SLC2A11
solute carrier family 2 member 11
Summary
This gene belongs to a family of proteins that mediate the transport of sugars across the cell membrane. The encoded protein transports glucose and fructose. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs184861968 | 22:24,203,332 | A/T | upstream gene variant | — |
| rs1308649604 | 22:24,204,316 | C/A | — | uncertain significance |
| rs202104377 | 22:24,204,349 | A/T | — | uncertain significance |
| rs138381486 | 22:24,204,438 | G/T | regulatory region variant | — |
| rs73160439 | 22:24,205,555 | G/A | intron variant | — |
| rs192481184 | 22:24,207,170 | C/T | intron variant | — |
| rs766163012 | 22:24,210,704 | C/T | — | uncertain significance |
| rs144757871 | 22:24,210,743 | A/G | — | likely benign |
| rs568447171 | 22:24,210,758 | G/A | — | uncertain significance |
| rs117035294 | 22:24,215,823 | G/A | intron variant | — |
| rs2517847784 | 22:24,217,311 | T/G | — | uncertain significance |
| rs2517847871 | 22:24,217,338 | G/A | — | uncertain significance |
| rs368747902 | 22:24,217,381 | C/T | — | uncertain significance |
| rs761282787 | 22:24,219,277 | A/T | — | uncertain significance |
| rs1568993172 | 22:24,219,314 | C/G | — | uncertain significance |
| rs772886467 | 22:24,219,925 | C/T | — | uncertain significance |
| rs141517261 | 22:24,220,011 | C/T | — | uncertain significance |
| rs148376745 | 22:24,220,044 | G/A | — | uncertain significance |
| rs74413288 | 22:24,221,683 | G/A | coding sequence variant | — |
| rs113201888 | 22:24,223,107 | A/G | — | — |
| rs766659555 | 22:24,224,652 | G/A | — | likely benign |
| rs753205664 | 22:24,224,654 | C/T | — | uncertain significance |
| rs572438357 | 22:24,224,723 | G/A | — | uncertain significance |
| rs780021102 | 22:24,224,735 | C/T | — | uncertain significance |
| rs150867325 | 22:24,224,738 | C/T | — | uncertain significance |
| rs376897328 | 22:24,224,742 | C/T | — | uncertain significance |
| rs775659722 | 22:24,224,762 | C/G | — | uncertain significance |
| rs139308916 | 22:24,224,763 | G/A | — | uncertain significance |
| rs1227563536 | 22:24,224,811 | T/C | — | uncertain significance |
| rs143899804 | 22:24,224,953 | C/G | — | uncertain significance |
| rs200581467 | 22:24,224,973 | C/T | — | uncertain significance |
| rs553658890 | 22:24,225,983 | C/T | — | uncertain significance |
| rs576534762 | 22:24,225,986 | C/T | — | uncertain significance |
| rs372590867 | 22:24,225,987 | G/A | — | uncertain significance |
| rs377301649 | 22:24,225,989 | G/A | — | uncertain significance |
| rs2032907464 | 22:24,225,993 | T/C | — | uncertain significance |
| rs140261431 | 22:24,226,055 | C/G | — | uncertain significance |
| rs2032927840 | 22:24,226,489 | C/G | — | uncertain significance |
| rs753628410 | 22:24,226,564 | C/T | — | uncertain significance |
| rs778889925 | 22:24,226,578 | A/T | — | uncertain significance |
| rs772563155 | 22:24,226,938 | C/G | — | uncertain significance |
| rs2517870394 | 22:24,226,948 | C/G | — | uncertain significance |
| rs41277537 | 22:24,227,149 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.