ZMIZ2
zinc finger MIZ-type containing 2
Summary
ZMIZ2 and ZMIZ1 (MIM 607159) are members of a PIAS (see MIM 603566)-like family of proteins that interact with nuclear hormone receptors. ZMIZ2 interacts with androgen receptor (AR; MIM 313700) and enhances AR-mediated transcription (Huang et al., 2005 [PubMed 16051670]).[supplied by OMIM, May 2010]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs55812947 | 7:44,790,807 | T/C | regulatory region variant | — |
| rs574652545 | 7:44,795,859 | T/C | — | uncertain significance |
| rs200135812 | 7:44,795,868 | T/G | — | uncertain significance |
| rs753030298 | 7:44,795,889 | C/T | — | uncertain significance |
| rs199684927 | 7:44,796,067 | G/A | — | uncertain significance |
| rs762226810 | 7:44,796,124 | G/A | — | uncertain significance |
| rs2485166631 | 7:44,796,135 | C/T | — | likely benign |
| rs756876987 | 7:44,796,702 | G/C | — | uncertain significance |
| rs367805690 | 7:44,796,712 | G/A | — | uncertain significance |
| rs200740396 | 7:44,796,747 | G/A | — | uncertain significance |
| rs751339057 | 7:44,796,987 | G/A | — | uncertain significance |
| rs201911821 | 7:44,796,990 | C/G | — | uncertain significance |
| rs752627717 | 7:44,796,991 | C/T | — | uncertain significance |
| rs926141225 | 7:44,797,003 | G/A | — | uncertain significance |
| rs375616323 | 7:44,797,008 | C/G | — | uncertain significance |
| rs769212250 | 7:44,797,037 | C/G | — | uncertain significance |
| rs764164101 | 7:44,797,075 | C/T | — | uncertain significance |
| rs368887424 | 7:44,797,159 | C/T | — | uncertain significance |
| rs1438883730 | 7:44,797,510 | G/A | — | uncertain significance |
| rs756543847 | 7:44,797,549 | A/G | — | uncertain significance |
| rs779714515 | 7:44,797,570 | C/G | — | uncertain significance |
| rs768411556 | 7:44,797,585 | C/T | — | uncertain significance |
| rs747778159 | 7:44,797,685 | G/C | — | uncertain significance |
| rs770915659 | 7:44,797,702 | T/G | — | uncertain significance |
| rs113585586 | 7:44,798,315 | G/T | intron variant | — |
| rs775499095 | 7:44,798,917 | A/G | — | uncertain significance |
| rs2485234279 | 7:44,798,944 | C/T | — | uncertain significance |
| rs777822165 | 7:44,799,781 | G/A | — | uncertain significance |
| rs200058478 | 7:44,799,787 | A/G | — | uncertain significance |
| rs371090113 | 7:44,800,031 | G/A | — | uncertain significance |
| rs1178022987 | 7:44,800,049 | C/T | — | uncertain significance |
| rs1429333565 | 7:44,800,052 | G/C | — | uncertain significance |
| rs577059407 | 7:44,801,053 | G/A | — | uncertain significance |
| rs373218484 | 7:44,801,092 | G/C | — | uncertain significance |
| rs2116815827 | 7:44,801,155 | C/T | — | uncertain significance |
| rs1350767422 | 7:44,801,167 | T/C | — | uncertain significance |
| rs948815746 | 7:44,801,312 | A/G | — | likely benign |
| rs376863416 | 7:44,801,412 | G/A | — | uncertain significance |
| rs1791210165 | 7:44,801,413 | A/G | — | uncertain significance |
| rs111363146 | 7:44,801,682 | T/C | regulatory region variant | — |
| rs762794949 | 7:44,802,519 | G/A | — | uncertain significance |
| rs530339068 | 7:44,802,576 | A/G | — | uncertain significance |
| rs758713337 | 7:44,802,875 | G/A | — | uncertain significance |
| rs79784917 | 7:44,803,944 | G/T | intron variant | — |
| rs11980575 | 7:44,804,062 | G/C | — | benign |
| rs2485384296 | 7:44,804,548 | C/G | — | uncertain significance |
| rs2485398097 | 7:44,804,962 | C/T | — | uncertain significance |
| rs886679537 | 7:44,804,966 | C/T | — | uncertain significance |
| rs367789981 | 7:44,804,981 | C/T | — | uncertain significance |
| rs769069807 | 7:44,805,009 | C/G | — | uncertain significance |
| rs535580978 | 7:44,805,041 | G/A | — | uncertain significance |
| rs201947872 | 7:44,805,112 | G/A | — | uncertain significance |
| rs768307925 | 7:44,805,128 | C/A | — | uncertain significance |
| rs763068838 | 7:44,805,139 | C/T | — | uncertain significance |
| rs2485423479 | 7:44,805,808 | C/A | — | uncertain significance |
| rs1791693653 | 7:44,805,844 | C/A | — | uncertain significance |
| rs1436578887 | 7:44,805,885 | A/G | — | uncertain significance |
| rs2485426201 | 7:44,805,913 | C/A | — | uncertain significance |
| rs773513282 | 7:44,806,044 | C/T | — | uncertain significance |
| rs202189418 | 7:44,806,078 | C/T | — | uncertain significance |
| rs746352345 | 7:44,806,140 | C/T | — | uncertain significance |
| rs567088827 | 7:44,806,185 | G/T | — | uncertain significance |
| rs777975265 | 7:44,806,206 | G/A | — | uncertain significance |
| rs1376123822 | 7:44,806,216 | C/T | — | uncertain significance |
| rs779297978 | 7:44,806,224 | A/G | — | uncertain significance |
| rs2485434470 | 7:44,806,245 | C/G | — | uncertain significance |
| rs372277555 | 7:44,807,178 | A/G | — | uncertain significance |
| rs1399305213 | 7:44,807,191 | A/G | — | uncertain significance |
| rs771705675 | 7:44,807,193 | G/A | — | uncertain significance |
| rs770369265 | 7:44,807,203 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.