APOM
apolipoprotein M
Summary
The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs55880811 | 6:31,622,531 | T/C | — | — |
| rs805297 | 6:31,622,606 | C/G | — | — |
| rs4947251 | 6:31,622,662 | A/G | — | — |
| rs9404941 | 6:31,622,816 | T/C | downstream gene variant | benign |
| rs805296 | 6:31,622,893 | T/A | — | — |
| rs76611345 | 6:31,623,074 | C/A | — | — |
| rs76794541 | 6:31,623,416 | G/A | regulatory region variant | — |
| rs748212498 | 6:31,623,813 | C/A | — | uncertain significance |
| rs805264 | 6:31,623,873 | G/A | regulatory region variant | — |
| rs116715239 | 6:31,624,170 | G/A | — | — |
| rs766882303 | 6:31,624,370 | C/T | — | uncertain significance |
| rs2536793100 | 6:31,624,374 | G/A | — | uncertain significance |
| rs369056786 | 6:31,624,400 | G/C | — | uncertain significance |
| rs113947529 | 6:31,624,465 | A/T | downstream gene variant | — |
| rs3117581 | 6:31,624,864 | A/G | downstream gene variant | — |
| rs34490746 | 6:31,625,008 | T/C | synonymous variant | — |
| rs552461480 | 6:31,625,217 | A/T | — | uncertain significance |
| rs570765318 | 6:31,625,234 | T/A | — | uncertain significance |
| rs2273612 | 6:31,625,334 | C/T | downstream gene variant | — |
| rs763927499 | 6:31,625,422 | G/A | — | likely benign |
| rs707921 | 6:31,625,541 | C/A | downstream gene variant | — |
| rs28432254 | 6:31,625,884 | G/C | — | — |
| rs114826514 | 6:31,625,986 | C/T | regulatory region variant | — |
| rs75629491 | 6:31,626,080 | C/T | upstream gene variant | — |
| rs1143030 | 6:31,626,127 | A/T | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.