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Results 1 - 10 of 10 for kcnq1
  1. KCNQ1 gene 
    The KCNQ1 gene belongs to a large family of genes that provide instructions for making potassium channels. These channels, which transport positively charged ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  2. KCNQ1OT1 gene 
    The KCNQ1OT1 gene is located within another gene, KCNQ1. Because the two genes share a region of ... DNA, the KCNQ1OT1 gene is also known as KCNQ1 overlapping transcript 1 or KCNQ1 opposite strand/antisense ...
    https://medlineplus.gov/genetics/gene/kcnq1ot1 - Genetics
  3. Short QT syndrome 
    ... experience symptoms. Mutations in the KCNH2, KCNJ2, and KCNQ1 genes can cause short QT syndrome. These genes ... normal rhythm. Mutations in the KCNH2, KCNJ2, or KCNQ1 gene increase the activity of the channels, which ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  4. Familial atrial fibrillation 
    ... to be associated with familial atrial fibrillation was KCNQ1, which provides instructions for making a channel that ... risk of developing atrial fibrillation. ABCC9 KCNH2 KCNJ2 KCNQ1 LMNA PRKAG2 RYR2 SCN5A Additional Information from NCBI ...
    https://medlineplus.gov/.../condition/familial-atrial-fibrillation - Genetics
  5. KCNE1 gene 
    ... called alpha subunits, which are produced from the KCNQ1 gene. One beta subunit, produced from the KCNE1 ... Marx SO, Karlin A, Kass RS. Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1. ...
    https://medlineplus.gov/genetics/gene/kcne1 - Genetics
  6. Jervell and Lange-Nielsen syndrome 
    ... is caused by mutations in the KCNE1 and KCNQ1 genes. These genes provide instructions for making proteins ... Nielsen syndrome are caused by mutations in the KCNQ1 gene; KCNE1 mutations are responsible for the remaining ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
  7. Romano-Ward syndrome 
    ... therefore may not be diagnosed. Mutations in the KCNQ1, KCNH2, and SCN5A genes are the most common ... very small percentage of cases. CAV3 KCNH2 KCNJ5 KCNQ1 SCN5A Additional Information from NCBI Gene: AKAP9 CALM1 ...
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  8. KCNH2 gene 
    ... G, Cohen N, Aerssens J. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  9. Gestational diabetes 
    ... risk of developing type 2 diabetes. GCK KCNJ11 KCNQ1 Additional Information from NCBI Gene: CDKAL1 IGF2BP2 IRS1 ...
    https://medlineplus.gov/genetics/condition/gestational-diabetes - Genetics
  10. SCN5A gene 
    ... G, Cohen N, Aerssens J. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics