CDON
cell adhesion associated, oncogene regulated
Summary
This gene encodes a cell surface receptor that is a member of the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells and positively regulates myogenesis. [provided by RefSeq, Aug 2011]
Known Variants576 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4937076 | 11:125,826,702 | G/A | downstream gene variant | benign |
| rs886047941 | 11:125,826,740 | T/C | — | uncertain significance |
| rs79685272 | 11:125,826,757 | C/T | — | benign |
| rs1230287167 | 11:125,826,774 | C/A | — | uncertain significance |
| rs3039 | 11:125,826,785 | G/A | — | benign |
| rs1945502699 | 11:125,826,830 | C/T | — | uncertain significance |
| rs79719160 | 11:125,826,837 | G/A | — | benign |
| rs142923654 | 11:125,826,865 | G/C | — | likely benign |
| rs1166335234 | 11:125,826,866 | C/T | — | uncertain significance |
| rs61917811 | 11:125,826,918 | A/G | — | likely benign |
| rs886047942 | 11:125,826,921 | C/T | — | uncertain significance |
| rs13424 | 11:125,826,953 | C/A | — | benign |
| rs73019367 | 11:125,826,975 | A/C | — | benign |
| rs116746244 | 11:125,827,007 | C/T | — | benign |
| rs74527873 | 11:125,827,060 | C/T | — | benign |
| rs1047070 | 11:125,827,072 | A/G | — | benign |
| rs1042404589 | 11:125,827,182 | A/G | — | uncertain significance |
| rs140783947 | 11:125,827,209 | G/C | — | benign |
| rs886047943 | 11:125,827,227 | G/A | — | uncertain significance |
| rs77815115 | 11:125,827,323 | T/C | — | benign |
| rs11220285 | 11:125,827,347 | A/G | — | benign |
| rs886047945 | 11:125,827,356 | G/A | — | uncertain significance |
| rs147791703 | 11:125,827,413 | A/G | — | benign |
| rs141160538 | 11:125,827,428 | A/C | — | benign |
| rs531690322 | 11:125,827,543 | T/C | — | uncertain significance |
| rs894728448 | 11:125,827,568 | C/G | — | uncertain significance |
| rs907381947 | 11:125,827,602 | C/T | — | uncertain significance |
| rs539903009 | 11:125,827,616 | T/C | — | likely benign |
| rs886047946 | 11:125,827,627 | T/C | — | uncertain significance |
| rs187258536 | 11:125,827,661 | G/C | — | likely benign |
| rs191432564 | 11:125,827,696 | T/C | — | likely benign |
| rs886047947 | 11:125,827,704 | T/A | — | uncertain significance |
| rs886047948 | 11:125,827,733 | A/G | — | uncertain significance |
| rs73019370 | 11:125,827,761 | A/T | — | benign |
| rs1045261392 | 11:125,827,777 | G/A | — | uncertain significance |
| rs1945529006 | 11:125,827,838 | G/A | — | uncertain significance |
| rs116579152 | 11:125,827,845 | A/G | — | benign |
| rs577809378 | 11:125,827,904 | G/A | — | uncertain significance |
| rs977950622 | 11:125,827,990 | C/A | — | uncertain significance |
| rs1065398 | 11:125,828,007 | T/C | — | benign |
| rs886047949 | 11:125,828,068 | C/T | — | uncertain significance |
| rs1945536687 | 11:125,828,077 | T/C | — | uncertain significance |
| rs188024207 | 11:125,828,082 | T/C | — | uncertain significance |
| rs76176354 | 11:125,828,088 | G/C | — | benign |
| rs2186754 | 11:125,828,097 | A/G | — | benign |
| rs12294405 | 11:125,828,103 | C/T | — | benign |
| rs531873614 | 11:125,828,107 | T/C | — | uncertain significance |
| rs12294553 | 11:125,828,120 | G/A | — | benign |
