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 		0.110 GeneticVariation disease BEFREE We identified a de novo KCND3 mutation causing the most marked change in Kv4.3's channel properties reported so far, which correlated with a severe and unique spinocerebellar ataxia (SCA) type 19/22 disease phenotype. 26189493 2015
Entrez Id: 3752
Gene Symbol: KCND3
KCND3 		0.110 Biomarker disease HPO