GOLGA4
golgin A4
Summary
The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This protein has been postulated to play a role in Rab6-regulated membrane-tethering events in the Golgi apparatus. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010]
Known Variants128 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201682914 | 3:37,292,887 | C/T | — | uncertain significance |
| rs1387423500 | 3:37,292,904 | A/G | — | uncertain significance |
| rs754033529 | 3:37,292,950 | T/C | — | uncertain significance |
| rs139183035 | 3:37,292,954 | T/A | — | uncertain significance |
| rs373401405 | 3:37,315,046 | C/T | — | uncertain significance |
| rs1279810359 | 3:37,315,082 | G/A | — | uncertain significance |
| rs60600531 | 3:37,323,459 | C/T | — | benign |
| rs140013994 | 3:37,323,488 | C/T | — | uncertain significance |
| rs7612972 | 3:37,323,489 | G/A | — | uncertain significance |
| rs372845682 | 3:37,323,570 | G/A | — | uncertain significance |
| rs748127866 | 3:37,323,624 | G/A | — | likely benign |
| rs2096836548 | 3:37,323,656 | G/A | — | uncertain significance |
| rs375883623 | 3:37,323,725 | G/A | — | uncertain significance |
| rs768238779 | 3:37,323,743 | T/A | — | uncertain significance |
| rs2480025030 | 3:37,337,638 | C/T | — | uncertain significance |
| rs200520226 | 3:37,337,681 | A/T | — | uncertain significance |
| rs184743517 | 3:37,337,707 | G/T | — | likely benign |
| rs772013857 | 3:37,340,335 | A/G | — | likely benign |
| rs759277142 | 3:37,340,377 | C/T | — | uncertain significance |
| rs368268747 | 3:37,340,399 | G/A | — | uncertain significance |
| rs1326616554 | 3:37,340,434 | T/C | — | uncertain significance |
| rs1400161981 | 3:37,340,789 | T/C | — | uncertain significance |
| rs140983166 | 3:37,343,751 | C/T | — | uncertain significance |
| rs1441051052 | 3:37,343,814 | G/A | — | uncertain significance |
| rs1209171773 | 3:37,360,619 | G/C | — | uncertain significance |
| rs540864530 | 3:37,360,621 | A/G | — | uncertain significance |
| rs867556525 | 3:37,360,632 | A/G | — | uncertain significance |
| rs372045264 | 3:37,360,669 | A/G | — | uncertain significance |
| rs2096955424 | 3:37,363,226 | A/G | — | uncertain significance |
| rs377320558 | 3:37,363,272 | A/C | — | uncertain significance |
| rs113898889 | 3:37,363,342 | C/T | — | uncertain significance |
| rs201915621 | 3:37,363,343 | G/A | — | likely benign |
| rs540853421 | 3:37,365,080 | G/A | — | uncertain significance |
| rs750176027 | 3:37,365,126 | C/G | — | uncertain significance |
| rs142972537 | 3:37,365,173 | A/T | — | benign |
| rs200887494 | 3:37,365,182 | A/G | — | uncertain significance |
| rs150028760 | 3:37,365,215 | A/G | — | uncertain significance |
| rs570208465 | 3:37,365,302 | T/G | — | uncertain significance |
| rs201417675 | 3:37,365,480 | C/A | — | uncertain significance |
| rs377325720 | 3:37,365,484 | C/G | — | uncertain significance |
| rs750976266 | 3:37,365,502 | G/A | — | likely benign |
| rs1348719097 | 3:37,365,511 | G/A | — | uncertain significance |
| rs191655781 | 3:37,365,599 | A/G | — | likely benign |
| rs1283315168 | 3:37,365,633 | G/T | — | uncertain significance |
| rs375999710 | 3:37,365,689 | A/T | — | uncertain significance |
| rs761611900 | 3:37,365,761 | A/G | — | uncertain significance |
| rs764806803 | 3:37,365,763 | G/A | — | uncertain significance |
| rs757309333 | 3:37,365,809 | A/G | — | uncertain significance |
