Gene: KCNQ4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9132
Gene Symbol: KCNQ4
KCNQ4 		0.010 GeneticVariation disease BEFREE The c.140T>C (p.Leu47Pro) mutation in KCNQ4 causes progressive NSHL; however, the defective channel activity of the mutant protein can be rescued using channel activators. 30556268 2019