SLC2A7
solute carrier family 2 member 7
Summary
SLC2A7 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Li et al., 2004). This family of transporters shows conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs193198026 | 1:9,062,686 | T/A | — | — |
| rs776616572 | 1:9,063,435 | T/C | — | uncertain significance |
| rs146720870 | 1:9,063,478 | A/T | — | uncertain significance |
| rs367693641 | 1:9,063,489 | T/C | — | uncertain significance |
| rs1313379876 | 1:9,063,565 | C/G | — | uncertain significance |
| rs372870693 | 1:9,063,568 | C/T | — | uncertain significance |
| rs1640628849 | 1:9,064,853 | C/A | — | uncertain significance |
| rs1257868935 | 1:9,064,876 | T/C | — | uncertain significance |
| rs772287606 | 1:9,064,926 | G/A | — | uncertain significance |
| rs760260995 | 1:9,064,930 | G/C | — | uncertain significance |
| rs140137998 | 1:9,065,903 | A/G | intron variant | — |
| rs142794704 | 1:9,067,164 | G/A | intron variant | — |
| rs769352024 | 1:9,067,389 | G/C | — | uncertain significance |
| rs371136367 | 1:9,067,390 | C/T | — | uncertain significance |
| rs376126148 | 1:9,067,399 | C/T | — | uncertain significance |
| rs113930491 | 1:9,067,408 | A/T | — | uncertain significance |
| rs138250900 | 1:9,070,196 | T/C | — | likely benign |
| rs1386015467 | 1:9,070,258 | C/T | — | uncertain significance |
| rs1408065266 | 1:9,070,263 | A/T | — | uncertain significance |
| rs754741264 | 1:9,070,270 | G/A | — | uncertain significance |
| rs370854911 | 1:9,070,276 | G/A | — | uncertain significance |
| rs374564551 | 1:9,070,279 | G/A | — | uncertain significance |
| rs1265865058 | 1:9,070,287 | C/T | — | uncertain significance |
| rs1299333336 | 1:9,070,289 | C/A | — | uncertain significance |
| rs79764084 | 1:9,073,591 | A/T | — | benign |
| rs543841758 | 1:9,073,600 | A/C | — | uncertain significance |
| rs373804911 | 1:9,073,610 | C/T | — | uncertain significance |
| rs201372175 | 1:9,073,613 | C/T | — | uncertain significance |
| rs777214714 | 1:9,073,660 | G/A | — | uncertain significance |
| rs147603199 | 1:9,074,794 | C/T | — | likely benign |
| rs772823908 | 1:9,074,810 | C/A | — | uncertain significance |
| rs148489455 | 1:9,074,847 | C/T | — | uncertain significance |
| rs779456894 | 1:9,074,855 | T/G | — | uncertain significance |
| rs78914166 | 1:9,074,869 | C/T | — | benign |
| rs780075652 | 1:9,074,870 | G/A | — | likely benign |
| rs144688962 | 1:9,074,903 | G/A | — | likely benign |
| rs781552889 | 1:9,075,196 | T/C | — | uncertain significance |
| rs1172704226 | 1:9,075,202 | T/C | — | uncertain significance |
| rs35776221 | 1:9,075,221 | G/A | — | likely benign |
| rs200878810 | 1:9,075,238 | A/G | — | uncertain significance |
| rs779216554 | 1:9,078,345 | C/T | — | uncertain significance |
| rs971271989 | 1:9,078,419 | G/A | — | uncertain significance |
| rs372549045 | 1:9,078,421 | G/T | — | uncertain significance |
| rs2522907704 | 1:9,078,428 | G/A | — | uncertain significance |
| rs200486584 | 1:9,079,349 | C/T | — | uncertain significance |
| rs773308377 | 1:9,082,981 | C/T | — | uncertain significance |
| rs199633115 | 1:9,082,989 | T/A | — | uncertain significance |
| rs201765487 | 1:9,082,998 | A/G | — | uncertain significance |
| rs372160828 | 1:9,083,047 | C/T | — | uncertain significance |
| rs528126954 | 1:9,083,050 | T/G | — | uncertain significance |
| rs142873567 | 1:9,083,080 | C/T | — | uncertain significance |
| rs61744620 | 1:9,083,094 | G/T | — | benign |
| rs755688872 | 1:9,083,095 | C/T | — | uncertain significance |
| rs779773770 | 1:9,083,096 | G/A | — | likely benign |
| rs1640938489 | 1:9,083,128 | A/C | — | uncertain significance |
| rs772699627 | 1:9,085,069 | C/G | — | uncertain significance |
| rs773898557 | 1:9,086,357 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.