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GENE - TERM ANNOTATION REPORT

45 Annotations Found.

An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by OMIM:609621
  • Original References(s): PMID:11278406, PMID:15051636, PMID:15159330, PMID:20436212, PMID:22581653


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:19716085, PMID:22581653, PMID:23392653, PMID:24033266, PMID:25741868, PMID:25854863, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:26168993


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:16109388, PMID:17999538, PMID:18599533, PMID:19841300, PMID:22250012, PMID:22581653, PMID:23375927, PMID:24006450, PMID:24818999, PMID:25348405, PMID:25974115, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:25741868


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14661677, PMID:15234419, PMID:19841300, PMID:22378279, PMID:22581653, PMID:2294929, PMID:22949429, PMID:24055113, PMID:25348405, PMID:25637381, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:10737999, PMID:11087258, PMID:12736279, PMID:14678125, PMID:17999538, PMID:19841300, PMID:22581653, PMID:22949429, PMID:24667783, PMID:25741868, PMID:27041150, PMID:27251404, PMID:28492532, PMID:28600177, PMID:30571187, PMID:9641694, PMID:9927399


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:19716085, PMID:22581653, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:10973849, PMID:11997281, PMID:14661677, PMID:14731347, PMID:15051636, PMID:15242738, PMID:16155735, PMID:16487223, PMID:17016049, PMID:17210839, PMID:17597962, PMID:19841300, PMID:22581653, PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:10807545, PMID:11761407, PMID:14661677, PMID:15028050, PMID:15500450, PMID:16038262, PMID:16487223, PMID:17016049, PMID:18426444, PMID:19841300, PMID:22378279, PMID:22581653, PMID:22949429, PMID:24033266, PMID:24284363, PMID:24388587, PMID:24762593, PMID:25741868, PMID:26159999, PMID:26385840, PMID:26467025, PMID:28492532, PMID:28704380, PMID:9799083


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14661677, PMID:19841300, PMID:22581653, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14678125, PMID:19716085, PMID:22581653, PMID:25741868, PMID:26077850, PMID:27159321, PMID:27650965, PMID:27884173, PMID:28438721, PMID:28492532, PMID:28944242, PMID:29197658


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:18752142, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:19716085, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14760488, PMID:16132053, PMID:24033266, PMID:25741868


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15913580, PMID:17210839, PMID:17470695, PMID:17999538, PMID:18222468, PMID:18611041, PMID:19490272, PMID:19716085, PMID:19815527, PMID:21185501, PMID:21215473, PMID:21778721, PMID:22581653, PMID:23304551, PMID:23465283, PMID:24033266, PMID:24920132, PMID:25637381, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15192825, PMID:24033266, PMID:25741868, PMID:26467025, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14661677, PMID:14678125, PMID:16556865, PMID:17161064, PMID:17210839, PMID:17470695, PMID:19841300, PMID:19862833, PMID:21185501, PMID:22581653, PMID:22677073, PMID:22949429, PMID:23571586, PMID:23861362, PMID:24033266, PMID:25741868, PMID:26498160, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14998624, PMID:19716085


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14661677, PMID:17210839, PMID:19841300, PMID:22581653, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:10482963, PMID:10704188, PMID:10737999, PMID:10973849, PMID:11530100, PMID:12736279, PMID:14510661, PMID:15935335, PMID:16556866, PMID:22309168, PMID:22539601, PMID:23098067, PMID:23392653, PMID:24033266, PMID:24052033, PMID:24552659, PMID:24912595, PMID:25236808, PMID:25705178, PMID:25741868, PMID:26019114, PMID:26546361, PMID:27451284, PMID:27816319, PMID:27831900, PMID:28438721, PMID:28492532, PMID:28720088, PMID:29247119, PMID:29379719, PMID:29740400, PMID:32238909


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15840476, PMID:19841300, PMID:22581653


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:16487223, PMID:21063070, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:19841300, PMID:22581653, PMID:25649125, PMID:25741868, PMID:25854863, PMID:26318259, PMID:28492532, PMID:29197658, PMID:31696929


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15840476, PMID:19716085, PMID:19841300, PMID:20851114, PMID:22581653, PMID:22949429, PMID:23098067, PMID:24606995, PMID:24667783, PMID:25351510, PMID:25741868, PMID:28588847, PMID:29197658


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15840476, PMID:22378279, PMID:22581653, PMID:24055113, PMID:25608792, PMID:25637381, PMID:25741868, PMID:28449774, PMID:28492532, PMID:29197658


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:12566525, PMID:22581653, PMID:24033266, PMID:24190995, PMID:25741868


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15547041, PMID:18752142, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:26467025


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:24033266


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:10807545, PMID:18426444, PMID:20851114, PMID:21779290, PMID:23890619, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:12402336, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:19716085, PMID:24033266, PMID:25741868, PMID:26704558, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:16487223, PMID:23890619, PMID:25741868, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:14661676, PMID:14661677, PMID:17016049, PMID:19841300, PMID:22581653, PMID:22947121, PMID:25348405, PMID:25741868, PMID:26118460, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:10704188, PMID:11530100, PMID:14510661, PMID:14678125, PMID:15051636, PMID:15935335, PMID:19716085, PMID:22629021, PMID:23174487, PMID:23392653, PMID:24357532, PMID:24606995, PMID:24912595, PMID:25705178, PMID:25741868, PMID:26669661, PMID:28492532


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:11668641, PMID:12175777, PMID:12402336, PMID:23098067, PMID:23935525, PMID:24033266, PMID:26467025, PMID:26937405, PMID:28302345, PMID:28360401


  • An association has been curated linking Kcnq1 and Short QT Syndrome 2 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 KCNQ1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Short QT Syndrome 2  (DOID:9001050)
  • 30 papers in CRRD have been used to annotate Kcnq1
  • Curation Notes: ClinVar Annotator: match by term: Short QT syndrome 2
  • Original References(s): PMID:15840476, PMID:22581653, PMID:24033266, PMID:25741868


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