TUBD1
tubulin delta 1
Summary
Predicted to enable GTP binding activity. Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in microtubule cytoskeleton organization; mitotic cell cycle; and positive regulation of smoothened signaling pathway. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7223057 | 17:57,936,438 | G/C | downstream gene variant | — |
| rs2509150137 | 17:57,937,694 | A/T | — | uncertain significance |
| rs2509150618 | 17:57,937,768 | T/C | — | uncertain significance |
| rs2509150834 | 17:57,937,785 | T/G | — | uncertain significance |
| rs143600797 | 17:57,941,166 | G/A | — | uncertain significance |
| rs2526358 | 17:57,942,585 | A/C | — | — |
| rs572341288 | 17:57,943,999 | C/T | — | uncertain significance |
| rs1345291281 | 17:57,944,066 | G/A | — | uncertain significance |
| rs186001883 | 17:57,944,072 | G/A | — | uncertain significance |
| rs67892093 | 17:57,945,784 | C/T | intron variant | — |
| rs59426030 | 17:57,950,688 | G/A | intron variant | — |
| rs200122426 | 17:57,951,932 | T/C | — | uncertain significance |
| rs983898580 | 17:57,955,475 | C/T | — | uncertain significance |
| rs369557664 | 17:57,955,500 | C/A | — | uncertain significance |
| rs767904487 | 17:57,955,535 | T/A | — | uncertain significance |
| rs1350676244 | 17:57,955,602 | T/C | — | uncertain significance |
| rs868415094 | 17:57,955,629 | G/A | — | uncertain significance |
| rs2040455664 | 17:57,958,284 | G/C | — | uncertain significance |
| rs773282613 | 17:57,958,421 | C/T | — | likely benign |
| rs2509256684 | 17:57,958,443 | C/T | — | uncertain significance |
| rs573936498 | 17:57,958,451 | C/T | — | likely benign |
| rs772857732 | 17:57,958,455 | G/A | — | uncertain significance |
| rs4047777 | 17:57,959,887 | A/T | upstream gene variant | — |
| rs765041198 | 17:57,963,480 | C/T | — | uncertain significance |
| rs2509279962 | 17:57,963,484 | A/G | — | uncertain significance |
| rs1292053 | 17:57,963,537 | A/G | missense variant | — |
| rs370691365 | 17:57,963,586 | T/C | — | likely benign |
| rs2040967076 | 17:57,968,202 | C/G | — | uncertain significance |
| rs76112765 | 17:57,968,208 | A/G | — | benign |
| rs758436504 | 17:57,968,258 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.