SYNPO2
synaptopodin 2
Summary
Enables alpha-actinin binding activity and filamin binding activity. Involved in positive regulation of actin filament bundle assembly; positive regulation of cell migration; and regulation of Rho-dependent protein serine/threonine kinase activity. Located in several cellular components, including Z disc; focal adhesion; and stress fiber. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10018977 | 4:119,785,229 | C/T | intergenic variant | — |
| rs116587722 | 4:119,790,517 | T/C | intergenic variant | — |
| rs752585023 | 4:119,810,209 | T/A | — | uncertain significance |
| rs371874744 | 4:119,810,259 | G/A | — | uncertain significance |
| rs1472066 | 4:119,863,476 | A/G | intron variant | — |
| rs769570941 | 4:119,947,852 | G/T | — | uncertain significance |
| rs2476544995 | 4:119,947,992 | G/C | — | uncertain significance |
| rs542980877 | 4:119,948,022 | G/C | — | uncertain significance |
| rs1737981454 | 4:119,948,116 | G/C | — | uncertain significance |
| rs755634036 | 4:119,948,131 | C/G | — | uncertain significance |
| rs753768167 | 4:119,948,139 | G/T | — | uncertain significance |
| rs200179576 | 4:119,948,170 | G/A | — | uncertain significance |
| rs2476545771 | 4:119,948,369 | C/T | — | uncertain significance |
| rs143767970 | 4:119,948,381 | T/C | — | uncertain significance |
| rs569699949 | 4:119,948,383 | A/C | — | uncertain significance |
| rs2476545837 | 4:119,948,393 | G/A | — | uncertain significance |
| rs200870694 | 4:119,948,512 | T/C | — | uncertain significance |
| rs1738009261 | 4:119,948,513 | C/T | — | uncertain significance |
| rs1341900721 | 4:119,948,528 | A/G | — | uncertain significance |
| rs199593703 | 4:119,948,543 | G/A | — | uncertain significance |
| rs2476549347 | 4:119,951,006 | G/A | — | uncertain significance |
| rs61745559 | 4:119,951,088 | T/G | — | benign |
| rs369424886 | 4:119,951,092 | A/T | — | uncertain significance |
| rs369985385 | 4:119,951,131 | C/T | — | uncertain significance |
| rs951901344 | 4:119,951,135 | G/A | — | uncertain significance |
| rs372848851 | 4:119,951,234 | T/C | — | uncertain significance |
| rs751055742 | 4:119,951,300 | C/A | — | uncertain significance |
| rs759691705 | 4:119,951,379 | G/A | — | uncertain significance |
| rs2476551069 | 4:119,951,447 | C/T | — | uncertain significance |
| rs144056756 | 4:119,951,453 | A/C | — | uncertain significance |
| rs148657710 | 4:119,951,464 | G/A | — | uncertain significance |
| rs141219187 | 4:119,951,524 | A/G | — | uncertain significance |
| rs150741126 | 4:119,951,578 | G/A | — | uncertain significance |
| rs7698598 | 4:119,951,647 | A/T | missense variant | — |
| rs375410311 | 4:119,951,693 | C/T | — | uncertain significance |
| rs1022435691 | 4:119,951,710 | G/T | — | uncertain significance |
| rs368294065 | 4:119,951,728 | G/T | — | uncertain significance |
| rs1403368975 | 4:119,951,788 | C/G | — | uncertain significance |
| rs150054203 | 4:119,951,812 | C/A | — | uncertain significance |
| rs2476553234 | 4:119,952,044 | G/A | — | uncertain significance |
| rs201894708 | 4:119,952,100 | G/A | — | uncertain significance |
| rs745805028 | 4:119,952,182 | C/T | — | uncertain significance |
| rs759959851 | 4:119,952,245 | C/T | — | uncertain significance |
| rs1049475650 | 4:119,952,278 | G/C | — | uncertain significance |
| rs1738232882 | 4:119,952,284 | C/A | — | uncertain significance |
| rs562890418 | 4:119,952,355 | G/T | — | uncertain significance |
| rs545390527 | 4:119,952,377 | C/T | — | uncertain significance |
| rs777838583 | 4:119,952,410 | C/T | — | uncertain significance |
| rs2476554571 | 4:119,952,457 | A/G | — | uncertain significance |
| rs141800282 | 4:119,952,496 | C/T | — | uncertain significance |
| rs777692059 | 4:119,952,518 | A/G | — | uncertain significance |
| rs115012720 | 4:119,952,589 | G/A | — | benign |
| rs201200646 | 4:119,952,719 | C/T | — | uncertain significance |
| rs753637222 | 4:119,952,723 | G/T | — | likely benign |
| rs1437669785 | 4:119,952,836 | C/G | — | uncertain significance |
| rs375644391 | 4:119,952,848 | A/G | — | uncertain significance |
| rs139205025 | 4:119,952,878 | A/G | — | uncertain significance |
| rs918346408 | 4:119,952,958 | C/T | — | uncertain significance |
| rs2476556908 | 4:119,952,961 | G/C | — | uncertain significance |
| rs769802322 | 4:119,952,980 | C/G | — | uncertain significance |
| rs201416335 | 4:119,953,015 | G/A | — | uncertain significance |
| rs572380117 | 4:119,953,033 | T/A | — | uncertain significance |
| rs1738289923 | 4:119,953,064 | G/A | — | uncertain significance |
| rs199921121 | 4:119,953,066 | G/A | — | uncertain significance |
| rs61733552 | 4:119,953,101 | A/C | — | benign |
| rs2476644369 | 4:119,978,556 | G/A | — | uncertain significance |
| rs754134859 | 4:119,978,565 | C/T | — | uncertain significance |
| rs201135815 | 4:119,978,601 | C/G | — | uncertain significance |
| rs201996079 | 4:119,978,602 | C/G | — | uncertain significance |
| rs200416625 | 4:119,978,670 | G/A | — | uncertain significance |
| rs1202147829 | 4:119,978,688 | C/G | — | uncertain significance |
| rs751444032 | 4:119,978,691 | A/G | — | uncertain significance |
| rs137992021 | 4:119,978,703 | G/A | — | benign |
| rs2476646061 | 4:119,978,749 | C/A | — | uncertain significance |
| rs773918484 | 4:119,978,770 | T/C | — | uncertain significance |
| rs745365878 | 4:119,978,832 | A/C | — | uncertain significance |
| rs2476646814 | 4:119,978,847 | T/A | — | uncertain significance |
| rs766431738 | 4:119,978,893 | A/C | — | uncertain significance |
| rs1445227597 | 4:119,978,908 | C/T | — | uncertain significance |
| rs372414505 | 4:119,978,984 | A/C | — | uncertain significance |
| rs17050126 | 4:119,979,001 | T/C | — | benign |
| rs147691876 | 4:119,979,047 | C/T | — | benign |
| rs1739266435 | 4:119,979,055 | A/G | — | uncertain significance |
| rs140963106 | 4:119,979,058 | C/T | — | uncertain significance |
| rs185497340 | 4:119,979,079 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.