SLC2A5
solute carrier family 2 member 5
Summary
The protein encoded by this gene is a fructose transporter responsible for fructose uptake by the small intestine. The encoded protein also is necessary for the increase in blood pressure due to high dietary fructose consumption. [provided by RefSeq, Jun 2016]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761999982 | 1:9,097,685 | T/C | — | uncertain significance |
| rs372826964 | 1:9,097,700 | A/G | — | uncertain significance |
| rs2522969624 | 1:9,097,758 | C/T | — | uncertain significance |
| rs1358637353 | 1:9,097,811 | A/C | — | uncertain significance |
| rs574081080 | 1:9,097,839 | C/T | — | uncertain significance |
| rs201668362 | 1:9,097,982 | C/T | — | uncertain significance |
| rs1251075567 | 1:9,098,011 | C/T | — | uncertain significance |
| rs875996 | 1:9,098,230 | T/C | — | benign |
| rs875995 | 1:9,098,272 | T/C | — | benign |
| rs11804164 | 1:9,098,331 | G/A | — | benign |
| rs11121306 | 1:9,098,742 | G/A | — | benign |
| rs1277255313 | 1:9,098,928 | G/A | — | likely benign |
| rs200768991 | 1:9,098,982 | C/T | — | uncertain significance |
| rs2522997564 | 1:9,099,657 | A/C | — | uncertain significance |
| rs910856917 | 1:9,099,678 | G/C | — | uncertain significance |
| rs747010390 | 1:9,099,688 | C/T | — | uncertain significance |
| rs769897 | 1:9,099,727 | A/G | — | benign |
| rs771448887 | 1:9,099,891 | T/G | — | uncertain significance |
| rs139477702 | 1:9,099,912 | G/A | — | likely benign |
| rs779760381 | 1:9,099,936 | G/A | — | association |
| rs1641252877 | 1:9,099,953 | G/C | — | uncertain significance |
| rs200930417 | 1:9,099,966 | C/G | — | uncertain significance |
| rs1641254482 | 1:9,099,996 | T/C | — | uncertain significance |
| rs754707926 | 1:9,100,032 | G/A | — | uncertain significance |
| rs1237876654 | 1:9,100,152 | T/G | — | uncertain significance |
| rs906629444 | 1:9,100,172 | G/T | — | uncertain significance |
| rs759519221 | 1:9,100,238 | G/C | — | uncertain significance |
| rs1060998 | 1:9,100,479 | G/A | — | benign |
| rs1445787696 | 1:9,101,873 | C/T | — | uncertain significance |
| rs2523024015 | 1:9,101,883 | G/C | — | uncertain significance |
| rs773127479 | 1:9,101,925 | C/G | — | uncertain significance |
| rs61737428 | 1:9,101,939 | C/T | — | uncertain significance |
| rs369582431 | 1:9,101,982 | C/T | — | uncertain significance |
| rs150090064 | 1:9,103,402 | A/G | intron variant | — |
| rs778328193 | 1:9,107,686 | A/G | — | uncertain significance |
| rs146964071 | 1:9,107,759 | T/C | — | benign |
| rs3737661 | 1:9,107,849 | G/T | — | benign |
| rs11121310 | 1:9,117,371 | A/G | — | benign |
| rs761342863 | 1:9,117,597 | G/A | — | uncertain significance |
| rs202244308 | 1:9,117,607 | A/T | — | uncertain significance |
| rs777932709 | 1:9,117,653 | A/C | — | uncertain significance |
| rs6680123 | 1:9,117,748 | T/C | — | benign |
| rs74595111 | 1:9,117,948 | T/C | — | benign |
| rs764313073 | 1:9,118,212 | A/C | — | uncertain significance |
| rs1312303033 | 1:9,118,231 | C/T | — | uncertain significance |
| rs77511432 | 1:9,118,247 | A/C | — | likely benign |
| rs2523174958 | 1:9,118,284 | G/A | — | uncertain significance |
| rs921695589 | 1:9,118,290 | G/A | — | uncertain significance |
| rs12145292 | 1:9,118,596 | C/A | — | benign |
| rs5438 | 1:9,129,620 | C/T | regulatory region variant | benign |
| rs3820034 | 1:9,129,867 | G/A | — | benign |
| rs770041 | 1:9,129,945 | A/G | — | benign |
| rs12080794 | 1:9,151,325 | C/T | upstream gene variant | — |
| rs116198061 | 1:9,152,571 | C/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.