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AKAP12 - A-kinase anchoring protein 12 Gene

Also Known as SSeCKS; AKAP250

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 9590

About AKAP12

Cytogenetic location: 6q25.1 Genomic coordinates (GRCh38): 6:151,239,967-151,358,559 (from NCBI)

This gene has 5 transcripts (splice variants) and 219 orthologues. Broad expression in testis (RPKM 48.0), fat (RPKM 27.1) and 20 other tissues.

Summary

The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. The encoded protein is expressed in endothelial cells, cultured fibroblasts, and osteosarcoma cells. It associates with protein kinases A and C and Phosphatase, and serves as a scaffold protein in signal transduction. This protein and RII PKA colocalize at the cell periphery. This protein is a cell growth-related protein. Antibodies to this protein can be produced by patients with myasthenia gravis. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

AKAP12 Products (3)

mRNA	Protein	Name
NM_001370346.1	NP_001357275.1	A-kinase anchor protein 12 isoform 3
NM_005100.4	NP_005091.2	A-kinase anchor protein 12 isoform 1
NM_144497.2	NP_653080.1	A-kinase anchor protein 12 isoform 2

Gene Ontology

Molecular Function
Biological Process

Molecular Function GO Annotation	Evidence	References	Source
enables adenylate cyclase binding	IPI IPI: Inferred from physical interaction	17081159	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	16642035	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway	IMP IMP: Inferred from mutant phenotype	17081159	GOA
involved in regulation of protein kinase A signaling	IMP IMP: Inferred from mutant phenotype	17081159	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

AKAP12 Protein Structure

WSK

RII_binding_1

0
300
600
900
1200
1500
1782 a.a.

Protein Preferred Names	Protein Names
A-kinase anchor protein 12	A kinase (PRKA) anchor protein 12

AKAP12 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	AKAP12	Q02952	PRKAR2A	Homo sapiens	P13861	Anti Tag CoIP	35271311
Intra	AKAP12	Q02952	PRKAR2A	Homo sapiens	P13861	Filter Binding	16642035
Intra	AKAP12	Q02952	EGFR	Homo sapiens	P00533	Ub Reconstruction	20029029
Intra	AKAP12	Q02952	FHL1	Homo sapiens	Q13642	Anti Tag CoIP	35271311
Intra	AKAP12	Q02952	FHL1	Homo sapiens	Q13642	Y2H Fragment Pooling	23414517
Intra	AKAP12	Q02952	FHL1	Homo sapiens	Q13642	Y2H	21900206

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Myasthenia Gravis	MG Acquired Myasthenia Autoimmune Myasthenia Gravis Erb-Goldflam Disease Mg - [Myasthenia Gravis] Myasthenia Gravis Nos Myasthenia
Myasthenic Syndrome, Congenital, 15	Congenital Myasthenic Syndrome 15 CMS15 Myasthenic Syndrome, Congenital, Without Tubular Aggregates Cmswta Myasthenic Syndrome, Congenital, 15, Without Tubular Aggregates Congenital Myasthenic Syndrome 15 Without Tubular Aggregates Myasthenic Syndrome, Congenital, Type 15, Without Tubular Aggregates
Myasthenic Syndrome, Congenital, 9, Associated With Acetylcholine Receptor Deficiency	Congenital Myasthenic Syndrome 9 CMS9 Congenital Myasthenic Syndrome 9, Associated With Acetylcholine Receptor Deficiency Myasthenic Syndrome, Congenital, Type 9, Associated With Acetylcholine Receptor Deficiency
Amyotrophic Lateral Sclerosis 1	Amyotrophic Lateral Sclerosis ALS Lou Gehrig Disease Amyotrophic Lateral Sclerosis Type 1 Charcot Disease ALS1 Amyotrophic Lateral Sclerosis, Susceptibility To Fals Lou Gehrig'S Disease Mnd Motor Neuron Disease Familial Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis 1, Familial Amyotrophic Lateral Sclerosis 1, Autosomal Dominant Motor Neuron Disease, Bulbar Motor Neurone Disease Amyotrophic Lateral Sclerosis With Dementia Dementia With Amyotrophic Lateral Sclerosis Motor Neuron Disease, Amyotrophic Lateral Sclerosis Sclerosis, Lateral, Amyotrophic Sclerosis, Lateral, Amyotrophic, Type 1 Amyotrophic Sclerosis Als - [Amyotrophic Lateral Sclerosis] Wasting Palsy Amyotrophic Paralysis Amyotrophy Lateral Sclerosis Wasting Paralysis Spinal Progressive Amyotrophy Progressive Atrophic Paralysis

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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS00515	AKAP12 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	AKAP12	RGD	RGD:70988
Macaca mulatta	AKAP12	VGNC	VGNC:69766
Bos taurus	AKAP12	VGNC	VGNC:25782
Canis familiaris	AKAP12	VGNC	VGNC:37754
Mus musculus	AKAP12	MGD	MGI:1932576
Others	AKAP12	NCBI