GOLGA1
golgin A1
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 encoded protein is associated with Sjogren's syndrome. [provided by RefSeq, Feb 2010]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143825735 | 9:127,642,826 | G/A | — | uncertain significance |
| rs748185454 | 9:127,642,858 | T/C | — | uncertain significance |
| rs1025595839 | 9:127,642,876 | C/G | — | uncertain significance |
| rs145763272 | 9:127,644,164 | G/A | — | uncertain significance |
| rs769477508 | 9:127,644,178 | A/G | — | uncertain significance |
| rs138765093 | 9:127,644,199 | C/T | — | uncertain significance |
| rs1023316762 | 9:127,650,574 | C/G | — | uncertain significance |
| rs16927704 | 9:127,650,631 | A/C | — | benign |
| rs34090990 | 9:127,651,449 | G/A | — | benign |
| rs2490815872 | 9:127,651,535 | C/G | — | uncertain significance |
| rs199534446 | 9:127,651,542 | G/A | — | likely benign |
| rs372990641 | 9:127,651,576 | T/C | — | uncertain significance |
| rs200756008 | 9:127,651,758 | C/T | — | uncertain significance |
| rs1048803619 | 9:127,651,761 | T/C | — | uncertain significance |
| rs774959189 | 9:127,651,769 | C/T | — | likely benign |
| rs201455650 | 9:127,652,660 | G/C | — | benign |
| rs150023063 | 9:127,652,750 | C/A | — | uncertain significance |
| rs761042816 | 9:127,660,829 | T/G | — | uncertain significance |
| rs145802446 | 9:127,660,869 | G/A | — | uncertain significance |
| rs1288450905 | 9:127,661,632 | G/T | — | uncertain significance |
| rs201106148 | 9:127,661,756 | G/A | — | likely benign |
| rs150137668 | 9:127,662,748 | T/C | — | likely benign |
| rs186493725 | 9:127,665,162 | C/T | intron variant | — |
| rs752034801 | 9:127,670,685 | C/T | — | uncertain significance |
| rs138783087 | 9:127,670,702 | G/A | — | uncertain significance |
| rs583134 | 9:127,674,200 | A/T | missense variant | — |
| rs774101149 | 9:127,674,233 | T/C | — | uncertain significance |
| rs148532217 | 9:127,674,305 | C/A | — | uncertain significance |
| rs1413424575 | 9:127,683,487 | T/G | — | uncertain significance |
| rs1269251175 | 9:127,684,093 | C/T | — | uncertain significance |
| rs755795939 | 9:127,685,376 | T/G | — | uncertain significance |
| rs749413063 | 9:127,685,460 | G/C | — | uncertain significance |
| rs1830710034 | 9:127,690,561 | G/A | — | uncertain significance |
| rs145566855 | 9:127,693,601 | G/T | — | uncertain significance |
| rs763271118 | 9:127,693,619 | G/A | — | uncertain significance |
| rs148050398 | 9:127,693,630 | T/C | — | uncertain significance |
| rs2491051871 | 9:127,700,873 | C/T | — | uncertain significance |
| rs755588954 | 9:127,700,960 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.