CEACAM16
CEA cell adhesion molecule 16, tectorial membrane component
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]
Known Variants193 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs117484881 | 19:45,201,694 | C/T | upstream gene variant | — |
| rs536360559 | 19:45,203,696 | C/T | — | — |
| rs1530268 | 19:45,204,298 | G/T | — | benign |
| rs2919847 | 19:45,204,322 | C/A | — | benign |
| rs189900455 | 19:45,204,623 | C/G | — | benign |
| rs182456186 | 19:45,204,692 | C/A | — | likely benign |
| rs374411449 | 19:45,204,712 | G/A | — | likely benign |
| rs1355072516 | 19:45,204,719 | G/A | — | uncertain significance |
| rs377750953 | 19:45,204,731 | C/T | — | conflicting classifications of pathogenicity |
| rs1040792995 | 19:45,204,761 | G/A | — | uncertain significance |
| rs1198256157 | 19:45,204,763 | G/T | — | pathogenic |
| rs747674339 | 19:45,204,770 | G/A | — | likely benign |
| rs571010129 | 19:45,204,801 | C/T | — | likely benign |
| rs116510010 | 19:45,206,510 | C/A | — | likely benign |
| rs2965167 | 19:45,206,532 | A/G | — | benign |
| rs114907619 | 19:45,206,624 | T/C | — | benign |
| rs202230938 | 19:45,206,632 | T/C | — | benign |
| rs368296153 | 19:45,206,642 | G/A | — | uncertain significance |
| rs1974380866 | 19:45,206,651 | A/C | — | uncertain significance |
| rs778614897 | 19:45,206,657 | C/G | — | uncertain significance |
| rs746286359 | 19:45,206,663 | C/G | — | uncertain significance |
| rs1456226708 | 19:45,206,672 | C/A | — | uncertain significance |
| rs769083688 | 19:45,206,673 | C/T | — | uncertain significance |
| rs186687142 | 19:45,206,676 | G/T | — | likely benign |
| rs191552868 | 19:45,206,677 | C/T | — | likely benign |
| rs773449918 | 19:45,206,678 | G/A | — | uncertain significance |
| rs201786853 | 19:45,206,689 | C/T | — | likely benign |
| rs894189 | 19:45,206,695 | G/A | — | benign |
| rs375722926 | 19:45,206,697 | T/A | — | conflicting classifications of pathogenicity |
| rs201593262 | 19:45,206,715 | C/T | — | uncertain significance |
| rs760535948 | 19:45,206,741 | T/C | — | uncertain significance |
| rs747360355 | 19:45,206,745 | C/T | — | conflicting classifications of pathogenicity |
| rs551887849 | 19:45,206,746 | G/A | — | likely benign |
| rs369512841 | 19:45,206,756 | C/T | — | uncertain significance |
| rs978272117 | 19:45,206,777 | G/A | — | uncertain significance |
| rs199924613 | 19:45,206,778 | C/T | — | conflicting classifications of pathogenicity |
| rs201182389 | 19:45,206,789 | G/A | — | uncertain significance |
| rs534225927 | 19:45,206,800 | C/T | — | likely benign |
| rs536837008 | 19:45,206,801 | G/A | — | uncertain significance |
| rs1974385839 | 19:45,206,809 | T/G | — | likely benign |
| rs73568059 | 19:45,206,815 | C/T | — | likely benign |
| rs535370616 | 19:45,206,818 | G/A | — | likely benign |
| rs776527204 | 19:45,206,826 | C/T | — | uncertain significance |
| rs761814983 | 19:45,206,827 | G/A | — | likely benign |
| rs750005713 | 19:45,206,831 | C/T | — | uncertain significance |
| rs373543716 | 19:45,206,843 | C/T | — | uncertain significance |
| rs752941421 | 19:45,206,848 | C/T | — | likely benign |
| rs778130089 | 19:45,206,862 | A/T | — | uncertain significance |
| rs1216516010 | 19:45,206,893 | C/T | — | uncertain significance |
| rs1018820441 | 19:45,206,900 | A/G | — | uncertain significance |
| rs753166718 | 19:45,206,932 | C/T | — | likely benign |
