KCNQ Potassium Channels

A family of delayed rectifier voltage-gated potassium channels that share homology with their founding member, KCNQ1 PROTEIN. KCNQ potassium channels have been implicated in a variety of diseases including LONG QT SYNDROME; DEAFNESS; and EPILEPSY.

Also Known As:

KvLQT Potassium Channels; Potassium Channels, KCNQ; Potassium Channels, KvLQT

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Carrier Proteins: 12999
    - Membrane Transport Proteins: 589
      - Ion Channels: 6731
        Potassium Channels: 2882
        Voltage-Gated Potassium Channels: 811
        Delayed Rectifier Potassium Channels: 14
        KCNQ Potassium Channels: 9
  - Membrane Proteins: 10078
    - Membrane Glycoproteins: 2252
      - Ion Channels: 6731
        Potassium Channels: 2882
        Voltage-Gated Potassium Channels: 811
        Delayed Rectifier Potassium Channels: 14
        KCNQ Potassium Channels: 9
    - Membrane Transport Proteins: 589
      - Ion Channels: 6731
        Potassium Channels: 2882
        Voltage-Gated Potassium Channels: 811
        Delayed Rectifier Potassium Channels: 14
        KCNQ Potassium Channels: 9

rat Kcnq5 protein

Bio-Agent Context: Research Results