ERMP1
endoplasmic reticulum metallopeptidase 1
Summary
Predicted to enable metal ion binding activity and metalloexopeptidase activity. Involved in cellular response to oxidative stress. Acts upstream of or within endoplasmic reticulum unfolded protein response. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200756546 | 9:5,787,152 | C/T | — | uncertain significance |
| rs776293176 | 9:5,787,154 | A/G | — | uncertain significance |
| rs1035894014 | 9:5,787,199 | G/T | — | uncertain significance |
| rs200810811 | 9:5,787,242 | C/T | — | uncertain significance |
| rs371806673 | 9:5,787,256 | T/G | — | uncertain significance |
| rs778417508 | 9:5,787,524 | T/C | — | uncertain significance |
| rs62638707 | 9:5,787,553 | C/T | — | benign |
| rs189400569 | 9:5,787,725 | A/G | intron variant | — |
| rs751027218 | 9:5,797,819 | G/A | — | uncertain significance |
| rs145639054 | 9:5,797,894 | C/T | — | uncertain significance |
| rs2537821112 | 9:5,798,828 | G/T | — | uncertain significance |
| rs747293708 | 9:5,798,849 | G/C | — | uncertain significance |
| rs1463543992 | 9:5,798,861 | C/G | — | uncertain significance |
| rs370992190 | 9:5,798,981 | C/T | — | uncertain significance |
| rs775344090 | 9:5,801,200 | C/T | — | likely benign |
| rs371939957 | 9:5,801,302 | G/C | — | uncertain significance |
| rs752157842 | 9:5,805,047 | T/C | — | uncertain significance |
| rs1828839492 | 9:5,805,613 | T/C | — | uncertain significance |
| rs2537836089 | 9:5,805,634 | A/C | — | uncertain significance |
| rs1227696868 | 9:5,805,647 | T/C | — | uncertain significance |
| rs374260134 | 9:5,805,661 | G/A | — | uncertain significance |
| rs141976024 | 9:5,805,682 | A/G | — | uncertain significance |
| rs765569318 | 9:5,805,684 | C/T | — | likely benign |
| rs35643913 | 9:5,805,741 | C/T | — | benign |
| rs2797512 | 9:5,807,444 | T/G | intron variant | — |
| rs543515732 | 9:5,810,030 | G/A | — | uncertain significance |
| rs559305338 | 9:5,810,081 | C/A | — | uncertain significance |
| rs755468335 | 9:5,810,171 | G/A | — | uncertain significance |
| rs202014818 | 9:5,811,135 | T/G | — | uncertain significance |
| rs754823307 | 9:5,811,147 | A/T | — | uncertain significance |
| rs192189369 | 9:5,811,155 | A/C | — | benign |
| rs149390224 | 9:5,811,183 | T/C | — | uncertain significance |
| rs115468892 | 9:5,811,226 | C/T | — | benign |
| rs140094646 | 9:5,811,257 | T/C | — | benign |
| rs200754622 | 9:5,811,279 | T/C | — | uncertain significance |
| rs2537851645 | 9:5,812,181 | T/C | — | uncertain significance |
| rs199824716 | 9:5,812,883 | A/G | — | likely benign |
| rs2537853472 | 9:5,812,972 | A/G | — | uncertain significance |
| rs2537853554 | 9:5,812,994 | C/G | — | uncertain significance |
| rs2537853616 | 9:5,813,009 | C/T | — | uncertain significance |
| rs773294457 | 9:5,823,899 | T/A | — | uncertain significance |
| rs1829640289 | 9:5,823,971 | A/T | — | uncertain significance |
| rs747273080 | 9:5,825,172 | G/A | — | uncertain significance |
| rs545806699 | 9:5,830,763 | C/T | — | uncertain significance |
| rs149335278 | 9:5,830,786 | T/C | — | uncertain significance |
| rs779437476 | 9:5,830,831 | T/C | — | uncertain significance |
| rs554983063 | 9:5,832,742 | C/G | — | uncertain significance |
| rs747748510 | 9:5,832,822 | G/C | — | uncertain significance |
| rs528252782 | 9:5,832,849 | G/A | — | likely benign |
| rs1830016719 | 9:5,832,917 | C/G | — | uncertain significance |
| rs372868521 | 9:5,832,963 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.