# terms

id: MOD:01475
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"O-phosphopantetheine-L-serine","termid":"MOD:00159"},{"relation_name":"is_a","term_name":"iodoacetamide derivatized residue","termid":"MOD:00397"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine","termid":"MOD:01475"}


id: GO:0090217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the frequency, rate or extent of the catalysis of the reaction: ATP + 1-phosphatidyl-1D-myo-inositol 4-phosphate = ADP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of 1-phosphatidylinositol-4-phosphate 5-kinase activity (obsolete GO:0090217)","termid":"GO:0090217"}


id: PBO:0030483
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_sodium_export","termid":"PBO:0030483"}


id: PBO:0062368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily A member 3 pseudogene","termid":"PBO:0062368"}


id: MONDO:0100501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare anomaly (1 in 14,000 to 42,000 pregnancies; 1 in 7500 fetuses from 10 to 14 weeks of gestation) characterized by a complex anomaly of the anterior abdominal wall, severe kyphoscoliosis, rudimentary umbilical cord, and anatomical defects of the pelvis and lower limbs.","definition_xrefs":["PMID:33115503"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abdominal wall malformation","termid":"MONDO:0100298"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"body-stalk anomaly","synonyms":[{"name":"BSA","type":"exact"},{"name":"LBWC","type":"narrow"},{"name":"body stalk anomaly","type":"exact"},{"name":"body stalk complex","type":"exact"},{"name":"limb body wall complex","type":"narrow"}],"termid":"MONDO:0100501","xrefs":{"Monarch":{"xref_id":"0100501"}}}


id: PBO:0045217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJC8 pseudogene 2","termid":"PBO:0045217"}


id: GO:0010479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the stele over time, from its formation to the mature structure. The stele is the central column of primary vascular tissue in the root and any tissue that it surrounds.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"},{"relation_name":"part_of","term_name":"root development","termid":"GO:0048364"}],"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":"stele development","termid":"GO:0010479"}


id: PBO:0079650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 T","termid":"PBO:0079650"}


id: GO:1903098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of the formation of nucleosomes containing the histone H3 variant CENP-A to form centromeric chromatin. This specialised chromatin occurs at centromeric region in point centromeres, and the central core in modular centromeres.","definition_xrefs":["PMID:24710126","GO_REF:0000058","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of CENP-A containing nucleosome assembly (obsolete GO:1903098)","synonyms":[{"name":"down regulation of CENP-A containing nucleosome assembly at centromere","type":"exact"},{"name":"down regulation of CENP-A deposition","type":"related"},{"name":"down regulation of CENP-A loading","type":"related"},{"name":"down regulation of CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"down regulation of DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"down regulation of centromere specific nucleosome exchange","type":"related"},{"name":"down regulation of centromere-specific histone exchange","type":"exact"},{"name":"down regulation of centromere-specific nucleosome assembly","type":"exact"},{"name":"down regulation of centromeric DNA replication-independent nucleosome assembly","type":"exact"},{"name":"down-regulation of CENP-A containing nucleosome assembly at centromere","type":"exact"},{"name":"down-regulation of CENP-A deposition","type":"related"},{"name":"down-regulation of CENP-A loading","type":"related"},{"name":"down-regulation of CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"down-regulation of DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"down-regulation of centromere specific nucleosome exchange","type":"related"},{"name":"down-regulation of centromere-specific histone exchange","type":"exact"},{"name":"down-regulation of centromere-specific nucleosome assembly","type":"exact"},{"name":"down-regulation of centromeric DNA replication-independent nucleosome assembly","type":"exact"},{"name":"downregulation of CENP-A containing nucleosome assembly at centromere","type":"exact"},{"name":"downregulation of CENP-A deposition","type":"related"},{"name":"downregulation of CENP-A loading","type":"related"},{"name":"downregulation of CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"downregulation of DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"downregulation of centromere specific nucleosome exchange","type":"related"},{"name":"downregulation of centromere-specific histone exchange","type":"exact"},{"name":"downregulation of centromere-specific nucleosome assembly","type":"exact"},{"name":"downregulation of centromeric DNA replication-independent nucleosome assembly","type":"exact"},{"name":"inhibition of CENP-A containing nucleosome assembly at centromere","type":"narrow"},{"name":"inhibition of CENP-A deposition","type":"related"},{"name":"inhibition of CENP-A loading","type":"related"},{"name":"inhibition of CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"inhibition of DNA replication-independent nucleosome assembly at centromere","type":"narrow"},{"name":"inhibition of centromere specific nucleosome exchange","type":"related"},{"name":"inhibition of centromere-specific histone exchange","type":"narrow"},{"name":"inhibition of centromere-specific nucleosome assembly","type":"narrow"},{"name":"inhibition of centromeric DNA replication-independent nucleosome assembly","type":"narrow"},{"name":"negative regulation of CENP-A deposition","type":"related"},{"name":"negative regulation of CENP-A loading","type":"related"},{"name":"negative regulation of CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"negative regulation of DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"negative regulation of centromere specific nucleosome exchange","type":"related"},{"name":"negative regulation of centromere-specific histone exchange","type":"exact"},{"name":"negative regulation of centromere-specific nucleosome assembly","type":"exact"},{"name":"negative regulation of centromeric DNA replication-independent nucleosome assembly","type":"exact"}],"termid":"GO:1903098"}


id: PR:Q9P7C3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11742:SF7","OMA:SCHPO01384","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":"endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2E1P5.01c","secondary_identifiers":["UniProtKB:Q9P7C3"],"synonyms":[{"name":"ER alpha-1,2-mannosidase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Man(9)-alpha-mannosidase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MAN1B1","type":"exact"}],"termid":"PR:Q9P7C3"}


id: MONDO:1010965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cauda equina syndrome that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cauda equina syndrome, non-human animal","termid":"MONDO:1010227"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cauda equina syndrome, dog","secondary_identifiers":["OMIA:000170-9615"],"termid":"MONDO:1010965","xrefs":{"Monarch":{"xref_id":"1010965"}}}


id: MONDO:0010187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Combined vitamin K-dependent clotting factors deficiency (VKCFD) is a congenital bleeding disorder resulting from variably decreased levels of coagulation factors II, VII, IX and X, as well as natural anticoagulants protein C, protein S and protein Z.","definition_xrefs":["Orphanet:98434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital vitamin K-dependent coagulation factors deficiency","termid":"MONDO:0015722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"vitamin K-dependent clotting factors, combined deficiency of, type 1","secondary_identifiers":["DOID:0112173","OMIM:277450","UMLS:C1848534","MESH:C564741","GARD:18195","MEDGEN:376381","SCTID:724356003"],"synonyms":[{"name":"FMFD 3","type":"related"},{"name":"GGCX congenital vitamin K-dependent coagulation factors combined deficiency","type":"exact"},{"name":"VKCFD1","type":"related"},{"name":"Vkcfd","type":"related"},{"name":"congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in GGCX","type":"exact"},{"name":"factors II, VII, IX, and X, combined deficiency of","type":"related"},{"name":"familial multiple coagulation Factor deficiency 3","type":"related"},{"name":"glutamic acid, deficient gamma-carboxylation of","type":"related"},{"name":"hereditary combined deficiency of factors II, VII, IX and X","type":"exact"},{"name":"hereditary combined deficiency of vitamin K-dependent clotting factors","type":"related"},{"name":"multiple coagulation Factor deficiency 3","type":"related"},{"name":"vitamin K-dependent clotting factors, combined deficiency of, 1","type":"related"},{"name":"vitamin K-dependent clotting factors, combined deficiency of, type 1","type":"exact"},{"name":"vitamin K-dependent coagulation defect","type":"related"}],"termid":"MONDO:0010187","xrefs":{"Monarch":{"xref_id":"0010187"}}}


