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GENE - TERM ANNOTATION REPORT

18 Annotations Found.

An association has been curated linking Kcnh2 and Short QT Syndrome 1 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 KCNH2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with KCNH2 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:18724381, PMID:29574456


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:16414944, PMID:22581653, PMID:25741868, PMID:26164358, PMID:28492532


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by OMIM:609620
  • 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 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:25741868


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:19862833, PMID:22581653, PMID:25741868, PMID:26958806, PMID:28492532


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:12925462, PMID:14676148, PMID:22581653


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:10973849, PMID:15051636, PMID:19716085, PMID:22581653, PMID:23861362, PMID:25741868, PMID:28492532, PMID:30246897, PMID:30758498, PMID:30996762


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:18776039, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:19716085, PMID:22581653, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:10973849, PMID:11468227, PMID:11668638, PMID:11854117, PMID:16432067, PMID:17905336, PMID:18808722, PMID:19716085, PMID:19841300, PMID:22573844, PMID:22581653, PMID:23303164, PMID:24606995, PMID:25417810, PMID:25741868, PMID:26063740, PMID:26496715, PMID:28492532, PMID:9544837


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:19716085, PMID:22581653, PMID:24033266, PMID:25741868, PMID:26743238, PMID:28492532


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:14661677, PMID:19841300, PMID:22581653, PMID:25649125, PMID:25741868, PMID:28492532, PMID:29752375


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:22677073, PMID:25741868, PMID:28492532, PMID:28988457


  • An association has been curated linking Kcnh2 and Short QT Syndrome 1 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]
  • 1 CRRD objects have been annotated to Short QT Syndrome 1  (DOID:9005764)
  • 21 papers in CRRD have been used to annotate Kcnh2
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 1
  • Original References(s): PMID:10483966, PMID:10862094, PMID:10973849, PMID:15840476, PMID:19490267, PMID:19716085, PMID:19841300, PMID:20659946, PMID:22581653, PMID:22949429, PMID:23098067, PMID:24033266, PMID:24606995, PMID:25741868, PMID:26063740, PMID:26187847, PMID:26958806, PMID:28431243, PMID:28492532


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