# terms

id: MONDO:0010019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"selective IgA deficiency disease","termid":"MONDO:0001341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"secretory component deficiency","secondary_identifiers":["SCTID:234554004","OMIM:269650","ICD9:279.03","MEDGEN:140769","MESH:C562869","UMLS:C0398709"],"synonyms":[{"name":"IgA deficiency, secretory","type":"related"},{"name":"secretory component deficiency","type":"exact"}],"termid":"MONDO:0010019","xrefs":{"Monarch":{"xref_id":"0010019"}}}


id: GO:1905115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lateral attachment of mitotic spindle microtubules to kinetochore.","definition_xrefs":["GOC:TermGenie","PMID:22375062","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of attachment of mitotic spindle microtubules to kinetochore","termid":"GO:1902423"},{"relation_name":"regulates","term_name":"lateral attachment of mitotic spindle microtubules to kinetochore","termid":"GO:0099607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0000070"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0000070","GO:0007049"],"is_obsolete":false,"name":"regulation of lateral attachment of mitotic spindle microtubules to kinetochore","termid":"GO:1905115"}


id: GO:1990447
data:
  {"annotated_genes":["SJAG_02558"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[114160],"is_not":false,"summary":null,"term":"GO:1990447"}]},"cv_name":"molecular_function","definition":"Binding to a U2 small nuclear ribonucleoprotein particle.","definition_xrefs":["PMID:14713954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNP binding","termid":"GO:0070990"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02558":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"U2 snRNP binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990447","terms_by_termid":{"GO:1990447":null}}


id: PBO:0064687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 23","termid":"PBO:0064687"}


id: PBO:0000341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin/PY protein 1 (predicted)","termid":"PBO:0000341"}


id: PBO:0060324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin IC","termid":"PBO:0060324"}


id: MONDO:0100463
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive inborn disorder of cobalamin metabolism caused by biallelic variants in MMADHC. Depending on the type and location of variants in MMADHC, patients may present with methylmalonic aciduria, homocystinuria, or both. MMADHC has been reported to result in the cblD complementation group of cobalamin disorders.","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of cobalamin metabolism and transport","termid":"MONDO:0019220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"methylmalonic aciduria and/or homocystinuria, cblD type","termid":"MONDO:0100463","xrefs":{"Monarch":{"xref_id":"0100463"}}}


id: MONDO:0957210
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":"neurooculorenal syndrome","secondary_identifiers":["UMLS:C5830377","MEDGEN:1841013","OMIM:620305"],"termid":"MONDO:0957210","xrefs":{"Monarch":{"xref_id":"0957210"}}}


id: MONDO:0008665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ptosis-vocal cord paralysis syndrome is a rare, hereditary disorder with ptosis characterized by the combination of congenital bilateral recurrent laryngeal nerve paralysis and congenital bilateral ptosis. There have been no further descriptions in the literature since 1983.","definition_xrefs":["Orphanet:2997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ptosis-vocal cord paralysis syndrome","secondary_identifiers":["MESH:C536923","UMLS:C1860403","GARD:427","OMIM:193240","MEDGEN:349807"],"synonyms":[{"name":"congenital bilateral recurrent nerve paralysis and ptosis","type":"related"},{"name":"ptosis vocal cord paralysis","type":"related"},{"name":"tucker syndrome","type":"exact"},{"name":"vocal cord paralysis and ptosis","type":"related"}],"termid":"MONDO:0008665","xrefs":{"Monarch":{"xref_id":"0008665"}}}


id: GO:0062124
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with 4-hydroxybutyrte to initiate a change in cell activity.","definition_xrefs":["PMID:17197387"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor activity","termid":"GO:0038023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"4-hydroxybutyrate receptor activity","synonyms":[{"name":"gamma-hydroxybutyrate receptor activity","type":"exact"}],"termid":"GO:0062124"}


id: GO:1905621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of alpha-(1->3)-fucosyltransferase activity.","definition_xrefs":["PMID:15364955","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of alpha-(1->3)-fucosyltransferase activity (obsolete GO:1905621)","synonyms":[{"name":"activation of alpha(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-(1->3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-1,3-fucosyltransferase activity","type":"narrow"},{"name":"positive regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"positive regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"positive regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-1,3-fucosyltransferase activity","type":"exact"}],"termid":"GO:1905621"}


id: PBO:0051590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 20 receptor subunit beta","termid":"PBO:0051590"}


id: PBO:0061039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIPA magnesium transporter 2","termid":"PBO:0061039"}


id: GO:0051466
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the regulated release of corticotropin-releasing hormone from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of corticotropin-releasing hormone secretion","termid":"GO:0043397"},{"relation_name":"is_a","term_name":"positive regulation of peptide hormone secretion","termid":"GO:0090277"},{"relation_name":"positively_regulates","term_name":"corticotropin-releasing hormone secretion","termid":"GO:0043396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of corticotropin-releasing hormone secretion","synonyms":[{"name":"activation of corticotropin-releasing hormone secretion","type":"narrow"},{"name":"positive regulation of CRF secretion","type":"exact"},{"name":"positive regulation of CRH secretion","type":"exact"},{"name":"positive regulation of corticotropin-releasing factor secretion","type":"exact"},{"name":"stimulation of corticotropin-releasing hormone secretion","type":"narrow"},{"name":"up regulation of corticotropin-releasing hormone secretion","type":"exact"},{"name":"up-regulation of corticotropin-releasing hormone secretion","type":"exact"},{"name":"upregulation of corticotropin-releasing hormone secretion","type":"exact"}],"termid":"GO:0051466"}


id: GO:0035126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after embryonic development, by which the anatomical structures of the genitalia are generated and organized.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genitalia morphogenesis","termid":"GO:0035112"}],"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":"post-embryonic genitalia morphogenesis","synonyms":[{"name":"post-embryonic genital morphogenesis","type":"related"}],"termid":"GO:0035126"}


id: MONDO:0975806
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fatal multiple mitochondrial dysfunctions syndrome","termid":"MONDO:0017338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0002525"],"is_obsolete":false,"name":"multiple mitochondrial dysfunctions syndrome 10","secondary_identifiers":["OMIM:620960"],"termid":"MONDO:0975806","xrefs":{"Monarch":{"xref_id":"0975806"}}}


id: PBO:0051021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor binding protein 1","termid":"PBO:0051021"}


id: MONDO:0010835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pterygium colli-intellectual disability-digital anomalies syndrome is characterized by pterygium colli, digital anomalies (abnormal small thumbs, widened interphalangeal joints, and broad terminal phalanges), and craniofacial abnormalities (brachycephaly, epicanthic folds, angulated eyebrows, upward slanting of the palpebral fissures, ptosis, hypertelorism, and prominent low-set, posteriorly rotated ears). It has been described in a woman and her son, but the manifestations were much less severe in the mother. The son also had intellectual deficit. The inheritance is either X-linked dominant or autosomal dominant.","definition_xrefs":["Orphanet:2988"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pterygium colli-intellectual disability-digital anomalies syndrome","secondary_identifiers":["SCTID:719256004","GARD:4568","OMIM:600159","UMLS:C1838562","MEDGEN:374001","MESH:C535831"],"synonyms":[{"name":"khalifa-Graham syndrome","type":"exact"},{"name":"pterygium colli and intellectual disability with facial and digital anomalies","type":"related"},{"name":"pterygium colli and mental retardation with facial and digital anomalies","type":"related"},{"name":"pterygium colli intellectual disability digital anomalies","type":"related"},{"name":"pterygium colli mental retardation digital anomalies","type":"related"}],"termid":"MONDO:0010835","xrefs":{"Monarch":{"xref_id":"0010835"}}}


id: PBO:0049351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 9","termid":"PBO:0049351"}


id: PBO:0110361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJC2 pseudogene 1","termid":"PBO:0110361"}


id: MONDO:0007570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign, congenital genetic skin disorder characterized by permanent and asymptomatic erythema of the palmar and, less frequently, the solar surfaces. In most cases, it presents with sharply demarcated redness of the thenar and hypothenar eminences, as well as the palmar aspect of the phalanges, with scattered telangiectasia spots that do not cause any discomfort (pain, itching or burning) to the patient.","definition_xrefs":["Orphanet:231031"],"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":"erythema palmare hereditarium","secondary_identifiers":["MEDGEN:343587","GARD:17157","SCTID:763767006","OMIM:133000","MESH:C565041","UMLS:C1851502"],"synonyms":[{"name":"Red palms disease","type":"exact"},{"name":"erythema palmare hereditarium","type":"exact"},{"name":"lane disease","type":"exact"}],"termid":"MONDO:0007570","xrefs":{"Monarch":{"xref_id":"0007570"}}}


id: PBO:0065909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB GTPase activating protein 1","termid":"PBO:0065909"}


id: PBO:0079001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon CGT) 1-1","termid":"PBO:0079001"}


id: GO:0022894
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of potassium by a channel with a unit conductance of 20 to 85 picoSiemens that opens in response to stimulus by internal calcium ions. Intermediate conductance calcium-activated potassium channels are more sensitive to calcium than are large conductance calcium-activated potassium channels. Transport by a channel involves catalysis of facilitated diffusion of a solute (by an energy-independent process) involving passage through a transmembrane aqueous pore or channel, without evidence for a carrier-mediated mechanism.","definition_xrefs":["GOC:mtg_transport","OMIM:602754"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium-activated potassium channel activity","termid":"GO:0015269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"intermediate conductance calcium-activated potassium channel activity","synonyms":[{"name":"IK KCa channels","type":"exact"},{"name":"IK calcium-activated potassium channel activity","type":"exact"},{"name":"intermediate conductance KCa channels","type":"exact"}],"termid":"GO:0022894"}


id: MONDO:0013189
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by repetitive pulling out of one's hair resulting in noticeable hair loss; the individual experiences a rising subjective sense of tension before pulling out the hair and a sense of gratification or relief when pulling out the hair.","definition_xrefs":["NCIT:C94336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impulse control disorder","termid":"MONDO:0001162"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trichotillomania","secondary_identifiers":["MESH:D014256","UMLS:C0040953","OMIM:613229","ICD9:312.39","SCTID:17155009","DOID:0050587","MEDGEN:21654","ICD10CM:F63.3","icd11.foundation:1253999657"],"synonyms":[{"name":"TTM","type":"related"},{"name":"trichotillomania","type":"exact"},{"name":"trichotillomania, multifactorial","type":"exact"}],"termid":"MONDO:0013189","xrefs":{"Monarch":{"xref_id":"0013189"}}}


id: MONDO:0016829
data:
  {"annotated_genes":["SJAG_03703","SJAG_02431"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86893,86892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859157"}]},"cv_name":"mondo","definition":"A rare hereditary myopathic degeneration of both gastrointestinal and urinary tracts that causes chronic intestinal pseudo-obstruction. It usually presents after the first decade of life with megaduodenum, megacystis and symptoms such as abdominal distension and/or pain, vomiting, constipation, diarrhea, dysphagia, and/or urinary tract infections.n.","definition_xrefs":["Orphanet:2604"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete megacystis-microcolon-intestinal hypoperistalsis syndrome (obsolete MONDO:0007960)","termid":"MONDO:0007960"},{"relation_name":"is_a","term_name":"visceral myopathy 1","termid":"MONDO:0020754"},{"relation_name":"is_a","term_name":"intestinal motility disease","termid":"MONDO:0021189"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"familial visceral myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1838806574","GARD:3443","SCTID:63684002","ICD9:359.89","MEDGEN:120590","UMLS:C0266833"],"synonyms":[{"name":"familial hollow visceral myopathy","type":"exact"},{"name":"hereditary hollow visceral myopathy","type":"exact"},{"name":"megaduodenum and/or megacystis","type":"exact"},{"name":"pseudoobstruction idiopathic intestinal","type":"related"},{"name":"visceral myopathy familial","type":"related"}],"termid":"MONDO:0016829","terms_by_termid":{"MONDO:0859157":null},"xrefs":{"Monarch":{"xref_id":"0016829"}}}


id: PBO:0005169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase activator Mob2","termid":"PBO:0005169"}


id: PBO:0082690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the heterotetrameric MHF histone-fold complex; in humans the MHF complex interacts with both DNA and Mph1p ortholog FANCM, a Fanconi anemia complementation group protein, to stabilize and remodel blocked replication forks and repair damaged DNA; mhf1 srs2 double mutants are MMS hypersensitive; ortholog of human centromere constitutive-associated network (CCAN) subunit CENP-S, also known as MHF1","termid":"PBO:0082690"}


id: PBO:0029954
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_microtubule_binding","termid":"PBO:0029954"}


id: PBO:0071391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L30 pseudogene 14","termid":"PBO:0071391"}


id: PBO:0049080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 135","termid":"PBO:0049080"}


id: MONDO:0019187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Axenfeld-Rieger syndrome (ARS) is a generic term used to designate overlapping genetic disorders, in which the major physical condition is anterior segment dysgenesis of the eye. Patients with ARS may also present with multiple variable congenital anomalies.","definition_xrefs":["Orphanet:782"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"},{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic developmental defect of the eye (obsolete MONDO:0015217)","termid":"MONDO:0015217"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic anorectal malformation (obsolete MONDO:0015246)","termid":"MONDO:0015246"},{"relation_name":"excluded_subClassOf","term_name":"non-acquired combined pituitary hormone deficiency","termid":"MONDO:0018762"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Axenfeld-Rieger syndrome","secondary_identifiers":["DOID:14686","NCIT:C131001","OMIMPS:180500","SCTID:47507006","UMLS:C3495488","GARD:5701","MedDRA:10059255","ICD9:743.44","MEDGEN:501192","NORD:1670","MESH:C535679"],"synonyms":[{"name":"Axenfeld syndrome","type":"exact"},{"name":"Axenfeldt-Rieger syndrome","type":"exact"},{"name":"Hagedoom syndrome","type":"related"},{"name":"RGS - Rieger syndrome","type":"exact"},{"name":"Rieger syndrome","type":"exact"},{"name":"Rieger's anomaly","type":"exact"},{"name":"anomaly, Rieger's","type":"exact"},{"name":"goniodysgenesis hypodontia","type":"related"},{"name":"iridogoniodysgenesis with somatic anomalies","type":"related"}],"termid":"MONDO:0019187","xrefs":{"Monarch":{"xref_id":"0019187"}}}


id: MONDO:0010505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intellectual disability-balding-patella luxation-acromicria syndrome is characterized by severe intellectual deficit, patella luxations, acromicria, hypogonadism, facial dysmorphism (including midface hypoplasia and premature frontotemporal balding). It has been described in three unrelated males.","definition_xrefs":["Orphanet:3041"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"acromelic dysplasia","termid":"MONDO:0019695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability-balding-patella luxation-acromicria syndrome","secondary_identifiers":["GARD:257","OMIM:300977","MESH:C536638","SCTID:722002002","MEDGEN:401129","UMLS:C1866985"],"synonyms":[{"name":"SCHOLTE syndrome","type":"related"},{"name":"SHLTS","type":"exact"},{"name":"Scholte syndrome","type":"exact"},{"name":"Scholte-Begeer-van Essen syndrome","type":"exact"},{"name":"early balding, patella luxation, acromicria and hypogonadism","type":"related"},{"name":"early balding, patella luxation, acromicria, and hypogonadism","type":"related"}],"termid":"MONDO:0010505","xrefs":{"Monarch":{"xref_id":"0010505"}}}


id: GO:0036479
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of peroxidase.","definition_xrefs":["GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"},{"relation_name":"negatively_regulates","term_name":"peroxidase activity","termid":"GO:0004601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"regulates","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"regulates","termid":"GO:0003824"},{"rel_name":"negatively_regulates","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0004857","GO:0016491","GO:0098772","GO:0030234","GO:0003824","GO:0140678","GO:0003674"],"is_obsolete":false,"name":"peroxidase inhibitor activity","termid":"GO:0036479"}


id: MONDO:0021321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the extrahepatic bile duct.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bile duct cancer","termid":"MONDO:0003059"},{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0002515"],"is_obsolete":false,"name":"malignant tumor of extrahepatic bile duct","secondary_identifiers":["NCIT:C7483","ICD9:156.1","MEDGEN:56304","UMLS:C0153453","ICD9:156.8","SCTID:363416002"],"synonyms":[{"name":"cancer of extrahepatic bile duct","type":"exact"},{"name":"extrahepatic bile duct cancer","type":"broad"},{"name":"malignant extrahepatic bile duct neoplasm","type":"exact"},{"name":"malignant extrahepatic bile duct tumor","type":"exact"},{"name":"malignant extrahepatic bile duct tumour","type":"exact"},{"name":"malignant neoplasm of extrahepatic bile duct","type":"exact"},{"name":"malignant neoplasm of the extrahepatic bile duct","type":"exact"},{"name":"malignant tumor of the extrahepatic bile duct","type":"exact"},{"name":"malignant tumour of the extrahepatic bile duct","type":"exact"}],"termid":"MONDO:0021321","xrefs":{"Monarch":{"xref_id":"0021321"}}}


id: GO:0102879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = (+)-thujopsene + diphosphoric acid.","definition_xrefs":["RHEA:30375","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"(+)-thujopsene synthase activity","secondary_identifiers":["MetaCyc:RXN-8418","EC:4.2.3.79"],"termid":"GO:0102879"}


id: PATO:0001157
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001157 absolute concentration value (obsolete PATO:0001157)","termid":"PATO:0001157"}


id: MOD:00735
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a hexosuronic acid group through a glycosidic bond.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylated residue","termid":"MOD:00693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"hexosuronylated","synonyms":[{"name":"HexA","type":"exact"}],"termid":"MOD:00735"}


id: GO:0090180
data:
  {"annotated_genes":["SJAG_03538","SJAG_02406"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89378,113988],"is_not":false,"summary":null,"term":"GO:0090180"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of thiamine.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of vitamin metabolic process","termid":"GO:0046136"},{"relation_name":"is_a","term_name":"positive regulation of sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"regulation of thiamine biosynthetic process","termid":"GO:0070623"},{"relation_name":"is_a","term_name":"positive regulation of alcohol biosynthetic process","termid":"GO:1902932"},{"relation_name":"positively_regulates","term_name":"thiamine biosynthetic process","termid":"GO:0009228"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02406":null,"SJAG_03538":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"positively_regulates","termid":"GO:0006766"},{"rel_name":"regulates","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006766","GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"positive regulation of thiamine biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"positive regulation of thiamin biosynthetic process","type":"exact"}],"termid":"GO:0090180","terms_by_termid":{"GO:0090180":null}}


id: MONDO:0019711
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dysostosis with predominant vertebral and costal involvement (obsolete MONDO:0019711)","secondary_identifiers":["icd11.foundation:395969787","Orphanet:93454"],"termid":"MONDO:0019711","xrefs":{"Monarch":{"xref_id":"0019711"}}}


id: PBO:0071494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 35","termid":"PBO:0071494"}


id: PBO:0051088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy joining 1","termid":"PBO:0051088"}


id: PR:O13339-2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A telomerase reverse transcriptase (Schizosaccharomyces pombe 972h-) that is a translation product of some mRNA giving rise to a protein with the amino acid sequence represented by UniProtKB:O13339-2.","definition_xrefs":["UniProtKB:O13339","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomerase reverse transcriptase (Schizosaccharomyces pombe 972h-)","termid":"PR:O13339"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomerase reverse transcriptase isoform 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1002.01","secondary_identifiers":["UniProtKB:O13339-2"],"synonyms":[{"name":"Spom972h-TERT/iso:2","type":"exact"}],"termid":"PR:O13339-2"}


id: PBO:0072833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAP18 pseudogene 3","termid":"PBO:0072833"}


id: PBO:0054170
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 1543","termid":"PBO:0054170"}


id: PATO:0000751
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000751 locomotor activity value (obsolete PATO:0000751)","termid":"PATO:0000751"}


id: SO:0001776
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant in the genetic material inherited from the father.","direct_ancestors":[{"relation_name":"is_a","term_name":"variant_origin","termid":"SO:0001762"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paternal_variant","synonyms":[{"name":"paternal variant","type":"exact"}],"termid":"SO:0001776"}


id: GO:1903068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to cell tip.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24554432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell tip","termid":"GO:1903066"},{"relation_name":"is_a","term_name":"positive regulation of protein localization","termid":"GO:1903829"},{"relation_name":"positively_regulates","term_name":"protein localization to cell tip","termid":"GO:1990151"}],"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 protein localization to cell tip","synonyms":[{"name":"activation of protein localisation to cell tip","type":"narrow"},{"name":"activation of protein localization to cell tip","type":"narrow"},{"name":"positive regulation of protein localisation to cell tip","type":"exact"},{"name":"up regulation of protein localisation to cell tip","type":"exact"},{"name":"up regulation of protein localization to cell tip","type":"exact"},{"name":"up-regulation of protein localisation to cell tip","type":"exact"},{"name":"up-regulation of protein localization to cell tip","type":"exact"},{"name":"upregulation of protein localisation to cell tip","type":"exact"},{"name":"upregulation of protein localization to cell tip","type":"exact"}],"termid":"GO:1903068"}


id: PBO:0068968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 212, pseudogene","termid":"PBO:0068968"}


id: PBO:0044471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 11 subfamily A member 1","termid":"PBO:0044471"}


id: PBO:0049323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTF2A1 antisense RNA 1","termid":"PBO:0049323"}


id: GO:0044503
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the activity of a G protein-coupled receptor in a second organism.","definition_xrefs":["GOC:jl","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of G protein-coupled receptor activity in another organism (obsolete GO:0044503)","synonyms":[{"name":"modulation of G protein-coupled receptor activity in other organism","type":"exact"},{"name":"modulation of G-protein coupled receptor activity in other organism","type":"exact"}],"termid":"GO:0044503"}


id: PBO:0058227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4517","termid":"PBO:0058227"}


id: GO:0048901
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the anterior lateral line neuromast over time, from its formation to the mature structure. The neuromast is the sensory receptor of the anterior lateral line system and is composed of a population of sensory hair cells, and nonsensory supporting cells and mantle cells. Neuromast are located superficially on the epithelium or in lateral line canals.","definition_xrefs":["ISBN:0125296509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromast development","termid":"GO:0048884"},{"relation_name":"part_of","term_name":"anterior lateral line development","termid":"GO:0048899"}],"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":"anterior lateral line neuromast development","termid":"GO:0048901"}


id: MONDO:1011475
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arthrogryposis multiplex congenita that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita, non-human animal","termid":"MONDO:1011455"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis multiplex congenita, pig","secondary_identifiers":["OMIA:001465-9823"],"termid":"MONDO:1011475","xrefs":{"Monarch":{"xref_id":"1011475"}}}


id: MONDO:0006508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infantile epileptic encephalopathy (obsolete MONDO:0006508)","termid":"MONDO:0006508","xrefs":{"Monarch":{"xref_id":"0006508"}}}


id: GO:0009933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Organization of a region of tissue in a plant that is composed of one or more undifferentiated cells capable of undergoing mitosis and differentiation, thereby effecting growth and development of a plant by giving rise to more meristem or specialized tissue.","definition_xrefs":["GOC:sm","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"meristem development","termid":"GO:0048507"}],"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":"meristem structural organization","synonyms":[{"name":"meristem organisation","type":"broad"},{"name":"meristem organization","type":"broad"}],"termid":"GO:0009933"}


id: PBO:0077888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPRG1 antisense RNA 2","termid":"PBO:0077888"}


id: MONDO:0014167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the CNTN2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign adult familial myoclonic epilepsy","termid":"MONDO:0019448"},{"relation_name":"is_a","term_name":"epilepsy, familial adult myoclonic","termid":"MONDO:0000160"}],"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":"epilepsy, familial adult myoclonic, 5","secondary_identifiers":["GARD:18086","MEDGEN:815704","OMIM:615400","UMLS:C3809374","DOID:0111691"],"synonyms":[{"name":"CNTN2 epilepsy, familial adult myoclonic","type":"exact"},{"name":"FAME5","type":"related"},{"name":"cortical myoclonic tremor with epilepsy, familial, 5","type":"related"},{"name":"epilepsy, familial ADULT myoclonic, 5","type":"related"},{"name":"epilepsy, familial adult myoclonic caused by mutation in CNTN2","type":"exact"},{"name":"epilepsy, familial adult myoclonic, 5","type":"exact"},{"name":"epilepsy, familial adult myoclonic, type 5","type":"exact"},{"name":"epilepsy, myoclonic, familial adult, 5","type":"exact"}],"termid":"MONDO:0014167","xrefs":{"Monarch":{"xref_id":"0014167"}}}


id: FYPO:0006520
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of cytoplasmic translation is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytoplasmic translation","termid":"FYPO:0003124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"increased cytoplasmic translation","synonyms":[{"name":"increased cytoplasmic translation during mitotic cell cycle","type":"related"},{"name":"increased cytoplasmic translation during vegetative growth","type":"exact"}],"termid":"FYPO:0006520"}


id: PBO:0054393
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 1789","termid":"PBO:0054393"}


id: FYPO:0005882
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of gamma-glutamyl-2-aminobutyrate (also called gamma-Glu-Abu) measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular gamma-glutamyl-2-aminobutyrate level","synonyms":[{"name":"increased cellular gamma-Glu-Abu level","type":"related"},{"name":"increased cellular gamma-Glu-Abu(1-) level","type":"exact"},{"name":"increased cellular gamma-glutamyl-2-aminobutyrate level during mitotic cell cycle","type":"related"},{"name":"increased cellular gamma-glutamyl-2-aminobutyrate level during vegetative growth","type":"exact"},{"name":"increased gamma-glutamyl-2-aminobutyrate accumulation","type":"related"}],"termid":"FYPO:0005882"}


id: GO:0032703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-2 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of interleukin-2 production","termid":"GO:0032663"},{"relation_name":"negatively_regulates","term_name":"interleukin-2 production","termid":"GO:0032623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of interleukin-2 production","secondary_identifiers":["GO:0045085","GO:1900041"],"synonyms":[{"name":"down regulation of interleukin-2 production","type":"exact"},{"name":"down-regulation of interleukin-2 production","type":"exact"},{"name":"downregulation of interleukin-2 production","type":"exact"},{"name":"inhibition of interleukin-2 production","type":"narrow"},{"name":"negative regulation of IL-2 production","type":"exact"},{"name":"negative regulation of interleukin-2 biosynthetic process","type":"narrow"},{"name":"negative regulation of interleukin-2 secretion","type":"narrow"}],"termid":"GO:0032703"}


id: PBO:0083382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps CUP1-1","termid":"PBO:0083382"}


id: PBO:0056570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCPH1 antisense RNA 1","termid":"PBO:0056570"}


id: PBO:0065096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase AMP-activated non-catalytic subunit gamma 3","termid":"PBO:0065096"}


id: PBO:0043553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COL4A2 antisense RNA 2","termid":"PBO:0043553"}


id: GO:0046520
data:
  {"annotated_genes":["SJAG_01057","SJAG_02429","SJAG_02305","SJAG_00880","SJAG_04178","SJAG_02706"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110023,77212,74052,97234,79244,106311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046512"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sphingoids, any of a class of compounds comprising sphinganine and its homologues and stereoisomers, and derivatives of these compounds.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphingolipid biosynthetic process","termid":"GO:0030148"},{"relation_name":"is_a","term_name":"sphingoid metabolic process","termid":"GO:0046519"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00880":null,"SJAG_01057":null,"SJAG_02305":null,"SJAG_02429":null,"SJAG_02706":null,"SJAG_04178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"sphingoid biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"sphingoid anabolism","type":"exact"},{"name":"sphingoid biosynthesis","type":"exact"},{"name":"sphingoid formation","type":"exact"},{"name":"sphingoid synthesis","type":"exact"}],"termid":"GO:0046520","terms_by_termid":{"GO:0046512":null}}


id: GO:2000982
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of inner ear receptor cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mechanoreceptor differentiation","termid":"GO:0045633"},{"relation_name":"is_a","term_name":"regulation of inner ear receptor cell differentiation","termid":"GO:2000980"},{"relation_name":"positively_regulates","term_name":"inner ear receptor cell differentiation","termid":"GO:0060113"}],"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 inner ear receptor cell differentiation","synonyms":[{"name":"positive regulation of inner ear hair cell differentiation","type":"exact"}],"termid":"GO:2000982"}


id: PBO:0018286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CMP deaminase family/ methyltransferase bifunctional enzyme involved in riboflavin biosynthesis and tRNA pseudouridine biosynthesis Rib2 (predicted)","termid":"PBO:0018286"}


id: GO:0003069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which acetylcholine signaling causes vasodilation, resulting in a change in blood pressure.","definition_xrefs":["GOC:rl","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of systemic arterial blood pressure","termid":"GO:0003085"},{"relation_name":"is_a","term_name":"vasodilation","termid":"GO:0042311"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by acetylcholine","termid":"GO:0003068"}],"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":"acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure","synonyms":[{"name":"vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure","type":"exact"}],"termid":"GO:0003069"}


id: FYPO:0007786
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the cell is longer than normal, and progression through the meiotic cell cycle is arrested at the G2/MI phase transition. A cell can elongate when arrested at the G2/MI transition if it overcomes the growth arrest that usually occurs.","definition_xrefs":["PomBase:mah","PomBase:jh","PMID:28476936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated cell","termid":"FYPO:0000017"},{"relation_name":"is_a","term_name":"abnormal cell cycle arrest at meiotic G2/MI transition","termid":"FYPO:0007785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000005","FYPO:0000631"],"is_obsolete":false,"name":"elongated cell with cell cycle arrest at meiotic G2/MI transition","synonyms":[{"name":"elongated cell with abnormal cell cycle arrest at G2/M1 transition","type":"exact"},{"name":"elongated cell with abnormal cell cycle arrest at G2/MI transition of meiotic cell cycle","type":"exact"},{"name":"elongated cell with abnormal cell cycle arrest at meiotic G2/MI phase transition","type":"exact"},{"name":"elongated cell with abnormal cell cycle arrest at meiotic G2/MI transition","type":"exact"},{"name":"elongated cell with abnormal cell cycle arrest at meiotic cell cycle G2/MI phase transition","type":"exact"},{"name":"elongated cell with abnormal meiotic cell cycle arrest at G2/MI phase transition","type":"exact"},{"name":"elongated cell with abnormal meiotic cell cycle arrest at G2/MI transition","type":"exact"},{"name":"elongated cells during meiotic G2/M1 arrest","type":"exact"},{"name":"elongated cells during meiotic G2/MI arrest","type":"exact"},{"name":"long cell with cell cycle arrest at meiotic G2/MI transition","type":"exact"}],"termid":"FYPO:0007786"}


id: GO:2001228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of response to gamma radiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to stimulus","termid":"GO:0048583"},{"relation_name":"regulates","term_name":"response to gamma radiation","termid":"GO:0010332"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of response to gamma radiation","synonyms":[{"name":"regulation of response to gamma ray","type":"related"},{"name":"regulation of response to gamma-ray photon","type":"related"}],"termid":"GO:2001228"}


id: GO:1901703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any protein localization that is involved in auxin polar transport.","definition_xrefs":["GOC:TermGenie","PMID:23163883"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"},{"relation_name":"part_of","term_name":"auxin polar transport","termid":"GO:0009926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization involved in auxin polar transport","synonyms":[{"name":"establishment and maintenance of protein localization involved in auxin polar transport","type":"exact"},{"name":"protein localisation involved in auxin polar transport","type":"exact"}],"termid":"GO:1901703"}


id: PBO:0034363
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-contributes_to_severity_of_condition","termid":"PBO:0034363"}


id: GO:0006610
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a ribosomal protein from the cytoplasm into the nucleus, across the nuclear membrane. At least some ribosomal proteins, including rpl12, uses the importin 11 pathway as a major route into the nucleus.","definition_xrefs":["GOC:ai","PMID:11809816"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein import into nucleus","termid":"GO:0006606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006913"},{"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","GO:0006913"],"is_obsolete":false,"name":"ribosomal protein import into nucleus","synonyms":[{"name":"ribosomal protein import into cell nucleus","type":"exact"},{"name":"ribosomal protein transport from cytoplasm to nucleus","type":"exact"},{"name":"ribosomal protein-nucleus import","type":"exact"}],"termid":"GO:0006610"}


id: MONDO:0020403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mitral valve agenesis is a rare congenital heart malformation defined as an agenesis or severe hypoplasia of both mitral valve leaflets (complete agenesis) or one of the leaflets (partial agenesis). Complete mitral valve agenesis presents in the neonatal period with symptoms of severe mitral regurgitation and is rapidly fatal unless surgically treated. It is frequently associated with other heart malformations. Partial mitral valve agenesis may present at various ages, usually with symptoms of mitral regurgitation.","definition_xrefs":["Orphanet:99062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital mitral valve insufficiency and/or stenosis","termid":"MONDO:0019817"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital mitral valve agenesis","secondary_identifiers":["GARD:19629","UMLS:C0685721","MEDGEN:672659"],"termid":"MONDO:0020403","xrefs":{"Monarch":{"xref_id":"0020403"}}}


id: PBO:0076820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminal nucleotidyltransferase 4A","termid":"PBO:0076820"}


id: PBO:0071451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 57","termid":"PBO:0071451"}


id: GO:0047657
data:
  {"annotated_genes":["SJAG_01028","SJAG_03057","SJAG_04184","SJAG_02916","SJAG_04236"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70984,71807,73756,73938,79012],"is_not":false,"summary":null,"term":"GO:0047657"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + [alpha-D-glucosyl-(1,3)]n = UDP + [alpha-D-glucosyl-(1,3)]n+1.","definition_xrefs":["MetaCyc:ALPHA-13-GLUCAN-SYNTHASE-RXN","EC:2.4.1.183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01028":null,"SJAG_02916":null,"SJAG_03057":null,"SJAG_04184":null,"SJAG_04236":null},"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"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"alpha-1,3-glucan synthase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:19749"],"synonyms":[{"name":"1,3-alpha-D-glucan synthase activity","type":"related"},{"name":"1,3-alpha-glucan synthase activity","type":"exact"},{"name":"UDP-glucose:alpha-D-(1->3)-glucan 3-alpha-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:alpha-D-(1->3)-glucan 3-alpha-D-glucosyltransferase activity","type":"related"},{"name":"a-1,3-glucan synthase activity","type":"exact"},{"name":"uridine diphosphoglucose-1,3-alpha-glucan glucosyltransferase activity","type":"related"}],"termid":"GO:0047657","terms_by_termid":{"GO:0047657":null}}


id: PBO:0050516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox D cluster","termid":"PBO:0050516"}


id: PBO:0002541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-protein coupled receptor Stm1","termid":"PBO:0002541"}


id: GO:0001060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis of RNA from a DNA template by RNA polymerase V, originating at a Pol V-specific promoter.","definition_xrefs":["GOC:txnOH","PMID:19110459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription","termid":"GO:0006351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150"],"is_obsolete":false,"name":"transcription by RNA polymerase V","synonyms":[{"name":"transcription from RNA pol V promoter","type":"exact"},{"name":"transcription from RNA polymerase V promoter","type":"exact"}],"termid":"GO:0001060"}


id: PBO:0089904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ThiJ domain protein, implicated in cellular detoxification","termid":"PBO:0089904"}


id: GO:0031717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a cannabinoid receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"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:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"cannabinoid receptor binding","synonyms":[{"name":"cannabinoid receptor ligand","type":"narrow"}],"termid":"GO:0031717"}