id: GO:0015127
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of bilirubin from one side of a membrane to the other. Bilirubin is a linear tetrapyrrole produced in the reticuloendothelial system from biliverdin and transported to the liver as a complex with serum albumin. In the liver, bilirubin is converted to bilirubin bisglucuronide, which is excreted in the bile.","definition_xrefs":["GOC:ai","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transmembrane transporter activity","termid":"GO:0005310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"bilirubin transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-5679041","Reactome:R-HSA-9661417","Reactome:R-HSA-5679031"],"termid":"GO:0015127"}


id: GO:0071541
data:
  {"annotated_genes":["SJAG_04891","SJAG_02164","SJAG_02995","SJAG_04900","SJAG_04744","SJAG_03472","SJAG_03147","SJAG_04981","SJAG_02628"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[59642,74733,75477,76040,95155,97209,98090,99288,105975],"is_not":false,"summary":null,"term":"GO:0071541"}]},"cv_name":"cellular_component","definition":"An eukaryotic translation initiation factor 3 complex that contains the PCI-domain protein eIF3m.","definition_xrefs":["PMID:15904532","PMID:19061185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eukaryotic translation initiation factor 3 complex","termid":"GO:0005852"}],"gene_count":9,"genes_by_uniquename":{"SJAG_02164":null,"SJAG_02628":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03472":null,"SJAG_04744":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 complex, eIF3m","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"eIF3m-containing eukaryotic translation initiation factor 3 complex","type":"exact"}],"termid":"GO:0071541","terms_by_termid":{"GO:0071541":null}}


id: PBO:0059238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L11","termid":"PBO:0059238"}


id: PBO:0072169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 6","termid":"PBO:0072169"}


id: GO:0070044
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptobrevin 2 (VAMP2), SNAP-25, and syntaxin 1a (or orthologs thereof).","definition_xrefs":["PMID:10336434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"synaptobrevin 2-SNAP-25-syntaxin-1a complex","synonyms":[{"name":"SNARE complex (Snap25, Stx1a, Vamp2)","type":"narrow"},{"name":"SNARE complex (Stx1a, SNAP25, VAMP)","type":"narrow"},{"name":"Snap25-Stx1a-Vamp2 complex","type":"narrow"},{"name":"Stx1a-SNAP25-VAMP complex","type":"narrow"}],"termid":"GO:0070044"}


id: PR:O94417
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cwf26 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94417"],"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":"pre-mRNA-splicing factor cwf26 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.10","synonyms":[{"name":"Spom972h-cwf26","type":"exact"},{"name":"complexed with cdc5 protein 26 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94417"}


id: GO:0003282
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the ventricular septum intermedium over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular septum development","termid":"GO:0003281"}],"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 septum intermedium development","termid":"GO:0003282"}


id: MONDO:0013109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"acute lymphoblastic leukemia","termid":"MONDO:0004967"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukemia, acute lymphocytic, susceptibility to, 2","secondary_identifiers":["UMLS:C2751593","MEDGEN:442766","OMIM:613067"],"synonyms":[{"name":"ALL2","type":"related"},{"name":"leukemia, acute lymphoblastic, susceptibility to, 2","type":"related"},{"name":"leukemia, acute lymphocytic, susceptibility to, 2","type":"exact"}],"termid":"MONDO:0013109","xrefs":{"Monarch":{"xref_id":"0013109"}}}


id: MONDO:0018172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Malignant sex cord stromal tumor (SCST) of ovary is a rare ovarian cancer arising from granulosa, theca, sertoli and leydig cells or stromal fibroblasts, occurring at any age and presenting with abdominal or pelvic mass, and characterized (with the exception of fibroma) by the production of sex steroids resulting in manifestations of hormone excess, with a relatively favorable prognosis.","definition_xrefs":["Orphanet:35808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant non-epithelial tumor of ovary","termid":"MONDO:0018365"},{"relation_name":"is_a","term_name":"ovarian sex cord-stromal tumor","termid":"MONDO:0021657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant sex cord stromal tumor of ovary","secondary_identifiers":["GARD:18816","MEDGEN:233667","NCIT:C8053","UMLS:C1334609"],"synonyms":[{"name":"malignant Sex cord-stromal tumor of ovary","type":"exact"},{"name":"malignant Sex cord-stromal tumor of the ovary","type":"exact"},{"name":"malignant Sex cord-stromal tumour of ovary","type":"exact"},{"name":"malignant Sex cord-stromal tumour of the ovary","type":"exact"},{"name":"malignant ovarian SCST","type":"exact"},{"name":"malignant ovarian Sex cord-stromal neoplasm","type":"exact"},{"name":"malignant ovarian Sex cord-stromal tumor","type":"exact"},{"name":"malignant ovarian Sex cord-stromal tumour","type":"exact"},{"name":"malignant ovarian sex cord-stromal tumor","type":"exact"},{"name":"malignant ovarian sex cord-stromal tumour","type":"exact"},{"name":"ovarian sex cord-stromal tumor, malignant","type":"exact"}],"termid":"MONDO:0018172","xrefs":{"Monarch":{"xref_id":"0018172"}}}


id: GO:0019643
data:
  {"annotated_genes":["SJAG_03920"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117141],"is_not":false,"summary":null,"term":"GO:0019643"}]},"cv_name":"biological_process","definition":"A pathway leading to the fixation of two molecules of CO2 and the production of one molecule of acetyl-CoA; essentially the oxidative TCA cycle running in reverse. Acetyl-CoA is reductively carboxylated to pyruvate, from which all other central metabolites can be formed. Most of the enzymes of reductive and oxidative TCA cycle are shared, with the exception of three key enzymes that allow the cycle to run in reverse: ATP citrate lyase, 2-oxoglutarate:ferredoxin oxidoreductase, and fumarate reductase. 2-oxoglutarate:ferredoxin oxidoreductase catalyzes the carboxylation of succinyl-CoA to 2-oxoglutarate, ATP citrate lyase the ATP-dependent cleavage of citrate to acetyl-CoA and oxaloacetate, and fumarate reductase the reduction of fumarate forming succinate.","definition_xrefs":["GOC:jl","PMID:15838028"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon fixation","termid":"GO:0015977"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03920":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"reductive tricarboxylic acid cycle","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0019644"],"synonyms":[{"name":"reductive Kreb's cycle","type":"exact"},{"name":"reductive TCA cycle","type":"exact"},{"name":"reductive carboxylate cycle","type":"exact"},{"name":"reductive carboxylic acid cycle","type":"exact"},{"name":"reductive citric acid pathway","type":"exact"}],"termid":"GO:0019643","terms_by_termid":{"GO:0019643":null}}


id: MONDO:0000170
data:
  {"annotated_genes":["SJAG_03497"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013783"}]},"cv_name":"mondo","definition":"A developmental disorder of the eye characterized by unilateral or bilateral microphthalmia associated with ocular coloboma.","definition_xrefs":["Orphanet:98938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"},{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03497":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"microphthalmia, isolated, with coloboma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:3644","MESH:C537463","MEDGEN:444071","OMIMPS:300345","UMLS:C2931500"],"synonyms":[{"name":"MAC","type":"exact"},{"name":"MCOPCB1","type":"related"},{"name":"colobomatous microphthalmia","type":"exact"},{"name":"microphthalmia associated with colobomatous cyst","type":"related"},{"name":"microphthalmia with colobomatous cyst","type":"exact"},{"name":"microphthalmia-anophthalmia-coloboma syndrome","type":"exact"},{"name":"microphthalmos bilateral, colobomatous orbital cyst","type":"related"}],"termid":"MONDO:0000170","terms_by_termid":{"MONDO:0013783":null},"xrefs":{"Monarch":{"xref_id":"0000170"}}}


