PDE9A Products

Description

The protein encoded by the PDE9A gene catalyzes the hydrolysis of cAMP and cGMP to their corresponding monophosphates. The encoded protein plays a role in signal transduction by regulating the intracellular concentration of these cyclic nucleotides. Multiple transcript variants encoding several different isoforms have been found for this gene. (provided by RefSeq)

Bioinformatics

Uniprot	O76083 Human O76083-13 Human NM_002606 Human NP_001001567 Human NP_001001567.1 Human AAH09047 Human
Product By Gene ID	5152
Alternate Names	EC 3.1.4.35 FLJ90181 CGMP-specific 3'-5'-cyclic phosphodiesterase type 9, EC 3.1.4.1710phosphodiesterase PDE9A21 high affinity cGMP-specific 3'-5'-cyclic phosphodiesterase 9A HSPDE9A2 CGMP-specific 3'-5'-cyclic phosphodiesterase type 9 phosphodiesterase 9A

Diseases related to PDE9A

Discover more about diseases related to PDE9A.

Alzheimer's Disease
Malnutrition
Anemia, Sickle Cell
Diabetes Mellitus
Down Syndrome
Malignant Neoplasms
Pain
Hereditary Diseases
Depressive Disorder
Impaired Cognition
Neurodegenerative Disorders
Nervousness
Bipolar Disorder
Complete Hearing Loss
Cognition Disorders
Tissue Adhesions
Erectile Dysfunction
Leukemia
Meningeal Disorder

Pathways for PDE9A

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Localization
Cognition
Cell Proliferation
Sensory Processing
Signal Transmission
Aging
Penile Erection
Intracellular Signal Transduction
Oocyte Maturation
Cellular Localization
Water Homeostasis
Phototransduction
Pathogenesis
Meiosis

Research Areas for PDE9A

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Lipid and Metabolism

PTMs for PDE9A

Learn more about PTMs related to PDE9A.

Phosphorylation
Methylation

Bioinformatics Tool for PDE9A

Discover related pathways, diseases and genes to PDE9A. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.