GNA12
G protein subunit alpha 12
Summary
Enables G protein activity; protein phosphatase 2A binding activity; and protein phosphatase activator activity. Involved in Rho-activating G protein-coupled receptor signaling pathway; regulation of TOR signaling; and regulation of proteasomal ubiquitin-dependent protein catabolic process. Located in lateral plasma membrane; neuron projection; and neuronal cell body. Is active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs749682380 | 7:2,770,886 | C/T | — | likely benign |
| rs560123937 | 7:2,770,898 | C/A | — | uncertain significance |
| rs140322696 | 7:2,770,936 | C/A | — | uncertain significance |
| rs755401911 | 7:2,770,955 | C/T | — | uncertain significance |
| rs777971344 | 7:2,770,975 | C/T | — | uncertain significance |
| rs61758983 | 7:2,770,983 | G/A | — | benign |
| rs2534620191 | 7:2,770,987 | T/G | — | uncertain significance |
| rs2534621473 | 7:2,771,176 | A/G | — | uncertain significance |
| rs201475988 | 7:2,771,312 | C/T | — | uncertain significance |
| rs3846991 | 7:2,781,249 | G/C | intron variant | — |
| rs798514 | 7:2,781,892 | T/C | intron variant | — |
| rs798513 | 7:2,782,493 | C/G | — | — |
| rs798510 | 7:2,783,338 | C/G | — | — |
| rs798507 | 7:2,783,929 | C/T | — | — |
| rs798506 | 7:2,788,912 | T/C | intron variant | — |
| rs798502 | 7:2,789,880 | A/C | regulatory region variant | — |
| rs798497 | 7:2,795,957 | A/G | intron variant | — |
| rs798496 | 7:2,796,763 | C/T | intron variant | — |
| rs798491 | 7:2,800,521 | A/G | regulatory region variant | — |
| rs798489 | 7:2,801,803 | C/T | intron variant | — |
| rs798488 | 7:2,802,522 | T/C | regulatory region variant | — |
| rs798487 | 7:2,802,943 | G/A | regulatory region variant | — |
| rs368699386 | 7:2,803,883 | T/C | — | — |
| rs798482 | 7:2,805,014 | A/T | intron variant | — |
| rs142567289 | 7:2,808,320 | A/C | — | — |
| rs13240877 | 7:2,808,324 | A/C | — | — |
| rs1182207 | 7:2,810,746 | G/A | intron variant | — |
| rs35957220 | 7:2,812,632 | C/G | regulatory region variant | — |
| rs7784066 | 7:2,819,727 | T/A | downstream gene variant | — |
| rs2260230 | 7:2,822,986 | T/C | — | — |
| rs774244411 | 7:2,834,581 | C/T | — | uncertain significance |
| rs766968121 | 7:2,834,621 | C/T | — | uncertain significance |
| rs752999465 | 7:2,834,633 | G/C | — | uncertain significance |
| rs145512130 | 7:2,834,726 | A/G | — | likely benign |
| rs1792626538 | 7:2,834,773 | G/A | — | uncertain significance |
| rs771273709 | 7:2,852,290 | C/A | — | — |
| rs151253462 | 7:2,853,995 | C/T | — | likely benign |
| rs2533879 | 7:2,859,847 | G/T | — | — |
| rs1182188 | 7:2,869,985 | T/C | intron variant | — |
| rs1182183 | 7:2,873,136 | C/A | — | — |
| rs1182176 | 7:2,874,601 | A/G | upstream gene variant | — |
| rs73033403 | 7:2,877,941 | G/C | — | — |
| rs577734383 | 7:2,881,732 | G/A | — | — |
| rs540524389 | 7:2,881,745 | G/A | — | — |
| rs2533872 | 7:2,883,004 | G/A | — | — |
| rs2533871 | 7:2,883,006 | C/A | — | — |
| rs1196221691 | 7:2,883,529 | C/G | — | likely benign |
| rs2534911410 | 7:2,883,538 | G/C | — | uncertain significance |
| rs766629746 | 7:2,883,624 | C/T | — | uncertain significance |
| rs1417455995 | 7:2,883,632 | C/T | — | uncertain significance |
| rs1300879649 | 7:2,883,636 | C/A | — | uncertain significance |
| rs1469782889 | 7:2,883,705 | C/T | — | uncertain significance |
| rs1636251 | 7:2,884,720 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.