"renal vesicle induction","termid":"GO:0072034"},{"relation_name":"positively_regulates","term_name":"mesonephric renal vesicle formation","termid":"GO:0061262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric renal vesicle induction","termid":"GO:0061294"}


id: GO:2001096
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a cellotrioseacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trisaccharide transport","termid":"GO:2001088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"cellotriose transport","termid":"GO:2001096"}


id: GO:0071292
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 silver (Ag+) ion stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to silver ion","termid":"GO:0010272"},{"relation_name":"is_a","term_name":"cellular response to metal ion","termid":"GO:0071248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to silver ion","termid":"GO:0071292"}


id: PBO:0065810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB3D, member RAS oncogene family","termid":"PBO:0065810"}


id: PBO:0034334
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-developmentally_contributes_to","termid":"PBO:0034334"}


id: PBO:0003141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate N-acetyltransferase (predicted)","termid":"PBO:0003141"}


id: PR:O94500
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03130","PRO:DNx","PANTHER:PTHR11780: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":"NADH-ubiquinone oxidoreductase 51 kDa subunit homolog SPBC18E5.10, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18E5.10","secondary_identifiers":["UniProtKB:O94500"],"synonyms":[{"name":"Spom972h-NDUFV1","type":"exact"}],"termid":"PR:O94500"}


id: SO:0000467
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing a gene sequence where the resulting protein is regulated by the stability of the resulting protein.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post_translationally_regulated","termid":"SO:0000130"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post_translationally_regulated_by_protein_stability","synonyms":[{"name":"post translationally regulated by protein stability","type":"exact"},{"name":"post-translationally regulated by protein stability","type":"exact"}],"termid":"SO:0000467"}


id: MONDO:0006087
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from glandular epithelial cells of the vermiform appendix.","direct_ancestors":[{"relation_name":"is_a","term_name":"appendix carcinoma","termid":"MONDO:0003196"},{"relation_name":"is_a","term_name":"cecum adenocarcinoma","termid":"MONDO:0006028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"appendix adenocarcinoma","secondary_identifiers":["DOID:3608","UMLS:C0238003","SCTID:413445002","ONCOTREE:APAD","MEDGEN:65942","NCIT:C7718","GARD:10564","EFO:1000088"],"synonyms":[{"name":"APAD","type":"related"},{"name":"adenocarcinoma of appendix","type":"exact"},{"name":"adenocarcinoma of the appendix","type":"exact"},{"name":"appendiceal adenocarcinoma","type":"exact"},{"name":"appendix adenocarcinoma","type":"exact"},{"name":"vermiform appendix adenocarcinoma","type":"exact"}],"termid":"MONDO:0006087","xrefs":{"Monarch":{"xref_id":"0006087"}}}


id: PBO:0063097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"par-6 family cell polarity regulator alpha","termid":"PBO:0063097"}


id: PBO:0062887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oviductal glycoprotein 1","termid":"PBO:0062887"}


id: PBO:0085894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; localized to the vacuolar outer membrane; predicted to be palmitoylated","termid":"PBO:0085894"}


id: GO:0004443
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-myo-inositol 3,4-bisphosphate + H2O = D-myo-inositol 3-monophosphate + phosphate.","definition_xrefs":["EC:3.1.3.66","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol-1,4,-bisphosphate 4-phosphatase (obsolete GO:0004443)","synonyms":[{"name":"inositol-1,4,-bisphosphate 4-phosphatase","type":"exact"}],"termid":"GO:0004443"}


id: PR:O43040
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ctf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43040"],"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":"cleavage and termination factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B9.11c","synonyms":[{"name":"Spom972h-ctf1","type":"exact"},{"name":"transcription termination factor ctf1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43040"}


id: PBO:0080256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 19 pseudogene","termid":"PBO:0080256"}


id: GO:0050640
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phenylacetyl-CoA + isopenicillin N + H2O = CoA + penicillin G + L-2-aminoadipate.","definition_xrefs":["RHEA:20720"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acyltransferase activity","termid":"GO:0016410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"isopenicillin-N N-acyltransferase activity","secondary_identifiers":["GO:0042319","EC:2.3.1.164","MetaCyc:2.3.1.164-RXN","GO:0045440"],"synonyms":[{"name":"acyl-CoA:isopenicillin N N-acyltransferase activity","type":"related"},{"name":"acyl-coenzyme A:6-aminopenicillanic-acid-acyltransferase activity","type":"related"},{"name":"acyl-coenzyme A:isopenicillin N acyltransferase activity","type":"related"},{"name":"isopenicillin N:acyl-CoA acyltransferase activity","type":"related"},{"name":"isopenicillin-N acyltransferase activity","type":"exact"}],"termid":"GO:0050640"}


id: MONDO:0003559
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cervical adenosquamous carcinoma (obsolete MONDO:0003559)","termid":"MONDO:0003559","xrefs":{"Monarch":{"xref_id":"0003559"}}}


id: PBO:0031423
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cell_population_phenotype","termid":"PBO:0031423"}


id: GO:0019622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 3-(3-hydroxy)phenylpropionate, a hydroxylated derivative of phenylpropionate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"},{"relation_name":"is_a","term_name":"3-(3-hydroxy)phenylpropionate metabolic process","termid":"GO:0046435"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0044281","GO:0044248","GO:0008150"],"is_obsolete":false,"name":"3-(3-hydroxy)phenylpropionate catabolic process","synonyms":[{"name":"3-(3-hydroxy)phenylpropionate breakdown","type":"exact"},{"name":"3-(3-hydroxy)phenylpropionate catabolism","type":"exact"},{"name":"3-(3-hydroxy)phenylpropionate degradation","type":"exact"}],"termid":"GO:0019622"}


id: PATO:0001831
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A female fertility which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"female fertile","termid":"PATO:0000888"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased female fertility","synonyms":[{"name":"high female fertility","type":"exact"}],"termid":"PATO:0001831"}


id: FYPO:0004670
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which macroautophagy is abnormal when the cell is subject to nitrogen starvation. Macroautophagy is the major pathway by which cells digest parts of their own cytoplasm.","definition_xrefs":["PomBase:mah","GO:0016236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal macroautophagy","termid":"FYPO:0000163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal macroautophagy during nitrogen starvation","synonyms":[{"name":"abnormal macroautophagy during cellular response to nitrogen starvation","type":"exact"},{"name":"abnormal macroautophagy during nitrogen depletion","type":"exact"},{"name":"abnormal macroautophagy during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0004670"}


id: GO:2000333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of blood microparticle formation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of blood microparticle formation","termid":"GO:2000332"},{"relation_name":"negatively_regulates","term_name":"blood microparticle formation","termid":"GO:0072564"}],"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 blood microparticle formation","synonyms":[{"name":"negative regulation of microparticle generation","type":"exact"},{"name":"negative regulation of microparticle release","type":"exact"}],"termid":"GO:2000333"}


id: PBO:0056174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAF bZIP transcription factor","termid":"PBO:0056174"}


id: GO:0000821
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving arginine, 2-amino-5-(carbamimidamido)pentanoic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid metabolic process","termid":"GO:0006521"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"arginine metabolic process","termid":"GO:0006525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"regulation of arginine metabolic process","synonyms":[{"name":"regulation of arginine metabolism","type":"exact"}],"termid":"GO:0000821"}


id: MONDO:0023273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of dermatofibrosarcoma protuberans characterized by the presence of melanin-pigmented dendritic cells.","definition_xrefs":["NCIT:C9430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatofibrosarcoma protuberans","termid":"MONDO:0011934"}],"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":"pigmented dermatofibrosarcoma protuberans","secondary_identifiers":["UMLS:C0334464","SCTID:398670003","MEDGEN:90786"],"synonyms":[{"name":"Bednar Tumor","type":"related"},{"name":"Bednar Tumour","type":"related"},{"name":"Bednar's Tumor","type":"related"},{"name":"Bednar's Tumour","type":"related"},{"name":"Bednars Tumor","type":"related"},{"name":"Bednars Tumour","type":"related"},{"name":"DFSP, Pigmented","type":"related"},{"name":"DFSPs, Pigmented","type":"related"},{"name":"Dermatofibrosarcoma Protuberan, Pigmented","type":"related"},{"name":"Dermatofibrosarcoma Protuberans, Pigmented","type":"related"},{"name":"Pigmented DFSP","type":"related"},{"name":"Pigmented DFSPs","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberan","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberans","type":"related"},{"name":"Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)","type":"related"},{"name":"Pigmented dermatofibrosarcoma","type":"related"},{"name":"Pigmented dermatofibrosarcoma protuberans","type":"related"},{"name":"Pigmented dermatofibrosarcoma protuberans of skin","type":"related"},{"name":"Pigmented storiform neurofibroma","type":"related"},{"name":"Protuberan, Pigmented Dermatofibrosarcoma","type":"related"},{"name":"Protuberans, Pigmented Dermatofibrosarcoma","type":"related"},{"name":"Tumor, Bednar","type":"related"},{"name":"Tumor, Bednar's","type":"related"},{"name":"bednar tumor","type":"exact"},{"name":"bednar tumour","type":"exact"},{"name":"pigmented dermatofibrosarcoma protuberans","type":"exact"},{"name":"pigmented dermatofibrosarcoma protuberans (bednar tumor)","type":"exact"}],"termid":"MONDO:0023273","xrefs":{"Monarch":{"xref_id":"0023273"}}}


id: PBO:0012580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit alpha 1 (predicted)","termid":"PBO:0012580"}


id: FYPO:0008104
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the cortical endoplasmic reticulum is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:36799444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0006378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000138","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to cortical endoplasmic reticulum","termid":"FYPO:0008104"}


id: PBO:0114487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Type I HSP40 co-chaperone; regulates HSP90 and HSP70 functions; acts as an adaptor that helps Rsp5p recognize and ubiquitinate misfolded, cytosolic proteins after heat shock; critical for determining cell size at Start as a function of growth rate; involved in protein translocation across membranes; forms cytotoxic amyloidogenic-like structures in vitro; DnaJ family member; chimeric protein in which the human p58IPK J domain replaces the yeast Ydj1p J domain can complement yeast ydj1 mutant","termid":"PBO:0114487"}


id: PBO:0056412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane associated ring-CH-type finger 9","termid":"PBO:0056412"}


id: PBO:0079320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 10","termid":"PBO:0079320"}


id: GO:0075081
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism modulates the frequency, rate or extent of transmembrane receptor-mediated signal transduction in the symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by host of symbiont transmembrane receptor-mediated signal transduction (obsolete GO:0075081)","termid":"GO:0075081"}


id: PBO:0109657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-type ATPase P5 type Cta5","termid":"PBO:0109657"}


id: MONDO:0003966
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A choriocarcinoma that arises from the testis and is characterized by the predominance of cytotrophoblastic and intermediate trophoblastic cells. Syncytiotrophoblastic cells are absent or not prominent.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choriocarcinoma of testis","termid":"MONDO:0003508"}],"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":"testicular monophasic choriocarcinoma","secondary_identifiers":["NCIT:C39935","MEDGEN:272841","UMLS:C1515290","DOID:6693"],"termid":"MONDO:0003966","xrefs":{"Monarch":{"xref_id":"0003966"}}}


id: GO:0050675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of urothelial cell proliferation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"regulates","term_name":"urothelial cell proliferation","termid":"GO:0050674"}],"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 urothelial cell proliferation","termid":"GO:0050675"}


id: MONDO:0033479
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia","termid":"MONDO:0020380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"spinocerebellar ataxia 44","secondary_identifiers":["DOID:0080286","MEDGEN:1611168","Orphanet:631095","OMIM:617691","UMLS:C4521563"],"synonyms":[{"name":"SCA44","type":"related"},{"name":"spinocerebellar ataxia 44","type":"exact"}],"termid":"MONDO:0033479","xrefs":{"Monarch":{"xref_id":"0033479"}}}


id: GO:0021822
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The intracellular signaling pathway that results in the cessation of cell movement involved in lamination of the cerebral cortex.","definition_xrefs":["PMID:12626695","GOC:dph","GOC:jid","GOC:tb","GOC:cls","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glial cell migration","termid":"GO:1903976"},{"relation_name":"negatively_regulates","term_name":"cell motility involved in cerebral cortex radial glia guided migration","termid":"GO:0021814"},{"relation_name":"part_of","term_name":"layer formation in cerebral cortex","termid":"GO:0021819"}],"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 motility involved in cerebral cortex radial glia guided migration","synonyms":[{"name":"down regulation of cell locomotion involved in cerebral cortex glial-mediated radial cell migration","type":"exact"},{"name":"down-regulation of cell locomotion involved in cerebral cortex glial-mediated radial cell migration","type":"exact"},{"name":"downregulation of cell locomotion involved in cerebral cortex glial-mediated radial cell migration","type":"exact"},{"name":"inhibition of cell locomotion involved in cerebral cortex glial-mediated radial cell migration","type":"narrow"},{"name":"negative regulation of cell locomotion involved in cerebral cortex glial-mediated radial migration","type":"exact"},{"name":"negative regulation of cell locomotion involved in cerebral cortex radial glia guided migration","type":"related"}],"termid":"GO:0021822"}


id: PBO:0030110
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_methionine_import","termid":"PBO:0030110"}


id: GO:0046805
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent linkage of heme and a protein via 1'-L-histidine (otherwise known as tau-heme-histidine, tele-heme-histidine).","definition_xrefs":["RESID:AA0329"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-heme linkage via 1'-L-histidine (obsolete GO:0046805)","synonyms":[{"name":"protein-haem linkage via 1'-L-histidine","type":"exact"}],"termid":"GO:0046805"}


id: GO:0035316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of non-sensory hairs. These hairs are polarized cellular extensions that cover much of the insect epidermis.","definition_xrefs":["GOC:mtg_sensu","PMID:11064425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection organization","termid":"GO:0120036"},{"relation_name":"part_of","term_name":"hair cell differentiation","termid":"GO:0035315"}],"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":"non-sensory hair organization","synonyms":[{"name":"non-sensory hair organization and biogenesis","type":"related"},{"name":"trichome organisation","type":"broad"},{"name":"trichome organization and biogenesis","type":"broad"}],"termid":"GO:0035316"}


id: PBO:0071227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 68","termid":"PBO:0071227"}


id: PBO:0083186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the uncharacterized gene CTS2/YDR371W; identified by expression profiling and mass spectrometry","termid":"PBO:0083186"}


id: MONDO:0002473
data:
  {"annotated_genes":["SJAG_03280","SJAG_00394"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010916"},{"annotations":[85248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031062"}]},"cv_name":"mondo","definition":"A congenital or acquired kidney disorder characterized by the presence of renal cysts.","definition_xrefs":["NCIT:C34750"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00394":null,"SJAG_03280":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"cystic kidney disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:Q61","MEDGEN:854361","UMLS:C3887499","NANDO:2200172","DOID:2975","MESH:D052177","SCTID:722223000","EFO:0008615"],"synonyms":[{"name":"cystic renal disease","type":"exact"},{"name":"kidney cyst","type":"exact"},{"name":"renal cyst","type":"exact"}],"termid":"MONDO:0002473","terms_by_termid":{"MONDO:0010916":null,"MONDO:0031062":null},"xrefs":{"Monarch":{"xref_id":"0002473"}}}


id: MONDO:0013201
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of Waardenburg syndrome type 4 (Waardenburg-Shah syndrome) caused by mutations in EDN3.","direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg-Shah syndrome","termid":"MONDO:0019518"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0004335"],"is_obsolete":false,"name":"Waardenburg syndrome type 4B","secondary_identifiers":["MESH:C567680","DOID:0110954","MEDGEN:412961","GARD:15641","OMIM:613265","UMLS:C2750457"],"synonyms":[{"name":"EDN3 Waardenburg syndrome","type":"exact"},{"name":"WS4B","type":"exact"},{"name":"Waardenburg syndrome caused by mutation in EDN3","type":"exact"},{"name":"Waardenburg syndrome type 4B","type":"exact"},{"name":"Waardenburg syndrome type IVB","type":"exact"},{"name":"Waardenburg syndrome with Hirschsprung disease type 4B","type":"exact"},{"name":"Waardenburg syndrome, type 4B","type":"related"},{"name":"Waardenburg syndrome, type 4B, with Hirschsprung disease","type":"related"}],"termid":"MONDO:0013201","xrefs":{"Monarch":{"xref_id":"0013201"}}}


id: PBO:0076511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 12 pseudogene","termid":"PBO:0076511"}


id: GO:0072035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell adhesion process in which mesenchyme cells adhere to one another in the initial stages of the formation of the pre-tubular aggregate, the earliest recognizable structure of the kidney.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion","termid":"GO:0098609"},{"relation_name":"part_of","term_name":"renal vesicle formation","termid":"GO:0072033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"pre-tubular aggregate formation","synonyms":[{"name":"mesenchymal cell condensation involved in renal vesicle formation","type":"exact"},{"name":"nephron epithelium formation","type":"related"}],"termid":"GO:0072035"}


id: GO:0006746
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the reduced form of flavin adenine dinucleotide.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavin adenine dinucleotide metabolic process","termid":"GO:0072387"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"FADH2 metabolic process","synonyms":[{"name":"FADH2 metabolism","type":"exact"},{"name":"reduced flavin adenine dinucleotide metabolic process","type":"exact"}],"termid":"GO:0006746"}


id: GO:0032670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-26 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-26 production","termid":"GO:0032630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of interleukin-26 production","secondary_identifiers":["GO:0045530"],"synonyms":[{"name":"regulation of IL-26 production","type":"exact"},{"name":"regulation of interleukin-26 biosynthetic process","type":"narrow"}],"termid":"GO:0032670"}


id: GO:0031821
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a metabotropic serotonin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"G protein-coupled serotonin receptor binding","synonyms":[{"name":"G-protein coupled serotonin receptor binding","type":"exact"},{"name":"metabotropic 5-hydroxytryptamine receptor binding","type":"exact"},{"name":"metabotropic serotonin receptor binding","type":"exact"},{"name":"metabotropic serotonin receptor ligand","type":"narrow"}],"termid":"GO:0031821"}


id: GO:1904200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which iodide is transported across a membrane.","definition_xrefs":["PMID:20392814","GO_REF:0000069","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iodide transport","termid":"GO:0015705"},{"relation_name":"is_a","term_name":"monoatomic anion transmembrane transport","termid":"GO:0098656"},{"relation_name":"is_a","term_name":"inorganic anion transmembrane transport","termid":"GO:0098661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"iodide transmembrane transport","termid":"GO:1904200"}


id: PBO:0045087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrolipoamide S-succinyltransferase","termid":"PBO:0045087"}


id: GO:0009146
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of purine nucleoside triphosphate, a compound consisting of a purine base linked to a ribose or deoxyribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate catabolic process","termid":"GO:0009143"},{"relation_name":"is_a","term_name":"purine nucleoside triphosphate metabolic process","termid":"GO:0009144"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"purine nucleoside triphosphate catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"purine nucleoside triphosphate breakdown","type":"exact"},{"name":"purine nucleoside triphosphate catabolism","type":"exact"},{"name":"purine nucleoside triphosphate degradation","type":"exact"}],"termid":"GO:0009146","terms_by_termid":{"GO:0035863":null}}


id: PBO:0058674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6802","termid":"PBO:0058674"}


id: MONDO:0100050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Usher syndrome in which the cause of the disease is a mutation in the CDH23 and PCDH15 genes.","definition_xrefs":["MONDO:patterns/OMIM_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Usher syndrome type 1","termid":"MONDO:0010168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Usher syndrome, type 1D/F","synonyms":[{"name":"USH1D/F, CDH23/PCDH15, digenic","type":"related"},{"name":"Usher syndrome, type 1D/F, CDH23/PCDH15, digenic","type":"exact"}],"termid":"MONDO:0100050","xrefs":{"Monarch":{"xref_id":"0100050"}}}


id: MONDO:0029143
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":"intellectual developmental disorder with hypertelorism and distinctive facies","secondary_identifiers":["OMIM:618147","UMLS:C4748381","MEDGEN:1648403"],"synonyms":[{"name":"IDDHDF","type":"related"},{"name":"INTELLECTUAL DEVELOPMENTAL disorder WITH HYPERTELORISM AND DISTINCTIVE FACIES","type":"related"},{"name":"chromosome 14q32 deletion syndrome","type":"related"}],"termid":"MONDO:0029143","xrefs":{"Monarch":{"xref_id":"0029143"}}}


id: GO:0046821
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"DNA structures that are not part of a chromosome.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular anatomical structure","termid":"GO:0005622"}],"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":"extrachromosomal DNA","secondary_identifiers":["Wikipedia:Extrachromosomal_DNA"],"termid":"GO:0046821"}


id: PBO:0082760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the SF3b subcomplex of the U2 snRNP; increases efficiency of first and second step pre-mRNA splicing; diploid mutants display a random budding pattern instead of the wild-type bipolar pattern; facilitates passage through G1/S Start, but is not required for G2/M transition or exit from mitosis","termid":"PBO:0082760"}


id: PBO:0051206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 4-34","termid":"PBO:0051206"}


id: MONDO:0011727
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":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anorexia nervosa, susceptibility to, 1","secondary_identifiers":["MEDGEN:376139","UMLS:C1847492","OMIM:606788"],"synonyms":[{"name":"AN","type":"related"},{"name":"ANON1","type":"exact"},{"name":"anon","type":"related"},{"name":"anorexia nervosa, susceptibility to","type":"related"},{"name":"anorexia nervosa, susceptibility to, 1","type":"exact"}],"termid":"MONDO:0011727","xrefs":{"Monarch":{"xref_id":"0011727"}}}


id: MONDO:0054565
data:
  {"annotated_genes":["SJAG_01370"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86307],"is_not":false,"summary":null,"term":"MONDO:0054565"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"short-rib thoracic dysplasia 17 with or without polydactyly","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4479416","MEDGEN:1372794","OMIM:617405"],"synonyms":[{"name":"SRTD17","type":"related"},{"name":"short-rib thoracic dysplasia 17 with or without POLYDACTYLY","type":"related"}],"termid":"MONDO:0054565","terms_by_termid":{"MONDO:0054565":null},"xrefs":{"Monarch":{"xref_id":"0054565"}}}


id: PBO:0063507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"p53 and DNA damage regulated 1","termid":"PBO:0063507"}


id: PBO:0111738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 19 member 4, pseudogene","termid":"PBO:0111738"}


id: PBO:0034400
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-requires_sequence_feature_(obsolete_requires_sequence_feature)","termid":"PBO:0034400"}


id: PBO:0046668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"estrogen related receptor alpha","termid":"PBO:0046668"}


id: MONDO:0013470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any generalized epilepsy with febrile seizures plus in which the cause of the disease is a mutation in the SCN9A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"generalized epilepsy with febrile seizures plus","termid":"MONDO:0018214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"generalized epilepsy with febrile seizures plus, type 7","secondary_identifiers":["UMLS:C2751778","GARD:18665","MESH:C567827","MEDGEN:416630","DOID:0111295","OMIM:613863"],"synonyms":[{"name":"GEFSP7","type":"related"},{"name":"Gefs+, type 7","type":"related"},{"name":"SCN9A generalised epilepsy with febrile seizures plus","type":"exact"},{"name":"SCN9A generalized epilepsy with febrile seizures plus","type":"exact"},{"name":"febrile seizures, familial, 3B","type":"related"},{"name":"generalised epilepsy with febrile seizures plus caused by mutation in SCN9A","type":"exact"},{"name":"generalized epilepsy with febrile seizures plus caused by mutation in SCN9A","type":"exact"},{"name":"generalized epilepsy with febrile seizures plus, type 7","type":"exact"}],"termid":"MONDO:0013470","xrefs":{"Monarch":{"xref_id":"0013470"}}}


id: PBO:0087435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit D of the V1 peripheral membrane domain of V-ATPase; part of the electrogenic proton pump found throughout the endomembrane system; plays a role in the coupling of proton transport and ATP hydrolysis; the V1 peripheral membrane domain of the vacuolar H+-ATPase (V-ATPase) has eight subunits","termid":"PBO:0087435"}


