CEACAM16 CEA cell adhesion molecule 16, tectorial membrane component
Gene ID: 388551, updated on 2-Nov-2024Gene type: protein coding
Also known as: CEAL2; DFNA4B; DFNB113
- See all available tests in GTR for this gene
- Go to complete Gene record for CEACAM16
- Go to Variation Viewer for CEACAM16 variants
Summary
The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Autosomal dominant nonsyndromic hearing loss 4B | not available |
| Hearing loss, autosomal recessive 113 | not available |
| SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. GeneReviews: Not available |
Genomic context
- Location:
- 19q13.31-q13.32
- Sequence:
- Chromosome: 19; NC_000019.10 (44699151..44710718)
- Total number of exons:
- 7
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CEACAM16 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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