GLG1
golgi glycoprotein 1
Summary
Predicted to enable fibroblast growth factor binding activity. Predicted to act upstream of or within several processes, including negative regulation of protein processing; negative regulation of transforming growth factor beta receptor signaling pathway; and regulation of chondrocyte differentiation. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs562331457 | 16:74,481,517 | G/T | coding sequence variant | — |
| rs150213948 | 16:74,486,009 | G/T | — | uncertain significance |
| rs1271235612 | 16:74,486,024 | T/G | — | uncertain significance |
| rs138842904 | 16:74,486,025 | G/A | — | likely benign |
| rs567614609 | 16:74,487,098 | G/A | — | likely benign |
| rs1397341177 | 16:74,487,170 | G/C | — | uncertain significance |
| rs1244624471 | 16:74,490,588 | G/A | — | uncertain significance |
| rs778360585 | 16:74,491,774 | C/T | — | uncertain significance |
| rs1432226434 | 16:74,491,799 | C/T | — | uncertain significance |
| rs755981823 | 16:74,493,589 | C/A | — | uncertain significance |
| rs763867401 | 16:74,493,681 | T/C | — | uncertain significance |
| rs147773944 | 16:74,496,062 | C/T | — | uncertain significance |
| rs753037950 | 16:74,496,431 | T/G | — | uncertain significance |
| rs1221101437 | 16:74,496,480 | G/A | — | uncertain significance |
| rs368508466 | 16:74,496,509 | C/T | — | uncertain significance |
| rs200896820 | 16:74,497,270 | C/G | — | uncertain significance |
| rs763542690 | 16:74,497,271 | T/A | — | uncertain significance |
| rs2543483025 | 16:74,497,284 | T/C | — | uncertain significance |
| rs2143189928 | 16:74,497,340 | T/C | — | uncertain significance |
| rs375250447 | 16:74,499,669 | G/C | — | uncertain significance |
| rs1023218360 | 16:74,502,863 | C/T | — | uncertain significance |
| rs754176332 | 16:74,502,935 | G/A | — | uncertain significance |
| rs2543501949 | 16:74,503,936 | A/T | — | uncertain significance |
| rs760108754 | 16:74,503,952 | C/T | — | uncertain significance |
| rs754994262 | 16:74,505,116 | C/G | — | uncertain significance |
| rs745901793 | 16:74,505,181 | C/T | — | uncertain significance |
| rs140352716 | 16:74,508,494 | C/G | — | uncertain significance |
| rs1448121110 | 16:74,511,359 | C/G | — | uncertain significance |
| rs2543522403 | 16:74,511,421 | T/A | — | uncertain significance |
| rs2015551429 | 16:74,514,171 | G/A | — | uncertain significance |
| rs2015553129 | 16:74,514,211 | T/G | — | uncertain significance |
| rs764943105 | 16:74,514,230 | C/A | — | uncertain significance |
| rs932614298 | 16:74,514,269 | T/G | — | uncertain significance |
| rs748301851 | 16:74,514,273 | G/A | — | uncertain significance |
| rs2543538825 | 16:74,516,961 | G/A | — | uncertain significance |
| rs775658494 | 16:74,516,964 | G/A | — | uncertain significance |
| rs781585464 | 16:74,519,784 | C/G | — | uncertain significance |
| rs2015965494 | 16:74,524,981 | T/C | — | uncertain significance |
| rs1313341380 | 16:74,524,998 | G/C | — | uncertain significance |
| rs140582641 | 16:74,525,019 | G/T | — | uncertain significance |
| rs766586113 | 16:74,525,020 | C/T | — | uncertain significance |
| rs758836765 | 16:74,525,045 | A/G | — | uncertain significance |
| rs371676824 | 16:74,528,728 | G/A | — | uncertain significance |
| rs528071772 | 16:74,530,490 | T/G | — | uncertain significance |
| rs187061091 | 16:74,530,499 | C/A | — | uncertain significance |
| rs538300970 | 16:74,537,424 | G/C | — | likely benign |
| rs4887772 | 16:74,537,591 | C/T | — | benign |
| rs778941649 | 16:74,542,792 | G/A | — | uncertain significance |
| rs199928841 | 16:74,566,058 | G/A | — | benign |
| rs9806812 | 16:74,589,192 | G/A | downstream gene variant | — |
| rs12924604 | 16:74,601,486 | G/A | intron variant | — |
| rs553399706 | 16:74,615,577 | G/A | — | — |
| rs200972392 | 16:74,640,577 | T/A | — | uncertain significance |
| rs1191349486 | 16:74,640,610 | T/G | — | uncertain significance |
| rs756615761 | 16:74,640,659 | G/C | — | uncertain significance |
| rs769755263 | 16:74,640,686 | C/T | — | uncertain significance |
| rs1830349041 | 16:74,640,700 | G/A | — | uncertain significance |
| rs769468827 | 16:74,640,767 | G/T | — | uncertain significance |
| rs780912700 | 16:74,640,858 | G/C | — | uncertain significance |
| rs1160448076 | 16:74,640,917 | C/T | — | uncertain significance |
| rs755962866 | 16:74,640,950 | C/A | — | uncertain significance |
| rs780009268 | 16:74,640,952 | G/A | — | uncertain significance |
| rs771156802 | 16:74,640,965 | T/A | — | uncertain significance |
| rs764483025 | 16:74,640,971 | G/C | — | uncertain significance |
| rs371279250 | 16:74,640,983 | A/C | — | uncertain significance |
| rs781349197 | 16:74,640,988 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.