| rs549903425 | 11:125,828,132 | G/A | — | uncertain significance |
| rs886047950 | 11:125,828,139 | A/G | — | uncertain significance |
| rs886047951 | 11:125,828,197 | T/C | — | uncertain significance |
| rs886047952 | 11:125,828,257 | C/G | — | uncertain significance |
| rs115327518 | 11:125,828,264 | C/T | — | benign |
| rs562083604 | 11:125,828,458 | A/G | — | benign |
| rs582224 | 11:125,828,460 | A/G | — | uncertain significance |
| rs12296046 | 11:125,828,462 | G/A | — | uncertain significance |
| rs371492744 | 11:125,828,464 | G/A | — | uncertain significance |
| rs61917812 | 11:125,828,488 | T/G | — | uncertain significance |
| rs58515733 | 11:125,828,490 | A/G | — | benign |
| rs58251767 | 11:125,828,492 | A/T | — | benign |
| rs1012078514 | 11:125,828,498 | A/T | — | uncertain significance |
| rs192250689 | 11:125,828,546 | A/G | — | benign |
| rs185017679 | 11:125,828,573 | G/A | — | benign |
| rs886047961 | 11:125,828,642 | C/T | — | uncertain significance |
| rs886047962 | 11:125,828,736 | T/C | — | uncertain significance |
| rs76179044 | 11:125,828,740 | C/T | — | benign |
| rs893725040 | 11:125,828,780 | C/T | — | uncertain significance |
| rs148239384 | 11:125,828,813 | G/A | — | benign |
| rs73019373 | 11:125,828,834 | G/C | — | benign |
| rs2509616 | 11:125,828,904 | T/C | — | benign |
| rs1945569001 | 11:125,828,963 | C/A | — | uncertain significance |
| rs947313022 | 11:125,829,003 | C/T | — | uncertain significance |
| rs776338493 | 11:125,829,021 | G/A | — | uncertain significance |
| rs574337524 | 11:125,829,032 | T/C | — | uncertain significance |
| rs886047963 | 11:125,829,034 | G/A | — | uncertain significance |
| rs886047964 | 11:125,829,037 | T/C | — | uncertain significance |
| rs886047965 | 11:125,829,092 | T/C | — | uncertain significance |
| rs886047966 | 11:125,829,101 | G/A | — | uncertain significance |
| rs7940762 | 11:125,829,166 | C/T | — | benign |
| rs192397582 | 11:125,829,176 | G/A | — | uncertain significance |
| rs867218141 | 11:125,829,248 | C/T | — | uncertain significance |
| rs367911589 | 11:125,829,265 | T/C | — | uncertain significance |
| rs886047967 | 11:125,829,320 | C/A | — | uncertain significance |
| rs886047968 | 11:125,829,329 | T/C | — | uncertain significance |
| rs141994408 | 11:125,829,380 | C/T | — | likely benign |
| rs886047970 | 11:125,829,408 | G/A | — | uncertain significance |
| rs77555036 | 11:125,829,505 | A/C | — | benign |
| rs886047971 | 11:125,829,510 | A/C | — | uncertain significance |
| rs539481575 | 11:125,829,530 | A/C | — | benign |
| rs757413144 | 11:125,829,621 | C/T | — | uncertain significance |
| rs886047973 | 11:125,829,626 | T/C | — | uncertain significance |
| rs780047854 | 11:125,829,686 | G/A | — | uncertain significance |
| rs181601254 | 11:125,829,775 | G/A | — | uncertain significance |
| rs114455813 | 11:125,829,776 | A/G | — | benign |
| rs545234191 | 11:125,829,821 | G/A | — | benign |
| rs76724574 | 11:125,829,854 | T/C | — | benign |
| rs79576369 | 11:125,829,921 | C/T | — | benign |
| rs369720108 | 11:125,829,926 | A/G | — | benign |
| rs563620294 | 11:125,829,940 | A/G | — | benign |
| rs148777681 | 11:125,829,966 | G/A | — | benign |
Showing 100 of 576 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.