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NCBI Description of KCTD7 |
This gene encodes 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. |
Community Annotation of KCTD7 Add / Edit KCTD7: Annotations
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Figure notes
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Data details