| KCNH1 | 
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| Identifiers | 
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| Aliases | KCNH1, EAG, EAG1, Kv10.1, h-eag, TMBTS, ZLS1, hEAG1, potassium voltage-gated channel subfamily H member 1, hEAG | 
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| External IDs | OMIM: 603305; MGI: 1341721; HomoloGene: 68242; GeneCards: KCNH1; OMA:KCNH1 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 1 (mouse) | 
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 |  |  | Band | 1|1 H6 | Start | 191,873,082 bp | 
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 | End | 192,192,467 bp | 
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| Wikidata | 
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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.