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KCTD7 is a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.
Gene Name: | potassium channel tetramerization domain containing 7 |
Synonyms: | KCTD7, EPM3, CLN14 |
Target Sequences: | Q96MP8 Q96MP8 |
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