id: GO:0038171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by a cannabinoid binding to its receptor on the cell surface, and ending with the regulation of a downstream cellular process, e.g. transcription. Cannabinoids are a class of diverse chemical compounds that include the endocannabinoids and the phytocannabinoids.","definition_xrefs":["Wikipedia:Cannabinoid","GOC:signaling","GOC:bf","GOC:jc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"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":"cannabinoid signaling pathway","synonyms":[{"name":"cannabinoid receptor signaling pathway","type":"exact"},{"name":"cannabinoid-activated signaling pathway","type":"exact"},{"name":"cannabinoid-mediated signaling pathway","type":"exact"}],"termid":"GO:0038171"}


id: GO:0170057
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the joining of an RNA with 3'-phosphate or 2',3'-cyclic-phosphate ends to an RNA with 5'-hydroxy ends according to either (i) a 3'-end 3'-phospho-ribonucleotide-RNA + a 5'-end dephospho-ribonucleoside-RNA + GTP = a ribonucleotidyl-ribonucleotide-RNA + diphosphate + GMP; or (ii) a 3'-end 2',3'-cyclophospho-ribonucleotide-RNA + a 5'-end dephospho-ribonucleoside-RNA + GTP + H2O = a ribonucleotidyl-ribonucleotide-RNA + diphosphate + GMP + H+.","definition_xrefs":["PMID:21311021","EC:6.5.1.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA ligase activity","termid":"GO:0008452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0140098","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"RNA ligase (GTP) activity","synonyms":[{"name":"3'-phosphate/5'-hydroxy nucleic acid ligase activity","type":"exact"}],"termid":"GO:0170057"}


id: GO:0071675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of mononuclear cell migration. Mononuclear cell migration is the movement of a mononuclear cell within or between different tissues and organs of the body.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte migration","termid":"GO:0002685"},{"relation_name":"regulates","term_name":"mononuclear cell migration","termid":"GO:0071674"}],"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 mononuclear cell migration","termid":"GO:0071675"}


id: GO:0018671
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-hydroxybenzoate + NAD(P)H + H+ + O2 = 3,4-dihydroxybenzoate + NAD(P)+ + H2O.","definition_xrefs":["EC:1.14.13.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"4-hydroxybenzoate 3-monooxygenase [NAD(P)H] activity","secondary_identifiers":["MetaCyc:1.14.13.33-RXN"],"synonyms":[{"name":"4-hydroxybenzoate 3-hydroxylase activity","type":"broad"},{"name":"4-hydroxybenzoate 3-monooxygenase (reduced nicotinamide adenine dinucleotide (phosphate))","type":"exact"},{"name":"4-hydroxybenzoate,NAD(P)H:oxygen oxidoreductase (3-hydroxylating)","type":"related"},{"name":"4-hydroxybenzoate-3-hydroxylase activity","type":"related"}],"termid":"GO:0018671"}


id: GO:1904855
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a proteasome regulatory particle.","definition_xrefs":["GOC:TermGenie","PMID:16096059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"proteasome regulatory particle binding","synonyms":[{"name":"19S regulatory particle binding","type":"narrow"},{"name":"PA700 proteasome activator binding","type":"narrow"},{"name":"PA700-dependent proteasome activator binding","type":"exact"},{"name":"modulator complex binding","type":"related"}],"termid":"GO:1904855"}


id: PBO:0044137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 3","termid":"PBO:0044137"}


id: GO:0050626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trimethylamine + 2 (ferricytochrome c)-subunit + H2O = trimethylamine-N-oxide + 2 (ferrocytochrome c)-subunit + 2 H+.","definition_xrefs":["EC:1.7.2.3","MetaCyc:1.7.2.3-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor","termid":"GO:0016662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"trimethylamine-N-oxide reductase (cytochrome c) activity","secondary_identifiers":["RHEA:24236","Wikipedia:Trimethylamine_N-oxide_reductase"],"synonyms":[{"name":"TMAO reductase activity","type":"related"},{"name":"TOR activity","type":"related"},{"name":"trimethylamine:cytochrome c oxidoreductase activity","type":"related"}],"termid":"GO:0050626"}


id: PBO:0078973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ser (anticodon GCT) 1-1","termid":"PBO:0078973"}


id: GO:0043513
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Heterodimeric hormone composed of an inhibin alpha subunit complexed with an inhibin beta-B subunit.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inhibin complex","termid":"GO:0043511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005576","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"inhibin B complex","termid":"GO:0043513"}


id: GO:0000754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"In organisms that undergo conjugation with cellular fusion, the process resulting in desensitization following exposure to pheromone stimulus that act to down-regulate further stimulation or block initial conjugation responses. An example of this is the adaptation to pheromone during conjugation with cellular fusion in Saccharomyces cerevisiae.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adaptation of signaling pathway","termid":"GO:0023058"},{"relation_name":"part_of","term_name":"response to pheromone triggering conjugation with cellular fusion","termid":"GO:0000749"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"adaptation of signaling pathway by response to pheromone involved in conjugation with cellular fusion","secondary_identifiers":["GO:0007331","GO:0030453"],"synonyms":[{"name":"adaptation of signalling pathway by response to pheromone involved in conjugation with cellular fusion","type":"exact"},{"name":"adaptation to pheromone during conjugation with cellular fusion","type":"related"},{"name":"desensitization to pheromone during conjugation with cellular fusion","type":"exact"}],"termid":"GO:0000754"}


id: GO:0060212
data:
  {"annotated_genes":["SJAG_02370"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91153],"is_not":false,"summary":null,"term":"GO:0060212"}]},"cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of poly(A) tail shortening of a nuclear-transcribed mRNA. Poly(A) tail shortening is the decrease in length of the poly(A) tail of an mRNA from full length to an oligo(A) length.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nuclear-transcribed mRNA poly(A) tail shortening","termid":"GO:0060211"},{"relation_name":"is_a","term_name":"negative regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:1900152"},{"relation_name":"negatively_regulates","term_name":"nuclear-transcribed mRNA poly(A) tail shortening","termid":"GO:0000289"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"negatively_regulates","termid":"GO:0016071"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0016071"],"is_obsolete":false,"name":"negative regulation of nuclear-transcribed mRNA poly(A) tail shortening","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"negative regulation of 3' to 5' mRNA deadenylation","type":"related"},{"name":"negative regulation of mRNA deadenylation","type":"related"},{"name":"negative regulation of nuclear mRNA poly(A) tail shortening","type":"related"}],"termid":"GO:0060212","terms_by_termid":{"GO:0060212":null}}


id: GO:1902084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving fumagillin.","definition_xrefs":["GOC:di","PMID:23488861","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"epoxide metabolic process","termid":"GO:0097176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"fumagillin metabolic process","synonyms":[{"name":"fumagillin metabolism","type":"exact"}],"termid":"GO:1902084"}


id: PBO:0072246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 21","termid":"PBO:0072246"}


id: GO:0052516
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the jasmonic acid-mediated defense response of 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 positive regulation by organism of symbiont jasmonic acid-mediated defense response (obsolete GO:0052516)","synonyms":[{"name":"induction by organism of symbiont JA-mediated defense response","type":"narrow"},{"name":"induction by organism of symbiont jasmonic acid-mediated defense response","type":"narrow"},{"name":"positive regulation by organism of symbiont JA-mediated defense response","type":"exact"},{"name":"positive regulation by organism of symbiont jasmonic acid-mediated defense response","type":"exact"}],"termid":"GO:0052516"}


id: PBO:0042481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 7","termid":"PBO:0042481"}


id: PBO:0043671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corin, serine peptidase","termid":"PBO:0043671"}


id: GO:0099540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling between presynapse and postsynapse mediated by a peptide ligand crossing the synaptic cleft.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trans-synaptic signaling","termid":"GO:0099537"},{"relation_name":"is_a","term_name":"synaptic signaling via neuropeptide","termid":"GO:0099538"}],"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":"trans-synaptic signaling by neuropeptide","termid":"GO:0099540"}


id: MONDO:0012431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital diaphragmatic hernia in which the cause of the disease is a mutation in the ZFPM2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital diaphragmatic hernia","termid":"MONDO:0005711"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diaphragmatic hernia 3","secondary_identifiers":["MESH:C565710","OMIM:610187","GARD:15474","UMLS:C1857781","MEDGEN:347546"],"synonyms":[{"name":"DIH3","type":"related"},{"name":"ZFPM2 congenital diaphragmatic hernia","type":"exact"},{"name":"congenital diaphragmatic hernia caused by mutation in ZFPM2","type":"exact"},{"name":"diaphragmatic hernia 3","type":"exact"},{"name":"diaphragmatic hernia type 3","type":"exact"}],"termid":"MONDO:0012431","xrefs":{"Monarch":{"xref_id":"0012431"}}}


id: PBO:0053775
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 1020","termid":"PBO:0053775"}


id: PBO:0091402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S12","termid":"PBO:0091402"}


id: PBO:0085410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane regulator of polyamine and carnitine transport; has similarity to transporters but lacks transport activity; may act as a sensor that transduces environmental signals; has a positive or negative regulatory effect on transcription of many transporter genes","termid":"PBO:0085410"}


id: MONDO:0009829
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pallidal degeneration, progressive, with retinitis pigmentosa (obsolete MONDO:0009829)","secondary_identifiers":["OMIM:260200","MESH:C564910"],"synonyms":[{"name":"pallidal degeneration, progressive, with retinitis pigmentosa","type":"exact"}],"termid":"MONDO:0009829","xrefs":{"Monarch":{"xref_id":"0009829"}}}


id: PBO:0084842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; conserved in metazoa, with similarity to human mitochondrial ribosomal protein MRPL49","termid":"PBO:0084842"}


id: GO:0100019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that regulates cAMP-mediated signaling.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cAMP-mediated signaling by transcription from RNA polymerase II promoter (obsolete GO:0100019)","termid":"GO:0100019"}


id: PBO:0065506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoserine phosphatase","termid":"PBO:0065506"}


id: PBO:0034775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanyl-nucleotide exchange factor, CUE domain absent Vps902","termid":"PBO:0034775"}


id: MONDO:0015437
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 21 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including growth retardation, developmental delay, intellectual disability, epilepsy, microcephaly, short stature, dysmorphic features, hypogammaglobulinemia, thrombocytopenia and unspecific skeletal anomalies (hemivertebrae, clinodactyly, syndactyly). In rare cases, it has been described in phenotypically normal individuals.","definition_xrefs":["Orphanet:1445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"},{"relation_name":"is_a","term_name":"chromosome 21 disorder","termid":"MONDO:0700124"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 21","secondary_identifiers":["UMLS:C2931422","NORD:947","GARD:6083","SCTID:31325007","MESH:C537109","MEDGEN:419409"],"synonyms":[{"name":"Chromosome 21 Ring","type":"exact"},{"name":"R21","type":"related"},{"name":"Ring 21","type":"related"},{"name":"Ring chromosome 21 syndrome","type":"related"},{"name":"Ring chromosome type 21","type":"exact"},{"name":"chromosome 21 en anneau","type":"exact"},{"name":"chromosome 21 ring","type":"related"}],"termid":"MONDO:0015437","xrefs":{"Monarch":{"xref_id":"0015437"}}}


id: PBO:0089673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multispanning 7TM plasma membrane rhodopsin family protein, implicated in signalling","termid":"PBO:0089673"}


id: GO:0002707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of lymphocyte mediated immunity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte mediated immunity","termid":"GO:0002704"},{"relation_name":"is_a","term_name":"regulation of lymphocyte mediated immunity","termid":"GO:0002706"},{"relation_name":"negatively_regulates","term_name":"lymphocyte mediated immunity","termid":"GO:0002449"}],"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 lymphocyte mediated immunity","synonyms":[{"name":"down regulation of lymphocyte mediated immunity","type":"exact"},{"name":"down-regulation of lymphocyte mediated immunity","type":"exact"},{"name":"downregulation of lymphocyte mediated immunity","type":"exact"},{"name":"inhibition of lymphocyte mediated immunity","type":"narrow"}],"termid":"GO:0002707"}


id: MOD:00115
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-palmitoyl-L-cysteine.","definition_xrefs":["PubMed:3166978","DeltaMass:303","PubMed:8180229","Unimod:47#C","PubMed:8824274","RESID:AA0106","PubMed:1872406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-palmitoylated residue","termid":"MOD:00653"},{"relation_name":"is_a","term_name":"palmitoylated-L-cysteine","termid":"MOD:01684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"},{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:00905","MOD:01155"],"is_obsolete":false,"name":"S-palmitoyl-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-(hexadecanoylsulfanyl)propanoic acid","type":"exact"},{"name":"2-amino-3-(hexadecanoylthio)propanoic acid","type":"exact"},{"name":"ACT_SITE S-palmitoyl cysteine intermediate","type":"exact"},{"name":"LIPID S-palmitoyl cysteine","type":"exact"},{"name":"Palmitoyl","type":"related"},{"name":"Palmitoylation","type":"related"},{"name":"S-hexadecanoylated L-cysteine","type":"exact"},{"name":"S-palmitoyl-L-cysteine","type":"exact"},{"name":"S-palmitoylated L-cysteine","type":"exact"},{"name":"S-palmityl Cystenyl","type":"exact"},{"name":"SPamCys","type":"exact"},{"name":"cysteine hexadecanoate thioester","type":"exact"},{"name":"cysteine palmitate thioester","type":"exact"}],"termid":"MOD:00115"}


id: MONDO:0001879
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the anus","direct_ancestors":[{"relation_name":"is_a","term_name":"anus neoplasm","termid":"MONDO:0003046"},{"relation_name":"is_a","term_name":"rectal cancer","termid":"MONDO:0006519"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"anus cancer","secondary_identifiers":["SCTID:363352004","UMLS:C0153446","DOID:14110","MEDGEN:56303","ICD9:154.3","NCIT:C7379","ICD9:154.2"],"synonyms":[{"name":"anus cancer","type":"exact"},{"name":"cancer of anus","type":"exact"},{"name":"malignant anal neoplasm","type":"exact"},{"name":"malignant anal tumor","type":"exact"},{"name":"malignant anal tumour","type":"exact"},{"name":"malignant anus neoplasm","type":"exact"},{"name":"malignant neoplasm of anus","type":"exact"},{"name":"malignant neoplasm of the anus","type":"exact"},{"name":"malignant tumor of anus","type":"exact"},{"name":"malignant tumor of the anus","type":"exact"},{"name":"malignant tumour of anus","type":"exact"},{"name":"malignant tumour of the anus","type":"exact"}],"termid":"MONDO:0001879","xrefs":{"Monarch":{"xref_id":"0001879"}}}


id: MONDO:0017460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndactyly type 6 is a rare, genetic, non-syndromic, congenital limb malformation characterized by unilateral fusion of second to fifth fingers, amalgamation of distal phalanges in a knot-like structure, and second- and third-toe fusion. Some individuals present only with webbing between second and third toes, without involvement of fingers.","definition_xrefs":["Orphanet:295012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic syndactyly","termid":"MONDO:0019530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndactyly type 6","secondary_identifiers":["SCTID:763624007","MEDGEN:1635950","UMLS:C4706525","icd11.foundation:2105806379","GARD:21201"],"synonyms":[{"name":"mitten hand","type":"exact"},{"name":"syndactyly, mitten type","type":"exact"},{"name":"unilateral syndactyly of digits 2-5","type":"exact"}],"termid":"MONDO:0017460","xrefs":{"Monarch":{"xref_id":"0017460"}}}


id: PBO:0067686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5.8S ribosomal 3","termid":"PBO:0067686"}


id: PBO:0071701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39","termid":"PBO:0071701"}


id: MONDO:0018887
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Cutaneous lupus erythematosus (CLE) is an autoimmune disease that denotes a heterogeneous spectrum of clinical manifestations affecting the skin and can be divided into 4 categories: acute CLE (ACLE); subacute CLE (SCLE); chronic CLE (CCLE; the most diverse form); and intermittent CLE (ICLE). CLE can either occur alone or associated with systemic lupus erythematosus (SLE).","definition_xrefs":["Orphanet:535"],"gene_count":0,"genotype_count":0,"name":"obsolete rare cutaneous lupus erythematosus (obsolete MONDO:0018887)","secondary_identifiers":["MedDRA:10056509","MESH:D008178"],"synonyms":[{"name":"rare cutaneous lupus erythematosus","type":"exact"}],"termid":"MONDO:0018887","xrefs":{"Monarch":{"xref_id":"0018887"}}}


id: FYPO:0007706
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 removal of tubulin dimers from a microtubule occurs to a lower extent than normal in the lateral part of the cell.","definition_xrefs":["PomBase:mah","PMID:26443240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule depolymerization during vegetative growth","termid":"FYPO:0000902"}],"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:0000054"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased microtubule depolymerization at cell side","synonyms":[{"name":"decreased microtubule catastrophe at cell side","type":"related"},{"name":"decreased microtubule depolymerisation at cell side","type":"exact"},{"name":"decreased microtubule depolymerization at cell side during mitotic cell cycle","type":"related"},{"name":"decreased microtubule depolymerization at cell side during vegetative growth","type":"exact"},{"name":"decreased microtubule depolymerization at lateral part of cell","type":"exact"},{"name":"reduced microtubule depolymerization at cell side","type":"exact"}],"termid":"FYPO:0007706"}


id: MONDO:0015602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete developmental delay-deafness syndrome, Hildebrand type (obsolete MONDO:0015602)","secondary_identifiers":["Orphanet:163988"],"termid":"MONDO:0015602","xrefs":{"Monarch":{"xref_id":"0015602"}}}


id: GO:0022615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial attachment of a protein to a target membrane, mediated by a proteins protruding from the target membrane. Docking requires only that the proteins come close enough to interact and adhere.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane docking","termid":"GO:0022406"}],"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":"protein to membrane docking","synonyms":[{"name":"protein-membrane docking","type":"exact"}],"termid":"GO:0022615"}


id: PBO:0027846
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-swollen_multinucleate_vegetative_cell","termid":"PBO:0027846"}


id: GO:0047530
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,4-diaminopentanoate + H2O + NAD(P)+ = 2-amino-4-oxopentanoate + NH3 + NAD(P)H + H+.","definition_xrefs":["EC:1.4.1.12","MetaCyc:24-DIAMINOPENTANOATE-DEHYDROGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor","termid":"GO:0016639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2,4-diaminopentanoate dehydrogenase activity","synonyms":[{"name":"2,4-diaminopentanoate:NAD(P)+ oxidoreductase (deaminating)","type":"related"},{"name":"2,4-diaminopentanoic acid C4 dehydrogenase activity","type":"related"}],"termid":"GO:0047530"}


id: PBO:0039633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amine oxidase copper containing 1","termid":"PBO:0039633"}


id: MONDO:0700064
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder consisting of the presence a chromosomal abnormality in which there is an addition or loss of chromosomes within a set.","definition_xrefs":["PMID:26126276","NCIT:C2873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal disorder","termid":"MONDO:0019040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneuploidy","secondary_identifiers":["UMLS:C0002938","MESH:D000782","MEDGEN:294"],"synonyms":[{"name":"chromosome number anomaly","type":"exact"}],"termid":"MONDO:0700064","xrefs":{"Monarch":{"xref_id":"0700064"}}}


id: PBO:0004120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C3HC4 type zinc finger","termid":"PBO:0004120"}


id: PBO:0069997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1292, pseudogene","termid":"PBO:0069997"}


id: PBO:0000039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"comment","termid":"PBO:0000039"}


id: PBO:0090302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate mutase/6-phosphofructo-2-kinase family","termid":"PBO:0090302"}


id: MONDO:0100541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital heart disease that is present at birth. Representative examples include tetralogy of fallot, bicuspid aortic valve, atrial septal defect, double outlet right ventricle, ventricular septal defect, and coarctation of the aorta, and atrioventricular canal.","definition_xrefs":["PMID:22641149","PMID:23031282","PMID:23289003","PMID:22961344","PMID:24638895"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart disease","termid":"MONDO:0005453"}],"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":"GATA5-related congenital heart defects","synonyms":[{"name":"GATA5 related congenital heart defects","type":"exact"}],"termid":"MONDO:0100541","xrefs":{"Monarch":{"xref_id":"0100541"}}}


id: MONDO:1012126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease, non-human animal","termid":"MONDO:1011724"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunodeficiency disease, domestic cat","secondary_identifiers":["OMIA:000550-9685"],"termid":"MONDO:1012126","xrefs":{"Monarch":{"xref_id":"1012126"}}}


id: GO:0040021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of sex and sexual phenotype in the germ line of a hermaphrodite.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germ-line sex determination","termid":"GO:0018992"}],"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":"hermaphrodite germ-line sex determination","secondary_identifiers":["GO:0042005"],"termid":"GO:0040021"}


