GPC5
glypican 5
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 Variants98 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7322083 | 13:92,050,246 | A/T | — | — |
| rs3759452 | 13:92,050,403 | A/G | regulatory region variant | — |
| rs778584986 | 13:92,051,307 | G/A | — | uncertain significance |
| rs769981633 | 13:92,051,320 | C/A | — | uncertain significance |
| rs368315924 | 13:92,051,322 | G/T | — | uncertain significance |
| rs1445942910 | 13:92,051,347 | T/C | — | uncertain significance |
| rs760668409 | 13:92,051,367 | C/A | — | uncertain significance |
| rs2501339406 | 13:92,051,379 | G/A | — | uncertain significance |
| rs928214742 | 13:92,051,430 | G/A | — | uncertain significance |
| rs145436207 | 13:92,051,453 | G/A | — | benign |
| rs12428047 | 13:92,061,359 | A/G | intron variant | — |
| rs116990124 | 13:92,069,998 | A/G | intron variant | — |
| rs114910989 | 13:92,078,522 | G/T | intron variant | — |
| rs118000667 | 13:92,083,635 | C/T | intron variant | — |
| rs559277707 | 13:92,101,090 | C/T | — | uncertain significance |
| rs142381235 | 13:92,101,123 | C/T | — | uncertain significance |
| rs1594103967 | 13:92,101,134 | A/G | — | likely benign |
| rs767268470 | 13:92,101,149 | A/G | — | uncertain significance |
| rs766037396 | 13:92,101,162 | C/T | — | uncertain significance |
| rs117624944 | 13:92,105,217 | T/C | intron variant | — |
| rs778681221 | 13:92,183,478 | A/G | — | — |
| rs16946160 | 13:92,203,813 | G/A | intron variant | — |
| rs190346813 | 13:92,216,232 | C/T | intron variant | — |
| rs9560827 | 13:92,224,273 | A/C | intron variant | — |
| rs189213343 | 13:92,284,278 | G/A | regulatory region variant | — |
| rs117342639 | 13:92,305,277 | T/C | regulatory region variant | — |
| rs150456039 | 13:92,323,929 | C/T | intron variant | — |
| rs554672393 | 13:92,340,929 | G/T | — | — |
| rs553717 | 13:92,345,579 | C/A | missense variant | — |
| rs144683011 | 13:92,345,598 | A/G | — | benign |
| rs2035801669 | 13:92,345,635 | G/C | — | uncertain significance |
| rs137912074 | 13:92,345,672 | G/T | — | uncertain significance |
| rs561761293 | 13:92,345,681 | A/G | — | uncertain significance |
| rs777139638 | 13:92,345,699 | G/A | — | uncertain significance |
| rs148285243 | 13:92,345,845 | T/G | — | likely benign |
| rs141328977 | 13:92,345,891 | C/G | — | likely benign |
| rs772070951 | 13:92,345,996 | C/G | — | uncertain significance |
| rs1261664128 | 13:92,346,014 | A/G | — | uncertain significance |
| rs1282598896 | 13:92,346,104 | C/T | — | uncertain significance |
| rs112827304 | 13:92,346,106 | C/T | — | benign |
| rs372453843 | 13:92,346,109 | C/G | — | uncertain significance |
| rs372530892 | 13:92,380,805 | G/A | — | likely benign |
| rs2503153350 | 13:92,380,913 | G/A | — | uncertain significance |
| rs1384334439 | 13:92,380,916 | G/T | — | uncertain significance |
| rs1332797715 | 13:92,408,653 | A/T | — | uncertain significance |
| rs3012004 | 13:92,435,818 | A/G | intron variant | — |
| rs3864180 | 13:92,436,488 | A/C | — | — |
| rs193208 | 13:92,437,430 | T/G | intron variant | — |
| rs431670 | 13:92,439,543 | G/T | — | — |
| rs187288494 | 13:92,442,145 | G/A | intron variant | — |
| rs2352028 | 13:92,445,229 | C/G | — | — |
| rs184187936 | 13:92,446,822 | T/G | intron variant | — |
| rs1929922 | 13:92,451,883 | G/A | intron variant | — |
| rs570154810 | 13:92,474,576 | C/A | — | — |
| rs192194001 | 13:92,488,750 | T/A | intron variant | — |
| rs532303181 | 13:92,490,257 | G/A | — | — |
| rs7328464 | 13:92,501,664 | C/T | intron variant | — |
| rs61966368 | 13:92,521,560 | G/C | — | — |
| rs1854739 | 13:92,537,670 | G/C | intron variant | — |
| rs1253568464 | 13:92,560,289 | A/G | — | uncertain significance |
| rs185606411 | 13:92,595,644 | T/C | intron variant | — |
| rs148582841 | 13:92,626,382 | C/G | intron variant | — |
| rs189634528 | 13:92,627,009 | A/G | intron variant | — |
| rs752073123 | 13:92,718,351 | G/A | — | — |
| rs776473093 | 13:92,797,130 | G/T | — | uncertain significance |
| rs759173637 | 13:92,797,132 | T/C | — | uncertain significance |
| rs1164190037 | 13:92,797,147 | G/A | — | uncertain significance |
| rs188610314 | 13:92,799,053 | G/A | intron variant | — |
| rs79320254 | 13:92,823,286 | A/G | intron variant | — |
| rs4771854 | 13:92,851,968 | C/G | — | — |
| rs138846693 | 13:92,856,629 | G/A | intron variant | — |
| rs61967888 | 13:92,862,063 | G/A | intron variant | — |
| rs72636856 | 13:92,882,799 | G/C | — | — |
| rs7987675 | 13:92,884,370 | C/T | intron variant | — |
| rs7986701 | 13:92,905,521 | C/G | intron variant | — |
| rs1831463 | 13:92,908,890 | T/C | — | — |
| rs9516053 | 13:92,945,884 | T/C | intron variant | — |
| rs7982677 | 13:92,988,323 | C/G | — | — |
| rs13378794 | 13:93,045,282 | C/T | intron variant | — |
| rs11842834 | 13:93,045,723 | C/A | — | — |
| rs4771859 | 13:93,088,651 | T/A | — | — |
| rs148586127 | 13:93,137,057 | G/T | — | — |
| rs1413191 | 13:93,213,476 | C/T | intron variant | — |
| rs17267292 | 13:93,323,146 | T/A | — | — |
| rs9516120 | 13:93,331,222 | G/A | intron variant | — |
| rs9523762 | 13:93,331,886 | G/C | — | — |
| rs72641050 | 13:93,345,170 | A/C | intron variant | — |
| rs9523787 | 13:93,363,760 | G/T | intron variant | — |
| rs2765717 | 13:93,432,646 | A/G | — | — |
| rs570881406 | 13:93,450,744 | A/G | — | — |
| rs7988257 | 13:93,465,539 | C/T | — | — |
| rs1460299993 | 13:93,518,564 | G/A | — | uncertain significance |
| rs543866919 | 13:93,518,606 | A/G | — | uncertain significance |
| rs377004057 | 13:93,518,610 | C/A | — | uncertain significance |
| rs141458785 | 13:93,518,636 | G/C | — | uncertain significance |
| rs750526647 | 13:93,518,643 | T/A | — | uncertain significance |
| rs542054228 | 13:93,518,651 | A/G | — | uncertain significance |
| rs766268211 | 13:93,518,652 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.