Gene: ESPN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83715
Gene Symbol: ESPN
ESPN 		0.300 Biomarker disease CTD_human Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation. 15930085 2006
Entrez Id: 83715
Gene Symbol: ESPN
ESPN 		0.300 Biomarker disease CTD_human Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction. 15286153 2004