CMYA5 Products

Description

CMYA5 was originally identified as the muscle-specific partner of dysbindin, (a component of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)), and as a Mef-2 target gene. CMYA5 interacts with desmin, and this association is important for the proper perinuclear localization of CMYA5 and potentially facilitates lysosome biogenesis and/or positioning. CMYA5 may also be a muscle-specific protein kinase A-anchoring protein that is dysregulated in Duchenne muscular dystrophy.

Bioinformatics

Entrez	202333 Human 76469 Mouse
Uniprot	Q8N3K9 Human NP_705838 Human
Product By Gene ID	202333
Alternate Names	myospryn C5orf10 DTNBP2 DKFZp451G223 cardiomyopathy-associated protein 5 tripartite motif-containing protein 76 SPRY domain-containing protein 2 DKFZp451G182 SPRYD2 genethonin-3 dystrobrevin-binding protein 2 cardiomyopathy associated 5

Diseases related to CMYA5

Discover more about diseases related to CMYA5.

Muscular Dystrophy, Duchenne
Dystrophy
Muscular Dystrophy
Schizophrenia
Cardiomyopathies
Hypertrophy
Myopathy
Heart Diseases
Dysequilibrium Syndrome
Muscular Dystrophy, Tibial
Myeloproliferative Syndrome, Transient
Abnormal Degeneration
Muscle Injury
Heart Failure
Cardiac Hypertrophy
Left Ventricular Hypertrophy
Hypertensive Disease
Aortic Aneurysm, Thoracic
Muscular Dystrophies, Limb-girdle

Pathways for CMYA5

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Localization
Pathogenesis
Regeneration
Muscle Hypertrophy
Translation
Autolysis

Bioinformatics Tool for CMYA5

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