Gene: KCND3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3752
Gene Symbol: KCND3
KCND3 		0.040 Biomarker disease BEFREE Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome. 18052691 2008
Entrez Id: 3752
Gene Symbol: KCND3
KCND3 		0.040 GeneticVariation disease BEFREE The data suggest that mutations in KCND2 and KCND3 are not a frequent cause of long QT syndrome. 15563876 2005
Entrez Id: 3752
Gene Symbol: KCND3
KCND3 		0.040 GeneticVariation disease BEFREE We report here 20 single-nucleotide polymorphisms (SNPs), including 15 novel ones, in six genes that are considered to be candidates for long QT syndrome (LQTS): 2 SNPs in KCNB1, 3 in KCND3, 3 in KCNJ11, 7 in ABCC9, 3 in ADRB1, and 2 in SLC18A2. 11310586 2001
Entrez Id: 3752
Gene Symbol: KCND3
KCND3 		0.040 GeneticVariation disease BEFREE This information should facilitate the systematic screening of KCND2 and KCND3 exons for mutations in (inherited) arrhythmia syndromes, such as LQTS and Brugada. 10942109 2000