Gene: CLDN14 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14 		0.010 GeneticVariation disease BEFREE Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. 27629923 2017