1. Gene
  2. PRKAR2A - protein kinase cAMP-dependent type II regulatory subunit alpha Gene

PRKAR2A - protein kinase cAMP-dependent type II regulatory subunit alpha Gene

Homo sapiens

Also known as PKR2; PRKAR2

Gene ID: 5576 | Gene type: protein coding

About PRKAR2A

Cytogenetic location: 3p21.31 Genomic coordinates (GRCh38): 3:48,744,591-48,847,874 (from NCBI)

This gene has 7 transcripts (splice variants), 283 orthologues and 4 paralogues. Ubiquitous expression in testis (RPKM 11.3), colon (RPKM 10.8) and 25 other tissues.

Summary

cAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. 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. The protein encoded by this gene is one of the regulatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. It may interact with various A-kinase anchoring proteins and determine the subcellular localization of cAMP-dependent protein kinase. This subunit has been shown to regulate protein transport from endosomes to the Golgi apparatus and further to the endoplasmic reticulum (ER). [provided by RefSeq, Jul 2008]

PRKAR2A Products(4)

mRNA Protein Name
NM_001321982.2 NP_001308911.1 cAMP-dependent protein kinase type II-alpha regulatory subunit isoform a
NM_001321983.2 NP_001308912.1 cAMP-dependent protein kinase type II-alpha regulatory subunit isoform b
NM_001321989.2 NP_001308918.1 cAMP-dependent protein kinase type II-alpha regulatory subunit isoform c
NM_004157.4 NP_004148.1 cAMP-dependent protein kinase type II-alpha regulatory subunit isoform a

PRKAR2A Protein Structure

RIIa

RIIa: Regulatory subunit of type II PKA R-subunit (9 - 45)

cNMP_binding

cNMP_binding: Cyclic nucleotide-binding domain (158 - 244)

cNMP_binding

cNMP_binding: Cyclic nucleotide-binding domain (280 - 372)

  • 0
  • 100
  • 200
  • 300
  • 404 a.a.
Protein Preferred Names Protein Names

cAMP-dependent protein kinase type II-alpha regulatory subunit

cAMP-dependent protein kinase regulatory subunit RII alpha

Related Diseases

Diseases Alias
Nivelon-Nivelon-Mabille Syndrome

Chondrodysplasia-Pseudohermaphroditism Syndrome

NNMS

Chondrodysplasia-Disorder Of Sex Development Syndrome

Nivelon Nivelon Mabille Syndrome

Carney Complex Variant

Carney Complex

Carney Syndrome

Carney Complex, Type 1

Lamb Syndrome

Name Syndrome

Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome

Carney Complex - Trismus - Pseudocamptodactyly Syndrome

Carney Complex, Type 2

Car

Cnc1

Carney Myxoma-Endocrine Complex

Myxoma - Spotty Pigmentation - Endocrine Overactivity

Myxoma, Spotty Pigmentation, And Endocrine Overactivity

Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome

Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome

Carney Complex-Trismus-Pseudocamptodactyly Syndrome

CACOV

Fibrolamellar Carcinoma

Fibrolamellar Hepatocellular Carcinoma

Fhcc

Fibrolamellar Hepatocarcinoma

Hepatocellular Carcinoma, Fibrolamellar

Oncocytic Hepatocellular Tumor

Eosinophilic Glassy Cell Hepatoma

Eosinophilic Hepatocellular Carcinoma With Lamellar Fibrosis

Fl-Hcc

Fibrolamellar Oncocytic Hepatoma

Hepatocellular Carcinoma With Increased Stromal Fibrosis

Polygonal Cell Hepatocellular Carcinoma With Fibrous Stroma

Primary Pigmented Nodular Adrenocortical Disease

Ppnad

Primary Pigmented Nodular Adrenal Dysplasia

Pigmented Nodular Adrenocortical Disease, Primary, 2

Pigmented Nodular Adrenocortical Disease, Primary, 1

Kallmann Syndrome

Hypogonadism With Anosmia

Kallman'S Syndrome

Anosmic Hypogonadism

Anosmic Idiopathic Hypogonadotropic Hypogonadism

Hypogonadotropic Hypogonadism And Anosmia

Hypogonadotropic Hypogonadism-Anosmia Syndrome

Olfacto-Genital Pathological Sequence

Familial Hypogonadism With Anosmia

Kallman Syndrome

Dysplasia Olfactogenitalis Of De Morsier

Kallmann'S Syndrome

Congenital Hypogonadotropic Hypogonadism With Anosmia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta PRKAR2A VGNC VGNC:76407
Mus musculus PRKAR2A MGD MGI:108025
Rattus norvegicus PRKAR2A RGD RGD:3393
Felis catus PRKAR2A VGNC VGNC:69053
Canis familiaris PRKAR2A VGNC VGNC:44976
Bos taurus PRKAR2A VGNC VGNC:33325