id: GO:0098827
data:
  {"annotated_genes":["SJAG_01307","SJAG_02839","SJAG_02085","SJAG_04231","SJAG_01570","SJAG_00557","SJAG_03333","SJAG_03509","SJAG_06425","SJAG_02264","SJAG_00437","SJAG_03812","SJAG_02196","SJAG_04913","SJAG_03506","SJAG_00295","SJAG_00131","SJAG_00554","SJAG_01857","SJAG_00895","SJAG_01642","SJAG_00790","SJAG_01860","SJAG_02044","SJAG_02716","SJAG_02080","SJAG_03115","SJAG_04471","SJAG_01069","SJAG_04345","SJAG_03657","SJAG_02354","SJAG_05022","SJAG_03235","SJAG_05327","SJAG_01558","SJAG_01803","SJAG_00068","SJAG_03750","SJAG_04513","SJAG_00893","SJAG_01233","SJAG_00846","SJAG_02683","SJAG_01127","SJAG_01435","SJAG_00426","SJAG_05016","SJAG_02717","SJAG_04413","SJAG_00681","SJAG_06514","SJAG_00284","SJAG_01785","SJAG_04451","SJAG_04938","SJAG_00064","SJAG_01416","SJAG_01356","SJAG_04608","SJAG_03018","SJAG_01991","SJAG_01491","SJAG_00919","SJAG_03878","SJAG_03850","SJAG_04954","SJAG_02827","SJAG_00339","SJAG_04975","SJAG_01078","SJAG_01709","SJAG_04952","SJAG_00334","SJAG_04915","SJAG_01939","SJAG_00924","SJAG_04316","SJAG_02056","SJAG_02446","SJAG_01527","SJAG_05414","SJAG_00999","SJAG_03670","SJAG_03930","SJAG_05306","SJAG_04162","SJAG_04740","SJAG_03672","SJAG_00175","SJAG_02842","SJAG_02590","SJAG_03929","SJAG_02903","SJAG_04986","SJAG_04319","SJAG_04417","SJAG_05013","SJAG_00360","SJAG_02640","SJAG_01537","SJAG_05274","SJAG_01223","SJAG_03795","SJAG_03943","SJAG_00906","SJAG_02120","SJAG_03292","SJAG_05278","SJAG_04294","SJAG_02032","SJAG_01563","SJAG_00825","SJAG_03261","SJAG_04592","SJAG_04337","SJAG_01957","SJAG_00603","SJAG_03831","SJAG_04904","SJAG_04615","SJAG_05348","SJAG_03281","SJAG_03955","SJAG_03933","SJAG_04384","SJAG_04119","SJAG_04821","SJAG_04883","SJAG_03609","SJAG_00831","SJAG_01227","SJAG_00261","SJAG_02914","SJAG_01168","SJAG_03841","SJAG_05219","SJAG_01389","SJAG_01180","SJAG_02982","SJAG_02019","SJAG_02586","SJAG_02595","SJAG_05311","SJAG_03247","SJAG_00784","SJAG_04049","SJAG_02418","SJAG_02804","SJAG_07010","SJAG_01460","SJAG_02867","SJAG_04217","SJAG_03244","SJAG_03066","SJAG_03656","SJAG_04435","SJAG_00785","SJAG_00812","SJAG_02532","SJAG_01051","SJAG_01999","SJAG_02489","SJAG_04018","SJAG_04023","SJAG_02523","SJAG_03715","SJAG_03032","SJAG_00328","SJAG_01160","SJAG_00810","SJAG_02065","SJAG_02706","SJAG_04127","SJAG_04363","SJAG_04165","SJAG_00453","SJAG_03718","SJAG_02719","SJAG_04956","SJAG_00880","SJAG_01422","SJAG_03737","SJAG_02204","SJAG_02588","SJAG_03170","SJAG_03801","SJAG_05296","SJAG_01564","SJAG_00948","SJAG_02488","SJAG_03992","SJAG_00519","SJAG_04701","SJAG_00959","SJAG_00394","SJAG_00355","SJAG_04270","SJAG_00053","SJAG_00730","SJAG_00771","SJAG_03162","SJAG_00530","SJAG_04792","SJAG_02613","SJAG_02694","SJAG_04583","SJAG_04110","SJAG_01750","SJAG_03396","SJAG_03311","SJAG_04103","SJAG_03024","SJAG_01134","SJAG_01950","SJAG_02776","SJAG_02437","SJAG_01626","SJAG_01300","SJAG_00434","SJAG_02102","SJAG_00630","SJAG_06383","SJAG_04550","SJAG_03315","SJAG_02885","SJAG_00370","SJAG_01899","SJAG_01782","SJAG_04053","SJAG_04881","SJAG_04059","SJAG_03345","SJAG_03330","SJAG_00747","SJAG_01990","SJAG_03056","SJAG_01329","SJAG_00222","SJAG_04810","SJAG_02330","SJAG_03774","SJAG_00717","SJAG_02913","SJAG_01321","SJAG_03764","SJAG_01006","SJAG_01848","SJAG_02208","SJAG_00277","SJAG_04090","SJAG_02980","SJAG_05189"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[106880,118695,118441,96945,94805,117027,111151,93724,118172,108127,109117,95165,102952,113892,105813,118373,111548,113673,115711,118694,88239,103870,100972,87946,89882,90965,118081,93149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032541"},{"annotations":[92569],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099021"},{"annotations":[89883,103871],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160219"},{"annotations":[93379,105328,94200,98179,94562,97840,109340,116231,101800],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098554"},{"annotations":[103011,91149,113880,104280,113329,111742,94314,100688],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0072546"},{"annotations":[111846,95675,108148,116233,87948,109531,105474,99739,93033,92026,90706,93872,97864,100266,103583,118121,106881,91497,118374,90049,87998,114728,106794,91630,99505,104471,88979,100724,107017,102503,88401,113823,93245,87311,115630,93012,88241,99721,102601,102906,103477,100973,103982,114275,107194,110574,107036,113894,59033,112611,117120,112044,92515,95824,114170,88034,115104,109565,110810,103272,93119,96941,100512,116877,96388,89140,107502,111860,90074,108217,95193,99787,107331,113676,100327,110796,111297,92428,95099,93151,107510,104704,90659,89307,91387,108772,109406,109603,91425,110395,94119,87706,117819,89772,92535,95909,96272,96449,59741,104096,104191,110318,100573,109290,115267,89133,113122,118299,93699,94999,116471,106208,93996,105374,89725,107908,102539,115352,114280,101103,95577,98093,112962,113702,98351,102610,91012,116044,113831,101039,111550,114707,97595,98322,109637,62329,99515,89027,94129,96033,97698,106981,103960,110476,60844,100840,97895,91288,114391,110233,88127,110945,112888,89040,102686,92348,101656,113685,117322,96827,87266,93246,112503,112025,108732,96197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005789"},{"annotations":[102954,114459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071782"},{"annotations":[118082,64192,118926,108128],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098826"},{"annotations":[116731,109420,92475,92565,108071,111090],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000506"},{"annotations":[113432,91710,86913,90879,103210],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042765"},{"annotations":[109057,104311,116650,103469,104789,107161,88731],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000836"},{"annotations":[88994],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990604"},{"annotations":[90609,97891,108779,89851,104493,94202,99283,99489],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098553"},{"annotations":[102069,116340,116812,94808,99524,99144,100850],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008250"},{"annotations":[90727,107886],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160005"},{"annotations":[115099,97293,100096,94203,86851,98158,105817],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990578"},{"annotations":[97541,108823,105658,107794],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005784"},{"annotations":[109120,95221,90063,109896],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031207"},{"annotations":[87121,112048,97914,103315],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005787"},{"annotations":[93763,109245],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005785"},{"annotations":[97542],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071261"},{"annotations":[103070,98181,97841],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043541"},{"annotations":[103472,88735],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034098"}]},"cv_name":"cellular_component","definition":"A distinct region of the endoplasmic reticulum.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle subcompartment","termid":"GO:0031984"},{"relation_name":"part_of","term_name":"endoplasmic reticulum","termid":"GO:0005783"}],"gene_count":253,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00064":null,"SJAG_00068":null,"SJAG_00131":null,"SJAG_00175":null,"SJAG_00222":null,"SJAG_00261":null,"SJAG_00277":null,"SJAG_00284":null,"SJAG_00295":null,"SJAG_00328":null,"SJAG_00334":null,"SJAG_00339":null,"SJAG_00355":null,"SJAG_00360":null,"SJAG_00370":null,"SJAG_00394":null,"SJAG_00426":null,"SJAG_00434":null,"SJAG_00437":null,"SJAG_00453":null,"SJAG_00519":null,"SJAG_00530":null,"SJAG_00554":null,"SJAG_00557":null,"SJAG_00603":null,"SJAG_00630":null,"SJAG_00681":null,"SJAG_00717":null,"SJAG_00730":null,"SJAG_00747":null,"SJAG_00771":null,"SJAG_00784":null,"SJAG_00785":null,"SJAG_00790":null,"SJAG_00810":null,"SJAG_00812":null,"SJAG_00825":null,"SJAG_00831":null,"SJAG_00846":null,"SJAG_00880":null,"SJAG_00893":null,"SJAG_00895":null,"SJAG_00906":null,"SJAG_00919":null,"SJAG_00924":null,"SJAG_00948":null,"SJAG_00959":null,"SJAG_00999":null,"SJAG_01006":null,"SJAG_01051":null,"SJAG_01069":null,"SJAG_01078":null,"SJAG_01127":null,"SJAG_01134":null,"SJAG_01160":null,"SJAG_01168":null,"SJAG_01180":null,"SJAG_01223":null,"SJAG_01227":null,"SJAG_01233":null,"SJAG_01300":null,"SJAG_01307":null,"SJAG_01321":null,"SJAG_01329":null,"SJAG_01356":null,"SJAG_01389":null,"SJAG_01416":null,"SJAG_01422":null,"SJAG_01435":null,"SJAG_01460":null,"SJAG_01491":null,"SJAG_01527":null,"SJAG_01537":null,"SJAG_01558":null,"SJAG_01563":null,"SJAG_01564":null,"SJAG_01570":null,"SJAG_01626":null,"SJAG_01642":null,"SJAG_01709":null,"SJAG_01750":null,"SJAG_01782":null,"SJAG_01785":null,"SJAG_01803":null,"SJAG_01848":null,"SJAG_01857":null,"SJAG_01860":null,"SJAG_01899":null,"SJAG_01939":null,"SJAG_01950":null,"SJAG_01957":null,"SJAG_01990":null,"SJAG_01991":null,"SJAG_01999":null,"SJAG_02019":null,"SJAG_02032":null,"SJAG_02044":null,"SJAG_02056":null,"SJAG_02065":null,"SJAG_02080":null,"SJAG_02085":null,"SJAG_02102":null,"SJAG_02120":null,"SJAG_02196":null,"SJAG_02204":null,"SJAG_02208":null,"SJAG_02264":null,"SJAG_02330":null,"SJAG_02354":null,"SJAG_02418":null,"SJAG_02437":null,"SJAG_02446":null,"SJAG_02488":null,"SJAG_02489":null,"SJAG_02523":null,"SJAG_02532":null,"SJAG_02586":null,"SJAG_02588":null,"SJAG_02590":null,"SJAG_02595":null,"SJAG_02613":null,"SJAG_02640":null,"SJAG_02683":null,"SJAG_02694":null,"SJAG_02706":null,"SJAG_02716":null,"SJAG_02717":null,"SJAG_02719":null,"SJAG_02776":null,"SJAG_02804":null,"SJAG_02827":null,"SJAG_02839":null,"SJAG_02842":null,"SJAG_02867":null,"SJAG_02885":null,"SJAG_02903":null,"SJAG_02913":null,"SJAG_02914":null,"SJAG_02980":null,"SJAG_02982":null,"SJAG_03018":null,"SJAG_03024":null,"SJAG_03032":null,"SJAG_03056":null,"SJAG_03066":null,"SJAG_03115":null,"SJAG_03162":null,"SJAG_03170":null,"SJAG_03235":null,"SJAG_03244":null,"SJAG_03247":null,"SJAG_03261":null,"SJAG_03281":null,"SJAG_03292":null,"SJAG_03311":null,"SJAG_03315":null,"SJAG_03330":null,"SJAG_03333":null,"SJAG_03345":null,"SJAG_03396":null,"SJAG_03506":null,"SJAG_03509":null,"SJAG_03609":null,"SJAG_03656":null,"SJAG_03657":null,"SJAG_03670":null,"SJAG_03672":null,"SJAG_03715":null,"SJAG_03718":null,"SJAG_03737":null,"SJAG_03750":null,"SJAG_03764":null,"SJAG_03774":null,"SJAG_03795":null,"SJAG_03801":null,"SJAG_03812":null,"SJAG_03831":null,"SJAG_03841":null,"SJAG_03850":null,"SJAG_03878":null,"SJAG_03929":null,"SJAG_03930":null,"SJAG_03933":null,"SJAG_03943":null,"SJAG_03955":null,"SJAG_03992":null,"SJAG_04018":null,"SJAG_04023":null,"SJAG_04049":null,"SJAG_04053":null,"SJAG_04059":null,"SJAG_04090":null,"SJAG_04103":null,"SJAG_04110":null,"SJAG_04119":null,"SJAG_04127":null,"SJAG_04162":null,"SJAG_04165":null,"SJAG_04217":null,"SJAG_04231":null,"SJAG_04270":null,"SJAG_04294":null,"SJAG_04316":null,"SJAG_04319":null,"SJAG_04337":null,"SJAG_04345":null,"SJAG_04363":null,"SJAG_04384":null,"SJAG_04413":null,"SJAG_04417":null,"SJAG_04435":null,"SJAG_04451":null,"SJAG_04471":null,"SJAG_04513":null,"SJAG_04550":null,"SJAG_04583":null,"SJAG_04592":null,"SJAG_04608":null,"SJAG_04615":null,"SJAG_04701":null,"SJAG_04740":null,"SJAG_04792":null,"SJAG_04810":null,"SJAG_04821":null,"SJAG_04881":null,"SJAG_04883":null,"SJAG_04904":null,"SJAG_04913":null,"SJAG_04915":null,"SJAG_04938":null,"SJAG_04952":null,"SJAG_04954":null,"SJAG_04956":null,"SJAG_04975":null,"SJAG_04986":null,"SJAG_05013":null,"SJAG_05016":null,"SJAG_05022":null,"SJAG_05189":null,"SJAG_05219":null,"SJAG_05274":null,"SJAG_05278":null,"SJAG_05296":null,"SJAG_05306":null,"SJAG_05311":null,"SJAG_05327":null,"SJAG_05348":null,"SJAG_05414":null,"SJAG_06383":null,"SJAG_06425":null,"SJAG_06514":null,"SJAG_07010":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005783"],"is_obsolete":false,"name":"endoplasmic reticulum subcompartment","references_by_uniquename":{"GO_REF:0000104":null,"GO_REF:0000107":null,"PMID:21802294":null,"PMID:33495454":null},"termid":"GO:0098827","terms_by_termid":{"GO:0000506":null,"GO:0000836":null,"GO:0005784":null,"GO:0005785":null,"GO:0005787":null,"GO:0005789":null,"GO:0008250":null,"GO:0031207":null,"GO:0032541":null,"GO:0034098":null,"GO:0042765":null,"GO:0043541":null,"GO:0071261":null,"GO:0071782":null,"GO:0072546":null,"GO:0098553":null,"GO:0098554":null,"GO:0098826":null,"GO:0099021":null,"GO:0160005":null,"GO:0160219":null,"GO:1990578":null,"GO:1990604":null}}


id: MONDO:0008132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Leber plus disease","termid":"MONDO:0020478"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"optic atrophy with demyelinating disease of CNS","secondary_identifiers":["DOID:0111756","GARD:15098","MESH:C563496","OMIM:165200","UMLS:C1833830","MEDGEN:322290"],"synonyms":[{"name":"optic atrophy with demyelinating disease of CNS","type":"exact"}],"termid":"MONDO:0008132","xrefs":{"Monarch":{"xref_id":"0008132"}}}


id: PBO:0002819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-phosphatidylinositol 4-kinase Pik1","termid":"PBO:0002819"}


id: PR:P39750
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A flap endonuclease 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02239","PANTHER:PTHR11081:SF9","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":"flap endonuclease 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3G6.06c","secondary_identifiers":["UniProtKB:P39750"],"synonyms":[{"name":"DNA repair protein rad2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"FEN-1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FEN1","type":"exact"},{"name":"flap structure-specific endonuclease 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P39750"}


id: FYPO:0007210
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 total volume of all mitochondria in the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitochondrial morphology","termid":"FYPO:0003896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal mitochondrial volume","synonyms":[{"name":"normal mitochondrial volume during mitotic cell cycle","type":"related"},{"name":"normal mitochondrial volume during vegetative growth","type":"exact"},{"name":"normal total mitochondrial volume","type":"exact"}],"termid":"FYPO:0007210"}


id: MONDO:0008789
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anemia, nonspherocytic hemolytic","termid":"MONDO:0000105"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane","secondary_identifiers":["UMLS:C1859786","MEDGEN:349245","OMIM:206300","MESH:C565953"],"synonyms":[{"name":"anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane","type":"exact"}],"termid":"MONDO:0008789","xrefs":{"Monarch":{"xref_id":"0008789"}}}


id: PBO:0070629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 like 1 pseudogene 13","termid":"PBO:0070629"}


id: GO:0045505
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an intermediate chain of the dynein complex.","definition_xrefs":["GOC:bf"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"dynein intermediate chain binding","termid":"GO:0045505"}


id: PBO:0044273
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 13","termid":"PBO:0044273"}


id: MONDO:0009113
data:
  {"annotated_genes":["SJAG_02009"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86556],"is_not":false,"summary":null,"term":"MONDO:0009113"}]},"cv_name":"mondo","definition":"A rare, autosomal recessive, inherited disorder caused by mutation of the BPGM gene. It is characterized by hemolytic anemia and splenomegaly.","definition_xrefs":["NCIT:C131638"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hemolytic anemia","termid":"MONDO:0003689"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"anemia due to erythrocyte enzyme disorder","termid":"MONDO:0020585"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02009":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280","MONDO:0005066"],"is_obsolete":false,"name":"hemolytic anemia due to diphosphoglycerate mutase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1291620","Orphanet:714","MEDGEN:489898","DOID:0111630","GARD:1874","OMIM:222800"],"synonyms":[{"name":"BPGM deficiency","type":"related"},{"name":"DPGM deficiency","type":"related"},{"name":"bisphosphoglycerate mutase deficiency","type":"related"},{"name":"bisphosphoglyceromutase deficiency","type":"related"},{"name":"diphosphoglycerate mutase deficiency of erythrocyte","type":"related"},{"name":"diphosphoglycerate phosphatase deficiency","type":"exact"},{"name":"erythrocytosis, familial, 8","type":"exact"}],"termid":"MONDO:0009113","terms_by_termid":{"MONDO:0009113":null},"xrefs":{"Monarch":{"xref_id":"0009113"}}}


id: PBO:0082833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Constituent of 66S pre-ribosomal particles; forms a complex with Nop7p and Ytm1p that is required for maturation of the large ribosomal subunit; required for maturation of the 25S and 5.8S ribosomal RNAs; binds RNA via its C-terminal domain; homologous to mammalian Bop1","termid":"PBO:0082833"}


id: GO:0071090
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaIIb-beta3 integrin complex bound to fibronectin and tissue transglutaminase.","definition_xrefs":["PMID:10684262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"alphaIIb-beta3 integrin-fibronectin-tissue transglutaminase complex","synonyms":[{"name":"ITGA2b-ITGB3-FN1-TGM2 complex","type":"narrow"}],"termid":"GO:0071090"}


id: PBO:0045152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAH8 divergent transcript","termid":"PBO:0045152"}


id: PBO:0090937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin cortical patch component, with EF hand and WH2 motif Panl","termid":"PBO:0090937"}


id: PBO:0114290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OCIA domain-containing protein, involved in endocytosis pathway","termid":"PBO:0114290"}


id: PBO:0034612
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_cell_periphery","termid":"PBO:0034612"}


id: GO:0008537
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multisubunit complex that activates the hydrolysis of small nonubiquitinated peptides by binding to the proteasome core complex.","definition_xrefs":["GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"proteasome accessory complex","termid":"GO:0022624"}],"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"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"proteasome activator complex","synonyms":[{"name":"PA28","type":"narrow"}],"termid":"GO:0008537"}


id: MONDO:0013233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, primary bone dysplasia characterized by three distinct phenotypes, namely: 1) patients of average height with painful, osteoarthritic changes of the hip joints and no spinal abnormalities, 2) short-statured patients with predominantly truncal shortening, arm span exceeding height, dyspalstic changes of hips and varying degrees of platyspondyly, and 3) patients with dwarfism, various associated skeletal abnormalities (particularly of the knees and hands) and severe epiphyseal dysplasia (of hips, knees, hands, wrists) associated with significant platyspondyly. Most patients cannot walk long distances, and many have decreased joint spaces and sclerotic and cystic changes on imaging.","definition_xrefs":["Orphanet:99642"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia","termid":"MONDO:0100510"}],"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":"spondyloepimetaphyseal dysplasia, Handigodu type","secondary_identifiers":["MEDGEN:461895","icd11.foundation:2048058677","UMLS:C3150545","OMIM:613343","GARD:10741"],"synonyms":[{"name":"Handigodu JOINT disease","type":"related"},{"name":"Hjd","type":"related"},{"name":"spondyloepimetaphyseal dysplasia, Handigodu type","type":"exact"}],"termid":"MONDO:0013233","xrefs":{"Monarch":{"xref_id":"0013233"}}}


id: MONDO:0006547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any change in the skin which affects its appearance or texture. A rash may be localized to one part of the body, or affect all the skin. Rashes may cause the skin to change color, itch, become warm, bumpy, dry, cracked or blistered, swell and may be painful.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"exanthem","secondary_identifiers":["MEDGEN:8732","MESH:D005076","DOID:0050486","SCTID:271807003","UMLS:C0015230","ICD9:782.1","Wikipedia:Exanthem","NCIT:C39594","HP:0000988","EFO:1000697"],"synonyms":[{"name":"Rash","type":"exact"},{"name":"cutaneous eruption","type":"exact"},{"name":"exanthem","type":"exact"},{"name":"exanthem (disease)","type":"exact"},{"name":"exanthema","type":"exact"},{"name":"skin Rash","type":"exact"},{"name":"skin eruption","type":"exact"}],"termid":"MONDO:0006547","xrefs":{"Monarch":{"xref_id":"0006547"}}}


id: GO:0004500
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-ascorbate + dopamine + O2 = (R)-noradrenaline + dehydroascorbate + H2O.","definition_xrefs":["EC:1.14.17.1","RHEA:19117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen","termid":"GO:0016715"}],"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":"dopamine beta-monooxygenase activity","secondary_identifiers":["Reactome:R-HSA-209891","MetaCyc:DOPAMINE-BETA-MONOOXYGENASE-RXN","KEGG_REACTION:R02535"],"synonyms":[{"name":"(3,4-dihydroxyphenethylamine)beta-mono-oxygenase activity","type":"related"},{"name":"3,4-dihydroxyphenethylamine beta-oxidase activity","type":"related"},{"name":"3,4-dihydroxyphenethylamine,ascorbate:oxygen oxidoreductase (beta-hydroxylating)","type":"related"},{"name":"4-(2-aminoethyl)pyrocatechol beta-oxidase activity","type":"related"},{"name":"MDBH (membrane-associated dopamine beta-monooxygenase)","type":"related"},{"name":"SDBH (soluble dopamine beta-monooxygenase)","type":"related"},{"name":"dopa beta-hydroxylase activity","type":"related"},{"name":"dopamine b-hydroxylase activity","type":"exact"},{"name":"dopamine beta-hydroxylase activity","type":"related"},{"name":"dopamine beta-oxidase activity","type":"related"},{"name":"dopamine hydroxylase activity","type":"related"},{"name":"dopamine-B-hydroxylase activity","type":"related"},{"name":"oxygenase, dopamine beta-mono-","type":"related"},{"name":"phenylamine beta-hydroxylase activity","type":"related"}],"termid":"GO:0004500"}


id: PBO:0004366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PKC subfamily","termid":"PBO:0004366"}


id: PBO:0017486
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-actively_participates_in","termid":"PBO:0017486"}


id: MONDO:0002785
data:
  {"annotated_genes":["SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the skull base.","definition_xrefs":["NCIT:C4676"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull neoplasm","termid":"MONDO:0024653"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"skull base neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:138208","MESH:D019292","DOID:3842","UMLS:C0376527"],"synonyms":[{"name":"basicranium neoplasm","type":"exact"},{"name":"basicranium neoplasm (disease)","type":"exact"},{"name":"basicranium tumor","type":"exact"},{"name":"basicranium tumour","type":"exact"},{"name":"neoplasm of basicranium","type":"exact"},{"name":"neoplasm of skull base","type":"exact"},{"name":"neoplasm of the skull base","type":"exact"},{"name":"skull base cancer","type":"related"},{"name":"skull base neoplasm","type":"exact"},{"name":"skull base tumor","type":"exact"},{"name":"skull base tumour","type":"exact"},{"name":"tumor of basicranium","type":"exact"},{"name":"tumor of skull base","type":"exact"},{"name":"tumor of the skull base","type":"exact"},{"name":"tumors of skull base","type":"exact"},{"name":"tumour of basicranium","type":"exact"},{"name":"tumour of skull base","type":"exact"},{"name":"tumour of the skull base","type":"exact"},{"name":"tumours of skull base","type":"exact"}],"termid":"MONDO:0002785","terms_by_termid":{"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0002785"}}}


id: PBO:0041052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing 7 pseudogene 3","termid":"PBO:0041052"}


id: PBO:0062492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily B member 8","termid":"PBO:0062492"}


id: MONDO:0030077
data:
  {"annotated_genes":["SJAG_02618"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85006],"is_not":false,"summary":null,"term":"MONDO:0030077"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital vertebral-cardiac-renal anomalies syndrome","termid":"MONDO:0020831"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02618":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005267"],"is_obsolete":false,"name":"vertebral, cardiac, renal, and limb defects syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5394250","OMIM:618845","GARD:18510","MEDGEN:1709064"],"synonyms":[{"name":"Congenital Nad Deficiency Disorder 3","type":"exact"},{"name":"VCRL3","type":"exact"},{"name":"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3","type":"exact"},{"name":"vertebral, cardiac, renal, and limb defects syndrome 3","type":"exact"}],"termid":"MONDO:0030077","terms_by_termid":{"MONDO:0030077":null},"xrefs":{"Monarch":{"xref_id":"0030077"}}}


id: GO:1903779
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac conduction.","definition_xrefs":["GO_REF:0000058","GOC:mtg_cardiac_conduct_nov11","GOC:BHF","GOC:TermGenie","PMID:12967627","GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart contraction","termid":"GO:0008016"},{"relation_name":"regulates","term_name":"cardiac conduction","termid":"GO:0061337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cardiac conduction","secondary_identifiers":["Reactome:R-HSA-5578768","Reactome:R-HSA-5578775"],"termid":"GO:1903779"}


id: GO:1901143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of insulin.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein catabolic process","termid":"GO:0030163"},{"relation_name":"is_a","term_name":"insulin metabolic process","termid":"GO:1901142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0030163","GO:0008150"],"is_obsolete":false,"name":"insulin catabolic process","synonyms":[{"name":"insulin breakdown","type":"exact"},{"name":"insulin catabolism","type":"exact"},{"name":"insulin degradation","type":"exact"}],"termid":"GO:1901143"}


id: PATO:0001436
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An attachment quality inhering in a flower by virtue of the bearer's lacking a stalk, as in flowers or leaves that grow directly from the stem.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Sessility_(botany)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment quality","termid":"PATO:0001435"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sessile (sensu botany)","termid":"PATO:0001436"}


id: PBO:0047869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(2)(q33)","termid":"PBO:0047869"}


