SLC2A13
solute carrier family 2 member 13
Summary
Enables ATPase binding activity; myo-inositol:proton symporter activity; and protease binding activity. Involved in myo-inositol transport and positive regulation of amyloid-beta formation. Located in cell body; cell projection; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2498669439 | 12:40,153,899 | A/G | — | uncertain significance |
| rs147724845 | 12:40,154,036 | G/A | — | uncertain significance |
| rs2498683378 | 12:40,158,301 | G/C | — | uncertain significance |
| rs768413141 | 12:40,158,346 | C/A | — | uncertain significance |
| rs2498683791 | 12:40,158,369 | A/C | — | uncertain significance |
| rs753861463 | 12:40,158,617 | C/T | — | uncertain significance |
| rs752709836 | 12:40,223,926 | G/A | — | uncertain significance |
| rs1010246332 | 12:40,223,978 | T/C | — | uncertain significance |
| rs1463455434 | 12:40,258,579 | G/A | — | uncertain significance |
| rs200242923 | 12:40,258,621 | C/T | — | uncertain significance |
| rs1005956 | 12:40,341,085 | T/C | intron variant | — |
| rs748960640 | 12:40,345,111 | C/A | — | uncertain significance |
| rs531725171 | 12:40,345,125 | C/A | — | uncertain significance |
| rs1259089546 | 12:40,345,161 | G/T | — | uncertain significance |
| rs10877840 | 12:40,352,996 | T/C | intron variant | — |
| rs11174478 | 12:40,354,244 | G/A | intron variant | — |
| rs28370649 | 12:40,399,149 | A/G | intron variant | — |
| rs28370650 | 12:40,399,948 | T/A | intron variant | — |
| rs515291 | 12:40,402,992 | G/A | intron variant | — |
| rs28370664 | 12:40,413,305 | C/A | intron variant | — |
| rs10877955 | 12:40,421,117 | G/A | intron variant | — |
| rs759358485 | 12:40,422,251 | C/A | — | uncertain significance |
| rs200980396 | 12:40,422,282 | G/C | — | uncertain significance |
| rs11174812 | 12:40,425,087 | C/T | intron variant | — |
| rs1994090 | 12:40,428,561 | G/C | — | — |
| rs368001135 | 12:40,441,874 | T/C | — | uncertain significance |
| rs976591878 | 12:40,441,883 | G/C | — | uncertain significance |
| rs2499046710 | 12:40,441,920 | T/G | — | uncertain significance |
| rs758683743 | 12:40,441,983 | T/C | — | uncertain significance |
| rs17483551 | 12:40,475,260 | T/C | intron variant | — |
| rs781326099 | 12:40,499,098 | C/G | — | uncertain significance |
| rs1001866833 | 12:40,499,123 | G/A | — | uncertain significance |
| rs2499214720 | 12:40,499,139 | A/G | — | uncertain significance |
| rs1484840929 | 12:40,499,192 | G/A | — | uncertain significance |
| rs2499215566 | 12:40,499,247 | G/C | — | uncertain significance |
| rs776190692 | 12:40,499,274 | G/A | — | uncertain significance |
| rs759063094 | 12:40,499,275 | C/A | — | uncertain significance |
| rs776070011 | 12:40,499,282 | T/C | — | uncertain significance |
| rs2499217020 | 12:40,499,442 | C/T | — | uncertain significance |
| rs538841712 | 12:40,499,444 | G/A | — | uncertain significance |
| rs2499217113 | 12:40,499,454 | T/C | — | likely benign |
| rs1592087932 | 12:40,499,466 | T/C | — | likely benign |
| rs1327530841 | 12:40,499,536 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.