IVL
involucrin
Summary
Involucrin, a component of the keratinocyte crosslinked envelope, is found in the cytoplasm and crosslinked to membrane proteins by transglutaminase. This gene is mapped to 1q21, among calpactin I light chain, trichohyalin, profillaggrin, loricrin, and calcyclin. [provided by RefSeq, Jul 2008]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201303454 | 1:152,882,302 | C/T | — | uncertain significance |
| rs145430176 | 1:152,882,359 | C/G | — | uncertain significance |
| rs923323615 | 1:152,882,361 | C/A | — | uncertain significance |
| rs910838819 | 1:152,882,423 | G/C | — | uncertain significance |
| rs868067456 | 1:152,882,454 | G/A | — | uncertain significance |
| rs572279454 | 1:152,882,648 | A/G | — | likely benign |
| rs756949313 | 1:152,882,674 | T/A | — | uncertain significance |
| rs142358562 | 1:152,882,760 | C/G | — | uncertain significance |
| rs114448437 | 1:152,882,765 | G/A | — | benign |
| rs756472719 | 1:152,882,767 | A/T | — | uncertain significance |
| rs11205135 | 1:152,882,786 | A/G | — | likely benign |
| rs541736259 | 1:152,882,800 | C/T | — | uncertain significance |
| rs11205136 | 1:152,882,801 | G/A | — | likely benign |
| rs2526582695 | 1:152,882,802 | G/C | — | uncertain significance |
| rs75111974 | 1:152,882,811 | G/A | — | benign |
| rs200516479 | 1:152,882,849 | G/T | — | uncertain significance |
| rs200916786 | 1:152,882,860 | C/T | — | likely benign |
| rs1363515668 | 1:152,882,897 | G/T | — | uncertain significance |
| rs1334180545 | 1:152,882,906 | G/A | — | likely benign |
| rs1254406982 | 1:152,882,928 | C/G | — | uncertain significance |
| rs7520711 | 1:152,882,982 | C/G | — | benign |
| rs1649931379 | 1:152,883,000 | C/G | — | uncertain significance |
| rs998511154 | 1:152,883,003 | G/C | — | uncertain significance |
| rs4459054 | 1:152,883,036 | C/T | — | benign |
| rs780252658 | 1:152,883,087 | C/A | — | uncertain significance |
| rs1446551963 | 1:152,883,129 | C/A | — | uncertain significance |
| rs180686771 | 1:152,883,137 | G/A | — | benign |
| rs374818807 | 1:152,883,141 | G/A | — | uncertain significance |
| rs184389068 | 1:152,883,155 | G/T | — | likely benign |
| rs1570914756 | 1:152,883,206 | G/A | — | likely benign |
| rs1000691868 | 1:152,883,224 | G/T | — | uncertain significance |
| rs370790605 | 1:152,883,230 | G/A | — | likely benign |
| rs755108500 | 1:152,883,240 | C/T | — | uncertain significance |
| rs557152744 | 1:152,883,241 | C/G | — | uncertain significance |
| rs1429598484 | 1:152,883,264 | G/A | — | uncertain significance |
| rs1208977433 | 1:152,883,299 | G/C | — | uncertain significance |
| rs182325885 | 1:152,883,317 | G/T | — | likely benign |
| rs367633832 | 1:152,883,348 | C/G | — | uncertain significance |
| rs201996963 | 1:152,883,381 | G/T | — | uncertain significance |
| rs904542233 | 1:152,883,421 | C/T | — | likely benign |
| rs559617080 | 1:152,883,438 | G/A | — | uncertain significance |
| rs1396410919 | 1:152,883,445 | G/A | — | uncertain significance |
| rs1053642694 | 1:152,883,447 | C/A | — | uncertain significance |
| rs1317641060 | 1:152,883,459 | C/G | — | uncertain significance |
| rs1251632595 | 1:152,883,482 | G/A | — | likely benign |
| rs368432151 | 1:152,883,487 | A/G | — | uncertain significance |
| rs1001758745 | 1:152,883,502 | A/T | — | uncertain significance |
| rs1374269393 | 1:152,883,516 | C/T | — | likely benign |
| rs1649970339 | 1:152,883,522 | G/A | — | uncertain significance |
| rs1454319459 | 1:152,883,555 | G/A | — | uncertain significance |
| rs139703221 | 1:152,883,573 | G/A | — | uncertain significance |
| rs773600947 | 1:152,883,579 | C/G | — | uncertain significance |
| rs61731340 | 1:152,883,620 | G/A | — | benign |
| rs116373638 | 1:152,883,621 | T/A | — | benign |
| rs754578993 | 1:152,883,626 | G/T | — | uncertain significance |
| rs146972484 | 1:152,883,647 | G/A | — | benign |
| rs185349036 | 1:152,883,681 | C/G | — | uncertain significance |
| rs146331989 | 1:152,883,687 | C/T | — | uncertain significance |
| rs761914993 | 1:152,883,772 | C/G | — | uncertain significance |
| rs149718823 | 1:152,883,786 | C/G | — | benign |
| rs141266953 | 1:152,883,789 | C/G | — | likely benign |
| rs747420489 | 1:152,883,810 | C/G | — | uncertain significance |
| rs138618991 | 1:152,883,825 | G/A | — | uncertain significance |
| rs1047739020 | 1:152,883,843 | G/A | — | uncertain significance |
| rs2526588616 | 1:152,883,943 | C/A | — | uncertain significance |
| rs372109143 | 1:152,883,950 | G/A | — | likely benign |
| rs145659686 | 1:152,883,983 | G/T | — | uncertain significance |
| rs768558009 | 1:152,883,987 | C/G | — | uncertain significance |
| rs368244218 | 1:152,884,023 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.