ULK3
unc-51 like kinase 3
Summary
Enables protein serine/threonine kinase activity. Involved in several processes, including fibroblast activation; protein autophosphorylation; and regulation of smoothened signaling pathway. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs55973697 | 15:75,129,584 | A/C | — | benign |
| rs2290573 | 15:75,129,594 | G/A | intron variant | — |
| rs769848635 | 15:75,129,727 | G/A | — | uncertain significance |
| rs757346294 | 15:75,129,763 | C/T | — | likely benign |
| rs2505705726 | 15:75,129,776 | T/C | — | uncertain significance |
| rs773968655 | 15:75,130,094 | T/C | — | uncertain significance |
| rs370060398 | 15:75,130,512 | C/T | — | uncertain significance |
| rs776746082 | 15:75,130,528 | G/A | — | uncertain significance |
| rs1385407531 | 15:75,130,529 | C/A | — | uncertain significance |
| rs774756261 | 15:75,130,657 | G/A | — | uncertain significance |
| rs2505720764 | 15:75,131,004 | G/A | — | uncertain significance |
| rs780377315 | 15:75,131,019 | A/C | — | uncertain significance |
| rs2141137614 | 15:75,131,032 | T/G | — | uncertain significance |
| rs1349452738 | 15:75,131,062 | C/T | — | uncertain significance |
| rs1446562926 | 15:75,131,068 | G/A | — | uncertain significance |
| rs1038886442 | 15:75,131,672 | C/A | — | uncertain significance |
| rs1254719633 | 15:75,131,710 | G/A | — | uncertain significance |
| rs1215287061 | 15:75,131,899 | T/C | — | likely benign |
| rs186759889 | 15:75,131,906 | C/T | — | uncertain significance |
| rs2505733466 | 15:75,131,931 | G/T | — | uncertain significance |
| rs2064170423 | 15:75,131,966 | T/C | — | uncertain significance |
| rs200157375 | 15:75,131,982 | G/A | — | uncertain significance |
| rs377255351 | 15:75,132,020 | C/T | — | uncertain significance |
| rs540997889 | 15:75,132,045 | G/C | — | uncertain significance |
| rs936229 | 15:75,132,319 | A/G | downstream gene variant | — |
| rs12908814 | 15:75,132,490 | C/G | regulatory region variant | — |
| rs749981080 | 15:75,132,583 | C/T | — | uncertain significance |
| rs373403457 | 15:75,132,602 | C/G | — | uncertain significance |
| rs772952582 | 15:75,132,615 | G/A | — | likely benign |
| rs377064776 | 15:75,132,875 | G/A | — | uncertain significance |
| rs757280306 | 15:75,132,878 | C/T | — | uncertain significance |
| rs759102107 | 15:75,132,920 | G/C | — | uncertain significance |
| rs35249396 | 15:75,132,921 | G/C | — | benign |
| rs375863086 | 15:75,132,954 | C/T | — | likely benign |
| rs531063819 | 15:75,132,986 | C/T | — | benign |
| rs1449005838 | 15:75,134,437 | G/A | — | uncertain significance |
| rs775347115 | 15:75,134,439 | G/A | — | uncertain significance |
| rs34945944 | 15:75,134,478 | C/T | — | benign |
| rs188373666 | 15:75,134,485 | G/A | — | likely benign |
| rs200940651 | 15:75,134,523 | T/C | — | uncertain significance |
| rs2505758150 | 15:75,134,529 | C/T | — | uncertain significance |
| rs774909124 | 15:75,135,354 | G/A | — | likely benign |
| rs373520078 | 15:75,135,367 | G/A | — | uncertain significance |
| rs2505766243 | 15:75,135,371 | C/T | — | uncertain significance |
| rs904230171 | 15:75,135,424 | G/A | — | uncertain significance |
| rs764806826 | 15:75,135,425 | G/A | — | uncertain significance |
| rs2064324232 | 15:75,135,427 | C/T | — | uncertain significance |
| rs2290574 | 15:75,135,447 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.