DPYSL3
dihydropyrimidinase like 3
Summary
Enables filamin binding activity. Predicted to be involved in several processes, including actin filament organization; regulation of plasma membrane bounded cell projection organization; and response to axon injury. Predicted to act upstream of or within nervous system development. Predicted to be located in several cellular components, including exocytic vesicle; growth cone; and lamellipodium. Predicted to be part of filamentous actin. Predicted to be active in cytosol and synapse. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs762162860 | 5:146,773,623 | C/T | — | uncertain significance |
| rs768220433 | 5:146,773,674 | T/G | — | uncertain significance |
| rs751361322 | 5:146,775,188 | G/A | — | uncertain significance |
| rs2480784679 | 5:146,775,256 | C/A | — | uncertain significance |
| rs776105614 | 5:146,775,266 | C/T | — | uncertain significance |
| rs962598779 | 5:146,775,279 | T/G | — | likely benign |
| rs200874080 | 5:146,777,264 | C/T | — | uncertain significance |
| rs748199099 | 5:146,777,331 | C/A | — | uncertain significance |
| rs35381274 | 5:146,778,717 | C/G | — | benign |
| rs2480792987 | 5:146,778,733 | T/C | — | uncertain significance |
| rs1324562094 | 5:146,780,266 | C/T | — | uncertain significance |
| rs368254542 | 5:146,780,338 | T/C | — | uncertain significance |
| rs58562158 | 5:146,780,406 | G/A | — | benign |
| rs941054021 | 5:146,781,116 | A/C | — | uncertain significance |
| rs1758309106 | 5:146,785,259 | A/G | — | uncertain significance |
| rs762723911 | 5:146,785,265 | A/G | — | uncertain significance |
| rs35891125 | 5:146,788,351 | G/C | — | benign |
| rs1751878449 | 5:146,792,221 | G/T | — | uncertain significance |
| rs377270433 | 5:146,792,232 | C/A | — | uncertain significance |
| rs772784218 | 5:146,792,242 | T/C | — | uncertain significance |
| rs1461179400 | 5:146,793,213 | G/C | — | uncertain significance |
| rs115541254 | 5:146,795,264 | G/A | — | benign |
| rs973954644 | 5:146,795,332 | C/G | — | uncertain significance |
| rs572434542 | 5:146,795,391 | T/C | — | uncertain significance |
| rs1183579974 | 5:146,798,010 | T/G | — | uncertain significance |
| rs201521252 | 5:146,798,038 | C/T | — | likely benign |
| rs958023861 | 5:146,798,150 | A/G | — | uncertain significance |
| rs751057179 | 5:146,804,468 | G/A | — | uncertain significance |
| rs137909376 | 5:146,833,124 | T/G | — | likely benign |
| rs12517529 | 5:146,871,535 | C/T | — | — |
| rs1383071576 | 5:146,889,366 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.