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 		0.120 GeneticVariation phenotype LHGDN A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family. 18973245 2008
Entrez Id: 83715
Gene Symbol: ESPN
ESPN 		0.120 Biomarker phenotype LHGDN 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 		0.120 CausalMutation phenotype CLINVAR