id: GO:1990664
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transcription factor complex formed by two or more subunits of Nkx-2.5. Nkx-2.5 is an evolutionary conserved transcription factor important for the specification and differentiation of cardiomyocytes during heart development. It is also required for spleen development. It binds DNA either as a monomer, or a homodimer, or a heterodimer complex to activate or inhibit expression of genes.","definition_xrefs":["PMID:22849347","GOC:ame"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"Nkx-2.5 complex","synonyms":[{"name":"NKX.2-5 homodimer complex","type":"related"},{"name":"NKX2.5 complex","type":"related"},{"name":"NKX2E homodimer complex","type":"related"},{"name":"Nkx-2.5 homodimer complex","type":"narrow"}],"termid":"GO:1990664"}


id: PBO:0087474
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of both RNase MRP and nuclear RNase P; RNase MRP cleaves pre-rRNA, while nuclear RNase P cleaves tRNA precursors to generate mature 5' ends and facilitates turnover of nuclear RNAs; binds to the RPR1 RNA subunit in RNase P","termid":"PBO:0087474"}


id: PBO:0056745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase 2A, methylcytidine","termid":"PBO:0056745"}


id: FYPO:0000223
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is longer, and has a greater length:diameter ratio, than normal, and has more than one septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"elongated septated vegetative cell","termid":"FYPO:0004750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000005","FYPO:0000032"],"is_obsolete":false,"name":"elongated multiseptate vegetative cell","synonyms":[{"name":"elongated multiseptate cell during mitotic cell cycle","type":"related"},{"name":"elongated multiseptate cells during vegetative growth","type":"exact"},{"name":"long multiseptate cells","type":"exact"}],"termid":"FYPO:0000223"}


id: PBO:0048149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FYN binding protein 1","termid":"PBO:0048149"}


id: GO:1990869
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 chemokine stimulus.","definition_xrefs":["PMID:11113082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"},{"relation_name":"is_a","term_name":"response to chemokine","termid":"GO:1990868"}],"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 chemokine","termid":"GO:1990869"}


id: GO:0047062
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+-)-trans-acenaphthene-1,2-diol + 2 NADP+ = acenaphthene-1,2-dione + 2 H+ + 2 NADPH.","definition_xrefs":["RHEA:22184","EC:1.10.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors, NAD or NADP as acceptor","termid":"GO:0016680"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"trans-acenaphthene-1,2-diol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04059","MetaCyc:1.10.1.1-RXN"],"synonyms":[{"name":"(+-)-trans-acenaphthene-1,2-diol:NADP+ oxidoreductase activity","type":"related"},{"name":"trans-1,2-acenaphthenediol dehydrogenase activity","type":"related"}],"termid":"GO:0047062"}


id: PBO:0063471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase complex component X","termid":"PBO:0063471"}


id: GO:0048635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of muscle development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle organ development","termid":"GO:0048634"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"muscle organ development","termid":"GO:0007517"}],"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 muscle organ development","synonyms":[{"name":"down regulation of muscle development","type":"exact"},{"name":"down-regulation of muscle development","type":"exact"},{"name":"downregulation of muscle development","type":"exact"},{"name":"inhibition of muscle development","type":"narrow"}],"termid":"GO:0048635"}


id: MONDO:0700105
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental defect during embryogenesis, non-human animal","termid":"MONDO:1011310"},{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"},{"relation_name":"is_a","term_name":"reproductive system disorder, non-human animal","termid":"MONDO:1011354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"difference of sexual differentiation, non-human animal","termid":"MONDO:0700105","xrefs":{"Monarch":{"xref_id":"0700105"}}}


id: MONDO:0020242
data:
  {"annotated_genes":["SJAG_02885","SJAG_04681","SJAG_01356"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[85590,85589],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010819"}]},"cv_name":"mondo","definition":"Macular dystrophy that is related to a change in a gene.","definition_xrefs":["NCIT:C140264"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null,"SJAG_04681":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"hereditary macular dystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:98664","MEDGEN:137919","NANDO:1200931","ICD10CM:H35.5","SCTID:276436007","UMLS:C0339508"],"synonyms":[{"name":"genetic macular dystrophy","type":"exact"},{"name":"genetic macular dystrophy (disease)","type":"exact"}],"termid":"MONDO:0020242","terms_by_termid":{"MONDO:0010819":null,"MONDO:0012099":null},"xrefs":{"Monarch":{"xref_id":"0020242"}}}


id: GO:0018260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of phospho-guanosine to a protein amino acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein nucleotidylation","termid":"GO:0018175"}],"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":"protein guanylylation","synonyms":[{"name":"protein amino acid guanylylation","type":"exact"}],"termid":"GO:0018260"}


id: GO:0032153
data:
  {"annotated_genes":["SJAG_04460","SJAG_01453","SJAG_02392","SJAG_02065","SJAG_04462","SJAG_02864","SJAG_01732","SJAG_02943","SJAG_00333","SJAG_03760","SJAG_00028","SJAG_00152","SJAG_03602","SJAG_02228","SJAG_05210","SJAG_00800","SJAG_00472","SJAG_00910","SJAG_01459","SJAG_04566","SJAG_04960","SJAG_01281","SJAG_05004","SJAG_04591","SJAG_03246","SJAG_01460","SJAG_03005","SJAG_04724","SJAG_00589","SJAG_02152","SJAG_02278","SJAG_04509","SJAG_01143","SJAG_01770","SJAG_02215","SJAG_00667","SJAG_03025","SJAG_02222","SJAG_02576","SJAG_03596","SJAG_03374","SJAG_00317","SJAG_03681","SJAG_04287","SJAG_00807","SJAG_03429","SJAG_01993","SJAG_03073","SJAG_04470","SJAG_02075","SJAG_04062","SJAG_01171","SJAG_01319","SJAG_03887","SJAG_01794","SJAG_02277","SJAG_02004","SJAG_01135","SJAG_01718","SJAG_02202","SJAG_03655","SJAG_03074","SJAG_01888","SJAG_04258","SJAG_04690","SJAG_00546","SJAG_07018","SJAG_02366","SJAG_00692","SJAG_00331","SJAG_03637","SJAG_00185","SJAG_02104","SJAG_01658","SJAG_04706","SJAG_00280","SJAG_02444","SJAG_04917","SJAG_04887","SJAG_05232","SJAG_04044","SJAG_01353","SJAG_03379","SJAG_04486","SJAG_03891","SJAG_03986","SJAG_01071","SJAG_04051","SJAG_02645","SJAG_03131","SJAG_02760","SJAG_01978","SJAG_00318","SJAG_00661","SJAG_04012","SJAG_01754","SJAG_04771","SJAG_03938","SJAG_02412","SJAG_02716","SJAG_00666","SJAG_01181","SJAG_04781","SJAG_02886","SJAG_01590","SJAG_02322","SJAG_04637","SJAG_00229","SJAG_04901","SJAG_02166","SJAG_02848","SJAG_01889","SJAG_00993","SJAG_00587","SJAG_02368","SJAG_03915","SJAG_04074","SJAG_04268","SJAG_01215","SJAG_01925","SJAG_01686","SJAG_03795","SJAG_01268","SJAG_00228","SJAG_04931","SJAG_04787","SJAG_04776","SJAG_02968","SJAG_02062","SJAG_04829","SJAG_02797","SJAG_01317","SJAG_00424","SJAG_04498","SJAG_04885","SJAG_04624","SJAG_03625","SJAG_03705","SJAG_03581","SJAG_01255","SJAG_04280","SJAG_00082","SJAG_02572","SJAG_02838","SJAG_04421","SJAG_03748","SJAG_02902","SJAG_02729","SJAG_01822","SJAG_04315","SJAG_04668","SJAG_03407","SJAG_01787","SJAG_00162","SJAG_05290","SJAG_03835","SJAG_01189","SJAG_03537","SJAG_03704","SJAG_00104","SJAG_00773","SJAG_03746","SJAG_04828","SJAG_04050","SJAG_04673","SJAG_01167","SJAG_01756","SJAG_04609","SJAG_00743","SJAG_01665","SJAG_02266","SJAG_02957","SJAG_01448","SJAG_02761","SJAG_01964","SJAG_00118","SJAG_04620","SJAG_03229","SJAG_01196","SJAG_01799","SJAG_02737","SJAG_03606","SJAG_05205","SJAG_01943","SJAG_03145","SJAG_03754","SJAG_03010","SJAG_01373","SJAG_00216","SJAG_02550","SJAG_01855","SJAG_00245","SJAG_05001","SJAG_04765","SJAG_01290","SJAG_01114","SJAG_03810","SJAG_01774","SJAG_02186","SJAG_02684","SJAG_03703","SJAG_00279","SJAG_03631","SJAG_03600","SJAG_02916","SJAG_02581","SJAG_03264","SJAG_03708","SJAG_01277","SJAG_01863","SJAG_02700","SJAG_04322","SJAG_01146","SJAG_00669","SJAG_04551","SJAG_00137","SJAG_02566","SJAG_04457","SJAG_01817","SJAG_04077","SJAG_03564","SJAG_02132","SJAG_02730","SJAG_01003","SJAG_04001","SJAG_01956","SJAG_00030","SJAG_04935","SJAG_01697","SJAG_02333","SJAG_00850","SJAG_02727","SJAG_02379","SJAG_00916","SJAG_04595","SJAG_03172","SJAG_04522","SJAG_02431","SJAG_03011","SJAG_04621","SJAG_03380","SJAG_02602","SJAG_02422","SJAG_04058","SJAG_00514","SJAG_05315","SJAG_03146","SJAG_04358","SJAG_03123","SJAG_04461","SJAG_05185","SJAG_00268","SJAG_02022","SJAG_02753","SJAG_03536","SJAG_04703","SJAG_05264","SJAG_03338","SJAG_04013","SJAG_04666","SJAG_03936","SJAG_05198","SJAG_02511","SJAG_00652","SJAG_03436","SJAG_04375","SJAG_01894","SJAG_02733","SJAG_03453","SJAG_03486","SJAG_01898","SJAG_04069","SJAG_00063","SJAG_00724","SJAG_01384","SJAG_01095","SJAG_04655","SJAG_00551","SJAG_00521","SJAG_02114","SJAG_04597","SJAG_04479","SJAG_03643","SJAG_03432","SJAG_00289","SJAG_02831","SJAG_01703","SJAG_03353","SJAG_00442","SJAG_05285","SJAG_00700","SJAG_01571","SJAG_00856","SJAG_01118","SJAG_01720","SJAG_02169","SJAG_00072","SJAG_04455","SJAG_03753","SJAG_03158","SJAG_02320","SJAG_03052","SJAG_01631","SJAG_01901","SJAG_03331","SJAG_01456","SJAG_01738","SJAG_02058","SJAG_01288","SJAG_00264","SJAG_01247","SJAG_03119","SJAG_02712","SJAG_02609","SJAG_05179","SJAG_02508","SJAG_00805","SJAG_01360","SJAG_03375","SJAG_05978","SJAG_01769","SJAG_01983","SJAG_01848","SJAG_03086","SJAG_00236","SJAG_00663","SJAG_00845","SJAG_03688","SJAG_00938","SJAG_02657","SJAG_02241","SJAG_03088","SJAG_01350","SJAG_03126","SJAG_00018","SJAG_03731","SJAG_00445","SJAG_00750","SJAG_00575","SJAG_00101","SJAG_00610","SJAG_00677","SJAG_03793","SJAG_04982"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[65136,86933,87006,87353,87462,87529,87608,87709,87727,87745,87937,88093,88233,88256,88425,88703,88807,88841,88906,89083,89178,89202,89285,89297,89329,89458,89686,89818,89943,89944,89945,89946,89947,89948,89949,89950,89951,90193,90222,90243,90317,90439,90546,90613,90637,90741,90958,91063,91072,91116,91233,91324,91588,91595,91667,91744,91753,91802,91812,91892,91987,92015,92058,92183,92509,92951,92978,93132,93321,93339,93354,93615,93708,93867,93881,93887,94055,94415,94426,94475,94764,94893,95142,95182,95327,95440,95754,95790,95802,95811,95895,95952,96060,96179,96283,96347,96423,96480,96511,96686,97037,97132,97728,97875,97947,98309,98318,98333,98391,98407,98497,98785,98815,99086,99178,99237,99256,99393,99626,99663,99852,99885,99940,100024,100100,100416,100425,100447,100453,100755,100843,100914,100967,101245,101260,101414,101639,101725,101817,101943,102109,102138,102158,102224,102239,102259,102339,102506,102746,102808,102951,102963,102987,103009,103024,103192,103213,103236,103414,104108,104138,104155,104219,104317,104633,104650,104665,104841,105112,105128,105403,105584,105607,105761,105841,105964,105969,106154,106160,106176,106328,106337,106498,106522,106589,106646,106670,106712,107440,107543,107611,107669,107776,107818,107848,108099,108126,108239,108279,108542,108857,108907,109002,109010,109088,109389,109592,109656,109667,110006,110062,110174,110243,110284,110349,110408,110535,110745,110916,110959,110984,111144,111164,111417,111436,111500,111627,111654,111789,111956,111965,112248,112262,112489,112538,112568,112702,112733,112845,112937,113153,113156,113262,113321,113528,113645,113660,113810,113863,114326,114404,114416,114442,114557,114787,114821,114957,115134,115303,115388,115553,115564,115576,115666,115685,115974,116225,116326,116414,116507,117000,117018,117224,117365,117386,117400,117490,117508,117821,117822,117921,118019,118037,118065,118080,118127,118220,118241,118281,118325,118359,118368,118470],"is_not":false,"summary":null,"term":"GO:0032153"},{"annotations":[118633,118634,118630,118640,101919,118632,118631,118785],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005826"},{"annotations":[115497,98496,102984,97923],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110115"},{"annotations":[99258,89331,87355,105586,106524,115305,91876],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032154"},{"annotations":[87464,90762],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090689"},{"annotations":[117388,102141,87010,90321,110465,104157,109595,102988,112570,96350,91877,93041,117402,90196,88526,90245,94059,101438,105610,110852,113532,87939,105764,100427,89205,87750,93215,113865,115307,95144,91748,101437,116056,91895,106714,99239,89334,96688,102341,99639,105587,90225,86992,99679],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000935"},{"annotations":[92842,118770,118641,118765,118772,118763],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990753"},{"annotations":[99574,105931,116428,100477,99864,100918,101820,112252,116680,108325,109090,110064],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000923"},{"annotations":[94061,97924,102561,104634,110008,87623,115671,117369,117389,91897,112541,87011,118370,107615,99398,107097,92017,97383,91804,102161,110245,97135,110285,118131,101263,116523,94850,102751,97211,98395,87941,106375,111356,104835,98819,97407],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031097"},{"annotations":[97384,100455,99605,107442,117370,112264,118132,103417,97308,101264],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036391"},{"annotations":[104668,100193,87746,95804,92063,115498,88429,97518,100758,105691,91805,116524,117371,97925,98499,93341,90198],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071341"},{"annotations":[113867,99853,92064,100172],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032178"},{"annotations":[88801,92018,94419,90246,93889,94769,96689,97787,100428,97519,101923,107617,89460,100194,111791,112848,93304,100759,105692,91806,116525,103195,118133,92065,110247,87362,118764,118766,118769,118331,118771,118773,90200,104844,106376,115394,106528,119033,110286,97136,87747,115310,117390,117138,94062,89288,100766,95805,117372],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110085"},{"annotations":[108546,117373,100195,100027,104635],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120106"},{"annotations":[100429,105693,93890,94420,108547,110287,112849,87748,103196,90247,117374,96690,89461,117391,111792,95331,95806],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120105"},{"annotations":[100457,97386,108548,106529,116432,116526,101924,103419,107618,92066,91807,99608,97520,117375,97137],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120104"},{"annotations":[115313,99641],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000936"},{"annotations":[115466,99611,105499,93988],"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":["PMID:16983191","PMID:15380095","PMID:12101122","GOC:krc","PMID:18165305","GOC:imk","GOC:bf","GOC:ns"],"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_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_03436":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_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_04885":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: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:0011508
data:
  {"annotated_genes":["SJAG_00980","SJAG_02460"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85668,85669],"is_not":false,"summary":null,"term":"MONDO:0011508"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-Hodgkin lymphoma","termid":"MONDO:0018908"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00980":null,"SJAG_02460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"lymphoma, non-Hodgkin, familial","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:118601006","OMIM:605027","ICD9:202.80","UMLS:C4721532","MEDGEN:1648388"],"synonyms":[{"name":"lymphoma, follicular, somatic","type":"exact"},{"name":"lymphoma, non-Hodgkin","type":"exact"},{"name":"lymphoma, non-Hodgkin, familial","type":"exact"},{"name":"lymphoma, non-Hodgkin, somatic","type":"exact"},{"name":"non-Hodgkin lymphoma","type":"related"}],"termid":"MONDO:0011508","terms_by_termid":{"MONDO:0011508":null},"xrefs":{"Monarch":{"xref_id":"0011508"}}}


id: PBO:0056133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysozyme like 2","termid":"PBO:0056133"}


id: GO:0060900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a camera-type eye from unspecified neurectoderm. This process begins with the differentiation of cells that form the optic field and ends when the optic cup has attained its shape.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"embryonic camera-type eye morphogenesis","termid":"GO:0048596"}],"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":"embryonic camera-type eye formation","termid":"GO:0060900"}


id: PBO:0056993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 34a","termid":"PBO:0056993"}


id: PBO:0084977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH-dependent aldehyde reductase; involved in detoxification of furfural; expression is upregulated in cells treated with the aldehydes furfural and glycolaldehyde, the mycotoxin patulin, and also the quinone methide triterpene celastrol; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm","termid":"PBO:0084977"}


id: GO:0016503
data:
  {"annotated_genes":["SJAG_01978","SJAG_01345"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004932"},{"annotations":[87619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036320"}]},"cv_name":"molecular_function","definition":"Combining with a pheromone to initiate a change in cell activity. A pheromone is a substance used in olfactory communication between organisms of the same species eliciting a change in sexual or social behavior.","definition_xrefs":["GOC:hjd","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01345":null,"SJAG_01978":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"pheromone receptor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0016503","terms_by_termid":{"GO:0004932":null,"GO:0036320":null}}


id: PBO:0045865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EEF1A lysine methyltransferase 4","termid":"PBO:0045865"}


id: GO:0001700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the embryo over time, from zygote formation through syncytial blastoderm to the hatching of the first instar larva. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryo development ending in birth or egg hatching","termid":"GO:0009792"}],"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":"embryonic development via the syncytial blastoderm","termid":"GO:0001700"}


id: GO:0051347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of transferase activity, the catalysis of the transfer of a group, e.g. a methyl group, glycosyl group, acyl group, phosphorus-containing, or other groups, from a donor compound to an acceptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catalytic activity","termid":"GO:0043085"},{"relation_name":"is_a","term_name":"regulation of transferase activity","termid":"GO:0051338"}],"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 transferase activity","synonyms":[{"name":"activation of transferase activity","type":"narrow"},{"name":"stimulation of transferase activity","type":"narrow"},{"name":"transferase activator","type":"exact"},{"name":"up regulation of transferase activity","type":"exact"},{"name":"up-regulation of transferase activity","type":"exact"},{"name":"upregulation of transferase activity","type":"exact"}],"termid":"GO:0051347"}


id: _global:immediately_causally_downstream_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_downstream_of","termid":"_global:causally_downstream_of"},{"relation_name":"is_a","term_name":"immediately_preceded_by","termid":"_global:immediately_preceded_by"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immediately_causally_downstream_of","secondary_identifiers":["RO:0002405"],"termid":"_global:immediately_causally_downstream_of"}


id: SO:0001828
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequencer read of a genomic DNA substrate.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"read","termid":"SO:0000150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genomic_DNA_read","synonyms":[{"name":"gDNA read","type":"exact"},{"name":"gDNA_read","type":"exact"},{"name":"genomic DNA read","type":"exact"}],"termid":"SO:0001828"}


id: FYPO:0001691
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 paraquat.","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:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002058","FYPO:0002057","FYPO:0000003","FYPO:0002060","FYPO:0000257"],"is_obsolete":false,"name":"normal growth on paraquat","synonyms":[{"name":"normal cell population growth in presence of paraquat","type":"exact"},{"name":"normal cell population growth on paraquat","type":"exact"},{"name":"normal cellular response to paraquat","type":"related"},{"name":"normal vegetative cell population growth on paraquat","type":"exact"}],"termid":"FYPO:0001691"}


id: GO:0031548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of signaling via the brain-derived neurotrophic factor receptor signaling pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"brain-derived neurotrophic factor receptor signaling pathway","termid":"GO:0031547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of brain-derived neurotrophic factor receptor signaling pathway","synonyms":[{"name":"regulation of BDNF receptor signaling pathway","type":"exact"},{"name":"regulation of BDNF receptor signalling pathway","type":"exact"},{"name":"regulation of brain-derived neurotrophic factor receptor signalling pathway","type":"exact"}],"termid":"GO:0031548"}


id: PBO:0051522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor accessory protein","termid":"PBO:0051522"}


id: GO:0102715
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A17 + 2-oxoglutarate + O2 = gibberellin A28 + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A17,oxoglutarate:oxygen oxidoreductase activity (obsolete GO:0102715)","termid":"GO:0102715"}


id: MONDO:0044787
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, keratinizing or non-keratinizing squamous cell carcinoma arising from the mucosal epithelium of the nasal cavity or the paranasal sinuses. It affects most often the maxillary sinus. Less frequently, it arises from the nasal cavity, ethmoid sinus, sphenoid sinus, and frontal sinus. Symptoms include nasal fullness, epistaxis, rhinorhea, pain, and paresthesia. Patients with nasal squamous cell carcinoma usually present earlier than patients with maxillary sinus carcinoma and have a better prognosis compared to the latter group.","definition_xrefs":["NCIT:C68611"],"direct_ancestors":[{"relation_name":"is_a","term_name":"head and neck squamous cell carcinoma","termid":"MONDO:0010150"},{"relation_name":"is_a","term_name":"nasal cavity and paranasal sinus carcinoma","termid":"MONDO:0056819"}],"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":"nasal cavity and paranasal sinus squamous cell carcinoma","secondary_identifiers":["UMLS:C0280332","MEDGEN:124722"],"synonyms":[{"name":"nasal cavity and paranasal sinus squamous cell cancer","type":"exact"},{"name":"nasal cavity and paranasal sinus squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0044787","xrefs":{"Monarch":{"xref_id":"0044787"}}}


id: MONDO:0014130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Dowling-Degos disease in which the cause of the disease is a mutation in the POFUT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Dowling-Degos disease","termid":"MONDO:0008371"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"Dowling-Degos disease 2","secondary_identifiers":["MEDGEN:815477","GARD:15944","UMLS:C3809147","OMIM:615327"],"synonyms":[{"name":"DDD2","type":"related"},{"name":"Dowling-Degos disease 2","type":"exact"},{"name":"Dowling-Degos disease caused by mutation in POFUT1","type":"exact"},{"name":"Dowling-Degos disease type 2","type":"exact"},{"name":"POFUT1 Dowling-Degos disease","type":"exact"}],"termid":"MONDO:0014130","xrefs":{"Monarch":{"xref_id":"0014130"}}}


id: MONDO:0006592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Parapsoriasis describes a group ofskin diseases that can be characterized by scaly patches or slightly elevated papules and/or plaques (red, scaly patches) that have a resemblance to psoriasis. However, this description includes several inflammatory cutaneous diseases that are unrelated with respect to pathogenesis, histopathology, and response to treatment. Because of the variation in clinical presentation and a lack of a specific diagnostic finding on histopathology, a uniformly accepted definition of parapsoriasis remains lacking. There are 2 general forms: a small plaque type, which is usually benign, and a large plaque type, which is a precursor of cutaneous T-cell lymphoma (CTCL).Treatment of small plaque parapsoriasis is unnecessary but can include emollients, topical tar preparations or corticosteroids, and/or phototherapy. Treatment of large plaque parapsoriasis is phototherapy or topical corticosteroids.","direct_ancestors":[{"relation_name":"is_a","term_name":"psoriasis","termid":"MONDO:0005083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"parapsoriasis","secondary_identifiers":["SCTID:88233000","MEDGEN:10579","ICD9:696.2","MESH:D010267","NCIT:C3312","Wikipedia:Parapsoriasis","DOID:9088","EFO:1000747","ICD10CM:L41","UMLS:C0030491"],"synonyms":[{"name":"digitate dermatosis","type":"related"},{"name":"parapsoriasis en plaque","type":"related"}],"termid":"MONDO:0006592","xrefs":{"Monarch":{"xref_id":"0006592"}}}


