Gene Gene information from NCBI Gene database.
Entrez ID 5138
Gene name Phosphodiesterase 2A
Gene symbol PDE2A
Synonyms (NCBI Gene)
CGS-PDEIDDPADSPDE2A1PED2A4cGSPDE
Chromosome 11
Chromosome location 11q13.4
miRNA miRNA information provided by mirtarbase database.
42
miRTarBase ID miRNA Experiments Reference
MIRT004169 hsa-miR-192-5p Microarray 16822819
MIRT017522 hsa-miR-335-5p Microarray 18185580
MIRT1220258 hsa-miR-103b CLIP-seq
MIRT1220259 hsa-miR-298 CLIP-seq
MIRT1220260 hsa-miR-3151 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
81
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 17329248
GO:0000166 Function Nucleotide binding IEA
GO:0000287 Function Magnesium ion binding IDA 15938621
GO:0003170 Process Heart valve development ISS
GO:0003281 Process Ventricular septum development ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602658 8777 ENSG00000186642
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O00408
Protein name cGMP-dependent 3',5'-cyclic phosphodiesterase (EC 3.1.4.17) (Cyclic GMP-stimulated phosphodiesterase) (CGS-PDE) (cGSPDE)
Protein function cGMP-activated cyclic nucleotide phosphodiesterase with a dual-specificity for the second messengers cAMP and cGMP, which are key regulators of many important physiological processes (PubMed:15938621, PubMed:29392776, PubMed:9210593). Has a high
PDB 1Z1L , 3IBJ , 3ITM , 3ITU , 4C1I , 4D08 , 4D09 , 4HTX , 4HTZ , 4JIB , 5TZ3 , 5TZA , 5TZC , 5TZH , 5TZW , 5TZX , 5TZZ , 5U00 , 5U7D , 5U7I , 5U7J , 5U7K , 5U7L , 5VP0 , 5VP1 , 5XKM , 6B96 , 6B97 , 6B98 , 6BLF , 6C7D , 6C7E , 6C7F , 6C7G , 6C7I , 6C7J , 6CYB , 6CYC , 6CYD , 6ZND , 6ZQZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01590 GAF 241 372 GAF domain Domain
PF01590 GAF 409 548 GAF domain Domain
PF00233 PDEase_I 655 889 Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed (PubMed:29392776, PubMed:9210593). Expressed in brain, with high expression observed in the corpus striatum (PubMed:29392776). Also expressed in heart, placenta, lung, skeletal muscle, kidney and pancreas (PubMed:29392
Sequence
MGQACGHSILCRSQQYPAARPAEPRGQQVFLKPDEPPPPPQPCADSLQDALLSLGSVIDI
SGLQRAVKEALSAVLPRVETVYTYLLDGESQLVCEDPPHELPQEGKVREAIISQKRLGCN
GLGFSDLPGKPLARLVAPLAPDTQVLVMPLADKEAGAVAAVILVHCGQLSDNEEWSLQAV
EKHTLVALRRVQVLQQRGPREAPRAVQNPPEGTAEDQKGGAAYTDRDRKILQLCGELYDL
DASSLQLKVLQYLQQETRASRCCLLLVSEDNLQLSCKVIGDKVLGEEVSFPLTGCLGQVV
EDKKSIQLKDLTSEDVQQLQSMLGCELQAMLCVPVISRATDQVVALACAFNKLEGDLFTD
EDEHVIQHCFHY
TSTVLTSTLAFQKEQKLKCECQALLQVAKNLFTHLDDVSVLLQEIITE
ARNLSNAEICSVFLLDQNELVAKVFDGGVVDDESYEIRIPADQGIAGHVATTGQILNIPD
AYAHPLFYRGVDDSTGFRTRNILCFPIKNENQEVIGVAELVNKINGPWFSKFDEDLATAF
SIYCGISI
AHSLLYKKVNEAQYRSHLANEMMMYHMKVSDDEYTKLLHDGIQPVAAIDSNF
ASFTYTPRSLPEDDTSMAILSMLQDMNFINNYKIDCPTLARFCLMVKKGYRDPPYHNWMH
AFSVSHFCYLLYKNLELTNYLEDIEIFALFISCMCHDLDHRGTNNSFQVASKSVLAALYS
SEGSVMERHHFAQAIAILNTHGCNIFDHFSRKDYQRMLDLMRDIILATDLAHHLRIFKDL
QKMAEVGYDRNNKQHHRLLLCLLMTSCDLSDQTKGWKTTRKIAELIYKEFFSQGDLEKAM
GNRPMEMMDREKAYIPELQISFMEHIAMPIYKLLQDLFPKAAELYERVA
SNREHWTKVSH
KFTIRGLPSNNSLDFLDEEYEVPDLDGTRAPINGCCSLDAE
Sequence length 941
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Purine metabolism
Metabolic pathways
cGMP-PKG signaling pathway
Olfactory transduction
Aldosterone synthesis and secretion
Morphine addiction
  cGMP effects
G alpha (s) signalling events
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
17
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Intellectual developmental disorder with paroxysmal dyskinesia or seizures Likely pathogenic; Pathogenic rs111657177, rs1591023585, rs1855880808, rs1855739332, rs987916591, rs1856914827 RCV002266781
RCV001290006
RCV001290005
RCV001290007
RCV001290008
RCV001290009
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
PDE2A-related disorder Likely benign rs190149811 RCV003969538
Sarcoma Benign rs12287467 RCV005911294
See cases Uncertain significance rs2135291663 RCV002252912
Squamous cell lung carcinoma Uncertain significance rs1263976937 RCV005934995
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Abnormalities Drug Induced Associate 32467598
Adrenal Hyperplasia Congenital Associate 33112806
Arthritis Rheumatoid Associate 23577190
Carcinoma Hepatocellular Associate 35800238, 36054420, 37622118, 39699377
Carcinoma Hepatocellular Inhibit 36611861
Cardiomyopathy Dilated Associate 26095046
Chorea Associate 32467598
Cognition Disorders Associate 32467598
Coronary Artery Disease Associate 26619243
Developmental Disabilities Associate 32467598