| rs183860695 | 19:45,206,933 | G/A | — | likely benign |
| rs979461820 | 19:45,206,940 | G/C | — | likely benign |
| rs577689341 | 19:45,206,951 | G/C | — | uncertain significance |
| rs73568061 | 19:45,206,984 | C/T | — | likely benign |
| rs575937266 | 19:45,207,036 | T/A | — | benign |
| rs71364503 | 19:45,207,037 | A/T | — | likely benign |
| rs201855875 | 19:45,207,283 | C/A | — | likely benign |
| rs565350614 | 19:45,207,293 | C/T | — | uncertain significance |
| rs1974397617 | 19:45,207,312 | T/C | — | uncertain significance |
| rs387907149 | 19:45,207,323 | A/C | missense variant | pathogenic |
| rs775017974 | 19:45,207,326 | G/C | — | uncertain significance |
| rs374742680 | 19:45,207,338 | C/T | — | uncertain significance |
| rs762263810 | 19:45,207,342 | G/A | — | uncertain significance |
| rs547346351 | 19:45,207,354 | G/A | — | uncertain significance |
| rs2122194539 | 19:45,207,364 | C/A | — | likely pathogenic |
| rs1974399490 | 19:45,207,380 | A/G | — | uncertain significance |
| rs781465343 | 19:45,207,382 | C/T | — | likely benign |
| rs753704474 | 19:45,207,383 | G/A | — | uncertain significance |
| rs770300041 | 19:45,207,407 | G/A | — | uncertain significance |
| rs876661405 | 19:45,207,410 | G/A | missense variant | pathogenic |
| rs200297676 | 19:45,207,413 | G/A | — | conflicting classifications of pathogenicity |
| rs767675963 | 19:45,207,421 | C/T | — | likely benign |
| rs756280582 | 19:45,207,422 | G/A | — | conflicting classifications of pathogenicity |
| rs114645388 | 19:45,207,424 | C/T | — | likely benign |
| rs750153629 | 19:45,207,425 | G/A | — | conflicting classifications of pathogenicity |
| rs780034057 | 19:45,207,428 | C/G | — | conflicting classifications of pathogenicity |
| rs1417666764 | 19:45,207,431 | C/T | — | uncertain significance |
| rs746541677 | 19:45,207,432 | G/A | — | conflicting classifications of pathogenicity |
| rs59028589 | 19:45,207,444 | C/T | — | benign |
| rs747829770 | 19:45,207,451 | C/A | — | uncertain significance |
| rs2122195063 | 19:45,207,454 | C/T | — | uncertain significance |
| rs577629047 | 19:45,207,456 | G/A | — | conflicting classifications of pathogenicity |
| rs370890913 | 19:45,207,470 | C/T | — | conflicting classifications of pathogenicity |
| rs767607056 | 19:45,207,472 | T/C | — | likely benign |
| rs544948409 | 19:45,207,480 | G/A | — | uncertain significance |
| rs376638197 | 19:45,207,482 | C/T | — | uncertain significance |
| rs1414459671 | 19:45,207,493 | C/T | — | likely benign |
| rs367891074 | 19:45,207,494 | G/A | — | conflicting classifications of pathogenicity |
| rs2122195213 | 19:45,207,495 | G/A | — | uncertain significance |
| rs372088113 | 19:45,207,496 | C/T | — | likely benign |
| rs754826882 | 19:45,207,497 | G/A | — | uncertain significance |
| rs1974403999 | 19:45,207,507 | G/T | — | uncertain significance |
| rs376972162 | 19:45,207,523 | G/A | — | likely benign |
| rs573717477 | 19:45,207,528 | G/A | — | uncertain significance |
| rs876657762 | 19:45,207,531 | T/A | — | uncertain significance |
| rs749658138 | 19:45,207,536 | C/T | — | uncertain significance |
| rs915972808 | 19:45,207,541 | C/T | — | uncertain significance |
| rs771309051 | 19:45,207,542 | G/A | — | uncertain significance |
| rs2513588731 | 19:45,207,553 | C/A | — | uncertain significance |
Showing 100 of 193 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.