DNAJC11
DnaJ heat shock protein family (Hsp40) member C11
Summary
Involved in cristae formation. Located in MICOS complex; SAM complex; and nuclear speck. Part of MIB complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2294532 | 1:6,694,927 | C/T | regulatory region variant | — |
| rs756082894 | 1:6,695,739 | C/T | — | uncertain significance |
| rs141309205 | 1:6,695,754 | C/T | — | uncertain significance |
| rs139166688 | 1:6,696,227 | A/G | — | uncertain significance |
| rs375527993 | 1:6,696,231 | C/T | — | uncertain significance |
| rs139008319 | 1:6,696,232 | G/A | — | benign |
| rs1341530241 | 1:6,696,267 | C/T | — | uncertain significance |
| rs774995067 | 1:6,697,271 | G/A | — | uncertain significance |
| rs12134083 | 1:6,697,285 | T/C | — | benign |
| rs200927563 | 1:6,697,530 | A/G | — | uncertain significance |
| rs139633039 | 1:6,698,357 | C/T | — | uncertain significance |
| rs773708089 | 1:6,698,375 | T/G | — | uncertain significance |
| rs745627956 | 1:6,698,396 | C/T | — | uncertain significance |
| rs781252102 | 1:6,700,001 | C/T | — | uncertain significance |
| rs1208728623 | 1:6,700,007 | A/C | — | uncertain significance |
| rs1252950956 | 1:6,700,008 | T/C | — | uncertain significance |
| rs148994820 | 1:6,700,035 | C/T | — | uncertain significance |
| rs767604148 | 1:6,704,634 | C/T | — | uncertain significance |
| rs1641937975 | 1:6,704,651 | A/G | — | uncertain significance |
| rs748488397 | 1:6,704,673 | C/T | — | uncertain significance |
| rs777281244 | 1:6,704,682 | T/C | — | uncertain significance |
| rs746745536 | 1:6,704,690 | T/G | — | uncertain significance |
| rs2522388115 | 1:6,705,150 | G/C | — | uncertain significance |
| rs543280345 | 1:6,705,157 | G/C | — | uncertain significance |
| rs2522388217 | 1:6,705,165 | C/T | — | uncertain significance |
| rs1313438159 | 1:6,705,920 | C/T | — | uncertain significance |
| rs140778277 | 1:6,705,986 | C/T | — | uncertain significance |
| rs115455042 | 1:6,706,030 | G/A | — | uncertain significance |
| rs12137032 | 1:6,708,246 | G/A | intron variant | — |
| rs371586809 | 1:6,711,607 | C/T | — | uncertain significance |
| rs201917830 | 1:6,712,926 | G/A | — | uncertain significance |
| rs1178647556 | 1:6,712,965 | G/A | — | uncertain significance |
| rs762207483 | 1:6,714,053 | T/C | — | uncertain significance |
| rs1553130273 | 1:6,738,509 | G/T | — | uncertain significance |
| rs2522500128 | 1:6,741,006 | G/A | — | uncertain significance |
| rs277685 | 1:6,749,761 | A/G | intron variant | — |
| rs770666056 | 1:6,761,833 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.