SIDT2
SID1 transmembrane family member 2
Summary
Predicted to enable several functions, including AP-1 adaptor complex binding activity; AP-2 adaptor complex binding activity; and RNA transmembrane transporter activity. Involved in RNA transport. Located in lysosomal membrane and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774874825 | 11:117,050,117 | G/C | — | uncertain significance |
| rs4938354 | 11:117,051,165 | A/T | — | — |
| rs2542714192 | 11:117,052,137 | G/C | — | uncertain significance |
| rs750749205 | 11:117,052,181 | C/T | — | uncertain significance |
| rs773432083 | 11:117,052,204 | C/A | — | uncertain significance |
| rs764867354 | 11:117,052,523 | G/A | — | uncertain significance |
| rs61729990 | 11:117,052,532 | C/A | synonymous variant | — |
| rs749420063 | 11:117,052,575 | C/T | — | uncertain significance |
| rs762616736 | 11:117,052,609 | A/C | — | uncertain significance |
| rs61729991 | 11:117,052,611 | G/A | — | uncertain significance |
| rs781014204 | 11:117,052,668 | A/G | — | uncertain significance |
| rs140766167 | 11:117,052,674 | G/A | — | uncertain significance |
| rs1160638203 | 11:117,053,242 | A/C | — | uncertain significance |
| rs78302783 | 11:117,053,270 | G/A | synonymous variant | — |
| rs1309515919 | 11:117,053,283 | G/A | — | uncertain significance |
| rs371165317 | 11:117,053,442 | C/G | — | uncertain significance |
| rs768818608 | 11:117,053,458 | A/G | — | uncertain significance |
| rs774287752 | 11:117,053,466 | G/A | — | uncertain significance |
| rs530885291 | 11:117,053,959 | G/A | — | — |
| rs568864021 | 11:117,054,495 | C/T | — | uncertain significance |
| rs2542721085 | 11:117,054,576 | T/G | — | uncertain significance |
| rs539243256 | 11:117,054,689 | T/A | — | — |
| rs7107152 | 11:117,056,080 | A/C | — | — |
| rs567689836 | 11:117,056,766 | G/A | — | — |
| rs143730905 | 11:117,057,294 | G/A | — | likely benign |
| rs143587311 | 11:117,057,329 | T/C | — | uncertain significance |
| rs945494947 | 11:117,058,098 | C/A | — | uncertain significance |
| rs956801595 | 11:117,058,364 | G/A | — | uncertain significance |
| rs148750007 | 11:117,058,405 | C/T | — | likely benign |
| rs553451865 | 11:117,058,895 | G/A | — | — |
| rs141277106 | 11:117,059,426 | C/T | — | uncertain significance |
| rs61729987 | 11:117,059,427 | G/A | — | uncertain significance |
| rs137941267 | 11:117,059,447 | A/G | — | uncertain significance |
| rs2030640452 | 11:117,060,671 | G/C | — | uncertain significance |
| rs771826709 | 11:117,060,882 | C/T | — | likely benign |
| rs375342078 | 11:117,061,341 | A/T | — | uncertain significance |
| rs1242229 | 11:117,062,370 | T/A | — | — |
| rs776956726 | 11:117,062,673 | C/T | — | likely benign |
| rs1251517395 | 11:117,062,979 | A/C | — | uncertain significance |
| rs12285035 | 11:117,062,989 | C/T | — | benign |
| rs17120425 | 11:117,063,003 | G/A | missense variant | — |
| rs12285062 | 11:117,063,020 | C/T | — | benign |
| rs146964701 | 11:117,063,046 | C/T | — | uncertain significance |
| rs758627899 | 11:117,063,293 | C/T | — | uncertain significance |
| rs1368743279 | 11:117,063,304 | C/T | — | uncertain significance |
| rs565574054 | 11:117,063,319 | G/A | — | uncertain significance |
| rs142171036 | 11:117,063,891 | C/T | — | likely benign |
| rs521171 | 11:117,064,693 | C/G | intron variant | — |
| rs1784042 | 11:117,065,476 | G/A | upstream gene variant | — |
| rs1794116 | 11:117,065,779 | T/C | upstream gene variant | — |
| rs768646260 | 11:117,066,566 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.