PRKACA Chromosome 19
Protein kinase cAMP-activated catalytic subunit alpha
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What This Gene Does
This gene encodes one of the catalytic subunits of protein kinase A, which exists as a tetrameric holoenzyme with two regulatory subunits and two catalytic subunits, in its inactive form. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. cAMP-dependent phosphorylation of proteins by protein kinase A is important to many cellular processes, including differentiation, proliferation, and apoptosis. Constitutive activation of this gene caused either by somatic mutations, or genomic duplications of regions that include this gene, have been associated with hyperplasias and adenomas of the adrenal cortex and are linked to corticotropin-independent Cushing's syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. Tissue-specific isoforms that differ at the N-terminus have been described, and these isoforms may differ in the post-translational modifications that occur at the N-terminus of some isoforms. [provided by RefSeq, Jan 2015]
Gene Info
Gene Group
"Protein kinase A subunits|Protein kinase A family"
Locus Type
gene with protein product
Location
19p13.12
Ensembl
ENSG00000072062
Associated Conditions (7)
Pigmented nodular adrenocortical disease
primary
4
Cardioacrofacial dysplasia 1
ACTH-independent adrenal Cushing syndrome
somatic
Adrenal cortex neoplasm
Key Variants
RS724160013
Pathogenic
Pigmented nodular adrenocortical disease, primary, 4
Health Risk
RS148280386
Pathogenic/Likely pathogenic
Cardioacrofacial dysplasia 1, Cardioacrofacial dysplasia 1
Health Risk
RS386352352
Pathogenic/Likely pathogenic
Pigmented nodular adrenocortical disease, primary, 4
Health Risk
All Variants (3)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS724160013 | Health Risk | Pathogenic | Pigmented nodular adrenocortical disease, primary, 4 |
| RS148280386 | Health Risk | Pathogenic/Likely pathogenic | Cardioacrofacial dysplasia 1, Cardioacrofacial dysplasia 1 |
| RS386352352 | Health Risk | Pathogenic/Likely pathogenic | Pigmented nodular adrenocortical disease, primary, 4 |