Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Kcnh2 and short QT 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 KCNH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to short QT syndrome  (DOID:0050793)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: short QT syndrome
  • Original References(s): PMID:18692916, PMID:19174314, PMID:22581653


  • An association has been curated linking Kcnh2 and short QT 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 KCNH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to short QT syndrome  (DOID:0050793)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: short QT syndrome
  • Original References(s): PMID:19340359, PMID:22581653


  • An association has been curated linking Kcnh2 and short QT 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 KCNH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to short QT syndrome  (DOID:0050793)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: short QT syndrome
  • Original References(s): PMID:11173780, PMID:12925462, PMID:14676148, PMID:15828882, PMID:19088443, PMID:19439805, PMID:19501051, PMID:22194679, PMID:22581653


  • An association has been curated linking Kcnh2 and short QT 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 KCNH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to short QT syndrome  (DOID:0050793)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: short QT syndrome
  • Original References(s): PMID:21130771, PMID:22581653


  • An association has been curated linking Kcnh2 and short QT 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 KCNH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 CRRD objects have been annotated to short QT syndrome  (DOID:0050793)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: short QT syndrome
  • Original References(s): PMID:12925462, PMID:14676148, PMID:22581653


  • An association has been curated linking Kcnh2 and short QT syndrome in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Kcnh2 (Mus musculus) [(IEA) inferred from electronic annotation]
  • 8 CRRD objects have been annotated to short QT syndrome  (DOID:0050793)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: OMIM:609620 | OMIM:609621 | OMIM:609622


  • Go Back to source page   Continue to Ontology report



    NHLBI Logo

    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.