CPEB4
cytoplasmic polyadenylation element binding protein 4
Summary
Enables RNA binding activity. Predicted to be involved in several processes, including cellular response to glucose starvation; negative regulation of cytoplasmic translation; and response to ischemia. Located in cytoplasm and nucleus. Biomarker of liver cirrhosis; portal hypertension; and primary biliary cholangitis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2532017589 | 5:173,316,749 | G/A | — | uncertain significance |
| rs774985810 | 5:173,316,852 | C/A | — | uncertain significance |
| rs2532018560 | 5:173,317,109 | G/C | — | uncertain significance |
| rs139234513 | 5:173,317,137 | G/A | — | uncertain significance |
| rs149568017 | 5:173,317,206 | C/A | — | uncertain significance |
| rs2532019081 | 5:173,317,320 | T/C | — | uncertain significance |
| rs748463752 | 5:173,317,380 | G/A | — | uncertain significance |
| rs771639094 | 5:173,317,557 | T/G | — | uncertain significance |
| rs2532019922 | 5:173,317,653 | A/G | — | uncertain significance |
| rs1438592549 | 5:173,317,758 | A/G | — | uncertain significance |
| rs758003370 | 5:173,317,781 | G/T | — | uncertain significance |
| rs373430313 | 5:173,317,860 | C/T | — | uncertain significance |
| rs72810983 | 5:173,318,254 | A/G | regulatory region variant | — |
| rs7705502 | 5:173,320,815 | G/A | intron variant | — |
| rs55646464 | 5:173,324,971 | G/T | intron variant | — |
| rs17694791 | 5:173,326,891 | C/T | intron variant | — |
| rs17694835 | 5:173,328,024 | G/T | intron variant | — |
| rs62376951 | 5:173,329,285 | T/C | intron variant | — |
| rs4867732 | 5:173,334,401 | C/T | — | — |
| rs17695092 | 5:173,337,853 | T/G | intron variant | — |
| rs112299234 | 5:173,339,531 | T/A | — | — |
| rs10516107 | 5:173,348,156 | G/A | regulatory region variant | — |
| rs17695555 | 5:173,351,081 | C/T | regulatory region variant | — |
| rs12519998 | 5:173,351,861 | G/T | intron variant | — |
| rs1106693 | 5:173,352,763 | G/C | — | — |
| rs72812818 | 5:173,356,752 | G/C | intron variant | — |
| rs6864691 | 5:173,358,154 | G/A | intron variant | — |
| rs17763373 | 5:173,359,331 | A/G | intron variant | — |
| rs6861681 | 5:173,362,458 | G/A | intron variant | — |
| rs17076724 | 5:173,363,667 | G/T | intron variant | — |
| rs17076726 | 5:173,363,889 | C/T | intron variant | — |
| rs750548380 | 5:173,371,974 | G/T | — | uncertain significance |
| rs376710749 | 5:173,372,017 | C/T | — | uncertain significance |
| rs1561630076 | 5:173,372,062 | T/G | — | uncertain significance |
| rs72812832 | 5:173,372,625 | G/A | intron variant | — |
| rs28391057 | 5:173,373,332 | A/G | regulatory region variant | — |
| rs1313241047 | 5:173,376,532 | G/A | — | uncertain significance |
| rs72812852 | 5:173,379,347 | G/T | intron variant | — |
| rs1758363739 | 5:173,382,971 | G/A | — | uncertain significance |
| rs12659398 | 5:173,386,203 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.