id: PBO:0039579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and zinc finger peptidyl tRNA hydrolase 1","termid":"PBO:0039579"}


id: GO:0005955
data:
  {"annotated_genes":["SJAG_03793","SJAG_03631"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73303,79866],"is_not":false,"summary":null,"term":"GO:0005955"}]},"cv_name":"cellular_component","definition":"A heterodimeric calcium ion and calmodulin dependent protein phosphatase composed of catalytic and regulatory subunits; the regulatory subunit is very similar in sequence to calmodulin.","definition_xrefs":["PMID:26794871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine phosphatase complex","termid":"GO:0008287"},{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03631":null,"SJAG_03793":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":"calcineurin complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"calcium-dependent protein serine/threonine phosphatase complex","type":"narrow"},{"name":"protein phosphatase type 2B complex","type":"exact"}],"termid":"GO:0005955","terms_by_termid":{"GO:0005955":null}}


id: MONDO:0019140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute ackee fruit intoxication (also referred to as Jamaican vomiting syndrome or sickness) is caused by the ingestion of unripe Blighia sapida fruits. It is a serious intoxication that is frequent in certain countries in the Caribbean and Western Africa. In contrast, it is rare in France and other Western countries. Intoxication leads to toxic hypoglycaemia and inhibition of neoglucogenesis. The hypoglycaemia is caused by the effect of hypoglycin A, which is found in the arils.","definition_xrefs":["Orphanet:73423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute ackee fruit intoxication","secondary_identifiers":["SCTID:49434001","ICD9:988.2","MESH:C537562","GARD:9299"],"synonyms":[{"name":"Jamaican vomiting sickness","type":"exact"},{"name":"Jamaican vomiting syndrome","type":"exact"},{"name":"ackee poisoning","type":"related"},{"name":"acute intoxication by Blighia sapida","type":"exact"}],"termid":"MONDO:0019140","xrefs":{"Monarch":{"xref_id":"0019140"}}}


id: GO:0061269
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of glomerular mesangial cells in the mesonephros, resulting in the expansion of the population.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell proliferation involved in mesonephros development","termid":"GO:0061209"},{"relation_name":"is_a","term_name":"glomerular mesangial cell proliferation","termid":"GO:0072110"},{"relation_name":"part_of","term_name":"mesonephric glomerular mesangium development","termid":"GO:0061247"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric glomerular mesangial cell proliferation involved in mesonephros development","termid":"GO:0061269"}


id: FYPO:0005433
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of meiotic recombination at one or more recombination hotspots is decreased to the background level. The basal rate of recombination (i.e. away from hotspots) may remain normal or may be decreased.","definition_xrefs":["PMID:12019258","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased meiotic recombination","termid":"FYPO:0000485"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"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:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000631","FYPO:0000293"],"is_obsolete":false,"name":"decreased meiotic recombination at hotspot","synonyms":[{"name":"decreased meiotic recombination at recombination hotspot","type":"exact"},{"name":"hotspot-specific decreased meiotic recombination","type":"exact"},{"name":"reduced meiotic recombination at hotspot","type":"exact"}],"termid":"FYPO:0005433"}


id: PBO:0091217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sub-telomeric 5Tm protein family","termid":"PBO:0091217"}


id: MONDO:0003996
data:
  {"annotated_genes":["SJAG_01270","SJAG_04757","SJAG_16459","SJAG_00078","SJAG_00063","SJAG_04404","SJAG_01317","SJAG_04545","SJAG_02106","SJAG_02397","SJAG_03866","SJAG_04840","SJAG_03900","SJAG_00233","SJAG_01229","SJAG_02695","SJAG_00421","SJAG_01039"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86146,86147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014796"},{"annotations":[86541,86540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011658"},{"annotations":[85587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014628"},{"annotations":[86156,86155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014233"},{"annotations":[87287,87286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"},{"annotations":[87685,87686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008199"},{"annotations":[87649],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013625"},{"annotations":[86735,86736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957576"},{"annotations":[86924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0036193"},{"annotations":[87456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030676"},{"annotations":[87098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008201"},{"annotations":[86200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010747"}]},"cv_name":"mondo","definition":"A disease involving the basal ganglia.","direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_00078":null,"SJAG_00233":null,"SJAG_00421":null,"SJAG_01039":null,"SJAG_01229":null,"SJAG_01270":null,"SJAG_01317":null,"SJAG_02106":null,"SJAG_02397":null,"SJAG_02695":null,"SJAG_03866":null,"SJAG_03900":null,"SJAG_04404":null,"SJAG_04545":null,"SJAG_04757":null,"SJAG_04840":null,"SJAG_16459":null},"genotype_count":0,"is_obsolete":false,"name":"basal ganglia disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["CSP:2057-3403","DOID:679","EFO:0009533","MEDGEN:1619147","MESH:D001480","SCTID:70835005","ICD9:333.0","UMLS:C4520981"],"synonyms":[{"name":"basal ganglia disease","type":"exact"},{"name":"collection of basal ganglia disease","type":"exact"},{"name":"collection of basal ganglia disease or disorder","type":"exact"},{"name":"disease of basal ganglia","type":"exact"},{"name":"disease of collection of basal ganglia","type":"exact"},{"name":"disease or disorder of collection of basal ganglia","type":"exact"},{"name":"disorder of basal ganglia","type":"related"},{"name":"disorder of collection of basal ganglia","type":"exact"}],"termid":"MONDO:0003996","terms_by_termid":{"MONDO:0008199":null,"MONDO:0008201":null,"MONDO:0010747":null,"MONDO:0011658":null,"MONDO:0011706":null,"MONDO:0013625":null,"MONDO:0014233":null,"MONDO:0014628":null,"MONDO:0014796":null,"MONDO:0030676":null,"MONDO:0036193":null,"MONDO:0957576":null},"xrefs":{"Monarch":{"xref_id":"0003996"}}}


id: GO:0034920
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: pyrene + 2 H+ + 2 e- + O2 = cis-4,5-dihydroxy-4,5-dihydropyrene.","definition_xrefs":["UM-BBD_reactionID:r0934"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrene dioxygenase activity (obsolete GO:0034920)","termid":"GO:0034920"}


id: GO:1903350
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 dopamine stimulus.","definition_xrefs":["PMID:11118945","GOC:mr","GOC:TermGenie","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to catecholamine","termid":"GO:0071869"}],"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 dopamine","termid":"GO:1903350"}


id: PBO:0028124
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-swollen_pear-shaped_vegetative_cell","termid":"PBO:0028124"}


id: GO:0036421
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of mycolate membrane consisting of gene products and protein complexes that are loosely bound to its external surface, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:md"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of external side of cell outer membrane","termid":"GO:0031242"},{"relation_name":"is_a","term_name":"extrinsic component of mycolate outer membrane","termid":"GO:0036420"},{"relation_name":"part_of","term_name":"external side of mycolate outer membrane","termid":"GO:0098568"}],"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":"extrinsic component of external side of mycolate outer membrane","synonyms":[{"name":"extrinsic to external side of MOM","type":"exact"},{"name":"extrinsic to external side of mycolate outer membrane","type":"narrow"},{"name":"extrinsic to external side of mycomembrane","type":"exact"}],"termid":"GO:0036421"}


id: PBO:0089159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L13","termid":"PBO:0089159"}


id: PBO:0086821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; YMR187C is not an essential gene","termid":"PBO:0086821"}


id: PBO:0090119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk13","termid":"PBO:0090119"}


id: MONDO:0005255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heart failure characterized by mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity.","definition_xrefs":["EFO:0003147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symptomatic heart failure","termid":"MONDO:0005254"}],"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":"mild heart failure","secondary_identifiers":["Wikipedia:New_York_Heart_Association_Functional_Classification"],"termid":"MONDO:0005255","xrefs":{"Monarch":{"xref_id":"0005255"}}}


id: MONDO:0009181
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal subtype of epidermolysis bullosa simplex (EBS) characterized by generalized blistering associated with muscular dystrophy.","definition_xrefs":["Orphanet:257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of plectin","termid":"MONDO:0016198"},{"relation_name":"is_a","term_name":"epidermolysis bullosa simplex","termid":"MONDO:0017610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005093","MONDO:0006025"],"is_obsolete":false,"name":"epidermolysis bullosa simplex 5B, with muscular dystrophy","secondary_identifiers":["OMIM:226670","MESH:C535955","DOID:0090017","GARD:2137","MEDGEN:418981","SCTID:723308003","UMLS:C2931072","NANDO:2201376"],"synonyms":[{"name":"EBS-MD","type":"exact"},{"name":"EBSMD","type":"related"},{"name":"Epidermolysa bullosa simplex and limb girdle muscular dystrophy","type":"related"},{"name":"Epidermolysa bullosa simplex with muscular dystrophy","type":"related"},{"name":"MD-EBS","type":"related"},{"name":"MDEBS","type":"related"},{"name":"epidermolysis bullosa simplex - limb girdle muscular dystrophy","type":"related"},{"name":"epidermolysis bullosa simplex 5B, with muscular dystrophy","type":"exact"},{"name":"epidermolysis bullosa simplex and limb-girdle muscular dystrophy","type":"exact"},{"name":"epidermolysis bullosa simplex with muscular dystrophy","type":"exact"},{"name":"limb-girdle muscular dystrophy with epidermolysis bullosa simplex","type":"exact"}],"termid":"MONDO:0009181","xrefs":{"Monarch":{"xref_id":"0009181"}}}


id: GO:0046939
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of introducing one or more phosphate groups into a nucleotide to produce a phosphorylated nucleoside.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleotide phosphorylation (obsolete GO:0046939)","termid":"GO:0046939"}


id: GO:0021545
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cranial nerves over time, from its formation to the mature structure. The cranial nerves are composed of twelve pairs of nerves that emanate from the nervous tissue of the hindbrain. These nerves are sensory, motor, or mixed in nature, and provide the motor and general sensory innervation of the head, neck and viscera. They mediate vision, hearing, olfaction and taste and carry the parasympathetic innervation of the autonomic ganglia that control visceral functions.","definition_xrefs":["GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nerve development","termid":"GO:0021675"}],"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":"cranial nerve development","termid":"GO:0021545"}


id: GO:0044022
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H3-serine (position 28) + ATP = histone H3-phosphoserine (position 28) + ADP. This reaction is the addition of a phosphate group to the serine residue at position 28 of histone H3.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"},{"relation_name":"is_a","term_name":"histone H3 kinase activity","termid":"GO:0140996"}],"gene_count":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:0140096"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0004672","GO:0016740","GO:0003824","GO:0140096","GO:0016301","GO:0003674"],"is_obsolete":false,"name":"histone H3S28 kinase activity","synonyms":[{"name":"histone kinase activity (H3-S28 specific)","type":"exact"},{"name":"histone serine kinase activity (H3-S28 specific)","type":"exact"},{"name":"histone-serine kinase activity (H3-S28 specific)","type":"exact"}],"termid":"GO:0044022"}


id: FYPO:0008372
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 cell surface is normal (i.e. indistinguishable from wild-type.","definition_xrefs":["PomBase:pb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000138","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to cell surface during vegetative growth","termid":"FYPO:0008372"}


id: PBO:0070950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18a pseudogene 5","termid":"PBO:0070950"}


id: GO:0033852
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + 3,5,3'-triiodo-L-thyronine = 3,5,3'-triiodothyropyruvate + L-glutamate.","definition_xrefs":["RHEA:19133","EC:2.6.1.26"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"thyroid-hormone transaminase activity","secondary_identifiers":["KEGG_REACTION:R03952","MetaCyc:THYROID-HORMONE-AMINOTRANSFERASE-RXN"],"synonyms":[{"name":"3,5-dinitrotyrosine aminotransferase activity","type":"related"},{"name":"3,5-dinitrotyrosine transaminase activity","type":"related"},{"name":"L-3,5,3'-triiodothyronine:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"thyroid hormone aminotransferase activity","type":"related"},{"name":"thyroid-hormone aminotransferase activity","type":"related"}],"termid":"GO:0033852"}


id: GO:0006074
data:
  {"annotated_genes":["SJAG_03587","SJAG_03705","SJAG_00610","SJAG_04483","SJAG_01290","SJAG_00876","SJAG_01787","SJAG_01255","SJAG_04771","SJAG_04462","SJAG_04659","SJAG_02222","SJAG_01835","SJAG_04666","SJAG_00218","SJAG_05285","SJAG_01288","SJAG_04668"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[106426,91935,71261,73432,113468,74863,76217,116119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[87860,92761],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[91109,105667,106239,92745,118207,103161,118334],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090334"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving (1->3)-beta-D-glucans, compounds composed of glucose residues linked by (1->3)-beta-D-glucosidic bonds.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-glucan metabolic process","termid":"GO:0051273"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00610":null,"SJAG_00876":null,"SJAG_01255":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01787":null,"SJAG_01835":null,"SJAG_02222":null,"SJAG_03587":null,"SJAG_03705":null,"SJAG_04462":null,"SJAG_04483":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"(1->3)-beta-D-glucan metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"1,3-beta-D-glucan metabolic process","type":"broad"},{"name":"1,3-beta-D-glucan metabolism","type":"exact"},{"name":"1,3-beta-glucan metabolic process","type":"broad"},{"name":"beta-1,3 glucan metabolic process","type":"exact"},{"name":"beta-1,3 glucan metabolism","type":"exact"}],"termid":"GO:0006074","terms_by_termid":{"GO:0034413":null,"GO:0071970":null,"GO:0090334":null,"GO:0140748":null}}


id: GO:0051964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of synapse assembly, the aggregation, arrangement and bonding together of a set of components to form a synapse.","definition_xrefs":["GOC:ai","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nervous system development","termid":"GO:0051961"},{"relation_name":"is_a","term_name":"regulation of synapse assembly","termid":"GO:0051963"},{"relation_name":"is_a","term_name":"negative regulation of cell junction assembly","termid":"GO:1901889"},{"relation_name":"is_a","term_name":"negative regulation of synapse organization","termid":"GO:1905809"},{"relation_name":"negatively_regulates","term_name":"synapse assembly","termid":"GO:0007416"}],"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 synapse assembly","synonyms":[{"name":"down regulation of synapse assembly","type":"exact"},{"name":"down-regulation of synapse assembly","type":"exact"},{"name":"downregulation of synapse assembly","type":"exact"},{"name":"inhibition of synapse assembly","type":"narrow"},{"name":"negative regulation of synapse biogenesis","type":"exact"},{"name":"negative regulation of synaptogenesis","type":"exact"}],"termid":"GO:0051964"}


id: PBO:0114283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal membrane E2 ubiquitin-conjugating activity activator Pex22","termid":"PBO:0114283"}


id: MOD:02070
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-histidine residue coordinated to one or more metal atoms or metal clusters.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metal or metal cluster coordinated L-histidine residue","termid":"MOD:02070"}


id: _global:assayed_using
data:
  {"annotation_feature_type":"gene","cv_name":"fypo_extension_relations","definition":"Relation between a phenotype and an entity, such as a gene product that acts as an enzyme or substrate, with which the phenotype was assayed.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assayed_using","termid":"_global:assayed_using"}


id: GO:0042676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the cone cells of the compound eye, the lens-secreting cells in the ommatidia, adopt pathways of differentiation that lead to the establishment of their distinct cell type.","definition_xrefs":["GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment","termid":"GO:0045165"},{"relation_name":"part_of","term_name":"compound eye cone cell differentiation","termid":"GO:0042675"}],"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":"compound eye cone cell fate commitment","secondary_identifiers":["GO:0007466"],"termid":"GO:0042676"}


id: GO:0061416
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a stimulus indicating the organism is under salt stress. The stress is usually an increase or decrease in the concentration of salt (particularly but not exclusively sodium and chloride ions) in the environment.","definition_xrefs":["GOC:dph","PMID:18667581"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter in response to salt stress (obsolete GO:0061416)","termid":"GO:0061416"}


id: FYPO:0003738
data:
  {"alleles_by_uniquename":{"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119457],"is_not":false,"summary":null,"term":"FYPO:0003738"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is arrested when cells have condensed chromosomes, but show no other signs of having entered mitosis or M phase, under conditions where arrest does not normally occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormally arrested mitotic cell cycle progression","termid":"FYPO:0000502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04464":null},"genotype_count":1,"genotypes_by_uniquename":{"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal mitotic cell cycle arrest with condensed chromosomes","references_by_uniquename":{"PMID:28954740":null},"single_locus_annotated_genes":["SJAG_04464"],"single_locus_genotype_uniquenames":["pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal cell cycle arrest with condensed chromosomes during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic cell cycle arrest with condensed chromosomes during vegetative growth","type":"exact"}],"termid":"FYPO:0003738","terms_by_termid":{"FYECO:0000004":null,"FYPO:0003738":null}}


id: PBO:0055525
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 2959","termid":"PBO:0055525"}


id: PBO:0070454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L3 pseudogene 11","termid":"PBO:0070454"}


id: PBO:0110259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase II complex subunit Rpb2","termid":"PBO:0110259"}


id: PBO:0089700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prevacuole/endosomal FYVE tethering component Pep7","termid":"PBO:0089700"}


id: MOD:00661
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to a methylated histidine, such as pros-methylhistidine, or tele-methylhistidine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated histidine","synonyms":[{"name":"MeHis","type":"exact"}],"termid":"MOD:00661"}


id: PBO:0070154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 68 pseudogene","termid":"PBO:0070154"}


id: MONDO:0014307
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 POGLUT1 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:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"Dowling-Degos disease 4","secondary_identifiers":["UMLS:C3810313","OMIM:615696","MEDGEN:816643","GARD:16002"],"synonyms":[{"name":"DDD4","type":"related"},{"name":"Dowling-Degos disease 4","type":"exact"},{"name":"Dowling-Degos disease caused by mutation in POGLUT1","type":"exact"},{"name":"Dowling-Degos disease type 4","type":"exact"},{"name":"POGLUT1 Dowling-Degos disease","type":"exact"}],"termid":"MONDO:0014307","xrefs":{"Monarch":{"xref_id":"0014307"}}}


id: GO:0030189
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Increases the activity of a molecular chaperone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete chaperone activator activity (obsolete GO:0030189)","synonyms":[{"name":"chaperone activator activity","type":"exact"}],"termid":"GO:0030189"}


id: PBO:0052222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kielin cysteine rich BMP regulator","termid":"PBO:0052222"}


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: PBO:0085587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in assembly of the RNA Pol III complex; high copy suppressor of Pol III assembly mutation and psk1 psk2 mutations that confer temperature-sensitivity for galactose utilization; physically interacts with Pol III; proposed to bind single-stranded nucleic acids via its R3H domain; capable of forming the prion [VTS1+]","termid":"PBO:0085587"}


id: PBO:0039759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APPBP2 divergent transcript","termid":"PBO:0039759"}


id: GO:0034419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-2-hydroxyglutarate + O2 = 2-oxoglutarate + hydrogen peroxide.","definition_xrefs":["PMID:18390652"],"gene_count":0,"genotype_count":0,"name":"obsolete L-2-hydroxyglutarate oxidase activity (obsolete GO:0034419)","termid":"GO:0034419"}


id: PBO:0075598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPNS lysolipid transporter 2, sphingosine-1-phosphate","termid":"PBO:0075598"}


id: PBO:0027674
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_wall_beta-glucan_level","termid":"PBO:0027674"}


id: PBO:0048517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDNF antisense RNA 1","termid":"PBO:0048517"}


id: PBO:0077308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 45A","termid":"PBO:0077308"}


id: PBO:0085989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; required for proliferation or remodeling of the ER that is caused by overexpression of Hmg2p; may interact with ribosomes, based on co-purification experiments; HER1 has a paralog, GIP3, that arose from the whole genome duplication","termid":"PBO:0085989"}


id: PBO:0065408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome subunit alpha 6 pseudogene 4","termid":"PBO:0065408"}


id: PBO:0044399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 2 subfamily C member 60, pseudogene","termid":"PBO:0044399"}


id: PBO:0057746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1825","termid":"PBO:0057746"}


id: FYPO:0008273
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of histone H4 binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type). The affected gene product may be encoded by the mutated gene, or by a different gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone binding","termid":"FYPO:0008271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000257","FYPO:0000652"],"is_obsolete":false,"name":"normal histone H4 binding","termid":"FYPO:0008273"}


id: PATO:0000973
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A permeability quality inhering in a bearer by virtue of the bearer's disposition to admit the passage of gas or liquid through pores or interstices.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"permeability","termid":"PATO:0000970"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"porosity","termid":"PATO:0000973"}


id: MONDO:0859167
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":"hypokalemic tubulopathy and deafness","secondary_identifiers":["MEDGEN:1785163","OMIM:619406","UMLS:C5543621"],"termid":"MONDO:0859167","xrefs":{"Monarch":{"xref_id":"0859167"}}}


id: MONDO:0958119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare central nervous system embryonal tumor characterized by embryonal cells arranged in multilayered rosettes and displaying one of three morphological patterns: embryonal tumor with abundant neuropil and true rosettes, ependymoblastoma, or medulloepithelioma. The tumors typically have a C19MC alteration or (rarely) a DICER1 mutation and correspond to WHO grade IV. They are mostly localized intracranially, rarely in the spinal cord, and commonly cause signs and symptoms of elevated intracranial pressure, sometimes seizures and focal neurological signs. Most cases occur in children during the first two years of life.","definition_xrefs":["Orphanet:656417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor","termid":"MONDO:0016713"}],"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":"embryonal tumor with multilayered rosettes","secondary_identifiers":["NCIT:C186534","GARD:6352","UMLS:C5575350","MEDGEN:1804732"],"termid":"MONDO:0958119","xrefs":{"Monarch":{"xref_id":"0958119"}}}


id: GO:1900806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of ergot alkaloid.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete ergot alkaloid catabolic process (obsolete GO:1900806)","synonyms":[{"name":"ergot alkaloid breakdown","type":"exact"},{"name":"ergot alkaloid catabolism","type":"exact"},{"name":"ergot alkaloid degradation","type":"exact"},{"name":"ergot alkaloids breakdown","type":"related"},{"name":"ergot alkaloids catabolic process","type":"related"},{"name":"ergot alkaloids catabolism","type":"related"},{"name":"ergot alkaloids degradation","type":"related"}],"termid":"GO:1900806"}


id: GO:0043304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of mast cell degranulation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of myeloid leukocyte mediated immunity","termid":"GO:0002886"},{"relation_name":"is_a","term_name":"regulation of leukocyte degranulation","termid":"GO:0043300"},{"relation_name":"regulates","term_name":"mast cell degranulation","termid":"GO:0043303"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of mast cell degranulation","synonyms":[{"name":"regulation of mast cell granule exocytosis","type":"exact"}],"termid":"GO:0043304"}


id: PBO:0034125
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_symptom","termid":"PBO:0034125"}


id: PBO:0002204
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-Alpha-Acetyltransferase","termid":"PBO:0002204"}


id: PBO:0072176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S16 pseudogene 3","termid":"PBO:0072176"}


id: PBO:0064279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology and RUN domain containing M1","termid":"PBO:0064279"}


id: SO:1000038
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A duplication that occurred within a chromosome.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"duplication","termid":"SO:1000035"},{"relation_name":"is_a","term_name":"intrachromosomal_mutation","termid":"SO:1000028"},{"relation_name":"is_a","term_name":"chromosomal_duplication","termid":"SO:1000037"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intrachromosomal_duplication","synonyms":[{"name":"intrachromosomal duplication","type":"exact"}],"termid":"SO:1000038"}


id: GO:1902855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of non-motile cilium assembly.","definition_xrefs":["GOC:cilia","GOC:kmv","GOC:TermGenie","PMID:23807208","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cilium assembly","termid":"GO:1902017"},{"relation_name":"regulates","term_name":"non-motile cilium assembly","termid":"GO:1905515"}],"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":"regulation of non-motile cilium assembly","synonyms":[{"name":"regulation of immotile primary cilium assembly","type":"related"},{"name":"regulation of nonmotile primary cilia assembly","type":"related"},{"name":"regulation of nonmotile primary cilium assembly","type":"related"},{"name":"regulation of sensory cilium assembly","type":"related"},{"name":"regulation of sensory cilium biogenesis","type":"related"}],"termid":"GO:1902855"}


id: _global:inheres_in
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"a relation between a specifically dependent continuant (the characteristic) and any other entity (the bearer), in which the characteristic depends on the bearer for its existence.","direct_ancestors":[{"relation_name":"is_a","term_name":"inheres_in_part_of","termid":"_global:inheres_in_part_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inheres_in","secondary_identifiers":["RO:0000052"],"termid":"_global:inheres_in"}


id: FYPO:0000607
data:
  {"alleles_by_uniquename":{"SJAG_00871:allele-1":{"allele_type":"amino_acid_mutation","description":"cut3-T19E","gene_uniquename":"SJAG_00871","name":"cut3-T19E","uniquename":"SJAG_00871:allele-1"},"SJAG_01956:allele-1":{"allele_type":"amino_acid_mutation","description":"E405K ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_03351:allele-1":{"allele_type":"amino_acid_mutation","description":"A186T ts","gene_uniquename":"SJAG_03351","name":"cut23-415","uniquename":"SJAG_03351:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"},"SJAG_04284:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04284","name":"nup61delta","uniquename":"SJAG_04284:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000619"}],"single_locus_phenotype":[{"annotations":[119463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000619"},{"annotations":[119776,119775,119774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000618"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through M phase of the mitotic cell cycle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle phase","termid":"FYPO:0002736"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00871":null,"SJAG_01956":null,"SJAG_03351":null,"SJAG_03575":null,"SJAG_04284":null,"SJAG_04464":null},"genotype_count":5,"genotypes_by_uniquename":{"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]}]},"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut23-415(A186T ts)","display_uniquename":"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03351:allele-1","expression":"Not assayed or wild type"}]}]},"cut3-T19E-cut3-T19E-amino_acid_mutation-expression-not_assayed_or_wild_type__pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut3-T19E(aa) pim1-R152C(aa)","display_uniquename":"cut3-T19E-cut3-T19E-amino_acid_mutation-expression-not_assayed_or_wild_type__pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00871:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]},"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"nuc2-1051(E405K ts)","display_uniquename":"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01956:allele-1","expression":"Not assayed or wild type"}]}]},"nup61delta":{"display_name":"nup61delta","display_uniquename":"nup61delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04284:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_00871","SJAG_04464"],"name":"abnormal mitotic M phase progression","references_by_uniquename":{"PMID:23786411":null,"PMID:28954740":null},"single_locus_annotated_genes":["SJAG_04284","SJAG_03351","SJAG_01956","SJAG_03575"],"single_locus_genotype_uniquenames":["cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","nup61delta","nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal M phase progression during mitotic cell cycle","type":"exact"},{"name":"abnormal mitotic M phase progression during vegetative growth","type":"exact"},{"name":"abnormal mitotic cell cycle progression in M","type":"exact"},{"name":"mitotic cell cycle progression in M phase: abnormal","type":"related"}],"termid":"FYPO:0000607","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000618":null,"FYPO:0000619":null,"FYPO_EXT:0000001":null}}


id: GO:0098641
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any cadherin binding that occurs as part of the process of cell-cell adhesion.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cadherin binding","termid":"GO:0045296"},{"relation_name":"is_a","term_name":"cell-cell adhesion mediator activity","termid":"GO:0098632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098631"}],"interesting_parent_ids":["GO:0098631","GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"cadherin binding involved in cell-cell adhesion","termid":"GO:0098641"}


id: GO:0009955
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process in which differences in cell differentiation along the adaxial/abaxial are generated. Adaxial refers to being situated toward an axis of an anatomical structure. Abaxial refers to being situated away from an axis of an anatomical structure.","definition_xrefs":["GOC:isa_complete","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"}],"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":"adaxial/abaxial pattern specification","synonyms":[{"name":"adaxial/abaxial pattern formation","type":"related"}],"termid":"GO:0009955"}


id: PBO:0046596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K3 member 6","termid":"PBO:0046596"}


id: GO:0042167
data:
  {"annotated_genes":["SJAG_00366"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106918],"is_not":false,"summary":null,"term":"GO:0042167"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of heme, any compound of iron complexed in a porphyrin (tetrapyrrole) ring.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin-containing compound catabolic process","termid":"GO:0006787"},{"relation_name":"is_a","term_name":"heme metabolic process","termid":"GO:0042168"},{"relation_name":"is_a","term_name":"pigment catabolic process","termid":"GO:0046149"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00366":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"heme catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-189483"],"synonyms":[{"name":"haem catabolic process","type":"exact"},{"name":"haem catabolism","type":"exact"},{"name":"heme breakdown","type":"exact"},{"name":"heme catabolism","type":"exact"},{"name":"heme degradation","type":"exact"}],"termid":"GO:0042167","terms_by_termid":{"GO:0042167":null}}


id: MONDO:0004068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disease of anatomical entity (obsolete MONDO:0004068)","termid":"MONDO:0004068","xrefs":{"Monarch":{"xref_id":"0004068"}}}


id: GO:0014890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process, occurring in smooth muscle, that is characterized by a decrease in protein content, fiber diameter, force production and fatigue resistance in response to different conditions such as starvation, aging and disuse.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smooth muscle adaptation","termid":"GO:0014805"},{"relation_name":"is_a","term_name":"muscle atrophy","termid":"GO:0014889"}],"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":"smooth muscle atrophy","termid":"GO:0014890"}


id: MONDO:0004580
data:
  {"annotated_genes":["SJAG_02063","SJAG_03592","SJAG_02955","SJAG_01422","SJAG_01634","SJAG_00643","SJAG_04745","SJAG_02295","SJAG_00737","SJAG_01630","SJAG_00495","SJAG_04529","SJAG_04637","SJAG_01756","SJAG_03588","SJAG_04681","SJAG_04334","SJAG_01526","SJAG_02163","SJAG_03258","SJAG_03557","SJAG_04003","SJAG_01298","SJAG_02946","SJAG_00531","SJAG_03795","SJAG_01152","SJAG_04296","SJAG_02623","SJAG_04225","SJAG_05342","SJAG_04495","SJAG_02889","SJAG_01356","SJAG_02885","SJAG_03827","SJAG_00742","SJAG_01897","SJAG_04497","SJAG_02712","SJAG_02150","SJAG_01998","SJAG_02947"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87637,87638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012419"},{"annotations":[86953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[87276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010557"},{"annotations":[86787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014372"},{"annotations":[85441],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014669"},{"annotations":[86798,86799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013802"},{"annotations":[87259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013454"},{"annotations":[85802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012990"},{"annotations":[87312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032794"},{"annotations":[85980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012056"},{"annotations":[85459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060650"},{"annotations":[87606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009624"},{"annotations":[86828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007918"},{"annotations":[87412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009796"},{"annotations":[86677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008379"},{"annotations":[86426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010828"},{"annotations":[86566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010806"},{"annotations":[86482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011075"},{"annotations":[87530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010723"},{"annotations":[87025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012363"},{"annotations":[85422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012477"},{"annotations":[87108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013468"},{"annotations":[85820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013516"},{"annotations":[86198,86199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013611"},{"annotations":[86183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014256"},{"annotations":[86949,86950,86948,86942,86946,86944,86947,86945,86943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014323"},{"annotations":[86630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014400"},{"annotations":[87184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015013"},{"annotations":[87064,87063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044320"},{"annotations":[86592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032604"},{"annotations":[85932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031007"},{"annotations":[86454,86453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010819"}]},"cv_name":"mondo","definition":"Degeneration of the retina.","definition_xrefs":["NCIT:C34979"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"gene_count":43,"genes_by_uniquename":{"SJAG_00495":null,"SJAG_00531":null,"SJAG_00643":null,"SJAG_00737":null,"SJAG_00742":null,"SJAG_01152":null,"SJAG_01298":null,"SJAG_01356":null,"SJAG_01422":null,"SJAG_01526":null,"SJAG_01630":null,"SJAG_01634":null,"SJAG_01756":null,"SJAG_01897":null,"SJAG_01998":null,"SJAG_02063":null,"SJAG_02150":null,"SJAG_02163":null,"SJAG_02295":null,"SJAG_02623":null,"SJAG_02712":null,"SJAG_02885":null,"SJAG_02889":null,"SJAG_02946":null,"SJAG_02947":null,"SJAG_02955":null,"SJAG_03258":null,"SJAG_03557":null,"SJAG_03588":null,"SJAG_03592":null,"SJAG_03795":null,"SJAG_03827":null,"SJAG_04003":null,"SJAG_04225":null,"SJAG_04296":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_04497":null,"SJAG_04529":null,"SJAG_04637":null,"SJAG_04681":null,"SJAG_04745":null,"SJAG_05342":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"retinal degeneration","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:95695004","MEDGEN:48432","MESH:D012162","UMLS:C0035304","DOID:8466"],"synonyms":[{"name":"degeneration of retina","type":"exact"},{"name":"retina degeneration","type":"exact"},{"name":"retina, Degeneration Of","type":"exact"}],"termid":"MONDO:0004580","terms_by_termid":{"MONDO:0007918":null,"MONDO:0008379":null,"MONDO:0009624":null,"MONDO:0009796":null,"MONDO:0010557":null,"MONDO:0010723":null,"MONDO:0010806":null,"MONDO:0010819":null,"MONDO:0010828":null,"MONDO:0011075":null,"MONDO:0012056":null,"MONDO:0012099":null,"MONDO:0012363":null,"MONDO:0012419":null,"MONDO:0012477":null,"MONDO:0012990":null,"MONDO:0013454":null,"MONDO:0013468":null,"MONDO:0013516":null,"MONDO:0013611":null,"MONDO:0013802":null,"MONDO:0014256":null,"MONDO:0014323":null,"MONDO:0014372":null,"MONDO:0014400":null,"MONDO:0014669":null,"MONDO:0015013":null,"MONDO:0031007":null,"MONDO:0032604":null,"MONDO:0032794":null,"MONDO:0044320":null,"MONDO:0060650":null},"xrefs":{"Monarch":{"xref_id":"0004580"}}}


id: PBO:0068619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 71, pseudogene","termid":"PBO:0068619"}


id: PATO:0000201
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000201 memory (obsolete PATO:0000201)","termid":"PATO:0000201"}


id: FYPO:0002022
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, and structure of actin cortical patches are normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal actin cortical patch morphology","synonyms":[{"name":"normal F-actin patch morphology","type":"exact"},{"name":"normal actin cortical patch morphology during mitotic cell cycle","type":"related"},{"name":"normal actin cortical patch morphology during vegetative growth","type":"exact"},{"name":"normal actin patch morphology","type":"exact"}],"termid":"FYPO:0002022"}


id: PBO:0002706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin depolymerizing factor, cofilin","termid":"PBO:0002706"}


id: PBO:0082807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of UDP-GlcNAc transferase; required for second step of dolichyl-linked oligosaccharide synthesis; anchors catalytic subunit Alg13p to ER membrane; similar to bacterial and human glycosyltransferases; both human homologs ALG13 and ALG14 are required to complement yeast alg14 mutant; mutations of human ALG14 cause congenital myasthenic syndrome","termid":"PBO:0082807"}


id: GO:0106027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a prolongation or process extending from a neuron, e.g. an axon, or a dendrite.","definition_xrefs":["PMID:11585923","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection organization","termid":"GO:0120036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neuron projection organization","termid":"GO:0106027"}


id: GO:0070487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The adhesion of one monocyte to one or more other monocytes via adhesion molecules.","definition_xrefs":["PMID:12972508","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte aggregation","termid":"GO:0070486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"monocyte aggregation","synonyms":[{"name":"mononuclear phagocyte aggregation","type":"exact"}],"termid":"GO:0070487"}