id: PBO:0004777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur protein Isa2","termid":"PBO:0004777"}


id: PBO:0049874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatic and glial cell adhesion molecule","termid":"PBO:0049874"}


id: MOD:01972
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl coenzyme A thioester.","definition_xrefs":["PubMed:20977214","PubMed:7915164","RESID:AA0614","PubMed:16253988"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur containing modified residue","termid":"MOD:00860"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-glutamyl coenzyme A thioester","synonyms":[{"name":"(2S)-2-amino-5-(2-[([3-([(2R)-2-hydroxy-3,3-dimethyl-4-([3'-phospho-adenosyl-5'-diphosphoryl]-oxy)-butanoyl]-amino)-propanoyl]-amino)-ethyl]-sulfanyl)-5-oxopentanoic acid","type":"exact"},{"name":"(2S)-2-amino-5-([2-(3-[(2R)-2-hydroxy-3,3-dimethyl-4-([3'-phospho-adenosyl-5'-diphosphoryl]-oxy)-butanamido]-propanamido)-ethyl]-sulfanyl)-5-oxopentanoic acid","type":"exact"},{"name":"5-glutamyl 4-[(3'-phospho-adenosyl-5'-diphosphoryl)oxy]pantetheine thioester","type":"exact"},{"name":"5-glutamyl coenzyme A thioester","type":"exact"},{"name":"5-glutamyl coenzyme A thioester intermediate","type":"exact"}],"termid":"MOD:01972"}


id: MONDO:0021178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity.","definition_xrefs":["NCIT:C3671"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"injury","secondary_identifiers":["EFO:0000546","MESH:D014947"],"synonyms":[{"name":"injury","type":"exact"},{"name":"trauma","type":"exact"},{"name":"traumatic injury","type":"exact"},{"name":"wound","type":"exact"}],"termid":"MONDO:0021178","xrefs":{"Monarch":{"xref_id":"0021178"}}}


id: GO:0034546
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,4-dichloroaniline + 2 H+ + 2 e- = 4-chloroaniline + HCl.","definition_xrefs":["UM-BBD_reactionID:r0819"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,4-dichloroaniline reductive dehalogenase activity (obsolete GO:0034546)","termid":"GO:0034546"}


id: PBO:0031217
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_DNA_replication","termid":"PBO:0031217"}


id: SO:0000863
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing an mRNA feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_attribute","termid":"SO:0000237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_attribute","synonyms":[{"name":"mRNA attribute","type":"exact"}],"termid":"SO:0000863"}


id: PBO:0051132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 2-70D","termid":"PBO:0051132"}


id: GO:0031510
data:
  {"annotated_genes":["SJAG_00604","SJAG_05032"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75975,98115],"is_not":false,"summary":null,"term":"GO:0031510"}]},"cv_name":"cellular_component","definition":"A conserved heterodimeric complex with SUMO activating enzyme activity.","definition_xrefs":["PMID:15601841"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00604":null,"SJAG_05032":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"SUMO activating enzyme complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"SAE","type":"exact"},{"name":"SUMO E1 activator enzyme complex","type":"exact"}],"termid":"GO:0031510","terms_by_termid":{"GO:0031510":null}}


id: PBO:0067482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 616, pseudogene","termid":"PBO:0067482"}


id: PBO:0111333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal nucleolar protein, implicated in rDNA metabolism or ribosome biogenesis","termid":"PBO:0111333"}


id: PATO:0002129
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A disposition inhering in a tumour by virtue of the bearer's disposition to invade surrounding tissues.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplastic","termid":"PATO:0002011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplastic, invasive","termid":"PATO:0002129"}


id: PBO:0090355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribose-phosphate pyrophosphokinase","termid":"PBO:0090355"}


id: MONDO:0002174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2) fibrocytes; and (3) retinal pigment epithelial cells. Localized epiretinal membranes may occur at the posterior pole of the eye without clinical signs or may cause marked loss of vision as a result of covering, distorting, or detaching the fovea centralis. Epiretinal membranes may cause vascular leakage and secondary retinal edema. In younger individuals some membranes appear to be developmental in origin and occur in otherwise normal eyes. The majority occur in association with retinal holes, ocular concussions, retinal inflammation, or after ocular surgery. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p291)","definition_xrefs":["MESH:D019773"],"direct_ancestors":[{"relation_name":"is_a","term_name":"degeneration of macula and posterior pole","termid":"MONDO:0002175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"preretinal fibrosis","secondary_identifiers":["SCTID:367649002","MEDGEN:87388","UMLS:C0339543","ICD9:362.89","ICD9:362.56","DOID:2006"],"synonyms":[{"name":"cellophane maculopathy","type":"exact"},{"name":"macular puckering of retina","type":"exact"},{"name":"macular retinal puckering","type":"exact"}],"termid":"MONDO:0002174","xrefs":{"Monarch":{"xref_id":"0002174"}}}


id: PBO:0001852
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.1.1.33","termid":"PBO:0001852"}


id: MONDO:0008941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, syndromic intellectual disability characterized by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnea. There have been no further descriptions in the literature since 1987.","definition_xrefs":["Orphanet:2031"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary parenchymatous liver disease (obsolete MONDO:0015508)","termid":"MONDO:0015508"},{"relation_name":"excluded_subClassOf","term_name":"familial cystic renal disease","termid":"MONDO:0019741"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatic fibrosis-renal cysts-intellectual disability syndrome","secondary_identifiers":["OMIM:213010","MESH:C565867","UMLS:C1859300","GARD:5177","MEDGEN:347120"],"synonyms":[{"name":"Thompson Baraitser syndrome","type":"exact"},{"name":"Thompson-Baraitser syndrome","type":"exact"},{"name":"cerebellar vermis aplasia with associated features suggesting SMITH-Lemli-Opitz syndrome and Meckel syndrome","type":"related"}],"termid":"MONDO:0008941","xrefs":{"Monarch":{"xref_id":"0008941"}}}


id: GO:0031481
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A myosin complex containing a dimer of class XI myosin heavy chains and associated light chains. Myosin XI heavy chain sizes are similar in molecular structure to the class V myosins with 5 to 6 IQ motifs and tail regions with predicted coiled coil domains (forming dimeric molecules) and large C-terminal regions.","definition_xrefs":["PMID:29307817","PMID:22973289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unconventional myosin complex","termid":"GO:0016461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0015629"],"is_obsolete":false,"name":"myosin XI complex","termid":"GO:0031481"}


id: MONDO:0000344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Ross River virus.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alphavirus infectious disease","termid":"MONDO:0005643"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ross river fever","secondary_identifiers":["DOID:0050518","MEDGEN:1673033","SCTID:602001","UMLS:C0919833"],"synonyms":[{"name":"Ross River virus caused disease or disorder","type":"exact"},{"name":"Ross River virus disease","type":"exact"},{"name":"Ross River virus disease or disorder","type":"exact"},{"name":"Ross River virus infectious disease","type":"exact"}],"termid":"MONDO:0000344","xrefs":{"Monarch":{"xref_id":"0000344"}}}


id: PBO:0112880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial dihydrolipoamide dehydrogenase (e3 component of oxoglutarate dehydrogenase complex) Dld1","termid":"PBO:0112880"}