id: FYPO:0004782
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which spores germinate to a greater extent than wild type following exposure to ionizing radiation.","definition_xrefs":["PMID:25533340","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell phenotype","termid":"FYPO:0003037"}],"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":"spores resistant to ionizing radiation","synonyms":[{"name":"resistant to ionizing radiation in spore phase","type":"exact"},{"name":"spores resistant to IR","type":"exact"}],"termid":"FYPO:0004782"}


id: GO:0051969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of transmission of a nerve impulse, the sequential electrochemical polarization and depolarization that travels across the membrane of a neuron in response to stimulation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"is_a","term_name":"regulation of nervous system process","termid":"GO:0031644"},{"relation_name":"regulates","term_name":"transmission of nerve impulse","termid":"GO:0019226"}],"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 transmission of nerve impulse","synonyms":[{"name":"regulation of conduction of nerve impulse","type":"exact"}],"termid":"GO:0051969"}


id: PBO:0051496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobin superfamily member 21","termid":"PBO:0051496"}


id: FYPO:0008175
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the amount of oxygen consumed by cells in a given time is normal.","direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative phenotype","termid":"FYPO:0001312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal oxygen consumption","termid":"FYPO:0008175"}


id: MONDO:0005955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete scrub typhus (obsolete MONDO:0005955)","termid":"MONDO:0005955","xrefs":{"Monarch":{"xref_id":"0005955"}}}


id: PBO:0072915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scavenger receptor class A member 5","termid":"PBO:0072915"}


id: MONDO:0018674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic fibrotic inflammatory process affecting the salivary gland. Signs and symptoms include firm and painful swelling of the salivary gland, often associated with the presence of salivary gland stones.","definition_xrefs":["NCIT:C82887"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease of ear, nose and throat","termid":"MONDO:0000587"},{"relation_name":"is_a","term_name":"IgG4-related disease","termid":"MONDO:0017287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"IgG4-related submandibular gland disease","secondary_identifiers":["UMLS:C5679995","SCTID:448131008","Orphanet:449432","MEDGEN:1830092","GARD:21884","icd11.foundation:588811750"],"synonyms":[{"name":"IgG4-related sialadenitis","type":"exact"},{"name":"Kuttner tumor","type":"exact"},{"name":"Kuttner tumour","type":"exact"},{"name":"Kuttner's tumor","type":"exact"},{"name":"Kuttner's tumour","type":"exact"},{"name":"Küttner tumor","type":"exact"},{"name":"Küttner tumour","type":"exact"},{"name":"chronic sclerosing sialadenitis","type":"exact"}],"termid":"MONDO:0018674","xrefs":{"Monarch":{"xref_id":"0018674"}}}


id: PBO:0081009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 45","termid":"PBO:0081009"}


id: PBO:0091862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF4504 family protein, human C1orf74 ortholog","termid":"PBO:0091862"}


id: GO:0045639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of myeloid cell differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of myeloid cell differentiation","termid":"GO:0045637"},{"relation_name":"positively_regulates","term_name":"myeloid cell differentiation","termid":"GO:0030099"}],"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 myeloid cell differentiation","synonyms":[{"name":"activation of myeloid cell differentiation","type":"narrow"},{"name":"stimulation of myeloid cell differentiation","type":"narrow"},{"name":"up regulation of myeloid cell differentiation","type":"exact"},{"name":"up-regulation of myeloid cell differentiation","type":"exact"},{"name":"upregulation of myeloid cell differentiation","type":"exact"}],"termid":"GO:0045639"}


id: PR:Q9Y813
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpr2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease P protein subunit rpr2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1105.16c","synonyms":[{"name":"RNA-processing protein rpr2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rpr2","type":"exact"}],"termid":"PR:Q9Y813"}


id: PBO:0005445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin Kap113","termid":"PBO:0005445"}


id: PBO:0039885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP42 pseudogene 2","termid":"PBO:0039885"}


id: MONDO:0016630
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated delta-storage pool disease is a rare, isolated, constitutional thrombocytopenia disorder characterized by defective formation and/or malfunction of platelet dense granules, as well as melanosomes in skin cells, resulting in variable manifestations ranging from mild bleeding and easy bruising to moderate mucous/cutaneous hemorrhagic diathesis and bleeding complications after surgery.","definition_xrefs":["Orphanet:248340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombocytopenia","termid":"MONDO:0100241"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"isolated delta-storage pool disease","secondary_identifiers":["GARD:20674","icd11.foundation:2133567182"],"synonyms":[{"name":"isolated delta-SPD","type":"exact"},{"name":"isolated dense-SPD","type":"exact"},{"name":"isolated dense-storage pool disease","type":"exact"}],"termid":"MONDO:0016630","xrefs":{"Monarch":{"xref_id":"0016630"}}}


id: PBO:0042207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin I family member 2","termid":"PBO:0042207"}


id: MONDO:0032689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066","MONDO:0005328"],"is_obsolete":false,"name":"retinitis pigmentosa 85","secondary_identifiers":["DOID:0112142","GARD:16342","MEDGEN:1682947","UMLS:C5193041","OMIM:618345"],"synonyms":[{"name":"RETINITIS PIGMENTOSA 85","type":"related"},{"name":"RP85","type":"related"}],"termid":"MONDO:0032689","xrefs":{"Monarch":{"xref_id":"0032689"}}}


id: GO:0050163
data:
  {"annotated_genes":["SJAG_00493"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106270],"is_not":false,"summary":null,"term":"GO:0050163"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: oxaloacetate = <stereo>enol</stereo>-oxaloacetate.","definition_xrefs":["EC:5.3.2.2","RHEA:16021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting keto- and enol-groups","termid":"GO:0016862"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00493":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"oxaloacetate tautomerase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:OXALOACETATE-TAUTOMERASE-RXN","KEGG_REACTION:R00363"],"synonyms":[{"name":"oxalacetic keto-enol isomerase activity","type":"related"},{"name":"oxaloacetate keto-enol tautomerase activity","type":"related"},{"name":"oxaloacetate keto-enol-isomerase activity","type":"related"}],"termid":"GO:0050163","terms_by_termid":{"GO:0050163":null}}


id: GO:0019008
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that possesses molybdopterin synthase activity. In E. coli, the complex is a heterotetramer consisting of two MoaD and two MoaE subunits.","definition_xrefs":["PMID:15709772","GOC:mah","PMID:12571227"],"gene_count":0,"genotype_count":0,"name":"obsolete molybdopterin synthase complex (obsolete GO:0019008)","synonyms":[{"name":"molybdopterin converting factor complex","type":"exact"}],"termid":"GO:0019008"}


id: GO:0004766
data:
  {"annotated_genes":["SJAG_04481"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102258],"is_not":false,"summary":null,"term":"GO:0004766"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosylmethioninamine + putrescine = 5'-methylthioadenosine + spermidine.","definition_xrefs":["EC:2.5.1.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04481":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016765"],"is_obsolete":false,"name":"spermidine synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-351215","RHEA:12721","MetaCyc:SPERMIDINESYN-RXN"],"synonyms":[{"name":"S-adenosylmethioninamine:putrescine 3-aminopropyltransferase activity","type":"related"},{"name":"SpeE","type":"related"},{"name":"aminopropyltransferase activity","type":"related"},{"name":"putrescine aminopropyltransferase activity","type":"related"},{"name":"spermidine synthetase activity","type":"related"}],"termid":"GO:0004766","terms_by_termid":{"GO:0004766":null}}


id: PBO:0076058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stonin 1","termid":"PBO:0076058"}


id: FYPO:0002607
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 histone H2A phosphorylation occurs to a greater extent than normal at tRNA genes (tDNA) in centromeric regions during S phase of the mitotic cell cycle. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H2A phosphorylation during vegetative growth","termid":"FYPO:0002596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased histone H2A phosphorylation at centromeric tDNA during mitotic S phase","synonyms":[{"name":"increased histone H2A phosphorylation at centromeric tDNA during mitotic S phase during vegetative growth","type":"exact"}],"termid":"FYPO:0002607"}


id: GO:0048088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of a pattern of pigment in males.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental pigmentation","termid":"GO:0048070"},{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"male pigmentation","termid":"GO:0048094"}],"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 male pigmentation","termid":"GO:0048088"}


id: GO:1902046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of Fas signaling pathway.","definition_xrefs":["GOC:TermGenie","PMID:17245429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of Fas signaling pathway","termid":"GO:1902044"},{"relation_name":"positively_regulates","term_name":"Fas signaling pathway","termid":"GO:0036337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of Fas signaling pathway","synonyms":[{"name":"activation of Apo-1 signaling pathway","type":"narrow"},{"name":"activation of CD95 signaling pathway","type":"narrow"},{"name":"activation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"activation of Fas receptor signaling pathway","type":"narrow"},{"name":"activation of Fas signaling pathway","type":"narrow"},{"name":"activation of Fas-FasL signaling pathway","type":"narrow"},{"name":"activation of FasL signaling pathway","type":"related"},{"name":"activation of FasR signaling pathway","type":"narrow"},{"name":"positive regulation of Apo-1 signaling pathway","type":"exact"},{"name":"positive regulation of CD95 signaling pathway","type":"exact"},{"name":"positive regulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"positive regulation of Fas receptor signaling pathway","type":"exact"},{"name":"positive regulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"positive regulation of FasL signaling pathway","type":"related"},{"name":"positive regulation of FasR signaling pathway","type":"exact"},{"name":"up regulation of Apo-1 signaling pathway","type":"exact"},{"name":"up regulation of CD95 signaling pathway","type":"exact"},{"name":"up regulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"up regulation of Fas receptor signaling pathway","type":"exact"},{"name":"up regulation of Fas signaling pathway","type":"exact"},{"name":"up regulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"up regulation of FasL signaling pathway","type":"related"},{"name":"up regulation of FasR signaling pathway","type":"exact"},{"name":"up-regulation of Apo-1 signaling pathway","type":"exact"},{"name":"up-regulation of CD95 signaling pathway","type":"exact"},{"name":"up-regulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"up-regulation of Fas receptor signaling pathway","type":"exact"},{"name":"up-regulation of Fas signaling pathway","type":"exact"},{"name":"up-regulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"up-regulation of FasL signaling pathway","type":"related"},{"name":"up-regulation of FasR signaling pathway","type":"exact"},{"name":"upregulation of Apo-1 signaling pathway","type":"exact"},{"name":"upregulation of CD95 signaling pathway","type":"exact"},{"name":"upregulation of FAS ligand-Fas signaling pathway","type":"narrow"},{"name":"upregulation of Fas receptor signaling pathway","type":"exact"},{"name":"upregulation of Fas signaling pathway","type":"exact"},{"name":"upregulation of Fas-FasL signaling pathway","type":"narrow"},{"name":"upregulation of FasL signaling pathway","type":"related"},{"name":"upregulation of FasR signaling pathway","type":"exact"}],"termid":"GO:1902046"}


id: FYPO:0001373
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"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118757],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"}],"single_locus_phenotype":[{"annotations":[118775,118776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000731"},{"annotations":[118754,118747,118758,118746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the medial cortex is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell cortex","termid":"FYPO:0006867"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01143":null,"SJAG_01665":null,"SJAG_02392":null,"SJAG_03596":null,"SJAG_03703":null,"SJAG_04498":null},"genotype_count":3,"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"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01143","SJAG_02392"],"name":"abnormal protein localization to medial cortex","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_01143","SJAG_02392"],"single_locus_genotype_uniquenames":["mid1delta","pom1delta"],"synonyms":[{"name":"abnormal protein localisation to medial cortex","type":"exact"},{"name":"abnormal protein localization to medial ring","type":"exact"}],"termid":"FYPO:0001373","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000731":null,"FYPO:0007177":null,"FYPO_EXT:0000001":null}}


id: PBO:0003076
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Tup11","termid":"PBO:0003076"}


id: GO:0035684
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a helper T cell from the blood vessels into the surrounding tissue. A helper T-cell is an effector T cell that provides help in the form of secreted cytokines to other immune cells.","definition_xrefs":["GOC:BHF","CL:0000912"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell extravasation","termid":"GO:0072683"}],"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":"helper T cell extravasation","synonyms":[{"name":"T-helper cell extravasation","type":"exact"},{"name":"helper T-cell extravasation","type":"exact"}],"termid":"GO:0035684"}


id: MONDO:0004473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that affects the epiglottis. The vast majority of cases are squamous cell carcinomas.","definition_xrefs":["NCIT:C4836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epiglottis neoplasm","termid":"MONDO:0004109"},{"relation_name":"is_a","term_name":"carcinoma of supraglottis","termid":"MONDO:0004357"},{"relation_name":"is_a","term_name":"hypopharyngeal carcinoma","termid":"MONDO:0005216"},{"relation_name":"is_a","term_name":"oropharyngeal carcinoma","termid":"MONDO:0044926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"epiglottis cancer","secondary_identifiers":["UMLS:C1112382","MEDGEN:249035","ICD10CM:C10.1","NCIT:C35697","DOID:8133","ICD9:146.4","SCTID:187681002"],"synonyms":[{"name":"cancer of epiglottis","type":"exact"},{"name":"epiglottic cancer","type":"exact"},{"name":"epiglottic carcinoma","type":"narrow"},{"name":"epiglottic throat cancer","type":"exact"},{"name":"epiglottis cancer","type":"exact"},{"name":"malignant Epiglottis neoplasm","type":"exact"},{"name":"malignant Epiglottis tumor","type":"exact"},{"name":"malignant Epiglottis tumour","type":"exact"},{"name":"malignant epiglottic neoplasm","type":"exact"},{"name":"malignant epiglottic tumor","type":"exact"},{"name":"malignant epiglottic tumour","type":"exact"},{"name":"malignant epiglottis neoplasm","type":"exact"},{"name":"malignant neoplasm of Epiglottis","type":"exact"},{"name":"malignant neoplasm of anterior aspect of epiglottis","type":"narrow"},{"name":"malignant neoplasm of anterior epiglottis","type":"exact"},{"name":"malignant neoplasm of anterior surface of epiglottis","type":"narrow"},{"name":"malignant neoplasm of epiglottis","type":"exact"},{"name":"malignant neoplasm of the Epiglottis","type":"exact"},{"name":"malignant tumor of Epiglottis","type":"exact"},{"name":"malignant tumor of the Epiglottis","type":"exact"},{"name":"malignant tumour of Epiglottis","type":"exact"},{"name":"malignant tumour of the Epiglottis","type":"exact"}],"termid":"MONDO:0004473","xrefs":{"Monarch":{"xref_id":"0004473"}}}


id: GO:0106419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-N6-lipoyl-L-lysyl-[protein] + H2O + NAD+ = 2''-O-lipoyl-ADP-D-ribose + L-lysyl-[protein] + nicotinamide.","definition_xrefs":["RHEA:63640","PMID:25525879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"NAD-dependent protein lipoamidase activity","secondary_identifiers":["MetaCyc:RXN-22964","EC:2.3.1.313"],"termid":"GO:0106419"}


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


id: PR:P87133
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug143 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87133"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 143 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC167.06c","synonyms":[{"name":"Spom972h-mug143","type":"exact"}],"termid":"PR:P87133"}


id: MONDO:0020309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Landau-Kleffner syndrome (obsolete MONDO:0020309)","termid":"MONDO:0020309","xrefs":{"Monarch":{"xref_id":"0020309"}}}


id: PBO:0051428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 3-7 (pseudogene)","termid":"PBO:0051428"}


id: PBO:0052265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 3B","termid":"PBO:0052265"}


id: PBO:0002633
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.3.46","termid":"PBO:0002633"}


id: PBO:0056799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitofusin 2","termid":"PBO:0056799"}


id: MONDO:0016096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor other than dysgerminoma that arises from the ovary.","definition_xrefs":["NCIT:C102870"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian primitive germ cell tumor","termid":"MONDO:0003408"},{"relation_name":"is_a","term_name":"nongerminomatous germ cell tumor","termid":"MONDO:0021656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant non-dysgerminomatous germ cell tumor of ovary","secondary_identifiers":["Orphanet:206538","MEDGEN:1826164","UMLS:C5679783","GARD:20349"],"synonyms":[{"name":"non-dysgerminomatous germ cell cancer of ovary","type":"exact"},{"name":"ovarian Nondysgerminomatous germ cell tumor","type":"exact"},{"name":"ovarian Nondysgerminomatous germ cell tumour","type":"exact"},{"name":"ovarian non-dysgerminomatous germ cell tumor","type":"exact"},{"name":"ovarian non-dysgerminomatous germ cell tumour","type":"exact"}],"termid":"MONDO:0016096","xrefs":{"Monarch":{"xref_id":"0016096"}}}


id: PBO:0042477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDH3 antisense RNA 1","termid":"PBO:0042477"}


id: MONDO:1010754
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary sparse hair and dental aplasia in dogs associated with a variation in the EDA gene.","definition_xrefs":["OMIA:000543-9615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease, non-human animal","termid":"MONDO:1012575"},{"relation_name":"is_a","term_name":"hypohidrotic ectodermal dysplasia, non-human animal","termid":"MONDO:1012576"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked hypohidrotic ectodermal dysplasia, EDA-related, dog","termid":"MONDO:1010754","xrefs":{"Monarch":{"xref_id":"1010754"}}}


id: PBO:0046472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERBIN divergent transcript","termid":"PBO:0046472"}


id: MONDO:1011944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple exostoses, non-human animal","secondary_identifiers":["OMIA:000354"],"termid":"MONDO:1011944","xrefs":{"Monarch":{"xref_id":"1011944"}}}


id: PBO:0057986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3912","termid":"PBO:0057986"}


id: PATO:0001601
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A rotation quality inhering in a bearer by virtue of being rotated towards the front of an organism.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rotated","termid":"PATO:0001599"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anteriorly rotated","termid":"PATO:0001601"}


id: MONDO:0007179
data:
  {"annotated_genes":["SJAG_04810","SJAG_01787","SJAG_03453","SJAG_03850","SJAG_00610"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[85308,85309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"},{"annotations":[86019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008218"},{"annotations":[85671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013276"}]},"cv_name":"mondo","definition":"A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis).","definition_xrefs":["NCIT:C2889"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hypersensitivity reaction disease","termid":"MONDO:0000605"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_03453":null,"SJAG_03850":null,"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OBI:1110054","OMIM:109100","SCTID:85828009","UMLS:C0004364","EFO:0005809","ICD9:720","DOID:417","MESH:D001327","ICD9:279.49","MEDGEN:2135","ICD9:279.4"],"synonyms":[{"name":"autoimmune disease","type":"exact"},{"name":"autoimmune disease or disorder","type":"exact"},{"name":"autoimmune disorder","type":"exact"},{"name":"autoimmune hypersensitivity disease","type":"related"},{"name":"disease, autoimmune","type":"exact"},{"name":"hypersensitivity reaction type II disease","type":"related"}],"termid":"MONDO:0007179","terms_by_termid":{"MONDO:0008218":null,"MONDO:0013276":null,"MONDO:0013767":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0007179"}}}


id: PBO:0063797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate dehydrogenase","termid":"PBO:0063797"}


id: PR:O60080
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent RNA helicase DDX56 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO05031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase dbp9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1494.06c","secondary_identifiers":["UniProtKB:O60080"],"synonyms":[{"name":"Spom972h-DDX56","type":"exact"}],"termid":"PR:O60080"}


id: FYECO:0000394
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which caspofungin was added to the medium or assay buffer in excess compared to standard medium or assay buffers at lethal dose for the assayed cell density.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ caspofungin SLD","termid":"FYECO:0000393"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ caspofungin LD","termid":"FYECO:0000394"}