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":["EC:2.5.1.7","RHEA:18681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016765","GO:0003674","GO:0016740"],"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: PBO:0028696
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_chromatin_silencing_at_telomere","termid":"PBO:0028696"}


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:0077541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 253","termid":"PBO:0077541"}


id: PBO:0077211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane 9 superfamily member 2","termid":"PBO:0077211"}


id: PBO:0057064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 147a","termid":"PBO:0057064"}


id: MONDO:1012149
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant hyperthermia, non-human animal","termid":"MONDO:1011713"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant hyperthermia, deer","secondary_identifiers":["OMIA:000621-9850"],"termid":"MONDO:1012149","xrefs":{"Monarch":{"xref_id":"1012149"}}}


id: GO:1990165
data:
  {"annotated_genes":["SJAG_04410","SJAG_16460"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77234,96214],"is_not":false,"summary":null,"term":"GO:1990165"}]},"cv_name":"molecular_function","definition":"Binding to damaged DNA containing single-strand breaks (SSBs).","definition_xrefs":["GOC:al","PMID:21984210"],"direct_ancestors":[{"relation_name":"is_a","term_name":"damaged DNA binding","termid":"GO:0003684"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04410":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003677","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"single-strand break-containing DNA binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"SSB-containing DNA binding","type":"exact"},{"name":"single-strand break-containing damaged DNA binding","type":"exact"}],"termid":"GO:1990165","terms_by_termid":{"GO:1990165":null}}


id: PBO:0078668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon TTT) 3-3","termid":"PBO:0078668"}


id: GO:0120107
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The rotor complex of the bacterial-type flagellum consists of a membrane-anchored ring and the motor switch complex, which participates in the conversion of proton/Na+ energy into the mechanical work of rotation and controls the direction of flagellar rotation.","definition_xrefs":["PMID:10572114","GOC:cilia","PMID:25251856","PMID:12624192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"bacterial-type flagellum motor","termid":"GO:0120100"}],"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":"bacterial-type flagellum rotor complex","termid":"GO:0120107"}


id: GO:1900152
data:
  {"annotated_genes":["SJAG_02370"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060212"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay.","definition_xrefs":["GOC:TermGenie","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:1900151"},{"relation_name":"is_a","term_name":"negative regulation of mRNA catabolic process","termid":"GO:1902373"},{"relation_name":"negatively_regulates","term_name":"nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:0000288"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"negatively_regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"negative regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"down regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"down regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"down-regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"down-regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"downregulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"downregulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"inhibition of deadenylation-dependent mRNA decay","type":"narrow"},{"name":"inhibition of mRNA breakdown, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of mRNA catabolic process, deadenylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolic process, deadenylylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolism, deadenylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolism, deadenylylation-dependent","type":"narrow"},{"name":"inhibition of mRNA degradation, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"narrow"},{"name":"negative regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"negative regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"negative regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"negative regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"negative regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"}],"termid":"GO:1900152","terms_by_termid":{"GO:0060212":null}}


id: GO:1902444
data:
  {"annotated_genes":["SJAG_02360"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110692],"is_not":false,"summary":null,"term":"GO:1902444"}]},"cv_name":"molecular_function","definition":"Binding to riboflavin.","definition_xrefs":["PMID:12083520","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02360":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"riboflavin binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1902444","terms_by_termid":{"GO:1902444":null}}


id: FYPO:0006134
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of 2-palmitoleoylglycerophosphoinositol measured in a cell is higher than normal.","definition_xrefs":["PMID:28667014","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased phospholipid level","termid":"FYPO:0001288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular 2-palmitoleoylglycerophosphoinositol level","synonyms":[{"name":"increased 2-palmitoleoylglycerophosphoinositol accumulation","type":"related"},{"name":"increased cellular 2-palmitoleoyl-sn-glycero-3-phospho-D-myo-inositol level during vegetative growth","type":"exact"},{"name":"increased cellular 2-palmitoleoylglycerophosphoinositol level during mitotic cell cycle","type":"related"},{"name":"increased cellular 2-palmitoleoylglycerophosphoinositol level during vegetative growth","type":"exact"}],"termid":"FYPO:0006134"}


id: PBO:0082220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-agglutinin of alpha-cells; binds to Aga1p during agglutination, N-terminal half is homologous to the immunoglobulin superfamily and contains binding site for a-agglutinin, C-terminal half is highly glycosylated and contains GPI anchor","termid":"PBO:0082220"}


id: MONDO:1010235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinal muscular atrophy that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease, non-human animal","termid":"MONDO:1012953"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"},{"relation_name":"is_a","term_name":"neuromuscular disease, non-human animal","termid":"MONDO:1012983"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal muscular atrophy, non-human animal","secondary_identifiers":["OMIA:000939"],"termid":"MONDO:1010235","xrefs":{"Monarch":{"xref_id":"1010235"}}}


id: GO:0044120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The progression of the symbiont from an initial condition to a later condition, occurring in a host vacuole. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete development of symbiont in host vacuole (obsolete GO:0044120)","synonyms":[{"name":"development of symbiont in host organelle","type":"broad"}],"termid":"GO:0044120"}


id: GO:0019676
data:
  {"annotated_genes":["SJAG_00359","SJAG_04054","SJAG_03266"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72583,94610,118033],"is_not":false,"summary":null,"term":"GO:0019676"}]},"cv_name":"biological_process","definition":"The pathway by which ammonia is processed and incorporated into a cell. In an energy-rich (glucose-containing), nitrogen-poor environment, glutamine synthetase and glutamate synthase form an ammonia assimilatory cycle, in which ammonia is incorporated into L-glutamate to form L-glutamine, which then combines with alpha-ketoglutarate to regenerate L-glutamate. This ATP-dependent cycle is essential for nitrogen-limited growth and for steady-state growth with some sources of nitrogen.","definition_xrefs":["MetaCyc:AMMASSIM-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate metabolic process","termid":"GO:0006536"},{"relation_name":"is_a","term_name":"glutamine metabolic process","termid":"GO:0006541"},{"relation_name":"is_a","term_name":"nitrogen utilization","termid":"GO:0019740"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00359":null,"SJAG_03266":null,"SJAG_04054":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"ammonia assimilation cycle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"glutamate metabolic process via glutamine and ammonia","type":"exact"},{"name":"glutamate metabolism via glutamine and ammonia","type":"exact"}],"termid":"GO:0019676","terms_by_termid":{"GO:0019676":null}}


id: PBO:0005648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf element Wtf18","termid":"PBO:0005648"}


id: PBO:0068756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5F small nuclear 1","termid":"PBO:0068756"}


id: PBO:0048916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A8 family member K","termid":"PBO:0048916"}


id: FYPO:0007821
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which vacuoles are larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vacuolar morphology","termid":"FYPO:0002257"}],"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":"large vacuoles","synonyms":[{"name":"enlarged vacuoles","type":"exact"}],"termid":"FYPO:0007821"}


id: MONDO:0022777
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":"cleft lip palate dysmorphism kumar type","termid":"MONDO:0022777","xrefs":{"Monarch":{"xref_id":"0022777"}}}


id: FYPO:0000360
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 RNA localization is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal RNA localization","termid":"FYPO:0003057"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal RNA localization during vegetative growth","synonyms":[{"name":"RNA localization: abnormal","type":"related"},{"name":"abnormal RNA localisation during vegetative growth","type":"exact"},{"name":"abnormal RNA localization during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000360"}


id: GO:0021519
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into an association neuron in an environment that is neutral with respect to the developmental pathway.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:cls","GO_REF:0000021","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron fate specification","termid":"GO:0048665"},{"relation_name":"part_of","term_name":"spinal cord association neuron differentiation","termid":"GO:0021527"}],"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":"spinal cord association neuron specification","termid":"GO:0021519"}


id: GO:0043097
data:
  {"annotated_genes":["SJAG_05029","SJAG_04264"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98065,114118],"is_not":false,"summary":null,"term":"GO:0043097"}]},"cv_name":"biological_process","definition":"Any process that generates a pyrimidine nucleoside, one of a family of organic molecules consisting of a pyrimidine base covalently bonded to a sugar ribose, from derivatives of it, without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine-containing compound salvage","termid":"GO:0008655"},{"relation_name":"is_a","term_name":"nucleoside salvage","termid":"GO:0043174"},{"relation_name":"is_a","term_name":"pyrimidine nucleoside biosynthetic process","termid":"GO:0046134"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04264":null,"SJAG_05029":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"pyrimidine nucleoside salvage","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-73614"],"termid":"GO:0043097","terms_by_termid":{"GO:0043097":null}}


id: PBO:0059607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 19","termid":"PBO:0059607"}


id: PR:O94668
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nse5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94668"],"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":"non-structural maintenance of chromosome element 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC651.10","synonyms":[{"name":"Spom972h-nse5","type":"exact"},{"name":"non-SMC element 5 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94668"}


id: SO:0001837
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of insertion where the inserted sequence is a mobile element.","definition_xrefs":["EBI:dvga"],"direct_ancestors":[{"relation_name":"contains","term_name":"mobile_genetic_element","termid":"SO:0001037"},{"relation_name":"is_a","term_name":"insertion","termid":"SO:0000667"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mobile_element_insertion","synonyms":[{"name":"mobile element insertion","type":"exact"}],"termid":"SO:0001837"}


id: MONDO:0009512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Larsen-like syndrome, lethal type, is characterized by multiple joint dislocation and respiratory insufficiency due to tracheomalacia and/or lung hypoplasia. It has been described in less than ten patients. Transmission is thought to be autosomal recessive. Brain dysplasia has been described in some patients and could result from systemic hypoxic-ischemic insults during the second half of pregnancy, although genetic factors have not been ruled out.","definition_xrefs":["Orphanet:2371"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal Larsen-like syndrome","secondary_identifiers":["icd11.foundation:1014532279","MESH:C537872","MEDGEN:343375","OMIM:245650","SCTID:719409004","GARD:3181","UMLS:C1855535"],"synonyms":[{"name":"Larsen-like multiple joint dislocation syndrome","type":"related"},{"name":"Larsen-like syndrome, lethal type","type":"related"}],"termid":"MONDO:0009512","xrefs":{"Monarch":{"xref_id":"0009512"}}}


id: PBO:0049814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase 6","termid":"PBO:0049814"}


id: _global:exists_during
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","direct_ancestors":[{"relation_name":"is_a","term_name":"during","termid":"_global:during"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exists_during","secondary_identifiers":["GOREL:0000032"],"synonyms":[{"name":"during","type":"broad"}],"termid":"_global:exists_during"}


id: FYPO:0003096
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which methylation of lysine at position 9 of histone H3 in centromere outer repeat regions occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000872"},{"relation_name":"is_a","term_name":"abnormal histone methylation at centromere during vegetative growth","termid":"FYPO:0007374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0002274","FYPO:0001320","FYPO:0002494","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H3-K9 methylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 methylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation at centromere otr during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"decreased histone H3-K9 methylation at centromeric dg repeats during vegetative growth","type":"narrow"},{"name":"decreased histone H3-K9 methylation at centromeric outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation at pericentric region during vegetative growth","type":"related"},{"name":"decreased histone H3-K9 methylation at pericentromeric region during vegetative growth","type":"related"},{"name":"decreased histone H3K9me at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 methylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 methylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0003096"}


id: PBO:0090509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase delta subunit Swp1","termid":"PBO:0090509"}


id: PBO:0047276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FA complementation group C","termid":"PBO:0047276"}


id: PBO:0074630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 25","termid":"PBO:0074630"}


id: PBO:0042128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical cancer associated DHX9 suppressive transcript","termid":"PBO:0042128"}


id: GO:0141097
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A DNA-binding transcription activator activity regulated by binding to a ligand and that activates the transcription of specific genes and gene sets.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding transcription activator activity","termid":"GO:0001216"},{"relation_name":"is_a","term_name":"ligand-modulated transcription factor activity","termid":"GO:0098531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003700"},{"rel_name":"is_a","termid":"GO:0140110"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0001216"}],"interesting_parent_ids":["GO:0003674","GO:0003700","GO:0001216","GO:0140110"],"is_obsolete":false,"name":"ligand-modulated transcription activator activity","synonyms":[{"name":"ligand-activated transcription activator activity","type":"narrow"}],"termid":"GO:0141097"}


id: PBO:0071508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 11","termid":"PBO:0071508"}


id: FYPO:0004813
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 termination of transcription by RNA polymerase II at tRNA genes (tDNA) is abnormal.","definition_xrefs":["PMID:25417108","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal termination of RNA polymerase II transcription","termid":"FYPO:0004811"}],"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:0000294"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000294","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal termination of RNA polymerase II transcription at tDNA","synonyms":[{"name":"abnormal RNA polymerase II release at tDNA","type":"related"},{"name":"abnormal RNA polymerase II transcription termination at tDNA","type":"exact"},{"name":"abnormal termination of RNA polymerase II transcription at tDNA during mitotic cell cycle","type":"related"},{"name":"abnormal termination of RNA polymerase II transcription at tDNA during vegetative growth","type":"exact"},{"name":"abnormal termination of RNA polymerase II transcription at transfer RNA genes","type":"related"}],"termid":"FYPO:0004813"}


id: PBO:0055377
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 2806","termid":"PBO:0055377"}


id: FYPO:0002214
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which all vegetative cells arising from a population of germinated spores are inviable, and have germ tubes with abnormal morphology (i.e. size, shape, or structure).","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable vegetative cell population after spore germination, abnormal germ tube morphology (obsolete FYPO:0002214)","synonyms":[{"name":"cell population inviable after spore germination, abnormal germ tube morphology","type":"exact"},{"name":"inviable germinated spore population, abnormal germ tube morphology","type":"exact"},{"name":"inviable population of undivided germinated spores with abnormal germ tube morphology","type":"exact"}],"termid":"FYPO:0002214"}


id: MONDO:0017258
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss.","definition_xrefs":["Orphanet:280921"],"direct_ancestors":[{"relation_name":"is_a","term_name":"panuveitis","termid":"MONDO:0017255"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"idiopathic panuveitis","secondary_identifiers":["GARD:21100","MEDGEN:1633708","SCTID:766933000","UMLS:C4707884"],"termid":"MONDO:0017258","xrefs":{"Monarch":{"xref_id":"0017258"}}}


id: GO:0047548
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-methyleneglutarate = 2-methylene-3-methylsuccinate.","definition_xrefs":["EC:5.4.99.4","RHEA:13793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"2-methyleneglutarate mutase activity","secondary_identifiers":["MetaCyc:2-METHYLENEGLUTARATE-MUTASE-RXN","KEGG_REACTION:R03908"],"synonyms":[{"name":"2-methyleneglutarate carboxy-methylenemethylmutase activity","type":"related"},{"name":"alpha-methyleneglutarate mutase activity","type":"related"}],"termid":"GO:0047548"}


id: PBO:0065837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB9A, member RAS oncogene family pseudogene 2","termid":"PBO:0065837"}


id: PBO:0111517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 7 open reading frame 78","termid":"PBO:0111517"}


id: PBO:0053171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"left-right determination factor 2","termid":"PBO:0053171"}


id: MONDO:0016214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pulmonary fibrosis - hepatic hyperplasia - bone marrow hypoplasia, also named Btrimorphic syndromeB (i.e. three (inherited) morbidities, pulmonary, hepatic and cytopenia), is a rare disease reported in 4 cases to date, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality.","definition_xrefs":["Orphanet:210136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease","termid":"MONDO:0015925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome","secondary_identifiers":["GARD:20449","UMLS:C4510085","MEDGEN:1385709"],"termid":"MONDO:0016214","xrefs":{"Monarch":{"xref_id":"0016214"}}}


id: GO:0004030
data:
  {"annotated_genes":["SJAG_03786","SJAG_00482","SJAG_02961"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140087"},{"annotations":[78956,76434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004029"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an aldehyde + NAD(P)+ + H2O = an acid + NAD(P)H + H+.","definition_xrefs":["EC:1.2.1.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00482":null,"SJAG_02961":null,"SJAG_03786":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"aldehyde dehydrogenase [NAD(P)+] activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6808464","MetaCyc:ALDEHYDE-DEHYDROGENASE-NADORNOP+-RXN","Reactome:R-HSA-5696080","Reactome:R-HSA-5692283"],"synonyms":[{"name":"ALDH","type":"related"},{"name":"aldehyde:NAD(P)+ oxidoreductase activity","type":"related"}],"termid":"GO:0004030","terms_by_termid":{"GO:0004029":null,"GO:0140087":null}}


id: GO:0098632
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding by a cell-adhesion protein on the cell surface to an extracellular matrix component, to mediate adhesion of the cell to another cell.","definition_xrefs":["Wikipedia:Cell_adhesion"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell adhesion mediator activity","termid":"GO:0098631"}],"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"},{"rel_name":"is_a","termid":"GO:0098631"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0098631","GO:0005488"],"is_obsolete":false,"name":"cell-cell adhesion mediator activity","synonyms":[{"name":"cell-cell adhesion molecule","type":"exact"},{"name":"protein binding involved in cell-cell adhesion","type":"exact"}],"termid":"GO:0098632"}


id: GO:0060624
data:
  {"annotated_genes":["SJAG_04666","SJAG_04771"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92761,87860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of ascospore wall (1->3)-beta-D-glucan biosynthetic process, the chemical reactions and pathways resulting in the formation of (1->3)-beta-D-glucans, compounds composed of glucose residues linked by (1->3)-beta-D--glucosidic bonds, found in the walls of ascospores.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ascospore wall beta-glucan biosynthetic process","termid":"GO:0060622"},{"relation_name":"is_a","term_name":"regulation of cell wall (1->3)-beta-D-glucan biosynthetic process","termid":"GO:0090334"},{"relation_name":"regulates","term_name":"ascospore wall (1->3)-beta-D-glucan biosynthetic process","termid":"GO:0034413"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04666":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0007049","GO:0005975","GO:0071554"],"is_obsolete":false,"name":"regulation of ascospore wall (1->3)-beta-D-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of ascospore wall 1,3-beta-D-glucan biosynthetic process","type":"broad"},{"name":"regulation of ascospore wall 1,3-beta-glucan biosynthetic process","type":"broad"}],"termid":"GO:0060624","terms_by_termid":{"GO:0140748":null}}


id: RO:0002157
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of derived by descent from","direct_ancestors":[{"relation_name":"is_a","term_name":"evolutionarily_related_to","termid":"RO:0002320"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_derived_by_descendant","termid":"RO:0002157"}


id: FYPO:0007234
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 central core of the centromeric region of a chromosome is normal (i.e. indistinguishable from wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to centromere during vegetative growth","termid":"FYPO:0002574"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000138","FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to centromere central core","synonyms":[{"name":"normal protein localisation to centromere central core","type":"exact"},{"name":"normal protein localization to centromere central core during mitotic cell cycle","type":"related"},{"name":"normal protein localization to centromere central core during vegetative growth","type":"exact"}],"termid":"FYPO:0007234"}


id: GO:0140712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a Frizzled Nuclear Import pathway.","definition_xrefs":["PMID:22510459","PMID:22579286"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Frizzled Nuclear Import pathway","termid":"GO:0140710"},{"relation_name":"is_a","term_name":"negative regulation of non-canonical Wnt signaling pathway","termid":"GO:2000051"},{"relation_name":"negatively_regulates","term_name":"Frizzled Nuclear Import pathway","termid":"GO:0140709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of Frizzled Nuclear Import pathway","synonyms":[{"name":"negative regulation of FNI","type":"broad"},{"name":"negative regulation of Frizzled Nuclear Import Wnt Pathway","type":"exact"}],"termid":"GO:0140712"}


id: PBO:0083226
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 with verified gene UBP16/YPL072W; may interact with ribosome based on co-purification experiments","termid":"PBO:0083226"}


id: MONDO:0000937
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An encephalitis caused by infection with Treponema.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Treponema infectious disease","termid":"MONDO:0007000"},{"relation_name":"is_a","term_name":"infectious encephalitis","termid":"MONDO:0020067"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syphilitic encephalitis","secondary_identifiers":["ICD9:094.81","SCTID:26135000","UMLS:C0153168","MEDGEN:509177","DOID:10081"],"synonyms":[{"name":"Treponema caused encephalitis","type":"exact"},{"name":"Treponema encephalitis","type":"exact"}],"termid":"MONDO:0000937","xrefs":{"Monarch":{"xref_id":"0000937"}}}


id: PBO:0030884
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cellular_metabolism_phenotype_during_vegetative_growth","termid":"PBO:0030884"}


id: MONDO:0019076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Circumscribed palmoplantar hypokeratosis is an ectodermal dysplasia characterized by circular, well-circumscribed patches of erythematous depressed skin.","definition_xrefs":["Orphanet:69744"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"circumscribed palmoplantar hypokeratosis","secondary_identifiers":["GARD:18898","UMLS:C0406762","MEDGEN:590662"],"termid":"MONDO:0019076","xrefs":{"Monarch":{"xref_id":"0019076"}}}


id: PBO:0090982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP1 regulatory subunit Sds22","termid":"PBO:0090982"}


id: PR:Q9USY1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1861.05 gene.","definition_xrefs":["UniProtKB:Q9USY1","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":"pseudouridine-metabolizing bifunctional protein C1861.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1861.05","synonyms":[{"name":"Spom972h-SPBC1861.05","type":"exact"}],"termid":"PR:Q9USY1"}


id: GO:0047592
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-pyridoxate + NADPH + O2 = 2-(acetamidomethylene)-3-(hydroxymethyl)succinate) + NADP+.","definition_xrefs":["RHEA:11152"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"5-pyridoxate dioxygenase activity","secondary_identifiers":["KEGG_REACTION:R04570","EC:1.14.13.241","MetaCyc:5-PYRIDOXATE-DIOXYGENASE-RXN"],"synonyms":[{"name":"5-pyridoxate oxidase activity","type":"related"}],"termid":"GO:0047592"}


id: GO:0098769
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a member of the Tissue inhibitors of metalloproteinases (TIMPs) family. TIMPs are endogenous protein regulators of the matrix metalloproteinase (MMPs) family.","definition_xrefs":["PMID:22078297"],"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:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"TIMP family protein binding","termid":"GO:0098769"}


id: PR:000027516
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcriptional regulator prz1 unmodified form in Schizosaccharomyces pombe.","definition_xrefs":["PMID:12637524","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptional regulator prz1","termid":"PR:000027513"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prz1/UnMod","pombase_gene_id":"SPAC4G8.13c","synonyms":[{"name":"PomBase_original_PRO_term_name: transcriptional regulator prz1 unmodified form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-prz1/UnMod","type":"exact"},{"name":"prz1/UnMod","type":"exact"}],"termid":"PR:000027516"}


id: PBO:0069786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1072, pseudogene","termid":"PBO:0069786"}


id: GO:1900210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiolipin metabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiolipin metabolic process","termid":"GO:1900208"},{"relation_name":"is_a","term_name":"positive regulation of phospholipid metabolic process","termid":"GO:1903727"},{"relation_name":"positively_regulates","term_name":"cardiolipin metabolic process","termid":"GO:0032048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cardiolipin metabolic process","synonyms":[{"name":"activation of cardiolipin metabolic process","type":"narrow"},{"name":"activation of cardiolipin metabolism","type":"exact"},{"name":"activation of diphosphatidylglycerol metabolic process","type":"related"},{"name":"activation of diphosphatidylglycerol metabolism","type":"related"},{"name":"positive regulation of cardiolipin metabolism","type":"exact"},{"name":"positive regulation of diphosphatidylglycerol metabolic process","type":"related"},{"name":"positive regulation of diphosphatidylglycerol metabolism","type":"related"},{"name":"up regulation of cardiolipin metabolic process","type":"exact"},{"name":"up regulation of cardiolipin metabolism","type":"exact"},{"name":"up regulation of diphosphatidylglycerol metabolic process","type":"related"},{"name":"up regulation of diphosphatidylglycerol metabolism","type":"related"},{"name":"up-regulation of cardiolipin metabolic process","type":"exact"},{"name":"up-regulation of cardiolipin metabolism","type":"exact"},{"name":"up-regulation of diphosphatidylglycerol metabolic process","type":"related"},{"name":"up-regulation of diphosphatidylglycerol metabolism","type":"related"},{"name":"upregulation of cardiolipin metabolic process","type":"exact"},{"name":"upregulation of cardiolipin metabolism","type":"exact"},{"name":"upregulation of diphosphatidylglycerol metabolic process","type":"related"},{"name":"upregulation of diphosphatidylglycerol metabolism","type":"related"}],"termid":"GO:1900210"}


id: GO:0005621
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Crater-like ring of chitinous scar tissue located on the surface of the mother cell. It is formed after the newly emerged daughter cell separates thereby marking the site of cytokinesis and septation. The number of bud scars that accumulate on the surface of a cell is a useful determinant of replicative age.","definition_xrefs":["GOC:rn","PMID:14600225","PMID:2005820"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"fungal-type cell wall","termid":"GO:0009277"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005618"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005618","GO:0005575"],"is_obsolete":false,"name":"cellular bud scar","termid":"GO:0005621"}


id: GO:1904988
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of endothelial cell activation.","definition_xrefs":["PMID:24255059","GOC:bc","GOC:TermGenie","GO_REF:0000058","GOC:BHF","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell activation","termid":"GO:0050866"},{"relation_name":"is_a","term_name":"regulation of endothelial cell activation","termid":"GO:1904987"},{"relation_name":"negatively_regulates","term_name":"endothelial cell activation","termid":"GO:0042118"}],"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 endothelial cell activation","synonyms":[{"name":"down regulation of endothelial cell activation","type":"exact"},{"name":"down-regulation of endothelial cell activation","type":"exact"},{"name":"downregulation of endothelial cell activation","type":"exact"},{"name":"inhibition of endothelial cell activation","type":"narrow"}],"termid":"GO:1904988"}


id: GO:0072305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the occurrence or rate of mesenchymal stem cell death by apoptotic process that contributes to the shaping of the nephron in the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:0072040"},{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process involved in metanephric nephron morphogenesis","termid":"GO:0072304"},{"relation_name":"is_a","term_name":"negative regulation of mesenchymal cell apoptotic process involved in metanephros development","termid":"GO:1900212"},{"relation_name":"negatively_regulates","term_name":"mesenchymal stem cell maintenance involved in metanephric nephron morphogenesis","termid":"GO:0072309"},{"relation_name":"negatively_regulates","term_name":"mesenchymal cell apoptotic process involved in metanephric nephron morphogenesis","termid":"GO:1901147"}],"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 mesenchymal cell apoptotic process involved in metanephric nephron morphogenesis","synonyms":[{"name":"negative regulation of mesenchymal stem cell apoptosis involved in metanephric nephron morphogenesis","type":"narrow"},{"name":"negative regulation of mesenchymal stem cell apoptotic process involved in metanephric nephron morphogenesis","type":"exact"}],"termid":"GO:0072305"}


id: GO:0033204
data:
  {"annotated_genes":["SJAG_03796","SJAG_01623"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76439,79621],"is_not":false,"summary":null,"term":"GO:0033204"}]},"cv_name":"molecular_function","definition":"Binding to RNA subunit of ribonuclease P.","definition_xrefs":["PMID:11455963","GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01623":null,"SJAG_03796":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"ribonuclease P RNA binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"RNase P RNA binding","type":"exact"}],"termid":"GO:0033204","terms_by_termid":{"GO:0033204":null}}


id: MONDO:0002172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory disease involving a pathogenic inflammatory response in the pharyngotympanic tube.","definition_xrefs":["MONDO:patterns/inflammatory_disease_by_site"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eustachian tube disorder","termid":"MONDO:0004866"},{"relation_name":"is_a","term_name":"otitis media","termid":"MONDO:0005441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otosalpingitis","secondary_identifiers":["ICD9:381.5","DOID:2000","ICD9:381.50","ICD10CM:H68.0","MEDGEN:509960","SCTID:270491006","UMLS:C0155428"],"synonyms":[{"name":"Eustachian salpingitis","type":"exact"},{"name":"Eustachian tube salpingitis","type":"exact"},{"name":"inflammation of pharyngotympanic tube","type":"exact"},{"name":"pharyngotympanic tube inflammation","type":"exact"}],"termid":"MONDO:0002172","xrefs":{"Monarch":{"xref_id":"0002172"}}}


id: FYPO:0004096
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cytoskeleton is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization","termid":"FYPO:0003627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to cytoskeleton","synonyms":[{"name":"normal protein localisation to cytoskeleton","type":"exact"}],"termid":"FYPO:0004096"}


id: GO:0110138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of imaginal disc-derived leg joint morphogenesis.","definition_xrefs":["PMID:25329825","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of imaginal disc-derived leg joint morphogenesis","termid":"GO:0110137"},{"relation_name":"positively_regulates","term_name":"imaginal disc-derived leg morphogenesis","termid":"GO:0007480"}],"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 imaginal disc-derived leg joint morphogenesis","termid":"GO:0110138"}


id: PBO:0043969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crystallin zeta like 2, pseudogene","termid":"PBO:0043969"}


id: PATO:0001523
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality which is equal to the quotient of the speed of a sound wave divided by its wavelength.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Sound_wavelength"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wavelength","termid":"PATO:0001242"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sound wavelength","termid":"PATO:0001523"}


id: GO:0021738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the fastigial nucleus over time, from its formation to the mature structure.","definition_xrefs":["GOC:cls","GOC:jid","GO_REF:0000021","GOC:curators","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"cerebellum development","termid":"GO:0021549"}],"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":"fastigial nucleus development","termid":"GO:0021738"}


id: PR:Q9Y7I3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC6C3.03c gene.","definition_xrefs":["UniProtKB:Q9Y7I3","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C6C3.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6C3.03c","synonyms":[{"name":"Spom972h-SPAC6C3.03c","type":"exact"}],"termid":"PR:Q9Y7I3"}


id: PBO:0041130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTB domain containing 10","termid":"PBO:0041130"}


id: null:local:null
data:
  {"annotation_feature_type":"gene","cv_name":"null","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"null","termid":"null:local:null"}


id: GO:0001869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of complement activation by the lectin pathway.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of complement activation, lectin pathway","termid":"GO:0001868"},{"relation_name":"is_a","term_name":"negative regulation of innate immune response","termid":"GO:0045824"},{"relation_name":"is_a","term_name":"negative regulation of complement activation","termid":"GO:0045916"},{"relation_name":"negatively_regulates","term_name":"complement activation, lectin pathway","termid":"GO:0001867"}],"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 complement activation, lectin pathway","synonyms":[{"name":"down regulation of complement activation, lectin pathway","type":"exact"},{"name":"down-regulation of complement activation, lectin pathway","type":"exact"},{"name":"downregulation of complement activation, lectin pathway","type":"exact"},{"name":"inhibition of complement activation, lectin pathway","type":"narrow"},{"name":"negative regulation of complement cascade, lectin pathway","type":"exact"}],"termid":"GO:0001869"}


id: GO:0050583
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + H2 = NADPH + H+.","definition_xrefs":["EC:1.12.1.3","MetaCyc:1.12.1.3-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on hydrogen as donor, NAD or NADP as acceptor","termid":"GO:0016696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"hydrogen dehydrogenase (NADP+) activity","secondary_identifiers":["RHEA:18637"],"synonyms":[{"name":"NADP-linked hydrogenase activity","type":"related"},{"name":"NADP-reducing hydrogenase activity","type":"related"},{"name":"hydrogen:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0050583"}


id: PBO:0078744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase 6 non-catalytic subunit","termid":"PBO:0078744"}


id: GO:0070568
data:
  {"annotated_genes":["SJAG_01724","SJAG_00890","SJAG_03188","SJAG_04233"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75826,103404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004475"},{"annotations":[75888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004484"},{"annotations":[73663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008193"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a guanylyl group to an acceptor.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotidyltransferase activity","termid":"GO:0016779"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00890":null,"SJAG_01724":null,"SJAG_03188":null,"SJAG_04233":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016779","GO:0003674"],"is_obsolete":false,"name":"guanylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0070568","terms_by_termid":{"GO:0004475":null,"GO:0004484":null,"GO:0008193":null}}


id: GO:0044278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disruption of the cell wall of another organism by a venom, leading to damage or temporary subversion of the cell wall.","definition_xrefs":["PMID:36738900"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated disruption of anatomical structure in another organism","termid":"GO:0140138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated disruption of cell wall in another organism","synonyms":[{"name":"cell wall disruption in another organism","type":"broad"},{"name":"cell wall disruption in other organism","type":"broad"}],"termid":"GO:0044278"}


id: PBO:0082295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arginyl-tRNA-protein transferase; catalyzes post-translational conjugation of arginine to the amino termini of acceptor proteins which are then subject to degradation via the N-end rule pathway; may have a role in regulating stress response","termid":"PBO:0082295"}


id: GO:0050488
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + ecdysteroid = UDP + glucosyl-ecdysteroid.","definition_xrefs":["PMID:10073711","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"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:0016740","GO:0003824","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"ecdysteroid UDP-glucosyltransferase activity","secondary_identifiers":["GO:0050489"],"synonyms":[{"name":"ecdysteroid UDP-glucosyl/UDP-glucuronosyl transferase activity","type":"related"}],"termid":"GO:0050488"}


id: PBO:0082494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of 1,3-beta-D-glucan synthase; functionally redundant with alternate catalytic subunit Gsc2p; binds to regulatory subunit Rho1p; involved in cell wall synthesis and maintenance; localizes to sites of cell wall remodeling; FKS1 has a paralog, GSC2, that arose from the whole genome duplication","termid":"PBO:0082494"}


id: PBO:0063711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PGM5 antisense RNA 1","termid":"PBO:0063711"}


id: PBO:0075280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 20","termid":"PBO:0075280"}


id: FYPO:0000497
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 rate, or speed, of mitochondrial transport is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial transport","termid":"FYPO:0000495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased rate of mitochondrial transport","synonyms":[{"name":"decreased rate of mitochondrial transport during mitotic cell cycle","type":"related"},{"name":"decreased rate of mitochondrial transport during vegetative growth","type":"exact"},{"name":"mitochondrial transport: decreased rate","type":"related"},{"name":"reduced rate of mitochondrial transport","type":"exact"}],"termid":"FYPO:0000497"}


id: GO:0048657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an anther cell wall tapetum cell. The tapetum is a layer of cells that provides a source of nutrition for the pollen grains as they mature.","definition_xrefs":["GOC:sm","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"anther wall tapetum formation","termid":"GO:0048656"}],"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":"anther wall tapetum cell differentiation","synonyms":[{"name":"tapetal cell differentiation","type":"broad"}],"termid":"GO:0048657"}


id: FYPO:0001927
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the regulation of the mitotic cell cycle in response to ionizing radiation is normal (i.e. indistinguishable from wild type). Normally, cell cycle progression is slowed or arrested transiently following exposure to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal regulation of mitotic cell cycle","termid":"FYPO:0001928"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal cell cycle regulation during cellular response to ionizing radiation","synonyms":[{"name":"normal cell cycle delay following ionizing radiation","type":"exact"},{"name":"normal cell cycle regulation during cellular response to gamma radiation","type":"narrow"},{"name":"normal cell cycle regulation during cellular response to ionizing radiation during mitotic cell cycle","type":"related"},{"name":"normal cell cycle regulation during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"normal cell cycle regulation in response to ionizing radiation","type":"exact"},{"name":"normal mitotic cell cycle regulation during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0001927"}


