Gene entry
KCTD7
potassium channel tetramerization domain containing 7
- Chromosome
- 7
- Cytoband
- 7q11.21
- Variants (rsID)
- 3
KCTD7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q11.21). Its official name is “potassium channel tetramerization domain containing 7”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs79736939Benignsingle nucleotide variantProgressive myoclonic epilepsy type 3
- rs145238250Conflicting interpretationssingle nucleotide variantProgressive myoclonic epilepsy type 3|Seizure
- rs372150992Conflicting interpretationssingle nucleotide variantSeizure|Progressive myoclonic epilepsy type 3
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.