CADM2
cell adhesion molecule 2
Summary
This gene encodes a member of the synaptic cell adhesion molecule 1 (SynCAM) family which belongs to the immunoglobulin (Ig) superfamily. The encoded protein has three Ig-like domains and a cytosolic protein 4.1 binding site near the C-terminus. Proteins belonging to the protein 4.1 family crosslink spectrin and interact with other cytoskeletal proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]
Known Variants150 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1248857 | 3:85,018,612 | G/A | intron variant | — |
| rs1248855 | 3:85,019,809 | C/T | intron variant | — |
| rs13082518 | 3:85,027,085 | G/A | intron variant | — |
| rs9831123 | 3:85,052,150 | C/A | — | — |
| rs2035562 | 3:85,056,521 | A/G | regulatory region variant | — |
| rs1872556 | 3:85,065,229 | A/T | — | — |
| rs7645787 | 3:85,085,714 | C/T | intron variant | — |
| rs9284802 | 3:85,095,766 | G/A | intron variant | — |
| rs6768559 | 3:85,100,901 | C/A | — | — |
| rs6791035 | 3:85,122,909 | C/T | intron variant | — |
| rs9309969 | 3:85,134,557 | T/C | — | — |
| rs34201102 | 3:85,137,499 | A/G | intron variant | — |
| rs66500121 | 3:85,137,683 | A/G | intron variant | — |
| rs9883252 | 3:85,138,818 | T/A | — | — |
| rs9819278 | 3:85,144,350 | G/A | intron variant | — |
| rs73843290 | 3:85,145,836 | T/C | intron variant | — |
| rs13064817 | 3:85,166,315 | G/T | intron variant | — |
| rs9309970 | 3:85,171,302 | C/T | intron variant | — |
| rs4856268 | 3:85,202,524 | T/G | — | — |
| rs73130739 | 3:85,287,296 | T/C | intron variant | — |
| rs2290339 | 3:85,362,016 | T/C | intron variant | — |
| rs818219 | 3:85,374,589 | T/C | intron variant | — |
| rs146071762 | 3:85,396,778 | T/C | — | — |
| rs9810488 | 3:85,396,964 | G/C | — | — |
| rs1368748 | 3:85,412,330 | A/T | — | — |
| rs9870448 | 3:85,416,384 | A/G | intron variant | — |
| rs9854869 | 3:85,420,724 | C/A | intron variant | — |
| rs4279114 | 3:85,421,737 | C/G | intron variant | — |
| rs73845475 | 3:85,433,074 | T/C | upstream gene variant | — |
| rs9863620 | 3:85,448,493 | T/C | intron variant | — |
| rs71626887 | 3:85,449,777 | G/T | intron variant | — |
| rs62250685 | 3:85,457,240 | A/C | — | — |
| rs77242693 | 3:85,462,759 | C/T | intron variant | — |
| rs4856570 | 3:85,466,861 | C/T | intron variant | — |
| rs62250686 | 3:85,468,446 | T/C | — | — |
| rs62250687 | 3:85,469,353 | T/A | intron variant | — |
| rs74664784 | 3:85,475,292 | T/C | — | — |
| rs11920427 | 3:85,477,685 | C/A | — | — |
| rs78841189 | 3:85,478,462 | T/A | intron variant | — |
| rs1865250 | 3:85,481,412 | T/C | intron variant | — |
| rs1025531 | 3:85,486,931 | T/A | intron variant | — |
| rs9825494 | 3:85,487,470 | A/C | intron variant | — |
| rs568187754 | 3:85,491,766 | A/G | — | — |
| rs9828679 | 3:85,497,198 | T/C | intron variant | — |
| rs11922956 | 3:85,497,807 | A/T | — | — |
| rs13323436 | 3:85,502,845 | T/A | intron variant | — |
| rs57630146 | 3:85,508,427 | G/C | — | — |
| rs6762267 | 3:85,513,115 | C/G | — | — |
| rs62250714 | 3:85,515,776 | G/A | intron variant | — |
| rs6800177 | 3:85,516,952 | A/T | intron variant | — |
| rs2875907 | 3:85,518,580 | A/C | — | — |
| rs62250717 | 3:85,521,990 | C/G | intron variant | — |
| rs11127893 | 3:85,524,170 | C/T | intron variant | — |
| rs67416405 | 3:85,539,234 | T/C | intron variant | — |
| rs76395182 | 3:85,547,337 | T/G | — | — |
| rs62250753 | 3:85,552,240 | C/G | — | — |
| rs4637303 | 3:85,552,787 | C/A | — | — |
| rs68102233 | 3:85,558,538 | G/T | — | — |
| rs1463202 | 3:85,564,781 | A/T | intron variant | — |
| rs62250759 | 3:85,569,026 | A/G | intron variant | — |
| rs113642272 | 3:85,579,472 | G/C | — | — |
| rs17516256 | 3:85,580,588 | G/A | intron variant | — |
| rs62252504 | 3:85,581,770 | C/A | — | — |
| rs113351222 | 3:85,581,991 | A/G | — | — |
| rs62252507 | 3:85,582,078 | C/A | — | — |
| rs10511076 | 3:85,583,193 | A/G | intron variant | — |
| rs10511075 | 3:85,583,403 | G/C | — | — |
| rs12629607 | 3:85,583,608 | T/C | intron variant | — |
| rs66625173 | 3:85,585,091 | A/G | intron variant | — |
| rs2167046 | 3:85,586,806 | G/A | intron variant | — |
| rs2122235 | 3:85,586,921 | C/G | — | — |
| rs35438712 | 3:85,588,205 | T/G | — | — |
| rs17457426 | 3:85,588,962 | A/C | intron variant | — |
| rs2326316 | 3:85,592,445 | C/G | — | — |
| rs6790090 | 3:85,592,750 | T/A | intron variant | — |
| rs6807666 | 3:85,594,428 | A/C | intron variant | — |
| rs12714629 | 3:85,598,424 | T/C | intron variant | — |
| rs6783138 | 3:85,599,920 | C/G | intron variant | — |
| rs7652683 | 3:85,603,462 | T/A | — | — |
| rs76084961 | 3:85,604,041 | T/G | — | — |
| rs17518584 | 3:85,604,923 | C/T | intron variant | — |
| rs1449371 | 3:85,607,323 | T/A | — | — |
| rs17459563 | 3:85,609,365 | G/C | — | — |
| rs72615727 | 3:85,609,398 | G/T | — | — |
| rs77852438 | 3:85,609,412 | C/A | — | — |
| rs78015688 | 3:85,610,907 | T/G | intron variant | — |
| rs1449382 | 3:85,612,053 | G/T | — | — |
| rs4856591 | 3:85,612,550 | T/G | intron variant | — |
| rs4856592 | 3:85,612,730 | G/A | intron variant | — |
| rs1375550 | 3:85,613,380 | A/C | — | — |
| rs62250491 | 3:85,616,009 | G/T | intron variant | — |
| rs542809491 | 3:85,617,378 | A/T | — | — |
| rs6790699 | 3:85,624,189 | A/T | — | — |
| rs1551042 | 3:85,630,551 | A/G | — | — |
| rs1972994 | 3:85,631,142 | A/C | — | — |
| rs35344466 | 3:85,633,021 | A/C | intron variant | — |
| rs6782190 | 3:85,639,672 | G/C | — | — |
| rs2029130 | 3:85,644,047 | T/C | — | — |
| rs55753638 | 3:85,644,482 | T/C | intron variant | — |
| rs1900917 | 3:85,646,059 | C/G | intron variant | — |
Showing 100 of 150 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.