Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3737
Gene Symbol: KCNA2
KCNA2
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation 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
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Voltage-sensing residues in the S2 and S4 segments of the Shaker K+ channel. 8663992

1996
Entrez Id: 3737
Gene Symbol: KCNA2
KCNA2
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Crystal structure of a mammalian voltage-dependent Shaker family K+ channel. 16002581

2005