id: PBO:0111846
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-ranBP","termid":"PBO:0111846"}


id: GO:0023030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a major histocompatibility complex class Ib molecules via the antigen binding groove.","definition_xrefs":["GOC:mtg_signal","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MHC class Ib protein binding","termid":"GO:0023029"},{"relation_name":"part_of","term_name":"MHC class Ib protein complex binding","termid":"GO:0023025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"MHC class Ib protein binding, via antigen binding groove","termid":"GO:0023030"}


id: GO:0047178
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-radyl-2-lyso-sn-glycero-3-phosphoethanolamine + 1-radyl-2-acyl-sn-glycero-3-phosphocholine = 1-radyl-2-lyso-sn-glycero-3-phosphocholine + 1-radyl-2-acyl-sn-glycero-3-phosphoethanolamine.","definition_xrefs":["MetaCyc:2.3.1.148-RXN","EC:2.3.1.148"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"glycerophospholipid acyltransferase (CoA-dependent) activity","secondary_identifiers":["RHEA:20972"],"synonyms":[{"name":"1-organyl-2-acyl-sn-glycero-3-phosphocholine:1-organyl-2-lyso-sn-glycero-3-phosphoethanolamine acyltransferase (CoA-dependent)","type":"related"}],"termid":"GO:0047178"}


id: PBO:0030787
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-aseptate","termid":"PBO:0030787"}


id: MOD:01583
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-121 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ8plex-121 reporter+balance reagent acylated residue","termid":"MOD:01577"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent O-acylated residue","termid":"MOD:01714"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-121 reporter+balance reagent O3-acylated threonine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"}],"termid":"MOD:01583"}


id: MONDO:0043512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Encephalopathy resulting from trauma.","definition_xrefs":["NCIT:C35542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"traumatic encephalopathy","secondary_identifiers":["MEDGEN:536661","UMLS:C0236959","icd11.foundation:1673722101","SCTID:230282000"],"synonyms":[{"name":"dementia due to head trauma","type":"narrow"},{"name":"post-traumatic brain syndrome","type":"narrow"},{"name":"post-traumatic dementia","type":"narrow"},{"name":"traumatic encephalopathy","type":"exact"}],"termid":"MONDO:0043512","xrefs":{"Monarch":{"xref_id":"0043512"}}}


id: PBO:0056403
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 1","termid":"PBO:0056403"}


id: MONDO:0017973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital lipoid adrenal hyperplasia due to STAR deficency","termid":"MONDO:0008725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066","MONDO:0005047"],"is_obsolete":false,"name":"non-classic congenital lipoid adrenal hyperplasia due to STAR deficency","secondary_identifiers":["GARD:21474","MEDGEN:1842170","Orphanet:325529","UMLS:C5680948"],"termid":"MONDO:0017973","xrefs":{"Monarch":{"xref_id":"0017973"}}}


id: PBO:0065794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"R3HDM2 divergent transcript","termid":"PBO:0065794"}


id: PBO:0010216
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"related to S. pombe SPAC521.02 and S. cerevisiae YHR134W, but has an additional N-terminal ubiquitin family domain","termid":"PBO:0010216"}


id: MONDO:0000348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete posterior polar cataract (obsolete MONDO:0000348)","secondary_identifiers":["DOID:0050537"],"synonyms":[{"name":"cataract, posterior polar","type":"exact"},{"name":"obsolete posterior polar cataract (disease)","type":"exact"}],"termid":"MONDO:0000348","xrefs":{"Monarch":{"xref_id":"0000348"}}}


id: PBO:0040844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bleomycin hydrolase","termid":"PBO:0040844"}


id: PBO:0117048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MBP antisense RNA 1","termid":"PBO:0117048"}


id: FYPO:0003970
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid segregation stops before completing separation of chromosomes, and partially separated DNA masses are connected by one or more bridges formed of chromatin.","definition_xrefs":["PomBase:mah","PMID:12455694"],"direct_ancestors":[{"relation_name":"is_a","term_name":"incomplete mitotic sister chromatid segregation","termid":"FYPO:0003757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0000337","FYPO:0005447","FYPO:0000641","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"incomplete mitotic sister chromatid segregation, with chromatin bridge","synonyms":[{"name":"incomplete mitotic sister chromatid segregation, with chromatin bridge, during vegetative growth","type":"exact"},{"name":"incomplete mitotic sister chromatid separation, with chromatin bridge","type":"related"},{"name":"incomplete sister chromatid segregation, with chromatin bridge during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003970"}


id: MONDO:0021948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"},{"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 tuberculosis","secondary_identifiers":["SCTID:66986005","UMLS:C0041309","icd11.foundation:625292625","MEDGEN:22515"],"synonyms":[{"name":"Cutaneous Tuberculoses","type":"related"},{"name":"Cutaneous Tuberculosis","type":"related"},{"name":"Cutaneous tuberculosis","type":"related"},{"name":"Skin Tuberculoses","type":"related"},{"name":"Skin Tuberculosis","type":"related"},{"name":"Tuberculoderma","type":"related"},{"name":"Tuberculoses, Cutaneous","type":"related"},{"name":"Tuberculoses, Skin","type":"related"},{"name":"Tuberculosis cutis","type":"related"},{"name":"Tuberculosis of skin","type":"related"},{"name":"Tuberculosis, Cutaneous","type":"related"},{"name":"Tuberculosis, Skin","type":"related"},{"name":"cutaneous tuberculosis","type":"exact"},{"name":"tuberculoderma","type":"related"},{"name":"tuberculosis cutis","type":"related"},{"name":"tuberculosis of skin","type":"exact"}],"termid":"MONDO:0021948","xrefs":{"Monarch":{"xref_id":"0021948"}}}


id: PBO:0044091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 45 member A11, pseudogene","termid":"PBO:0044091"}


id: PBO:0072410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 15","termid":"PBO:0072410"}


id: MONDO:0850201
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":"hereditary alpha tryptasemia syndrome","secondary_identifiers":["DOID:0080714","MEDGEN:1797172","UMLS:C5565749"],"termid":"MONDO:0850201","xrefs":{"Monarch":{"xref_id":"0850201"}}}


id: SO:0001692
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A site where restriction enzymes can cleave that will produce an overhang or 'sticky end'.","direct_ancestors":[{"relation_name":"is_a","term_name":"restriction_enzyme_recognition_site","termid":"SO:0001687"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sticky_end_restriction_enzyme_cleavage_site","synonyms":[{"name":"sticky end restriction enzyme cleavage site","type":"related"}],"termid":"SO:0001692"}


id: GO:0102739
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A36 + O2 + 2-oxoglutarate = H+ + gibberellin A4 + succinate + 2 carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete (gibberellin-36), 2-oxoglutarate:oxygen oxidoreductase activity (obsolete GO:0102739)","termid":"GO:0102739"}


id: PBO:0067250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 323, pseudogene","termid":"PBO:0067250"}


id: GO:0003222
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the trabecular cardiac ventricle muscle are generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular cardiac muscle tissue morphogenesis","termid":"GO:0055010"},{"relation_name":"is_a","term_name":"heart trabecula morphogenesis","termid":"GO:0061384"}],"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":"ventricular trabecula myocardium morphogenesis","synonyms":[{"name":"trabecula carnea morphogenesis","type":"related"}],"termid":"GO:0003222"}


id: GO:0003301
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The enlargement or overgrowth of all or part of the heart muscle due to an increase in size of cardiac muscle cells without cell division. This process contributes to the developmental growth of the heart.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physiological muscle hypertrophy","termid":"GO:0003298"},{"relation_name":"is_a","term_name":"cardiac muscle hypertrophy","termid":"GO:0003300"},{"relation_name":"part_of","term_name":"cardiac muscle tissue growth","termid":"GO:0055017"}],"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":"physiological cardiac muscle hypertrophy","termid":"GO:0003301"}


id: SO:0002348
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Plastid LSU rRNA is an RNA component of the large subunit of plastid (such as chloroplast) ribosomes.","definition_xrefs":["PMID:3044395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid_rRNA","termid":"SO:0002346"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plastid_LSU_rRNA","synonyms":[{"name":"plastid LSU rRNA","type":"exact"},{"name":"plastid large subunit rRNA","type":"exact"}],"termid":"SO:0002348"}


id: PBO:0080404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS35 endosomal protein sorting factor like","termid":"PBO:0080404"}


id: GO:0120133
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the assembly of actin cortical patches.","definition_xrefs":["PMID:19962315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin cytoskeleton organization","termid":"GO:0032956"},{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"negatively_regulates","term_name":"actin cortical patch assembly","termid":"GO:0000147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0030036"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0044085","GO:0008150","GO:0030036"],"is_obsolete":false,"name":"negative regulation of actin cortical patch assembly","synonyms":[{"name":"down regulation of actin cortical patch assembly","type":"exact"},{"name":"down-regulation of actin cortical patch assembly","type":"exact"},{"name":"downregulation of actin cortical patch assembly","type":"exact"},{"name":"inhibition of actin cortical patch assembly","type":"narrow"}],"termid":"GO:0120133"}


id: GO:0099149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocytosis of neurotransmitter receptor at the postsynapse.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of receptor internalization","termid":"GO:0002090"},{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"},{"relation_name":"regulates","term_name":"postsynaptic neurotransmitter receptor internalization","termid":"GO:0098884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of postsynaptic neurotransmitter receptor internalization","synonyms":[{"name":"regulation of postsynaptic neurotransmitter receptor endocytosis","type":"exact"}],"termid":"GO:0099149"}


id: PBO:0067812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 114","termid":"PBO:0067812"}


id: PBO:0070571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 37","termid":"PBO:0070571"}


id: PR:Q9P7M5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An H/ACA ribonucleoprotein complex subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13305:SF0","PRO:DNx","OMA:SCHPO00663"],"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":"H/ACA ribonucleoprotein complex subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.13c","secondary_identifiers":["UniProtKB:Q9P7M5"],"synonyms":[{"name":"Spom972h-NOP10","type":"exact"},{"name":"nucleolar protein 10 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"nucleolar protein family A member 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"snoRNP protein nop10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7M5"}


id: GO:0000103
data:
  {"annotated_genes":["SJAG_04060","SJAG_01192","SJAG_01702","SJAG_00084","SJAG_01693","SJAG_03475","SJAG_04953","SJAG_05027","SJAG_01786"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58874,66980,75340,79323,88108,98126,117777],"is_not":false,"summary":null,"term":"GO:0000103"},{"annotations":[80287,100327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019379"}]},"cv_name":"biological_process","definition":"The pathways by which inorganic sulfate is processed and incorporated into sulfated compounds.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00084":null,"SJAG_01192":null,"SJAG_01693":null,"SJAG_01702":null,"SJAG_01786":null,"SJAG_03475":null,"SJAG_04060":null,"SJAG_04953":null,"SJAG_05027":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0006790"],"is_obsolete":false,"name":"sulfate assimilation","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0019378"],"synonyms":[{"name":"sulfate assimilation, phosphoadenylyl sulfate reduction by an oxidoreductase, acting on sulfur group of donors, NAD or NADP as acceptor","type":"narrow"},{"name":"sulphate assimilation","type":"exact"},{"name":"sulphate assimilation, phosphoadenylyl sulphate reduction by an oxidoreductase, acting on sulphur group of donors, NAD or NADP as acceptor","type":"narrow"}],"termid":"GO:0000103","terms_by_termid":{"GO:0000103":null,"GO:0019379":null}}


id: PBO:0043388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLYBL antisense RNA 2","termid":"PBO:0043388"}


id: SO:0000217
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding glutamyl tRNA (SO:0000260).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine_tRNA_primary_transcript","synonyms":[{"name":"glutamine tRNA primary transcript","type":"exact"}],"termid":"SO:0000217"}


id: GO:0005810
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete endocytotic transport vesicle (obsolete GO:0005810)","synonyms":[{"name":"endocytotic transport vesicle","type":"exact"}],"termid":"GO:0005810"}


id: PBO:0061581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-terminal Xaa-Pro-Lys N-methyltransferase 2","termid":"PBO:0061581"}


id: GO:0090374
data:
  {"annotated_genes":["SJAG_02602"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75986],"is_not":false,"summary":null,"term":"GO:0090374"}]},"cv_name":"biological_process","definition":"The process in which an oligopeptide is transported out of the mitochondrial matrix. Oligopeptides are molecules that contain a small number (2 to 20) of amino-acid residues connected by peptide linkages.","definition_xrefs":["PMID:11251115"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligopeptide transmembrane transport","termid":"GO:0035672"},{"relation_name":"is_a","term_name":"export from the mitochondrion","termid":"GO:0170037"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02602":null},"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"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"oligopeptide export from mitochondrion","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0090374","terms_by_termid":{"GO:0090374":null}}


id: PBO:0040030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo repeat containing X-linked 5","termid":"PBO:0040030"}


id: SO:0000388
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The Rev response element (RRE) is encoded within the HIV-env gene. Rev is an essential regulatory protein of HIV that binds an internal loop of the RRE leading, encouraging further Rev-RRE binding. This RNP complex is critical for mRNA export and hence for expression of the HIV structural proteins.","direct_ancestors":[{"relation_name":"is_a","term_name":"small_regulatory_ncRNA","termid":"SO:0000370"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRE_RNA","synonyms":[{"name":"RRE RNA","type":"exact"}],"termid":"SO:0000388"}


id: GO:1900950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of 18-methylnonadec-1-ene biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of olefin biosynthetic process","termid":"GO:1900911"},{"relation_name":"is_a","term_name":"regulation of 18-methylnonadec-1-ene metabolic process","termid":"GO:1900953"},{"relation_name":"regulates","term_name":"18-methylnonadec-1-ene biosynthetic process","termid":"GO:1900881"}],"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 18-methylnonadec-1-ene biosynthetic process","synonyms":[{"name":"regulation of 18-methylnonadec-1-ene anabolism","type":"exact"},{"name":"regulation of 18-methylnonadec-1-ene biosynthesis","type":"exact"},{"name":"regulation of 18-methylnonadec-1-ene formation","type":"exact"},{"name":"regulation of 18-methylnonadec-1-ene synthesis","type":"exact"}],"termid":"GO:1900950"}


id: PATO:0002355
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a physical object that is currently realizing none of its functions.","definition_xrefs":["PATOC:RH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activation quality","termid":"PATO:0002353"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inactive","termid":"PATO:0002355"}


id: MONDO:0020215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A corneal dystrophy (disease) that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"gene_count":0,"genotype_count":0,"name":"obsolete syndromic corneal dystrophy (obsolete MONDO:0020215)","secondary_identifiers":["Orphanet:98628"],"synonyms":[{"name":"syndrome associated with corneal dystrophy (disease)","type":"exact"},{"name":"syndromic corneal dystrophy (disease)","type":"exact"}],"termid":"MONDO:0020215","xrefs":{"Monarch":{"xref_id":"0020215"}}}


id: MONDO:0012738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any long QT syndrome in which the cause of the disease is a mutation in the AKAP9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"long QT syndrome","termid":"MONDO:0002442"},{"relation_name":"is_a","term_name":"familial long QT syndrome","termid":"MONDO:0019171"}],"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":"long QT syndrome 11","secondary_identifiers":["DOID:0110652","GARD:10437","MEDGEN:437218","UMLS:C2678483","OMIM:611820","MESH:C567513"],"synonyms":[{"name":"AKAP9 long QT syndrome","type":"exact"},{"name":"LQT11","type":"exact"},{"name":"long QT syndrome 11","type":"exact"},{"name":"long QT syndrome caused by mutation in AKAP9","type":"exact"},{"name":"long QT syndrome type 11","type":"exact"}],"termid":"MONDO:0012738","xrefs":{"Monarch":{"xref_id":"0012738"}}}


id: PBO:0031282
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_mitotic_cell_cycle","termid":"PBO:0031282"}


id: PBO:0086214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that binds to DNA mismatches; forms heterodimers with Msh3p and Msh6p that bind to DNA mismatches to initiate the mismatch repair process; contains a Walker ATP-binding motif required for repair activity and involved in interstrand cross-link repair; Msh2p-Msh6p binds to and hydrolyzes ATP; required for silencing at the silent mating-type loci and telomeres","termid":"PBO:0086214"}


id: PBO:0072532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 62","termid":"PBO:0072532"}


id: GO:0016564
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any transcription regulator activity that prevents or downregulates transcription.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription repressor activity (obsolete GO:0016564)","synonyms":[{"name":"negative transcriptional regulator activity","type":"exact"},{"name":"transcription repressor activity","type":"exact"},{"name":"transcriptional repressor activity","type":"exact"}],"termid":"GO:0016564"}


id: PBO:0043771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly factor COX20","termid":"PBO:0043771"}


id: GO:0070268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A type of programmed cell death that occurs in the epidermis, morphologically and biochemically distinct from apoptosis. It leads to the formation of corneocytes, i.e. dead keratinocytes containing an amalgam of specific proteins (e.g., keratin, loricrin, SPR and involucrin) and lipids (e.g., fatty acids and ceramides), which are necessary for the function of the cornified skin layer (mechanical resistance, elasticity, water repellence and structural stability).","definition_xrefs":["GOC:krc","PMID:18846107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"programmed cell death","termid":"GO:0012501"},{"relation_name":"part_of","term_name":"keratinization","termid":"GO:0031424"}],"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":"cornification","secondary_identifiers":["Reactome:R-HSA-6809371"],"termid":"GO:0070268"}


id: MONDO:0009691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors.","definition_xrefs":["Orphanet:2584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary cutaneous T-cell non-Hodgkin lymphoma","termid":"MONDO:0000607"},{"relation_name":"is_a","term_name":"mycosis fungoides and variants","termid":"MONDO:0015821"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"mycosis fungoides","secondary_identifiers":["icd11.foundation:901411509","NORD:1479","GARD:3863","MESH:D009182","ICDO:9700/3","OMIM:254400","NCIT:C3246","ONCOTREE:MYCF","ICD10CM:C84.0","DOID:8691","ICD9:202.1","SCTID:118618005","MedDRA:10028483","MEDGEN:7771","EFO:1001051","UMLS:C0026948"],"synonyms":[{"name":"Alibert-Bazin syndrome","type":"related"},{"name":"CTCL/ mycosis fungoides","type":"exact"},{"name":"MF","type":"exact"},{"name":"classic mycosis fungoides","type":"related"},{"name":"cutaneous T-cell lymphoma/mycosis fungoides","type":"exact"},{"name":"granuloma fungoides","type":"related"},{"name":"mycosis fungoides","type":"exact"},{"name":"mycosis fungoides (morphologic abnormality)","type":"exact"},{"name":"mycosis fungoides NOS (morphologic abnormality)","type":"exact"},{"name":"mycosis fungoides lymphoma","type":"exact"},{"name":"mycosis fungoides of unspecified site","type":"exact"},{"name":"mycosis fungoides, Alibert-Bazin type","type":"exact"},{"name":"mycosis fungoides, unspecified site, extranodal and solid organ sites","type":"exact"}],"termid":"MONDO:0009691","xrefs":{"Monarch":{"xref_id":"0009691"}}}


id: MONDO:0008891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A progressive motor neuron disorder characterized by respiratory insufficiency, sensorineural deafness and progressive ponto-bulbar palsy.","definition_xrefs":["Orphanet:97229"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete bulbospinal muscular atrophy of childhood (obsolete MONDO:0016114)","termid":"MONDO:0016114"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic genetic hearing loss (obsolete MONDO:0019589)","termid":"MONDO:0019589"},{"relation_name":"is_a","term_name":"hereditary motor neuron disease","termid":"MONDO:0024257"}],"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":"riboflavin transporter deficiency","secondary_identifiers":["MEDGEN:1634394","GARD:9993","MESH:C537111","NORD:1960","DOID:0050694","SCTID:699866005","UMLS:C4551777","OMIMPS:211530"],"synonyms":[{"name":"BVVLS","type":"related"},{"name":"BVVLS1","type":"related"},{"name":"Brown-Vialetto-Van Laere syndrome 1","type":"narrow"},{"name":"Brown-Vialetto-van Laere syndrome","type":"exact"},{"name":"Fazio-Londe syndrome","type":"exact"},{"name":"disorder of riboflavin transmembrane transporter activity","type":"exact"},{"name":"pontobulbar palsy and neurosensory deafness","type":"related"},{"name":"progressive bulbar palsy with sensorineural deafness","type":"related"},{"name":"riboflavin transmembrane transporter activity disease","type":"exact"},{"name":"sensorineural hearing loss-pontobulbar palsy syndrome","type":"exact"}],"termid":"MONDO:0008891","xrefs":{"Monarch":{"xref_id":"0008891"}}}


id: GO:0004343
data:
  {"annotated_genes":["SJAG_00519"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71157],"is_not":false,"summary":null,"term":"GO:0004343"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucosamine 6-phosphate + acetyl-CoA = N-acetyl-D-glucosamine 6-phosphate + CoA + H+.","definition_xrefs":["EC:2.3.1.4","RHEA:10292"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetyltransferase activity","termid":"GO:0008080"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00519":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"glucosamine 6-phosphate N-acetyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-449734","KEGG_REACTION:R02058","MetaCyc:GLUCOSAMINEPNACETYLTRANS-RXN"],"synonyms":[{"name":"D-glucosamine-6-P N-acetyltransferase activity","type":"related"},{"name":"N-acetylglucosamine-6-phosphate synthase activity","type":"related"},{"name":"acetyl-CoA:D-glucosamine-6-phosphate N-acetyltransferase activity","type":"related"},{"name":"aminodeoxyglucosephosphate acetyltransferase activity","type":"related"},{"name":"glucosamine 6-phosphate acetylase activity","type":"related"},{"name":"glucosamine-6-phosphate acetylase activity","type":"related"},{"name":"glucosamine-phosphate N-acetyltransferase activity","type":"exact"},{"name":"phosphoglucosamine N-acetylase activity","type":"related"},{"name":"phosphoglucosamine acetylase activity","type":"related"},{"name":"phosphoglucosamine transacetylase activity","type":"related"}],"termid":"GO:0004343","terms_by_termid":{"GO:0004343":null}}


id: GO:0017067
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phospho-5'-adenylyl sulfate + L-tyrosine methyl ester = L-tyrosine methyl ester 4-sulfate + adenosine 3',5'-diphosphate + H+.","definition_xrefs":["RHEA:19977","EC:2.8.2.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfotransferase activity","termid":"GO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016782"],"is_obsolete":false,"name":"tyrosine-ester sulfotransferase activity","secondary_identifiers":["GO:0008128","KEGG_REACTION:R04213","MetaCyc:TYROSINE-ESTER-SULFOTRANSFERASE-RXN"],"synonyms":[{"name":"3'-phosphoadenylyl-sulfate:L-tyrosine-methyl-ester sulfotransferase activity","type":"related"},{"name":"L-tyrosine methyl ester sulfotransferase activity","type":"related"},{"name":"aryl sulfotransferase IV","type":"related"},{"name":"tyrosine-ester sulphotransferase activity","type":"exact"}],"termid":"GO:0017067"}


id: GO:0110137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of imaginal disc-derived leg joint morphogenesis, the process in which the anatomical structure of the imaginal disc-derived leg joint is generated and organized.","definition_xrefs":["PMID:25329825","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"regulates","term_name":"imaginal disc-derived leg morphogenesis","termid":"GO:0007480"}],"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 imaginal disc-derived leg joint morphogenesis","termid":"GO:0110137"}


id: PR:O94645
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A thymocyte nuclear protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03612","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C21.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21.03c","secondary_identifiers":["UniProtKB:O94645"],"synonyms":[{"name":"Spom972h-THYN1","type":"exact"}],"termid":"PR:O94645"}


id: PBO:0063466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet derived growth factor receptor like 2, pseudogene","termid":"PBO:0063466"}


id: GO:0004908
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-1 to initiate a change in cell activity. Interleukin-1 is produced mainly by activated macrophages and is involved in the inflammatory response.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"interleukin-1 receptor activity","secondary_identifiers":["Wikipedia:Interleukin-1_receptor"],"synonyms":[{"name":"IL-1 receptor activity","type":"exact"},{"name":"IL-1R","type":"exact"}],"termid":"GO:0004908"}


id: PBO:0066076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid receptor responder 2 pseudogene 4","termid":"PBO:0066076"}


id: GO:0140326
data:
  {"annotated_genes":["SJAG_01731","SJAG_02943","SJAG_00589","SJAG_00669","SJAG_03050","SJAG_02132","SJAG_00587","SJAG_03774","SJAG_01095","SJAG_02581","SJAG_05209","SJAG_02516","SJAG_02897","SJAG_01945","SJAG_02957","SJAG_02114","SJAG_00018"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90875,90876,90877,90878,90879,90880,90881,90882,90883,102655,105406],"is_not":false,"summary":null,"term":"GO:0140326"},{"annotations":[112863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034202"},{"annotations":[94764,98257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140351"},{"annotations":[99803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180013"},{"annotations":[98259,94766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140345"},{"annotations":[98260,94767,100520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090554"},{"annotations":[94768,98261,99805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090555"},{"annotations":[99806,112806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140346"},{"annotations":[98262,112807,94769,99807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090556"}]},"cv_name":"molecular_function","definition":"Catalysis of the movement of lipids from one membrane leaflet to the other, driven by ATP hydrolysis. This includes flippases and floppases.","definition_xrefs":["PMID:16828084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramembrane lipid transporter activity","termid":"GO:0140303"},{"relation_name":"is_a","term_name":"ATP-dependent activity","termid":"GO:0140657"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00669":null,"SJAG_01095":null,"SJAG_01731":null,"SJAG_01945":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02516":null,"SJAG_02581":null,"SJAG_02897":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_03050":null,"SJAG_03774":null,"SJAG_05209":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0140303"],"is_obsolete":false,"name":"ATPase-coupled intramembrane lipid transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:7.6.2.1","GO:0004012","MetaCyc:3.6.3.1-RXN","Reactome:R-HSA-939763","Reactome:R-HSA-947591","GO:0008557"],"synonyms":[{"name":"ATPase-coupled phospholipid transporter activity","type":"related"},{"name":"ATPase-dependent phospholipid transporter activity","type":"related"},{"name":"aminophospholipid-transporting ATPase","type":"related"},{"name":"phospholipid flippase activity","type":"narrow"},{"name":"phospholipid translocating ATPase activity","type":"related"},{"name":"phospholipid-translocating ATPase activity","type":"related"},{"name":"phospholipid-transporting ATPase activity","type":"related"}],"termid":"GO:0140326","terms_by_termid":{"GO:0034202":null,"GO:0090554":null,"GO:0090555":null,"GO:0090556":null,"GO:0140326":null,"GO:0140345":null,"GO:0140346":null,"GO:0140351":null,"GO:0180013":null}}


id: GO:2000881
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of starch catabolic process.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"is_a","term_name":"regulation of starch metabolic process","termid":"GO:2000904"},{"relation_name":"regulates","term_name":"starch catabolic process","termid":"GO:0005983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"regulation of starch catabolic process","synonyms":[{"name":"regulation of starch breakdown","type":"exact"},{"name":"regulation of starch catabolism","type":"exact"},{"name":"regulation of starch degradation","type":"exact"}],"termid":"GO:2000881"}


id: PBO:0087414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit (60 kDa) of TFIID and SAGA complexes; involved in transcription initiation of RNA polymerase II and in chromatin modification, similar to histone H4; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0087414"}


id: PBO:0047038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 104 member A","termid":"PBO:0047038"}


id: PBO:0072546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 76","termid":"PBO:0072546"}


id: SO:0000434
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence of the target DNA that is duplicated when a transposable element or phage inserts; usually found at each end the insertion.","direct_ancestors":[{"relation_name":"derives_from","term_name":"transposable_element","termid":"SO:0000101"},{"relation_name":"is_a","term_name":"direct_repeat","termid":"SO:0000314"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target_site_duplication","synonyms":[{"name":"target site duplication","type":"exact"}],"termid":"SO:0000434"}


id: MONDO:0018522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acinar cell carcinoma of pancreas (obsolete MONDO:0018522)","termid":"MONDO:0018522","xrefs":{"Monarch":{"xref_id":"0018522"}}}


id: MONDO:1010601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hypothyroidism that occurs in chicken.","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":"congenital hypothyroidism, non-human animal","termid":"MONDO:1010057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypothyroidism, chicken","secondary_identifiers":["OMIA:000536-9031"],"termid":"MONDO:1010601","xrefs":{"Monarch":{"xref_id":"1010601"}}}


id: GO:0072072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the kidney stroma over time, from its formation to the mature structure. The kidney stroma is the mesenchyme of the mature kidney.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue development","termid":"GO:0061448"},{"relation_name":"is_a","term_name":"kidney mesenchyme development","termid":"GO:0072074"}],"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":"kidney stroma development","termid":"GO:0072072"}


id: GO:0048348
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a paraxial mesoderm cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesodermal cell fate specification","termid":"GO:0007501"},{"relation_name":"part_of","term_name":"paraxial mesodermal cell fate commitment","termid":"GO:0048343"}],"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":"paraxial mesodermal cell fate specification","termid":"GO:0048348"}


id: PBO:0041797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase recruitment domain family member 6","termid":"PBO:0041797"}


id: PBO:0083041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Delta subunit of the translation initiation factor eIF2B; the guanine-nucleotide exchange factor for eIF2; activity subsequently regulated by phosphorylated eIF2; first identified as a negative regulator of GCN4 expression","termid":"PBO:0083041"}


id: GO:0016601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signaling cassette in which a small monomeric GTPase of the Rac subfamily relays a signal.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small GTPase-mediated signal transduction","termid":"GO:0007264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"Rac protein signal transduction","secondary_identifiers":["Reactome:R-HSA-428540"],"synonyms":[{"name":"Rac mediated signal transduction","type":"exact"}],"termid":"GO:0016601"}


id: MONDO:0020771
data:
  {"annotated_genes":["SJAG_04418","SJAG_03923","SJAG_02242"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011801"},{"annotations":[86967,86966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018996"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"},{"relation_name":"is_a","term_name":"DNA repair disease","termid":"MONDO:0021190"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02242":null,"SJAG_03923":null,"SJAG_04418":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025","MONDO:0005066","MONDO:0021190"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:607250","MEDGEN:337609","UMLS:C1846574"],"synonyms":[{"name":"SCAN","type":"exact"}],"termid":"MONDO:0020771","terms_by_termid":{"MONDO:0011801":null,"MONDO:0018996":null},"xrefs":{"Monarch":{"xref_id":"0020771"}}}


id: GO:0014905
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which non-proliferating myoblasts, after migrating to the site of injury, fuse into existing damaged fibers or fuse to myotubes to form new fibers, as part of the process of skeletal muscle regeneration. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["CL:0000056","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoblast fusion","termid":"GO:0007520"},{"relation_name":"part_of","term_name":"myotube differentiation involved in skeletal muscle regeneration","termid":"GO:0014908"}],"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":"myoblast fusion involved in skeletal muscle regeneration","termid":"GO:0014905"}


id: PBO:0058780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7114","termid":"PBO:0058780"}


id: MONDO:0008758
data:
  {"annotated_genes":["SJAG_02658"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87401],"is_not":false,"summary":null,"term":"MONDO:0008758"}]},"cv_name":"mondo","definition":"A cerebrohepatopathy and a rare and severe form of mitochondrial DNA (mtDNA) depletion syndrome characterized by the triad of progressive developmental regression, intractable seizures, and hepatic failure.","definition_xrefs":["Orphanet:726"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic epilepsy","termid":"MONDO:0100033"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"},{"relation_name":"is_a","term_name":"mitochondrial DNA depletion syndrome, hepatocerebral form","termid":"MONDO:0100512"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02658":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0005066","MONDO:0005559","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial DNA depletion syndrome 4a","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:60012","DOID:1442","NCIT:C35257","OMIM:203700","NORD:752","DOID:0080122","GARD:5783","ICD9:330.8","MedDRA:10062943","SCTID:20415001","UMLS:C0205710"],"synonyms":[{"name":"AHD","type":"exact"},{"name":"AHS","type":"exact"},{"name":"Alper syndrome","type":"exact"},{"name":"Alper's disease","type":"exact"},{"name":"Alper's syndrome","type":"exact"},{"name":"Alpers Disease","type":"exact"},{"name":"Alpers Huttenlocher disease","type":"exact"},{"name":"Alpers Huttenlocher syndrome","type":"exact"},{"name":"Alpers diffuse Degeneration of cerebral Gray matter with hepatic cirrhosis","type":"related"},{"name":"Alpers diffuse Degeneration of cerebral Grey matter with hepatic cirrhosis","type":"related"},{"name":"Alpers disease","type":"exact"},{"name":"Alpers progressive infantile poliodystrophy","type":"exact"},{"name":"Alpers progressive sclerosing poliodystrophy","type":"exact"},{"name":"Alpers syndrome","type":"exact"},{"name":"Alpers' disease or gray-matter degeneration","type":"exact"},{"name":"Alpers-Huttenlocher","type":"exact"},{"name":"Alpers-Huttenlocher syndrome","type":"exact"},{"name":"MTDPS4A","type":"related"},{"name":"PNDC","type":"related"},{"name":"Poliodystrophia cerebri progressiva","type":"related"},{"name":"diffuse cerebral degeneration in infancy","type":"related"},{"name":"infantile poliodystrophy","type":"related"},{"name":"mitochondrial DNA depletion syndrome 4A","type":"exact"},{"name":"mitochondrial DNA depletion syndrome 4A (Alpers type)","type":"related"},{"name":"mitochondrial DNA depletion syndrome type 4a","type":"exact"},{"name":"neuronal Degeneration of childhood with liver disease, progressive","type":"related"},{"name":"progressive cerebral poliodystrophy","type":"related"},{"name":"progressive neuronal degeneration of childhood with liver disease","type":"exact"},{"name":"progressive sclerosing poliodystrophy","type":"exact"}],"termid":"MONDO:0008758","terms_by_termid":{"MONDO:0008758":null},"xrefs":{"Monarch":{"xref_id":"0008758"}}}


id: MONDO:0859379
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lymphatic malformation","termid":"MONDO:0019313"}],"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":"lymphatic malformation 13","secondary_identifiers":["MEDGEN:1840915","UMLS:C5830279","OMIM:620244"],"termid":"MONDO:0859379","xrefs":{"Monarch":{"xref_id":"0859379"}}}


id: GO:0051563
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maintenance of an internal steady state of calcium ions within the smooth endoplasmic reticulum of a cell or between the smooth endoplasmic reticulum and its surroundings.","definition_xrefs":["GOC:ai","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum calcium ion homeostasis","termid":"GO:0032469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098771"],"is_obsolete":false,"name":"smooth endoplasmic reticulum calcium ion homeostasis","synonyms":[{"name":"calcium ion homeostasis in smooth ER","type":"exact"},{"name":"calcium ion homeostasis in smooth endoplasmic reticulum","type":"exact"},{"name":"regulation of calcium ion concentration in smooth ER","type":"exact"},{"name":"regulation of calcium ion concentration in smooth endoplasmic reticulum","type":"exact"},{"name":"regulation of smooth ER calcium ion concentration","type":"exact"},{"name":"regulation of smooth endoplasmic reticulum calcium ion concentration","type":"exact"},{"name":"smooth ER calcium ion concentration regulation","type":"exact"},{"name":"smooth ER calcium ion homeostasis","type":"exact"},{"name":"smooth endoplasmic reticulum calcium ion concentration regulation","type":"exact"}],"termid":"GO:0051563"}


