Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 340990
Gene Symbol: OTOG
OTOG
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN Delayed Otolith Development Does Not Impair Vestibular Circuit Formation in Zebrafish. 28332011

2017
Entrez Id: 340990
Gene Symbol: OTOG
OTOG
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment. 26636018

2015
Entrez Id: 340990
Gene Symbol: OTOG
OTOG
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment. 23122587

2012
Entrez Id: 340990
Gene Symbol: OTOG
OTOG
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN Spatiotemporal expression of otogelin in the developing and adult mouse inner ear. 11506947

2001
Entrez Id: 340990
Gene Symbol: OTOG
OTOG
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN Targeted disruption of otog results in deafness and severe imbalance. 10655058

2000
Entrez Id: 340990
Gene Symbol: OTOG
OTOG
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN Otogelin: a glycoprotein specific to the acellular membranes of the inner ear. 9405633

1997