SIGLEC9
sialic acid binding Ig like lectin 9
Summary
Predicted to enable monosaccharide binding activity and sialic acid binding activity. Predicted to be involved in cell adhesion. Predicted to act upstream of or within negative regulation of inflammatory response and negative regulation of phagocytosis, engulfment. Predicted to be located in external side of plasma membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs137991548 | 19:51,623,113 | C/T | upstream gene variant | — |
| rs200563478 | 19:51,628,249 | G/A | — | likely benign |
| rs769074663 | 19:51,628,319 | A/T | — | uncertain significance |
| rs376638487 | 19:51,628,320 | C/T | — | uncertain significance |
| rs199616534 | 19:51,628,332 | G/C | — | uncertain significance |
| rs2513822493 | 19:51,628,343 | C/T | — | uncertain significance |
| rs749869743 | 19:51,628,374 | A/G | — | uncertain significance |
| rs2091967746 | 19:51,628,381 | G/C | — | uncertain significance |
| rs2513822614 | 19:51,628,382 | A/G | — | uncertain significance |
| rs144549146 | 19:51,628,395 | C/T | — | uncertain significance |
| rs779222990 | 19:51,628,430 | A/G | — | uncertain significance |
| rs146058640 | 19:51,628,431 | A/G | — | uncertain significance |
| rs2513822799 | 19:51,628,467 | C/T | — | uncertain significance |
| rs1396738331 | 19:51,628,590 | G/A | — | uncertain significance |
| rs200658 | 19:51,628,605 | G/A | — | benign |
| rs16988910 | 19:51,628,622 | A/C | missense variant | — |
| rs273687 | 19:51,628,873 | C/G | missense variant | — |
| rs377233936 | 19:51,628,958 | C/T | — | uncertain significance |
| rs200142428 | 19:51,628,985 | G/A | — | uncertain significance |
| rs150601072 | 19:51,629,151 | C/T | downstream gene variant | — |
| rs186620214 | 19:51,629,264 | G/A | downstream gene variant | — |
| rs202208227 | 19:51,629,379 | G/A | — | uncertain significance |
| rs373039771 | 19:51,630,443 | C/T | — | uncertain significance |
| rs273688 | 19:51,630,485 | C/A | missense variant | — |
| rs758761342 | 19:51,630,507 | G/T | — | uncertain significance |
| rs1293174736 | 19:51,630,510 | C/A | — | uncertain significance |
| rs751743147 | 19:51,630,517 | G/A | — | uncertain significance |
| rs763446784 | 19:51,631,251 | G/C | — | uncertain significance |
| rs1175655363 | 19:51,631,257 | C/T | — | uncertain significance |
| rs192799402 | 19:51,631,694 | C/T | — | uncertain significance |
| rs61739656 | 19:51,631,709 | C/T | — | uncertain significance |
| rs867190 | 19:51,631,710 | G/A | — | benign |
| rs746271295 | 19:51,631,724 | C/T | — | uncertain significance |
| rs144700400 | 19:51,631,743 | C/T | — | benign |
| rs138401485 | 19:51,631,763 | C/T | — | uncertain significance |
| rs2569444 | 19:51,632,416 | T/G | regulatory region variant | — |
| rs2569446 | 19:51,633,052 | T/C | intron variant | — |
| rs118147512 | 19:51,635,701 | A/G | regulatory region variant | — |
| rs139528466 | 19:51,636,818 | G/A | upstream gene variant | — |
| rs144178553 | 19:51,637,626 | G/C | upstream gene variant | — |
| rs116993226 | 19:51,638,043 | G/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.