CTU1
cytosolic thiouridylase subunit 1
Summary
Predicted to enable tRNA binding activity. Predicted to be involved in tRNA wobble position uridine thiolation. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113294466 | 19:51,601,363 | C/T | 3 prime UTR variant | — |
| rs551731574 | 19:51,601,869 | G/A | — | uncertain significance |
| rs975063361 | 19:51,601,890 | G/A | — | uncertain significance |
| rs939361549 | 19:51,601,941 | G/C | — | uncertain significance |
| rs1339692634 | 19:51,601,964 | C/T | — | uncertain significance |
| rs1044354349 | 19:51,601,998 | C/A | — | uncertain significance |
| rs1185941198 | 19:51,602,018 | C/T | — | uncertain significance |
| rs999673397 | 19:51,602,019 | G/T | — | uncertain significance |
| rs2514420305 | 19:51,602,057 | C/G | — | likely benign |
| rs1018653314 | 19:51,602,060 | G/C | — | uncertain significance |
| rs1203223621 | 19:51,602,069 | G/T | — | uncertain significance |
| rs920483360 | 19:51,602,073 | C/T | — | uncertain significance |
| rs2091899495 | 19:51,602,187 | C/T | — | uncertain significance |
| rs1255736998 | 19:51,602,274 | G/C | — | uncertain significance |
| rs773312410 | 19:51,602,291 | C/T | — | uncertain significance |
| rs770771525 | 19:51,602,295 | C/A | — | uncertain significance |
| rs767210453 | 19:51,602,301 | C/T | — | uncertain significance |
| rs765696186 | 19:51,602,315 | C/T | — | uncertain significance |
| rs1294782839 | 19:51,602,349 | G/A | — | uncertain significance |
| rs2514421080 | 19:51,602,396 | C/T | — | uncertain significance |
| rs66717916 | 19:51,607,151 | A/T | intron variant | — |
| rs2091913623 | 19:51,607,366 | G/C | — | uncertain significance |
| rs966864399 | 19:51,607,367 | C/G | — | uncertain significance |
| rs554596578 | 19:51,607,435 | G/A | — | uncertain significance |
| rs1461795571 | 19:51,607,619 | C/T | — | uncertain significance |
| rs748854150 | 19:51,607,655 | C/T | — | uncertain significance |
| rs1026519079 | 19:51,607,681 | G/A | — | uncertain significance |
| rs562481846 | 19:51,607,771 | G/A | — | uncertain significance |
| rs1193474464 | 19:51,607,776 | G/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.