TMPRSS11E
transmembrane serine protease 11E
Summary
Predicted to enable serine-type peptidase activity. Involved in cognition. Predicted to be located in extracellular region and membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs373417678 | 4:69,313,240 | C/T | — | uncertain significance |
| rs34956644 | 4:69,315,905 | A/G | intron variant | — |
| rs1554891 | 4:69,317,078 | G/C | — | — |
| rs62317541 | 4:69,317,873 | G/A | regulatory region variant | — |
| rs34168560 | 4:69,325,415 | C/G | intron variant | — |
| rs4694077 | 4:69,326,683 | C/T | intron variant | — |
| rs2475916974 | 4:69,327,585 | G/A | — | uncertain significance |
| rs747882820 | 4:69,327,597 | G/A | — | likely benign |
| rs36028307 | 4:69,327,932 | A/G | intron variant | — |
| rs2123886 | 4:69,328,887 | A/C | intron variant | — |
| rs1003300852 | 4:69,332,425 | G/T | — | uncertain significance |
| rs2603192 | 4:69,333,810 | T/A | — | — |
| rs34243356 | 4:69,334,413 | C/A | intron variant | — |
| rs1336577571 | 4:69,337,201 | C/T | — | uncertain significance |
| rs543569632 | 4:69,337,233 | A/G | — | uncertain significance |
| rs376867140 | 4:69,337,272 | G/A | — | uncertain significance |
| rs145069161 | 4:69,337,337 | T/G | — | uncertain significance |
| rs969114 | 4:69,338,311 | A/C | — | — |
| rs34872892 | 4:69,339,257 | A/G | intron variant | — |
| rs35662434 | 4:69,339,933 | A/G | intron variant | — |
| rs925013905 | 4:69,340,463 | C/A | — | uncertain significance |
| rs368614631 | 4:69,340,491 | A/G | — | likely benign |
| rs4860948 | 4:69,340,991 | T/A | intron variant | — |
| rs976058 | 4:69,341,487 | T/C | intron variant | — |
| rs1367463951 | 4:69,341,994 | G/C | — | uncertain significance |
| rs1053035381 | 4:69,342,134 | A/G | — | uncertain significance |
| rs983745 | 4:69,342,169 | G/C | regulatory region variant | — |
| rs754101412 | 4:69,343,199 | C/G | — | uncertain significance |
| rs2475958300 | 4:69,343,203 | A/G | — | uncertain significance |
| rs1286498716 | 4:69,343,220 | G/A | — | uncertain significance |
| rs1408461900 | 4:69,343,286 | T/C | — | likely benign |
| rs976002 | 4:69,343,287 | A/G | — | benign |
| rs139089250 | 4:69,343,298 | C/G | — | uncertain significance |
| rs765721404 | 4:69,343,307 | G/A | — | uncertain significance |
| rs3100651 | 4:69,343,724 | C/G | intron variant | — |
| rs2109701732 | 4:69,344,581 | C/G | — | uncertain significance |
| rs149891396 | 4:69,344,588 | G/A | — | uncertain significance |
| rs775611549 | 4:69,344,644 | A/G | — | uncertain significance |
| rs1377870 | 4:69,345,132 | A/G | intron variant | — |
| rs551938386 | 4:69,348,845 | T/G | — | — |
| rs1117816 | 4:69,349,018 | A/C | intron variant | — |
| rs2708697 | 4:69,349,034 | T/A | — | — |
| rs2331415 | 4:69,349,677 | C/A | intron variant | — |
| rs35065844 | 4:69,352,321 | T/C | intron variant | — |
| rs10020631 | 4:69,353,863 | G/A | intron variant | — |
| rs2708674 | 4:69,354,095 | A/G | intron variant | — |
| rs34109652 | 4:69,354,350 | G/A | intron variant | — |
| rs34164133 | 4:69,355,334 | C/T | intron variant | — |
| rs62317882 | 4:69,355,709 | T/C | intron variant | — |
| rs35088884 | 4:69,357,050 | A/T | — | — |
| rs4694429 | 4:69,358,041 | A/G | intron variant | — |
| rs34638591 | 4:69,359,223 | T/C | intron variant | — |
| rs34103191 | 4:69,359,280 | A/G | intron variant | — |
| rs34728672 | 4:69,359,821 | G/C | — | — |
| rs34594059 | 4:69,360,760 | C/T | intron variant | — |
| rs35307342 | 4:69,361,389 | C/T | intron variant | — |
| rs35473170 | 4:69,361,441 | G/A | intron variant | — |
| rs35777071 | 4:69,361,445 | T/C | intron variant | — |
| rs3792631 | 4:69,362,088 | A/T | — | — |
| rs2278921 | 4:69,362,301 | T/G | intron variant | — |
| rs200962479 | 4:69,362,409 | T/C | — | uncertain significance |
| rs752390593 | 4:69,362,438 | T/G | — | uncertain significance |
| rs2278919 | 4:69,362,690 | A/T | — | — |
| rs2708672 | 4:69,363,598 | C/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.