Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family. 25589040

2015
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN Mutations in CEACAM16 cause autosomal dominant nonsyndromic hearing loss (DFNA4B). 26648831

2015
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies. 22544735

2012
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN In aggregate, these data identify CEACAM16 as an α-tectorin-interacting protein that concentrates at the point of attachment of the TM to the stereocilia and, when mutated, results in ADNSHL at the DFNA4 locus. 21368133

2011