DTX2
deltex E3 ubiquitin ligase 2
Summary
DTX2 functions as an E3 ubiquitin ligase (Takeyama et al., 2003 [PubMed 12670957]).[supplied by OMIM, Nov 2009]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1799179 | 7:76,108,927 | T/C | — | — |
| rs377456527 | 7:76,109,156 | A/T | — | — |
| rs368803468 | 7:76,109,860 | G/A | — | uncertain significance |
| rs754368794 | 7:76,109,915 | C/T | — | uncertain significance |
| rs1809072208 | 7:76,109,929 | A/G | — | uncertain significance |
| rs2690589 | 7:76,109,938 | G/A | — | uncertain significance |
| rs766952685 | 7:76,109,988 | T/G | — | uncertain significance |
| rs2116364336 | 7:76,110,019 | T/G | — | uncertain significance |
| rs370872905 | 7:76,110,082 | C/T | — | uncertain significance |
| rs1359328082 | 7:76,110,091 | A/C | — | uncertain significance |
| rs150857694 | 7:76,111,831 | T/C | missense variant | — |
| rs1584182484 | 7:76,111,849 | A/G | — | uncertain significance |
| rs747694774 | 7:76,111,887 | G/A | — | uncertain significance |
| rs777578252 | 7:76,111,905 | G/A | — | uncertain significance |
| rs565972500 | 7:76,111,961 | G/T | — | uncertain significance |
| rs777415062 | 7:76,111,982 | C/T | — | likely benign |
| rs759267168 | 7:76,112,020 | A/G | — | uncertain significance |
| rs947478547 | 7:76,112,025 | A/G | — | likely benign |
| rs2536481770 | 7:76,112,056 | G/T | — | uncertain significance |
| rs138102519 | 7:76,112,076 | C/T | — | uncertain significance |
| rs1474475420 | 7:76,112,077 | G/A | — | uncertain significance |
| rs543279359 | 7:76,112,115 | G/T | — | uncertain significance |
| rs192290514 | 7:76,112,122 | C/T | — | uncertain significance |
| rs1367772269 | 7:76,112,176 | C/T | — | uncertain significance |
| rs368500347 | 7:76,112,184 | G/A | — | uncertain significance |
| rs751158935 | 7:76,112,193 | C/G | — | uncertain significance |
| rs778090809 | 7:76,112,203 | A/G | — | uncertain significance |
| rs779291726 | 7:76,112,212 | C/T | — | uncertain significance |
| rs140118064 | 7:76,112,241 | C/G | — | uncertain significance |
| rs151329883 | 7:76,112,246 | C/T | — | likely benign |
| rs758670196 | 7:76,112,250 | C/T | — | uncertain significance |
| rs764351511 | 7:76,112,293 | C/T | — | uncertain significance |
| rs145151450 | 7:76,112,299 | A/G | missense variant | — |
| rs1809469573 | 7:76,112,305 | C/T | — | uncertain significance |
| rs142474507 | 7:76,112,316 | G/A | — | uncertain significance |
| rs142155908 | 7:76,112,398 | G/A | — | uncertain significance |
| rs776357746 | 7:76,112,422 | C/A | — | uncertain significance |
| rs1380948012 | 7:76,121,495 | A/C | — | uncertain significance |
| rs760631730 | 7:76,126,704 | C/T | — | uncertain significance |
| rs137896500 | 7:76,126,705 | G/A | — | uncertain significance |
| rs764883046 | 7:76,126,707 | G/A | — | uncertain significance |
| rs142067417 | 7:76,129,302 | C/T | — | — |
| rs2536580292 | 7:76,129,772 | C/G | — | uncertain significance |
| rs573134039 | 7:76,129,800 | A/G | — | likely benign |
| rs771655815 | 7:76,131,622 | T/A | — | uncertain significance |
| rs6958774 | 7:76,131,650 | G/A | — | likely benign |
| rs773707841 | 7:76,131,688 | G/T | — | uncertain significance |
| rs762997466 | 7:76,131,690 | T/C | — | likely benign |
| rs141623125 | 7:76,131,706 | A/G | — | likely benign |
| rs2536594758 | 7:76,131,727 | C/T | — | uncertain significance |
| rs150141824 | 7:76,131,762 | A/G | — | uncertain significance |
| rs368597411 | 7:76,132,738 | G/C | — | benign |
| rs73703182 | 7:76,132,805 | C/G | — | benign |
| rs545565669 | 7:76,132,851 | C/T | — | uncertain significance |
| rs1277120224 | 7:76,132,897 | G/A | — | uncertain significance |
| rs17855260 | 7:76,132,898 | T/C | — | likely benign |
| rs1453368261 | 7:76,133,693 | C/G | — | likely benign |
| rs746771647 | 7:76,133,724 | C/T | — | uncertain significance |
| rs1041875636 | 7:76,133,747 | C/T | — | likely benign |
| rs779458207 | 7:76,134,832 | G/A | — | uncertain significance |
| rs1812253497 | 7:76,134,863 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.