PRR5L
proline rich 5 like
Summary
Enables ubiquitin protein ligase binding activity. Involved in several processes, including TORC2 signaling; regulation of fibroblast migration; and regulation of primary metabolic process. Part of TORC2 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79627555 | 11:36,322,401 | G/A | regulatory region variant | — |
| rs12364550 | 11:36,362,125 | C/G | intron variant | — |
| rs10836538 | 11:36,365,253 | G/T | intron variant | — |
| rs2592555 | 11:36,371,757 | T/C | intron variant | — |
| rs112013938 | 11:36,372,432 | C/T | intron variant | — |
| rs9630171 | 11:36,422,679 | G/A | — | benign |
| rs144807940 | 11:36,422,687 | G/A | — | uncertain significance |
| rs771993504 | 11:36,422,716 | G/T | — | uncertain significance |
| rs567974104 | 11:36,422,793 | C/A | — | uncertain significance |
| rs537019006 | 11:36,422,795 | C/T | — | uncertain significance |
| rs1895839 | 11:36,424,342 | C/T | — | — |
| rs866924836 | 11:36,424,900 | G/A | — | uncertain significance |
| rs141071283 | 11:36,424,917 | C/T | — | benign |
| rs6484847 | 11:36,427,292 | C/A | — | — |
| rs734903 | 11:36,428,410 | A/T | — | — |
| rs28520436 | 11:36,428,447 | C/T | intron variant | — |
| rs74688172 | 11:36,430,658 | G/A | intron variant | — |
| rs56403503 | 11:36,431,969 | G/C | — | — |
| rs747676828 | 11:36,453,415 | G/A | — | uncertain significance |
| rs755502225 | 11:36,458,944 | G/T | — | uncertain significance |
| rs62621409 | 11:36,458,997 | G/A | — | benign |
| rs1430225611 | 11:36,467,913 | G/A | — | uncertain significance |
| rs141937897 | 11:36,472,840 | G/A | — | uncertain significance |
| rs1430555922 | 11:36,472,852 | G/C | — | uncertain significance |
| rs111844956 | 11:36,472,874 | C/T | — | uncertain significance |
| rs749777257 | 11:36,483,898 | G/A | — | uncertain significance |
| rs2494600335 | 11:36,483,902 | C/T | — | likely benign |
| rs2494600483 | 11:36,483,945 | C/T | — | uncertain significance |
| rs367619940 | 11:36,483,963 | C/T | — | uncertain significance |
| rs572962420 | 11:36,484,068 | T/G | — | uncertain significance |
| rs61754948 | 11:36,484,070 | G/A | — | benign |
| rs34680620 | 11:36,484,115 | G/T | — | benign |
| rs780657900 | 11:36,484,117 | G/T | — | uncertain significance |
| rs149035838 | 11:36,484,126 | C/A | — | uncertain significance |
| rs2494601728 | 11:36,484,176 | C/A | — | uncertain significance |
| rs141033911 | 11:36,484,179 | C/T | — | uncertain significance |
| rs150254725 | 11:36,484,203 | A/G | — | uncertain significance |
| rs745852254 | 11:36,484,221 | G/A | — | uncertain significance |
| rs1056425134 | 11:36,484,233 | G/A | — | uncertain significance |
| rs2494602159 | 11:36,484,270 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.