DCAF5
DDB1 and CUL4 associated factor 5
Summary
Predicted to be involved in negative regulation of fatty acid biosynthetic process. Part of Cul4-RING E3 ubiquitin ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs754319970 | 14:69,520,608 | T/G | — | uncertain significance |
| rs2505107236 | 14:69,520,652 | A/T | — | uncertain significance |
| rs2505107730 | 14:69,520,677 | C/T | — | uncertain significance |
| rs200458341 | 14:69,520,743 | T/G | — | uncertain significance |
| rs2037852520 | 14:69,520,774 | T/G | — | uncertain significance |
| rs1390379624 | 14:69,520,801 | C/G | — | uncertain significance |
| rs772864002 | 14:69,520,861 | C/T | — | uncertain significance |
| rs199498666 | 14:69,520,870 | G/T | — | uncertain significance |
| rs376979140 | 14:69,521,109 | G/A | — | uncertain significance |
| rs2505117727 | 14:69,521,167 | C/A | — | uncertain significance |
| rs145705724 | 14:69,521,181 | G/A | — | uncertain significance |
| rs529216482 | 14:69,521,205 | A/G | — | uncertain significance |
| rs200156447 | 14:69,521,232 | G/A | — | uncertain significance |
| rs148942004 | 14:69,521,251 | G/T | — | uncertain significance |
| rs908070174 | 14:69,521,311 | G/A | — | uncertain significance |
| rs1447245955 | 14:69,521,446 | T/C | — | uncertain significance |
| rs775595255 | 14:69,521,464 | C/G | — | uncertain significance |
| rs182427634 | 14:69,521,466 | C/T | — | uncertain significance |
| rs185370559 | 14:69,521,474 | T/G | — | uncertain significance |
| rs374855442 | 14:69,521,515 | T/C | — | likely benign |
| rs575827797 | 14:69,521,559 | T/C | — | uncertain significance |
| rs2505126388 | 14:69,521,671 | G/C | — | uncertain significance |
| rs2505129356 | 14:69,521,805 | G/A | — | uncertain significance |
| rs1054470398 | 14:69,521,851 | G/A | — | uncertain significance |
| rs2139824583 | 14:69,522,003 | C/T | — | uncertain significance |
| rs2505134839 | 14:69,522,151 | A/G | — | uncertain significance |
| rs750737328 | 14:69,522,190 | C/T | — | uncertain significance |
| rs200862680 | 14:69,522,279 | C/T | — | uncertain significance |
| rs2505195806 | 14:69,529,226 | C/T | — | uncertain significance |
| rs2505300788 | 14:69,542,115 | C/A | — | uncertain significance |
| rs116735454 | 14:69,554,235 | T/C | regulatory region variant | — |
| rs2502838131 | 14:69,558,521 | G/T | — | uncertain significance |
| rs1710990 | 14:69,575,054 | A/G | intron variant | — |
| rs61981649 | 14:69,577,140 | G/C | — | — |
| rs2502958918 | 14:69,583,183 | C/G | — | uncertain significance |
| rs747834181 | 14:69,584,865 | G/A | — | uncertain significance |
| rs1275411 | 14:69,594,913 | T/C | intron variant | — |
| rs12432645 | 14:69,599,483 | G/A | — | — |
| rs80255237 | 14:69,610,201 | G/A | downstream gene variant | — |
| rs766931980 | 14:69,619,578 | C/T | — | uncertain significance |
| rs2041753096 | 14:69,619,625 | T/C | — | uncertain significance |
| rs2503089571 | 14:69,619,679 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.