URGCP
upregulator of cell proliferation
Summary
URG4 is upregulated in the presence of hepatitis B virus (HBV)-encoded X antigen (HBxAg) and may contribute to the development of hepatocellular carcinoma by promoting hepatocellular growth and survival (Tufan et al., 2002 [PubMed 12082552]).[supplied by OMIM, Mar 2008]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750425699 | 7:43,916,273 | C/T | — | uncertain significance |
| rs61732517 | 7:43,916,413 | G/A | — | benign |
| rs1010442688 | 7:43,916,424 | C/T | — | uncertain significance |
| rs376195109 | 7:43,916,490 | C/A | — | uncertain significance |
| rs1436243858 | 7:43,916,546 | A/G | — | uncertain significance |
| rs372174530 | 7:43,916,618 | T/C | — | uncertain significance |
| rs200059472 | 7:43,916,708 | G/A | — | uncertain significance |
| rs375921236 | 7:43,916,714 | T/C | — | uncertain significance |
| rs375907049 | 7:43,916,777 | G/A | — | uncertain significance |
| rs2232107 | 7:43,916,782 | G/A | — | benign |
| rs767321555 | 7:43,916,923 | A/C | — | uncertain significance |
| rs780354948 | 7:43,916,970 | C/T | — | uncertain significance |
| rs201208471 | 7:43,917,048 | C/T | — | uncertain significance |
| rs2095846616 | 7:43,917,053 | A/G | — | likely benign |
| rs761170285 | 7:43,917,137 | C/T | — | uncertain significance |
| rs2232104 | 7:43,917,259 | G/A | — | benign |
| rs374359699 | 7:43,917,309 | G/A | — | uncertain significance |
| rs2232101 | 7:43,917,334 | C/T | — | benign |
| rs2232100 | 7:43,917,343 | G/T | — | benign |
| rs374090073 | 7:43,917,440 | C/A | — | uncertain significance |
| rs7807549 | 7:43,917,465 | G/A | — | benign |
| rs746473611 | 7:43,917,473 | C/T | — | uncertain significance |
| rs1259090153 | 7:43,917,532 | C/A | — | uncertain significance |
| rs2232098 | 7:43,917,604 | C/T | — | benign |
| rs755401456 | 7:43,917,638 | C/T | — | uncertain significance |
| rs368227707 | 7:43,917,759 | C/A | — | uncertain significance |
| rs549475424 | 7:43,917,780 | C/G | — | uncertain significance |
| rs201654703 | 7:43,917,785 | C/T | — | uncertain significance |
| rs368948970 | 7:43,917,792 | T/C | — | uncertain significance |
| rs2543356712 | 7:43,917,846 | G/C | — | uncertain significance |
| rs367764896 | 7:43,917,929 | T/C | — | likely benign |
| rs201996150 | 7:43,918,208 | G/A | — | uncertain significance |
| rs2543358636 | 7:43,918,215 | G/A | — | uncertain significance |
| rs571911766 | 7:43,918,266 | C/T | — | uncertain significance |
| rs114117271 | 7:43,918,278 | C/T | — | benign |
| rs766647021 | 7:43,918,311 | G/A | — | uncertain significance |
| rs201612221 | 7:43,918,355 | A/T | — | uncertain significance |
| rs565422675 | 7:43,918,526 | G/A | — | uncertain significance |
| rs549264023 | 7:43,918,600 | C/A | — | uncertain significance |
| rs768794584 | 7:43,918,811 | G/A | — | likely benign |
| rs188483654 | 7:43,933,634 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.