PABPC4L
poly(A) binding protein cytoplasmic 4 like
Summary
Predicted to enable mRNA 3'-UTR binding activity; poly(A) binding activity; and poly(U) RNA binding activity. Predicted to be part of ribonucleoprotein complex. Predicted to be active in cytoplasmic stress granule; cytosol; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1494978 | 4:134,947,801 | G/A | intergenic variant | — |
| rs1348296909 | 4:135,121,067 | G/A | — | likely benign |
| rs1333293489 | 4:135,121,139 | T/C | — | uncertain significance |
| rs2531020304 | 4:135,121,200 | C/A | — | uncertain significance |
| rs2531020653 | 4:135,121,247 | G/C | — | uncertain significance |
| rs748098961 | 4:135,121,409 | T/C | — | uncertain significance |
| rs1430775638 | 4:135,121,459 | C/T | — | uncertain significance |
| rs775758642 | 4:135,121,468 | C/G | — | uncertain significance |
| rs764605454 | 4:135,121,484 | C/A | — | uncertain significance |
| rs547997386 | 4:135,121,526 | G/C | — | uncertain significance |
| rs1047100036 | 4:135,121,569 | A/T | — | uncertain significance |
| rs756824527 | 4:135,121,570 | T/A | — | uncertain significance |
| rs1729822702 | 4:135,121,646 | C/A | — | uncertain significance |
| rs1223039061 | 4:135,121,703 | T/C | — | uncertain significance |
| rs116807401 | 4:135,121,721 | T/C | missense variant | — |
| rs2530102306 | 4:135,121,763 | C/T | — | uncertain significance |
| rs2530102391 | 4:135,121,766 | T/C | — | uncertain significance |
| rs1160108827 | 4:135,121,855 | T/C | — | uncertain significance |
| rs142016147 | 4:135,121,886 | T/G | — | uncertain significance |
| rs1729838838 | 4:135,121,924 | A/G | — | uncertain significance |
| rs1293188666 | 4:135,121,961 | T/C | — | uncertain significance |
| rs753715778 | 4:135,122,024 | G/T | — | uncertain significance |
| rs757838503 | 4:135,122,045 | C/T | — | uncertain significance |
| rs2125710410 | 4:135,122,069 | C/T | — | uncertain significance |
| rs1228920813 | 4:135,122,119 | G/A | — | uncertain significance |
| rs373743585 | 4:135,122,158 | T/C | — | uncertain significance |
| rs1448762549 | 4:135,122,174 | T/C | — | uncertain significance |
| rs761517220 | 4:135,122,193 | G/C | — | uncertain significance |
| rs541577955 | 4:135,122,225 | C/T | — | likely benign |
| rs1729865568 | 4:135,122,263 | T/G | — | uncertain significance |
| rs532372537 | 4:135,122,342 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.