ELOVL7
ELOVL fatty acid elongase 7
Summary
Enables fatty acid elongase activity. Involved in fatty acid elongation, polyunsaturated fatty acid; fatty acid elongation, saturated fatty acid; and very long-chain fatty acid biosynthetic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1741422748 | 5:60,050,470 | C/T | — | uncertain significance |
| rs374457003 | 5:60,050,506 | C/T | — | uncertain significance |
| rs2531406846 | 5:60,050,599 | T/A | — | uncertain significance |
| rs748545912 | 5:60,050,626 | T/C | — | uncertain significance |
| rs1462731009 | 5:60,050,660 | C/A | — | uncertain significance |
| rs773675782 | 5:60,053,355 | T/C | — | uncertain significance |
| rs372397313 | 5:60,053,430 | T/G | — | uncertain significance |
| rs375929224 | 5:60,060,113 | T/C | — | uncertain significance |
| rs764734594 | 5:60,060,143 | C/T | — | uncertain significance |
| rs762385054 | 5:60,062,406 | C/G | — | uncertain significance |
| rs779998858 | 5:60,063,669 | C/T | — | likely benign |
| rs142412675 | 5:60,063,683 | A/C | — | uncertain significance |
| rs200699082 | 5:60,063,694 | G/A | stop gained | — |
| rs759883343 | 5:60,063,715 | A/G | — | uncertain significance |
| rs199955250 | 5:60,067,776 | G/A | — | uncertain significance |
| rs1742625129 | 5:60,067,843 | C/A | — | uncertain significance |
| rs373511341 | 5:60,067,854 | T/C | — | uncertain significance |
| rs921897 | 5:60,089,137 | G/A | intron variant | — |
| rs10076679 | 5:60,090,951 | C/T | — | — |
| rs7709444 | 5:60,095,726 | T/C | intron variant | — |
| rs4482855 | 5:60,096,497 | T/C | intron variant | — |
| rs193080529 | 5:60,098,469 | C/T | — | likely benign |
| rs13184554 | 5:60,103,564 | C/T | intron variant | — |
| rs61160187 | 5:60,111,579 | A/G | intron variant | — |
| rs11747856 | 5:60,113,649 | G/C | — | — |
| rs3936423 | 5:60,118,961 | T/A | — | — |
| rs62372074 | 5:60,121,470 | A/T | intron variant | — |
| rs4410607 | 5:60,126,266 | T/C | intron variant | — |
| rs4700396 | 5:60,135,121 | G/T | — | — |
| rs34741733 | 5:60,139,548 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.