PM20D1
peptidase M20 domain containing 1
Summary
Enables hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides. Involved in several processes, including amide biosynthetic process; amide catabolic process; and amino acid metabolic process. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs568448704 | 1:205,797,146 | C/T | — | — |
| rs372031384 | 1:205,797,798 | G/T | — | uncertain significance |
| rs961576738 | 1:205,797,810 | A/C | — | uncertain significance |
| rs142122998 | 1:205,797,858 | T/G | — | uncertain significance |
| rs749953295 | 1:205,799,409 | G/A | — | uncertain significance |
| rs202094864 | 1:205,799,454 | T/A | — | uncertain significance |
| rs751958717 | 1:205,799,498 | A/G | — | uncertain significance |
| rs1772143 | 1:205,799,987 | T/A | intron variant | — |
| rs142013357 | 1:205,801,749 | G/A | — | uncertain significance |
| rs114776144 | 1:205,801,756 | T/C | — | benign |
| rs142134039 | 1:205,801,765 | C/T | — | likely benign |
| rs200541177 | 1:205,801,773 | C/T | — | uncertain significance |
| rs757926550 | 1:205,801,806 | G/A | — | uncertain significance |
| rs199717760 | 1:205,801,816 | C/T | — | likely benign |
| rs1440555455 | 1:205,801,819 | G/T | — | uncertain significance |
| rs1361754 | 1:205,801,872 | A/G | — | benign |
| rs112676812 | 1:205,804,437 | T/C | intron variant | — |
| rs11240572 | 1:205,808,013 | C/T | — | — |
| rs369049170 | 1:205,809,409 | G/A | — | uncertain significance |
| rs371652298 | 1:205,809,447 | T/C | — | uncertain significance |
| rs561916224 | 1:205,809,803 | C/T | — | — |
| rs757590554 | 1:205,810,970 | G/T | — | uncertain significance |
| rs779831025 | 1:205,812,798 | C/T | — | uncertain significance |
| rs1249874235 | 1:205,812,822 | A/G | — | uncertain significance |
| rs776728245 | 1:205,812,847 | A/C | — | uncertain significance |
| rs139066269 | 1:205,812,879 | A/G | — | likely benign |
| rs75574362 | 1:205,813,139 | C/A | intron variant | — |
| rs373311318 | 1:205,813,219 | C/T | — | uncertain significance |
| rs1166953221 | 1:205,813,225 | G/A | — | uncertain significance |
| rs538991994 | 1:205,813,252 | C/T | — | uncertain significance |
| rs2526737492 | 1:205,813,296 | C/T | — | uncertain significance |
| rs138275090 | 1:205,813,320 | A/T | — | uncertain significance |
| rs116474384 | 1:205,813,812 | C/T | intron variant | — |
| rs139168724 | 1:205,814,470 | C/T | — | likely benign |
| rs557183892 | 1:205,814,476 | G/C | — | uncertain significance |
| rs143000907 | 1:205,814,529 | A/T | — | uncertain significance |
| rs189235498 | 1:205,814,604 | G/A | — | uncertain significance |
| rs2526741539 | 1:205,814,640 | A/G | — | uncertain significance |
| rs544230377 | 1:205,815,389 | T/C | — | — |
| rs755780561 | 1:205,817,031 | C/T | — | uncertain significance |
| rs779931686 | 1:205,817,032 | G/A | — | likely benign |
| rs765058539 | 1:205,819,056 | C/G | — | uncertain significance |
| rs780382315 | 1:205,819,085 | A/T | — | uncertain significance |
| rs2526751921 | 1:205,819,100 | T/C | — | uncertain significance |
| rs1484485947 | 1:205,819,185 | C/T | — | uncertain significance |
| rs61822643 | 1:205,820,282 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.