Version 5.4
| Homo sapiens Protein: CEACAM16 | |||||
|---|---|---|---|---|---|
| Summary | |||||
| InnateDB Protein | IDBP-294364.6 | ||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||
| Gene Symbol | CEACAM16 | ||||
| Protein Name | carcinoembryonic antigen-related cell adhesion molecule 16 | ||||
| Synonyms | |||||
| Species | Homo sapiens | ||||
| Ensembl Protein | ENSP00000385576 | ||||
| InnateDB Gene | IDBG-236850 (CEACAM16) | ||||
| Protein Structure |
|
||||
| UniProt Annotation | |||||
| Function | May play a role in maintaining the integrity of the tectorial membrane. | ||||
| Subcellular Localization | Secreted. Note=Localizes to the tip of cochlear outer hair cells and to the tectorial membrane. {ECO:0000250}. | ||||
| Disease Associations | Deafness, autosomal dominant, 4B (DFNA4B) [MIM:614614]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. {ECO:0000269PubMed:21368133}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||
| Tissue Specificity | |||||
| Comments | |||||
| Interactions | |||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
|
||||
| Gene Ontology | |||||
Molecular Function |
|
||||
| Biological Process |
|
||||
| Cellular Component |
|
||||
| Protein Structure and Domains | |||||
| PDB ID | |||||
| InterPro |
IPR003598
Immunoglobulin subtype 2 IPR003599 Immunoglobulin subtype IPR007110 Immunoglobulin-like domain IPR013106 Immunoglobulin V-set domain |
||||
| PFAM |
PF07686
|
||||
| PRINTS | |||||
| PIRSF | |||||
| SMART |
SM00408
SM00409 |
||||
| TIGRFAMs | |||||
| Post-translational Modifications | |||||
| Modification | |||||
| Cross-References | |||||
| SwissProt | Q2WEN9 | ||||
| PhosphoSite | PhosphoSite-Q2WEN9 | ||||
| TrEMBL | |||||
| UniProt Splice Variant | |||||
| Entrez Gene | 388551 | ||||
| UniGene | Hs.456381 | ||||
| RefSeq | |||||
| HUGO | HGNC:31948 | ||||
| OMIM | 614591 | ||||
| CCDS | CCDS54278 | ||||
| HPRD | |||||
| IMGT | |||||
| EMBL | AC092066 AF479646 BC144608 EU021223 | ||||
| GenPept | AAQ05841 ABS52739 | ||||