Gene: KCNAB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8514
Gene Symbol: KCNAB2
KCNAB2 		0.300 Biomarker phenotype CTD_human Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome. 11580756 2001