XKR9
XK related 9
Summary
Predicted to enable phospholipid scramblase activity. Predicted to be involved in phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7017914 | 8:71,591,203 | A/G | intron variant | — |
| rs200842167 | 8:71,593,497 | G/C | — | uncertain significance |
| rs773274225 | 8:71,593,553 | G/A | — | uncertain significance |
| rs6988746 | 8:71,598,021 | A/G | intron variant | — |
| rs34737624 | 8:71,607,982 | T/G | — | — |
| rs76156096 | 8:71,609,171 | T/C | — | — |
| rs13254770 | 8:71,610,255 | C/A | — | — |
| rs140607007 | 8:71,619,168 | G/T | — | uncertain significance |
| rs147819305 | 8:71,619,185 | A/G | — | uncertain significance |
| rs751295987 | 8:71,619,200 | C/A | — | uncertain significance |
| rs548816589 | 8:71,619,209 | A/C | — | likely benign |
| rs747314955 | 8:71,619,234 | C/A | — | uncertain significance |
| rs2491601887 | 8:71,619,246 | A/C | — | uncertain significance |
| rs115282615 | 8:71,619,253 | C/A | — | uncertain significance |
| rs1805747003 | 8:71,619,326 | G/A | — | uncertain significance |
| rs758504730 | 8:71,619,353 | T/C | — | uncertain significance |
| rs200806311 | 8:71,619,374 | C/T | — | uncertain significance |
| rs145832461 | 8:71,646,036 | G/A | — | uncertain significance |
| rs2491678532 | 8:71,646,072 | A/G | — | uncertain significance |
| rs115507207 | 8:71,646,084 | C/T | — | benign |
| rs138399526 | 8:71,646,086 | A/C | — | uncertain significance |
| rs115882259 | 8:71,646,136 | G/A | — | likely benign |
| rs746989442 | 8:71,646,141 | A/C | — | uncertain significance |
| rs144673829 | 8:71,646,188 | G/A | — | uncertain significance |
| rs2491679724 | 8:71,646,211 | T/A | — | uncertain significance |
| rs1221879525 | 8:71,646,274 | C/T | — | uncertain significance |
| rs370452618 | 8:71,646,324 | T/C | — | uncertain significance |
| rs763326499 | 8:71,646,360 | T/G | — | uncertain significance |
| rs760215423 | 8:71,646,445 | C/G | — | uncertain significance |
| rs372821070 | 8:71,646,456 | G/A | — | uncertain significance |
| rs752979133 | 8:71,646,537 | C/T | — | uncertain significance |
| rs62530847 | 8:71,650,448 | A/C | — | — |
| rs1838392 | 8:71,682,583 | T/G | intron variant | — |
| rs7003794 | 8:71,789,146 | C/A | intergenic variant | — |
| rs192390871 | 8:71,806,742 | T/C | intergenic variant | — |
| rs2639945 | 8:71,912,539 | G/T | intergenic variant | — |
| rs2035927 | 8:71,913,560 | C/G | intergenic variant | — |
| rs2639953 | 8:71,925,660 | G/A | intergenic variant | — |
| rs12675159 | 8:71,945,274 | G/A | intergenic variant | — |
| rs62506027 | 8:71,954,909 | T/A | — | — |
| rs17698944 | 8:71,961,026 | G/A | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.