id: MONDO:0019269
data:
  {"annotated_genes":["SJAG_02085","SJAG_02326","SJAG_02842","SJAG_01307"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85646,85647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014010"},{"annotations":[86229,86230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100221"}]},"cv_name":"mondo","definition":"Disorders of cornification that are characterized by visible scaling and/or hyperkeratosis of most or all of the skin. Inherited ichthyoses, defined as the generalized form of Mendelian disorders of cornification, affect most or all of the skin. This etiologically and phenotypically heterogenous group of conditions is caused by mutations in various different genes important for keratinocyte differentiation and epidermal barrier function. Acquired forms of ichthyosis can be observed with certain autoimmune, inflammatory, metabolic, endocrine, or infectious diseases or with malignancies.","definition_xrefs":["PMID:22739337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal disease","termid":"MONDO:0019268"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01307":null,"SJAG_02085":null,"SJAG_02326":null,"SJAG_02842":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ichthyosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:1200618","MedDRA:10021198","MESH:D007057","UMLS:C0020757","GARD:18985","HP:0008064","DOID:1697","NCIT:C84776","Orphanet:79354","MEDGEN:7002"],"synonyms":[{"name":"DOC","type":"exact"},{"name":"disorder of cornification","type":"exact"},{"name":"fish scale disease","type":"exact"},{"name":"fish skin disease","type":"exact"},{"name":"ichthyoses","type":"exact"},{"name":"ichthyosis","type":"exact"},{"name":"ichthyosis (disease)","type":"exact"},{"name":"non-syndromic ichthyosis","type":"related"}],"termid":"MONDO:0019269","terms_by_termid":{"MONDO:0014010":null,"MONDO:0100221":null},"xrefs":{"Monarch":{"xref_id":"0019269"}}}


id: PBO:0088752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHREC complex intermodule linker subunit Clr1","termid":"PBO:0088752"}


id: MONDO:0014997
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nephronophthisis in which the cause of the disease is a mutation in the MAPKBP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephronophthisis","termid":"MONDO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"nephronophthisis 20","secondary_identifiers":["MEDGEN:934607","OMIM:617271","DOID:0111127","GARD:18181","UMLS:C4310640"],"synonyms":[{"name":"MAPKBP1 nephronophthisis (disease)","type":"exact"},{"name":"NPHP20","type":"exact"},{"name":"nephronophthisis (disease) caused by mutation in MAPKBP1","type":"exact"},{"name":"nephronophthisis 20","type":"exact"},{"name":"nephronophthisis type 20","type":"exact"}],"termid":"MONDO:0014997","xrefs":{"Monarch":{"xref_id":"0014997"}}}


id: PATO:0001261
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of red hue and low brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"red","termid":"PATO:0000322"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dark red","termid":"PATO:0001261"}


id: GO:0047047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycerate + CO2 + NAD(P)+ = NAD(P)H + H+ + 2-hydroxy-3-oxosuccinate.","definition_xrefs":["EC:1.1.1.92","MetaCyc:1.1.1.92-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"oxaloglycolate reductase (decarboxylating) activity","synonyms":[{"name":"D-glycerate:NAD(P)+ oxidoreductase (carboxylating)","type":"related"}],"termid":"GO:0047047"}


id: PBO:0047727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FN1 divergent transcript","termid":"PBO:0047727"}


id: PBO:0041676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CADM2 antisense RNA 2","termid":"PBO:0041676"}


id: MONDO:0002970
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the ciliary body.","direct_ancestors":[{"relation_name":"is_a","term_name":"iris disorder","termid":"MONDO:0002289"}],"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":"ciliary body disorder","secondary_identifiers":["NCIT:C35775","DOID:4353","MEDGEN:124384","SCTID:68575007","UMLS:C0271100"],"synonyms":[{"name":"ciliary body disease","type":"exact"},{"name":"ciliary body disease or disorder","type":"exact"},{"name":"ciliary body disorder","type":"exact"},{"name":"disease of ciliary body","type":"exact"},{"name":"disease or disorder of ciliary body","type":"exact"},{"name":"disorder of ciliary body","type":"exact"}],"termid":"MONDO:0002970","xrefs":{"Monarch":{"xref_id":"0002970"}}}


id: GO:0015050
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses methane monooxygenase activity; dimeric and trimeric complexes have been characterized.","definition_xrefs":["GOC:mah","PMID:15544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"methane monooxygenase complex","termid":"GO:0015050"}


id: PR:O60016
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- clr4 gene.","definition_xrefs":["UniProtKB:O60016","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":"histone-lysine N-methyltransferase, H3 lysine-9 specific (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.08c","synonyms":[{"name":"H3-K9-HMTase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-clr4","type":"exact"},{"name":"cryptic loci regulator 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"histone H3-K9 methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"lysine N-methyltransferase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60016"}


id: PBO:0051616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin like domain containing receptor 1","termid":"PBO:0051616"}


id: MONDO:0019452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This subgroup of myeloproliferative neoplasms includes cases which do not meet the morphologic criteria of any of the defined myeloproliferative neoplasms, or which have characteristics that overlap at least two of the myeloproliferative neoplasms.","definition_xrefs":["NCIT:C27350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloproliferative neoplasm","termid":"MONDO:0020076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"myeloproliferative neoplasm, unclassifiable","secondary_identifiers":["ICDO:9975/3","UMLS:C1333046","GARD:16764","MEDGEN:232365","Orphanet:86830"],"synonyms":[{"name":"CMPD, U","type":"exact"},{"name":"CMPD-U","type":"exact"},{"name":"MPN, U","type":"exact"},{"name":"MPN-U","type":"exact"},{"name":"chronic myeloproliferative disease, unclassifiable","type":"exact"},{"name":"chronic myeloproliferative disorder, unclassifiable","type":"exact"},{"name":"myeloproliferative neoplasm, unclassifiable","type":"exact"},{"name":"unclassifiable chronic myeloproliferative disease","type":"exact"},{"name":"unclassifiable chronic myeloproliferative disorder","type":"exact"},{"name":"undifferentiated myeloproliferative disease","type":"exact"}],"termid":"MONDO:0019452","xrefs":{"Monarch":{"xref_id":"0019452"}}}


id: MONDO:8000006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).","definition_xrefs":["Orphanet:51636"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutional neutropenia","termid":"MONDO:0015134"},{"relation_name":"is_a","term_name":"WHIM syndrome","termid":"MONDO:0023880"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"WHIM syndrome 1","secondary_identifiers":["NORD:1849","MESH:C536697","UMLS:C5542296","SCTID:234571003","DOID:0060591","GARD:9297","MEDGEN:1778124","OMIM:193670"],"synonyms":[{"name":"WHIM Syndrome","type":"exact"},{"name":"WHIM syndrome","type":"broad"},{"name":"WHIMS","type":"exact"},{"name":"WILM","type":"exact"},{"name":"Warts, hypogammaglobulinemia, infections, and myelokathexis","type":"exact"},{"name":"Warts, hypogammaglobulinemia, infections, and myelokathexis syndrome","type":"exact"},{"name":"Warts-hypogammaglobulinemia-infections-myelokathexis syndrome","type":"exact"},{"name":"Warts-infections-leukopenia-myelokatexis syndrome","type":"exact"},{"name":"myelokathexis, isolated","type":"exact"}],"termid":"MONDO:8000006","xrefs":{"Monarch":{"xref_id":"8000006"}}}


id: GO:0030766
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + 11-O-demethyl-17-O-deacetylvindoline = S-adenosyl-L-homocysteine + 17-O-deacetylvindoline.","definition_xrefs":["EC:2.1.1.94"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016741","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"11-O-demethyl-17-O-deacetylvindoline O-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.94-RXN","RHEA:20992"],"synonyms":[{"name":"11-demethyl-17-deacetylvindoline 11-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:11-O-demethyl-17-O-deacetylvindoline 11-O-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:16-hydroxytabersonine 16-O-methyltransferase activity","type":"related"},{"name":"tabersonine 16-O-methyltransferase activity","type":"related"}],"termid":"GO:0030766"}


