LGALS9
galectin 9
Summary
The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. The protein encoded by this gene is an S-type lectin. It is overexpressed in Hodgkin's disease tissue and might participate in the interaction between the H&RS cells with their surrounding cells and might thus play a role in the pathogenesis of this disease and/or its associated immunodeficiency. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374384119 | 17:25,958,303 | C/A | — | uncertain significance |
| rs767013575 | 17:25,958,313 | G/T | — | uncertain significance |
| rs200324450 | 17:25,965,343 | A/T | — | uncertain significance |
| rs745502360 | 17:25,967,680 | G/A | — | uncertain significance |
| rs371890240 | 17:25,967,692 | A/G | — | uncertain significance |
| rs531082359 | 17:25,967,693 | C/T | — | uncertain significance |
| rs2544961889 | 17:25,967,699 | A/C | — | uncertain significance |
| rs138238711 | 17:25,967,719 | G/A | — | uncertain significance |
| rs369758477 | 17:25,967,758 | C/T | — | uncertain significance |
| rs753596905 | 17:25,969,304 | G/A | — | uncertain significance |
| rs777812677 | 17:25,969,319 | G/A | — | uncertain significance |
| rs2544965388 | 17:25,969,358 | C/T | — | uncertain significance |
| rs747504001 | 17:25,970,605 | C/T | — | uncertain significance |
| rs199701061 | 17:25,970,635 | C/T | — | uncertain significance |
| rs74321993 | 17:25,971,978 | G/A | — | — |
| rs759516143 | 17:25,972,365 | C/T | — | uncertain significance |
| rs752765910 | 17:25,972,373 | A/T | — | uncertain significance |
| rs766865902 | 17:25,972,905 | A/T | — | uncertain significance |
| rs2544972031 | 17:25,973,577 | C/A | — | uncertain significance |
| rs1436144317 | 17:25,974,057 | C/T | — | uncertain significance |
| rs377135808 | 17:25,974,135 | G/T | — | uncertain significance |
| rs143800774 | 17:25,974,387 | G/A | — | likely benign |
| rs2544973966 | 17:25,974,394 | C/T | — | uncertain significance |
| rs151095310 | 17:25,974,408 | G/A | — | uncertain significance |
| rs552176742 | 17:25,974,424 | G/A | — | uncertain significance |
| rs199922464 | 17:25,974,441 | C/T | — | uncertain significance |
| rs142653327 | 17:25,974,442 | G/A | — | benign |
| rs747803291 | 17:25,975,879 | A/C | — | likely benign |
| rs141993094 | 17:25,975,901 | G/A | — | uncertain significance |
| rs145626584 | 17:25,975,908 | G/A | — | uncertain significance |
| rs2544976203 | 17:25,975,916 | C/G | — | uncertain significance |
| rs763182758 | 17:25,975,935 | G/A | — | uncertain significance |
| rs767755654 | 17:25,975,965 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.