Gene: EPS8L2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64787
Gene Symbol: EPS8L2
EPS8L2 		0.300 Biomarker disease CLINGEN Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss. 28281779 2017
Entrez Id: 64787
Gene Symbol: EPS8L2
EPS8L2 		0.300 Biomarker disease CLINGEN EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss. 26282398 2015
Entrez Id: 64787
Gene Symbol: EPS8L2
EPS8L2 		0.300 Biomarker disease CLINGEN Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2. 23918390 2013