id: PBO:0078580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 53C, pseudogene","termid":"PBO:0078580"}


id: GO:0022608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a multicellular organism to a substrate or other organism.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"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":"multicellular organism adhesion","termid":"GO:0022608"}


id: GO:0061108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the seminal vesicle epithelium over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"tube development","termid":"GO:0035295"},{"relation_name":"is_a","term_name":"epithelium development","termid":"GO:0060429"},{"relation_name":"part_of","term_name":"seminal vesicle development","termid":"GO:0061107"}],"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":"seminal vesicle epithelium development","termid":"GO:0061108"}


id: MONDO:0001855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"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":"rubeosis iridis","secondary_identifiers":["ICD9:364.42","MEDGEN:488789","DOID:14000","SCTID:51995000","UMLS:C0154916"],"termid":"MONDO:0001855","xrefs":{"Monarch":{"xref_id":"0001855"}}}


id: GO:0045658
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neutrophil differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of granulocyte differentiation","termid":"GO:0030852"},{"relation_name":"regulates","term_name":"neutrophil differentiation","termid":"GO:0030223"}],"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 neutrophil differentiation","termid":"GO:0045658"}


id: PBO:0084279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein of the endoplasmic reticulum; required for normal content of cell wall beta-1,6-glucan","termid":"PBO:0084279"}


id: PBO:0027478
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cytokinesis_checkpoint","termid":"PBO:0027478"}


id: GO:0021933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The inward migration of postmitotic granule cells along a radial glial cell from the external granule layer to the internal granule cell layer.","definition_xrefs":["PMID:15157725","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:jid","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hindbrain radial glia guided cell migration","termid":"GO:0021932"}],"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":"radial glia guided migration of cerebellar granule cell","termid":"GO:0021933"}


id: PBO:0004797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM22 inner membrane protein import complex subunit Tim54 (predicted)","termid":"PBO:0004797"}


id: GO:0010962
data:
  {"annotated_genes":["SJAG_03705","SJAG_01255","SJAG_04668","SJAG_02278","SJAG_04509","SJAG_04659","SJAG_01787","SJAG_04462","SJAG_04771","SJAG_00963","SJAG_01376","SJAG_00610","SJAG_04666","SJAG_00424"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79221,77548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"},{"annotations":[87875,92785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"},{"annotations":[88252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032951"},{"annotations":[92769,106289,103209,105715,118420,118290,91132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090334"},{"annotations":[95307,89801,92791,103211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of glucan biosynthesis. Glucan biosynthetic processes are the chemical reactions and pathways resulting in the formation of glucans, polysaccharides consisting only of glucose residues.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide biosynthetic process","termid":"GO:0032885"},{"relation_name":"regulates","term_name":"glucan biosynthetic process","termid":"GO:0009250"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00424":null,"SJAG_00610":null,"SJAG_00963":null,"SJAG_01255":null,"SJAG_01376":null,"SJAG_01787":null,"SJAG_02278":null,"SJAG_03705":null,"SJAG_04462":null,"SJAG_04509":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0010962","terms_by_termid":{"GO:0032951":null,"GO:0045719":null,"GO:0070610":null,"GO:0090334":null,"GO:0140748":null}}


id: MONDO:0001824
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder affecting more than one nerve.","definition_xrefs":["NCIT:C26951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral neuropathy","termid":"MONDO:0005244"}],"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":"polyneuropathy","secondary_identifiers":["icd11.foundation:58868923","UMLS:C0152025","MEDGEN:57502","ICD9:356.9","SCTID:42345000","DOID:1389","ICD9:357.4","MESH:D011115","EFO:0009562"],"synonyms":[{"name":"polyneuropathy","type":"exact"}],"termid":"MONDO:0001824","xrefs":{"Monarch":{"xref_id":"0001824"}}}


id: PBO:0056476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule associated tyrosine carboxypeptidase 2","termid":"PBO:0056476"}


id: PBO:0070006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1303, pseudogene","termid":"PBO:0070006"}


id: MOD:01533
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ8plex-113 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ8plex-113 reporter+balance reagent acylated residue","termid":"MOD:01528"},{"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-serine","termid":"MOD:02003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-113 reporter+balance reagent O3-acylated serine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"Representative mass and accurate mass for 113, 114, 116 & 117","type":"related"},{"name":"iTRAQ8plex","type":"related"},{"name":"iTRAQ8plex:13C(7)15N(1)","type":"related"}],"termid":"MOD:01533"}


id: FYPO:0000145
data:
  {"alleles_by_uniquename":{"SJAG_00370:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00370","name":"erg1delta","uniquename":"SJAG_00370:allele-1"},"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_01330:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01330","name":"mad2delta","uniquename":"SJAG_01330:allele-1"},"SJAG_03360:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03360","name":"shc1delta","uniquename":"SJAG_03360: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":[119656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000619"}],"single_locus_phenotype":[{"annotations":[119657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000619"},{"annotations":[119513,119514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006545"},{"annotations":[119989,119644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004318"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype that affects the regulation of a molecular function, biological process, or biological quality.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process phenotype","termid":"FYPO:0000114"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00370":null,"SJAG_00871":null,"SJAG_01330":null,"SJAG_03360":null,"SJAG_04284":null,"SJAG_04464":null},"genotype_count":5,"genotypes_by_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":{"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"}]}]},"erg1delta":{"display_name":"erg1delta","display_uniquename":"erg1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00370:allele-1","expression":"Null"}]}]},"mad2delta":{"display_name":"mad2delta","display_uniquename":"mad2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01330:allele-1","expression":"Null"}]}]},"nup61delta":{"display_name":"nup61delta","display_uniquename":"nup61delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04284:allele-1","expression":"Null"}]}]},"shc1delta":{"display_name":"shc1delta","display_uniquename":"shc1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03360:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04464","SJAG_00871"],"name":"regulation phenotype","references_by_uniquename":{"PMID:21802294":null,"PMID:28954740":null,"PMID:32109380":null,"PMID:40195311":null},"single_locus_annotated_genes":["SJAG_03360","SJAG_04284","SJAG_01330","SJAG_00370"],"single_locus_genotype_uniquenames":["erg1delta","nup61delta","mad2delta","shc1delta"],"synonyms":[{"name":"fission yeast regulation phenotype","type":"exact"}],"termid":"FYPO:0000145","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYPO:0000619":null,"FYPO:0004318":null,"FYPO:0006545":null,"FYPO_EXT:0000001":null}}


id: FYPO:0001451
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which cells show decreased sensitivity to freezing.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"resistance to cold","termid":"FYPO:0001450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"resistance to freezing","synonyms":[{"name":"increased growth during cellular response to freezing","type":"exact"},{"name":"increased vegetative cell population growth during cellular response to freezing","type":"exact"},{"name":"resistance to freezing during mitotic cell cycle","type":"related"},{"name":"resistance to freezing during vegetative growth","type":"exact"},{"name":"resistant to freeze-thawing","type":"related"},{"name":"resistant to freezing","type":"exact"}],"termid":"FYPO:0001451"}


id: GO:0005965
data:
  {"annotated_genes":["SJAG_04923","SJAG_02583"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71706,73947],"is_not":false,"summary":null,"term":"GO:0005965"}]},"cv_name":"cellular_component","definition":"A protein complex that possesses protein farnesyltransferase activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02583":null,"SJAG_04923":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"protein farnesyltransferase complex","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0005965","terms_by_termid":{"GO:0005965":null}}


