Gene: KCNA2 ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3737
Gene Symbol: KCNA2
KCNA2 		0.100 CausalMutation phenotype CLINVAR Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy. 25477152 2015
Entrez Id: 3737
Gene Symbol: KCNA2
KCNA2 		0.100 CausalMutation phenotype CLINVAR Voltage-sensing residues in the S2 and S4 segments of the Shaker K+ channel. 8663992 1996
Entrez Id: 3737
Gene Symbol: KCNA2
KCNA2 		0.100 CausalMutation phenotype CLINVAR Crystal structure of a mammalian voltage-dependent Shaker family K+ channel. 16002581 2005