id: PR:O42842
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An adenine phosphoribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11776: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":"adenine phosphoribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.03","secondary_identifiers":["UniProtKB:O42842"],"synonyms":[{"name":"APRT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC23A1.03","type":"related"},{"name":"Spom972h-APRT","type":"exact"}],"termid":"PR:O42842"}


id: FYPO:0003550
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell during one or both meiotic nuclear divisions is lower than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during meiotic cell cycle","termid":"FYPO:0004991"}],"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":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein level during meiosis","synonyms":[{"name":"decreased protein accumulation during meiosis","type":"related"},{"name":"decreased protein level during meiotic nuclear division","type":"exact"},{"name":"reduced protein level during meiosis","type":"exact"}],"termid":"FYPO:0003550"}


id: GO:0030365
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A factor is necessary for cleavage but not for poly(A) addition in mRNA 3' end processing; can stimulate poly(A) addition on substrates with a CstF binding site upstream of the AAUAAA hexanucleotide.","definition_xrefs":["PMID:10357856"],"gene_count":0,"genotype_count":0,"name":"obsolete cleavage stimulation factor activity (obsolete GO:0030365)","synonyms":[{"name":"CstF","type":"exact"},{"name":"cleavage stimulation factor activity","type":"exact"}],"termid":"GO:0030365"}


id: GO:0019575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of sucrose, catalyzed by the enzyme beta-fructofuranosidase (EC:3.2.1.26).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete sucrose catabolic process, using beta-fructofuranosidase (obsolete GO:0019575)","synonyms":[{"name":"sucrose breakdown, using beta-fructofuranosidase","type":"exact"},{"name":"sucrose catabolic process, using beta-fructofuranosidase","type":"exact"},{"name":"sucrose catabolism, using beta-fructofuranosidase","type":"exact"},{"name":"sucrose degradation, using beta-fructofuranosidase","type":"exact"}],"termid":"GO:0019575"}


id: PBO:0052198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium calcium-activated channel subfamily N member 2","termid":"PBO:0052198"}


id: MONDO:0008608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Down syndrome is a chromosomal abnormality caused by the presence of a third (partial or total) copy of the chromosome 21 genetic material and that is characterized by variable intellectual disability, muscular hypotonia, and joint laxity, often associated with a characteristic facial dysmorphism and various anomalies such as cardiac, gastrointestinal, or endocrine defects.","definition_xrefs":["Orphanet:870"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare syndrome with cardiac malformations (obsolete MONDO:0015506)","termid":"MONDO:0015506"},{"relation_name":"excluded_subClassOf","term_name":"obsolete chromosomal anomaly with epilepsy as a major feature (obsolete MONDO:0015652)","termid":"MONDO:0015652"},{"relation_name":"excluded_subClassOf","term_name":"obsolete Moyamoya syndrome (obsolete MONDO:0018792)","termid":"MONDO:0018792"},{"relation_name":"excluded_subClassOf","term_name":"chromosomal disorder","termid":"MONDO:0019040"},{"relation_name":"is_a","term_name":"chromosome 21 disorder","termid":"MONDO:0700124"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Down syndrome","secondary_identifiers":["MedDRA:10044688","UMLS:C0013080","MESH:D004314","MEDGEN:4385","EFO:0001064","NIFSTD:nlx_dys_20090502","OMIM:190685","SCTID:41040004","NANDO:2200965","DOID:14250","icd11.foundation:1624623908","ICD9:758.0","NCIT:C2993"],"synonyms":[{"name":"Down syndrome","type":"exact"},{"name":"Down syndrome chromosome region","type":"related"},{"name":"Down syndrome critical region","type":"related"},{"name":"Down syndrome, Isolated cases","type":"exact"},{"name":"Down's syndrome","type":"exact"},{"name":"Down's syndrome - trisomy 21","type":"exact"},{"name":"Downs syndrome","type":"exact"},{"name":"G trisomy","type":"exact"},{"name":"complete trisomy 21 syndrome","type":"narrow"},{"name":"leukemia, megakaryoblastic, of Down syndrome","type":"related"},{"name":"leukemia, megakaryoblastic, with or without Down syndrome, somatic","type":"exact"},{"name":"transient myeloproliferative disorder of Down syndrome","type":"related"},{"name":"trisomy 21","type":"narrow"},{"name":"trisomy 21 (Down syndrome)","type":"exact"},{"name":"trisomy 21 syndrome","type":"narrow"}],"termid":"MONDO:0008608","xrefs":{"Monarch":{"xref_id":"0008608"}}}


id: MONDO:0017855
data:
  {"annotated_genes":["SJAG_04199","SJAG_02038","SJAG_02527"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012650"},{"annotations":[87419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011686"},{"annotations":[86001],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009973"}]},"cv_name":"mondo","definition":"T-B- severe combined immunodeficiency (SCID) is a group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T and B lymphocytes, resulting in recurrent early-onset severe respiratory viral, bacterial or fungal infections, diarrhea and failure to thrive. Hypersensitivity to ionizing radiation is a characteristic feature of some of its sub-types.","definition_xrefs":["Orphanet:317419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"severe combined immunodeficiency","termid":"MONDO:0015974"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02038":null,"SJAG_02527":null,"SJAG_04199":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"T-B- severe combined immunodeficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:21406","MEDGEN:1842252","UMLS:C5679893"],"synonyms":[{"name":"T-B- SCID","type":"exact"}],"termid":"MONDO:0017855","terms_by_termid":{"MONDO:0009973":null,"MONDO:0011686":null,"MONDO:0012650":null},"xrefs":{"Monarch":{"xref_id":"0017855"}}}


id: PBO:0048075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin heavy chain 1 pseudogene 26","termid":"PBO:0048075"}


id: MONDO:0013151
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central areolar choroidal dystrophy","termid":"MONDO:0008982"}],"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":"choroidal dystrophy, central areolar, 3","secondary_identifiers":["MESH:C567729","OMIM:613144","UMLS:C2751055","MEDGEN:442631","GARD:15623"],"synonyms":[{"name":"CACD3","type":"exact"},{"name":"choroidal dystrophy, central areolar, 3","type":"exact"},{"name":"choroidal dystrophy, central areolar, with or without drusen","type":"related"}],"termid":"MONDO:0013151","xrefs":{"Monarch":{"xref_id":"0013151"}}}


id: GO:0030717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chromosome organization process in which meiotic chromosomes in the oocyte nucleus cluster together to form a compact spherical structure called the karyosome.","definition_xrefs":["PMID:11700288","PMID:18039935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"karyosome formation","termid":"GO:0061988"},{"relation_name":"part_of","term_name":"oogenesis","termid":"GO:0048477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"oocyte karyosome formation","termid":"GO:0030717"}


id: PBO:0028608
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-RNA_absent_from_cell_during_cellular_response_to_thiamine_starvation","termid":"PBO:0028608"}


id: GO:0021551
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the central nervous system is generated and organized. The central nervous system is the core nervous system that serves an integrating and coordinating function. In vertebrates it consists of the brain and spinal cord. In those invertebrates with a central nervous system it typically consists of a brain, cerebral ganglia and a nerve cord.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:cls","GOC:dph","ISBN:0582227089","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"central nervous system development","termid":"GO:0007417"}],"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":"central nervous system morphogenesis","termid":"GO:0021551"}


id: SO:0000003
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"G-quartets are unusual nucleic acid structures consisting of a planar arrangement where each guanine is hydrogen bonded by hoogsteen pairing to another guanine in the quartet.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_secondary_structure","termid":"SO:0000002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G_quartet","secondary_identifiers":["http://en.wikipedia.org/wiki/G-quadruplex"],"synonyms":[{"name":"G quartet","type":"exact"},{"name":"G tetrad","type":"exact"},{"name":"G-quadruplex","type":"exact"},{"name":"G-quartet","type":"exact"},{"name":"G-tetrad","type":"exact"},{"name":"G_quadruplex","type":"exact"},{"name":"guanine tetrad","type":"exact"}],"termid":"SO:0000003"}


id: GO:1904336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ductus arteriosus closure.","definition_xrefs":["GOC:TermGenie","PMID:16303610","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ductus arteriosus closure","termid":"GO:1904335"},{"relation_name":"is_a","term_name":"negative regulation of artery morphogenesis","termid":"GO:1905652"},{"relation_name":"negatively_regulates","term_name":"ductus arteriosus closure","termid":"GO:0097070"}],"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 ductus arteriosus closure","synonyms":[{"name":"down regulation of ductus arteriosus closure","type":"exact"},{"name":"down-regulation of ductus arteriosus closure","type":"exact"},{"name":"downregulation of ductus arteriosus closure","type":"exact"},{"name":"inhibition of ductus arteriosus closure","type":"narrow"}],"termid":"GO:1904336"}


id: GO:0055041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cyclopentanol + NAD+ = cyclopentanone + H+ + NADH.","definition_xrefs":["RHEA:11728","EC:1.1.1.163"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"cyclopentanol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R02553","MetaCyc:CYCLOPENTANOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"cyclopentanol:NAD+ oxidoreductase activity","type":"related"},{"name":"cyclopentanol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0055041"}


id: GO:0047874
data:
  {"annotated_genes":["SJAG_02056"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74007],"is_not":false,"summary":null,"term":"GO:0047874"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: dolichyl diphosphate + H2O = dolichyl phosphate + phosphate.","definition_xrefs":["EC:3.6.1.43","MetaCyc:DOLICHYLDIPHOSPHATASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02056":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"dolichyldiphosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-446200","RHEA:14385"],"synonyms":[{"name":"dolichol diphosphatase activity","type":"related"},{"name":"dolichyl diphosphate phosphohydrolase activity","type":"related"},{"name":"dolichyl pyrophosphatase activity","type":"related"},{"name":"dolichyl-diphosphate phosphohydrolase activity","type":"related"}],"termid":"GO:0047874","terms_by_termid":{"GO:0047874":null}}


id: PBO:0059367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S18B pseudogene 2","termid":"PBO:0059367"}


id: GO:0060923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to specific cardiac muscle cell fates and their capacity to differentiate into cardiac muscle cells. Cardiac muscle cells are striated muscle cells that are responsible for heart contraction.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle cell fate commitment","termid":"GO:0042693"},{"relation_name":"is_a","term_name":"cardiac cell fate commitment","termid":"GO:0060911"},{"relation_name":"part_of","term_name":"cardiac muscle cell differentiation","termid":"GO:0055007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac muscle cell fate commitment","synonyms":[{"name":"cardiomyocyte cell fate commitment","type":"exact"},{"name":"heart muscle cell fate commitment","type":"exact"}],"termid":"GO:0060923"}


id: PBO:0054509
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 1909","termid":"PBO:0054509"}


id: PBO:0074196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 6","termid":"PBO:0074196"}


id: GO:0031525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of menthol, the monoterpene 2-isopropyl-5-methylcyclohexanol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoterpenoid biosynthetic process","termid":"GO:0016099"},{"relation_name":"is_a","term_name":"menthol metabolic process","termid":"GO:0031524"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"menthol biosynthetic process","synonyms":[{"name":"menthol anabolism","type":"exact"},{"name":"menthol biosynthesis","type":"exact"},{"name":"menthol formation","type":"exact"},{"name":"menthol synthesis","type":"exact"}],"termid":"GO:0031525"}


id: PBO:0083127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-ribulokinase; carbohydrate kinase that specifically converts D-ribulose to D-ribulose 5-phosphate during pentose metabolism; null mutant accumulates D-ribulose and the precursor ribitol; proposed to function as a D-ribulose metabolic repair enzyme; member of the FGGY family of carbohydrate kinases; human homolog, FGGY, is involved in both D-ribulose and ribitol metabolism; human FGGY has been linked to both sporadic amyotrophic lateral sclerosis and bipolar disorder","termid":"PBO:0083127"}


id: PBO:0050159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 15","termid":"PBO:0050159"}


id: GO:0060376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of mast cell differentiation, the process in which a relatively unspecialized myeloid precursor cell acquires the specialized features of a mast cell. A mast cell is a cell that is found in almost all tissues containing numerous basophilic granules and capable of releasing large amounts of histamine and heparin upon activation.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of myeloid leukocyte differentiation","termid":"GO:0002763"},{"relation_name":"is_a","term_name":"regulation of mast cell differentiation","termid":"GO:0060375"},{"relation_name":"positively_regulates","term_name":"mast cell differentiation","termid":"GO:0060374"}],"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 mast cell differentiation","termid":"GO:0060376"}


id: PBO:0070860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13 pseudogene 13","termid":"PBO:0070860"}


id: PBO:0056785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microfibril associated protein 2","termid":"PBO:0056785"}


id: PBO:0011425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NuA4 complex phosphatidylinositol pseudokinase complex subunit Tra2","termid":"PBO:0011425"}


id: GO:0045037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The targeting and import of proteins into the chloroplast stroma. Import depends on ATP hydrolysis catalyzed by stromal chaperones. Chloroplast stromal proteins, such as the S subunit of rubisco, have a N-terminal stromal-import sequence of about 44 amino acids which is cleaved from the protein precursor after import.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transmembrane transport","termid":"GO:0071806"},{"relation_name":"is_a","term_name":"establishment of protein localization to chloroplast","termid":"GO:0072596"}],"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"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"protein import into chloroplast stroma","synonyms":[{"name":"chloroplast stroma protein import","type":"exact"},{"name":"protein transport into chloroplast stroma","type":"exact"}],"termid":"GO:0045037"}


id: PBO:0028074
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_single_or_double_cell_division,_arrest_with_cut","termid":"PBO:0028074"}


id: MONDO:0014227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"}],"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":"hypopigmentation-punctate palmoplantar keratoderma syndrome","secondary_identifiers":["OMIM:615522","SCTID:711154007","MEDGEN:816111","Orphanet:324561","UMLS:C3809781","GARD:12384","ICD9:757.39"],"synonyms":[{"name":"COLE disease","type":"related"},{"name":"COLED","type":"related"},{"name":"Cole disease","type":"exact"},{"name":"guttate hypopigmentation","type":"related"},{"name":"guttate hypopigmentation and punctate palmoplantar keratoderma","type":"exact"},{"name":"guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification","type":"related"},{"name":"hypopigmentation and punctate keratosis of the palms and soles","type":"exact"},{"name":"punctate palmoplantar keratoderma with or without ectopic calcification","type":"related"}],"termid":"MONDO:0014227","xrefs":{"Monarch":{"xref_id":"0014227"}}}


id: GO:0042780
data:
  {"annotated_genes":["SJAG_04885","SJAG_01704","SJAG_02288","SJAG_00997","SJAG_03761","SJAG_00195","SJAG_02993"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93368,98804,99267],"is_not":false,"summary":null,"term":"GO:0042780"},{"annotations":[80699,88077,70474,118223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990180"},{"annotations":[70624,75284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001680"}]},"cv_name":"biological_process","definition":"The process in which the 3' end of a pre-tRNA molecule is converted to that of a mature tRNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA processing","termid":"GO:0008033"},{"relation_name":"is_a","term_name":"RNA 3'-end processing","termid":"GO:0031123"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00997":null,"SJAG_01704":null,"SJAG_02288":null,"SJAG_02993":null,"SJAG_03761":null,"SJAG_04885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"tRNA 3'-end processing","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"tRNA 3' processing","type":"exact"}],"termid":"GO:0042780","terms_by_termid":{"GO:0001680":null,"GO:0042780":null,"GO:1990180":null}}


id: MONDO:0010551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked Charcot-Marie-Tooth disease type 3 is a rare, genetic, peripheral sensorimotor neuropathy characterized by an X-linked recessive inheritance pattern and the childhood- to adolescent-onset of progressive, distal muscle weakness and atrophy (beginning in the lower extremities and then affecting the upper extremities), as well as distal, pansensory loss in the upper and lower extremities, pes cavus, and absent or reduced distal tendon reflexes. Pain and paresthesia are frequently the initial sensory symptoms. Spastic paraparesis (manifested by clasp-knife sign, hyperactive deep-tendon reflexes, and Babinski sign) has also been reported.","definition_xrefs":["Orphanet:101077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type X","termid":"MONDO:0018994"}],"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":"Charcot-Marie-Tooth disease X-linked recessive 3","secondary_identifiers":["SCTID:763458005","UMLS:C1844865","DOID:0110211","MESH:C535303","MEDGEN:375530","GARD:1244","OMIM:302802"],"synonyms":[{"name":"CMT3X","type":"exact"},{"name":"CMTX 3","type":"exact"},{"name":"CMTX3","type":"exact"},{"name":"Charcot Marie Tooth disease X-linked recessive 3","type":"exact"},{"name":"Charcot-Marie-Tooth disease X-linked recessive type 3","type":"exact"},{"name":"Charcot-Marie-Tooth disease, X-linked recessive, 3","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy X-linked recessive 3","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, X-linked recessive, 3","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, X-linked recessive, 3, X-linked recessive","type":"exact"},{"name":"X-linked Charcot-Marie-Tooth disease type 3","type":"exact"}],"termid":"MONDO:0010551","xrefs":{"Monarch":{"xref_id":"0010551"}}}


id: GO:0034042
data:
  {"annotated_genes":["SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96478],"is_not":false,"summary":null,"term":"GO:0034042"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of 5-formyluracil bases by cleaving the N-C1' glycosidic bond between the oxidized pyrimidine and the deoxyribose sugar.","definition_xrefs":["PMID:17641464","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity","termid":"GO:0000703"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140097","GO:0003824","GO:0016798","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"5-formyluracil DNA N-glycosylase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"5-foU DNA N-glycosylase activity","type":"exact"}],"termid":"GO:0034042","terms_by_termid":{"GO:0034042":null}}


id: PBO:0064187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group XIIA pseudogene 1","termid":"PBO:0064187"}


