SLAMF8
SLAM family member 8
Summary
This gene encodes a member of the CD2 family of cell surface proteins involved in lymphocyte activation. These proteins are characterized by Ig domains. This protein is expressed in lymphoid tissues, and studies of a similar protein in mouse suggest that it may function during B cell lineage commitment. The gene is found in a region of chromosome 1 containing many CD2 genes. [provided by RefSeq, Jul 2008]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs931245451 | 1:159,796,711 | G/A | — | uncertain significance |
| rs377124328 | 1:159,799,671 | C/T | — | uncertain significance |
| rs762647287 | 1:159,799,688 | G/A | — | uncertain significance |
| rs138614766 | 1:159,799,706 | G/A | — | uncertain significance |
| rs943112449 | 1:159,799,707 | G/A | — | likely benign |
| rs748211205 | 1:159,799,734 | C/G | — | uncertain significance |
| rs769924299 | 1:159,799,743 | T/C | — | uncertain significance |
| rs2524925728 | 1:159,799,832 | C/T | — | uncertain significance |
| rs763656998 | 1:159,799,850 | C/G | — | uncertain significance |
| rs148009811 | 1:159,799,886 | G/A | — | likely benign |
| rs1571134790 | 1:159,799,913 | A/C | — | uncertain significance |
| rs141870216 | 1:159,800,116 | A/T | regulatory region variant | — |
| rs866550708 | 1:159,802,704 | G/A | — | uncertain significance |
| rs372242041 | 1:159,802,711 | G/A | — | uncertain significance |
| rs267598116 | 1:159,802,792 | G/A | — | uncertain significance |
| rs759722110 | 1:159,802,794 | C/T | — | uncertain significance |
| rs186733189 | 1:159,802,795 | G/T | — | uncertain significance |
| rs2524945357 | 1:159,802,811 | C/G | — | uncertain significance |
| rs765154247 | 1:159,802,948 | G/T | — | uncertain significance |
| rs149383951 | 1:159,802,965 | G/A | — | uncertain significance |
| rs747086552 | 1:159,803,085 | T/C | — | uncertain significance |
| rs776775459 | 1:159,803,088 | T/A | — | uncertain significance |
| rs548898106 | 1:159,803,103 | C/T | — | uncertain significance |
| rs367765736 | 1:159,803,155 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.