MEP1A
meprin A subunit alpha
Summary
Enables metallodipeptidase activity. Involved in epidermal growth factor receptor ligand maturation. Located in extracellular exosome. Part of meprin A complex. Is active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200179875 | 6:46,761,203 | C/T | — | uncertain significance |
| rs202088854 | 6:46,766,853 | A/G | — | uncertain significance |
| rs1407846400 | 6:46,787,388 | C/T | — | uncertain significance |
| rs201724464 | 6:46,787,394 | C/T | — | uncertain significance |
| rs766690241 | 6:46,787,400 | G/T | — | uncertain significance |
| rs6922686 | 6:46,788,191 | G/A | intron variant | — |
| rs757969989 | 6:46,793,021 | A/G | — | uncertain significance |
| rs754692574 | 6:46,793,033 | A/G | — | uncertain significance |
| rs781068330 | 6:46,793,035 | G/A | — | uncertain significance |
| rs372727410 | 6:46,793,063 | C/T | — | uncertain significance |
| rs767337393 | 6:46,793,138 | C/A | — | uncertain significance |
| rs138133276 | 6:46,793,144 | A/G | — | uncertain significance |
| rs769018940 | 6:46,793,170 | G/C | — | uncertain significance |
| rs143801305 | 6:46,793,192 | C/T | — | uncertain significance |
| rs758348379 | 6:46,794,103 | C/G | — | uncertain significance |
| rs2532883183 | 6:46,794,174 | G/A | — | uncertain significance |
| rs761608750 | 6:46,794,191 | C/G | — | uncertain significance |
| rs1320200907 | 6:46,794,193 | G/A | — | uncertain significance |
| rs768329749 | 6:46,794,214 | A/G | — | uncertain significance |
| rs1268302620 | 6:46,797,144 | C/G | — | uncertain significance |
| rs1768029771 | 6:46,797,257 | G/T | — | likely benign |
| rs376559870 | 6:46,797,272 | A/G | — | uncertain significance |
| rs763186687 | 6:46,800,818 | T/C | — | likely benign |
| rs756828283 | 6:46,800,846 | G/C | — | uncertain significance |
| rs748068549 | 6:46,800,870 | C/T | — | uncertain significance |
| rs142227340 | 6:46,800,897 | G/A | — | uncertain significance |
| rs766186999 | 6:46,800,924 | T/A | — | uncertain significance |
| rs756011676 | 6:46,800,976 | C/A | — | uncertain significance |
| rs545809127 | 6:46,801,009 | C/G | — | uncertain significance |
| rs1386229821 | 6:46,801,039 | G/A | — | uncertain significance |
| rs138587712 | 6:46,801,069 | G/T | — | uncertain significance |
| rs1206090590 | 6:46,801,080 | T/A | — | uncertain significance |
| rs200393800 | 6:46,801,158 | G/A | — | uncertain significance |
| rs780184381 | 6:46,801,182 | G/A | — | uncertain significance |
| rs142787710 | 6:46,801,214 | T/A | missense variant | — |
| rs545693270 | 6:46,802,369 | C/T | — | uncertain significance |
| rs139350018 | 6:46,802,428 | A/C | — | uncertain significance |
| rs774870617 | 6:46,803,121 | C/A | — | uncertain significance |
| rs372102824 | 6:46,803,151 | G/A | — | uncertain significance |
| rs1219370805 | 6:46,803,249 | G/A | — | uncertain significance |
| rs373369685 | 6:46,803,278 | G/A | — | likely benign |
| rs769344979 | 6:46,806,736 | T/G | — | uncertain significance |
| rs773829790 | 6:46,806,748 | G/T | — | uncertain significance |
| rs143826629 | 6:46,806,802 | G/A | — | uncertain significance |
| rs2532906165 | 6:46,806,811 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.