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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8555857 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2
  • Original References(s): PMID:10739754 PMID:17846994


  • An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:9589540 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2
  • Original References(s): PMID:25056293


  • An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:13539441 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:8690527 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:401738824 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2


  • An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:151713606 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SLC9B1 and Wolfram syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:15195868 (Homo sapiens)
  • 4 RGD objects have been annotated to Wolfram syndrome 2  (DOID:0110630)
  • 2 papers in RGD have been used to annotate SLC9B1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


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