Details
| Type | Protein Coding |
| Official Symbol | KCNQ2 |
| Official Name | potassium voltage-gated channel subfamily Q member 2 [Source:HGNC Symbol;Acc:HGNC:6296] |
| Ensembl ID | ENSG00000281151 |
| Bio databases IDs | |
| Aliases | potassium voltage-gated channel subfamily Q member 2 |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the KCNQ2 gene in human plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7
- SEIZURES BENIGN FAMILIAL NEONATAL 1
- BENIGN NEONATAL EPILEPSY TYPE 1
- EPILEPTIC ENCEPHALOPATHY EARLY INFANTILE TYPE 7