C11orf65
chromosome 11 open reading frame 65
Summary
Predicted to be involved in negative regulation of mitochondrial fission and negative regulation of protein targeting to mitochondrion. Predicted to be located in cytosol and mitochondrial outer membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7934935 | 11:108,245,098 | T/G | — | — |
| rs227080 | 11:108,247,888 | A/G | intron variant | — |
| rs227079 | 11:108,248,686 | C/G | — | — |
| rs192022 | 11:108,248,774 | C/T | — | — |
| rs2028155 | 11:108,267,430 | A/T | — | — |
| rs4754318 | 11:108,271,607 | G/A | intron variant | — |
| rs773626523 | 11:108,277,863 | T/C | — | uncertain significance |
| rs11212617 | 11:108,283,161 | C/A | intron variant | — |
| rs35244261 | 11:108,283,808 | A/C | intron variant | — |
| rs1961319 | 11:108,293,879 | G/T | intron variant | — |
| rs7121112 | 11:108,297,408 | T/C | intron variant | — |
| rs28861227 | 11:108,298,323 | T/C | intron variant | — |
| rs112568268 | 11:108,298,581 | A/G | intron variant | — |
| rs61913875 | 11:108,298,852 | A/G | intron variant | — |
| rs765276152 | 11:108,302,532 | T/A | — | uncertain significance |
| rs10890837 | 11:108,303,021 | T/C | regulatory region variant | — |
| rs10890839 | 11:108,306,236 | C/A | intron variant | — |
| rs147995785 | 11:108,308,471 | A/T | intron variant | — |
| rs7103222 | 11:108,309,239 | C/T | intron variant | — |
| rs4754322 | 11:108,311,655 | T/C | intron variant | — |
| rs11212637 | 11:108,311,989 | G/C | — | — |
| rs12222950 | 11:108,313,599 | T/C | intron variant | — |
| rs6589018 | 11:108,314,128 | C/A | — | — |
| rs4255510 | 11:108,314,362 | A/C | — | — |
| rs4460776 | 11:108,314,363 | C/A | — | — |
| rs60639858 | 11:108,314,886 | A/G | intron variant | — |
| rs2118308 | 11:108,315,463 | C/T | — | — |
| rs10890841 | 11:108,317,951 | C/T | — | — |
| rs147992152 | 11:108,320,094 | A/G | intron variant | — |
| rs139122788 | 11:108,336,636 | T/G | — | — |
| rs61913892 | 11:108,340,216 | T/C | coding sequence variant | — |
| rs10749917 | 11:108,341,554 | C/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.