DCT
dopachrome tautomerase
Summary
Predicted to enable dopachrome isomerase activity. Involved in response to blue light. Located in intracellular membrane-bounded organelle and plasma membrane. Implicated in oculocutaneous albinism. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748569533 | 13:95,092,159 | T/C | — | uncertain significance |
| rs376877447 | 13:95,092,172 | T/C | — | uncertain significance |
| rs146204093 | 13:95,092,181 | T/G | — | uncertain significance |
| rs764655568 | 13:95,092,305 | C/T | — | pathogenic |
| rs201705606 | 13:95,092,309 | C/A | — | uncertain significance |
| rs759177137 | 13:95,095,789 | G/A | — | uncertain significance |
| rs762269122 | 13:95,095,795 | G/C | — | uncertain significance |
| rs756489816 | 13:95,095,801 | T/C | — | uncertain significance |
| rs185229004 | 13:95,095,834 | G/A | — | likely benign |
| rs776329439 | 13:95,095,850 | C/T | — | uncertain significance |
| rs1407995 | 13:95,096,013 | C/T | — | association |
| rs746252950 | 13:95,097,989 | G/A | — | uncertain significance |
| rs770446816 | 13:95,098,002 | T/C | — | uncertain significance |
| rs727299 | 13:95,108,501 | C/T | intron variant | — |
| rs757947053 | 13:95,112,347 | C/T | — | uncertain significance |
| rs772228009 | 13:95,112,383 | C/T | — | uncertain significance |
| rs770964531 | 13:95,112,392 | C/A | — | uncertain significance |
| rs138973003 | 13:95,112,399 | G/T | — | uncertain significance |
| rs1300126891 | 13:95,112,416 | T/G | — | uncertain significance |
| rs1883691702 | 13:95,112,454 | G/T | — | uncertain significance |
| rs2501623967 | 13:95,114,280 | A/C | — | uncertain significance |
| rs1425828472 | 13:95,114,393 | C/T | — | uncertain significance |
| rs201692579 | 13:95,114,431 | G/T | — | pathogenic |
| rs1029675720 | 13:95,114,439 | C/A | — | uncertain significance |
| rs150712681 | 13:95,117,894 | A/G | — | uncertain significance |
| rs981625388 | 13:95,117,917 | C/T | — | uncertain significance |
| rs34139115 | 13:95,117,926 | C/T | — | benign |
| rs1187769005 | 13:95,117,947 | T/C | — | uncertain significance |
| rs770558686 | 13:95,117,977 | G/A | — | uncertain significance |
| rs144365832 | 13:95,117,993 | C/T | — | likely benign |
| rs143672390 | 13:95,118,052 | C/A | — | uncertain significance |
| rs377490914 | 13:95,118,840 | T/C | — | uncertain significance |
| rs369095389 | 13:95,118,846 | C/T | — | uncertain significance |
| rs749032774 | 13:95,118,847 | G/A | — | uncertain significance |
| rs754411804 | 13:95,118,859 | C/T | — | uncertain significance |
| rs530574255 | 13:95,118,904 | G/A | — | uncertain significance |
| rs34332656 | 13:95,121,086 | T/G | — | uncertain significance |
| rs1266129896 | 13:95,121,194 | C/T | — | uncertain significance |
| rs2501672395 | 13:95,121,209 | T/A | — | likely pathogenic |
| rs1367925937 | 13:95,121,240 | C/T | — | uncertain significance |
| rs200478079 | 13:95,121,252 | C/T | — | uncertain significance |
| rs34723994 | 13:95,121,253 | G/A | — | benign |
| rs144460082 | 13:95,121,261 | C/A | — | uncertain significance |
| rs777291106 | 13:95,131,250 | G/T | — | uncertain significance |
| rs763411727 | 13:95,131,263 | G/A | — | uncertain significance |
| rs758102115 | 13:95,131,298 | C/T | — | pathogenic |
| rs1885297366 | 13:95,131,327 | G/C | — | pathogenic |
| rs1885298359 | 13:95,131,334 | C/A | — | pathogenic |
| rs140411565 | 13:95,131,385 | G/A | — | uncertain significance |
| rs370729240 | 13:95,131,392 | A/T | — | pathogenic |
| rs751557518 | 13:95,131,397 | T/G | — | uncertain significance |
| rs567859263 | 13:95,131,410 | T/G | — | uncertain significance |
| rs749992341 | 13:95,131,430 | C/T | — | uncertain significance |
| rs9561570 | 13:95,156,198 | G/T | intergenic variant | — |
| rs717769 | 13:95,162,362 | T/A | — | — |
| rs7334485 | 13:95,184,243 | G/A | intergenic variant | — |
| rs6492711 | 13:95,196,559 | C/T | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.