| rs2480604873 | 3:37,365,826 | T/C | — | uncertain significance |
| rs2096963767 | 3:37,365,869 | T/C | — | uncertain significance |
| rs1201827162 | 3:37,365,997 | A/C | — | uncertain significance |
| rs749123349 | 3:37,366,120 | C/A | — | uncertain significance |
| rs770506566 | 3:37,366,127 | G/T | — | uncertain significance |
| rs778570684 | 3:37,366,132 | G/A | — | uncertain significance |
| rs1377347235 | 3:37,366,136 | A/G | — | uncertain significance |
| rs1412479585 | 3:37,366,251 | A/C | — | uncertain significance |
| rs148519799 | 3:37,366,288 | A/C | — | uncertain significance |
| rs2480622706 | 3:37,366,432 | T/A | — | uncertain significance |
| rs754434429 | 3:37,366,509 | A/G | — | uncertain significance |
| rs1366388105 | 3:37,366,513 | A/G | — | likely benign |
| rs749628809 | 3:37,366,533 | T/A | — | uncertain significance |
| rs773176430 | 3:37,366,600 | G/C | — | uncertain significance |
| rs754293342 | 3:37,366,760 | A/G | — | uncertain significance |
| rs138942611 | 3:37,366,814 | C/G | — | uncertain significance |
| rs150509071 | 3:37,366,918 | A/G | — | uncertain significance |
| rs2096967468 | 3:37,366,978 | G/A | — | uncertain significance |
| rs141111369 | 3:37,367,018 | C/T | — | uncertain significance |
| rs142152509 | 3:37,367,020 | A/G | — | likely benign |
| rs757433351 | 3:37,367,041 | A/G | — | uncertain significance |
| rs752958030 | 3:37,367,143 | C/T | — | likely benign |
| rs1187889659 | 3:37,367,247 | T/G | — | uncertain significance |
| rs1312239812 | 3:37,367,277 | A/T | — | uncertain significance |
| rs2480652183 | 3:37,367,291 | A/G | — | uncertain significance |
| rs2480653600 | 3:37,367,321 | G/A | — | uncertain significance |
| rs763942726 | 3:37,367,461 | C/T | — | uncertain significance |
| rs765149200 | 3:37,367,696 | A/G | — | uncertain significance |
| rs1187057111 | 3:37,367,810 | A/G | — | uncertain significance |
| rs199741470 | 3:37,367,856 | A/C | — | uncertain significance |
| rs201034947 | 3:37,367,858 | G/T | — | uncertain significance |
| rs1347008991 | 3:37,367,859 | A/T | — | uncertain significance |
| rs372401906 | 3:37,367,937 | A/C | — | uncertain significance |
| rs2480675668 | 3:37,367,977 | A/G | — | likely benign |
| rs9840779 | 3:37,368,032 | A/G | — | benign |
| rs765757657 | 3:37,368,205 | C/T | — | uncertain significance |
| rs139538082 | 3:37,368,206 | A/G | — | uncertain significance |
| rs146639243 | 3:37,368,209 | T/G | — | uncertain significance |
| rs745625948 | 3:37,368,260 | G/A | — | uncertain significance |
| rs137974637 | 3:37,368,395 | A/G | — | uncertain significance |
| rs2480695877 | 3:37,368,496 | A/G | — | likely benign |
| rs1213036569 | 3:37,368,568 | C/A | — | uncertain significance |
| rs2096973866 | 3:37,368,625 | A/G | — | uncertain significance |
| rs761996909 | 3:37,368,671 | C/T | — | uncertain significance |
| rs766208650 | 3:37,368,674 | A/G | — | uncertain significance |
| rs752502981 | 3:37,368,688 | T/C | — | uncertain significance |
| rs369048363 | 3:37,368,734 | A/G | — | uncertain significance |
| rs759461026 | 3:37,368,749 | A/G | — | uncertain significance |
| rs62241896 | 3:37,368,755 | T/A | missense variant | — |
| rs151318279 | 3:37,368,756 | G/C | — | uncertain significance |
| rs780735137 | 3:37,368,794 | A/G | — | uncertain significance |
| rs767873424 | 3:37,368,812 | T/G | — | uncertain significance |
Showing 100 of 128 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.