id: GO:0044391
data:
  {"annotated_genes":["SJAG_01364","SJAG_01609","SJAG_04168","SJAG_04490","SJAG_02184","SJAG_02755","SJAG_02479","SJAG_01045","SJAG_00628","SJAG_04204","SJAG_04814","SJAG_03919","SJAG_03584","SJAG_04847","SJAG_02870","SJAG_01303","SJAG_04998","SJAG_02359","SJAG_02522","SJAG_01287","SJAG_01226","SJAG_03762","SJAG_02477","SJAG_03040","SJAG_06612","SJAG_00749","SJAG_03065","SJAG_01468","SJAG_03254","SJAG_03262","SJAG_00944","SJAG_02243","SJAG_03636","SJAG_00537","SJAG_03335","SJAG_03922","SJAG_00034","SJAG_02546","SJAG_01512","SJAG_01322","SJAG_00069","SJAG_01630","SJAG_03053","SJAG_01829","SJAG_01588","SJAG_06110","SJAG_02121","SJAG_03192","SJAG_04244","SJAG_03425","SJAG_00921","SJAG_02890","SJAG_04066","SJAG_02283","SJAG_00799","SJAG_02020","SJAG_00148","SJAG_00733","SJAG_00765","SJAG_02871","SJAG_04176","SJAG_03133","SJAG_02081","SJAG_00155","SJAG_03159","SJAG_02531","SJAG_02340","SJAG_02224","SJAG_05216","SJAG_04476","SJAG_03176","SJAG_04746","SJAG_01387","SJAG_04174","SJAG_04414","SJAG_00465","SJAG_03297","SJAG_05221","SJAG_02280","SJAG_01413","SJAG_03034","SJAG_02201","SJAG_02452","SJAG_01365","SJAG_02611","SJAG_04478","SJAG_06253","SJAG_04494","SJAG_01478","SJAG_04378","SJAG_02643","SJAG_04342","SJAG_00060","SJAG_02046","SJAG_03284","SJAG_00503","SJAG_02891","SJAG_04173","SJAG_02324","SJAG_00384","SJAG_00726","SJAG_02802","SJAG_00889","SJAG_03326","SJAG_04672","SJAG_01721","SJAG_00220","SJAG_01676","SJAG_04534","SJAG_02894","SJAG_05244","SJAG_05320","SJAG_04164","SJAG_01608","SJAG_03043","SJAG_07014","SJAG_01296","SJAG_00166","SJAG_01548","SJAG_00086","SJAG_02312","SJAG_02861","SJAG_00513","SJAG_00105","SJAG_05248","SJAG_00544","SJAG_02904","SJAG_02597","SJAG_02335","SJAG_02682","SJAG_01411","SJAG_03197","SJAG_03122","SJAG_04897","SJAG_04689","SJAG_03364","SJAG_01568","SJAG_05218","SJAG_04889","SJAG_03424","SJAG_00315","SJAG_05270","SJAG_04207","SJAG_04788","SJAG_01767","SJAG_04281","SJAG_01473","SJAG_02840","SJAG_07013","SJAG_00497","SJAG_02253","SJAG_02067","SJAG_01551","SJAG_01719","SJAG_02535","SJAG_04626","SJAG_00748","SJAG_02749","SJAG_04160","SJAG_04020","SJAG_05573","SJAG_01366","SJAG_03383","SJAG_04324","SJAG_03859","SJAG_03423","SJAG_04188","SJAG_04304","SJAG_01591","SJAG_03459","SJAG_02071","SJAG_00844","SJAG_01580","SJAG_02836","SJAG_07009","SJAG_01632","SJAG_01132","SJAG_04918","SJAG_04475","SJAG_04695","SJAG_04753","SJAG_02777","SJAG_00860","SJAG_03568","SJAG_03402","SJAG_04216","SJAG_02762","SJAG_04663","SJAG_00468","SJAG_01565","SJAG_03971","SJAG_01853","SJAG_03422","SJAG_01727","SJAG_01087","SJAG_03649","SJAG_00782","SJAG_01202","SJAG_00940","SJAG_02585","SJAG_02803","SJAG_00523","SJAG_04019","SJAG_01128","SJAG_01463","SJAG_04893","SJAG_02510","SJAG_02207","SJAG_04256","SJAG_01734","SJAG_04029","SJAG_00629","SJAG_01520","SJAG_01194","SJAG_03127","SJAG_03666","SJAG_04493"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[110222,113004,96565,113005,98582,117456,114670,110526,89714,87150,101168,118289,87552,96315,91961,101396,106576,111813,87571,117154,99373,90529,96969,111873,111812,99922,116925,109325,113973,105043,116379,100705,90503,96316,98669,108107,107359,87149,103601,117095,117153,97705,96932,100404,107674,107675,96954,110221,104292,87570,90530,96970,111688,114018,111117,111508,89713,100283,107697,109326,118290,100284,117768,117096,113405,96651,89079,107476,114849,109777,87572,93056,101966,101984,93095,116264,111687,116378,89577,98668,96931,111607,95682,98583,100818,111608,89578,111874,101983,117271,105215,96660,114669,94364,101967,113974,114019,109023,114848,117144,113404,94365,96953,110525,99374,111116,112989,100861,93057,110595,91960,106577,115213,117769,101395,103602,90505,100817,97706,111430,116066,107696,105214,100860,111509,118402,101167,116926,108106,99923,118459,93094,113515,96659,118460,90504,88847,95681,107806,107807,116265,116067,110594,109778,118403,87654,109022,113516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022625"},{"annotations":[99537,104892,95830,105160,105545,98657,88404,93002,107400,110897,111097,106196,115791,103308,105171,88154,113691,114045,112597,109476,115927,101223,103746,118202,98162,101221,103937,105575,90848,93156,90490,98656,99290,97832,103353,106289,114044,94041,105546,111825,116906,98133,98134,94391,99963,97833,92495,99153,88405,93157,104893,104919,88153,88117,90491,88118,93003,94241,94390,87135,95916,95157,101050,98852,100273,101222,104918,74273,99152,99538,105159,105172,92494,105052,91083,100274,106195,94042,95829,103359,107401,101049,90041,110898,111098,93158,111824,112919,112920,112921,106288,113690,111096,112598,115792,116912,103745,96900,98163,96899,95917,87136,99291,90040,95158,96054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022627"},{"annotations":[98150,100591,101432,96083,111714,116493,110264,105196,114732,117418,107712,87826,97453,88952,105344,103865,95711,109334,95748,102117,102832,110589,112212,114206,90949,102939,104355,113804,114913,107665,103186,111949,112942,114866,115760,116608,106242,114088,97474,112387,88499,96385,115651,107566,98598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005762"},{"annotations":[103505,89407,117576,93136,102858,93961,93974,93676,108074,101812,111849,109624,96116,97717,94829,97478,97477,105520,108846,102579,89353,103435,115510,91562,110154,107570,107825,105885,107430,115086,109875,95412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005763"}]},"cv_name":"cellular_component","definition":"Either of the two subunits of a ribosome: the ribosomal large subunit or the ribosomal small subunit.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein complex","termid":"GO:1990904"},{"relation_name":"part_of","term_name":"ribosome","termid":"GO:0005840"}],"gene_count":217,"genes_by_uniquename":{"SJAG_00034":null,"SJAG_00060":null,"SJAG_00069":null,"SJAG_00086":null,"SJAG_00105":null,"SJAG_00148":null,"SJAG_00155":null,"SJAG_00166":null,"SJAG_00220":null,"SJAG_00315":null,"SJAG_00384":null,"SJAG_00465":null,"SJAG_00468":null,"SJAG_00497":null,"SJAG_00503":null,"SJAG_00513":null,"SJAG_00523":null,"SJAG_00537":null,"SJAG_00544":null,"SJAG_00628":null,"SJAG_00629":null,"SJAG_00726":null,"SJAG_00733":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00765":null,"SJAG_00782":null,"SJAG_00799":null,"SJAG_00844":null,"SJAG_00860":null,"SJAG_00889":null,"SJAG_00921":null,"SJAG_00940":null,"SJAG_00944":null,"SJAG_01045":null,"SJAG_01087":null,"SJAG_01128":null,"SJAG_01132":null,"SJAG_01194":null,"SJAG_01202":null,"SJAG_01226":null,"SJAG_01287":null,"SJAG_01296":null,"SJAG_01303":null,"SJAG_01322":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01387":null,"SJAG_01411":null,"SJAG_01413":null,"SJAG_01463":null,"SJAG_01468":null,"SJAG_01473":null,"SJAG_01478":null,"SJAG_01512":null,"SJAG_01520":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01565":null,"SJAG_01568":null,"SJAG_01580":null,"SJAG_01588":null,"SJAG_01591":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01630":null,"SJAG_01632":null,"SJAG_01676":null,"SJAG_01719":null,"SJAG_01721":null,"SJAG_01727":null,"SJAG_01734":null,"SJAG_01767":null,"SJAG_01829":null,"SJAG_01853":null,"SJAG_02020":null,"SJAG_02046":null,"SJAG_02067":null,"SJAG_02071":null,"SJAG_02081":null,"SJAG_02121":null,"SJAG_02184":null,"SJAG_02201":null,"SJAG_02207":null,"SJAG_02224":null,"SJAG_02243":null,"SJAG_02253":null,"SJAG_02280":null,"SJAG_02283":null,"SJAG_02312":null,"SJAG_02324":null,"SJAG_02335":null,"SJAG_02340":null,"SJAG_02359":null,"SJAG_02452":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02510":null,"SJAG_02522":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02546":null,"SJAG_02585":null,"SJAG_02597":null,"SJAG_02611":null,"SJAG_02643":null,"SJAG_02682":null,"SJAG_02749":null,"SJAG_02755":null,"SJAG_02762":null,"SJAG_02777":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02836":null,"SJAG_02840":null,"SJAG_02861":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02904":null,"SJAG_03034":null,"SJAG_03040":null,"SJAG_03043":null,"SJAG_03053":null,"SJAG_03065":null,"SJAG_03122":null,"SJAG_03127":null,"SJAG_03133":null,"SJAG_03159":null,"SJAG_03176":null,"SJAG_03192":null,"SJAG_03197":null,"SJAG_03254":null,"SJAG_03262":null,"SJAG_03284":null,"SJAG_03297":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03364":null,"SJAG_03383":null,"SJAG_03402":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03459":null,"SJAG_03568":null,"SJAG_03584":null,"SJAG_03636":null,"SJAG_03649":null,"SJAG_03666":null,"SJAG_03762":null,"SJAG_03859":null,"SJAG_03919":null,"SJAG_03922":null,"SJAG_03971":null,"SJAG_04019":null,"SJAG_04020":null,"SJAG_04029":null,"SJAG_04066":null,"SJAG_04160":null,"SJAG_04164":null,"SJAG_04168":null,"SJAG_04173":null,"SJAG_04174":null,"SJAG_04176":null,"SJAG_04188":null,"SJAG_04204":null,"SJAG_04207":null,"SJAG_04216":null,"SJAG_04244":null,"SJAG_04256":null,"SJAG_04281":null,"SJAG_04304":null,"SJAG_04324":null,"SJAG_04342":null,"SJAG_04378":null,"SJAG_04414":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04478":null,"SJAG_04490":null,"SJAG_04493":null,"SJAG_04494":null,"SJAG_04534":null,"SJAG_04626":null,"SJAG_04663":null,"SJAG_04672":null,"SJAG_04689":null,"SJAG_04695":null,"SJAG_04746":null,"SJAG_04753":null,"SJAG_04788":null,"SJAG_04814":null,"SJAG_04847":null,"SJAG_04889":null,"SJAG_04893":null,"SJAG_04897":null,"SJAG_04918":null,"SJAG_04998":null,"SJAG_05216":null,"SJAG_05218":null,"SJAG_05221":null,"SJAG_05244":null,"SJAG_05248":null,"SJAG_05270":null,"SJAG_05320":null,"SJAG_05573":null,"SJAG_06110":null,"SJAG_06253":null,"SJAG_06612":null,"SJAG_07009":null,"SJAG_07013":null,"SJAG_07014":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"ribosomal subunit","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0044391","terms_by_termid":{"GO:0005762":null,"GO:0005763":null,"GO:0022625":null,"GO:0022627":null}}


id: GO:0060575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a columnar/cuboidal epithelial cell of the intestine.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell differentiation","termid":"GO:0002065"},{"relation_name":"part_of","term_name":"digestive tract development","termid":"GO:0048565"}],"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":"intestinal epithelial cell differentiation","termid":"GO:0060575"}


id: PBO:0074867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 51","termid":"PBO:0074867"}


id: GO:0005962
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Mitochondrial complex that possesses isocitrate dehydrogenase (NAD+) activity.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial isocitrate dehydrogenase complex (NAD+) (obsolete GO:0005962)","termid":"GO:0005962"}


id: PBO:0028404
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ubiquinone_binding","termid":"PBO:0028404"}


id: PBO:0058498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5692a-1","termid":"PBO:0058498"}


id: GO:0061907
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of AMPA glutamate receptor activity.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:20739563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ion transmembrane transporter activity","termid":"GO:0032413"},{"relation_name":"is_a","term_name":"negative regulation of glutamate receptor signaling pathway","termid":"GO:1900450"},{"relation_name":"is_a","term_name":"negative regulation of signaling receptor activity","termid":"GO:2000272"},{"relation_name":"is_a","term_name":"regulation of AMPA receptor activity","termid":"GO:2000311"}],"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:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of AMPA receptor activity","termid":"GO:0061907"}


id: PR:Q9P6I1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubc16 gene.","definition_xrefs":["UniProtKB:Q9P6I1","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-conjugating enzyme E2 16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.09","synonyms":[{"name":"E2 ubiquitin-conjugating enzyme 16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ubc16","type":"exact"},{"name":"ubiquitin carrier protein 16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-protein ligase 16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6I1"}


id: PBO:0070933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 41","termid":"PBO:0070933"}


id: PBO:0001733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal-ubiquitin fusion protein","termid":"PBO:0001733"}


id: PBO:0034560
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_binding_during_mitotic_S_phase","termid":"PBO:0034560"}


id: PBO:0001604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar serine protease Isp6","termid":"PBO:0001604"}


id: PBO:0041649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CACNA2D3 antisense RNA 1","termid":"PBO:0041649"}


id: PR:O74522
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- adn3 gene.","definition_xrefs":["UniProtKB:O74522","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":"adhesion defective protein 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1494.10","synonyms":[{"name":"LisH domain-containing protein adn3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-adn3","type":"exact"}],"termid":"PR:O74522"}


id: MONDO:0023204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"muscular dystrophy","termid":"MONDO:0020121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"Fukuda-Miyanomae-Nakata syndrome","secondary_identifiers":["GARD:2411","Orphanet:2060"],"synonyms":[{"name":"Cerebromuscular dystrophy, Fukuyama type","type":"related"},{"name":"FCMD","type":"related"},{"name":"Fukuyama type muscular dystrophy","type":"related"},{"name":"muscular dystrophy, congenital progressive, with intellectual disability","type":"related"},{"name":"muscular dystrophy, congenital progressive, with mental retardation","type":"related"},{"name":"muscular dystrophy, congenital, Fukuyama type","type":"related"},{"name":"muscular dystrophy, congenital, with central nervous system involvement","type":"related"}],"termid":"MONDO:0023204","xrefs":{"Monarch":{"xref_id":"0023204"}}}


id: GO:0097303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways by which N-acyl transfer leads to formation of a water-soluble protein-lipid complex.","definition_xrefs":["UniPathway:UPA00666","GOC:pde","GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete lipoprotein biosynthetic process via N-acyl transfer (obsolete GO:0097303)","synonyms":[{"name":"lipoprotein biosynthesis (N-acyl transfer)","type":"exact"}],"termid":"GO:0097303"}


id: GO:0098645
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A supramolecular complex that consists of collagen triple helices associated to form a network.","definition_xrefs":["GOC:dos","PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex of collagen trimers","termid":"GO:0098644"},{"relation_name":"is_a","term_name":"supramolecular polymer","termid":"GO:0099081"}],"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":"collagen network","termid":"GO:0098645"}


id: PBO:0056344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase kinase 3","termid":"PBO:0056344"}


id: PBO:0040876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMP2K divergent transcript","termid":"PBO:0040876"}


id: PBO:0057174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR325 host gene","termid":"PBO:0057174"}


id: PBO:0049702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"highly accelerated region 1B","termid":"PBO:0049702"}


id: GO:0008760
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phosphoenolpyruvate + UDP-N-acetyl-alpha-D-glucosamine = phosphate + UDP-N-acetyl-3-O-(1-carboxyvinyl)-D-glucosamine.","definition_xrefs":["RHEA:18681","EC:2.5.1.7"],"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:0016765"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016765","GO:0003824"],"is_obsolete":false,"name":"UDP-N-acetylglucosamine 1-carboxyvinyltransferase activity","secondary_identifiers":["KEGG_REACTION:R00660","MetaCyc:UDPNACETYLGLUCOSAMENOLPYRTRANS-RXN"],"synonyms":[{"name":"MurA transferase activity","type":"narrow"},{"name":"UDP-N-acetylglucosamine 1-carboxyvinyl-transferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine enoylpyruvyltransferase activity","type":"related"},{"name":"enoylpyruvate transferase activity","type":"related"},{"name":"phosphoenolpyruvate-UDP-acetylglucosamine-3-enolpyruvyltransferase activity","type":"related"},{"name":"phosphoenolpyruvate:UDP-2-acetamido-2-deoxy-D-glucose 2-enoyl-1-carboxyethyltransferase activity","type":"related"},{"name":"phosphoenolpyruvate:UDP-N-acetyl-D-glucosamine 1-carboxyvinyltransferase activity","type":"related"},{"name":"phosphoenolpyruvate:uridine diphosphate N-acetylglucosamine enolpyruvyltransferase activity","type":"related"},{"name":"phosphoenolpyruvate:uridine-5'-diphospho-N-acetyl-2-amino-2-deoxyglucose 3-enolpyruvyltransferase activity","type":"related"},{"name":"phosphopyruvate-uridine diphosphoacetylglucosamine pyruvatetransferase activity","type":"related"},{"name":"pyruvate-UDP-acetylglucosamine transferase activity","type":"related"},{"name":"pyruvate-uridine diphospho-N-acetyl-glucosamine transferase activity","type":"related"},{"name":"pyruvate-uridine diphospho-N-acetylglucosamine transferase activity","type":"related"},{"name":"pyruvic-uridine diphospho-N-acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0008760"}


id: MONDO:0024559
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial thoracic aortic aneurysm and aortic dissection","termid":"MONDO:0019625"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic aneurysm, familial thoracic 1","secondary_identifiers":["MEDGEN:91038","MESH:C562834","OMIM:607086","GARD:15408","Orphanet:229","UMLS:C0345050"],"synonyms":[{"name":"AAT1","type":"exact"},{"name":"Erdheim cystic medial necrosis of aorta","type":"related"},{"name":"FAA1","type":"related"},{"name":"aneurysm, thoracic aortic","type":"related"},{"name":"annuloaortic ectasia","type":"related"},{"name":"aortic aneurysm, familial thoracic","type":"related"},{"name":"aortic dissection, familial","type":"related"}],"termid":"MONDO:0024559","xrefs":{"Monarch":{"xref_id":"0024559"}}}


id: GO:0097550
data:
  {"annotated_genes":["SJAG_01523","SJAG_03206","SJAG_03120"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89384,89736,102568],"is_not":false,"summary":null,"term":"GO:0097550"}]},"cv_name":"cellular_component","definition":"A protein-DNA complex composed of proteins binding promoter DNA to form the transcriptional preinitiation complex (PIC), the formation of which is a prerequisite for transcription.","definition_xrefs":["PMID:22751016","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex","termid":"GO:0032993"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01523":null,"SJAG_03120":null,"SJAG_03206":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"transcription preinitiation complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA-templated transcriptional preinitiation complex","type":"exact"},{"name":"PIC","type":"narrow"},{"name":"preinitiation complex","type":"narrow"},{"name":"transcriptional pre-initiation complex","type":"exact"},{"name":"transcriptional preinitiation complex","type":"exact"}],"termid":"GO:0097550","terms_by_termid":{"GO:0097550":null}}


id: GO:0021563
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Various sensory and motor branches of the glossopharyngeal nerve supply nerve connections to the pharynx and back of the tongue. The branchial motor component contains motor fibers that innervate muscles that elevate the pharynx and larynx, and the tympanic branch supplies parasympathetic fibers to the otic ganglion.","definition_xrefs":["ISBN:0838580343","GOC:cls","GOC:jid","GO_REF:0000021","GOC:dph","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve development","termid":"GO:0021545"}],"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":"glossopharyngeal nerve development","synonyms":[{"name":"CN IX development","type":"related"},{"name":"cranial nerve 9 development","type":"exact"},{"name":"cranial nerve IX development","type":"exact"}],"termid":"GO:0021563"}


id: PBO:0004463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Dbp3 (predicted)","termid":"PBO:0004463"}


id: GO:0051554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving flavonols, a member of a class of vascular pigments formed by consecutive oxidative processes from the flavonoid intermediates flavanones and dihydroflavonols. Flavonols are the most widespread of the flavonoids and have a wide array of physiological activities.","definition_xrefs":["PMID:11402179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavone metabolic process","termid":"GO:0051552"}],"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":"flavonol metabolic process","synonyms":[{"name":"flavonol metabolism","type":"exact"}],"termid":"GO:0051554"}


id: PBO:0046392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelial PAS domain protein 1","termid":"PBO:0046392"}


id: MONDO:0000066
data:
  {"annotated_genes":["SJAG_00601","SJAG_01490","SJAG_06002","SJAG_04450","SJAG_00080","SJAG_02480","SJAG_01503","SJAG_01368","SJAG_00354","SJAG_03490","SJAG_02504","SJAG_04639","SJAG_06392","SJAG_02646","SJAG_00217","SJAG_04560","SJAG_04348","SJAG_03099","SJAG_00852","SJAG_00755","SJAG_05305","SJAG_01355","SJAG_03046","SJAG_03296","SJAG_03322","SJAG_04553","SJAG_03782","SJAG_03114","SJAG_06046","SJAG_03173","SJAG_01077","SJAG_01820","SJAG_01405","SJAG_03550","SJAG_02564","SJAG_01190"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032617"},{"annotations":[85739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032630"},{"annotations":[85741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032631"},{"annotations":[85727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032609"},{"annotations":[85730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032612"},{"annotations":[86184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032909"},{"annotations":[85204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859321"},{"annotations":[85229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033639"},{"annotations":[85231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033645"},{"annotations":[85230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033649"},{"annotations":[85242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033651"},{"annotations":[85236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033653"},{"annotations":[85238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033654"},{"annotations":[85239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033655"},{"annotations":[85244,85245,85243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033656"},{"annotations":[85221],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033635"},{"annotations":[85218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033636"},{"annotations":[85227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033637"},{"annotations":[85228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033638"},{"annotations":[85841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020858"},{"annotations":[85959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007415"},{"annotations":[84620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014063"},{"annotations":[84621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014064"},{"annotations":[84619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014065"},{"annotations":[84623],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014066"},{"annotations":[85423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014194"},{"annotations":[85907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014356"},{"annotations":[85913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014364"},{"annotations":[86187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014496"},{"annotations":[86696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0700250"},{"annotations":[86030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859160"},{"annotations":[86066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859520"},{"annotations":[84597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014091"},{"annotations":[84984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011421"},{"annotations":[84938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012992"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial metabolism disorder","termid":"MONDO:0004069"}],"gene_count":36,"genes_by_uniquename":{"SJAG_00080":null,"SJAG_00217":null,"SJAG_00354":null,"SJAG_00601":null,"SJAG_00755":null,"SJAG_00852":null,"SJAG_01077":null,"SJAG_01190":null,"SJAG_01355":null,"SJAG_01368":null,"SJAG_01405":null,"SJAG_01490":null,"SJAG_01503":null,"SJAG_01820":null,"SJAG_02480":null,"SJAG_02504":null,"SJAG_02564":null,"SJAG_02646":null,"SJAG_03046":null,"SJAG_03099":null,"SJAG_03114":null,"SJAG_03173":null,"SJAG_03296":null,"SJAG_03322":null,"SJAG_03490":null,"SJAG_03550":null,"SJAG_03782":null,"SJAG_04348":null,"SJAG_04450":null,"SJAG_04553":null,"SJAG_04560":null,"SJAG_04639":null,"SJAG_05305":null,"SJAG_06002":null,"SJAG_06046":null,"SJAG_06392":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex deficiency","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0000066","terms_by_termid":{"MONDO:0007415":null,"MONDO:0011421":null,"MONDO:0012992":null,"MONDO:0014063":null,"MONDO:0014064":null,"MONDO:0014065":null,"MONDO:0014066":null,"MONDO:0014091":null,"MONDO:0014194":null,"MONDO:0014356":null,"MONDO:0014364":null,"MONDO:0014496":null,"MONDO:0020858":null,"MONDO:0032609":null,"MONDO:0032612":null,"MONDO:0032617":null,"MONDO:0032630":null,"MONDO:0032631":null,"MONDO:0032909":null,"MONDO:0033635":null,"MONDO:0033636":null,"MONDO:0033637":null,"MONDO:0033638":null,"MONDO:0033639":null,"MONDO:0033645":null,"MONDO:0033649":null,"MONDO:0033651":null,"MONDO:0033653":null,"MONDO:0033654":null,"MONDO:0033655":null,"MONDO:0033656":null,"MONDO:0700250":null,"MONDO:0859160":null,"MONDO:0859321":null,"MONDO:0859520":null},"xrefs":{"Monarch":{"xref_id":"0000066"}}}


id: PBO:0002842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme Ubc14 (predicted)","termid":"PBO:0002842"}


id: GO:0120181
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of a focal adhesion into its constituent components. A focal adhesion is a complex of intracellular signaling and structural proteins that provides a structural link between the internal actin cytoskeleton and the ECM, and also functions as a locus of signal transduction activity.","definition_xrefs":["PMID:25490267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-substrate junction disassembly","termid":"GO:0120180"}],"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":"focal adhesion disassembly","termid":"GO:0120181"}


id: PBO:0001678
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.11.2","termid":"PBO:0001678"}


id: PBO:0072730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingosine-1-phosphate receptor 1","termid":"PBO:0072730"}


id: PBO:0082998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic protein required for sporulation","termid":"PBO:0082998"}


id: MONDO:0014303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare and complex form of hereditary spastic paraplegia (see this term), reported in only 4 patients from 2 families to date, characterized by spastic paraplegia (presenting between the ages of 1 to 4 years with abnormal gait) associated with microcephaly, amyotrophy, cerebellar signs (e.g. dysarthria) aggressiveness, delayed puberty and mild to moderate intellectual disability. SPG64 is due to mutations in the ENTPD1 gene (10q24.1), encoding ectonucleoside triphosphate diphosphohydrolase 1.","definition_xrefs":["Orphanet:401810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"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":"hereditary spastic paraplegia 64","secondary_identifiers":["GARD:17659","OMIM:615683","DOID:0110815","SCTID:726609005","UMLS:C3810289","MEDGEN:816619"],"synonyms":[{"name":"ENTPD1 autosomal recessive complex spastic paraplegia","type":"exact"},{"name":"SPG64","type":"exact"},{"name":"autosomal recessive complex spastic paraplegia caused by mutation in ENTPD1","type":"exact"},{"name":"autosomal recessive spastic paraplegia 64","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 64","type":"exact"},{"name":"hereditary spastic paraplegia type 64","type":"exact"},{"name":"spastic paraplegia 64, autosomal recessive","type":"related"}],"termid":"MONDO:0014303","xrefs":{"Monarch":{"xref_id":"0014303"}}}


