LUZP2
leucine zipper protein 2
Summary
This gene encodes a leucine zipper protein. This protein is deleted in some patients with Wilms tumor-Aniridia-Genitourinary anomalies-mental Retardation (WAGR) syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2011]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79103986 | 11:24,517,030 | A/C | upstream gene variant | — |
| rs183154732 | 11:24,587,782 | T/C | intron variant | — |
| rs12285422 | 11:24,591,463 | G/A | — | — |
| rs12284708 | 11:24,596,273 | C/A | — | — |
| rs34578313 | 11:24,601,495 | G/C | — | — |
| rs931964 | 11:24,607,322 | A/G | intron variant | — |
| rs12361953 | 11:24,611,130 | C/G | intron variant | — |
| rs10834400 | 11:24,611,220 | G/C | intron variant | — |
| rs4561213 | 11:24,678,819 | T/C | — | — |
| rs111563973 | 11:24,697,396 | G/A | — | — |
| rs2494325712 | 11:24,750,784 | G/C | — | uncertain significance |
| rs1186534695 | 11:24,750,807 | T/C | — | uncertain significance |
| rs753486369 | 11:24,759,816 | A/G | — | uncertain significance |
| rs553637019 | 11:24,759,840 | C/G | — | uncertain significance |
| rs570443460 | 11:24,759,844 | C/T | — | uncertain significance |
| rs2631418 | 11:24,768,199 | C/A | — | — |
| rs10834489 | 11:24,837,801 | C/T | intron variant | — |
| rs10500991 | 11:24,849,566 | C/T | intron variant | — |
| rs1242066829 | 11:24,927,538 | A/G | — | uncertain significance |
| rs141661368 | 11:24,936,078 | A/T | — | uncertain significance |
| rs144319132 | 11:24,936,080 | T/A | — | uncertain significance |
| rs1268699195 | 11:24,940,042 | T/C | — | — |
| rs1279501275 | 11:24,998,143 | C/A | — | uncertain significance |
| rs1856087835 | 11:25,004,697 | A/T | — | uncertain significance |
| rs1856088670 | 11:25,004,712 | G/T | — | uncertain significance |
| rs1269061237 | 11:25,004,723 | G/T | — | uncertain significance |
| rs141562546 | 11:25,004,730 | G/A | — | uncertain significance |
| rs200569816 | 11:25,004,747 | C/G | — | uncertain significance |
| rs145329776 | 11:25,004,813 | C/G | — | uncertain significance |
| rs755294404 | 11:25,004,814 | T/C | — | uncertain significance |
| rs140789355 | 11:25,004,836 | C/G | — | uncertain significance |
| rs11028323 | 11:25,009,896 | A/T | — | — |
| rs1446209 | 11:25,062,398 | A/T | intron variant | — |
| rs1596854 | 11:25,064,297 | A/G | intron variant | — |
| rs767639836 | 11:25,079,841 | C/A | — | — |
| rs201686624 | 11:25,098,885 | C/T | — | uncertain significance |
| rs750539577 | 11:25,098,914 | C/T | — | uncertain significance |
| rs758064203 | 11:25,100,115 | C/T | — | uncertain significance |
| rs773564969 | 11:25,100,161 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.