Gene: GJB6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.110 GeneticVariation disease BEFREE There are significant differences in the clinical picture of two rare autosomal dominant syndromes: keratitis-ichthyosis-deafness (KID) syndrome and hidrotic ectodermal dysplasia (Clouston syndrome), which are caused by GJB2 and GJB6 mutations, respectively. 25575739 2015
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.110 Biomarker disease HPO