The GNA11 gene (GNA11 stands for "G Protein Subunit Alpha 11") is a protein coding gene located on chromosome 19p13.3Z.
Diseases associated with GNA11 include:
- Hypocalciuric Hypercalcemia, Familial, Type II (HH2).
- Hypocalcemia, Autosomal Dominant 2 (HYPOC2)
- Aldosterone-producing adenomas (Zhou J et al. 2021)
- Choroidal melanomas
Related signaling pathways include thromboxane signaling through the TP receptor and activation of ERK by developmental angiotensin. An important paralog of this gene is the GNAQ gene.