Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 3784
  • Symbol: KCNQ1
  • Description: potassium voltage-gated channel subfamily Q member 1

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Disease_Term Source Rank Other Values
Long QT syndrome 1, 192500 (3) OMIM high
  • Genome region : 11p15.5-p15.4
  • OMIM_ID : 192500 OMIM phenotype ID
  • OMIM_ID : 607542 OMIM gene ID
{Long QT syndrome 1, acquired, susceptibility to}, 192500 (3) OMIM high
  • Genome region : 11p15.5-p15.4
  • OMIM_ID : 192500 OMIM phenotype ID
  • OMIM_ID : 607542 OMIM gene ID
Short QT syndrome 2, 609621 (3) OMIM high
  • Genome region : 11p15.5-p15.4
  • OMIM_ID : 607542 OMIM gene ID
  • OMIM_ID : 609621 OMIM phenotype ID
Atrial fibrillation, familial, 3, 607554 (3) OMIM high
  • Genome region : 11p15.5-p15.4
  • OMIM_ID : 607542 OMIM gene ID
  • OMIM_ID : 607554 OMIM phenotype ID
Jervell and Lange-Nielsen syndrome, 220400 (3) OMIM high
  • Genome region : 11p15.5-p15.4
  • OMIM_ID : 220400 OMIM phenotype ID
  • OMIM_ID : 607542 OMIM gene ID
Blood pressure measurement (high sodium intervention) GWAS high
Protein quantitative trait loci GWAS high
Glucose homeostasis traits GWAS high
Body mass index GWAS high
QT interval GWAS high
Gout GWAS high
Plasma amyloid beta peptide concentrations (ABx-40) GWAS high
Electrocardiographic traits GWAS high
Height GWAS high
Platelet aggregation GWAS high
Glomerular filtration rate in non diabetics (creatinine) GWAS high
Type 2 diabetes GWAS high