id: GO:0005829
data:
  {"annotated_genes":["SJAG_04652","SJAG_02959","SJAG_07011","SJAG_01267","SJAG_04249","SJAG_01088","SJAG_04352","SJAG_04174","SJAG_03034","SJAG_01063","SJAG_05009","SJAG_01166","SJAG_04015","SJAG_04179","SJAG_03373","SJAG_04656","SJAG_02832","SJAG_01187","SJAG_04463","SJAG_03854","SJAG_01630","SJAG_02771","SJAG_04964","SJAG_01833","SJAG_03936","SJAG_01651","SJAG_00069","SJAG_02224","SJAG_02098","SJAG_16457","SJAG_03697","SJAG_02720","SJAG_04275","SJAG_02597","SJAG_01055","SJAG_01776","SJAG_03603","SJAG_01663","SJAG_04107","SJAG_02004","SJAG_04466","SJAG_04760","SJAG_02760","SJAG_03794","SJAG_03185","SJAG_05029","SJAG_00733","SJAG_00955","SJAG_02692","SJAG_02696","SJAG_00807","SJAG_02950","SJAG_04114","SJAG_03476","SJAG_03541","SJAG_03179","SJAG_04077","SJAG_00365","SJAG_00534","SJAG_00120","SJAG_02213","SJAG_03722","SJAG_03842","SJAG_03616","SJAG_02253","SJAG_00147","SJAG_00822","SJAG_02091","SJAG_02708","SJAG_02047","SJAG_02065","SJAG_03209","SJAG_01986","SJAG_00420","SJAG_03990","SJAG_01047","SJAG_00864","SJAG_02292","SJAG_03849","SJAG_00390","SJAG_00690","SJAG_01261","SJAG_03022","SJAG_01582","SJAG_02689","SJAG_07000","SJAG_03888","SJAG_00660","SJAG_04554","SJAG_02218","SJAG_00449","SJAG_00463","SJAG_04083","SJAG_00359","SJAG_01266","SJAG_04827","SJAG_03730","SJAG_01628","SJAG_04890","SJAG_00485","SJAG_04408","SJAG_04544","SJAG_02145","SJAG_01748","SJAG_02817","SJAG_03215","SJAG_02811","SJAG_03758","SJAG_01229","SJAG_04400","SJAG_04858","SJAG_03821","SJAG_00150","SJAG_00172","SJAG_01942","SJAG_04626","SJAG_05290","SJAG_01151","SJAG_00290","SJAG_02283","SJAG_00049","SJAG_02038","SJAG_04169","SJAG_04617","SJAG_03781","SJAG_04505","SJAG_04778","SJAG_04168","SJAG_00815","SJAG_02477","SJAG_03872","SJAG_04969","SJAG_00615","SJAG_04521","SJAG_00581","SJAG_05329","SJAG_03815","SJAG_03423","SJAG_01508","SJAG_04021","SJAG_01438","SJAG_02769","SJAG_02580","SJAG_03153","SJAG_01191","SJAG_02745","SJAG_04371","SJAG_04311","SJAG_00248","SJAG_06355","SJAG_02009","SJAG_01488","SJAG_01853","SJAG_00401","SJAG_03932","SJAG_03589","SJAG_01126","SJAG_03799","SJAG_03228","SJAG_05343","SJAG_00683","SJAG_01658","SJAG_03137","SJAG_04576","SJAG_04657","SJAG_03775","SJAG_00072","SJAG_01841","SJAG_01121","SJAG_01588","SJAG_00161","SJAG_03643","SJAG_01087","SJAG_02479","SJAG_04219","SJAG_03293","SJAG_02386","SJAG_04070","SJAG_04177","SJAG_00892","SJAG_01760","SJAG_04326","SJAG_04516","SJAG_00746","SJAG_04783","SJAG_00947","SJAG_04274","SJAG_00242","SJAG_04776","SJAG_04817","SJAG_04651","SJAG_00505","SJAG_03325","SJAG_04175","SJAG_00004","SJAG_01830","SJAG_00465","SJAG_02673","SJAG_04590","SJAG_03082","SJAG_02857","SJAG_00430","SJAG_04987","SJAG_01618","SJAG_00512","SJAG_04354","SJAG_02789","SJAG_02339","SJAG_02462","SJAG_00486","SJAG_03475","SJAG_03907","SJAG_03188","SJAG_01134","SJAG_00106","SJAG_03037","SJAG_01325","SJAG_03383","SJAG_02352","SJAG_00027","SJAG_04473","SJAG_04190","SJAG_04055","SJAG_01480","SJAG_00661","SJAG_00063","SJAG_02295","SJAG_00333","SJAG_04765","SJAG_00472","SJAG_04161","SJAG_03164","SJAG_02688","SJAG_00166","SJAG_01132","SJAG_03298","SJAG_00219","SJAG_01859","SJAG_03677","SJAG_04157","SJAG_05228","SJAG_03632","SJAG_04088","SJAG_00888","SJAG_02808","SJAG_03409","SJAG_05230","SJAG_00137","SJAG_05015","SJAG_00450","SJAG_01694","SJAG_04170","SJAG_05210","SJAG_00144","SJAG_01818","SJAG_02802","SJAG_00894","SJAG_01213","SJAG_03374","SJAG_04658","SJAG_04845","SJAG_00376","SJAG_01548","SJAG_05198","SJAG_01061","SJAG_02415","SJAG_04084","SJAG_01122","SJAG_04938","SJAG_01839","SJAG_03098","SJAG_02422","SJAG_04106","SJAG_04628","SJAG_01590","SJAG_00691","SJAG_00956","SJAG_00572","SJAG_00764","SJAG_04551","SJAG_01914","SJAG_00758","SJAG_01919","SJAG_01199","SJAG_02951","SJAG_03361","SJAG_03955","SJAG_02956","SJAG_04343","SJAG_04602","SJAG_03438","SJAG_00119","SJAG_01127","SJAG_01231","SJAG_01698","SJAG_02753","SJAG_02170","SJAG_02998","SJAG_00786","SJAG_01209","SJAG_00040","SJAG_03576","SJAG_02179","SJAG_03624","SJAG_00594","SJAG_04475","SJAG_03689","SJAG_00186","SJAG_02684","SJAG_02169","SJAG_04181","SJAG_00954","SJAG_02340","SJAG_00859","SJAG_03733","SJAG_04307","SJAG_01496","SJAG_03321","SJAG_00489","SJAG_04474","SJAG_04495","SJAG_02686","SJAG_03167","SJAG_03760","SJAG_02294","SJAG_04891","SJAG_00972","SJAG_04452","SJAG_03937","SJAG_03009","SJAG_03798","SJAG_02502","SJAG_01995","SJAG_04649","SJAG_04859","SJAG_02731","SJAG_00986","SJAG_03384","SJAG_03147","SJAG_04970","SJAG_02902","SJAG_04567","SJAG_01543","SJAG_01479","SJAG_00686","SJAG_04027","SJAG_00479","SJAG_02420","SJAG_01354","SJAG_03626","SJAG_02070","SJAG_00599","SJAG_00032","SJAG_02040","SJAG_04963","SJAG_05240","SJAG_02166","SJAG_05000","SJAG_04292","SJAG_03243","SJAG_02822","SJAG_02211","SJAG_00356","SJAG_02659","SJAG_00622","SJAG_02171","SJAG_03094","SJAG_03231","SJAG_00033","SJAG_01070","SJAG_01415","SJAG_03921","SJAG_04091","SJAG_03482","SJAG_03142","SJAG_04907","SJAG_02313","SJAG_00400","SJAG_03181","SJAG_04531","SJAG_01540","SJAG_04309","SJAG_03558","SJAG_03544","SJAG_01425","SJAG_00988","SJAG_02191","SJAG_02843","SJAG_00685","SJAG_04814","SJAG_05243","SJAG_04932","SJAG_02535","SJAG_02285","SJAG_03653","SJAG_01529","SJAG_02611","SJAG_03786","SJAG_04176","SJAG_01003","SJAG_04156","SJAG_03257","SJAG_00179","SJAG_00102","SJAG_02177","SJAG_03501","SJAG_02066","SJAG_01362","SJAG_06440","SJAG_01411","SJAG_03367","SJAG_04980","SJAG_03562","SJAG_03548","SJAG_02540","SJAG_01214","SJAG_02697","SJAG_01680","SJAG_04097","SJAG_03582","SJAG_02297","SJAG_03495","SJAG_03350","SJAG_02878","SJAG_00809","SJAG_01136","SJAG_02164","SJAG_02886","SJAG_02186","SJAG_02874","SJAG_00208","SJAG_02515","SJAG_02428","SJAG_01655","SJAG_03751","SJAG_01375","SJAG_01645","SJAG_00045","SJAG_03089","SJAG_01154","SJAG_00856","SJAG_04287","SJAG_01270","SJAG_02013","SJAG_04581","SJAG_04480","SJAG_04541","SJAG_01587","SJAG_02797","SJAG_03408","SJAG_04123","SJAG_00092","SJAG_04060","SJAG_00796","SJAG_03529","SJAG_02493","SJAG_04920","SJAG_02645","SJAG_04837","SJAG_00931","SJAG_02592","SJAG_01079","SJAG_02734","SJAG_00983","SJAG_04762","SJAG_03095","SJAG_02267","SJAG_00229","SJAG_03453","SJAG_02845","SJAG_00821","SJAG_03862","SJAG_04758","SJAG_00457","SJAG_02376","SJAG_01026","SJAG_02270","SJAG_01812","SJAG_00424","SJAG_00036","SJAG_04681","SJAG_03081","SJAG_03234","SJAG_01039","SJAG_01714","SJAG_03662","SJAG_01487","SJAG_03581","SJAG_03364","SJAG_02069","SJAG_00269","SJAG_04565","SJAG_02786","SJAG_00692","SJAG_01139","SJAG_02366","SJAG_00726","SJAG_01333","SJAG_00756","SJAG_00537","SJAG_00967","SJAG_04519","SJAG_00038","SJAG_00384","SJAG_00917","SJAG_00938","SJAG_02269","SJAG_01703","SJAG_00788","SJAG_04682","SJAG_01475","SJAG_00533","SJAG_03013","SJAG_02740","SJAG_00188","SJAG_03063","SJAG_01161","SJAG_02434","SJAG_02485","SJAG_01617","SJAG_02491","SJAG_04699","SJAG_03605","SJAG_03288","SJAG_01175","SJAG_01313","SJAG_00678","SJAG_03019","SJAG_02393","SJAG_00837","SJAG_01149","SJAG_02043","SJAG_03839","SJAG_02833","SJAG_00095","SJAG_01797","SJAG_01238","SJAG_04388","SJAG_01461","SJAG_04841","SJAG_02233","SJAG_00574","SJAG_02547","SJAG_05027","SJAG_01580","SJAG_04304","SJAG_03262","SJAG_02237","SJAG_00808","SJAG_04928","SJAG_02012","SJAG_01781","SJAG_00084","SJAG_05205","SJAG_04950","SJAG_04973","SJAG_02879","SJAG_01918","SJAG_01852","SJAG_00352","SJAG_03655","SJAG_00778","SJAG_00605","SJAG_02736","SJAG_03106","SJAG_00052","SJAG_03124","SJAG_03119","SJAG_01159","SJAG_01075","SJAG_02503","SJAG_02861","SJAG_04728","SJAG_04211","SJAG_03922","SJAG_02702","SJAG_05314","SJAG_03432","SJAG_01310","SJAG_01474","SJAG_04772","SJAG_03669","SJAG_04032","SJAG_00526","SJAG_03892","SJAG_00381","SJAG_04375","SJAG_02864","SJAG_03319","SJAG_01404","SJAG_00341","SJAG_03051","SJAG_00093","SJAG_04192","SJAG_01292","SJAG_06270","SJAG_05260","SJAG_04036","SJAG_04407","SJAG_03617","SJAG_03784","SJAG_02870","SJAG_04202","SJAG_02239","SJAG_03856","SJAG_03246","SJAG_00296","SJAG_04085","SJAG_05346","SJAG_04974","SJAG_02647","SJAG_00642","SJAG_00913","SJAG_04944","SJAG_04548","SJAG_03811","SJAG_04709","SJAG_05225","SJAG_02718","SJAG_05193","SJAG_04631","SJAG_04289","SJAG_05214","SJAG_04897","SJAG_00991","SJAG_01207","SJAG_01128","SJAG_01501","SJAG_00126","SJAG_04093","SJAG_03701","SJAG_02518","SJAG_02281","SJAG_01365","SJAG_04214","SJAG_01181","SJAG_02082","SJAG_00067","SJAG_03893","SJAG_01944","SJAG_04248","SJAG_01443","SJAG_01954","SJAG_00379","SJAG_01765","SJAG_04118","SJAG_04496","SJAG_04016","SJAG_01351","SJAG_02093","SJAG_00107","SJAG_03219","SJAG_02573","SJAG_00331","SJAG_06592","SJAG_03377","SJAG_03668","SJAG_01531","SJAG_04303","SJAG_02725","SJAG_00580","SJAG_01696","SJAG_00100","SJAG_03108","SJAG_04183","SJAG_01801","SJAG_04256","SJAG_04901","SJAG_01943","SJAG_02723","SJAG_03487","SJAG_01386","SJAG_02756","SJAG_02405","SJAG_03859","SJAG_03005","SJAG_02918","SJAG_01472","SJAG_00898","SJAG_01339","SJAG_02450","SJAG_02268","SJAG_02997","SJAG_01434","SJAG_01637","SJAG_00230","SJAG_01551","SJAG_00350","SJAG_03126","SJAG_04261","SJAG_01722","SJAG_04299","SJAG_01248","SJAG_04403","SJAG_00306","SJAG_01937","SJAG_00968","SJAG_04870","SJAG_03278","SJAG_00718","SJAG_01528","SJAG_04710","SJAG_02387","SJAG_04972","SJAG_00423","SJAG_03189","SJAG_03186","SJAG_04030","SJAG_01408","SJAG_00270","SJAG_00840","SJAG_04627","SJAG_04818","SJAG_01858","SJAG_02508","SJAG_01799","SJAG_02589","SJAG_01193","SJAG_03678","SJAG_05211","SJAG_01148","SJAG_01358","SJAG_07014","SJAG_04573","SJAG_02765","SJAG_04946","SJAG_04771","SJAG_05351","SJAG_05245","SJAG_01389","SJAG_01216","SJAG_02154","SJAG_02591","SJAG_03241","SJAG_00280","SJAG_00037","SJAG_00414","SJAG_00065","SJAG_02035","SJAG_01163","SJAG_01184","SJAG_03130","SJAG_05008","SJAG_00521","SJAG_04109","SJAG_00881","SJAG_01675","SJAG_00696","SJAG_03266","SJAG_02481","SJAG_04266","SJAG_04013","SJAG_02225","SJAG_03620","SJAG_00129","SJAG_02921","SJAG_01502","SJAG_04660","SJAG_03362","SJAG_00653","SJAG_03002","SJAG_04746","SJAG_05216","SJAG_01826","SJAG_03492","SJAG_01697","SJAG_00682","SJAG_04587","SJAG_04153","SJAG_00560","SJAG_00191","SJAG_01162","SJAG_03320","SJAG_01624","SJAG_03144","SJAG_02289","SJAG_00317","SJAG_03356","SJAG_03349","SJAG_03720","SJAG_03087","SJAG_02482","SJAG_04612","SJAG_04130","SJAG_04815","SJAG_00203","SJAG_01226","SJAG_02288","SJAG_03272","SJAG_00853","SJAG_03791","SJAG_01625","SJAG_01382","SJAG_04611","SJAG_02741","SJAG_00251","SJAG_03782","SJAG_02106","SJAG_01477","SJAG_01172","SJAG_03055","SJAG_03133","SJAG_02785","SJAG_02852","SJAG_03696","SJAG_03684","SJAG_02522","SJAG_01794","SJAG_02474","SJAG_03352","SJAG_00609","SJAG_04704","SJAG_03971","SJAG_01444","SJAG_01194","SJAG_00964","SJAG_01664","SJAG_03026","SJAG_00214","SJAG_04563","SJAG_02172","SJAG_02695","SJAG_04960","SJAG_04379","SJAG_04204","SJAG_02664","SJAG_02648","SJAG_02231","SJAG_03398","SJAG_04086","SJAG_04268","SJAG_04092","SJAG_02304","SJAG_03128","SJAG_00202","SJAG_04534","SJAG_03886","SJAG_03753","SJAG_03868","SJAG_04188","SJAG_02813","SJAG_00916","SJAG_04166","SJAG_02994","SJAG_02570","SJAG_01360","SJAG_00432","SJAG_00921","SJAG_00987","SJAG_00743","SJAG_02426","SJAG_03172","SJAG_03498","SJAG_01844","SJAG_03224","SJAG_04108","SJAG_01458","SJAG_04491","SJAG_02995","SJAG_04470","SJAG_00228","SJAG_01784","SJAG_01482","SJAG_02890","SJAG_02713","SJAG_04454","SJAG_00309","SJAG_01926","SJAG_03132","SJAG_06636","SJAG_04385","SJAG_04436","SJAG_02465","SJAG_01497","SJAG_02569","SJAG_00563","SJAG_01690","SJAG_02840","SJAG_01135","SJAG_02499","SJAG_03545","SJAG_04427","SJAG_03275","SJAG_00443","SJAG_00960","SJAG_04025","SJAG_05184","SJAG_04297","SJAG_02184","SJAG_04453","SJAG_04023","SJAG_01900","SJAG_00321","SJAG_04253","SJAG_04825","SJAG_03519","SJAG_01002","SJAG_02075","SJAG_04399","SJAG_02594","SJAG_02206","SJAG_06588","SJAG_03403","SJAG_02287","SJAG_03312","SJAG_03743","SJAG_00125","SJAG_04383","SJAG_00982","SJAG_04082","SJAG_00337","SJAG_00757","SJAG_02699","SJAG_05032","SJAG_00504","SJAG_00409","SJAG_03227","SJAG_00918","SJAG_01397","SJAG_02763","SJAG_01562","SJAG_01376","SJAG_04220","SJAG_03882","SJAG_01992","SJAG_03049","SJAG_04501","SJAG_04486","SJAG_01686","SJAG_00546","SJAG_00422","SJAG_01762","SJAG_04511","SJAG_02988","SJAG_04242","SJAG_02546","SJAG_00629","SJAG_05014","SJAG_05023","SJAG_04935","SJAG_00413","SJAG_02608","SJAG_00573","SJAG_04074","SJAG_02290","SJAG_02444","SJAG_02022","SJAG_00249","SJAG_03306","SJAG_03223","SJAG_04688","SJAG_03659","SJAG_03876","SJAG_02801","SJAG_04990","SJAG_02400","SJAG_01371","SJAG_03986","SJAG_02277","SJAG_03422","SJAG_01430","SJAG_02370","SJAG_03225","SJAG_04368","SJAG_02096","SJAG_00245","SJAG_01886","SJAG_03756","SJAG_06599","SJAG_03732","SJAG_02977","SJAG_03336","SJAG_04360","SJAG_03238","SJAG_02561","SJAG_02850","SJAG_00173","SJAG_00550","SJAG_01251","SJAG_03158","SJAG_04227","SJAG_00074","SJAG_00480","SJAG_00436","SJAG_04948","SJAG_01644","SJAG_03091","SJAG_01218","SJAG_00509","SJAG_00910","SJAG_04467","SJAG_02315","SJAG_03533","SJAG_03793","SJAG_02630","SJAG_00246","SJAG_00663","SJAG_04724","SJAG_02210","SJAG_03891","SJAG_04404","SJAG_02486","SJAG_02541","SJAG_04066","SJAG_04981","SJAG_01599","SJAG_04559","SJAG_04414","SJAG_01385","SJAG_04912","SJAG_00766","SJAG_01467","SJAG_03335","SJAG_00113","SJAG_02048","SJAG_05304","SJAG_00806","SJAG_01428","SJAG_00843","SJAG_00805","SJAG_06309","SJAG_04366","SJAG_04381","SJAG_01364","SJAG_03434","SJAG_01020","SJAG_03580","SJAG_02390","SJAG_00795","SJAG_02887","SJAG_01150","SJAG_02585","SJAG_02214","SJAG_05185","SJAG_01366","SJAG_02421","SJAG_03708","SJAG_00858","SJAG_00471","SJAG_03825","SJAG_04125","SJAG_05276","SJAG_02312","SJAG_03197","SJAG_04460","SJAG_01788","SJAG_00707","SJAG_04417","SJAG_01746","SJAG_01864","SJAG_03597","SJAG_00958","SJAG_04609","SJAG_03074","SJAG_03575","SJAG_04939","SJAG_04449","SJAG_02851","SJAG_03845","SJAG_04936","SJAG_04286","SJAG_03424","SJAG_02871","SJAG_00320","SJAG_02655","SJAG_02627","SJAG_01131","SJAG_04476","SJAG_02146","SJAG_01987","SJAG_01010","SJAG_01737","SJAG_01018","SJAG_04270","SJAG_02121","SJAG_03549","SJAG_04029","SJAG_03762","SJAG_04131","SJAG_02309","SJAG_01259","SJAG_01744","SJAG_04042","SJAG_03614","SJAG_01535","SJAG_04999","SJAG_03556","SJAG_01786","SJAG_04283","SJAG_04273","SJAG_03340","SJAG_01533","SJAG_02226","SJAG_04465","SJAG_01850","SJAG_04384","SJAG_00490","SJAG_02954","SJAG_04089","SJAG_02531","SJAG_03537","SJAG_03706","SJAG_02621","SJAG_00234","SJAG_00980","SJAG_03193","SJAG_04394","SJAG_04191","SJAG_03309","SJAG_03136","SJAG_04781","SJAG_00252","SJAG_05303","SJAG_00225","SJAG_02945","SJAG_03797","SJAG_02923","SJAG_04487","SJAG_00382","SJAG_04844","SJAG_03896","SJAG_00091","SJAG_03629","SJAG_03122","SJAG_03096","SJAG_05334","SJAG_03469","SJAG_02748","SJAG_04197","SJAG_01359","SJAG_02408","SJAG_01869","SJAG_01917","SJAG_04054","SJAG_05316","SJAG_04966","SJAG_01245","SJAG_02891","SJAG_01312","SJAG_02033","SJAG_04751","SJAG_04756","SJAG_00447","SJAG_02282","SJAG_01556","SJAG_01581","SJAG_03090","SJAG_01089","SJAG_04390","SJAG_00118","SJAG_04312","SJAG_01197","SJAG_03658","SJAG_00637","SJAG_01870","SJAG_00706","SJAG_04344","SJAG_02193","SJAG_03752","SJAG_04332","SJAG_01308","SJAG_02215","SJAG_04429","SJAG_01427","SJAG_04072","SJAG_02911","SJAG_07013","SJAG_03072","SJAG_04518","SJAG_00729","SJAG_02894","SJAG_00220","SJAG_05287","SJAG_04461","SJAG_02798","SJAG_04147","SJAG_04459","SJAG_00742","SJAG_04539","SJAG_00937","SJAG_05312","SJAG_03258","SJAG_00584","SJAG_03570","SJAG_01279","SJAG_04478","SJAG_01901","SJAG_03592","SJAG_00791","SJAG_01030","SJAG_02470","SJAG_02610","SJAG_04663","SJAG_00293","SJAG_00614","SJAG_04031","SJAG_03070","SJAG_01440","SJAG_01772","SJAG_01791","SJAG_01734","SJAG_03690","SJAG_04848","SJAG_00644","SJAG_04458","SJAG_00377","SJAG_03802","SJAG_01449","SJAG_00498","SJAG_01662","SJAG_01620","SJAG_02805","SJAG_04282","SJAG_02467","SJAG_02107","SJAG_04499","SJAG_00765","SJAG_00281","SJAG_01768","SJAG_03010","SJAG_02973","SJAG_00803","SJAG_04481","SJAG_02576","SJAG_02509","SJAG_05266","SJAG_02583","SJAG_02453","SJAG_01328","SJAG_02378","SJAG_01320","SJAG_01650","SJAG_02799","SJAG_03472","SJAG_04888","SJAG_00777","SJAG_04198","SJAG_00287","SJAG_02375","SJAG_03998","SJAG_03964","SJAG_03404","SJAG_03473","SJAG_00611","SJAG_02235","SJAG_01608","SJAG_00035","SJAG_00600","SJAG_05277","SJAG_04264","SJAG_04357","SJAG_02788","SJAG_01058","SJAG_00301","SJAG_00948","SJAG_00503","SJAG_00541","SJAG_04650","SJAG_00112","SJAG_00190","SJAG_02234","SJAG_01114","SJAG_04148","SJAG_05003","SJAG_03977","SJAG_00508","SJAG_00839","SJAG_01383","SJAG_04633","SJAG_00207","SJAG_01974","SJAG_00529","SJAG_04849","SJAG_01016","SJAG_06576","SJAG_01142","SJAG_01298","SJAG_03950","SJAG_04549","SJAG_00487","SJAG_04896","SJAG_04410","SJAG_02755","SJAG_02335","SJAG_03958","SJAG_02176","SJAG_00491","SJAG_01436","SJAG_00441","SJAG_04355","SJAG_02271","SJAG_03863","SJAG_03159","SJAG_00702","SJAG_03357","SJAG_04978","SJAG_02026","SJAG_01659","SJAG_04580","SJAG_01185","SJAG_01379","SJAG_03627","SJAG_03433","SJAG_03043","SJAG_01447","SJAG_01014","SJAG_05021","SJAG_04674","SJAG_02198","SJAG_02506","SJAG_03631","SJAG_02667","SJAG_00419","SJAG_01074","SJAG_01072","SJAG_01515","SJAG_01874","SJAG_03852","SJAG_00482","SJAG_01372","SJAG_02770","SJAG_01897","SJAG_02189","SJAG_02180","SJAG_03717","SJAG_01481","SJAG_01233","SJAG_04291","SJAG_02456","SJAG_02471","SJAG_00134","SJAG_03470","SJAG_02404","SJAG_02730","SJAG_04711","SJAG_03694","SJAG_01384","SJAG_01367","SJAG_02905","SJAG_02728","SJAG_01202","SJAG_05331","SJAG_01255","SJAG_00343","SJAG_01851","SJAG_01361","SJAG_00206","SJAG_00668","SJAG_00878","SJAG_00221","SJAG_00314","SJAG_04160","SJAG_00993","SJAG_05256","SJAG_03508","SJAG_01342","SJAG_02687","SJAG_03718","SJAG_02364","SJAG_02207","SJAG_00469","SJAG_03865","SJAG_02174","SJAG_03838","SJAG_01827","SJAG_02307","SJAG_00289","SJAG_05283","SJAG_01955","SJAG_03411","SJAG_01810","SJAG_05019","SJAG_00395","SJAG_00971","SJAG_02984","SJAG_02510","SJAG_00748","SJAG_02791","SJAG_01808","SJAG_03883","SJAG_00969","SJAG_00738","SJAG_00592","SJAG_00941","SJAG_04482","SJAG_03067","SJAG_04927","SJAG_02876","SJAG_05192","SJAG_03233","SJAG_04434","SJAG_00455","SJAG_03131","SJAG_02992","SJAG_00975","SJAG_03488","SJAG_03345","SJAG_00178","SJAG_01302","SJAG_04051","SJAG_04865","SJAG_04894","SJAG_04044","SJAG_03102","SJAG_04335","SJAG_04201","SJAG_03835","SJAG_04988","SJAG_04324","SJAG_00854","SJAG_05206","SJAG_00461","SJAG_01805","SJAG_02542","SJAG_04863","SJAG_00298","SJAG_01742","SJAG_04878","SJAG_04020","SJAG_00940","SJAG_04672","SJAG_02279","SJAG_02625","SJAG_01715","SJAG_03903","SJAG_01341","SJAG_05007","SJAG_01631","SJAG_02790","SJAG_03499","SJAG_05248","SJAG_02783","SJAG_02024","SJAG_00633","SJAG_02151","SJAG_01789","SJAG_01809","SJAG_02562","SJAG_03686","SJAG_04877","SJAG_02858","SJAG_00439","SJAG_00857","SJAG_00181","SJAG_02182","SJAG_04372","SJAG_01198","SJAG_03326","SJAG_02926","SJAG_04337","SJAG_01721","SJAG_02000","SJAG_00326","SJAG_01352","SJAG_00435","SJAG_00043","SJAG_03283","SJAG_00117","SJAG_04369","SJAG_00903","SJAG_00527","SJAG_04187","SJAG_05018","SJAG_03828","SJAG_02904","SJAG_01641","SJAG_01027","SJAG_00226","SJAG_01545","SJAG_03277","SJAG_03210","SJAG_03230","SJAG_03523","SJAG_00135","SJAG_02020","SJAG_01673","SJAG_04144","SJAG_04784","SJAG_01652","SJAG_01666","SJAG_00104","SJAG_00053","SJAG_03245","SJAG_02005","SJAG_03291","SJAG_00103","SJAG_04618","SJAG_01775","SJAG_03035","SJAG_01622","SJAG_01704","SJAG_01605","SJAG_02704","SJAG_01908","SJAG_04880","SJAG_03017","SJAG_00704","SJAG_01938","SJAG_02116","SJAG_03693","SJAG_00719","SJAG_03229","SJAG_00579","SJAG_03276","SJAG_00596","SJAG_00624","SJAG_00474","SJAG_00874","SJAG_01822","SJAG_03704","SJAG_01774","SJAG_02203","SJAG_02439","SJAG_01432","SJAG_05195","SJAG_01228","SJAG_03890","SJAG_04128","SJAG_03431","SJAG_04695","SJAG_05024","SJAG_01322","SJAG_01693","SJAG_01317","SJAG_03504","SJAG_03254","SJAG_03934","SJAG_04741","SJAG_04953","SJAG_00467","SJAG_02046","SJAG_04607","SJAG_02063","SJAG_03949","SJAG_00338","SJAG_02605","SJAG_01708","SJAG_01558","SJAG_04359","SJAG_04726","SJAG_01222","SJAG_01186","SJAG_03666","SJAG_03884","SJAG_04477","SJAG_01314","SJAG_04338","SJAG_00327","SJAG_00283","SJAG_04754","SJAG_02425","SJAG_04212","SJAG_04998","SJAG_00355","SJAG_05252","SJAG_04456","SJAG_04860","SJAG_01566","SJAG_04665","SJAG_00957","SJAG_01335","SJAG_02042","SJAG_01596","SJAG_00845","SJAG_02814","SJAG_00114","SJAG_00223","SJAG_01457","SJAG_00169","SJAG_02181","SJAG_02349","SJAG_02766","SJAG_04577","SJAG_04764","SJAG_02618","SJAG_02135","SJAG_05004","SJAG_00378","SJAG_01418","SJAG_03248","SJAG_02978","SJAG_02715","SJAG_00850","SJAG_02640","SJAG_01346","SJAG_03237","SJAG_01284","SJAG_03463","SJAG_01898","SJAG_01338","SJAG_04306","SJAG_02265","SJAG_01240","SJAG_00632","SJAG_02700","SJAG_03086","SJAG_01783","SJAG_04112","SJAG_04484","SJAG_03045","SJAG_06622","SJAG_04846","SJAG_01268","SJAG_02912","SJAG_02245","SJAG_04043","SJAG_06621","SJAG_03651","SJAG_01311","SJAG_00483","SJAG_00827","SJAG_00578","SJAG_03036","SJAG_01609","SJAG_04163","SJAG_04213","SJAG_02010","SJAG_03285","SJAG_01118","SJAG_03673","SJAG_00162","SJAG_00662","SJAG_03191","SJAG_00779","SJAG_01825","SJAG_04747","SJAG_00978","SJAG_03182","SJAG_05337","SJAG_03214","SJAG_05332","SJAG_03881","SJAG_04847","SJAG_03771","SJAG_03682","SJAG_00501","SJAG_05011","SJAG_00800","SJAG_04653","SJAG_04271","SJAG_00712","SJAG_02030","SJAG_01958","SJAG_04320","SJAG_00995","SJAG_04079","SJAG_04843","SJAG_01561","SJAG_01979","SJAG_02661","SJAG_04842","SJAG_04334","SJAG_02768","SJAG_01635","SJAG_02803","SJAG_01544","SJAG_00963","SJAG_02764","SJAG_02374","SJAG_02337","SJAG_02251","SJAG_02498","SJAG_01146","SJAG_01301","SJAG_03571","SJAG_00908","SJAG_04679","SJAG_04232","SJAG_03264","SJAG_01522","SJAG_03113","SJAG_03692","SJAG_02749","SJAG_03021","SJAG_02812","SJAG_02369","SJAG_03140","SJAG_02671","SJAG_01453","SJAG_04234","SJAG_04159","SJAG_02553","SJAG_01137","SJAG_03376","SJAG_01565","SJAG_02017","SJAG_04535","SJAG_03688","SJAG_04121","SJAG_00823","SJAG_03313","SJAG_05978","SJAG_04061","SJAG_01665","SJAG_03855","SJAG_01519","SJAG_02682","SJAG_02794","SJAG_02419","SJAG_02436","SJAG_03963","SJAG_00256","SJAG_03547","SJAG_02275","SJAG_01611","SJAG_05413","SJAG_00316","SJAG_03041","SJAG_01885","SJAG_01455","SJAG_03761","SJAG_04520","SJAG_01387","SJAG_00466","SJAG_04350","SJAG_04874","SJAG_01949","SJAG_05694","SJAG_01521","SJAG_00495","SJAG_04100","SJAG_03534","SJAG_05197","SJAG_01621","SJAG_03062","SJAG_00366","SJAG_03901","SJAG_02034","SJAG_16460","SJAG_02738","SJAG_01081","SJAG_01510","SJAG_04943","SJAG_01606","SJAG_04655","SJAG_00039","SJAG_04129","SJAG_02194","SJAG_01576","SJAG_04472","SJAG_02380","SJAG_00762","SJAG_02061","SJAG_03107","SJAG_03540","SJAG_00184","SJAG_04149","SJAG_03996","SJAG_04002","SJAG_01054","SJAG_00532","SJAG_03726","SJAG_03681","SJAG_01220","SJAG_00885","SJAG_02551","SJAG_02256","SJAG_00189","SJAG_04713","SJAG_00514","SJAG_01269","SJAG_03500","SJAG_02512","SJAG_02314","SJAG_03638","SJAG_01492","SJAG_03847","SJAG_03532","SJAG_01656","SJAG_03665","SJAG_02138","SJAG_02165","SJAG_01499","SJAG_00871","SJAG_00325","SJAG_03375","SJAG_02596","SJAG_02712","SJAG_00141","SJAG_01042","SJAG_01024","SJAG_00585","SJAG_02505","SJAG_03554","SJAG_00674","SJAG_00591","SJAG_00176","SJAG_03455","SJAG_01500","SJAG_01182","SJAG_00128","SJAG_02549","SJAG_05926","SJAG_00567","SJAG_01283","SJAG_05223","SJAG_02057","SJAG_01274","SJAG_03222","SJAG_01575","SJAG_04774","SJAG_01277","SJAG_04007","SJAG_04540","SJAG_01287","SJAG_02321","SJAG_04595","SJAG_02490","SJAG_02733","SJAG_00164","SJAG_01291","SJAG_04009","SJAG_02300","SJAG_03204","SJAG_00145","SJAG_02672","SJAG_02520","SJAG_06612","SJAG_03919","SJAG_00869","SJAG_03915","SJAG_04977","SJAG_02041","SJAG_02461","SJAG_02885","SJAG_00353","SJAG_00155","SJAG_00749","SJAG_00586","SJAG_02197","SJAG_01534","SJAG_00989","SJAG_03267","SJAG_02342","SJAG_00768","SJAG_00115","SJAG_02320","SJAG_03494","SJAG_03127","SJAG_03151","SJAG_04290","SJAG_02575","SJAG_03857","SJAG_05208","SJAG_03630","SJAG_00167","SJAG_02746","SJAG_02619","SJAG_03250","SJAG_03354","SJAG_04126","SJAG_04069","SJAG_01840","SJAG_03407","SJAG_04233","SJAG_03371","SJAG_02442","SJAG_02750","SJAG_04347","SJAG_03380","SJAG_04380","SJAG_01053","SJAG_03714","SJAG_04012","SJAG_01710","SJAG_01910","SJAG_04879","SJAG_05232","SJAG_02329","SJAG_01817","SJAG_03588","SJAG_02828","SJAG_00374","SJAG_04866","SJAG_03012","SJAG_01203","SJAG_02889","SJAG_04285","SJAG_00798","SJAG_02058","SJAG_02796","SJAG_01167","SJAG_03085","SJAG_04634","SJAG_04150","SJAG_02572","SJAG_02863","SJAG_01733","SJAG_03486","SJAG_04263","SJAG_01083","SJAG_02101","SJAG_00670","SJAG_00476","SJAG_02938","SJAG_03323","SJAG_01117","SJAG_02868","SJAG_04744","SJAG_01064","SJAG_02663","SJAG_03723","SJAG_03561","SJAG_01824","SJAG_00464","SJAG_00820","SJAG_02595","SJAG_02016","SJAG_00811","SJAG_00243","SJAG_00427","SJAG_01153","SJAG_05261","SJAG_01370","SJAG_03528","SJAG_00832","SJAG_02230","SJAG_02752","SJAG_00720","SJAG_04638","SJAG_03525","SJAG_00694","SJAG_03551","SJAG_03924","SJAG_00468","SJAG_04735","SJAG_02558","SJAG_01512","SJAG_00724","SJAG_02148","SJAG_01632","SJAG_04033","SJAG_04397","SJAG_01997","SJAG_05222","SJAG_02774","SJAG_00034","SJAG_04763","SJAG_01293","SJAG_01048","SJAG_00448","SJAG_01740","SJAG_02609","SJAG_03703","SJAG_03014","SJAG_02081","SJAG_03454","SJAG_01000","SJAG_02306","SJAG_02243","SJAG_01610","SJAG_04586","SJAG_02015","SJAG_04172","SJAG_02600","SJAG_02819","SJAG_03568","SJAG_02517","SJAG_01646","SJAG_00645","SJAG_02240","SJAG_02280","SJAG_02401","SJAG_01598","SJAG_03425","SJAG_02593","SJAG_01702","SJAG_04536","SJAG_04455","SJAG_05030","SJAG_02681","SJAG_02747","SJAG_03788","SJAG_04155","SJAG_00237","SJAG_02414","SJAG_03634","SJAG_03166","SJAG_03029","SJAG_04824","SJAG_03663","SJAG_04871","SJAG_06284","SJAG_04011","SJAG_05253","SJAG_03263","SJAG_01884","SJAG_00544","SJAG_03805","SJAG_02202","SJAG_00801","SJAG_04693","SJAG_04968","SJAG_00440","SJAG_00143","SJAG_00041","SJAG_00739","SJAG_03879","SJAG_00890","SJAG_02705","SJAG_01022","SJAG_01516","SJAG_03959","SJAG_05010","SJAG_00044","SJAG_00728","SJAG_00524","SJAG_02679","SJAG_02441","SJAG_03279","SJAG_04182","SJAG_03479","SJAG_02601","SJAG_00059","SJAG_04921","SJAG_02869","SJAG_04902","SJAG_04062","SJAG_02424","SJAG_01720","SJAG_01629","SJAG_01012","SJAG_03507","SJAG_00689","SJAG_00561","SJAG_02524","SJAG_02582","SJAG_03810","SJAG_01787","SJAG_02379","SJAG_00244","SJAG_01489","SJAG_03150","SJAG_00364","SJAG_00656","SJAG_05179","SJAG_03983","SJAG_03889","SJAG_00577","SJAG_01252","SJAG_02347","SJAG_02854","SJAG_04457","SJAG_02972","SJAG_00531","SJAG_03174","SJAG_00324","SJAG_04235","SJAG_03346","SJAG_02497","SJAG_02178","SJAG_02866","SJAG_00814","SJAG_02327","SJAG_00507","SJAG_00571","SJAG_02604","SJAG_04629","SJAG_01679","SJAG_04861","SJAG_00902","SJAG_05333","SJAG_02044","SJAG_00942","SJAG_03646","SJAG_04917","SJAG_03601","SJAG_00518","SJAG_04229","SJAG_01667","SJAG_04276","SJAG_04579","SJAG_04666","SJAG_03818","SJAG_02323","SJAG_00736","SJAG_01547","SJAG_02357","SJAG_00397","SJAG_01296","SJAG_02726","SJAG_03211","SJAG_00523","SJAG_03623","SJAG_03789","SJAG_04431","SJAG_04022","SJAG_00272","SJAG_02266","SJAG_00925","SJAG_00990","SJAG_04700","SJAG_01759","SJAG_02895","SJAG_00224","SJAG_01643","SJAG_02367","SJAG_02336","SJAG_03485","SJAG_02358","SJAG_01235","SJAG_07017","SJAG_04003","SJAG_01568","SJAG_03660","SJAG_05033","SJAG_04300","SJAG_03679","SJAG_01676","SJAG_03527","SJAG_04342","SJAG_03457","SJAG_03618"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[57188,57831,58090,58340,59075,59169,59202,59447,59481,59513,59518,59564,59666,60087,60179,60638,61227,61577,61714,61726,61932,62234,62269,62794,64174,64307,64545,64780,65660,65908,66129,66264,66313,66374,66563,66668,66746,67375,67995,68748,69169,69259,69300,69463,70175,70210,70217,70234,70284,70343,70360,70377,70404,70434,70441,70442,70448,70460,70496,70514,70570,70637,70775,70813,70840,70845,70900,70927,71014,71040,71068,71076,71300,71330,71335,71446,71450,71452,71483,71532,71708,71849,71857,71895,71924,71946,71983,71990,72020,72026,72186,72191,72218,72258,72271,72299,72317,72340,72457,72460,72519,72558,72563,72593,72800,72806,72850,72877,72910,72918,72926,72976,72987,72991,73009,73048,73165,73257,73272,73343,73367,73380,73391,73409,73417,73506,73556,73692,73700,73723,73726,73749,73758,73776,73801,73999,74086,74111,74119,74121,74155,74168,74198,74230,74290,74333,74338,74369,74385,74410,74420,74517,74539,74606,74642,74723,74750,74782,74836,74897,74898,75001,75010,75024,75067,75078,75082,75131,75179,75193,75222,75249,75255,75324,75373,75396,75414,75485,75502,75519,75523,75571,75605,75609,75629,75644,75683,75721,75764,75786,75847,75905,75930,75974,76025,76085,76094,76127,76168,76278,76296,76301,76317,76378,76380,76476,76491,76530,76634,76665,76723,76777,76850,76861,76873,76882,76917,76949,76961,77092,77142,77152,77157,77259,77284,77421,77462,77477,77479,77487,77533,77554,77620,77626,77669,77760,77764,77847,77868,77967,78010,78082,78110,78157,78202,78221,78239,78291,78299,78358,78378,78493,78497,78504,78514,78543,78629,78658,78753,78792,78830,78850,78866,78913,78937,78947,78964,78976,78989,79015,79081,79088,79125,79136,79172,79210,79224,79268,79281,79293,79342,79359,79370,79397,79408,79425,79431,79501,79531,79567,79573,79575,79627,79631,79667,79709,79719,79745,79803,79841,79848,79882,79889,79904,80004,80014,80036,80043,80153,80262,80284,80309,80318,80338,80479,80507,80548,80692,80705,80716,80728,80741,80773,87723,87746,87771,87780,87803,87808,87811,87822,87855,87863,87873,87939,87970,87988,87993,88053,88069,88075,88083,88106,88125,88130,88139,88148,88188,88257,88284,88304,88312,88331,88338,88349,88387,88413,88468,88513,88531,88541,88566,88577,88579,88631,88636,88640,88648,88659,88677,88689,88696,88698,88702,88725,88745,88759,88788,88819,88855,88870,88897,88906,88913,88919,88925,88939,88959,88965,88994,89028,89047,89066,89070,89111,89117,89122,89138,89143,89150,89173,89181,89193,89210,89219,89231,89251,89258,89301,89397,89494,89548,89573,89640,89645,89661,89683,89723,89733,89753,89763,89802,89810,89823,89842,89866,89881,89884,89909,89924,89948,89976,89983,89988,90009,90017,90035,90053,90079,90089,90118,90125,90132,90138,90163,90174,90197,90225,90233,90237,90241,90259,90266,90278,90289,90357,90417,90430,90505,90508,90524,90538,90549,90590,90617,90638,90648,90666,90672,90696,90727,90739,90745,90765,90770,90779,90795,90889,90925,90940,90946,90960,90968,90982,91000,91009,91029,91046,91053,91082,91089,91102,91142,91164,91178,91201,91212,91276,91314,91325,91339,91400,91405,91410,91414,91437,91473,91497,91544,91552,91572,91587,91593,91622,91657,91663,91693,91741,91765,91774,91776,91785,91791,91794,91807,91814,91825,91835,91860,91881,91887,91901,91913,91917,91951,91954,91999,92008,92043,92065,92089,92107,92112,92150,92172,92206,92257,92270,92294,92308,92319,92333,92336,92343,92355,92365,92420,92424,92438,92445,92451,92472,92508,92524,92537,92542,92545,92550,92555,92559,92567,92601,92632,92670,92680,92690,92701,92782,92797,92802,92805,92811,92840,92848,92855,92863,92937,92976,93001,93006,93012,93029,93033,93104,93143,93151,93179,93188,93209,93217,93226,93248,93255,93272,93294,93309,93317,93332,93348,93364,93373,93431,93462,93463,93474,93514,93556,93579,93591,93599,93604,93637,93648,93659,93666,93690,93693,93703,93724,93731,93736,93740,93747,93792,93806,93817,93827,93830,93836,93847,93878,93887,93929,93969,93987,93996,94032,94046,94058,94089,94124,94165,94241,94273,94296,94332,94344,94381,94409,94427,94440,94446,94454,94468,94487,94493,94501,94506,94517,94523,94561,94574,94590,94608,94624,94628,94636,94649,94670,94684,94692,94699,94735,94789,94829,94846,94857,94874,94902,94909,94922,94931,94956,94994,95017,95025,95029,95035,95086,95119,95146,95158,95169,95234,95254,95281,95302,95320,95324,95329,95334,95348,95360,95367,95378,95383,95401,95409,95421,95467,95481,95486,95505,95521,95528,95561,95567,95583,95598,95629,95676,95686,95698,95719,95745,95751,95758,95769,95776,95794,95819,95825,95860,95865,95872,95894,95901,95917,95920,95940,95954,95966,95973,95989,96021,96048,96065,96082,96088,96119,96126,96205,96234,96240,96260,96272,96275,96281,96286,96292,96301,96367,96373,96379,96388,96393,96409,96424,96433,96462,96535,96547,96561,96567,96601,96608,96638,96643,96649,96658,96663,96709,96719,96742,96770,96793,96809,96815,96834,96841,96849,96859,96866,96905,96913,96920,96936,96997,97032,97054,97077,97084,97127,97139,97150,97191,97241,97266,97273,97278,97282,97302,97316,97333,97357,97369,97392,97394,97425,97431,97438,97460,97466,97470,97477,97510,97532,97540,97555,97566,97599,97630,97691,97726,97802,97837,97843,97844,97845,97846,97847,97886,97901,97909,97945,98005,98022,98030,98036,98054,98062,98068,98081,98112,98123,98143,98154,98166,98168,98173,98182,98218,98235,98263,98269,98275,98292,98361,98392,98431,98470,98476,98508,98558,98564,98568,98578,98591,98605,98609,98629,98637,98638,98639,98640,98641,98668,98678,98704,98764,98785,98788,98796,98866,98909,98910,99015,99048,99061,99122,99135,99139,99160,99167,99173,99180,99210,99217,99234,99251,99312,99322,99338,99344,99359,99460,99470,99511,99588,99594,99612,99656,99662,99666,99672,99702,99706,99718,99756,99808,99813,99823,99848,99872,99880,99902,99918,99931,99967,99988,99996,100005,100018,100034,100075,100093,100136,100185,100243,100252,100262,100291,100312,100387,100393,100401,100416,100423,100431,100478,100486,100493,100522,100534,100543,100553,100559,100571,100586,100619,100629,100643,100663,100672,100713,100739,100769,100832,100837,100853,100866,100883,100887,100889,100895,100929,100938,100949,100961,100981,100990,101002,101014,101017,101037,101042,101045,101052,101060,101121,101148,101160,101165,101184,101189,101212,101218,101239,101254,101259,101270,101275,101286,101311,101322,101343,101373,101378,101422,101429,101463,101467,101478,101501,101523,101539,101551,101555,101564,101572,101579,101598,101624,101634,101704,101739,101765,101835,101848,101863,101902,101903,101953,102001,102071,102082,102089,102098,102101,102110,102120,102151,102174,102185,102195,102202,102235,102244,102276,102296,102373,102393,102414,102415,102424,102436,102457,102515,102530,102543,102576,102619,102643,102656,102727,102735,102757,102772,102854,102869,102879,102888,102893,102898,102902,102955,102965,102984,102994,103004,103023,103040,103050,103062,103098,103105,103138,103182,103188,103203,103255,103260,103279,103302,103376,103401,103412,103444,103475,103491,103528,103551,103584,103602,103626,103650,103660,103663,103677,103686,103691,103739,103786,103814,103825,103844,103876,103892,103909,103925,103928,103933,103939,103972,104000,104009,104029,104034,104052,104070,104116,104136,104140,104181,104194,104199,104255,104264,104270,104277,104283,104348,104355,104372,104384,104435,104450,104456,104463,104531,104570,104585,104620,104626,104633,104640,104657,104663,104668,104712,104730,104746,104767,104820,104855,104868,104881,104887,104891,104908,104919,104945,104993,105018,105028,105034,105044,105046,105050,105061,105075,105088,105102,105120,105133,105142,105152,105155,105163,105212,105232,105251,105262,105286,105291,105336,105344,105349,105364,105373,105378,105380,105392,105395,105433,105442,105450,105475,105482,105491,105497,105515,105537,105552,105567,105570,105576,105594,105601,105624,105650,105657,105673,105688,105696,105716,105732,105739,105764,105807,105824,105832,105841,105855,105865,105888,105890,105923,105933,105940,105945,106033,106040,106065,106075,106092,106104,106110,106130,106154,106211,106237,106245,106254,106290,106345,106363,106387,106403,106433,106444,106450,106459,106470,106475,106499,106560,106562,106569,106601,106615,106653,106672,106684,106718,106728,106736,106754,106759,106777,106794,106800,106808,106842,106851,106852,106884,106916,106919,106928,106959,106984,106996,107013,107055,107077,107088,107101,107106,107111,107134,107139,107148,107155,107160,107170,107183,107214,107241,107253,107275,107288,107323,107330,107334,107355,107378,107387,107417,107433,107439,107447,107467,107487,107519,107528,107598,107612,107621,107676,107714,107734,107783,107795,107797,107809,107820,107825,107847,107856,107887,107910,107913,107937,107949,107966,107987,108074,108113,108171,108177,108189,108265,108313,108353,108356,108365,108377,108413,108437,108484,108495,108584,108606,108648,108667,108690,108753,108767,108794,108803,108810,108815,108837,108842,108884,108911,108922,108945,108989,109004,109024,109029,109059,109067,109088,109108,109115,109138,109144,109175,109186,109290,109301,109322,109329,109334,109387,109409,109428,109450,109458,109468,109469,109512,109527,109559,109573,109617,109653,109658,109689,109694,109695,109698,109700,109773,109789,109802,109810,109828,109834,109872,109883,109889,109904,109923,109928,109946,109954,110003,110013,110025,110042,110049,110058,110084,110091,110122,110129,110177,110190,110237,110246,110281,110307,110308,110341,110358,110369,110411,110440,110448,110459,110464,110468,110475,110482,110485,110515,110542,110551,110572,110584,110629,110650,110672,110699,110702,110722,110727,110732,110743,110774,110814,110822,110827,110842,110847,110874,110883,110923,110928,110942,110967,110982,110987,111002,111019,111025,111102,111127,111157,111165,111177,111187,111188,111193,111224,111232,111251,111254,111265,111286,111316,111330,111336,111358,111375,111400,111426,111429,111434,111460,111464,111471,111536,111550,111558,111569,111572,111602,111621,111642,111668,111677,111701,111708,111755,111760,111768,111779,111792,111817,111823,111828,111837,111843,111852,111871,111901,111943,111953,111963,111983,111996,112018,112080,112089,112104,112125,112131,112136,112146,112203,112217,112234,112257,112283,112317,112380,112386,112397,112432,112444,112477,112481,112522,112534,112541,112576,112592,112596,112621,112659,112670,112683,112700,112728,112734,112758,112771,112776,112867,112940,112946,112956,112964,112975,112981,113000,113022,113042,113066,113128,113150,113220,113224,113284,113292,113327,113336,113365,113390,113426,113430,113456,113487,113522,113547,113579,113629,113651,113661,113749,113762,113766,113778,113784,113825,113832,113853,113865,113881,113938,113946,113980,113993,114015,114097,114112,114116,114126,114132,114146,114151,114170,114248,114272,114298,114304,114309,114314,114358,114367,114377,114413,114420,114445,114467,114514,114549,114559,114569,114577,114627,114654,114658,114667,114711,114719,114741,114806,114868,114879,114888,114900,114923,114930,114942,114947,114962,114967,114975,114991,115007,115023,115068,115076,115106,115113,115117,115122,115142,115147,115151,115164,115167,115213,115226,115251,115258,115279,115289,115296,115318,115340,115363,115401,115420,115429,115436,115453,115484,115500,115544,115551,115561,115563,115604,115627,115637,115644,115664,115674,115681,115683,115692,115699,115713,115721,115730,115738,115753,115777,115809,115820,115840,115847,115853,115871,115876,115913,115932,115942,115956,115969,115981,116001,116022,116027,116034,116039,116058,116069,116081,116094,116099,116124,116132,116136,116177,116194,116210,116265,116277,116325,116342,116349,116356,116368,116381,116386,116389,116399,116411,116425,116437,116447,116451,116488,116493,116529,116546,116560,116609,116628,116632,116660,116666,116671,116676,116694,116733,116742,116749,116754,116776,116790,116795,116819,116898,116920,116930,116936,116943,117018,117039,117059,117079,117118,117121,117190,117198,117206,117210,117217,117219,117247,117280,117289,117300,117311,117345,117373,117381,117383,117388,117425,117432,117462,117466,117474,117521,117564,117581,117586,117597,117615,117631,117638,117655,117683,117699,117717,117740,117752,117782,117803,117811,117841,117861,117869,117910,117916,117989,118036,118060,118096,118098,118132,118141,118166,118185,118221,118239,118268,118276,118285,118297,118317,118322,118331,118357,118363,118372,118384,118475,118481,118510,118516,118522,118578,118584,118593,118610,118649,118658,118669,118678,118725,118766,118767,118768,118784,118801,118808,118840,118868,118896,118904,118912,118940,118946,118966,118968,119012,119021,119037,119117,119128,119162,119187,119210,119216,119242,119251,119289,119296,119403],"is_not":false,"summary":null,"term":"GO:0005829"},{"annotations":[78206],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005945"},{"annotations":[78521,78423,76571,73063,70134,80147,74014,77022],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005832"},{"annotations":[99258,100355],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904564"},{"annotations":[79723,89306,71871,68436],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097361