SLC35E4
solute carrier family 35 member E4
Summary
Predicted to enable antiporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530160904 | 22:31,032,456 | G/C | — | uncertain significance |
| rs2517935906 | 22:31,032,475 | T/A | — | uncertain significance |
| rs557398990 | 22:31,032,490 | T/C | — | likely benign |
| rs764196135 | 22:31,032,495 | G/A | — | uncertain significance |
| rs751840191 | 22:31,032,496 | C/A | — | uncertain significance |
| rs747807094 | 22:31,032,580 | G/A | — | uncertain significance |
| rs758154841 | 22:31,032,693 | C/A | — | uncertain significance |
| rs754965757 | 22:31,032,763 | G/T | — | uncertain significance |
| rs1295464598 | 22:31,032,868 | C/T | — | uncertain significance |
| rs763699549 | 22:31,032,874 | T/C | — | uncertain significance |
| rs199715618 | 22:31,032,926 | G/T | — | uncertain significance |
| rs536806187 | 22:31,035,508 | G/A | — | — |
| rs190112018 | 22:31,040,095 | G/A | intron variant | — |
| rs113062185 | 22:31,041,987 | A/C | intron variant | — |
| rs142448568 | 22:31,042,632 | G/A | — | uncertain significance |
| rs141444677 | 22:31,042,663 | C/A | — | uncertain significance |
| rs151306839 | 22:31,042,702 | C/T | — | uncertain significance |
| rs2517946402 | 22:31,042,750 | G/A | — | uncertain significance |
| rs2517946421 | 22:31,042,758 | T/G | — | uncertain significance |
| rs2517946456 | 22:31,042,794 | G/T | — | uncertain significance |
| rs2088139104 | 22:31,042,801 | C/T | — | uncertain significance |
| rs201986232 | 22:31,042,833 | C/T | — | uncertain significance |
| rs753029619 | 22:31,042,839 | G/A | — | uncertain significance |
| rs146783483 | 22:31,042,863 | C/T | — | uncertain significance |
| rs373949868 | 22:31,042,864 | G/A | — | uncertain significance |
| rs771540555 | 22:31,042,902 | G/A | — | uncertain significance |
| rs148910498 | 22:31,042,968 | G/A | — | uncertain significance |
| rs778754550 | 22:31,042,971 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.