id: PBO:0062845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoclastogenesis associated transmembrane protein 1","termid":"PBO:0062845"}


id: PBO:0047178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 199, X-linked","termid":"PBO:0047178"}


id: PBO:0091906
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human AGO2","termid":"PBO:0091906"}


id: GO:0036015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-3 stimulus.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"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 interleukin-3","synonyms":[{"name":"response to IL-3","type":"exact"}],"termid":"GO:0036015"}


id: MONDO:1012683
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any X-linked chondrodysplasia characterized by spondylosis and arthrosis that occurs in dogs.","definition_xrefs":["PMID:17212747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia, dog","termid":"MONDO:1011194"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylo-epiphyseal dysplasia tarda, X-linked, dog","secondary_identifiers":["OMIA:001448-9615"],"synonyms":[{"name":"spondyloepiphyseal dysplasia, congenital type, dog","type":"related"}],"termid":"MONDO:1012683","xrefs":{"Monarch":{"xref_id":"1012683"}}}


id: GO:0050293
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + testololactone = H+ + testolate.","definition_xrefs":["RHEA:13721","EC:3.1.1.37"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"steroid-lactonase activity","secondary_identifiers":["KEGG_REACTION:R03641","MetaCyc:STEROID-LACTONASE-RXN"],"synonyms":[{"name":"testololactone lactonohydrolase activity","type":"related"}],"termid":"GO:0050293"}


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


# genes

id: HGNC:100
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"ASIC1","product":"acid sensing ion channel subunit 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:100"}


id: HGNC:10000
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS4","product":"regulator of G protein signaling 4","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10000"}


id: HGNC:10001
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS5","product":"regulator of G protein signaling 5","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10001"}


id: HGNC:10002
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS6","product":"regulator of G protein signaling 6","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10002"}


id: HGNC:10003
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS7","product":"regulator of G protein signaling 7","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10003"}


id: HGNC:10004
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS9","product":"regulator of G protein signaling 9","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10004"}


id: HGNC:10006
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"genes_by_uniquename":{"HGNC:10006":null,"SJAG_04731":null},"has_protein_features":false,"name":"RHAG","ortholog_annotations":[{"gene_uniquename":"HGNC:10006","ortholog_taxonid":4897,"ortholog_uniquename":"SJAG_04731","reference_uniquename":"PMID:29761456"}],"product":"Rh associated glycoprotein","references_by_uniquename":{"PMID:29761456":null},"split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10006"}


id: HGNC:10007
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RHBDL1","product":"rhomboid like 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10007"}


id: HGNC:10008
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"genes_by_uniquename":{"HGNC:10008":null,"SJAG_04731":null},"has_protein_features":false,"name":"RHCE","ortholog_annotations":[{"gene_uniquename":"HGNC:10008","ortholog_taxonid":4897,"ortholog_uniquename":"SJAG_04731","reference_uniquename":"PMID:29761456"}],"product":"Rh blood group CcEe antigens","references_by_uniquename":{"PMID:29761456":null},"split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10008"}


id: HGNC:10009
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"genes_by_uniquename":{"HGNC:10009":null,"SJAG_04731":null},"has_protein_features":false,"name":"RHD","ortholog_annotations":[{"gene_uniquename":"HGNC:10009","ortholog_taxonid":4897,"ortholog_uniquename":"SJAG_04731","reference_uniquename":"PMID:29761456"}],"product":"Rh blood group D antigen","references_by_uniquename":{"PMID:29761456":null},"split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10009"}


id: HGNC:1001
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"BCL6","product":"BCL6 transcription repressor","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:1001"}


id: HGNC:10010
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RHEBP1","product":"RHEB pseudogene 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10010"}


id: HGNC:10011
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"genes_by_uniquename":{"HGNC:10011":null,"SJAG_02605":null},"has_protein_features":false,"name":"RHEB","ortholog_annotations":[{"gene_uniquename":"HGNC:10011","ortholog_taxonid":4897,"ortholog_uniquename":"SJAG_02605","reference_uniquename":"PMID:29761456"}],"product":"Ras homolog, mTORC1 binding","references_by_uniquename":{"PMID:29761456":null},"split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10011"}


id: HGNC:10012
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RHO","product":"rhodopsin","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10012"}


id: HGNC:10013
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"GRK1","product":"G protein-coupled receptor kinase 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10013"}


id: HGNC:10017
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RIT2","product":"Ras like without CAAX 2","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10017"}


id: HGNC:10018
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RING1","product":"ring finger protein 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10018"}


id: HGNC:10019
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RIPK1","product":"receptor interacting serine/threonine kinase 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10019"}


id: HGNC:1002
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"BCL6B","product":"BCL6B transcription repressor","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:1002"}


id: HGNC:10020
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RIPK2","product":"receptor interacting serine/threonine kinase 2","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10020"}


id: HGNC:10021
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RIPK3","product":"receptor interacting serine/threonine kinase 3","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10021"}


id: HGNC:10023
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RIT1","product":"Ras like without CAAX 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10023"}


