SYNPO2L
synaptopodin 2 like
Summary
Predicted to enable actin binding activity. Predicted to be involved in several processes, including positive regulation of Rho protein signal transduction; positive regulation of stress fiber assembly; and sarcomere organization. Predicted to be located in cytoplasm and cytoskeleton. Predicted to be active in Z disc; actin cytoskeleton; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11000728 | 10:75,404,300 | C/A | — | — |
| rs140354250 | 10:75,406,498 | C/T | — | uncertain significance |
| rs532637767 | 10:75,406,532 | C/T | — | uncertain significance |
| rs1000630062 | 10:75,406,612 | G/T | — | uncertain significance |
| rs760585476 | 10:75,406,697 | T/C | — | uncertain significance |
| rs373834932 | 10:75,406,804 | G/C | — | uncertain significance |
| rs761659998 | 10:75,406,811 | C/T | — | uncertain significance |
| rs755094886 | 10:75,406,828 | A/G | — | uncertain significance |
| rs34163229 | 10:75,406,912 | G/T | missense variant | — |
| rs148367718 | 10:75,407,021 | G/C | — | uncertain significance |
| rs577750788 | 10:75,407,116 | C/A | — | uncertain significance |
| rs145644342 | 10:75,407,212 | C/T | — | uncertain significance |
| rs748283757 | 10:75,407,224 | G/A | — | uncertain significance |
| rs1214059186 | 10:75,407,261 | T/C | — | uncertain significance |
| rs769070146 | 10:75,407,281 | G/A | — | uncertain significance |
| rs3812629 | 10:75,407,290 | G/C | missense variant | — |
| rs768668437 | 10:75,407,291 | G/A | — | uncertain significance |
| rs1477710940 | 10:75,407,341 | A/G | — | uncertain significance |
| rs371822690 | 10:75,407,416 | G/A | — | uncertain significance |
| rs770274328 | 10:75,407,615 | G/C | — | uncertain significance |
| rs2547539812 | 10:75,407,642 | G/A | — | uncertain significance |
| rs1182129085 | 10:75,407,684 | T/C | — | uncertain significance |
| rs1465565690 | 10:75,407,750 | C/T | — | uncertain significance |
| rs779548300 | 10:75,407,839 | C/T | — | uncertain significance |
| rs767671228 | 10:75,407,896 | G/A | — | uncertain significance |
| rs2547540216 | 10:75,407,899 | G/T | — | uncertain significance |
| rs762086092 | 10:75,408,025 | C/A | — | uncertain significance |
| rs760049196 | 10:75,408,128 | C/G | — | uncertain significance |
| rs139351387 | 10:75,408,140 | G/C | — | uncertain significance |
| rs756968415 | 10:75,408,182 | G/A | — | uncertain significance |
| rs372513761 | 10:75,408,307 | G/A | — | uncertain significance |
| rs138501611 | 10:75,408,319 | G/A | — | uncertain significance |
| rs201100488 | 10:75,408,421 | G/A | — | uncertain significance |
| rs539614829 | 10:75,408,425 | G/A | — | uncertain significance |
| rs775780283 | 10:75,408,433 | C/T | — | uncertain significance |
| rs367837231 | 10:75,408,578 | T/C | — | uncertain significance |
| rs527349946 | 10:75,408,599 | T/C | — | uncertain significance |
| rs1415201889 | 10:75,408,605 | T/C | — | uncertain significance |
| rs568841082 | 10:75,412,924 | T/A | — | uncertain significance |
| rs1460068041 | 10:75,412,935 | T/A | — | uncertain significance |
| rs746388075 | 10:75,413,029 | G/T | — | uncertain significance |
| rs983104393 | 10:75,413,050 | C/T | — | uncertain significance |
| rs977884516 | 10:75,413,076 | C/T | — | uncertain significance |
| rs774559890 | 10:75,413,169 | G/A | — | uncertain significance |
| rs575621227 | 10:75,413,367 | A/G | — | uncertain significance |
| rs1375413385 | 10:75,413,376 | G/A | — | uncertain significance |
| rs1355877220 | 10:75,413,923 | T/C | — | uncertain significance |
| rs2547544354 | 10:75,413,969 | C/A | — | uncertain significance |
| rs759026761 | 10:75,415,604 | T/C | — | uncertain significance |
| rs2081875894 | 10:75,415,655 | A/G | — | uncertain significance |
| rs2547545303 | 10:75,415,658 | A/T | — | uncertain significance |
| rs60632610 | 10:75,415,677 | C/T | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.