SLC45A3
solute carrier family 45 member 3
Summary
Predicted to enable sucrose:proton symporter activity. Predicted to be involved in positive regulation of small molecule metabolic process; regulation of oligodendrocyte differentiation; and sucrose transport. Predicted to be located in plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774937348 | 1:205,628,387 | C/T | — | uncertain significance |
| rs151018622 | 1:205,628,442 | C/T | — | likely benign |
| rs142259819 | 1:205,628,568 | G/A | — | uncertain significance |
| rs200659267 | 1:205,628,573 | G/A | — | uncertain significance |
| rs760168590 | 1:205,628,589 | C/T | — | uncertain significance |
| rs765881137 | 1:205,628,612 | C/T | — | uncertain significance |
| rs137949511 | 1:205,628,616 | C/T | — | likely benign |
| rs140263007 | 1:205,628,648 | G/A | — | uncertain significance |
| rs780661012 | 1:205,628,676 | C/T | — | uncertain significance |
| rs745563098 | 1:205,628,678 | C/T | — | uncertain significance |
| rs768293551 | 1:205,628,718 | T/C | — | uncertain significance |
| rs1023644413 | 1:205,628,720 | G/C | — | uncertain significance |
| rs2527361743 | 1:205,628,799 | C/T | — | uncertain significance |
| rs762670191 | 1:205,631,182 | C/T | — | uncertain significance |
| rs140557323 | 1:205,631,252 | C/T | — | uncertain significance |
| rs773057305 | 1:205,631,993 | G/A | — | likely benign |
| rs750557568 | 1:205,632,122 | C/T | — | uncertain significance |
| rs779497295 | 1:205,632,143 | C/T | — | uncertain significance |
| rs377389106 | 1:205,632,144 | G/A | — | uncertain significance |
| rs777513989 | 1:205,632,156 | C/T | — | uncertain significance |
| rs759535515 | 1:205,632,159 | C/A | — | uncertain significance |
| rs757965831 | 1:205,632,208 | C/A | — | uncertain significance |
| rs745673426 | 1:205,632,240 | C/T | — | uncertain significance |
| rs760773350 | 1:205,632,254 | G/A | — | likely benign |
| rs747108852 | 1:205,632,428 | T/C | — | uncertain significance |
| rs150450020 | 1:205,632,464 | C/T | — | uncertain significance |
| rs367899036 | 1:205,632,465 | G/A | — | uncertain significance |
| rs558070897 | 1:205,632,655 | G/C | — | uncertain significance |
| rs772584733 | 1:205,632,669 | G/A | — | uncertain significance |
| rs2527370306 | 1:205,632,701 | G/A | — | uncertain significance |
| rs758617674 | 1:205,633,777 | T/C | — | uncertain significance |
| rs4951018 | 1:205,636,334 | A/T | — | — |
| rs1573104 | 1:205,636,907 | A/C | intron variant | — |
| rs12409639 | 1:205,638,222 | G/A | regulatory region variant | — |
| rs16856139 | 1:205,638,464 | C/T | regulatory region variant | — |
| rs4951255 | 1:205,645,063 | C/A | intron variant | — |
| rs1772139 | 1:205,647,155 | T/G | intron variant | — |
| rs6689008 | 1:205,649,173 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.