id: HGNC:10024
data:
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id: HGNC:10025
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id: HGNC:10026
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id: HGNC:10027
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id: HGNC:10031
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id: HGNC:10037
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id: HGNC:10038
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id: HGNC:10039
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id: HGNC:1004
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id: HGNC:10040
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id: HGNC:10041
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id: HGNC:10042
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id: HGNC:10043
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id: HGNC:10044
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id: HGNC:10045
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id: HGNC:10046
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id: HGNC:10047
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id: HGNC:10048
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id: HGNC:10049
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id: HGNC:1005
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id: HGNC:10050
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id: HGNC:10055
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id: HGNC:10056
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id: HGNC:10057
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id: HGNC:10058
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id: HGNC:10059
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id: HGNC:1006
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id: HGNC:10060
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id: HGNC:10061
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id: HGNC:10062
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id: HGNC:10063
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id: HGNC:10064
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id: HGNC:10065
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id: HGNC:10066
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id: HGNC:10067
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id: HGNC:10068
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id: HGNC:10069
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id: HGNC:1007
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id: HGNC:10070
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id: HGNC:10071
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id: HGNC:10072
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id: HGNC:10073
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id: HGNC:10074
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id: HGNC:10075
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id: HGNC:10078
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id: HGNC:10079
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id: HGNC:1008
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id: HGNC:10080
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id: HGNC:10082
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id: HGNC:10083
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id: HGNC:10084
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id: HGNC:10085
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id: HGNC:10086
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id: HGNC:10096
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id: HGNC:10097
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id: HGNC:10098
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id: HGNC:10099
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id: HGNC:101
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id: HGNC:10100
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id: HGNC:10101
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id: HGNC:10103
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id: HGNC:10104
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id: HGNC:10105
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id: HGNC:10106
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id: HGNC:10107
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id: HGNC:10108
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id: HGNC:10109
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id: HGNC:10110
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id: HGNC:10111
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id: HGNC:10112
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id: HGNC:10113
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id: HGNC:10114
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id: HGNC:10115
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id: HGNC:10116
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id: HGNC:10118
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id: HGNC:10119
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id: HGNC:1012
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id: HGNC:10120
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id: HGNC:10123
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id: HGNC:10128
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id: HGNC:10130
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id: HGNC:10133
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id: HGNC:10137
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id: HGNC:10139
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id: HGNC:1014
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id: HGNC:10140
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id: HGNC:10142
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id: HGNC:10143
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id: HGNC:10144
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id: HGNC:10145
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id: HGNC:10146
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id: HGNC:10147
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id: HGNC:10148
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id: HGNC:10149
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id: HGNC:1015
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id: HGNC:10150
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id: HGNC:10151
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id: HGNC:10152
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id: HGNC:10153
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id: HGNC:10154
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id: HGNC:10155
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id: HGNC:10157
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id: HGNC:10158
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id: HGNC:10159
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id: HGNC:1016
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id: HGNC:10160
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id: HGNC:10161
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id: HGNC:10162
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id: HGNC:10163
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id: HGNC:10164
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id: HGNC:10165
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id: HGNC:10166
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id: HGNC:10168
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id: HGNC:1017
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id: HGNC:10175
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id: HGNC:10177
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id: HGNC:10178
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id: HGNC:10179
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id: HGNC:1018
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id: HGNC:10180
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id: HGNC:10181
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id: HGNC:10182
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id: HGNC:10183
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id: HGNC:10184
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id: HGNC:10185
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id: HGNC:10186
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id: HGNC:10187
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id: HGNC:10188
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id: HGNC:10189
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id: HGNC:10192
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id: HGNC:10193
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id: HGNC:10194
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id: HGNC:10195
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id: HGNC:10196
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id: HGNC:10197
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id: HGNC:10198
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id: HGNC:10199
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id: HGNC:102
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id: HGNC:1020
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id: HGNC:10200
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id: HGNC:10201
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id: HGNC:10202
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id: HGNC:10203
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id: HGNC:10204
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id: HGNC:10205
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id: HGNC:10206
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id: HGNC:10207
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id: HGNC:10208
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id: HGNC:10209
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id: HGNC:10210
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id: HGNC:10211
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id: HGNC:10212
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id: HGNC:10214
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id: HGNC:10215
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id: HGNC:10216
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id: HGNC:10217
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id: HGNC:10218
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id: HGNC:10219
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id: HGNC:1022
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id: HGNC:10220
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id: HGNC:10221
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id: HGNC:10222
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id: HGNC:10223
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id: HGNC:10224
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id: HGNC:10225
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id: HGNC:10226
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id: HGNC:10227
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id: HGNC:10228
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id: HGNC:10229
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id: HGNC:1023
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id: HGNC:10230
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id: HGNC:10231
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id: HGNC:10232
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id: HGNC:10233
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id: HGNC:10234
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id: HGNC:10235
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id: HGNC:10236
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id: HGNC:10237
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id: HGNC:10239
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id: HGNC:1024
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id: HGNC:10240
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id: HGNC:10241
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id: HGNC:10242
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id: HGNC:10243
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id: HGNC:10244
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id: HGNC:10245
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id: HGNC:10246
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id: HGNC:10247
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id: HGNC:10248
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id: HGNC:10249
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id: HGNC:10250
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id: HGNC:10251
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id: HGNC:10252
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id: HGNC:10253
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id: HGNC:10254
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id: HGNC:10256
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id: HGNC:10257
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id: HGNC:10258
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id: HGNC:10259
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id: HGNC:10260
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id: HGNC:10261
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id: HGNC:10263
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id: HGNC:1027
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id: HGNC:10274
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id: HGNC:10288
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id: HGNC:10289
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id: HGNC:1029
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id: HGNC:10290
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id: HGNC:10291
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id: HGNC:10293
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id: HGNC:10294
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id: HGNC:10295
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id: HGNC:10296
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id: HGNC:10297
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id: HGNC:10298
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id: HGNC:10299
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id: HGNC:103
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id: HGNC:1030
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id: HGNC:10300
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id: HGNC:10301
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id: HGNC:10302
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id: HGNC:10303
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id: HGNC:10304
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id: HGNC:10305
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id: HGNC:10306
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id: HGNC:10307
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id: HGNC:10310
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id: HGNC:10311
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id: HGNC:10312
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id: HGNC:10313
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id: HGNC:10314
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id: HGNC:10315
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id: HGNC:10316
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id: HGNC:10317
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id: HGNC:10318
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id: HGNC:10319
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id: HGNC:10320
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id: HGNC:10321
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id: HGNC:10322
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id: HGNC:10324
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id: HGNC:10325
data:
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id: HGNC:10327
data:
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id: HGNC:10328
data:
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id: HGNC:10329
data:
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id: HGNC:1033
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id: HGNC:10330
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id: HGNC:10331
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id: HGNC:10332
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id: HGNC:10333
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id: HGNC:10334
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id: HGNC:10335
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id: HGNC:10336
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id: HGNC:10337
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id: HGNC:10338
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id: HGNC:10339
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id: HGNC:1034
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id: HGNC:10340
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id: HGNC:10341
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id: HGNC:10342
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id: HGNC:10343
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id: HGNC:10344
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id: HGNC:10345
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id: HGNC:10346
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id: HGNC:10347
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id: HGNC:10348
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id: HGNC:10349
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id: HGNC:10350
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id: HGNC:10351
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id: HGNC:10352
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id: HGNC:10353
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id: HGNC:10354
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id: HGNC:10355
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id: HGNC:10356
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id: HGNC:10357
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id: HGNC:10358
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id: HGNC:10359
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id: HGNC:1036
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id: HGNC:10360
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id: HGNC:10361
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id: HGNC:10362
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id: HGNC:10363
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id: HGNC:10364
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id: HGNC:10367
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id: HGNC:10368
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id: HGNC:10369
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id: HGNC:1037
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id: HGNC:10371
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id: HGNC:10372
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id: HGNC:10377
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id: HGNC:10378
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id: HGNC:10379
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id: HGNC:10380
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id: HGNC:10381
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id: HGNC:10382
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id: HGNC:10383
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id: HGNC:10384
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id: HGNC:10385
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id: HGNC:10386
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id: HGNC:10387
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id: HGNC:10388
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id: HGNC:10389
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id: HGNC:10396
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id: HGNC:10397
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id: HGNC:10398
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id: HGNC:10399
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id: HGNC:104
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id: HGNC:1040
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id: HGNC:10401
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id: HGNC:10402
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id: HGNC:10404
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id: HGNC:10405
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id: HGNC:10406
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id: HGNC:10407
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id: HGNC:10408
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id: HGNC:10409
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id: HGNC:1041
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id: HGNC:10410
data:
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id: HGNC:10411
data:
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id: HGNC:10412
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id: HGNC:10413
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id: HGNC:10414
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id: HGNC:10415
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id: HGNC:10416
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id: HGNC:10417
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id: HGNC:10418
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id: HGNC:10419
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id: HGNC:10420
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id: HGNC:10421
