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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Wfs1 and Wolfram syndrome in Heterocephalus glaber.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with WFS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 0 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: Diabetes mellitus AND insipidus with optic atrophy AND deafness | ClinVar Annotator: match by term: Wolfram syndrome
  • Original References(s): PMID:10521293 PMID:11161832 PMID:11244483 PMID:1161832 PMID:12754709 PMID:12955714 PMID:15151504 PMID:15277431 PMID:16806192 PMID:17568405 PMID:17603484 PMID:18060660 PMID:19344068 PMID:20301750 PMID:20738327 PMID:21446023 PMID:21602428 PMID:22226368 PMID:22238590 PMID:23429432 PMID:23596069 PMID:24033266 PMID:24890733 PMID:25133958 PMID:25741868 PMID:26435059 PMID:26875006 PMID:27395765 PMID:28432734 PMID:28492532 PMID:29207974 PMID:30014265 PMID:30245029 PMID:30773290 PMID:30957632 PMID:31264968 PMID:31567480 PMID:31980526 PMID:32141364 PMID:33046911 PMID:33763535 PMID:33841295 PMID:33879153 PMID:34404380 PMID:34426522 PMID:35018440 PMID:35469785 PMID:36098976 PMID:36208030 PMID:36227502 PMID:37508961 PMID:37510321


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