UNC5CL
unc-5 family C-terminal like
Summary
Enables peptidase activity. Acts upstream of or within positive regulation of JNK cascade and positive regulation of canonical NF-kappaB signal transduction. Located in centrosome; cytosol; and membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768224851 | 6:40,996,167 | G/T | — | uncertain significance |
| rs759771505 | 6:40,996,184 | G/C | — | likely benign |
| rs760167010 | 6:40,996,221 | C/T | — | uncertain significance |
| rs779967649 | 6:40,996,227 | A/G | — | uncertain significance |
| rs147879961 | 6:40,998,128 | G/A | — | uncertain significance |
| rs148783840 | 6:40,998,157 | G/A | — | uncertain significance |
| rs742493 | 6:40,998,167 | T/C | missense variant | — |
| rs780992462 | 6:40,998,212 | G/A | — | uncertain significance |
| rs200374920 | 6:40,998,223 | A/G | — | uncertain significance |
| rs201016286 | 6:40,998,409 | G/T | — | uncertain significance |
| rs370431682 | 6:40,998,430 | G/A | — | uncertain significance |
| rs369228384 | 6:40,999,787 | G/A | — | uncertain significance |
| rs752797482 | 6:40,999,801 | C/A | — | uncertain significance |
| rs142690624 | 6:40,999,802 | G/A | — | uncertain significance |
| rs529775453 | 6:41,000,703 | C/T | — | uncertain significance |
| rs920429480 | 6:41,000,746 | C/T | — | uncertain significance |
| rs780549004 | 6:41,000,754 | G/A | — | uncertain significance |
| rs565836218 | 6:41,000,775 | C/T | — | uncertain significance |
| rs2532500686 | 6:41,000,788 | G/C | — | uncertain significance |
| rs542781347 | 6:41,000,842 | G/A | — | uncertain significance |
| rs140534558 | 6:41,001,644 | C/G | — | uncertain significance |
| rs145770641 | 6:41,001,653 | C/T | — | uncertain significance |
| rs1382921138 | 6:41,001,728 | G/T | — | uncertain significance |
| rs148670174 | 6:41,001,731 | C/T | — | uncertain significance |
| rs1762488082 | 6:41,001,791 | G/C | — | uncertain significance |
| rs778884917 | 6:41,001,813 | C/A | — | uncertain significance |
| rs1762501202 | 6:41,002,540 | T/C | — | likely benign |
| rs1561830707 | 6:41,002,585 | C/G | — | uncertain significance |
| rs749414913 | 6:41,002,671 | C/A | — | uncertain significance |
| rs200511540 | 6:41,002,690 | C/A | — | uncertain significance |
| rs145836484 | 6:41,002,744 | C/A | — | uncertain significance |
| rs778037261 | 6:41,002,774 | G/C | — | uncertain significance |
| rs1260314882 | 6:41,002,776 | A/G | — | uncertain significance |
| rs2294693 | 6:41,005,502 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.