SIGLEC10
sialic acid binding Ig like lectin 10
Summary
SIGLECs are members of the immunoglobulin superfamily that are expressed on the cell surface. Most SIGLECs have 1 or more cytoplasmic immune receptor tyrosine-based inhibitory motifs, or ITIMs. SIGLECs are typically expressed on cells of the innate immune system, with the exception of the B-cell expressed SIGLEC6 (MIM 604405).[supplied by OMIM, Jul 2002]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs376276104 | 19:51,914,381 | G/A | — | uncertain significance |
| rs778351914 | 19:51,914,441 | G/A | — | uncertain significance |
| rs1456097107 | 19:51,914,487 | G/C | — | uncertain significance |
| rs775255585 | 19:51,914,489 | G/A | — | uncertain significance |
| rs200329927 | 19:51,914,516 | G/A | — | uncertain significance |
| rs763829345 | 19:51,914,586 | G/C | — | uncertain significance |
| rs768583087 | 19:51,914,592 | T/C | — | uncertain significance |
| rs761620466 | 19:51,914,600 | G/T | — | likely benign |
| rs374391800 | 19:51,914,625 | C/T | — | uncertain significance |
| rs545174330 | 19:51,915,736 | G/A | — | — |
| rs61741686 | 19:51,916,979 | G/T | — | benign |
| rs1407489346 | 19:51,917,001 | C/G | — | uncertain significance |
| rs61741687 | 19:51,917,008 | C/T | — | likely benign |
| rs1568495565 | 19:51,917,052 | T/C | — | uncertain significance |
| rs1285290633 | 19:51,917,077 | G/A | — | likely benign |
| rs545140583 | 19:51,917,734 | C/T | — | uncertain significance |
| rs139586458 | 19:51,917,748 | G/A | — | uncertain significance |
| rs145650287 | 19:51,918,088 | C/G | — | benign |
| rs1335048323 | 19:51,918,464 | T/C | — | uncertain significance |
| rs11882566 | 19:51,918,475 | T/A | — | benign |
| rs769528072 | 19:51,918,507 | C/T | — | uncertain significance |
| rs141231631 | 19:51,918,636 | A/G | — | likely benign |
| rs751830001 | 19:51,918,640 | G/C | — | uncertain significance |
| rs771597192 | 19:51,918,668 | G/A | — | uncertain significance |
| rs1323367217 | 19:51,918,843 | C/T | — | uncertain significance |
| rs112584540 | 19:51,919,231 | A/G | — | likely benign |
| rs201089294 | 19:51,919,235 | T/C | — | likely benign |
| rs199590261 | 19:51,919,237 | C/T | — | likely benign |
| rs371815585 | 19:51,919,256 | C/T | — | likely benign |
| rs2513849636 | 19:51,919,262 | G/A | — | uncertain significance |
| rs752106767 | 19:51,919,379 | G/A | — | likely benign |
| rs557047713 | 19:51,919,938 | C/A | — | uncertain significance |
| rs1988712616 | 19:51,919,958 | C/G | — | uncertain significance |
| rs61741677 | 19:51,919,998 | T/C | — | benign |
| rs770768237 | 19:51,920,051 | G/T | — | uncertain significance |
| rs142651280 | 19:51,920,065 | G/A | — | likely benign |
| rs766952654 | 19:51,920,079 | C/T | — | likely benign |
| rs1433213259 | 19:51,920,135 | C/A | — | uncertain significance |
| rs150721520 | 19:51,920,160 | G/A | — | uncertain significance |
| rs1599907772 | 19:51,920,177 | A/G | — | uncertain significance |
| rs202177835 | 19:51,920,210 | A/G | — | likely benign |
| rs757317742 | 19:51,920,489 | A/G | — | uncertain significance |
| rs201146870 | 19:51,920,498 | G/A | — | uncertain significance |
| rs762039627 | 19:51,920,513 | C/G | — | uncertain significance |
| rs1988793787 | 19:51,920,566 | A/G | — | uncertain significance |
| rs143232171 | 19:51,920,605 | G/A | — | uncertain significance |
| rs756010274 | 19:51,920,630 | A/G | — | uncertain significance |
| rs372246670 | 19:51,920,686 | C/T | — | likely benign |
| rs150439142 | 19:51,920,692 | C/A | — | uncertain significance |
| rs1346664961 | 19:51,920,704 | T/C | — | uncertain significance |
| rs201054656 | 19:51,920,810 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.