id: GO:0004784
data:
  {"annotated_genes":["SJAG_03303","SJAG_00668","SJAG_04788","SJAG_01734"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88460,99656,103510,109630],"is_not":false,"summary":null,"term":"GO:0004784"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 superoxide + 2 H+ = O2 + hydrogen peroxide.","definition_xrefs":["EC:1.15.1.1","PMID:15064408","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antioxidant activity","termid":"GO:0016209"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on superoxide radicals as acceptor","termid":"GO:0016721"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00668":null,"SJAG_01734":null,"SJAG_03303":null,"SJAG_04788":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"superoxide dismutase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0004785","Reactome:R-HSA-3777112","RHEA:20696","MetaCyc:SUPEROX-DISMUT-RXN","GO:0008383","GO:0008382","GO:0016954","Reactome:R-HSA-1222469","Reactome:R-HSA-3299680","Reactome:R-HSA-3299682","Reactome:R-HSA-3299691","Reactome:R-HSA-1222462"],"synonyms":[{"name":"Cu,Zn-SOD","type":"related"},{"name":"Cu-Zn superoxide dismutase activity","type":"narrow"},{"name":"Fe-SOD","type":"related"},{"name":"Mn, Fe superoxide dismutase","type":"narrow"},{"name":"Mn-SOD","type":"related"},{"name":"SOD","type":"related"},{"name":"SOD-1","type":"related"},{"name":"SOD-2","type":"related"},{"name":"SOD-3","type":"related"},{"name":"SOD-4","type":"related"},{"name":"SODF","type":"related"},{"name":"SODS","type":"related"},{"name":"copper, zinc superoxide dismutase activity","type":"narrow"},{"name":"cuprein","type":"related"},{"name":"cytocuprein","type":"related"},{"name":"erythrocuprein","type":"related"},{"name":"ferrisuperoxide dismutase activity","type":"narrow"},{"name":"hemocuprein","type":"related"},{"name":"hepatocuprein","type":"related"},{"name":"iron superoxide dismutase activity","type":"narrow"},{"name":"iron superoxide oxidoreductase","type":"related"},{"name":"manganese superoxide dismutase activity","type":"narrow"},{"name":"manganese superoxide oxidoreductase","type":"related"},{"name":"nickel superoxide dismutase activity","type":"narrow"},{"name":"nickel superoxide oxidoreductase","type":"related"},{"name":"superoxide dismutase I","type":"related"},{"name":"superoxide dismutase II","type":"related"},{"name":"superoxide:superoxide oxidoreductase activity","type":"exact"},{"name":"zinc superoxide oxidoreductase","type":"related"}],"termid":"GO:0004784","terms_by_termid":{"GO:0004784":null}}


id: GO:0018273
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-lysine to form N6-retinal-L-lysine.","definition_xrefs":["RESID:AA0120"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-chromophore linkage via peptidyl-N6-retinal-L-lysine (obsolete GO:0018273)","termid":"GO:0018273"}


id: GO:0005637
data:
  {"annotated_genes":["SJAG_01263","SJAG_05226","SJAG_03491","SJAG_01745","SJAG_03449","SJAG_00680","SJAG_03657","SJAG_05196"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88548,90819,93318,102314,102907,105440,117056,117667],"is_not":false,"summary":null,"term":"GO:0005637"},{"annotations":[117057,105441],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990862"}]},"cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the nuclear envelope.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle inner membrane","termid":"GO:0019866"},{"relation_name":"is_a","term_name":"nuclear membrane","termid":"GO:0031965"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00680":null,"SJAG_01263":null,"SJAG_01745":null,"SJAG_03449":null,"SJAG_03491":null,"SJAG_03657":null,"SJAG_05196":null,"SJAG_05226":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"nuclear inner membrane","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["NIF_Subcellular:sao1612527463"],"synonyms":[{"name":"inner envelope","type":"broad"},{"name":"inner nuclear membrane","type":"exact"},{"name":"nucleus inner membrane","type":"exact"}],"termid":"GO:0005637","terms_by_termid":{"GO:0005637":null,"GO:1990862":null}}


id: GO:0006662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving glycerol ethers, any anhydride formed between two organic hydroxy compounds, one of which is glycerol.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"glycerol ether metabolic process","synonyms":[{"name":"glycerol ether metabolism","type":"exact"}],"termid":"GO:0006662"}


id: PBO:0002213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane amino acid permease Per1","termid":"PBO:0002213"}


id: PBO:0045745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous Bornavirus like nucleoprotein 2","termid":"PBO:0045745"}


id: PBO:0050502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXC cluster antisense RNA 2","termid":"PBO:0050502"}


id: PBO:0058728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6856","termid":"PBO:0058728"}


id: FYPO:0004792
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the distance between one or more telomeres and the nuclear envelope is smaller than normal during G2 phase of the mitotic cell cycle.","definition_xrefs":["PMID:22959349","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere-nuclear envelope distance during vegetative growth","termid":"FYPO:0004790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased telomere-nuclear envelope distance during mitotic G2 phase","synonyms":[{"name":"decreased distance between telomeres and nuclear envelope during mitotic G2 phase","type":"exact"},{"name":"decreased telomere-nuclear envelope distance during G2 phase during mitotic cell cycle","type":"related"},{"name":"decreased telomere-nuclear envelope distance during mitotic G2 phase during vegetative growth","type":"exact"},{"name":"reduced telomere-nuclear envelope distance during mitotic G2 phase","type":"exact"}],"termid":"FYPO:0004792"}


id: GO:0021550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the medulla oblongata over time, from its formation to the mature structure. The medulla oblongata lies directly above the spinal cord and controls vital autonomic functions such as digestion, breathing and the control of heart rate.","definition_xrefs":["ISBN:0838580343","GOC:jid","GOC:cls","GOC:dgh","GO_REF:0000021","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"hindbrain development","termid":"GO:0030902"}],"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":"medulla oblongata development","synonyms":[{"name":"medulla development","type":"related"},{"name":"myelencephalon development","type":"related"}],"termid":"GO:0021550"}


id: PBO:0017499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane nicotinic acid transmembrane transporter (predicted)","termid":"PBO:0017499"}


id: PBO:0001300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mdm10/Mdm12/Mmm1 complex subunit Mdm10 (predicted)","termid":"PBO:0001300"}


id: GO:2000623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mRNA catabolic process","termid":"GO:1902373"},{"relation_name":"is_a","term_name":"regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay","termid":"GO:2000622"},{"relation_name":"negatively_regulates","term_name":"nuclear-transcribed mRNA catabolic process, nonsense-mediated decay","termid":"GO:0000184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"negatively_regulates","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay","synonyms":[{"name":"negative regulation of mRNA breakdown, nonsense-mediated decay","type":"exact"},{"name":"negative regulation of mRNA catabolic process, nonsense-mediated","type":"exact"},{"name":"negative regulation of mRNA catabolism, nonsense-mediated","type":"exact"},{"name":"negative regulation of mRNA degradation, nonsense-mediated decay","type":"exact"},{"name":"negative regulation of nonsense-mediated mRNA decay","type":"exact"},{"name":"negative regulation of nuclear mRNA catabolic process, nonsense-mediated decay","type":"exact"}],"termid":"GO:2000623"}


id: GO:0060071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A type of non-canonical Wnt signaling pathway in which Wnt binding to its receptor on the surface of a target cell results in the activation small G proteins such as Rho, Rac, and Cdc42 which, in turn activate effectors, including C-Jun N-terminal kinase (JNK) and Rho kinase (Rok). The signaling ends with change in the transcription of target genes and/or reorganisation of the cytoskeleton.","definition_xrefs":["PMID:25349257","PMID:28293032","PMID:37804416","PMID:11532397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-canonical Wnt signaling pathway","termid":"GO:0035567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"Wnt signaling pathway, planar cell polarity pathway","secondary_identifiers":["Reactome:R-HSA-4086400"],"synonyms":[{"name":"PCP pathway","type":"exact"},{"name":"Wnt receptor signaling pathway, planar cell polarity pathway","type":"exact"},{"name":"Wnt receptor signalling pathway, planar cell polarity pathway","type":"exact"},{"name":"Wnt-JNK signaling pathway","type":"related"},{"name":"Wnt-PCP signaling pathway","type":"related"},{"name":"Wnt-activated signaling pathway, planar cell polarity pathway","type":"exact"},{"name":"non-canonical Wnt signaling pathway","type":"related"},{"name":"planar cell polarity pathway","type":"exact"}],"termid":"GO:0060071"}


id: GO:1900874
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving heptadec-1-ene.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkene metabolic process","termid":"GO:0043449"}],"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":"heptadec-1-ene metabolic process","synonyms":[{"name":"heptadec-1-ene metabolism","type":"exact"}],"termid":"GO:1900874"}


id: PATO:0002359
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's width being notably higher than its length.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"broad","termid":"PATO:0002359"}


id: PBO:0064935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase targeting COQ7","termid":"PBO:0064935"}


id: PBO:0059789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 15","termid":"PBO:0059789"}


id: PBO:0065042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELID1 pseudogene 7","termid":"PBO:0065042"}


id: PBO:0062684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily A member 5 pseudogene","termid":"PBO:0062684"}


id: GO:0006143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete purine metabolic process (obsolete GO:0006143)","synonyms":[{"name":"purine metabolic process","type":"exact"}],"termid":"GO:0006143"}


id: PR:Q9UUC9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mdm34 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUC9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial distribution and morphology protein 34 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.11c","synonyms":[{"name":"Spom972h-mdm34","type":"exact"}],"termid":"PR:Q9UUC9"}


id: PBO:0040506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"advillin","termid":"PBO:0040506"}


id: PBO:0078734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Met (anticodon CAT) 6-1","termid":"PBO:0078734"}


id: MONDO:0009037
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":"craniosynostosis with anomalies of the cranial base and digits","secondary_identifiers":["MEDGEN:347469","MESH:C565666","OMIM:218530","UMLS:C1857493"],"synonyms":[{"name":"craniosynostosis with anomalies of the cranial base and digits","type":"exact"}],"termid":"MONDO:0009037","xrefs":{"Monarch":{"xref_id":"0009037"}}}


id: MONDO:0100308
data:
  {"annotated_genes":["SJAG_03692","SJAG_04641","SJAG_00526","SJAG_02196","SJAG_02885","SJAG_04110","SJAG_02377","SJAG_00059","SJAG_00421","SJAG_00863","SJAG_16456","SJAG_00087","SJAG_05212","SJAG_01854","SJAG_02084","SJAG_01400","SJAG_00686","SJAG_01317","SJAG_02457","SJAG_00773","SJAG_01286","SJAG_00380","SJAG_04533","SJAG_01417","SJAG_01179","SJAG_00645","SJAG_04418","SJAG_04622","SJAG_02680","SJAG_01168","SJAG_00721","SJAG_02242","SJAG_04822","SJAG_02119","SJAG_01356","SJAG_03862","SJAG_04233","SJAG_00797","SJAG_03393","SJAG_03923","SJAG_05332","SJAG_01438","SJAG_00933","SJAG_01945"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014744"},{"annotations":[84918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014557"},{"annotations":[86352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008980"},{"annotations":[85395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0016163"},{"annotations":[86283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011397"},{"annotations":[85680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012166"},{"annotations":[85796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012784"},{"annotations":[86516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013392"},{"annotations":[86196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014503"},{"annotations":[84653],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008943"},{"annotations":[84766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014601"},{"annotations":[85944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044720"},{"annotations":[84508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014104"},{"annotations":[85658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013886"},{"annotations":[86272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011402"},{"annotations":[85033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100340"},{"annotations":[85570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958009"},{"annotations":[86232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[84979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012664"},{"annotations":[86545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013354"},{"annotations":[86155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013776"},{"annotations":[85289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014803"},{"annotations":[85484],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033482"},{"annotations":[85171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011330"},{"annotations":[84734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011439"},{"annotations":[85249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011781"},{"annotations":[86752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008458"},{"annotations":[84686,84687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012246"},{"annotations":[84672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012450"},{"annotations":[85133,85134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007574"},{"annotations":[85329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013594"},{"annotations":[85778,85779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014417"},{"annotations":[86642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014934"},{"annotations":[84912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033115"},{"annotations":[84983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032923"},{"annotations":[86052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030312"},{"annotations":[85814,85815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030318"},{"annotations":[85821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030323"},{"annotations":[85091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011801"},{"annotations":[86102,86103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018996"},{"annotations":[85106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010547"},{"annotations":[85237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010524"}]},"cv_name":"mondo","definition":"A central nervous system disease that consists of gait impairment, unclear (“scanning”) speech, visual blurring due to nystagmus, hand incoordination, and tremor with movement.","definition_xrefs":["ISBN-13:978-1-259-64403-0"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"central nervous system disorder","termid":"MONDO:0002602"},{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":44,"genes_by_uniquename":{"SJAG_00059":null,"SJAG_00087":null,"SJAG_00380":null,"SJAG_00421":null,"SJAG_00526":null,"SJAG_00645":null,"SJAG_00686":null,"SJAG_00721":null,"SJAG_00773":null,"SJAG_00797":null,"SJAG_00863":null,"SJAG_00933":null,"SJAG_01168":null,"SJAG_01179":null,"SJAG_01286":null,"SJAG_01317":null,"SJAG_01356":null,"SJAG_01400":null,"SJAG_01417":null,"SJAG_01438":null,"SJAG_01854":null,"SJAG_01945":null,"SJAG_02084":null,"SJAG_02119":null,"SJAG_02196":null,"SJAG_02242":null,"SJAG_02377":null,"SJAG_02457":null,"SJAG_02680":null,"SJAG_02885":null,"SJAG_03393":null,"SJAG_03692":null,"SJAG_03862":null,"SJAG_03923":null,"SJAG_04110":null,"SJAG_04233":null,"SJAG_04418":null,"SJAG_04533":null,"SJAG_04622":null,"SJAG_04641":null,"SJAG_04822":null,"SJAG_05212":null,"SJAG_05332":null,"SJAG_16456":null},"genotype_count":0,"is_obsolete":false,"name":"atactic disorder","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"ataxia","type":"related"},{"name":"ataxic disorder","type":"exact"}],"termid":"MONDO:0100308","terms_by_termid":{"MONDO:0007574":null,"MONDO:0008458":null,"MONDO:0008943":null,"MONDO:0008980":null,"MONDO:0010524":null,"MONDO:0010547":null,"MONDO:0011330":null,"MONDO:0011397":null,"MONDO:0011402":null,"MONDO:0011439":null,"MONDO:0011781":null,"MONDO:0011801":null,"MONDO:0012166":null,"MONDO:0012246":null,"MONDO:0012450":null,"MONDO:0012651":null,"MONDO:0012664":null,"MONDO:0012784":null,"MONDO:0013354":null,"MONDO:0013392":null,"MONDO:0013594":null,"MONDO:0013776":null,"MONDO:0013886":null,"MONDO:0014104":null,"MONDO:0014417":null,"MONDO:0014503":null,"MONDO:0014557":null,"MONDO:0014601":null,"MONDO:0014744":null,"MONDO:0014803":null,"MONDO:0014934":null,"MONDO:0016163":null,"MONDO:0018996":null,"MONDO:0030312":null,"MONDO:0030318":null,"MONDO:0030323":null,"MONDO:0032923":null,"MONDO:0033115":null,"MONDO:0033482":null,"MONDO:0044720":null,"MONDO:0100340":null,"MONDO:0958009":null},"xrefs":{"Monarch":{"xref_id":"0100308"}}}


id: GO:0039596
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any viral process that modulates the frequency, rate or extent of dephosphorylation of a host protein.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by virus of host protein dephosphorylation (obsolete GO:0039596)","termid":"GO:0039596"}


id: SO:0000728
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a peptide that is able to excise itself and rejoin the remaining portions with a peptide bond.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleaved_peptide_region","termid":"SO:0100011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"intein","secondary_identifiers":["http://en.wikipedia.org/wiki/Intein"],"synonyms":[{"name":"protein intron","type":"related"}],"termid":"SO:0000728"}


id: PBO:0017408
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-improper_part_of","termid":"PBO:0017408"}


id: PBO:0074418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 17","termid":"PBO:0074418"}


id: PBO:0075864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family pseudogene 4","termid":"PBO:0075864"}


id: PBO:0082223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-arrestin, component of the Rsp5p E3-ubiquitin ligase complex; ubiquitin-binding adaptor involved in intracellular amino acid permease sorting, functions in heat shock element mediated gene expression, essential for growth in stress conditions; BUL2 has a paralog, BUL1, that arose from the whole genome duplication","termid":"PBO:0082223"}


id: GO:0061597
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction GTP = cyclic pyranopterin phosphate + diphosphate.","definition_xrefs":["PMID:18154309","EC:4.1.99.18","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete cyclic pyranopterin monophosphate synthase activity (obsolete GO:0061597)","termid":"GO:0061597"}


id: PBO:0000673
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.4.2.29","termid":"PBO:0000673"}


id: PBO:0030722
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_phosphatidylinositol-4-phosphate_level","termid":"PBO:0030722"}


id: PBO:0070569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 35","termid":"PBO:0070569"}


id: PBO:0045614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 25 (pseudogene)","termid":"PBO:0045614"}


id: SO:1000041
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome structure variation whereby a transposition occurred within a chromosome.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"translocation","termid":"SO:0000199"},{"relation_name":"has_part","term_name":"duplication","termid":"SO:1000035"},{"relation_name":"is_a","term_name":"chromosomal_transposition","termid":"SO:0000453"},{"relation_name":"is_a","term_name":"intrachromosomal_duplication","termid":"SO:1000038"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intrachromosomal_transposition","synonyms":[{"name":"(Drosophila)Tp","type":"related"},{"name":"intrachromosomal transposition","type":"exact"}],"termid":"SO:1000041"}


id: GO:0070761
data:
  {"annotated_genes":["SJAG_05223","SJAG_00752"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[97436,117167],"is_not":false,"summary":null,"term":"GO:0070761"}]},"cv_name":"cellular_component","definition":"A ribonucleoprotein complex that contains a precursor small nucleolar RNA (pre-snoRNA) and associated proteins, and forms during small nucleolar ribonucleoprotein complex (snoRNP) assembly. Pre-snoRNP complexes may contain proteins not found in the corresponding mature snoRNP complexes.","definition_xrefs":["PMID:17709390","GOC:mah","PMID:17636026","GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein complex","termid":"GO:1990904"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00752":null,"SJAG_05223":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"pre-snoRNP complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pre-small nucleolar ribonucleoprotein complex","type":"exact"}],"termid":"GO:0070761","terms_by_termid":{"GO:0070761":null}}


id: PBO:0088197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc finger transcription factor involved in multidrug resistance; Zn(2)-Cys(6) zinc finger transcription factor; activates genes involved in multidrug resistance; paralog of Yrr1p, acting on an overlapping set of target genes","termid":"PBO:0088197"}


id: PBO:0068934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 177, pseudogene","termid":"PBO:0068934"}


id: PBO:0039505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 26 pseudogene 3","termid":"PBO:0039505"}


id: GO:0016457
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The aggregation, arrangement and bonding together of proteins on DNA to form the complex that mediates dosage compensation on the X chromosome of the heterogametic sex, ultimately resulting in a two-fold increase in transcription from this chromosome. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete dosage compensation complex assembly involved in dosage compensation by hyperactivation of X chromosome (obsolete GO:0016457)","synonyms":[{"name":"dosage compensation complex assembly during dosage compensation by hyperactivation of X chromosome","type":"related"}],"termid":"GO:0016457"}


id: GO:0046605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the centrosome cycle, the processes of centrosome duplication and separation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of microtubule-based process","termid":"GO:0032886"},{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"centrosome cycle","termid":"GO:0007098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of centrosome cycle","termid":"GO:0046605"}


id: PBO:0084160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity zinc transporter of the plasma membrane; responsible for the majority of zinc uptake; transcription is induced under low-zinc conditions by the Zap1p transcription factor","termid":"PBO:0084160"}


id: MONDO:0006287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant tumor that arises from the bone. It is characterized by the presence of an area of high grade sarcoma in an otherwise typical giant cell tumor (primary malignancy in giant cell tumor), or the presence of sarcoma in which the pre-existing giant cell tumor may or may not be apparent (secondary malignancy in giant cell tumor).","definition_xrefs":["NCIT:C4304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant giant cell tumor","termid":"MONDO:0002402"},{"relation_name":"is_a","term_name":"bone sarcoma","termid":"MONDO:0021054"}],"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":"malignancy in giant cell tumor of bone","secondary_identifiers":["NANDO:2200052","DOID:4719","EFO:1000347","MEDGEN:87263","UMLS:C0334552","ICDO:9250/3"],"synonyms":[{"name":"Dedifferentiated giant cell tumor","type":"exact"},{"name":"Dedifferentiated giant cell tumour","type":"exact"},{"name":"OSTEOCLASTOMA, malignant","type":"exact"},{"name":"bone giant cell sarcoma","type":"exact"},{"name":"giant cell bone sarcoma","type":"exact"},{"name":"giant cell sarcoma of bone","type":"exact"},{"name":"giant cell sarcoma of the bone","type":"exact"},{"name":"giant cell tumor of bone, malignant","type":"exact"},{"name":"giant cell tumor of bone, malignant (morphologic abnormality)","type":"exact"},{"name":"giant cell tumour of bone, malignant","type":"exact"},{"name":"giant cell tumour of bone, malignant (morphologic abnormality)","type":"exact"},{"name":"malignancy in giant cell tumor of bone","type":"exact"},{"name":"malignancy in giant cell tumor of the bone","type":"exact"},{"name":"malignancy in giant cell tumour of the bone","type":"exact"},{"name":"malignant giant cell tumor of bone","type":"exact"},{"name":"malignant giant cell tumour of bone","type":"exact"}],"termid":"MONDO:0006287","xrefs":{"Monarch":{"xref_id":"0006287"}}}


id: PBO:0090061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial conserved fungal membrane protein Mug99","termid":"PBO:0090061"}


id: PBO:0026719
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H2B_localization_to_chromatin_at_protein_coding_gene","termid":"PBO:0026719"}


id: GO:0034321
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: octanoyl-CoA + an alcohol = CoA + an octyl ester.","definition_xrefs":["GOC:mah","PMID:16361250"],"gene_count":0,"genotype_count":0,"name":"obsolete alcohol O-octanoyltransferase activity (obsolete GO:0034321)","termid":"GO:0034321"}


id: GO:0000482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maturation of a precursor 5S ribosomal RNA (rRNA) molecule into a mature 5S rRNA molecule from the pre-rRNA molecule originally produced as a tetracistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, Large Subunit (LSU) the 4.5S rRNA, and the 5S rRNA in that order from 5' to 3' along the primary transcript.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturation of 5S rRNA","termid":"GO:0000481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0042254","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"maturation of 5S rRNA from tetracistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)","termid":"GO:0000482"}


id: PBO:0054353
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 1746","termid":"PBO:0054353"}


id: PBO:0072722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RXYLT1 antisense RNA 1","termid":"PBO:0072722"}


id: GO:0031727
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a CCR2 chemokine receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CCR chemokine receptor binding","termid":"GO:0048020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"CCR2 chemokine receptor binding","synonyms":[{"name":"CCR2 chemokine receptor ligand","type":"narrow"},{"name":"monocyte chemoattractant protein 1 receptor binding","type":"exact"}],"termid":"GO:0031727"}


id: GO:0003816
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of component C4 to C4a and C4b (Arg-Ala bond), and component C2 to C2a and C2b (Lys-Lys or Arg-Lys bond).","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete complement component C1s activity (obsolete GO:0003816)","synonyms":[{"name":"C1 esterase activity","type":"related"},{"name":"C1s esterase activity","type":"related"},{"name":"activated complement C1s","type":"related"},{"name":"complement C1s","type":"related"},{"name":"complement component C1s activity","type":"exact"},{"name":"complement subcomponent C1s","type":"related"}],"termid":"GO:0003816"}


id: PR:Q01475
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding protein SAR1b 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":"small COPII coat GTPase sar1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC31F10.06c","secondary_identifiers":["UniProtKB:Q01475"],"synonyms":[{"name":"SPBC31F10.06c","type":"related"},{"name":"Spom972h-SAR1B","type":"exact"}],"termid":"PR:Q01475"}


id: PBO:0077899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptase alpha/beta 1","termid":"PBO:0077899"}


id: PBO:0067664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 842, pseudogene","termid":"PBO:0067664"}


id: MONDO:0011143
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy","termid":"MONDO:0015993"},{"relation_name":"is_a","term_name":"GUCY2D retinopathy","termid":"MONDO:0100454"}],"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":"cone-rod dystrophy 6","secondary_identifiers":["GARD:10656","DOID:0111011","OMIM:601777","UMLS:C1866293","MEDGEN:400963","MESH:C538363"],"synonyms":[{"name":"CORD6","type":"exact"},{"name":"GUCY2D cone-rod dystrophy","type":"exact"},{"name":"RCD2","type":"exact"},{"name":"cone-rod dystrophy 6","type":"exact"},{"name":"cone-rod dystrophy caused by mutation in GUCY2D","type":"exact"},{"name":"cone-rod dystrophy type 6","type":"exact"},{"name":"retinal cone dystrophy 2","type":"exact"}],"termid":"MONDO:0011143","xrefs":{"Monarch":{"xref_id":"0011143"}}}


id: PR:O94595
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC622.05 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized membrane protein C622.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC622.05","synonyms":[{"name":"Spom972h-SPCC622.05","type":"exact"}],"termid":"PR:O94595"}


