CREB3L2
cAMP responsive element binding protein 3 like 2
Summary
This gene encodes a member of the oasis bZIP transcription factor family. Members of this family can dimerize but form homodimers only. The encoded protein is a transcriptional activator. Translocations between this gene on chromosome 7 and the gene fused in sarcoma on chromosome 16 can be found in some tumors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs73729083 | 7:137,559,799 | T/C | regulatory region variant | — |
| rs57979055 | 7:137,560,320 | G/A | 3 prime UTR variant | — |
| rs73729085 | 7:137,561,861 | A/G | 3 prime UTR variant | — |
| rs73729087 | 7:137,562,668 | T/C | 3 prime UTR variant | — |
| rs3735018 | 7:137,562,744 | G/C | 3 prime UTR variant | — |
| rs1301579805 | 7:137,565,293 | T/C | — | uncertain significance |
| rs369276139 | 7:137,565,295 | A/T | — | uncertain significance |
| rs6980335 | 7:137,566,421 | T/G | — | — |
| rs2535879795 | 7:137,567,204 | C/T | — | uncertain significance |
| rs375939444 | 7:137,567,239 | G/A | — | uncertain significance |
| rs750933727 | 7:137,567,291 | C/T | — | uncertain significance |
| rs145388881 | 7:137,567,314 | G/A | — | uncertain significance |
| rs768358209 | 7:137,567,332 | G/A | — | likely benign |
| rs376688758 | 7:137,567,333 | G/T | — | uncertain significance |
| rs199561057 | 7:137,567,341 | T/C | — | uncertain significance |
| rs778451113 | 7:137,569,744 | C/T | — | uncertain significance |
| rs1300445623 | 7:137,569,818 | T/C | — | uncertain significance |
| rs574310470 | 7:137,569,846 | C/T | — | uncertain significance |
| rs539159443 | 7:137,570,189 | G/A | — | uncertain significance |
| rs775525222 | 7:137,570,225 | T/C | — | uncertain significance |
| rs750056999 | 7:137,570,248 | C/G | — | uncertain significance |
| rs747050072 | 7:137,593,008 | G/A | — | uncertain significance |
| rs776621858 | 7:137,593,044 | C/T | — | uncertain significance |
| rs375749577 | 7:137,593,059 | G/C | — | uncertain significance |
| rs1585613637 | 7:137,593,146 | G/A | — | uncertain significance |
| rs273960 | 7:137,597,005 | T/A | — | — |
| rs201981192 | 7:137,600,626 | G/T | — | uncertain significance |
| rs201136941 | 7:137,600,663 | C/T | — | uncertain significance |
| rs747211957 | 7:137,600,753 | C/T | — | uncertain significance |
| rs273952 | 7:137,605,247 | A/T | — | — |
| rs273946 | 7:137,611,296 | G/C | — | — |
| rs2535933231 | 7:137,612,925 | T/C | — | uncertain significance |
| rs756310062 | 7:137,612,937 | G/C | — | uncertain significance |
| rs754799812 | 7:137,612,946 | C/T | — | uncertain significance |
| rs199993400 | 7:137,612,947 | G/A | — | uncertain significance |
| rs200716 | 7:137,614,547 | A/G | intron variant | — |
| rs7795277 | 7:137,614,569 | C/A | — | — |
| rs147545797 | 7:137,686,360 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.