NCAM2
neural cell adhesion molecule 2
Summary
The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein and may function in selective fasciculation and zone-to-zone projection of the primary olfactory axons. [provided by RefSeq, Jul 2008]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1368157918 | 21:22,370,928 | G/A | — | uncertain significance |
| rs116546079 | 21:22,370,929 | C/T | — | likely benign |
| rs150332667 | 21:22,400,228 | G/A | intron variant | — |
| rs185618424 | 21:22,417,258 | A/G | intron variant | — |
| rs116844215 | 21:22,430,303 | C/G | intron variant | — |
| rs141580342 | 21:22,452,847 | C/T | intron variant | — |
| rs12483272 | 21:22,480,541 | G/T | intron variant | — |
| rs2826659 | 21:22,487,854 | A/T | — | — |
| rs545323979 | 21:22,547,518 | G/A | — | — |
| rs563875257 | 21:22,559,251 | T/G | — | — |
| rs868203661 | 21:22,582,923 | C/A | — | likely benign |
| rs556299601 | 21:22,582,962 | G/A | — | likely benign |
| rs75625065 | 21:22,652,978 | T/C | — | benign |
| rs371967791 | 21:22,656,588 | G/C | — | uncertain significance |
| rs182642680 | 21:22,656,629 | T/C | — | likely benign |
| rs767308325 | 21:22,658,612 | G/A | — | uncertain significance |
| rs2516987658 | 21:22,658,616 | C/T | — | uncertain significance |
| rs748510401 | 21:22,658,685 | C/T | — | likely benign |
| rs770305591 | 21:22,658,687 | G/A | — | uncertain significance |
| rs774494067 | 21:22,658,703 | A/G | — | uncertain significance |
| rs373022329 | 21:22,658,723 | A/G | — | uncertain significance |
| rs762586053 | 21:22,664,424 | A/G | — | uncertain significance |
| rs751188340 | 21:22,664,427 | G/A | — | uncertain significance |
| rs145537614 | 21:22,664,446 | C/T | — | benign |
| rs2517017224 | 21:22,664,447 | A/G | — | uncertain significance |
| rs371793861 | 21:22,664,480 | G/T | — | uncertain significance |
| rs761740603 | 21:22,664,516 | G/A | — | uncertain significance |
| rs990255529 | 21:22,664,549 | G/A | — | uncertain significance |
| rs189711623 | 21:22,669,253 | A/G | intron variant | — |
| rs11088859 | 21:22,689,344 | G/C | — | — |
| rs232464 | 21:22,695,321 | T/A | — | — |
| rs763784898 | 21:22,696,804 | G/A | — | likely benign |
| rs1360579692 | 21:22,696,811 | C/T | — | uncertain significance |
| rs554440628 | 21:22,707,850 | G/A | — | uncertain significance |
| rs780643681 | 21:22,707,859 | A/T | — | uncertain significance |
| rs772671391 | 21:22,707,889 | G/A | — | uncertain significance |
| rs760767027 | 21:22,707,905 | A/G | — | uncertain significance |
| rs373865162 | 21:22,710,781 | C/T | — | uncertain significance |
| rs35654962 | 21:22,710,849 | G/A | — | benign |
| rs575430945 | 21:22,725,486 | G/A | — | — |
| rs232518 | 21:22,746,187 | T/C | — | benign |
| rs372471672 | 21:22,746,196 | G/A | — | uncertain significance |
| rs1340678477 | 21:22,746,210 | G/A | — | uncertain significance |
| rs1030161443 | 21:22,746,330 | G/A | — | uncertain significance |
| rs232423 | 21:22,755,223 | G/A | intron variant | — |
| rs866523167 | 21:22,782,756 | G/A | — | uncertain significance |
| rs986371 | 21:22,790,831 | T/C | — | benign |
| rs1214721154 | 21:22,790,850 | A/T | — | uncertain significance |
| rs2077359690 | 21:22,804,451 | G/T | — | uncertain significance |
| rs760268583 | 21:22,804,590 | A/G | — | uncertain significance |
| rs2077364378 | 21:22,804,591 | T/G | — | uncertain significance |
| rs551217096 | 21:22,816,012 | C/G | — | — |
| rs116800392 | 21:22,817,514 | G/C | — | — |
| rs565689408 | 21:22,824,187 | G/T | — | — |
| rs759393821 | 21:22,838,935 | G/A | — | uncertain significance |
| rs1192983313 | 21:22,841,003 | A/G | — | uncertain significance |
| rs2518006995 | 21:22,841,027 | A/G | — | uncertain significance |
| rs2518007012 | 21:22,841,028 | A/G | — | uncertain significance |
| rs192393333 | 21:22,841,450 | T/C | intron variant | — |
| rs150089513 | 21:22,842,348 | T/G | intron variant | — |
| rs180894612 | 21:22,842,426 | C/T | intron variant | — |
| rs11700959 | 21:22,845,008 | G/A | intron variant | — |
| rs189693383 | 21:22,848,052 | A/G | intron variant | — |
| rs149390445 | 21:22,848,802 | G/A | intron variant | — |
| rs201923816 | 21:22,849,618 | A/G | — | uncertain significance |
| rs1199652566 | 21:22,849,626 | C/A | — | uncertain significance |
| rs143579715 | 21:22,849,672 | T/C | — | benign |
| rs748814453 | 21:22,849,696 | G/T | — | uncertain significance |
| rs80026670 | 21:22,852,055 | A/G | — | — |
| rs564715921 | 21:22,867,027 | C/T | — | — |
| rs59586716 | 21:22,875,049 | C/A | — | — |
| rs201600701 | 21:22,881,163 | C/A | — | likely benign |
| rs2017705 | 21:22,881,251 | A/G | — | benign |
| rs199849179 | 21:22,881,335 | T/G | — | uncertain significance |
| rs200071566 | 21:22,881,350 | A/C | — | uncertain significance |
| rs1988186615 | 21:22,881,351 | C/A | — | uncertain significance |
| rs139508557 | 21:22,882,411 | C/T | intron variant | — |
| rs1263547199 | 21:22,906,881 | T/G | — | uncertain significance |
| rs757705447 | 21:22,906,896 | C/G | — | uncertain significance |
| rs2518228222 | 21:22,906,908 | G/T | — | uncertain significance |
| rs2826891 | 21:22,910,116 | C/A | — | — |
| rs749135738 | 21:22,910,186 | G/A | — | uncertain significance |
| rs1369495827 | 21:22,910,195 | A/G | — | uncertain significance |
| rs2518237797 | 21:22,910,196 | A/C | — | uncertain significance |
| rs376541267 | 21:22,910,240 | G/A | — | uncertain significance |
| rs150466591 | 21:22,910,249 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.