SIGLEC11
sialic acid binding Ig like lectin 11
Summary
This gene encodes a member of the sialic acid-binding immunoglobulin-like lectin family. These cell surface lectins are characterized by structural motifs in the immunoglobulin (Ig)-like domains and sialic acid recognition sites in the first Ig V set domain. This family member mediates anti-inflammatory and immunosuppressive signaling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201746673 | 19:50,453,306 | A/C | — | uncertain significance |
| rs201942673 | 19:50,453,351 | G/A | — | uncertain significance |
| rs374770988 | 19:50,453,432 | G/C | — | uncertain significance |
| rs368679072 | 19:50,453,447 | G/A | — | uncertain significance |
| rs149680238 | 19:50,453,464 | G/C | — | uncertain significance |
| rs200595712 | 19:50,453,472 | C/T | — | uncertain significance |
| rs1047234518 | 19:50,455,159 | G/T | — | uncertain significance |
| rs748219124 | 19:50,455,184 | C/T | — | likely benign |
| rs112796514 | 19:50,455,202 | G/A | — | benign |
| rs140702198 | 19:50,455,562 | C/T | — | likely benign |
| rs767835963 | 19:50,455,595 | C/T | — | likely benign |
| rs1038111334 | 19:50,455,639 | T/C | — | likely benign |
| rs919777 | 19:50,461,447 | C/T | intron variant | — |
| rs767478430 | 19:50,461,576 | C/T | — | uncertain significance |
| rs777794233 | 19:50,461,581 | A/G | — | uncertain significance |
| rs138849107 | 19:50,461,612 | C/T | — | uncertain significance |
| rs988238286 | 19:50,461,618 | T/C | — | uncertain significance |
| rs774700270 | 19:50,461,629 | T/G | — | uncertain significance |
| rs569790579 | 19:50,461,660 | C/T | — | uncertain significance |
| rs749874555 | 19:50,461,675 | T/A | — | uncertain significance |
| rs759718197 | 19:50,461,681 | C/T | — | uncertain significance |
| rs200767146 | 19:50,461,734 | C/G | — | uncertain significance |
| rs57682421 | 19:50,461,735 | G/C | — | benign |
| rs761548091 | 19:50,461,743 | G/C | — | uncertain significance |
| rs765843318 | 19:50,461,824 | G/A | — | uncertain significance |
| rs144054317 | 19:50,461,920 | G/A | — | uncertain significance |
| rs369288400 | 19:50,461,947 | T/C | — | uncertain significance |
| rs376222513 | 19:50,461,959 | G/A | — | uncertain significance |
| rs771866761 | 19:50,461,972 | C/T | — | uncertain significance |
| rs547243506 | 19:50,461,982 | T/A | — | uncertain significance |
| rs747814700 | 19:50,461,988 | G/A | — | likely benign |
| rs780898655 | 19:50,462,040 | T/C | — | uncertain significance |
| rs772490728 | 19:50,462,049 | C/T | — | likely benign |
| rs149136670 | 19:50,462,124 | G/A | — | uncertain significance |
| rs142292396 | 19:50,462,137 | C/T | — | uncertain significance |
| rs374104181 | 19:50,462,138 | G/T | — | uncertain significance |
| rs577987618 | 19:50,462,143 | C/T | — | likely benign |
| rs2514930791 | 19:50,462,152 | C/T | — | uncertain significance |
| rs62113133 | 19:50,462,298 | G/C | — | benign |
| rs2514931732 | 19:50,462,299 | C/T | — | uncertain significance |
| rs147064231 | 19:50,462,320 | G/C | — | uncertain significance |
| rs750055282 | 19:50,462,342 | G/A | — | likely benign |
| rs751178318 | 19:50,462,619 | T/A | — | uncertain significance |
| rs150164114 | 19:50,462,682 | C/T | — | uncertain significance |
| rs769673458 | 19:50,462,683 | G/A | — | uncertain significance |
| rs1245376830 | 19:50,462,700 | C/T | — | likely benign |
| rs201747553 | 19:50,462,709 | C/G | — | likely benign |
| rs773748696 | 19:50,462,823 | C/T | — | uncertain significance |
| rs201740168 | 19:50,463,030 | C/A | — | benign |
| rs1411027244 | 19:50,463,033 | A/T | — | uncertain significance |
| rs200380048 | 19:50,463,034 | C/T | — | likely benign |
| rs199756638 | 19:50,463,044 | T/C | — | benign |
| rs1253286759 | 19:50,463,402 | C/T | — | uncertain significance |
| rs1344155822 | 19:50,463,412 | C/T | — | uncertain significance |
| rs764395821 | 19:50,463,463 | G/A | — | uncertain significance |
| rs779205214 | 19:50,463,624 | G/A | — | uncertain significance |
| rs2514938327 | 19:50,463,625 | G/C | — | uncertain significance |
| rs77553517 | 19:50,463,670 | T/G | — | benign |
| rs751895660 | 19:50,463,854 | C/T | — | uncertain significance |
| rs2076238604 | 19:50,463,896 | C/T | — | uncertain significance |
| rs376315578 | 19:50,463,908 | C/T | — | uncertain significance |
| rs2514940017 | 19:50,463,945 | A/T | — | uncertain significance |
| rs1192258338 | 19:50,463,952 | G/A | — | uncertain significance |
| rs769247998 | 19:50,463,970 | C/T | — | uncertain significance |
| rs753065493 | 19:50,463,979 | A/G | — | uncertain significance |
| rs568916513 | 19:50,463,985 | A/G | — | uncertain significance |
| rs748856612 | 19:50,464,039 | C/T | — | uncertain significance |
| rs556232816 | 19:50,464,091 | G/A | — | uncertain significance |
| rs574890050 | 19:50,464,115 | C/T | — | uncertain significance |
| rs201377938 | 19:50,464,144 | A/C | — | uncertain significance |
| rs2514941697 | 19:50,464,166 | T/C | — | uncertain significance |
| rs562231084 | 19:50,464,275 | C/T | — | likely benign |
| rs371271734 | 19:50,464,330 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.