ATP10D
ATPase phospholipid transporting 10D (putative)
Summary
Enables glycosylceramide flippase activity. Predicted to be involved in phospholipid translocation. Located in endoplasmic reticulum; nucleoplasm; and plasma membrane. Part of phospholipid-translocating ATPase complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1344930454 | 4:47,514,634 | G/A | — | uncertain significance |
| rs375980643 | 4:47,514,637 | C/G | — | uncertain significance |
| rs138139630 | 4:47,514,646 | A/G | — | uncertain significance |
| rs199950421 | 4:47,514,652 | C/T | — | uncertain significance |
| rs1438407498 | 4:47,514,842 | T/A | — | uncertain significance |
| rs757700600 | 4:47,517,531 | A/G | — | uncertain significance |
| rs1290706431 | 4:47,517,612 | A/C | — | uncertain significance |
| rs770945581 | 4:47,517,633 | G/A | — | uncertain significance |
| rs2475655854 | 4:47,517,641 | A/G | — | uncertain significance |
| rs889046802 | 4:47,517,681 | A/G | — | uncertain significance |
| rs527490096 | 4:47,520,260 | A/G | — | — |
| rs114311534 | 4:47,525,088 | G/A | — | benign |
| rs371624169 | 4:47,525,102 | G/A | — | uncertain significance |
| rs764432218 | 4:47,525,203 | G/C | — | uncertain significance |
| rs201697796 | 4:47,527,650 | G/A | — | uncertain significance |
| rs146578598 | 4:47,537,546 | G/A | — | uncertain significance |
| rs185611178 | 4:47,537,548 | G/A | — | uncertain significance |
| rs759172595 | 4:47,537,967 | G/A | — | uncertain significance |
| rs755089954 | 4:47,538,466 | G/T | — | uncertain significance |
| rs2475037560 | 4:47,538,473 | C/A | — | uncertain significance |
| rs745700006 | 4:47,538,484 | A/G | — | uncertain significance |
| rs771471852 | 4:47,538,760 | T/C | — | uncertain significance |
| rs772847899 | 4:47,538,766 | A/G | — | uncertain significance |
| rs759945258 | 4:47,538,796 | A/G | — | uncertain significance |
| rs200358319 | 4:47,538,816 | G/T | — | uncertain significance |
| rs371369194 | 4:47,548,680 | A/T | — | uncertain significance |
| rs1718449193 | 4:47,548,685 | G/A | — | uncertain significance |
| rs201342683 | 4:47,548,731 | C/T | — | uncertain significance |
| rs1300826153 | 4:47,548,742 | A/G | — | uncertain significance |
| rs771042542 | 4:47,548,746 | G/A | — | uncertain significance |
| rs201603122 | 4:47,548,878 | T/C | — | uncertain significance |
| rs13106975 | 4:47,551,863 | T/G | intron variant | — |
| rs9790720 | 4:47,554,488 | T/A | downstream gene variant | — |
| rs557426590 | 4:47,556,777 | A/G | — | uncertain significance |
| rs757458517 | 4:47,556,800 | C/T | — | uncertain significance |
| rs369968292 | 4:47,556,924 | G/A | — | uncertain significance |
| rs1296683648 | 4:47,559,703 | G/A | — | uncertain significance |
| rs202127870 | 4:47,559,760 | G/A | — | uncertain significance |
| rs755937043 | 4:47,559,778 | C/T | — | uncertain significance |
| rs201572653 | 4:47,559,895 | G/A | — | uncertain significance |
| rs199600119 | 4:47,559,904 | C/T | — | uncertain significance |
| rs753682058 | 4:47,559,960 | G/A | — | uncertain significance |
| rs201846331 | 4:47,559,964 | G/C | — | uncertain significance |
| rs992491743 | 4:47,559,981 | G/A | — | uncertain significance |
| rs909732631 | 4:47,560,032 | G/A | — | uncertain significance |
| rs756861814 | 4:47,560,095 | C/T | — | uncertain significance |
| rs375583564 | 4:47,560,125 | G/C | — | uncertain significance |
| rs200095375 | 4:47,560,135 | G/A | — | uncertain significance |
| rs2475071802 | 4:47,560,143 | A/G | — | uncertain significance |
| rs142329918 | 4:47,563,064 | G/A | — | uncertain significance |
| rs10938494 | 4:47,563,448 | G/A | regulatory region variant | — |
| rs769294120 | 4:47,565,646 | T/C | — | uncertain significance |
| rs147847026 | 4:47,565,657 | C/A | — | uncertain significance |
| rs903422570 | 4:47,565,669 | A/G | — | uncertain significance |
| rs371722384 | 4:47,565,711 | G/A | — | uncertain significance |
| rs114229642 | 4:47,566,860 | T/C | regulatory region variant | — |
| rs199756910 | 4:47,570,881 | A/G | — | uncertain significance |
| rs753524004 | 4:47,570,965 | C/G | — | uncertain significance |
| rs372690498 | 4:47,571,044 | A/G | — | uncertain significance |
| rs138541186 | 4:47,571,089 | G/A | — | uncertain significance |
| rs1719989818 | 4:47,574,240 | G/T | — | uncertain significance |
| rs761170058 | 4:47,574,244 | G/T | — | uncertain significance |
| rs376165524 | 4:47,574,913 | G/A | — | likely benign |
| rs10002592 | 4:47,578,191 | A/C | — | — |
| rs777425761 | 4:47,578,822 | C/G | — | uncertain significance |
| rs750573173 | 4:47,578,928 | G/A | — | uncertain significance |
| rs2351791 | 4:47,582,387 | A/T | — | — |
| rs779597466 | 4:47,582,461 | A/G | — | uncertain significance |
| rs375013581 | 4:47,584,026 | A/T | — | uncertain significance |
| rs776140901 | 4:47,589,061 | T/C | — | likely benign |
| rs777503185 | 4:47,589,162 | A/G | — | uncertain significance |
| rs2475113804 | 4:47,589,180 | T/A | — | uncertain significance |
| rs2475113814 | 4:47,589,186 | G/A | — | uncertain significance |
| rs556426025 | 4:47,589,199 | C/T | — | uncertain significance |
| rs202051358 | 4:47,593,082 | G/A | — | uncertain significance |
| rs780172839 | 4:47,593,262 | T/C | — | uncertain significance |
| rs568660794 | 4:47,593,294 | A/G | — | likely benign |
| rs140236295 | 4:47,593,297 | G/C | — | uncertain significance |
| rs780438747 | 4:47,593,312 | T/C | — | likely benign |
| rs765003197 | 4:47,593,385 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.