Gene: CEACAM16 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16 		0.320 Biomarker disease 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 		0.320 Biomarker disease CLINGEN Mutations in CEACAM16 cause autosomal dominant nonsyndromic hearing loss (DFNA4B). 26648831 2015
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16 		0.320 GeneticVariation disease BEFREE 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 		0.320 Biomarker disease 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 		0.320 Biomarker disease 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
Entrez Id: 388551
Gene Symbol: CEACAM16
CEACAM16 		0.320 Biomarker disease BEFREE 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