PPM1J
protein phosphatase, Mg2+/Mn2+ dependent 1J
Summary
This gene encodes the serine/threonine protein phosphatase. The mouse homolog of this gene apparently belongs to the protein phosphatase 2C family of genes. The exact function of this gene is not yet known. [provided by RefSeq, Jul 2008]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2525066067 | 1:113,252,850 | G/C | — | uncertain significance |
| rs201204322 | 1:113,252,876 | C/T | — | uncertain significance |
| rs1284638104 | 1:113,253,100 | T/C | — | uncertain significance |
| rs757215867 | 1:113,253,106 | G/C | — | uncertain significance |
| rs2525067614 | 1:113,253,137 | C/A | — | uncertain significance |
| rs2525067908 | 1:113,253,211 | T/G | — | uncertain significance |
| rs767675603 | 1:113,253,214 | G/A | — | uncertain significance |
| rs754940696 | 1:113,253,378 | G/C | — | likely benign |
| rs369486057 | 1:113,253,380 | A/C | — | uncertain significance |
| rs765169509 | 1:113,253,458 | T/C | — | uncertain significance |
| rs145597332 | 1:113,253,638 | C/T | — | uncertain significance |
| rs778451937 | 1:113,253,689 | A/G | — | uncertain significance |
| rs772963847 | 1:113,253,889 | A/G | — | uncertain significance |
| rs149099760 | 1:113,253,909 | C/T | — | uncertain significance |
| rs748270752 | 1:113,253,951 | C/T | — | uncertain significance |
| rs771962023 | 1:113,253,952 | G/A | — | uncertain significance |
| rs201233160 | 1:113,254,612 | C/T | — | uncertain significance |
| rs374615983 | 1:113,254,636 | C/T | — | uncertain significance |
| rs115193797 | 1:113,254,664 | G/C | — | uncertain significance |
| rs974469975 | 1:113,254,672 | A/G | — | uncertain significance |
| rs2525075198 | 1:113,254,992 | A/G | — | uncertain significance |
| rs770337211 | 1:113,255,004 | G/T | — | uncertain significance |
| rs542707419 | 1:113,255,022 | G/C | — | uncertain significance |
| rs373932983 | 1:113,255,371 | G/T | — | uncertain significance |
| rs753719488 | 1:113,255,388 | A/G | — | uncertain significance |
| rs34611728 | 1:113,255,456 | C/A | — | benign |
| rs765263339 | 1:113,255,497 | T/C | — | uncertain significance |
| rs1455603342 | 1:113,255,520 | G/C | — | uncertain significance |
| rs769571465 | 1:113,255,575 | G/A | — | uncertain significance |
| rs140892250 | 1:113,255,584 | G/A | — | uncertain significance |
| rs761423740 | 1:113,255,586 | G/A | — | uncertain significance |
| rs1309252998 | 1:113,255,591 | C/T | — | uncertain significance |
| rs1329032236 | 1:113,256,130 | T/G | — | uncertain significance |
| rs1482084514 | 1:113,256,222 | G/A | — | uncertain significance |
| rs12724682 | 1:113,256,368 | G/T | — | — |
| rs760958860 | 1:113,257,619 | G/A | — | uncertain significance |
| rs1675169231 | 1:113,257,749 | T/C | — | uncertain significance |
| rs546905517 | 1:113,257,809 | C/A | — | uncertain significance |
| rs974000209 | 1:113,257,821 | G/A | — | uncertain significance |
| rs566807547 | 1:113,257,829 | G/A | — | uncertain significance |
| rs765446734 | 1:113,257,845 | C/T | — | uncertain significance |
| rs1675174365 | 1:113,257,866 | G/T | — | uncertain significance |
| rs1675174473 | 1:113,257,868 | G/C | — | uncertain significance |
| rs2525089108 | 1:113,257,882 | G/C | — | uncertain significance |
| rs903865806 | 1:113,257,892 | T/G | — | uncertain significance |
| rs12736457 | 1:113,258,293 | C/G | regulatory region variant | — |
| rs12722725 | 1:113,258,681 | T/C | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.