PHACTR2
phosphatase and actin regulator 2
Summary
Predicted to enable actin binding activity. Predicted to be involved in actin cytoskeleton organization. Predicted to be located in plasma membrane and platelet alpha granule membrane. Implicated in Parkinson's disease and multiple sclerosis. Biomarker of Alzheimer's disease. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1890402 | 6:143,856,734 | C/T | upstream gene variant | — |
| rs9403501 | 6:143,859,014 | C/A | intron variant | — |
| rs140398128 | 6:143,871,436 | C/T | downstream gene variant | — |
| rs145600344 | 6:143,871,451 | G/A | downstream gene variant | — |
| rs181635149 | 6:143,873,045 | G/A | downstream gene variant | — |
| rs12199775 | 6:143,898,894 | A/G | intron variant | — |
| rs191388453 | 6:143,911,531 | T/C | intron variant | — |
| rs150302918 | 6:143,914,125 | C/T | intron variant | — |
| rs191867719 | 6:143,916,591 | C/T | intron variant | — |
| rs529347848 | 6:143,917,116 | G/A | — | — |
| rs73003380 | 6:143,922,264 | G/C | intron variant | — |
| rs9390123 | 6:143,943,314 | T/C | intron variant | — |
| rs370627774 | 6:143,948,886 | G/A | — | — |
| rs577247541 | 6:143,952,343 | T/C | — | — |
| rs11155313 | 6:143,961,577 | A/G | intron variant | — |
| rs556081816 | 6:143,965,477 | C/T | — | — |
| rs9403521 | 6:143,994,199 | T/C | regulatory region variant | — |
| rs183580821 | 6:143,995,136 | C/A | — | — |
| rs6570573 | 6:144,012,842 | A/G | intron variant | — |
| rs187295122 | 6:144,023,604 | G/C | intron variant | — |
| rs112390177 | 6:144,026,090 | G/A | intron variant | — |
| rs10457751 | 6:144,026,125 | G/A | intron variant | — |
| rs538065802 | 6:144,027,693 | A/G | — | — |
| rs1203570523 | 6:144,033,167 | A/C | — | uncertain significance |
| rs749125256 | 6:144,033,213 | C/G | — | uncertain significance |
| rs78144562 | 6:144,039,779 | A/C | intron variant | — |
| rs1779243142 | 6:144,075,031 | C/G | — | uncertain significance |
| rs184592604 | 6:144,079,516 | G/A | intron variant | — |
| rs6931865 | 6:144,079,854 | A/G | regulatory region variant | — |
| rs760782112 | 6:144,081,546 | G/A | — | uncertain significance |
| rs370477271 | 6:144,081,560 | A/C | — | uncertain significance |
| rs368126366 | 6:144,081,570 | G/A | — | uncertain significance |
| rs202069880 | 6:144,081,585 | C/G | — | uncertain significance |
| rs1779410831 | 6:144,081,604 | C/T | — | uncertain significance |
| rs778193518 | 6:144,081,729 | C/A | — | uncertain significance |
| rs760658535 | 6:144,081,742 | C/T | — | uncertain significance |
| rs371888907 | 6:144,081,763 | C/T | — | uncertain significance |
| rs191299662 | 6:144,084,440 | G/A | intron variant | — |
| rs374075677 | 6:144,086,425 | C/T | — | uncertain significance |
| rs566532922 | 6:144,086,473 | G/A | — | uncertain significance |
| rs533895829 | 6:144,086,481 | G/A | — | uncertain significance |
| rs549285501 | 6:144,086,482 | C/G | — | uncertain significance |
| rs2533510672 | 6:144,086,575 | C/G | — | uncertain significance |
| rs2533510895 | 6:144,086,612 | A/T | — | uncertain significance |
| rs577746587 | 6:144,086,644 | T/G | — | uncertain significance |
| rs2533511040 | 6:144,086,653 | A/G | — | uncertain significance |
| rs200977430 | 6:144,086,665 | C/T | — | uncertain significance |
| rs199622615 | 6:144,086,718 | C/G | — | uncertain significance |
| rs765120539 | 6:144,086,748 | C/T | — | uncertain significance |
| rs761913315 | 6:144,086,779 | C/T | — | uncertain significance |
| rs766160688 | 6:144,086,797 | T/G | — | uncertain significance |
| rs200196216 | 6:144,086,829 | G/A | — | uncertain significance |
| rs200791181 | 6:144,086,895 | T/C | — | uncertain significance |
| rs2533530260 | 6:144,093,424 | C/T | — | uncertain significance |
| rs567848575 | 6:144,093,459 | G/A | — | uncertain significance |
| rs777928424 | 6:144,093,481 | C/T | — | uncertain significance |
| rs1436276902 | 6:144,093,552 | G/A | — | uncertain significance |
| rs769604911 | 6:144,095,219 | C/T | — | uncertain significance |
| rs2533534830 | 6:144,095,309 | G/C | — | uncertain significance |
| rs143073766 | 6:144,096,484 | G/A | intron variant | — |
| rs2533545023 | 6:144,098,484 | A/G | — | uncertain significance |
| rs190212593 | 6:144,109,983 | C/T | — | uncertain significance |
| rs1160303818 | 6:144,128,231 | C/T | — | uncertain significance |
| rs150273716 | 6:144,142,191 | A/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.