PLEKHM3
pleckstrin homology domain containing M3
Summary
Predicted to enable zinc ion binding activity. Predicted to be involved in myoblast differentiation. Predicted to be located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs781575909 | 2:208,693,167 | G/C | — | uncertain significance |
| rs113537648 | 2:208,711,011 | G/C | — | — |
| rs571437750 | 2:208,713,846 | C/T | — | — |
| rs61624605 | 2:208,722,898 | G/C | — | — |
| rs2470478222 | 2:208,725,831 | G/C | — | uncertain significance |
| rs200896303 | 2:208,725,840 | A/C | — | uncertain significance |
| rs1296865966 | 2:208,725,841 | A/G | — | uncertain significance |
| rs778046594 | 2:208,725,854 | G/A | — | uncertain significance |
| rs1266904915 | 2:208,725,877 | C/T | — | uncertain significance |
| rs762422346 | 2:208,725,979 | T/C | — | uncertain significance |
| rs11896555 | 2:208,756,352 | C/A | — | — |
| rs1471528 | 2:208,761,102 | A/G | — | — |
| rs2468840744 | 2:208,795,743 | A/C | — | uncertain significance |
| rs202021467 | 2:208,811,126 | G/A | — | uncertain significance |
| rs2105968903 | 2:208,811,161 | C/T | — | uncertain significance |
| rs753418017 | 2:208,811,201 | C/T | — | uncertain significance |
| rs1370146591 | 2:208,811,233 | C/A | — | uncertain significance |
| rs554420928 | 2:208,824,108 | C/T | — | — |
| rs200046449 | 2:208,841,425 | G/A | — | uncertain significance |
| rs762229483 | 2:208,841,455 | G/C | — | uncertain significance |
| rs753970574 | 2:208,841,488 | C/T | — | uncertain significance |
| rs1173496556 | 2:208,841,500 | T/C | — | uncertain significance |
| rs779273690 | 2:208,841,501 | T/C | — | uncertain significance |
| rs1691329154 | 2:208,841,579 | T/A | — | uncertain significance |
| rs201268173 | 2:208,841,591 | C/T | — | uncertain significance |
| rs369158949 | 2:208,841,599 | C/T | — | uncertain significance |
| rs765459423 | 2:208,841,611 | C/T | — | uncertain significance |
| rs1013506201 | 2:208,841,699 | C/A | — | uncertain significance |
| rs868708982 | 2:208,841,786 | C/T | — | uncertain significance |
| rs2468929852 | 2:208,841,833 | A/G | — | uncertain significance |
| rs746708061 | 2:208,841,849 | G/C | — | uncertain significance |
| rs1163987591 | 2:208,841,920 | G/A | — | uncertain significance |
| rs112176910 | 2:208,841,954 | T/C | — | uncertain significance |
| rs756408624 | 2:208,842,046 | G/A | — | uncertain significance |
| rs771200556 | 2:208,842,250 | T/C | — | uncertain significance |
| rs1417145488 | 2:208,842,278 | T/C | — | uncertain significance |
| rs17640594 | 2:208,850,232 | C/A | intron variant | — |
| rs537974055 | 2:208,865,781 | T/G | — | uncertain significance |
| rs180671227 | 2:208,865,900 | G/T | — | uncertain significance |
| rs772528902 | 2:208,866,203 | A/G | — | uncertain significance |
| rs950859081 | 2:208,866,219 | C/T | — | uncertain significance |
| rs756976770 | 2:208,866,239 | A/C | — | uncertain significance |
| rs1559278439 | 2:208,866,327 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.