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GENE - TERM ANNOTATION REPORT

20 Annotations Found.

An association has been curated linking KCNAB2 and genetic disease 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:401719349 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:13532087 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156307881 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:401750190 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:329396227 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:329349915 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:329391565 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:329364600 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:329381086 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156287812 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:155908683 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156033467 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156058717 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156365697 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156000292 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156136618 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156385788 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:156293336 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:42723667 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNAB2 and genetic disease 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:155915040 (Homo sapiens)
  • 32751 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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