Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5138
Gene name Gene Name - the full gene name approved by the HGNC.
Phosphodiesterase 2A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PDE2A
Synonyms (NCBI Gene) Gene synonyms aliases
CGS-PDE, IDDPADS, PDE2A1, PED2A4, cGSPDE
Disease Acronyms (UniProt) Disease acronyms from UniProt database
IDDPADS
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.4
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 17329248
GO:0000287 Function Magnesium ion binding IDA 15938621
GO:0003170 Process Heart valve development ISS
GO:0003281 Process Ventricular septum development ISS
GO:0004114 Function 3',5'-cyclic-nucleotide phosphodiesterase activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602658 8777 ENSG00000186642
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
View all (309 more)
12972520
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
12972520
Marfan syndrome Mammary Carcinoma, Human rs137854456, rs137854457, rs267606796, rs137854458, rs137854459, rs137854460, rs137854470, rs137854471, rs267606797, rs137854461, rs137854462, rs137854463, rs869025419, rs137854464, rs137854465
View all (942 more)
12972520
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 22446963
Unknown
Disease term Disease name Evidence References Source
Convulsions And Choreoathetosis infantile convulsions and choreoathetosis GenCC
Insomnia Insomnia GWAS
Associations from Text Mining
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