Gene: CLDN9 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9080
Gene Symbol: CLDN9
CLDN9 		0.010 GeneticVariation disease BEFREE Through whole-genome sequencing, we identified a one base pair deletion (c.86delT) in CLDN9 in a consanguineous family from Turkey with autosomal recessive nonsyndromic hearing loss. 31175426 2019