Gene: EPS8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.300 Biomarker disease CLINGEN Distinct roles of Eps8 in the maturation of cochlear and vestibular hair cells. 27132230 2016
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.300 Biomarker disease CLINGEN Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. 27344577 2016
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.300 Biomarker disease CLINGEN Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia. 27117407 2016
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.300 Biomarker disease CLINGEN EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness. 24741995 2014
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.300 Biomarker disease CLINGEN Regulation of stereocilia length by myosin XVa and whirlin depends on the actin-regulatory protein Eps8. 21236676 2011
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.300 Biomarker disease CLINGEN Eps8 regulates hair bundle length and functional maturation of mammalian auditory hair cells. 21526224 2011