Gene: KCNJ8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3764
Gene Symbol: KCNJ8
KCNJ8 		0.300 Biomarker phenotype GENOMICS_ENGLAND Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome. 21836131 2011