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Results 1 - 5 of 5 for KCNQ1
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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