id: MONDO:0043125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ptosis","termid":"MONDO:0000728"}],"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":"mcpherson robertson cammarano syndrome","secondary_identifiers":["UMLS:C2931751","MESH:C538161","MEDGEN:419888"],"synonyms":[{"name":"dominantly inherited ptosis, strabismus and ectopic pupils","type":"related"}],"termid":"MONDO:0043125","xrefs":{"Monarch":{"xref_id":"0043125"}}}


id: GO:0035614
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a stem-loop in a small nuclear RNA (snRNA). An RNA stem-loop is a secondary RNA structure consisting of a double-stranded RNA (dsRNA) stem and a terminal loop.","definition_xrefs":["PMID:16568238","GOC:sart","PMID:20455544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA binding","termid":"GO:0017069"},{"relation_name":"is_a","term_name":"RNA stem-loop binding","termid":"GO:0035613"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"snRNA stem-loop binding","synonyms":[{"name":"small nuclear RNA stem-loop binding","type":"exact"},{"name":"snRNA hairpin binding","type":"exact"},{"name":"snRNA hairpin loop binding","type":"exact"}],"termid":"GO:0035614"}


id: PBO:0029214
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-galactose_absent_from_cell_wall","termid":"PBO:0029214"}


id: FYPO:0007299
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein aggregate center formation is decreased. Protein aggregate centers are composed of chaperones and misfolded proteins, and are reversibly formed in the nucleus and cytosol to shield thermosensitive proteins from degradation until conditions allow disaggregation and refolding.","definition_xrefs":["PMID:32075773","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein aggregate center formation","termid":"FYPO:0007298"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein aggregate center formation","synonyms":[{"name":"decreased PAC formation","type":"exact"},{"name":"decreased protein aggregate center formation during mitotic cell cycle","type":"related"},{"name":"decreased protein aggregate center formation during vegetative growth","type":"exact"},{"name":"decreased protein aggregate centre formation","type":"exact"},{"name":"reduced protein aggregate center formation","type":"exact"}],"termid":"FYPO:0007299"}


id: GO:0000704
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the removal of pyrimidine dimers by removing the 5' pyrimidine of the dimer by cleaving the N-C1' glycosidic bond between the 5' pyrimidine of the dimer and the deoxyribose sugar. The reaction releases the 5' pyrimidine of the dimer and leaves an apurinic (AP) site. The reaction involves the formation of a covalent enzyme substrate intermediate. Release of the enzyme and free base by a beta-elimination or a beta, gamma-elimination mechanism results in the cleavage of the DNA backbone 3' of the apyrimidinic (AP) site.","definition_xrefs":["PMID:9224623","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA N-glycosylase activity","termid":"GO:0019104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016798","GO:0140097","GO:0016787"],"is_obsolete":false,"name":"pyrimidine dimer DNA N-glycosylase activity","termid":"GO:0000704"}


id: GO:0045829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of isotype switching.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immunoglobulin production","termid":"GO:0002638"},{"relation_name":"is_a","term_name":"negative regulation of immunoglobulin mediated immune response","termid":"GO:0002890"},{"relation_name":"is_a","term_name":"regulation of isotype switching","termid":"GO:0045191"},{"relation_name":"is_a","term_name":"negative regulation of DNA recombination","termid":"GO:0045910"},{"relation_name":"is_a","term_name":"negative regulation of B cell activation","termid":"GO:0050869"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"negatively_regulates","term_name":"isotype switching","termid":"GO:0045190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"negatively_regulates","termid":"GO:0006310"},{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006259","GO:0006310"],"is_obsolete":false,"name":"negative regulation of isotype switching","synonyms":[{"name":"down regulation of isotype switching","type":"exact"},{"name":"down-regulation of isotype switching","type":"exact"},{"name":"downregulation of isotype switching","type":"exact"},{"name":"inhibition of isotype switching","type":"narrow"},{"name":"negative regulation of class switch recombination","type":"exact"},{"name":"negative regulation of class switching","type":"exact"},{"name":"negative regulation of isotype switch recombination","type":"exact"}],"termid":"GO:0045829"}


id: GO:0010443
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The asymmetric cell division by which a meristemoid mother cells (MMC) give rise to a meristemoid and another cell. The other cell may itself become a MMC or may generate an epidermal cell. Any cell that undergoes this type of division is a MMC.","definition_xrefs":["GOC:expert_db","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokinesis by cell plate formation","termid":"GO:0000911"},{"relation_name":"part_of","term_name":"stomatal lineage progression","termid":"GO:0010440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"meristemoid mother cell division","synonyms":[{"name":"meristemoid division","type":"related"}],"termid":"GO:0010443"}


id: PR:Q9USP5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GPI-anchor transamidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04689","PANTHER:PTHR12000: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":"GPI-anchor transamidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC11E10.02c","secondary_identifiers":["UniProtKB:Q9USP5"],"synonyms":[{"name":"GPI transamidase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PIGK","type":"exact"}],"termid":"PR:Q9USP5"}


id: PBO:0049314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase theta 2B","termid":"PBO:0049314"}


id: GO:2000110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of macrophage apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of myeloid cell apoptotic process","termid":"GO:0033033"},{"relation_name":"is_a","term_name":"negative regulation of leukocyte apoptotic process","termid":"GO:2000107"},{"relation_name":"is_a","term_name":"regulation of macrophage apoptotic process","termid":"GO:2000109"},{"relation_name":"negatively_regulates","term_name":"macrophage apoptotic process","termid":"GO:0071888"}],"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 macrophage apoptotic process","synonyms":[{"name":"negative regulation of AICD","type":"related"},{"name":"negative regulation of activation-induced cell death","type":"related"},{"name":"negative regulation of macrophage apoptosis","type":"narrow"}],"termid":"GO:2000110"}


id: MONDO:0005650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Virus diseases caused by the arenaviridae.","definition_xrefs":["MESH:D001117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arenaviridae infectious disease","secondary_identifiers":["EFO:0007150","SCTID:3303004","ICD9:078.89","DOID:3944"],"synonyms":[{"name":"Arenaviridae caused disease or disorder","type":"exact"},{"name":"Arenaviridae disease or disorder","type":"exact"},{"name":"Arenaviridae infection","type":"related"},{"name":"arenavirus infection","type":"related"},{"name":"arenavirus infections","type":"related"},{"name":"arenavirus infectious disease","type":"exact"},{"name":"disease caused by arenavirus","type":"related"},{"name":"disease due to arenavirus","type":"exact"},{"name":"infection, Arenaviridae","type":"related"},{"name":"infection, arenavirus","type":"related"},{"name":"infections, Arenaviridae","type":"related"},{"name":"infections, arenavirus","type":"related"}],"termid":"MONDO:0005650","xrefs":{"Monarch":{"xref_id":"0005650"}}}


id: GO:0008041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete storage protein of fat body (sensu Insecta) (obsolete GO:0008041)","synonyms":[{"name":"storage protein of fat body (sensu Insecta)","type":"exact"}],"termid":"GO:0008041"}


id: GO:0042296
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of ISG15 from one protein to another via the reaction X-ISG15 + Y = Y-ISG15 + X, where both X-ISG15 and Y-ISG15 are covalent linkages.","definition_xrefs":["GOC:mah","PMID:12826404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein transferase activity","termid":"GO:0019787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0019787"}],"interesting_parent_ids":["GO:0019787","GO:0140096","GO:0003824","GO:0016746","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"ISG15 transferase activity","secondary_identifiers":["Reactome:R-HSA-9927247","Reactome:R-HSA-5653754"],"synonyms":[{"name":"ISG15 conjugating enzyme activity","type":"narrow"}],"termid":"GO:0042296"}


id: GO:0003227
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the right ventricular myocardium are generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"right ventricular cardiac muscle tissue morphogenesis","termid":"GO:0003221"},{"relation_name":"is_a","term_name":"ventricular trabecula myocardium morphogenesis","termid":"GO:0003222"}],"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":"right ventricular trabecular myocardium morphogenesis","termid":"GO:0003227"}


id: GO:0052479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism stops, prevents, or reduces the frequency, rate or extent of symbiont ethylene-mediated signal transduction pathways during the symbiont defense response. 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 negative regulation by organism of defense-related symbiont ethylene-mediated signal transduction pathway (obsolete GO:0052479)","synonyms":[{"name":"negative regulation by organism of defense-related symbiont ethylene-mediated signal transduction pathway","type":"exact"},{"name":"suppression by organism of defense-related symbiont ethylene-mediated signal transduction pathway","type":"exact"}],"termid":"GO:0052479"}


id: GO:0099160
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The intermediate filament cytoskeleton that is part of a postsynapse.","definition_xrefs":["GOC:dos","PMID:25869803"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament cytoskeleton","termid":"GO:0045111"},{"relation_name":"is_a","term_name":"postsynaptic cytoskeleton","termid":"GO:0099571"}],"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":"postsynaptic intermediate filament cytoskeleton","termid":"GO:0099160"}


id: PBO:0088819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-methyltransferase","termid":"PBO:0088819"}


id: GO:2000207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of ribosomal small subunit export from nucleus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ribosomal subunit export from nucleus","termid":"GO:2000201"},{"relation_name":"is_a","term_name":"regulation of ribosomal small subunit export from nucleus","termid":"GO:2000206"},{"relation_name":"negatively_regulates","term_name":"ribosomal small subunit export from nucleus","termid":"GO:0000056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0042254"},{"rel_name":"negatively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0042254"},{"rel_name":"negatively_regulates","termid":"GO:0006913"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006913"}],"interesting_parent_ids":["GO:0006810","GO:0044085","GO:0006913","GO:0008150","GO:0042254"],"is_obsolete":false,"name":"negative regulation of ribosomal small subunit export from nucleus","synonyms":[{"name":"negative regulation of 30S ribosomal subunit export from nucleus","type":"related"},{"name":"negative regulation of 40S ribosomal subunit export from nucleus","type":"related"},{"name":"negative regulation of ribosomal small subunit export from cell nucleus","type":"exact"},{"name":"negative regulation of ribosomal small subunit export out of nucleus","type":"exact"},{"name":"negative regulation of ribosomal small subunit transport from nucleus to cytoplasm","type":"exact"},{"name":"negative regulation of ribosomal small subunit-nucleus export","type":"exact"}],"termid":"GO:2000207"}


id: PATO:0001959
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's in which bundles of aligned anatomical fibers have become separated.","definition_xrefs":["PATOC:mw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fasciculation","termid":"PATO:0002013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defasciculated","termid":"PATO:0001959"}


id: GO:0048575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change from vegetative to reproductive phase as a result of detection of, or exposure to, a period of light that falls short of the critical day length. The critical day length varies between species. Although the term is short-day is used, most species actually respond to the duration of the night, so that the response will occur when a period of darkness exceeds the number of hours defined by 24 minus the critical day length.","definition_xrefs":["GOC:jid","ISBN:0582015952","ISBN:0697037754","ISBN:0709408862","GOC:pj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short-day photoperiodism","termid":"GO:0048572"},{"relation_name":"is_a","term_name":"photoperiodism, flowering","termid":"GO:0048573"}],"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":"short-day photoperiodism, flowering","synonyms":[{"name":"long-night photoperiodism, flowering","type":"exact"},{"name":"response to long-night, flowering","type":"exact"},{"name":"response to short-day, flowering","type":"exact"},{"name":"short-day photoperiodic control of flowering","type":"exact"},{"name":"short-day photoperiodic control of flowering time","type":"exact"},{"name":"short-day photoperiodic control of inflorescence development","type":"exact"}],"termid":"GO:0048575"}


id: PBO:0048193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GA binding protein transcription factor subunit beta 1","termid":"PBO:0048193"}


id: MONDO:0023005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double uterus-hemivagina-renal agenesis","secondary_identifiers":["UMLS:C4302552","MEDGEN:928221"],"termid":"MONDO:0023005","xrefs":{"Monarch":{"xref_id":"0023005"}}}


id: PBO:0085913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; may interact with ribosomes, based on co-purification experiments; YJL118W is a non-essential gene; deletion enhances the toxicity of heterologously expressed human alpha-synuclein","termid":"PBO:0085913"}


id: PBO:0066759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 57","termid":"PBO:0066759"}


id: PBO:0079587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 D3","termid":"PBO:0079587"}


id: MONDO:0018963
data:
  {"annotated_genes":["SJAG_04217","SJAG_00235","SJAG_03929"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009606"},{"annotations":[85026,85027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009605"}]},"cv_name":"mondo","definition":"Methemoglobinemia inherited in an autosomal recessive pattern. It is caused by deficiency of the enzyme NADH methemoglobin reductase or the presence of abnormal hemoglobin M. It presents with cyanosis early in life. There is no evidence of cardiopulmonary disease present.","definition_xrefs":["NCIT:C98898"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methemoglobinemia","termid":"MONDO:0001117"},{"relation_name":"is_a","term_name":"anemia","termid":"MONDO:0002280"},{"relation_name":"is_a","term_name":"inherited hemoglobinopathy","termid":"MONDO:0019050"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00235":null,"SJAG_03929":null,"SJAG_04217":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"hereditary methemoglobinemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:267550008","Orphanet:621","MEDGEN:473013","icd11.foundation:586921197","MESH:C580280","GARD:2659","UMLS:C0272087"],"synonyms":[{"name":"autosomal recessive methemoglobinemia","type":"exact"},{"name":"congenital methemoglobinemia","type":"exact"},{"name":"hereditary methemoglobinemia","type":"exact"}],"termid":"MONDO:0018963","terms_by_termid":{"MONDO:0009605":null,"MONDO:0009606":null},"xrefs":{"Monarch":{"xref_id":"0018963"}}}


id: PBO:0030252
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_trehalose_level","termid":"PBO:0030252"}


id: PBO:0047491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferrochelatase pseudogene 1","termid":"PBO:0047491"}


id: MOD:00973
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oxidation of proline (to glutamic acid)","termid":"MOD:00973"}


id: GO:0019760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving glucosinolates, substituted thioglucosides found in rapeseed products and related cruciferae. They are metabolized to a variety of toxic products which are most likely the cause of hepatocytic necrosis in animals and humans.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-glycoside metabolic process","termid":"GO:0016143"},{"relation_name":"is_a","term_name":"oxoacid metabolic process","termid":"GO:0043436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006790"],"is_obsolete":false,"name":"glucosinolate metabolic process","synonyms":[{"name":"glucosinolate metabolism","type":"exact"}],"termid":"GO:0019760"}


id: PBO:0080159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variable charge X-linked","termid":"PBO:0080159"}


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


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


id: GO:0061599
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction adenylyl-molybdopterin + molybdate = molybdenum cofactor + AMP.","definition_xrefs":["EC:2.10.1.1","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"}],"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:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"molybdopterin molybdotransferase activity","secondary_identifiers":["Reactome:R-HSA-947531","RHEA:35047"],"termid":"GO:0061599"}


id: PBO:0005226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human leukocyte receptor 1 ortholog","termid":"PBO:0005226"}


id: PBO:0082257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-tubulin folding protein; similar to mammalian cofactor B; Alf1p-GFP localizes to cytoplasmic microtubules; required for the folding of alpha-tubulin and may play an additional role in microtubule maintenance","termid":"PBO:0082257"}


id: PBO:0082038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-deoxyglucose-6-phosphate phosphatase; member of a family of low molecular weight phosphatases; confers 2-deoxyglucose resistance when overexpressed; DOG1 has a paralog, DOG2, that arose from a single-locus duplication; the last half of DOG1 and DOG2 are subject to gene conversions among S. cerevisiae, S. paradoxus, and S. mikatae","termid":"PBO:0082038"}


id: MONDO:0006718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous lesions arising from infection with Treponema pallidum. In the primary stage, 18-21 days following infection, one or more chancres appear. If untreated, the subsequent stages of the disease appear as syphilids. These eruptions are superficial, nondestructive, exanthematic, transient, macular roseolas that may later be maculopapular or papular polymorphous or scaly, pustular, pigmented eruptions.(Arnold, Odom, and James, Andrew's Diseases of the Skin, 8th ed, p409)","definition_xrefs":["MESH:D013591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syphilis","termid":"MONDO:0005976"},{"relation_name":"is_a","term_name":"skin disease caused by bacterial infection","termid":"MONDO:0024295"}],"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 syphilis","secondary_identifiers":["UMLS:C0039132","EFO:1000887","MEDGEN:52623"],"synonyms":[{"name":"Treponema pallidum caused skin disease caused by bacterial infection","type":"exact"},{"name":"Treponema pallidum skin disease caused by bacterial infection","type":"exact"}],"termid":"MONDO:0006718","xrefs":{"Monarch":{"xref_id":"0006718"}}}


id: PBO:0031294
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cellular_physical_quality_phenotype","termid":"PBO:0031294"}


id: FYPO:0007359
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 heavy water (D2O) 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:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002682","FYPO:0001985","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"resistance to heavy water","synonyms":[{"name":"resistance to D2O","type":"exact"},{"name":"resistance to dideuterium oxide","type":"exact"},{"name":"resistance to heavy water during mitotic cell cycle","type":"related"},{"name":"resistance to heavy water during vegetative growth","type":"exact"},{"name":"resistant to heavy water","type":"exact"}],"termid":"FYPO:0007359"}


id: PBO:0077990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transformer 2 beta homolog","termid":"PBO:0077990"}


id: GO:0150014
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any dendrite in a dendritic tree that emerges near the apical pole of a neuron, and which is farthest away from the neuronal cell body (the soma).","definition_xrefs":["GO:bc","GOC:aruk","PMID:20629984","PMID:9214543","PMID:1720142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apical dendrite","termid":"GO:0097440"},{"relation_name":"is_a","term_name":"distal dendrite","termid":"GO:0150002"}],"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":"apical distal dendrite","termid":"GO:0150014"}


id: PBO:0062243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily BJ member 1 pseudogene","termid":"PBO:0062243"}


id: MONDO:0016674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"46,XY partial gonadal dysgenesis (46,XY PGD) is a disorder of sex development (DSD) associated with anomalies in gonadal development that results in genital ambiguity of variable degree ranging from almost female phenotype to almost male phenotype in a patient carrying a male 46,XY karyotype.","definition_xrefs":["Orphanet:251510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"46,XY partial gonadal dysgenesis","secondary_identifiers":["MEDGEN:1388250","SCTID:725045004","GARD:17211","UMLS:C4510744"],"synonyms":[{"name":"46,XY PGD","type":"exact"},{"name":"46,XY partial testicular dysgenesis","type":"exact"}],"termid":"MONDO:0016674","xrefs":{"Monarch":{"xref_id":"0016674"}}}


id: GO:0039505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont inhibits or disrupts the normal processing and presentation of a peptide antigen on its cell surface in association with an MHC class II protein complex.","definition_xrefs":["VZ:820","GOC:bf","GOC:add","PMID:27832589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host antigen processing and presentation","termid":"GO:0039588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host antigen processing and presentation of peptide antigen via MHC class II","synonyms":[{"name":"inhibition of host MHC class II molecule presentation by virus","type":"narrow"},{"name":"suppression by virus of host antigen processing and presentation of peptide antigen via MHC class II","type":"narrow"}],"termid":"GO:0039505"}


id: GO:0030787
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine(1+) + myo-inositol = 1D-4-O-methyl-myo-inositol + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["RHEA:23248","EC:2.1.1.129"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0003824","GO:0016741","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"inositol 4-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.129-RXN","KEGG_REACTION:R01190"],"synonyms":[{"name":"S-adenosyl-L-methionine:1D-myo-inositol 4-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:myo-inositol 4-O-methyltransferase activity","type":"related"},{"name":"myo-inositol 4-O-methyltransferase activity","type":"related"},{"name":"myo-inositol 6-O-methyltransferase activity","type":"related"}],"termid":"GO:0030787"}


id: PBO:0018161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase, involved in cytoplasmic translational initiation (predicted)","termid":"PBO:0018161"}


id: MOD:01293
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to L-aspartic acid with one (18)O.","definition_xrefs":["PubMed:8382902","OMSSA:139","Unimod:366#N"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"deamidated L-asparagine","termid":"MOD:00684"},{"relation_name":"is_a","term_name":"1x(18)O labeled deamidated residue","termid":"MOD:00852"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1x(18)O labeled deamidated L-asparagine","synonyms":[{"name":"Deamidated:18O(1)","type":"related"},{"name":"Deamidation in presence of O18","type":"related"},{"name":"oxy18","type":"exact"}],"termid":"MOD:01293"}


id: PATO:0001411
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's having distinct structure.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structured","termid":"PATO:0001411"}


id: MONDO:0004279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diseases of the ninth cranial (glossopharyngeal) nerve or its nuclei in the medulla. The nerve may be injured by diseases affecting the lower brain stem, floor of the posterior fossa, jugular foramen, or the nerve's extracranial course. Clinical manifestations include loss of sensation from the pharynx, decreased salivation, and syncope. Glossopharyngeal neuralgia refers to a condition that features recurrent unilateral sharp pain in the tongue, angle of the jaw, external auditory meatus and throat that may be associated with syncope. Episodes may be triggered by cough, sneeze, swallowing, or pressure on the tragus of the ear. (Adams et al., Principles of Neurology, 6th ed, p1390)","definition_xrefs":["MESH:D020435"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"motor nerve neuritis","termid":"MONDO:0004004"},{"relation_name":"is_a","term_name":"motor peripheral neuropathy","termid":"MONDO:0002316"},{"relation_name":"is_a","term_name":"glossopharyngeal nerve disorder","termid":"MONDO:0002639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"glossopharyngeal motor neuropathy","secondary_identifiers":["MEDGEN:155662","UMLS:C0751942","DOID:7558","NCIT:C27212"],"synonyms":[{"name":"glossopharyngeal nerve motor peripheral neuropathy","type":"exact"},{"name":"motor peripheral neuropathy of glossopharyngeal nerve","type":"exact"}],"termid":"MONDO:0004279","xrefs":{"Monarch":{"xref_id":"0004279"}}}


id: PR:Q9USH7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- psy1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USH7"],"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":"syntaxin-like protein psy1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC825.03c","synonyms":[{"name":"Spom972h-psy1","type":"exact"}],"termid":"PR:Q9USH7"}


id: PBO:0041246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 131","termid":"PBO:0041246"}


id: GO:1905268
data:
  {"annotated_genes":["SJAG_02723","SJAG_04369"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061188"},{"annotations":[107979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060906"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of chromatin organization.","definition_xrefs":["GO_REF:0000058","GOC:vw","GOC:pr","GOC:TermGenie","PMID:654321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of chromatin organization","termid":"GO:1902275"},{"relation_name":"negatively_regulates","term_name":"chromatin organization","termid":"GO:0006325"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02723":null,"SJAG_04369":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0008150","GO:0006325"],"is_obsolete":false,"name":"negative regulation of chromatin organization","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0045798","GO:1903309"],"synonyms":[{"name":"down regulation of chromatin assembly or disassembly","type":"related"},{"name":"down regulation of chromatin organisation","type":"exact"},{"name":"down regulation of chromatin organization","type":"exact"},{"name":"down regulation of establishment or maintenance of chromatin architecture","type":"exact"},{"name":"down-regulation of chromatin assembly or disassembly","type":"related"},{"name":"down-regulation of chromatin organisation","type":"exact"},{"name":"down-regulation of chromatin organization","type":"exact"},{"name":"down-regulation of establishment or maintenance of chromatin architecture","type":"exact"},{"name":"downregulation of chromatin assembly or disassembly","type":"related"},{"name":"downregulation of chromatin organisation","type":"exact"},{"name":"downregulation of chromatin organization","type":"exact"},{"name":"downregulation of establishment or maintenance of chromatin architecture","type":"exact"},{"name":"inhibition of chromatin assembly or disassembly","type":"narrow"},{"name":"inhibition of chromatin organisation","type":"narrow"},{"name":"inhibition of chromatin organization","type":"narrow"},{"name":"inhibition of establishment or maintenance of chromatin architecture","type":"narrow"},{"name":"negative regulation of chromatin assembly or disassembly","type":"related"},{"name":"negative regulation of chromatin assembly/disassembly","type":"exact"},{"name":"negative regulation of chromatin modification","type":"related"},{"name":"negative regulation of chromatin organisation","type":"exact"},{"name":"negative regulation of establishment or maintenance of chromatin architecture","type":"exact"}],"termid":"GO:1905268","terms_by_termid":{"GO:0060906":null,"GO:0061188":null}}


