| KCNH1 |
|---|
|
|
| Identifiers |
|---|
| Aliases | KCNH1, EAG, EAG1, Kv10.1, h-eag, TMBTS, ZLS1, hEAG1, potassium voltage-gated channel subfamily H member 1, hEAG |
|---|
| External IDs | OMIM: 603305; MGI: 1341721; HomoloGene: 68242; GeneCards: KCNH1; OMA:KCNH1 - orthologs |
|---|
|
| Gene location (Mouse) |
|---|
| | Chr. | Chromosome 1 (mouse) |
|---|
| | Band | 1|1 H6 | Start | 191,873,082 bp |
|---|
| End | 192,192,467 bp |
|---|
|
|
|
|
| Wikidata |
|
Potassium voltage-gated channel subfamily H member 1 (KV10.1, EAG1) is a protein that in humans is encoded by the KCNH1 gene. Mutations in KCNH1 cause genetic epilepsy and developmental encephalopathies, and aberant expression is associated with tumor progression.