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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by OMIM:614296
  • Original References(s): PMID:21538838


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with WFS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:19877185 PMID:20069065 PMID:24033266


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:10679252 PMID:24033266 PMID:25388789 PMID:25741868


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11295831 PMID:19877185 PMID:20875904 PMID:21067485 PMID:21143470 PMID:21538838 PMID:22238590 PMID:24033266 PMID:24890733 PMID:26435059 PMID:26467025 PMID:26875006 PMID:27395765 PMID:28432734 PMID:29529044


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:16648378 PMID:17492394 PMID:18544103 PMID:21917145 PMID:24033266


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:15605410 PMID:24033266 PMID:25741868


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:24033266 PMID:25133958 PMID:25741868


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant


    • An association has been curated linking Wfs1 and autosomal dominant Wolfram syndrome in Rattus norvegicus.        

  • 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]
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 31 papers in RGD have been used to annotate Wfs1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:18544103 PMID:24033266 PMID:25133958 PMID:25741868 PMID:28492532


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