data:
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id: HGNC:10422
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id: HGNC:10424
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id: HGNC:10425
data:
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id: HGNC:10426
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id: HGNC:10427
data:
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id: HGNC:10428
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id: HGNC:10429
data:
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id: HGNC:1043
data:
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id: HGNC:10430
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id: HGNC:10431
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id: HGNC:10432
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id: HGNC:10433
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id: HGNC:10434
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id: HGNC:10435
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id: HGNC:10436
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id: HGNC:10437
data:
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id: HGNC:10439
data:
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id: HGNC:1044
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id: HGNC:10440
data:
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id: HGNC:10441
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id: HGNC:10442
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id: HGNC:10443
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id: HGNC:10445
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id: HGNC:10446
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id: HGNC:10447
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id: HGNC:10448
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id: HGNC:10449
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id: HGNC:10450
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id: HGNC:10451
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id: HGNC:10452
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id: HGNC:10454
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id: HGNC:10455
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id: HGNC:10456
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id: HGNC:10457
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id: HGNC:10458
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id: HGNC:1046
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id: HGNC:10461
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id: HGNC:10464
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id: HGNC:10466
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id: HGNC:10467
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id: HGNC:10468
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id: HGNC:10469
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id: HGNC:1047
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id: HGNC:10471
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id: HGNC:10472
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id: HGNC:10473
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id: HGNC:10474
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id: HGNC:10475
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id: HGNC:10477
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id: HGNC:10478
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id: HGNC:10479
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id: HGNC:1048
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id: HGNC:10480
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id: HGNC:10481
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id: HGNC:10482
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id: HGNC:10483
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id: HGNC:10484
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id: HGNC:10485
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id: HGNC:10486
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id: HGNC:10487
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id: HGNC:10488
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id: HGNC:10489
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id: HGNC:1049
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id: HGNC:10490
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id: HGNC:10491
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id: HGNC:10492
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id: HGNC:10493
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id: HGNC:10494
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id: HGNC:10495
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id: HGNC:10496
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id: HGNC:10497
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id: HGNC:10498
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id: HGNC:10499
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id: HGNC:105
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id: HGNC:1050
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id: HGNC:10500
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id: HGNC:10504
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id: HGNC:1051
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id: HGNC:10513
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id: HGNC:10514
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id: HGNC:10515
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id: HGNC:10516
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id: HGNC:10518
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id: HGNC:10519
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id: HGNC:1052
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id: HGNC:10520
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id: HGNC:10521
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id: HGNC:10522
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id: HGNC:10524
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id: HGNC:10525
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id: HGNC:10526
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id: HGNC:10527
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id: HGNC:10528
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id: HGNC:1053
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id: HGNC:10530
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id: HGNC:10532
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id: HGNC:10534
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id: HGNC:10535
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id: HGNC:10536
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id: HGNC:10537
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id: HGNC:10538
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id: HGNC:10539
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id: HGNC:1054
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id: HGNC:10540
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id: HGNC:10541
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id: HGNC:10542
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id: HGNC:10545
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id: HGNC:10546
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id: HGNC:10547
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id: HGNC:10548
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id: HGNC:10549
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id: HGNC:1055
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id: HGNC:10555
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id: HGNC:10560
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id: HGNC:10561
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id: HGNC:10563
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id: HGNC:10564
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id: HGNC:10565
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id: HGNC:10566
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id: HGNC:10567
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id: HGNC:10569
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id: HGNC:1057
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id: HGNC:10570
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id: HGNC:10571
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id: HGNC:10572
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id: HGNC:10573
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id: HGNC:10575
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id: HGNC:10576
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id: HGNC:10577
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id: HGNC:1058
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id: HGNC:10580
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id: HGNC:10581
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id: HGNC:10582
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id: HGNC:10583
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id: HGNC:10585
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id: HGNC:10586
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id: HGNC:10588
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id: HGNC:10589
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id: HGNC:1059
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id: HGNC:10590
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id: HGNC:10591
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id: HGNC:10592
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id: HGNC:10593
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id: HGNC:10594
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id: HGNC:10596
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id: HGNC:10597
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id: HGNC:10599
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id: HGNC:1060
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id: HGNC:10600
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id: HGNC:10601
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id: HGNC:10602
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id: HGNC:10603
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id: HGNC:10604
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id: HGNC:10606
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id: HGNC:10607
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id: HGNC:10608
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id: HGNC:10609
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id: HGNC:10610
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id: HGNC:10611
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id: HGNC:10612
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id: HGNC:10613
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id: HGNC:10614
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id: HGNC:10615
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id: HGNC:10616
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id: HGNC:10617
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id: HGNC:10618
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id: HGNC:10619
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id: HGNC:1062
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id: HGNC:10620
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id: HGNC:10621
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id: HGNC:10622
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id: HGNC:10623
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id: HGNC:10624
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id: HGNC:10625
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id: HGNC:10626
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id: HGNC:10627
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id: HGNC:10628
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id: HGNC:10629
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id: HGNC:1063
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id: HGNC:10630
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id: HGNC:10631
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id: HGNC:10632
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id: HGNC:10634
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id: HGNC:10635
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id: HGNC:10637
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id: HGNC:10638
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id: HGNC:10639
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id: HGNC:10640
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id: HGNC:10641
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id: HGNC:10642
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id: HGNC:10643
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id: HGNC:10645
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id: HGNC:10646
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id: HGNC:10647
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id: HGNC:10648
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id: HGNC:1065
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id: HGNC:10658
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id: HGNC:10659
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id: HGNC:1066
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id: HGNC:10660
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id: HGNC:10661
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id: HGNC:10662
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id: HGNC:10663
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id: HGNC:10664
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id: HGNC:10665
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id: HGNC:10666
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id: HGNC:10667
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id: HGNC:10668
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id: HGNC:10669
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id: HGNC:1067
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id: HGNC:10671
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id: HGNC:10672
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id: HGNC:10675
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id: HGNC:10676
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id: HGNC:1068
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id: HGNC:10680
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id: HGNC:10681
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id: HGNC:10682
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id: HGNC:10683
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id: HGNC:10684
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id: HGNC:10685
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id: HGNC:10686
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id: HGNC:10687
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id: HGNC:10688
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id: HGNC:10689
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id: HGNC:1069
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id: HGNC:10690
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id: HGNC:10691
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id: HGNC:10696
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id: HGNC:10697
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id: HGNC:10698
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id: HGNC:10699
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id: HGNC:1070
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id: HGNC:10700
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id: HGNC:10701
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id: HGNC:10702
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id: HGNC:10703
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id: HGNC:10704
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id: HGNC:10705
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id: HGNC:10706
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id: HGNC:10707
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id: HGNC:1071
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id: HGNC:10710
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id: HGNC:10711
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id: HGNC:10712
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id: HGNC:10713
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id: HGNC:10714
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id: HGNC:10715
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id: HGNC:10716
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id: HGNC:10717
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id: HGNC:10718
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id: HGNC:10719
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id: HGNC:1072
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id: HGNC:10720
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id: HGNC:10721
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id: HGNC:10722
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id: HGNC:10723
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id: HGNC:10724
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id: HGNC:10725
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id: HGNC:10726
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id: HGNC:10727
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id: HGNC:10728
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id: HGNC:10729
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id: HGNC:1073
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id: HGNC:10730
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id: HGNC:10731
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id: HGNC:10732
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id: HGNC:10734
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id: HGNC:10735
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id: HGNC:10736
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id: HGNC:10737
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id: HGNC:10738
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id: HGNC:10739
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id: HGNC:1074
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id: HGNC:10740
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id: HGNC:10741
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id: HGNC:10742
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id: HGNC:10743
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id: HGNC:1075
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id: HGNC:10750
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id: HGNC:10751
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id: HGNC:10752
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id: HGNC:10753
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id: HGNC:10755
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id: HGNC:10756
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id: HGNC:10757
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id: HGNC:10759
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id: HGNC:1076
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id: HGNC:10760
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id: HGNC:10761
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id: HGNC:10762
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id: HGNC:10763
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id: HGNC:10765
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id: HGNC:10766
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id: HGNC:10767
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id: HGNC:10768
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id: HGNC:10769
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id: HGNC:1077
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id: HGNC:10770
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id: HGNC:10771
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id: HGNC:10773
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id: HGNC:10774
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id: HGNC:10775
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id: HGNC:10776
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id: HGNC:10777
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id: HGNC:10778
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id: HGNC:10779
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id: HGNC:1078
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id: HGNC:10780
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id: HGNC:10781
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id: HGNC:10782
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id: HGNC:10783
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id: HGNC:10784
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id: HGNC:10785
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id: HGNC:10786
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id: HGNC:10787
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id: HGNC:10788
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id: HGNC:10789
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id: HGNC:1079
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id: HGNC:10790
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id: HGNC:10791
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id: HGNC:10792
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id: HGNC:10798
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id: HGNC:10799
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id: HGNC:108
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id: HGNC:1080
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