GPC1
glypican 1
Summary
Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. [provided by RefSeq, Jul 2008]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs529077716 | 2:241,374,632 | A/G | — | — |
| rs753510735 | 2:241,375,345 | C/T | — | uncertain significance |
| rs1427085751 | 2:241,375,354 | G/A | — | uncertain significance |
| rs778500540 | 2:241,375,372 | G/A | — | uncertain significance |
| rs2469887518 | 2:241,375,468 | A/G | — | uncertain significance |
| rs73102036 | 2:241,378,196 | T/G | regulatory region variant | — |
| rs71428439 | 2:241,395,500 | A/G | coding sequence variant | — |
| rs2292832 | 2:241,395,503 | T/C | coding sequence variant | — |
| rs13430967 | 2:241,397,326 | G/A | — | — |
| rs565369538 | 2:241,398,518 | C/T | — | uncertain significance |
| rs1481468257 | 2:241,398,542 | G/A | — | uncertain significance |
| rs146749086 | 2:241,398,563 | G/A | — | uncertain significance |
| rs138434031 | 2:241,398,578 | C/T | — | uncertain significance |
| rs61737161 | 2:241,401,663 | C/T | — | benign |
| rs140826218 | 2:241,401,707 | G/A | — | uncertain significance |
| rs531757424 | 2:241,401,709 | G/A | — | uncertain significance |
| rs771344419 | 2:241,401,727 | C/T | — | uncertain significance |
| rs138375141 | 2:241,401,728 | G/A | — | likely benign |
| rs767152299 | 2:241,401,800 | G/A | — | uncertain significance |
| rs367907059 | 2:241,401,896 | C/T | — | uncertain significance |
| rs200794161 | 2:241,401,910 | C/T | — | uncertain significance |
| rs768758570 | 2:241,401,916 | C/T | — | uncertain significance |
| rs545177373 | 2:241,401,917 | G/A | — | uncertain significance |
| rs143813409 | 2:241,401,926 | G/A | — | likely benign |
| rs2529016462 | 2:241,402,783 | G/A | — | uncertain significance |
| rs771408100 | 2:241,402,824 | C/G | — | uncertain significance |
| rs763227743 | 2:241,402,839 | G/A | — | uncertain significance |
| rs771573745 | 2:241,402,899 | G/A | — | uncertain significance |
| rs144394036 | 2:241,402,908 | G/A | — | likely benign |
| rs138318645 | 2:241,404,072 | C/T | — | uncertain significance |
| rs753065473 | 2:241,404,077 | G/A | — | uncertain significance |
| rs1435472054 | 2:241,404,085 | T/G | — | uncertain significance |
| rs200045063 | 2:241,404,098 | G/A | — | uncertain significance |
| rs911643531 | 2:241,404,129 | C/T | — | uncertain significance |
| rs540457331 | 2:241,404,288 | G/A | — | uncertain significance |
| rs1320591064 | 2:241,404,300 | G/A | — | uncertain significance |
| rs886101948 | 2:241,404,333 | C/T | — | uncertain significance |
| rs879506095 | 2:241,404,334 | G/A | — | uncertain significance |
| rs774918426 | 2:241,404,340 | G/A | — | uncertain significance |
| rs759479706 | 2:241,404,370 | C/T | — | uncertain significance |
| rs200248156 | 2:241,404,379 | C/A | — | uncertain significance |
| rs367854249 | 2:241,404,579 | T/C | — | uncertain significance |
| rs1213175751 | 2:241,404,599 | C/T | — | uncertain significance |
| rs1383057748 | 2:241,404,600 | G/A | — | uncertain significance |
| rs2228329 | 2:241,404,914 | C/T | — | benign |
| rs776391105 | 2:241,404,940 | C/G | — | uncertain significance |
| rs544444707 | 2:241,405,018 | G/A | — | uncertain significance |
| rs541996291 | 2:241,405,024 | G/A | — | uncertain significance |
| rs972321554 | 2:241,405,043 | C/T | — | likely benign |
| rs781304341 | 2:241,405,047 | G/A | — | uncertain significance |
| rs775242022 | 2:241,405,062 | G/A | — | uncertain significance |
| rs1126920 | 2:241,405,479 | C/A | missense variant | — |
| rs750462373 | 2:241,405,484 | G/A | — | uncertain significance |
| rs149996819 | 2:241,405,501 | G/A | — | uncertain significance |
| rs137923533 | 2:241,405,613 | A/C | — | uncertain significance |
| rs751446559 | 2:241,405,634 | C/T | — | uncertain significance |
| rs376967801 | 2:241,405,637 | A/G | — | uncertain significance |
| rs1280397022 | 2:241,405,682 | C/G | — | uncertain significance |
| rs1574782377 | 2:241,405,685 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.