CPEB3
cytoplasmic polyadenylation element binding protein 3
Summary
Enables mRNA 3'-UTR binding activity and translation factor activity, RNA binding. Involved in cellular response to amino acid stimulus and regulation of gene expression. Located in several cellular components, including cytosol; midbody; and nucleoplasm. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61875182 | 10:93,808,142 | T/A | — | — |
| rs1227931366 | 10:93,811,991 | T/G | — | uncertain significance |
| rs1194373530 | 10:93,812,024 | G/A | — | uncertain significance |
| rs762404398 | 10:93,812,064 | C/A | — | uncertain significance |
| rs833385 | 10:93,831,646 | C/G | upstream gene variant | — |
| rs61875203 | 10:93,888,810 | C/T | intron variant | — |
| rs773585852 | 10:93,902,837 | C/T | — | uncertain significance |
| rs760189725 | 10:93,902,866 | G/A | — | uncertain significance |
| rs2133844567 | 10:93,904,815 | T/C | — | uncertain significance |
| rs2134175514 | 10:93,952,237 | C/T | — | uncertain significance |
| rs762421634 | 10:93,952,294 | A/G | — | uncertain significance |
| rs771847381 | 10:93,952,393 | C/T | — | uncertain significance |
| rs7920520 | 10:93,969,270 | C/G | intron variant | — |
| rs72807264 | 10:93,988,790 | A/T | intron variant | — |
| rs7091853 | 10:93,997,695 | G/T | — | — |
| rs2493682784 | 10:93,999,264 | C/A | — | uncertain significance |
| rs115735799 | 10:93,999,268 | G/A | — | benign |
| rs377693834 | 10:93,999,282 | C/T | — | uncertain significance |
| rs761634354 | 10:93,999,315 | C/T | — | uncertain significance |
| rs1210592738 | 10:93,999,336 | G/T | — | uncertain significance |
| rs377049402 | 10:93,999,348 | C/G | — | uncertain significance |
| rs376818546 | 10:93,999,349 | G/T | — | uncertain significance |
| rs1240508039 | 10:93,999,431 | A/G | — | likely benign |
| rs547574003 | 10:93,999,462 | T/C | — | uncertain significance |
| rs987623986 | 10:93,999,493 | G/C | — | uncertain significance |
| rs943429286 | 10:93,999,515 | T/C | — | uncertain significance |
| rs2493693154 | 10:93,999,561 | G/C | — | uncertain significance |
| rs748420860 | 10:93,999,567 | G/T | — | uncertain significance |
| rs374239608 | 10:93,999,655 | G/C | — | uncertain significance |
| rs1301797491 | 10:93,999,696 | T/C | — | uncertain significance |
| rs2493698084 | 10:93,999,756 | C/T | — | uncertain significance |
| rs2493698502 | 10:93,999,780 | T/C | — | uncertain significance |
| rs140884766 | 10:93,999,797 | G/A | — | uncertain significance |
| rs1215982191 | 10:93,999,818 | G/A | — | uncertain significance |
| rs61735093 | 10:93,999,831 | G/A | — | uncertain significance |
| rs1851766757 | 10:93,999,890 | A/G | — | uncertain significance |
| rs761306247 | 10:93,999,921 | G/C | — | uncertain significance |
| rs2493702962 | 10:93,999,926 | G/A | — | uncertain significance |
| rs1477844383 | 10:94,000,007 | T/C | — | uncertain significance |
| rs2493708301 | 10:94,000,094 | A/G | — | uncertain significance |
| rs371048794 | 10:94,040,124 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.