SLC30A9
solute carrier family 30 member 9
Summary
Enables zinc ion transmembrane transporter activity. Involved in intracellular zinc ion homeostasis; regulation of mitochondrion organization; and zinc ion transport. Located in several cellular components, including cytoplasmic vesicle; endoplasmic reticulum; and mitochondrial membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2581434 | 4:41,992,677 | C/G | — | benign |
| rs577403817 | 4:41,992,701 | C/G | — | uncertain significance |
| rs368704320 | 4:41,992,719 | C/T | — | likely benign |
| rs16853872 | 4:41,992,752 | G/C | — | benign |
| rs1047626 | 4:42,003,671 | A/G | missense variant | benign |
| rs1239172014 | 4:42,003,701 | A/T | — | uncertain significance |
| rs115329927 | 4:42,003,775 | A/T | — | benign |
| rs2581453 | 4:42,003,835 | C/G | — | benign |
| rs2581423 | 4:42,020,142 | G/A | — | benign |
| rs15857 | 4:42,022,464 | C/A | — | benign |
| rs13107768 | 4:42,024,982 | A/G | — | benign |
| rs1412346108 | 4:42,025,334 | G/A | — | likely pathogenic |
| rs752882508 | 4:42,037,319 | G/A | — | uncertain significance |
| rs758117426 | 4:42,051,408 | G/T | — | uncertain significance |
| rs2153138452 | 4:42,051,497 | G/A | — | likely pathogenic |
| rs759507930 | 4:42,062,213 | A/T | — | uncertain significance |
| rs1222039958 | 4:42,062,224 | G/A | — | uncertain significance |
| rs375750615 | 4:42,065,022 | C/T | — | uncertain significance |
| rs1717929006 | 4:42,065,053 | G/A | — | uncertain significance |
| rs772760872 | 4:42,065,122 | T/C | — | uncertain significance |
| rs769629339 | 4:42,069,094 | A/G | — | uncertain significance |
| rs773628644 | 4:42,069,203 | A/G | — | uncertain significance |
| rs1307549674 | 4:42,072,596 | A/G | — | likely benign |
| rs146045214 | 4:42,072,621 | C/G | — | uncertain significance |
| rs1482446659 | 4:42,072,633 | C/T | — | uncertain significance |
| rs139981842 | 4:42,072,655 | G/C | — | uncertain significance |
| rs752883251 | 4:42,072,671 | C/T | — | uncertain significance |
| rs909489751 | 4:42,077,687 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.