SLC9C2
solute carrier family 9 member C2 (putative)
Summary
Predicted to enable potassium:proton antiporter activity and sodium:proton antiporter activity. Predicted to be involved in potassium ion transmembrane transport; regulation of intracellular pH; and sodium ion import across plasma membrane. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146614979 | 1:173,475,997 | G/C | — | uncertain significance |
| rs1377028792 | 1:173,476,170 | A/T | — | uncertain significance |
| rs747161909 | 1:173,478,795 | G/A | — | likely benign |
| rs373428010 | 1:173,486,698 | A/G | — | likely benign |
| rs147272652 | 1:173,486,716 | C/T | — | uncertain significance |
| rs751648052 | 1:173,490,523 | C/T | — | uncertain significance |
| rs151318411 | 1:173,490,525 | A/T | — | uncertain significance |
| rs747923378 | 1:173,493,167 | T/C | — | uncertain significance |
| rs2526889902 | 1:173,493,230 | G/A | — | uncertain significance |
| rs1661084598 | 1:173,493,988 | G/A | — | uncertain significance |
| rs764739922 | 1:173,494,006 | C/T | — | uncertain significance |
| rs771141059 | 1:173,499,063 | A/T | — | uncertain significance |
| rs1269191815 | 1:173,499,082 | G/T | — | uncertain significance |
| rs1661466886 | 1:173,499,174 | A/T | — | uncertain significance |
| rs377240801 | 1:173,499,181 | T/A | — | likely benign |
| rs905661425 | 1:173,502,787 | C/T | — | likely benign |
| rs780556489 | 1:173,502,810 | G/A | — | uncertain significance |
| rs965721456 | 1:173,502,898 | C/A | — | uncertain significance |
| rs377658375 | 1:173,503,706 | T/C | — | uncertain significance |
| rs1661916399 | 1:173,505,027 | T/C | — | uncertain significance |
| rs754463303 | 1:173,505,034 | T/C | — | likely benign |
| rs2527000596 | 1:173,505,078 | T/C | — | uncertain significance |
| rs2527009000 | 1:173,506,088 | G/C | — | uncertain significance |
| rs775523749 | 1:173,506,159 | C/G | — | uncertain significance |
| rs140112573 | 1:173,516,907 | T/C | — | uncertain significance |
| rs758586787 | 1:173,517,624 | T/C | — | uncertain significance |
| rs114617044 | 1:173,517,632 | G/T | — | uncertain significance |
| rs2527097930 | 1:173,517,687 | C/A | — | uncertain significance |
| rs769639295 | 1:173,523,911 | T/A | — | uncertain significance |
| rs145922237 | 1:173,526,484 | G/T | — | benign |
| rs994648548 | 1:173,526,629 | T/G | — | uncertain significance |
| rs4916371 | 1:173,533,572 | C/G | — | — |
| rs143195788 | 1:173,541,300 | A/G | intron variant | — |
| rs1664950711 | 1:173,542,366 | G/C | — | likely benign |
| rs540891244 | 1:173,545,824 | G/A | — | uncertain significance |
| rs762640428 | 1:173,545,837 | A/C | — | uncertain significance |
| rs142884761 | 1:173,551,102 | A/G | — | uncertain significance |
| rs765393938 | 1:173,552,702 | C/T | — | likely benign |
| rs147559775 | 1:173,556,912 | C/T | — | uncertain significance |
| rs115678523 | 1:173,558,837 | G/A | intron variant | — |
| rs765976977 | 1:173,569,311 | G/A | — | uncertain significance |
| rs752647057 | 1:173,569,354 | G/A | — | likely benign |
| rs749560382 | 1:173,570,809 | C/G | — | uncertain significance |
| rs2527470290 | 1:173,570,900 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.