PPIL6
peptidylprolyl isomerase like 6
Summary
Predicted to enable RNA polymerase II CTD heptapeptide repeat P3 isomerase activity and RNA polymerase II CTD heptapeptide repeat P6 isomerase activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13219952 | 6:109,712,287 | C/G | — | — |
| rs775997628 | 6:109,714,066 | A/G | — | uncertain significance |
| rs148088638 | 6:109,714,130 | C/T | — | uncertain significance |
| rs758158097 | 6:109,714,132 | A/G | — | uncertain significance |
| rs759583408 | 6:109,721,302 | C/T | — | uncertain significance |
| rs757338986 | 6:109,721,314 | G/A | — | uncertain significance |
| rs1297342302 | 6:109,721,322 | T/C | — | uncertain significance |
| rs769257444 | 6:109,721,366 | G/T | — | uncertain significance |
| rs112077923 | 6:109,721,368 | T/C | — | uncertain significance |
| rs6920372 | 6:109,723,939 | G/A | intron variant | — |
| rs1303804634 | 6:109,724,249 | T/A | — | uncertain significance |
| rs1400987342 | 6:109,724,261 | C/G | — | uncertain significance |
| rs9320286 | 6:109,724,937 | G/A | intron variant | — |
| rs13192476 | 6:109,725,154 | G/A | intron variant | — |
| rs61076041 | 6:109,741,530 | C/T | — | — |
| rs9487094 | 6:109,742,015 | G/A | regulatory region variant | — |
| rs1035426241 | 6:109,748,317 | T/C | — | uncertain significance |
| rs2482643007 | 6:109,748,329 | C/T | — | uncertain significance |
| rs372432146 | 6:109,748,350 | C/A | — | uncertain significance |
| rs144421142 | 6:109,752,416 | C/T | — | uncertain significance |
| rs2482668881 | 6:109,752,517 | G/A | — | uncertain significance |
| rs755543484 | 6:109,757,339 | C/T | — | uncertain significance |
| rs200986902 | 6:109,757,392 | T/C | — | likely benign |
| rs12213313 | 6:109,757,893 | C/T | — | — |
| rs367562291 | 6:109,761,661 | C/T | — | uncertain significance |
| rs371321942 | 6:109,761,699 | A/T | — | uncertain significance |
| rs749949559 | 6:109,761,726 | G/A | — | uncertain significance |
| rs766000276 | 6:109,761,744 | G/T | — | likely benign |
| rs754766224 | 6:109,761,768 | G/A | — | uncertain significance |
| rs1207216750 | 6:109,761,780 | T/C | — | uncertain significance |
| rs1315993048 | 6:109,761,783 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.