PCOLCE2
procollagen C-endopeptidase enhancer 2
Summary
Enables collagen binding activity; heparin binding activity; and peptidase activator activity. Predicted to act upstream of or within cellular response to leukemia inhibitory factor. Predicted to be located in extracellular region. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs373839458 | 3:142,537,231 | C/T | — | uncertain significance |
| rs368076904 | 3:142,537,244 | C/T | — | uncertain significance |
| rs2473172506 | 3:142,537,287 | C/T | — | uncertain significance |
| rs369551955 | 3:142,539,805 | C/G | — | uncertain significance |
| rs762887486 | 3:142,539,852 | C/T | — | uncertain significance |
| rs1347780534 | 3:142,542,409 | C/T | — | uncertain significance |
| rs564490873 | 3:142,545,086 | T/C | — | — |
| rs551242432 | 3:142,548,536 | G/A | — | uncertain significance |
| rs775143491 | 3:142,548,575 | G/C | — | uncertain significance |
| rs146863701 | 3:142,548,656 | A/G | — | uncertain significance |
| rs139818603 | 3:142,557,655 | C/T | — | uncertain significance |
| rs770868528 | 3:142,561,770 | T/C | — | uncertain significance |
| rs761025963 | 3:142,561,804 | C/T | — | uncertain significance |
| rs762365871 | 3:142,561,822 | G/A | — | uncertain significance |
| rs1464442258 | 3:142,561,855 | A/C | — | uncertain significance |
| rs2473204285 | 3:142,567,071 | G/A | — | uncertain significance |
| rs376768304 | 3:142,567,080 | C/T | — | uncertain significance |
| rs781197401 | 3:142,567,106 | C/T | — | uncertain significance |
| rs202177059 | 3:142,567,175 | C/T | — | uncertain significance |
| rs41267845 | 3:142,567,203 | G/A | — | uncertain significance |
| rs374060736 | 3:142,567,229 | A/G | — | uncertain significance |
| rs41267847 | 3:142,567,275 | T/C | — | uncertain significance |
| rs770509532 | 3:142,567,308 | C/T | — | uncertain significance |
| rs34516933 | 3:142,603,861 | T/A | intron variant | — |
| rs200265284 | 3:142,606,602 | C/A | — | uncertain significance |
| rs769413675 | 3:142,606,606 | A/T | — | uncertain significance |
| rs777136521 | 3:142,607,677 | G/A | — | uncertain significance |
| rs368648610 | 3:142,607,702 | G/T | — | uncertain significance |
| rs764665094 | 3:142,607,723 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.