"},{"annotations":[58259,75034,77292,75795,95242,79347,78492,71584,76138,71545,77186,75112,74786,73654,73296,74456,78797,74646,71574,80419,74627,70389,71462,75283,97489,77310,73974,70183,74478,68041,76866,78748,72055,72291,74095,80572,79482,74351,72265,112502,72534,75808,70699,70529,76759,91362,74003,80718,88418,78417,75733,91361,99489,70633,73537,91360,105970,105971,78530,114780,114824,72830,75307,114823,95241,72546,117180,74445,112503,70662,73593,78777,76818,117725,72452,72109,77074,77962,80176,97407,77787,72354,76437],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022625"},{"annotations":[108207],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022626"},{"annotations":[79454,105748,74871,73161,78996,74407,70774,74103,72308,75497,73785,58961,75087,80243,105749,114500,105722,76261,116594,107024,74806,73617,76277,78809,71541,100365,74873,114499,80603,80589,100115,71479,70197,74022,74026,78726,101870,116593,70367,95092,74711,77584,77015,100116,75576,77443,74212,113732,75580,101871,75096,105723,71559,76938,71293,91939,73646,77992,113734,69247],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022627"},{"annotations":[77890,106180],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002144"},{"annotations":[92033,95293,64846,118850],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090730"},{"annotations":[114174,98584,107195,109988,103421,93299,93529],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099128"},{"annotations":[105081,110170,93117,118151],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120510"},{"annotations":[70145,70715,77353],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000015"},{"annotations":[107570,76840],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005971"},{"annotations":[79871,115394],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0072380"},{"annotations":[70493,80179,73523],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033596"}]},"cv_name":"cellular_component","definition":"The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.","definition_xrefs":["GOC:hjd","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":2113,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00032":null,"SJAG_00033":null,"SJAG_00034":null,"SJAG_00035":null,"SJAG_00036":null,"SJAG_00037":null,"SJAG_00038":null,"SJAG_00039":null,"SJAG_00040":null,"SJAG_00041":null,"SJAG_00043":null,"SJAG_00044":null,"SJAG_00045":null,"SJAG_00049":null,"SJAG_00052":null,"SJAG_00053":null,"SJAG_00059":null,"SJAG_00063":null,"SJAG_00065":null,"SJAG_00067":null,"SJAG_00069":null,"SJAG_00072":null,"SJAG_00074":null,"SJAG_00084":null,"SJAG_00091":null,"SJAG_00092":null,"SJAG_00093":null,"SJAG_00095":null,"SJAG_00100":null,"SJAG_00102":null,"SJAG_00103":null,"SJAG_00104":null,"SJAG_00106":null,"SJAG_00107":null,"SJAG_00112":null,"SJAG_00113":null,"SJAG_00114":null,"SJAG_00115":null,"SJAG_00117":null,"SJAG_00118":null,"SJAG_00119":null,"SJAG_00120":null,"SJAG_00125":null,"SJAG_00126":null,"SJAG_00128":null,"SJAG_00129":null,"SJAG_00134":null,"SJAG_00135":null,"SJAG_00137":null,"SJAG_00141":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00145":null,"SJAG_00147":null,"SJAG_00150":null,"SJAG_00155":null,"SJAG_00161":null,"SJAG_00162":null,"SJAG_00164":null,"SJAG_00166":null,"SJAG_00167":null,"SJAG_00169":null,"SJAG_00172":null,"SJAG_00173":null,"SJAG_00176":null,"SJAG_00178":null,"SJAG_00179":null,"SJAG_00181":null,"SJAG_00184":null,"SJAG_00186":null,"SJAG_00188":null,"SJAG_00189":null,"SJAG_00190":null,"SJAG_00191":null,"SJAG_00202":null,"SJAG_00203":null,"SJAG_00206":null,"SJAG_00207":null,"SJAG_00208":null,"SJAG_00214":null,"SJAG_00219":null,"SJAG_00220":null,"SJAG_00221":null,"SJAG_00223":null,"SJAG_00224":null,"SJAG_00225":null,"SJAG_00226":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00230":null,"SJAG_00234":null,"SJAG_00237":null,"SJAG_00242":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00245":null,"SJAG_00246":null,"SJAG_00248":null,"SJAG_00249":null,"SJAG_00251":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00269":null,"SJAG_00270":null,"SJAG_00272":null,"SJAG_00280":null,"SJAG_00281":null,"SJAG_00283":null,"SJAG_00287":null,"SJAG_00289":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00298":null,"SJAG_00301":null,"SJAG_00306":null,"SJAG_00309":null,"SJAG_00314":null,"SJAG_00316":null,"SJAG_00317":null,"SJAG_00320":null,"SJAG_00321":null,"SJAG_00324":null,"SJAG_00325":null,"SJAG_00326":null,"SJAG_00327":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00337":null,"SJAG_00338":null,"SJAG_00341":null,"SJAG_00343":null,"SJAG_00350":null,"SJAG_00352":null,"SJAG_00353":null,"SJAG_00355":null,"SJAG_00356":null,"SJAG_00359":null,"SJAG_00364":null,"SJAG_00365":null,"SJAG_00366":null,"SJAG_00374":null,"SJAG_00376":null,"SJAG_00377":null,"SJAG_00378":null,"SJAG_00379":null,"SJAG_00381":null,"SJAG_00382":null,"SJAG_00384":null,"SJAG_00390":null,"SJAG_00395":null,"SJAG_00397":null,"SJAG_00400":null,"SJAG_00401":null,"SJAG_00409":null,"SJAG_00413":null,"SJAG_00414":null,"SJAG_00419":null,"SJAG_00420":null,"SJAG_00422":null,"SJAG_00423":null,"SJAG_00424":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00432":null,"SJAG_00435":null,"SJAG_00436":null,"SJAG_00439":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00448":null,"SJAG_00449":null,"SJAG_00450":null,"SJAG_00455":null,"SJAG_00457":null,"SJAG_00461":null,"SJAG_00463":null,"SJAG_00464":null,"SJAG_00465":null,"SJAG_00466":null,"SJAG_00467":null,"SJAG_00468":null,"SJAG_00469":null,"SJAG_00471":null,"SJAG_00472":null,"SJAG_00474":null,"SJAG_00476":null,"SJAG_00479":null,"SJAG_00480":null,"SJAG_00482":null,"SJAG_00483":null,"SJAG_00485":null,"SJAG_00486":null,"SJAG_00487":null,"SJAG_00489":null,"SJAG_00490":null,"SJAG_00491":null,"SJAG_00495":null,"SJAG_00498":null,"SJAG_00501":null,"SJAG_00503":null,"SJAG_00504":null,"SJAG_00505":null,"SJAG_00507":null,"SJAG_00508":null,"SJAG_00509":null,"SJAG_00512":null,"SJAG_00514":null,"SJAG_00518":null,"SJAG_00521":null,"SJAG_00523":null,"SJAG_00524":null,"SJAG_00526":null,"SJAG_00527":null,"SJAG_00529":null,"SJAG_00531":null,"SJAG_00532":null,"SJAG_00533":null,"SJAG_00534":null,"SJAG_00537":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00546":null,"SJAG_00550":null,"SJAG_00560":null,"SJAG_00561":null,"SJAG_00563":null,"SJAG_00567":null,"SJAG_00571":null,"SJAG_00572":null,"SJAG_00573":null,"SJAG_00574":null,"SJAG_00577":null,"SJAG_00578":null,"SJAG_00579":null,"SJAG_00580":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00585":null,"SJAG_00586":null,"SJAG_00591":null,"SJAG_00592":null,"SJAG_00594":null,"SJAG_00596":null,"SJAG_00599":null,"SJAG_00600":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00611":null,"SJAG_00614":null,"SJAG_00615":null,"SJAG_00622":null,"SJAG_00624":null,"SJAG_00629":null,"SJAG_00632":null,"SJAG_00633":null,"SJAG_00637":null,"SJAG_00642":null,"SJAG_00644":null,"SJAG_00645":null,"SJAG_00653":null,"SJAG_00656":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00668":null,"SJAG_00670":null,"SJAG_00674":null,"SJAG_00678":null,"SJAG_00682":null,"SJAG_00683":null,"SJAG_00685":null,"SJAG_00686":null,"SJAG_00689":null,"SJAG_00690":null,"SJAG_00691":null,"SJAG_00692":null,"SJAG_00694":null,"SJAG_00696":null,"SJAG_00702":null,"SJAG_00704":null,"SJAG_00706":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00718":null,"SJAG_00719":null,"SJAG_00720":null,"SJAG_00724":null,"SJAG_00726":null,"SJAG_00728":null,"SJAG_00729":null,"SJAG_00733":null,"SJAG_00736":null,"SJAG_00738":null,"SJAG_00739":null,"SJAG_00742":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00758":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00765":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00777":null,"SJAG_00778":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00788":null,"SJAG_00791":null,"SJAG_00795":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00800":null,"SJAG_00801":null,"SJAG_00803":null,"SJAG_00805":null,"SJAG_00806":null,"SJAG_00807":null,"SJAG_00808":null,"SJAG_00809":null,"SJAG_00811":null,"SJAG_00814":null,"SJAG_00815":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00822":null,"SJAG_00823":null,"SJAG_00827":null,"SJAG_00832":null,"SJAG_00837":null,"SJAG_00839":null,"SJAG_00840":null,"SJAG_00843":null,"SJAG_00845":null,"SJAG_00850":null,"SJAG_00853":null,"SJAG_00854":null,"SJAG_00856":null,"SJAG_00857":null,"SJAG_00858":null,"SJAG_00859":null,"SJAG_00864":null,"SJAG_00869":null,"SJAG_00871":null,"SJAG_00874":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00885":null,"SJAG_00888":null,"SJAG_00890":null,"SJAG_00892":null,"SJAG_00894":null,"SJAG_00898":null,"SJAG_00902":null,"SJAG_00903":null,"SJAG_00908":null,"SJAG_00910":null,"SJAG_00913":null,"SJAG_00916":null,"SJAG_00917":null,"SJAG_00918":null,"SJAG_00921":null,"SJAG_00925":null,"SJAG_00931":null,"SJAG_00937":null,"SJAG_00938":null,"SJAG_00940":null,"SJAG_00941":null,"SJAG_00942":null,"SJAG_00947":null,"SJAG_00948":null,"SJAG_00954":null,"SJAG_00955":null,"SJAG_00956":null,"SJAG_00957":null,"SJAG_00958":null,"SJAG_00960":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00967":null,"SJAG_00968":null,"SJAG_00969":null,"SJAG_00971":null,"SJAG_00972":null,"SJAG_00975":null,"SJAG_00978":null,"SJAG_00980":null,"SJAG_00982":null,"SJAG_00983":null,"SJAG_00986":null,"SJAG_00987":null,"SJAG_00988":null,"SJAG_00989":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01003":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01014":null,"SJAG_01016":null,"SJAG_01018":null,"SJAG_01020":null,"SJAG_01022":null,"SJAG_01024":null,"SJAG_01026":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01042":null,"SJAG_01047":null,"SJAG_01048":null,"SJAG_01053":null,"SJAG_01054":null,"SJAG_01055":null,"SJAG_01058":null,"SJAG_01061":null,"SJAG_01063":null,"SJAG_01064":null,"SJAG_01070":null,"SJAG_01072":null,"SJAG_01074":null,"SJAG_01075":null,"SJAG_01079":null,"SJAG_01081":null,"SJAG_01083":null,"SJAG_01087":null,"SJAG_01088":null,"SJAG_01089":null,"SJAG_01114":null,"SJAG_01117":null,"SJAG_01118":null,"SJAG_01121":null,"SJAG_01122":null,"SJAG_01126":null,"SJAG_01127":null,"SJAG_01128":null,"SJAG_01131":null,"SJAG_01132":null,"SJAG_01134":null,"SJAG_01135":null,"SJAG_01136":null,"SJAG_01137":null,"SJAG_01139":null,"SJAG_01142":null,"SJAG_01146":null,"SJAG_01148":null,"SJAG_01149":null,"SJAG_01150":null,"SJAG_01151":null,"SJAG_01153":null,"SJAG_01154":null,"SJAG_01159":null,"SJAG_01161":null,"SJAG_01162":null,"SJAG_01163":null,"SJAG_01166":null,"SJAG_01167":null,"SJAG_01172":null,"SJAG_01175":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01184":null,"SJAG_01185":null,"SJAG_01186":null,"SJAG_01187":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01194":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01199":null,"SJAG_01202":null,"SJAG_01203":null,"SJAG_01207":null,"SJAG_01209":null,"SJAG_01213":null,"SJAG_01214":null,"SJAG_01216":null,"SJAG_01218":null,"SJAG_01220":null,"SJAG_01222":null,"SJAG_01226":null,"SJAG_01228":null,"SJAG_01229":null,"SJAG_01231":null,"SJAG_01233":null,"SJAG_01235":null,"SJAG_01238":null,"SJAG_01240":null,"SJAG_01245":null,"SJAG_01248":null,"SJAG_01251":null,"SJAG_01252":null,"SJAG_01255":null,"SJAG_01259":null,"SJAG_01261":null,"SJAG_01266":null,"SJAG_01267":null,"SJAG_01268":null,"SJAG_01269":null,"SJAG_01270":null,"SJAG_01274":null,"SJAG_01277":null,"SJAG_01279":null,"SJAG_01283":null,"SJAG_01284":null,"SJAG_01287":null,"SJAG_01291":null,"SJAG_01292":null,"SJAG_01293":null,"SJAG_01296":null,"SJAG_01298":null,"SJAG_01301":null,"SJAG_01302":null,"SJAG_01308":null,"SJAG_01310":null,"SJAG_01311":null,"SJAG_01312":null,"SJAG_01313":null,"SJAG_01314":null,"SJAG_01317":null,"SJAG_01320":null,"SJAG_01322":null,"SJAG_01325":null,"SJAG_01328":null,"SJAG_01333":null,"SJAG_01335":null,"SJAG_01338":null,"SJAG_01339":null,"SJAG_01341":null,"SJAG_01342":null,"SJAG_01346":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01359":null,"SJAG_01360":null,"SJAG_01361":null,"SJAG_01362":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01367":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01372":null,"SJAG_01375":null,"SJAG_01376":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01383":null,"SJAG_01384":null,"SJAG_01385":null,"SJAG_01386":null,"SJAG_01387":null,"SJAG_01389":null,"SJAG_01397":null,"SJAG_01404":null,"SJAG_01408":null,"SJAG_01411":null,"SJAG_01415":null,"SJAG_01418":null,"SJAG_01425":null,"SJAG_01427":null,"SJAG_01428":null,"SJAG_01430":null,"SJAG_01432":null,"SJAG_01434":null,"SJAG_01436":null,"SJAG_01438":null,"SJAG_01440":null,"SJAG_01443":null,"SJAG_01444":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01453":null,"SJAG_01455":null,"SJAG_01457":null,"SJAG_01458":null,"SJAG_01461":null,"SJAG_01467":null,"SJAG_01472":null,"SJAG_01474":null,"SJAG_01475":null,"SJAG_01477":null,"SJAG_01479":null,"SJAG_01480":null,"SJAG_01481":null,"SJAG_01482":null,"SJAG_01487":null,"SJAG_01488":null,"SJAG_01489":null,"SJAG_01492":null,"SJAG_01496":null,"SJAG_01497":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01501":null,"SJAG_01502":null,"SJAG_01508":null,"SJAG_01510":null,"SJAG_01512":null,"SJAG_01515":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01521":null,"SJAG_01522":null,"SJAG_01528":null,"SJAG_01529":null,"SJAG_01531":null,"SJAG_01533":null,"SJAG_01534":null,"SJAG_01535":null,"SJAG_01540":null,"SJAG_01543":null,"SJAG_01544":null,"SJAG_01545":null,"SJAG_01547":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01556":null,"SJAG_01558":null,"SJAG_01561":null,"SJAG_01562":null,"SJAG_01565":null,"SJAG_01566":null,"SJAG_01568":null,"SJAG_01575":null,"SJAG_01576":null,"SJAG_01580":null,"SJAG_01581":null,"SJAG_01582":null,"SJAG_01587":null,"SJAG_01588":null,"SJAG_01590":null,"SJAG_01596":null,"SJAG_01598":null,"SJAG_01599":null,"SJAG_01605":null,"SJAG_01606":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01617":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01621":null,"SJAG_01622":null,"SJAG_01624":null,"SJAG_01625":null,"SJAG_01628":null,"SJAG_01629":null,"SJAG_01630":null,"SJAG_01631":null,"SJAG_01632":null,"SJAG_01635":null,"SJAG_01637":null,"SJAG_01641":null,"SJAG_01643":null,"SJAG_01644":null,"SJAG_01645":null,"SJAG_01646":null,"SJAG_01650":null,"SJAG_01651":null,"SJAG_01652":null,"SJAG_01655":null,"SJAG_01656":null,"SJAG_01658":null,"SJAG_01659":null,"SJAG_01662":null,"SJAG_01663":null,"SJAG_01664":null,"SJAG_01665":null,"SJAG_01666":null,"SJAG_01667":null,"SJAG_01673":null,"SJAG_01675":null,"SJAG_01676":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01686":null,"SJAG_01690":null,"SJAG_01693":null,"SJAG_01694":null,"SJAG_01696":null,"SJAG_01697":null,"SJAG_01698":null,"SJAG_01702":null,"SJAG_01703":null,"SJAG_01704":null,"SJAG_01708":null,"SJAG_01710":null,"SJAG_01714":null,"SJAG_01715":null,"SJAG_01720":null,"SJAG_01721":null,"SJAG_01722":null,"SJAG_01733":null,"SJAG_01734":null,"SJAG_01737":null,"SJAG_01740":null,"SJAG_01742":null,"SJAG_01744":null,"SJAG_01746":null,"SJAG_01748":null,"SJAG_01759":null,"SJAG_01760":null,"SJAG_01762":null,"SJAG_01765":null,"SJAG_01768":null,"SJAG_01772":null,"SJAG_01774":null,"SJAG_01775":null,"SJAG_01776":null,"SJAG_01781":null,"SJAG_01783":null,"SJAG_01784":null,"SJAG_01786":null,"SJAG_01787":null,"SJAG_01788":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01794":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01801":null,"SJAG_01805":null,"SJAG_01808":null,"SJAG_01809":null,"SJAG_01810":null,"SJAG_01812":null,"SJAG_01817":null,"SJAG_01818":null,"SJAG_01822":null,"SJAG_01824":null,"SJAG_01825":null,"SJAG_01826":null,"SJAG_01827":null,"SJAG_01830":null,"SJAG_01833":null,"SJAG_01839":null,"SJAG_01840":null,"SJAG_01841":null,"SJAG_01844":null,"SJAG_01850":null,"SJAG_01851":null,"SJAG_01852":null,"SJAG_01853":null,"SJAG_01858":null,"SJAG_01859":null,"SJAG_01864":null,"SJAG_01869":null,"SJAG_01870":null,"SJAG_01874":null,"SJAG_01884":null,"SJAG_01885":null,"SJAG_01886":null,"SJAG_01897":null,"SJAG_01898":null,"SJAG_01900":null,"SJAG_01901":null,"SJAG_01908":null,"SJAG_01910":null,"SJAG_01914":null,"SJAG_01917":null,"SJAG_01918":null,"SJAG_01919":null,"SJAG_01926":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01943":null,"SJAG_01944":null,"SJAG_01949":null,"SJAG_01954":null,"SJAG_01955":null,"SJAG_01958":null,"SJAG_01974":null,"SJAG_01979":null,"SJAG_01986":null,"SJAG_01987":null,"SJAG_01992":null,"SJAG_01995":null,"SJAG_01997":null,"SJAG_02000":null,"SJAG_02004":null,"SJAG_02005":null,"SJAG_02009":null,"SJAG_02010":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02015":null,"SJAG_02016":null,"SJAG_02017":null,"SJAG_02020":null,"SJAG_02022":null,"SJAG_02024":null,"SJAG_02026":null,"SJAG_02030":null,"SJAG_02033":null,"SJAG_02034":null,"SJAG_02035":null,"SJAG_02038":null,"SJAG_02040":null,"SJAG_02041":null,"SJAG_02042":null,"SJAG_02043":null,"SJAG_02044":null,"SJAG_02046":null,"SJAG_02047":null,"SJAG_02048":null,"SJAG_02057":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02063":null,"SJAG_02065":null,"SJAG_02066":null,"SJAG_02069":null,"SJAG_02070":null,"SJAG_02075":null,"SJAG_02081":null,"SJAG_02082":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02096":null,"SJAG_02098":null,"SJAG_02101":null,"SJAG_02106":null,"SJAG_02107":null,"SJAG_02116":null,"SJAG_02121":null,"SJAG_02135":null,"SJAG_02138":null,"SJAG_02145":null,"SJAG_02146":null,"SJAG_02148":null,"SJAG_02151":null,"SJAG_02154":null,"SJAG_02164":null,"SJAG_02165":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02170":null,"SJAG_02171":null,"SJAG_02172":null,"SJAG_02174":null,"SJAG_02176":null,"SJAG_02177":null,"SJAG_02178":null,"SJAG_02179":null,"SJAG_02180":null,"SJAG_02181":null,"SJAG_02182":null,"SJAG_02184":null,"SJAG_02186":null,"SJAG_02189":null,"SJAG_02191":null,"SJAG_02193":null,"SJAG_02194":null,"SJAG_02197":null,"SJAG_02198":null,"SJAG_02202":null,"SJAG_02203":null,"SJAG_02206":null,"SJAG_02207":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02213":null,"SJAG_02214":null,"SJAG_02215":null,"SJAG_02218":null,"SJAG_02224":null,"SJAG_02225":null,"SJAG_02226":null,"SJAG_02230":null,"SJAG_02231":null,"SJAG_02233":null,"SJAG_02234":null,"SJAG_02235":null,"SJAG_02237":null,"SJAG_02239":null,"SJAG_02240":null,"SJAG_02243":null,"SJAG_02245":null,"SJAG_02251":null,"SJAG_02253":null,"SJAG_02256":null,"SJAG_02265":null,"SJAG_02266":null,"SJAG_02267":null,"SJAG_02268":null,"SJAG_02269":null,"SJAG_02270":null,"SJAG_02271":null,"SJAG_02275":null,"SJAG_02277":null,"SJAG_02279":null,"SJAG_02280":null,"SJAG_02281":null,"SJAG_02282":null,"SJAG_02283":null,"SJAG_02285":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02289":null,"SJAG_02290":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02300":null,"SJAG_02304":null,"SJAG_02306":null,"SJAG_02307":null,"SJAG_02309":null,"SJAG_02312":null,"SJAG_02313":null,"SJAG_02314":null,"SJAG_02315":null,"SJAG_02320":null,"SJAG_02321":null,"SJAG_02323":null,"SJAG_02327":null,"SJAG_02329":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02337":null,"SJAG_02339":null,"SJAG_02340":null,"SJAG_02342":null,"SJAG_02347":null,"SJAG_02349":null,"SJAG_02352":null,"SJAG_02357":null,"SJAG_02358":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02367":null,"SJAG_02369":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02375":null,"SJAG_02376":null,"SJAG_02378":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02386":null,"SJAG_02387":null,"SJAG_02390":null,"SJAG_02393":null,"SJAG_02400":null,"SJAG_02401":null,"SJAG_02404":null,"SJAG_02405":null,"SJAG_02408":null,"SJAG_02414":null,"SJAG_02415":null,"SJAG_02419":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02422":null,"SJAG_02424":null,"SJAG_02425":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02434":null,"SJAG_02436":null,"SJAG_02439":null,"SJAG_02441":null,"SJAG_02442":null,"SJAG_02444":null,"SJAG_02450":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02461":null,"SJAG_02462":null,"SJAG_02465":null,"SJAG_02467":null,"SJAG_02470":null,"SJAG_02471":null,"SJAG_02474":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02481":null,"SJAG_02482":null,"SJAG_02485":null,"SJAG_02486":null,"SJAG_02490":null,"SJAG_02491":null,"SJAG_02493":null,"SJAG_02497":null,"SJAG_02498":null,"SJAG_02499":null,"SJAG_02502":null,"SJAG_02503":null,"SJAG_02505":null,"SJAG_02506":null,"SJAG_02508":null,"SJAG_02509":null,"SJAG_02510":null,"SJAG_02512":null,"SJAG_02515":null,"SJAG_02517":null,"SJAG_02518":null,"SJAG_02520":null,"SJAG_02522":null,"SJAG_02524":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02540":null,"SJAG_02541":null,"SJAG_02542":null,"SJAG_02546":null,"SJAG_02547":null,"SJAG_02549":null,"SJAG_02551":null,"SJAG_02553":null,"SJAG_02558":null,"SJAG_02561":null,"SJAG_02562":null,"SJAG_02569":null,"SJAG_02570":null,"SJAG_02572":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02583":null,"SJAG_02585":null,"SJAG_02589":null,"SJAG_02591":null,"SJAG_02592":null,"SJAG_02593":null,"SJAG_02594":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02597":null,"SJAG_02600":null,"SJAG_02601":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02608":null,"SJAG_02609":null,"SJAG_02610":null,"SJAG_02611":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02621":null,"SJAG_02625":null,"SJAG_02627":null,"SJAG_02630":null,"SJAG_02640":null,"SJAG_02645":null,"SJAG_02647":null,"SJAG_02648":null,"SJAG_02655":null,"SJAG_02659":null,"SJAG_02661":null,"SJAG_02663":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02671":null,"SJAG_02672":null,"SJAG_02673":null,"SJAG_02679":null,"SJAG_02681":null,"SJAG_02682":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02687":null,"SJAG_02688":null,"SJAG_02689":null,"SJAG_02692":null,"SJAG_02695":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02699":null,"SJAG_02700":null,"SJAG_02702":null,"SJAG_02704":null,"SJAG_02705":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02715":null,"SJAG_02718":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02726":null,"SJAG_02728":null,"SJAG_02730":null,"SJAG_02731":null,"SJAG_02733":null,"SJAG_02734":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02740":null,"SJAG_02741":null,"SJAG_02745":null,"SJAG_02746":null,"SJAG_02747":null,"SJAG_02748":null,"SJAG_02749":null,"SJAG_02750":null,"SJAG_02752":null,"SJAG_02753":null,"SJAG_02755":null,"SJAG_02756":null,"SJAG_02760":null,"SJAG_02763":null,"SJAG_02764":null,"SJAG_02765":null,"SJAG_02766":null,"SJAG_02768":null,"SJAG_02769":null,"SJAG_02770":null,"SJAG_02771":null,"SJAG_02774":null,"SJAG_02783":null,"SJAG_02785":null,"SJAG_02786":null,"SJAG_02788":null,"SJAG_02789":null,"SJAG_02790":null,"SJAG_02791":null,"SJAG_02794":null,"SJAG_02796":null,"SJAG_02797":null,"SJAG_02798":null,"SJAG_02799":null,"SJAG_02801":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02805":null,"SJAG_02808":null,"SJAG_02811":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02814":null,"SJAG_02817":null,"SJAG_02819":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_02832":null,"SJAG_02833":null,"SJAG_02840":null,"SJAG_02843":null,"SJAG_02845":null,"SJAG_02850":null,"SJAG_02851":null,"SJAG_02852":null,"SJAG_02854":null,"SJAG_02857":null,"SJAG_02858":null,"SJAG_02861":null,"SJAG_02863":null,"SJAG_02864":null,"SJAG_02866":null,"SJAG_02868":null,"SJAG_02869":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02874":null,"SJAG_02876":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02885":null,"SJAG_02886":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02895":null,"SJAG_02902":null,"SJAG_02904":null,"SJAG_02905":null,"SJAG_02911":null,"SJAG_02912":null,"SJAG_02918":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02938":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_02956":null,"SJAG_02959":null,"SJAG_02972":null,"SJAG_02973":null,"SJAG_02977":null,"SJAG_02978":null,"SJAG_02984":null,"SJAG_02988":null,"SJAG_02992":null,"SJAG_02994":null,"SJAG_02995":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03009":null,"SJAG_03010":null,"SJAG_03012":null,"SJAG_03013":null,"SJAG_03014":null,"SJAG_03017":null,"SJAG_03019":null,"SJAG_03021":null,"SJAG_03022":null,"SJAG_03026":null,"SJAG_03029":null,"SJAG_03034":null,"SJAG_03035":null,"SJAG_03036":null,"SJAG_03037":null,"SJAG_03041":null,"SJAG_03043":null,"SJAG_03045":null,"SJAG_03049":null,"SJAG_03051":null,"SJAG_03055":null,"SJAG_03062":null,"SJAG_03063":null,"SJAG_03067":null,"SJAG_03070":null,"SJAG_03072":null,"SJAG_03074":null,"SJAG_03081":null,"SJAG_03082":null,"SJAG_03085":null,"SJAG_03086":null,"SJAG_03087":null,"SJAG_03089":null,"SJAG_03090":null,"SJAG_03091":null,"SJAG_03094":null,"SJAG_03095":null,"SJAG_03096":null,"SJAG_03098":null,"SJAG_03102":null,"SJAG_03106":null,"SJAG_03107":null,"SJAG_03108":null,"SJAG_03113":null,"SJAG_03119":null,"SJAG_03122":null,"SJAG_03124":null,"SJAG_03126":null,"SJAG_03127":null,"SJAG_03128":null,"SJAG_03130":null,"SJAG_03131":null,"SJAG_03132":null,"SJAG_03133":null,"SJAG_03136":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03142":null,"SJAG_03144":null,"SJAG_03147":null,"SJAG_03150":null,"SJAG_03151":null,"SJAG_03153":null,"SJAG_03158":null,"SJAG_03159":null,"SJAG_03164":null,"SJAG_03166":null,"SJAG_03167":null,"SJAG_03172":null,"SJAG_03174":null,"SJAG_03179":null,"SJAG_03181":null,"SJAG_03182":null,"SJAG_03185":null,"SJAG_03186":null,"SJAG_03188":null,"SJAG_03189":null,"SJAG_03191":null,"SJAG_03193":null,"SJAG_03197":null,"SJAG_03204":null,"SJAG_03209":null,"SJAG_03210":null,"SJAG_03211":null,"SJAG_03214":null,"SJAG_03215":null,"SJAG_03219":null,"SJAG_03222":null,"SJAG_03223":null,"SJAG_03224":null,"SJAG_03225":null,"SJAG_03227":null,"SJAG_03228":null,"SJAG_03229":null,"SJAG_03230":null,"SJAG_03231":null,"SJAG_03233":null,"SJAG_03234":null,"SJAG_03237":null,"SJAG_03238":null,"SJAG_03241":null,"SJAG_03243":null,"SJAG_03245":null,"SJAG_03246":null,"SJAG_03248":null,"SJAG_03250":null,"SJAG_03254":null,"SJAG_03257":null,"SJAG_03258":null,"SJAG_03262":null,"SJAG_03263":null,"SJAG_03264":null,"SJAG_03266":null,"SJAG_03267":null,"SJAG_03272":null,"SJAG_03275":null,"SJAG_03276":null,"SJAG_03277":null,"SJAG_03278":null,"SJAG_03279":null,"SJAG_03283":null,"SJAG_03285":null,"SJAG_03288":null,"SJAG_03291":null,"SJAG_03293":null,"SJAG_03298":null,"SJAG_03306":null,"SJAG_03309":null,"SJAG_03312":null,"SJAG_03313":null,"SJAG_03319":null,"SJAG_03320":null,"SJAG_03321":null,"SJAG_03323":null,"SJAG_03325":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03336":null,"SJAG_03340":null,"SJAG_03345":null,"SJAG_03346":null,"SJAG_03349":null,"SJAG_03350":null,"SJAG_03352":null,"SJAG_03354":null,"SJAG_03356":null,"SJAG_03357":null,"SJAG_03361":null,"SJAG_03362":null,"SJAG_03364":null,"SJAG_03367":null,"SJAG_03371":null,"SJAG_03373":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03376":null,"SJAG_03377":null,"SJAG_03380":null,"SJAG_03383":null,"SJAG_03384":null,"SJAG_03398":null,"SJAG_03403":null,"SJAG_03404":null,"SJAG_03407":null,"SJAG_03408":null,"SJAG_03409":null,"SJAG_03411":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03431":null,"SJAG_03432":null,"SJAG_03433":null,"SJAG_03434":null,"SJAG_03438":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03455":null,"SJAG_03457":null,"SJAG_03463":null,"SJAG_03469":null,"SJAG_03470":null,"SJAG_03472":null,"SJAG_03473":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03482":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03487":null,"SJAG_03488":null,"SJAG_03492":null,"SJAG_03494":null,"SJAG_03495":null,"SJAG_03498":null,"SJAG_03499":null,"SJAG_03500":null,"SJAG_03501":null,"SJAG_03504":null,"SJAG_03507":null,"SJAG_03508":null,"SJAG_03519":null,"SJAG_03523":null,"SJAG_03525":null,"SJAG_03527":null,"SJAG_03528":null,"SJAG_03529":null,"SJAG_03532":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03537":null,"SJAG_03540":null,"SJAG_03541":null,"SJAG_03544":null,"SJAG_03545":null,"SJAG_03547":null,"SJAG_03548":null,"SJAG_03549":null,"SJAG_03551":null,"SJAG_03554":null,"SJAG_03556":null,"SJAG_03558":null,"SJAG_03561":null,"SJAG_03562":null,"SJAG_03568":null,"SJAG_03570":null,"SJAG_03571":null,"SJAG_03575":null,"SJAG_03576":null,"SJAG_03580":null,"SJAG_03581":null,"SJAG_03582":null,"SJAG_03588":null,"SJAG_03589":null,"SJAG_03592":null,"SJAG_03597":null,"SJAG_03601":null,"SJAG_03603":null,"SJAG_03605":null,"SJAG_03614":null,"SJAG_03616":null,"SJAG_03617":null,"SJAG_03618":null,"SJAG_03620":null,"SJAG_03623":null,"SJAG_03624":null,"SJAG_03626":null,"SJAG_03627":null,"SJAG_03629":null,"SJAG_03630":null,"SJAG_03631":null,"SJAG_03632":null,"SJAG_03634":null,"SJAG_03638":null,"SJAG_03643":null,"SJAG_03646":null,"SJAG_03651":null,"SJAG_03653":null,"SJAG_03655":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03662":null,"SJAG_03663":null,"SJAG_03665":null,"SJAG_03666":null,"SJAG_03668":null,"SJAG_03669":null,"SJAG_03673":null,"SJAG_03677":null,"SJAG_03678":null,"SJAG_03679":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03686":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03690":null,"SJAG_03692":null,"SJAG_03693":null,"SJAG_03694":null,"SJAG_03696":null,"SJAG_03697":null,"SJAG_03701":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03706":null,"SJAG_03708":null,"SJAG_03714":null,"SJAG_03717":null,"SJAG_03718":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03723":null,"SJAG_03726":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03733":null,"SJAG_03743":null,"SJAG_03751":null,"SJAG_03752":null,"SJAG_03753":null,"SJAG_03756":null,"SJAG_03758":null,"SJAG_03760":null,"SJAG_03761":null,"SJAG_03762":null,"SJAG_03771":null,"SJAG_03775":null,"SJAG_03781":null,"SJAG_03782":null,"SJAG_03784":null,"SJAG_03786":null,"SJAG_03788":null,"SJAG_03789":null,"SJAG_03791":null,"SJAG_03793":null,"SJAG_03794":null,"SJAG_03797":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03805":null,"SJAG_03810":null,"SJAG_03811":null,"SJAG_03815":null,"SJAG_03818":null,"SJAG_03821":null,"SJAG_03825":null,"SJAG_03828":null,"SJAG_03835":null,"SJAG_03838":null,"SJAG_03839":null,"SJAG_03842":null,"SJAG_03845":null,"SJAG_03847":null,"SJAG_03849":null,"SJAG_03852":null,"SJAG_03854":null,"SJAG_03855":null,"SJAG_03856":null,"SJAG_03857":null,"SJAG_03859":null,"SJAG_03862":null,"SJAG_03863":null,"SJAG_03865":null,"SJAG_03868":null,"SJAG_03872":null,"SJAG_03876":null,"SJAG_03879":null,"SJAG_03881":null,"SJAG_03882":null,"SJAG_03883":null,"SJAG_03884":null,"SJAG_03886":null,"SJAG_03888":null,"SJAG_03889":null,"SJAG_03890":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03901":null,"SJAG_03903":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03919":null,"SJAG_03921":null,"SJAG_03922":null,"SJAG_03924":null,"SJAG_03932":null,"SJAG_03934":null,"SJAG_03936":null,"SJAG_03937":null,"SJAG_03949":null,"SJAG_03950":null,"SJAG_03955":null,"SJAG_03958":null,"SJAG_03959":null,"SJAG_03963":null,"SJAG_03964":null,"SJAG_03971":null,"SJAG_03977":null,"SJAG_03983":null,"SJAG_03986":null,"SJAG_03990":null,"SJAG_03996":null,"SJAG_03998":null,"SJAG_04002":null,"SJAG_04003":null,"SJAG_04007":null,"SJAG_04009":null,"SJAG_04011":null,"SJAG_04012":null,"SJAG_04013":null,"SJAG_04015":null,"SJAG_04016":null,"SJAG_04020":null,"SJAG_04021":null,"SJAG_04022":null,"SJAG_04023":null,"SJAG_04025":null,"SJAG_04027":null,"SJAG_04029":null,"SJAG_04030":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04033":null,"SJAG_04036":null,"SJAG_04042":null,"SJAG_04043":null,"SJAG_04044":null,"SJAG_04051":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04060":null,"SJAG_04061":null,"SJAG_04062":null,"SJAG_04066":null,"SJAG_04069":null,"SJAG_04070":null,"SJAG_04072":null,"SJAG_04074":null,"SJAG_04077":null,"SJAG_04079":null,"SJAG_04082":null,"SJAG_04083":null,"SJAG_04084":null,"SJAG_04085":null,"SJAG_04086":null,"SJAG_04088":null,"SJAG_04089":null,"SJAG_04091":null,"SJAG_04092":null,"SJAG_04093":null,"SJAG_04097":null,"SJAG_04100":null,"SJAG_04106":null,"SJAG_04107":null,"SJAG_04108":null,"SJAG_04109":null,"SJAG_04112":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04123":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04128":null,"SJAG_04129":null,"SJAG_04130":null,"SJAG_04131":null,"SJAG_04144":null,"SJAG_04147":null,"SJAG_04148":null,"SJAG_04149":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04155":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04159":null,"SJAG_04160":null,"SJAG_04161":null,"SJAG_04163":null,"SJAG_04166":null,"SJAG_04168":null,"SJAG_04169":null,"SJAG_04170":null,"SJAG_04172":null,"SJAG_04174":null,"SJAG_04175":null,"SJAG_04176":null,"SJAG_04177":null,"SJAG_04179":null,"SJAG_04181":null,"SJAG_04182":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04188":null,"SJAG_04190":null,"SJAG_04191":null,"SJAG_04192":null,"SJAG_04197":null,"SJAG_04198":null,"SJAG_04201":null,"SJAG_04202":null,"SJAG_04204":null,"SJAG_04211":null,"SJAG_04212":null,"SJAG_04213":null,"SJAG_04214":null,"SJAG_04219":null,"SJAG_04220":null,"SJAG_04227":null,"SJAG_04229":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04234":null,"SJAG_04235":null,"SJAG_04242":null,"SJAG_04248":null,"SJAG_04249":null,"SJAG_04253":null,"SJAG_04256":null,"SJAG_04261":null,"SJAG_04263":null,"SJAG_04264":null,"SJAG_04266":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04271":null,"SJAG_04273":null,"SJAG_04274":null,"SJAG_04275":null,"SJAG_04276":null,"SJAG_04282":null,"SJAG_04283":null,"SJAG_04285":null,"SJAG_04286":null,"SJAG_04287":null,"SJAG_04289":null,"SJAG_04290":null,"SJAG_04291":null,"SJAG_04292":null,"SJAG_04297":null,"SJAG_04299":null,"SJAG_04300":null,"SJAG_04303":null,"SJAG_04304":null,"SJAG_04306":null,"SJAG_04307":null,"SJAG_04309":null,"SJAG_04311":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04324":null,"SJAG_04326":null,"SJAG_04332":null,"SJAG_04334":null,"SJAG_04335":null,"SJAG_04337":null,"SJAG_04338":null,"SJAG_04342":null,"SJAG_04343":null,"SJAG_04344":null,"SJAG_04347":null,"SJAG_04350":null,"SJAG_04352":null,"SJAG_04354":null,"SJAG_04355":null,"SJAG_04357":null,"SJAG_04359":null,"SJAG_04360":null,"SJAG_04366":null,"SJAG_04368":null,"SJAG_04369":null,"SJAG_04371":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04379":null,"SJAG_04380":null,"SJAG_04381":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04385":null,"SJAG_04388":null,"SJAG_04390":null,"SJAG_04394":null,"SJAG_04397":null,"SJAG_04399":null,"SJAG_04400":null,"SJAG_04403":null,"SJAG_04404":null,"SJAG_04407":null,"SJAG_04408":null,"SJAG_04410":null,"SJAG_04414":null,"SJAG_04417":null,"SJAG_04427":null,"SJAG_04429":null,"SJAG_04431":null,"SJAG_04434":null,"SJAG_04436":null,"SJAG_04449":null,"SJAG_04452":null,"SJAG_04453":null,"SJAG_04454":null,"SJAG_04455":null,"SJAG_04456":null,"SJAG_04457":null,"SJAG_04458":null,"SJAG_04459":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04463":null,"SJAG_04465":null,"SJAG_04466":null,"SJAG_04467":null,"SJAG_04470":null,"SJAG_04472":null,"SJAG_04473":null,"SJAG_04474":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04477":null,"SJAG_04478":null,"SJAG_04480":null,"SJAG_04481":null,"SJAG_04482":null,"SJAG_04484":null,"SJAG_04486":null,"SJAG_04487":null,"SJAG_04491":null,"SJAG_04495":null,"SJAG_04496":null,"SJAG_04499":null,"SJAG_04501":null,"SJAG_04505":null,"SJAG_04511":null,"SJAG_04516":null,"SJAG_04518":null,"SJAG_04519":null,"SJAG_04520":null,"SJAG_04521":null,"SJAG_04531":null,"SJAG_04534":null,"SJAG_04535":null,"SJAG_04536":null,"SJAG_04539":null,"SJAG_04540":null,"SJAG_04541":null,"SJAG_04544":null,"SJAG_04548":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04554":null,"SJAG_04559":null,"SJAG_04563":null,"SJAG_04565":null,"SJAG_04567":null,"SJAG_04573":null,"SJAG_04576":null,"SJAG_04577":null,"SJAG_04579":null,"SJAG_04580":null,"SJAG_04581":null,"SJAG_04586":null,"SJAG_04587":null,"SJAG_04590":null,"SJAG_04595":null,"SJAG_04602":null,"SJAG_04607":null,"SJAG_04609":null,"SJAG_04611":null,"SJAG_04612":null,"SJAG_04617":null,"SJAG_04618":null,"SJAG_04626":null,"SJAG_04627":null,"SJAG_04628":null,"SJAG_04629":null,"SJAG_04631":null,"SJAG_04633":null,"SJAG_04634":null,"SJAG_04638":null,"SJAG_04649":null,"SJAG_04650":null,"SJAG_04651":null,"SJAG_04652":null,"SJAG_04653":null,"SJAG_04655":null,"SJAG_04656":null,"SJAG_04657":null,"SJAG_04658":null,"SJAG_04660":null,"SJAG_04663":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04672":null,"SJAG_04674":null,"SJAG_04679":null,"SJAG_04681":null,"SJAG_04682":null,"SJAG_04688":null,"SJAG_04693":null,"SJAG_04695":null,"SJAG_04699":null,"SJAG_04700":null,"SJAG_04704":null,"SJAG_04709":null,"SJAG_04710":null,"SJAG_04711":null,"SJAG_04713":null,"SJAG_04724":null,"SJAG_04726":null,"SJAG_04728":null,"SJAG_04735":null,"SJAG_04741":null,"SJAG_04744":null,"SJAG_04746":null,"SJAG_04747":null,"SJAG_04751":null,"SJAG_04754":null,"SJAG_04756":null,"SJAG_04758":null,"SJAG_04760":null,"SJAG_04762":null,"SJAG_04763":null,"SJAG_04764":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04772":null,"SJAG_04774":null,"SJAG_04776":null,"SJAG_04778":null,"SJAG_04781":null,"SJAG_04783":null,"SJAG_04784":null,"SJAG_04814":null,"SJAG_04815":null,"SJAG_04817":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04827":null,"SJAG_04837":null,"SJAG_04841":null,"SJAG_04842":null,"SJAG_04843":null,"SJAG_04844":null,"SJAG_04845":null,"SJAG_04846":null,"SJAG_04847":null,"SJAG_04848":null,"SJAG_04849":null,"SJAG_04858":null,"SJAG_04859":null,"SJAG_04860":null,"SJAG_04861":null,"SJAG_04863":null,"SJAG_04865":null,"SJAG_04866":null,"SJAG_04870":null,"SJAG_04871":null,"SJAG_04874":null,"SJAG_04877":null,"SJAG_04878":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04888":null,"SJAG_04890":null,"SJAG_04891":null,"SJAG_04894":null,"SJAG_04896":null,"SJAG_04897":null,"SJAG_04901":null,"SJAG_04902":null,"SJAG_04907":null,"SJAG_04912":null,"SJAG_04917":null,"SJAG_04920":null,"SJAG_04921":null,"SJAG_04927":null,"SJAG_04928":null,"SJAG_04932":null,"SJAG_04935":null,"SJAG_04936":null,"SJAG_04938":null,"SJAG_04939":null,"SJAG_04943":null,"SJAG_04944":null,"SJAG_04946":null,"SJAG_04948":null,"SJAG_04950":null,"SJAG_04953":null,"SJAG_04960":null,"SJAG_04963":null,"SJAG_04964":null,"SJAG_04966":null,"SJAG_04968":null,"SJAG_04969":null,"SJAG_04970":null,"SJAG_04972":null,"SJAG_04973":null,"SJAG_04974":null,"SJAG_04977":null,"SJAG_04978":null,"SJAG_04980":null,"SJAG_04981":null,"SJAG_04987":null,"SJAG_04988":null,"SJAG_04990":null,"SJAG_04998":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05004":null,"SJAG_05007":null,"SJAG_05008":null,"SJAG_05009":null,"SJAG_05010":null,"SJAG_05011":null,"SJAG_05014":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05021":null,"SJAG_05023":null,"SJAG_05024":null,"SJAG_05027":null,"SJAG_05029":null,"SJAG_05030":null,"SJAG_05032":null,"SJAG_05033":null,"SJAG_05179":null,"SJAG_05184":null,"SJAG_05185":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05195":null,"SJAG_05197":null,"SJAG_05198":null,"SJAG_05205":null,"SJAG_05206":null,"SJAG_05208":null,"SJAG_05210":null,"SJAG_05211":null,"SJAG_05214":null,"SJAG_05216":null,"SJAG_05222":null,"SJAG_05223":null,"SJAG_05225":null,"SJAG_05228":null,"SJAG_05230":null,"SJAG_05232":null,"SJAG_05240":null,"SJAG_05243":null,"SJAG_05245":null,"SJAG_05248":null,"SJAG_05252":null,"SJAG_05253":null,"SJAG_05256":null,"SJAG_05260":null,"SJAG_05261":null,"SJAG_05266":null,"SJAG_05276":null,"SJAG_05277":null,"SJAG_05283":null,"SJAG_05287":null,"SJAG_05290":null,"SJAG_05303":null,"SJAG_05304":null,"SJAG_05312":null,"SJAG_05314":null,"SJAG_05316":null,"SJAG_05329":null,"SJAG_05331":null,"SJAG_05332":null,"SJAG_05333":null,"SJAG_05334":null,"SJAG_05337":null,"SJAG_05343":null,"SJAG_05346":null,"SJAG_05351":null,"SJAG_05413":null,"SJAG_05694":null,"SJAG_05926":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_06284":null,"SJAG_06309":null,"SJAG_06355":null,"SJAG_06440":null,"SJAG_06576":null,"SJAG_06588":null,"SJAG_06592":null,"SJAG_06599":null,"SJAG_06612":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06636":null,"SJAG_07000":null,"SJAG_07011":null,"SJAG_07013":null,"SJAG_07014":null,"SJAG_07017":null,"SJAG_16457":null,"SJAG_16460":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cytosol","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"PMID:31956022":null},"secondary_identifiers":["Wikipedia:Cytosol","NIF_Subcellular:sao101633890"],"termid":"GO:0005829","terms_by_termid":{"GO:0000015":null,"GO:0002144":null,"GO:0005829":null,"GO:0005832":null,"GO:0005945":null,"GO:0005971":null,"GO:0022625":null,"GO:0022626":null,"GO:0022627":null,"GO:0033596":null,"GO:0072380":null,"GO:0090730":null,"GO:0097361":null,"GO:0099128":null,"GO:0120510":null,"GO:1904564":null}}


