Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 785
Gene Symbol: CACNB4
CACNB4
0.320 GeneticVariation phenotype BEFREE These findings oppose an essential role of the β(4) distal C-terminus in nuclear targeting and challenge the idea that the nuclear function of calcium channel β(4) subunits is critically involved in the etiology of epilepsy and ataxia in patients and mouse models with mutations in the CACNB4 gene. 24875574 2014
Entrez Id: 785
Gene Symbol: CACNB4
CACNB4
0.320 Biomarker phenotype CTD_human To determine the role of the calcium-channel beta4-subunit gene CACNB4 on chromosome 2q22-23 in related human disorders, we screened for mutations in small pedigrees with familial epilepsy and ataxia. 10762541 2000
Entrez Id: 785
Gene Symbol: CACNB4
CACNB4
0.320 GeneticVariation phenotype BEFREE To determine the role of the calcium-channel beta4-subunit gene CACNB4 on chromosome 2q22-23 in related human disorders, we screened for mutations in small pedigrees with familial epilepsy and ataxia. 10762541 2000