Details
| Type | Protein Coding |
| Official Symbol | KCNQ1 |
| Official Name | potassium voltage-gated channel subfamily Q member 1 [Source:HGNC Symbol;Acc:HGNC:6294] |
| Ensembl ID | ENSG00000282076 |
| Bio databases IDs | |
| Aliases | potassium voltage-gated channel subfamily Q member 1 |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- ATRIAL FIBRILLATION FAMILIAL 3
- BECKWITH-WIEDEMANN SYNDROME
- JERVELL AND LANGE-NIELSEN SYNDROME 1
- LONG QT SYNDROME 1
- SHORT QT SYNDROME 2
- Jervell and Lange-Nielsen syndrome type 1