GNB3 Chromosome 12
G protein subunit beta 3
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What This Gene Does
Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit which belongs to the WD repeat G protein beta family. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. A single-nucleotide polymorphism (C825T) in this gene is associated with essential hypertension and obesity. This polymorphism is also associated with the occurrence of the splice variant GNB3-s, which appears to have increased activity. GNB3-s is an example of alternative splicing caused by a nucleotide change outside of the splice donor and acceptor sites. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Jul 2014]
Gene Info
Gene Group
"WD repeat domain containing|G protein subunits beta"
Locus Type
gene with protein product
Location
12p13.31
Ensembl
ENSG00000111664
Associated Conditions (4)
Inborn genetic diseases
Clear cell carcinoma of kidney
Ovarian serous cystadenocarcinoma
Congenital stationary night blindness 1H
Key Variants
RS112732503
Conflicting classifications of pathogenicity
Health Risk
RS61747607
Conflicting classifications of pathogenicity
Inborn genetic diseases, Clear cell carcinoma of kidney, Ovarian serous cystadenocarcinoma
Health Risk
RS879253773
Pathogenic
Congenital stationary night blindness 1H, Congenital stationary night blindness 1H
Health Risk
RS879253774
Pathogenic
Congenital stationary night blindness 1H, Congenital stationary night blindness 1H
Health Risk
All Variants (4)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS112732503 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS61747607 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Clear cell carcinoma of kidney, Ovarian serous cystadenocarcinoma |
| RS879253773 | Health Risk | Pathogenic | Congenital stationary night blindness 1H, Congenital stationary night blindness 1H |
| RS879253774 | Health Risk | Pathogenic | Congenital stationary night blindness 1H, Congenital stationary night blindness 1H |