id: GO:0102742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + 3,4-dihydroxyphenylpyruvate + NADPH = (2R)-3-(3,4-dihydroxyphenyl)lactate + NADP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete R(+)-3,4-dihydroxyphenyllactate:NADP+ oxidoreductase activity (obsolete GO:0102742)","termid":"GO:0102742"}


id: PR:O43058
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sep1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43058"],"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":"forkhead protein sep1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4C3.12","synonyms":[{"name":"Spom972h-sep1","type":"exact"}],"termid":"PR:O43058"}


id: GO:0061330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a Malpighian tubule stellate cell. A Malpighian tubule stellate cell is a specialized epithelial secretory cell that moves chloride ions and water across the tubule epithelium.","definition_xrefs":["PMID:19783135","GOC:mtg_kidney_jan10","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell differentiation","termid":"GO:0030855"},{"relation_name":"part_of","term_name":"Malpighian tubule development","termid":"GO:0072002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"Malpighian tubule stellate cell differentiation","termid":"GO:0061330"}


id: MONDO:0003334
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polyneuropathy that is characterized by demyelination of axons.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyneuropathy","termid":"MONDO:0001824"},{"relation_name":"is_a","term_name":"demyelinating disease","termid":"MONDO:0002562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"demyelinating polyneuropathy","secondary_identifiers":["MEDGEN:82859","UMLS:C0270922","DOID:5214","ICD9:356.9","NCIT:C27062","SCTID:23414001"],"synonyms":[{"name":"peripheral demyelinating neuropathy","type":"exact"}],"termid":"MONDO:0003334","xrefs":{"Monarch":{"xref_id":"0003334"}}}


id: PBO:0089811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Swr1 complex histone chaperone module subunit Swc3","termid":"PBO:0089811"}


id: GO:0036035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a osteoclast from its formation to the mature structure. Cell development does not include the steps involved in committing a cell to a specific fate. An osteoclast is a specialized phagocytic cell associated with the absorption and removal of the mineralized matrix of bone tissue.","definition_xrefs":["GOC:yaf","CL:0000092","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid cell development","termid":"GO:0061515"},{"relation_name":"is_a","term_name":"bone cell development","termid":"GO:0098751"},{"relation_name":"part_of","term_name":"osteoclast differentiation","termid":"GO:0030316"}],"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":"osteoclast development","synonyms":[{"name":"osteoclast cell development","type":"exact"}],"termid":"GO:0036035"}


id: GO:0002537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis or release of nitric oxide following a stimulus as part of an inflammatory response, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator involved in inflammatory response","termid":"GO:0002532"}],"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":"nitric oxide production involved in inflammatory response","synonyms":[{"name":"nitric oxide production involved in acute inflammatory response","type":"broad"},{"name":"production of nitric oxide involved in acute inflammatory response","type":"broad"},{"name":"production of nitric oxide involved in inflammatory response","type":"exact"}],"termid":"GO:0002537"}


id: PBO:0042843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 47","termid":"PBO:0042843"}


id: PBO:0113379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative ferric reductase with similarity to Fre2p; expression induced by low iron levels; targeted to vacuole via AP-3 pathway","termid":"PBO:0113379"}


id: PBO:0061889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OPCML intronic transcript 2","termid":"PBO:0061889"}


id: GO:0070743
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is composed of an interleukin-23 alpha (p19, product of the IL23A gene) and an interleukin-12 beta (p40, product of the IL12B gene) subunit and is secreted into the extracellular space.","definition_xrefs":["PMID:15999093","GOC:add","PMID:11114383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005576","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"interleukin-23 complex","synonyms":[{"name":"IL-23 complex","type":"exact"},{"name":"IL12B","type":"narrow"},{"name":"IL23A","type":"narrow"},{"name":"p19","type":"narrow"},{"name":"p40","type":"narrow"}],"termid":"GO:0070743"}


id: PBO:0082558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ceramide-activated, type 2A-related serine-threonine phosphatase; functions in G1/S transition of mitotic cycle; controls lifespan, mitochondrial function, cell cycle progression by regulating HXK2 phosphorylation; regulator of COPII coat dephosphorylation; required for ER to Golgi traffic; interacts with Hrr25p kinase; cytoplasmic and nuclear protein that modulates functions mediated by Pkc1p including cell wall and actin cytoskeleton organization; similar to human PP6","termid":"PBO:0082558"}


id: RO:HOM0000037
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Historical homology that involves a structure that has no other homologs in the species in which it is defined, and several homologous structures in another species.","definition_xrefs":["BGEE:curator"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in_historical_homology_relationship_with","termid":"RO:HOM0000007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_1_to_many_homology_relationship_with","synonyms":[{"name":"1 to many homologous to","type":"exact"},{"name":"1:many homology","type":"related"},{"name":"one-to-many homology","type":"exact"}],"termid":"RO:HOM0000037"}


id: GO:0141043
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont avoids recognition by host's innate immune response by altering, concealing or destroying a conserved symbiont molecule recognized by the host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:22131330","PMID:15014080","PMID:26502908","PMID:29101229"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated evasion of host immune response","termid":"GO:0042783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated evasion of host innate immune response","synonyms":[{"name":"evasion of host innate immune recognition","type":"related"},{"name":"evasion of host innate immune response","type":"exact"}],"termid":"GO:0141043"}


id: PBO:0003264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-N (predicted)","termid":"PBO:0003264"}


id: PBO:0081116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger AN1-type containing 5","termid":"PBO:0081116"}


id: PBO:0077865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin 3 pseudogene 6","termid":"PBO:0077865"}


id: PBO:0028104
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_cell_population_growth_on_galactose_carbon_source","termid":"PBO:0028104"}


id: MONDO:0013536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of porphyrin metabolism","termid":"MONDO:0017754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"heme oxygenase 1 deficiency","secondary_identifiers":["GARD:17995","MESH:C564200","Orphanet:562509","MEDGEN:333882","OMIM:614034","UMLS:C1841651"],"synonyms":[{"name":"HMOX1D","type":"related"},{"name":"heme oxygenase 1 deficiency","type":"exact"},{"name":"heme oxygenase-1 deficiency","type":"exact"}],"termid":"MONDO:0013536","xrefs":{"Monarch":{"xref_id":"0013536"}}}


id: PBO:0004987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidase family M20 protein","termid":"PBO:0004987"}


id: PBO:0030847
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cell_cycle_arrest_in_mitotic_G2_phase_during_response_to_DNA_damage","termid":"PBO:0030847"}


id: PBO:0048135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FMR1 autosomal homolog 1","termid":"PBO:0048135"}


id: MONDO:0019043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic skin disease (obsolete MONDO:0019043)","secondary_identifiers":["Orphanet:68346"],"synonyms":[{"name":"rare genodermatosis","type":"exact"}],"termid":"MONDO:0019043","xrefs":{"Monarch":{"xref_id":"0019043"}}}


id: MONDO:0005804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormally high level of prolactin in the blood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperpituitarism","termid":"MONDO:0006793"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperprolactinemia","secondary_identifiers":["UMLS:C0020514","HP:0000870","MEDGEN:5698","NANDO:2100115","ICD9:253.1","NANDO:2200322","ICD10CM:E22.1","MESH:D006966","EFO:0007319","SCTID:237662005"],"synonyms":[{"name":"hyperprolactinaemia","type":"exact"},{"name":"hyperprolactinemia","type":"exact"},{"name":"hyperprolactinemia (disease)","type":"exact"},{"name":"hyperprolactinemias","type":"related"},{"name":"hypersecretion syndrome, prolactin","type":"related"},{"name":"inappropriate prolactin secretion","type":"related"},{"name":"inappropriate prolactin secretion syndrome","type":"related"},{"name":"inappropriate secretion prolactin","type":"related"},{"name":"prolactin hypersecretion syndrome","type":"related"},{"name":"prolactin secretion, inappropriate","type":"related"},{"name":"prolactin, inappropriate secretion","type":"related"},{"name":"secretion prolactin, inappropriate","type":"related"},{"name":"secretion, inappropriate prolactin","type":"related"},{"name":"syndrome, prolactin hypersecretion","type":"related"}],"termid":"MONDO:0005804","xrefs":{"Monarch":{"xref_id":"0005804"}}}


id: PBO:0039847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 15","termid":"PBO:0039847"}


id: PBO:0026850
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_chromatin_at_rRNA_gene","termid":"PBO:0026850"}


id: PBO:0064075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 109","termid":"PBO:0064075"}


id: PBO:0001726
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.2.1.24","termid":"PBO:0001726"}


id: PBO:0050113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 23","termid":"PBO:0050113"}


id: PBO:0059012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMEL1 antisense RNA 1","termid":"PBO:0059012"}


id: PBO:0061132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD3 ribosome export adaptor pseudogene 2","termid":"PBO:0061132"}


id: PBO:0070060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 17, pseudogene","termid":"PBO:0070060"}


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


id: PBO:0071413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 19","termid":"PBO:0071413"}


id: GO:0002833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of a response to biotic stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to biotic stimulus","termid":"GO:0002831"},{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"positively_regulates","term_name":"response to biotic stimulus","termid":"GO:0009607"}],"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 response to biotic stimulus","synonyms":[{"name":"activation of response to biotic stimulus","type":"narrow"},{"name":"stimulation of response to biotic stimulus","type":"narrow"},{"name":"up regulation of response to biotic stimulus","type":"exact"},{"name":"up-regulation of response to biotic stimulus","type":"exact"},{"name":"upregulation of response to biotic stimulus","type":"exact"}],"termid":"GO:0002833"}


id: PBO:0082159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adenine phosphoribosyltransferase; catalyzes the formation of AMP from adenine and 5-phosphoribosylpyrophosphate; involved in the salvage pathway of purine nucleotide biosynthesis; APT1 has a paralog, APT2, that arose from the whole genome duplication","termid":"PBO:0082159"}


id: GO:0106200
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of amino acids and peptides linked to the hydrolysis of a nucleoside triphosphate.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocase activity acting on amio acids and peptides linked to the hydrolysis of a nucleoside triphosphate (obsolete GO:0106200)","termid":"GO:0106200"}


id: PBO:0040192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argininosuccinate synthetase 1 pseudogene 5","termid":"PBO:0040192"}


id: PBO:0080446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-set and immunoglobulin domain containing 4","termid":"PBO:0080446"}


id: GO:0019558
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-histidine into other compounds, including 2-oxoglutarate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate metabolic process","termid":"GO:0006103"},{"relation_name":"is_a","term_name":"L-histidine catabolic process","termid":"GO:0006548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"L-histidine catabolic process to 2-oxoglutarate","synonyms":[{"name":"histidine breakdown to 2-oxoglutarate","type":"exact"},{"name":"histidine catabolic process to 2-ketoglutarate","type":"exact"},{"name":"histidine catabolic process to 2-oxoglutarate","type":"broad"},{"name":"histidine catabolic process to alpha-ketoglutarate","type":"exact"},{"name":"histidine catabolic process to alpha-oxoglutarate","type":"exact"},{"name":"histidine catabolism to 2-ketoglutarate","type":"exact"},{"name":"histidine catabolism to alpha-ketoglutarate","type":"exact"},{"name":"histidine catabolism to alpha-oxoglutarate","type":"exact"},{"name":"histidine degradation to 2-oxoglutarate","type":"exact"}],"termid":"GO:0019558"}


id: PBO:0077678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF superfamily member 9","termid":"PBO:0077678"}


id: GO:0044020
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + (histone H4)-arginine (position 3) = S-adenosyl-L-homocysteine + (histone H4)-N-methyl-arginine (position 3). This reaction is the addition of a methyl group to the arginine residue at position 3 of histone H4, producing histone H4R3me.","definition_xrefs":["GOC:mah","PMID:17898714"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-arginine N-methyltransferase activity","termid":"GO:0016274"},{"relation_name":"is_a","term_name":"histone H4 methyltransferase activity","termid":"GO:0140939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0008276","GO:0140096","GO:0016741","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"histone H4R3 methyltransferase activity","synonyms":[{"name":"histone H4KR3 methylation","type":"exact"},{"name":"histone H4R3 arginine methylase activity","type":"exact"},{"name":"histone methylase activity (H4-R3 specific)","type":"exact"},{"name":"histone methyltransferase activity (H4-R3 specific)","type":"exact"},{"name":"histone-arginine N-methyltransferase activity (H4-R3 specific)","type":"exact"}],"termid":"GO:0044020"}


id: MONDO:0013924
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta in which the cause of the disease is a mutation in the BMP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta","termid":"MONDO:0019019"}],"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":"osteogenesis imperfecta type 13","secondary_identifiers":["UMLS:C3553887","GARD:15856","DOID:0110342","OMIM:614856","MEDGEN:766801"],"synonyms":[{"name":"BMP1 osteogenesis imperfecta","type":"exact"},{"name":"OI, type 13","type":"related"},{"name":"OI13","type":"exact"},{"name":"osteogenesis imperfecta caused by mutation in BMP1","type":"exact"},{"name":"osteogenesis imperfecta type XIII","type":"exact"},{"name":"osteogenesis imperfecta, type 13","type":"related"},{"name":"osteogenesis imperfecta, type XIII","type":"related"}],"termid":"MONDO:0013924","xrefs":{"Monarch":{"xref_id":"0013924"}}}


id: FYPO:0007448
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which autophagic degradation of the endoplasmic reticulum is normal (i.e. indistinguishable from wild type) when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah","PMID:32735772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process","termid":"FYPO:0000627"},{"relation_name":"is_a","term_name":"abnormal macroautophagy during nitrogen starvation","termid":"FYPO:0004670"},{"relation_name":"is_a","term_name":"abnormal reticulophagy","termid":"FYPO:0008083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"normal reticulophagy during nitrogen starvation","synonyms":[{"name":"normal ER autophagy during nitrogen starvation","type":"exact"},{"name":"normal ER degradation during nitrogen starvation","type":"related"},{"name":"normal ER-phagy during nitrogen starvation","type":"exact"},{"name":"normal endoplasmic reticulum autophagy during nitrogen starvation","type":"exact"},{"name":"normal reticulophagy during nitrogen depletion","type":"exact"},{"name":"normal reticulophagy during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0007448"}


id: GO:1905009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of L-lysine import into cell.","definition_xrefs":["PMID:7499219","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organic acid transport","termid":"GO:0032891"},{"relation_name":"is_a","term_name":"negative regulation of transmembrane transport","termid":"GO:0034763"},{"relation_name":"is_a","term_name":"negative regulation of amino acid transport","termid":"GO:0051956"},{"relation_name":"is_a","term_name":"regulation of L-lysine import across plasma membrane","termid":"GO:1905008"},{"relation_name":"negatively_regulates","term_name":"L-lysine import across plasma membrane","termid":"GO:0097639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"negative regulation of L-lysine import across plasma membrane","secondary_identifiers":["GO:0010806"],"synonyms":[{"name":"down regulation of L-lysine import into cell","type":"exact"},{"name":"down-regulation of L-lysine import into cell","type":"exact"},{"name":"downregulation of L-lysine import into cell","type":"exact"},{"name":"inhibition of L-lysine import into cell","type":"narrow"},{"name":"negative regulation of L-lysine import into cell","type":"exact"},{"name":"negative regulation of lysine import","type":"broad"},{"name":"negative regulation of lysine uptake","type":"exact"}],"termid":"GO:1905009"}


id: PBO:0079293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTLL10 antisense RNA 1","termid":"PBO:0079293"}


id: GO:0007089
data:
  {"annotated_genes":["SJAG_01401","SJAG_03681","SJAG_04140","SJAG_01210","SJAG_01825","SJAG_03591"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75157,77087,92085,109209,115641,116204],"is_not":false,"summary":null,"term":"GO:0007089"}]},"cv_name":"biological_process","definition":"A cell cycle process by which a cell commits to entering S phase via a positive feedback mechanism between the regulation of transcription and G1 CDK activity.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of G1/S transition of mitotic cell cycle","termid":"GO:1900087"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01210":null,"SJAG_01401":null,"SJAG_01825":null,"SJAG_03591":null,"SJAG_03681":null,"SJAG_04140":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0044772"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0044772"}],"interesting_parent_ids":["GO:0007049","GO:0044772","GO:0008150"],"is_obsolete":false,"name":"traversing start control point of mitotic cell cycle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0000081"],"termid":"GO:0007089","terms_by_termid":{"GO:0007089":null}}


id: GO:0120084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of a filopodium, a thin, stiff protrusion extended by the endothelial tip cell of a vascular sprout.","definition_xrefs":["PMID:28264837","GOC:cvs"],"direct_ancestors":[{"relation_name":"is_a","term_name":"filopodium assembly","termid":"GO:0046847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"endothelial tip cell filopodium assembly","termid":"GO:0120084"}


id: FYPO:0008015
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of glucose into the cell is decreased with respect to wild-type.","definition_xrefs":["PMID:35781263","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glucose import","termid":"FYPO:0001827"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased glucose import","termid":"FYPO:0008015"}


id: MONDO:0800460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The spectrum of ASAH1-related disorders ranges from Farber disease (FD) to spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). The diagnosis of an ASAH1-related disorder is established in a proband with suggestive clinical findings by identification of biallelic pathogenic variants in ASAH1 and/or decreased activity of the enzyme acid ceramidase in peripheral blood leukocytes or cultured skin fibroblasts.","definition_xrefs":["PMID:29595935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"ASAH1-related disorders","synonyms":[{"name":"ASAH1-related disorders","type":"exact"}],"termid":"MONDO:0800460","xrefs":{"Monarch":{"xref_id":"0800460"}}}


id: GO:1902414
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a cell junction.","definition_xrefs":["GOC:TermGenie","PMID:18332111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to cell junction","synonyms":[{"name":"protein localisation in cell junction","type":"exact"},{"name":"protein localisation to cell junction","type":"exact"},{"name":"protein localization in cell junction","type":"exact"}],"termid":"GO:1902414"}


id: PBO:0063119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase family member 4 pseudogene 1","termid":"PBO:0063119"}


id: GO:0031983
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane or protein that forms a vesicle.","definition_xrefs":["GOC:mah","GOC:vesicles"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle lumen","termid":"GO:0043233"},{"relation_name":"part_of","term_name":"vesicle","termid":"GO:0031982"}],"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":"vesicle lumen","secondary_identifiers":["NIF_Subcellular:sao797538226"],"termid":"GO:0031983"}


id: GO:0015789
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of UDP-N-acetylgalactosamine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. UDP-N-acetylgalactosamine is a substance composed of N-acetylgalactosamine, a common structural unit of oligosaccharides, in glycosidic linkage with uridine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"pyrimidine nucleotide-sugar transmembrane transport","termid":"GO:0090481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"UDP-N-acetylgalactosamine transmembrane transport","synonyms":[{"name":"UDP-N-acetylgalactosamine transport","type":"related"}],"termid":"GO:0015789"}


id: MONDO:0000696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete juvenile absence epilepsy (obsolete MONDO:0000696)","termid":"MONDO:0000696","xrefs":{"Monarch":{"xref_id":"0000696"}}}


id: PBO:0069763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1046, pseudogene","termid":"PBO:0069763"}


id: PBO:0045241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 9","termid":"PBO:0045241"}


