OTOG, otogelin, 340990

N. diseases: 10; N. variants: 9
Disease: Nonsyndromic Deafness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker disease CLINGEN Delayed Otolith Development Does Not Impair Vestibular Circuit Formation in Zebrafish. 28332011 2017
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker disease CLINGEN A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment. 26636018 2015
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker disease CLINGEN Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment. 23122587 2012
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker disease CLINGEN Spatiotemporal expression of otogelin in the developing and adult mouse inner ear. 11506947 2001
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker disease CLINGEN Targeted disruption of otog results in deafness and severe imbalance. 10655058 2000
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker disease CLINGEN Otogelin: a glycoprotein specific to the acellular membranes of the inner ear. 9405633 1997