Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5593
Gene name Gene Name - the full gene name approved by the HGNC.
Protein kinase cGMP-dependent 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PRKG2
Synonyms (NCBI Gene) Gene synonyms aliases
AMD4, PKG2, PRKGR2, SMDP, cGK2, cGKII
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q21.21
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that belongs to the serine/threonine protein kinase family of proteins. The encoded protein binds to and inhibits the activation of several receptor tyrosine kinases. The membrane-bound protein is a regulator of intestinal secr
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018075 hsa-miR-335-5p Microarray 18185580
MIRT023857 hsa-miR-1-3p Microarray 18668037
MIRT618399 hsa-miR-548a-5p HITS-CLIP 23824327
MIRT618398 hsa-miR-548ab HITS-CLIP 23824327
MIRT618397 hsa-miR-548ad-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004672 Function Protein kinase activity TAS 8607838
GO:0004674 Function Protein serine/threonine kinase activity IEA
GO:0004692 Function CGMP-dependent protein kinase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601591 9416 ENSG00000138669
Protein
UniProt ID Q13237
Protein name cGMP-dependent protein kinase 2 (cGK 2) (cGK2) (EC 2.7.11.12) (cGMP-dependent protein kinase II) (cGKII)
Protein function Crucial regulator of intestinal secretion and bone growth. Phosphorylates and activates CFTR on the plasma membrane. Plays a key role in intestinal secretion by regulating cGMP-dependent translocation of CFTR in jejunum (PubMed:33106379). Acts d
PDB 5BV6 , 5C6C , 5C8W , 5JIX , 5JIZ , 6BQ8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00027 cNMP_binding 186 269 Cyclic nucleotide-binding domain Domain
PF00027 cNMP_binding 304 393 Cyclic nucleotide-binding domain Domain
PF00069 Pkinase 453 711 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly concentrated in brain, lung and intestinal mucosa.
Sequence
MGNGSVKPKHSKHPDGHSGNLTTDALRNKVTELERELRRKDAEIQEREYHLKELREQLSK
QTVAIAELTEELQNKCIQLNKLQDVVHMQGGSPLQASPDKVPLEVHRKTSGLVSLHSRRG
AKAGVSAEPTTRTYDLNKPPEFSFEKARVRKDSSEKKLITDALNKNQFLKRLDPQQIKDM
VECMYGRNYQQGSYIIKQGEPGNHIFVLAEGRLEVFQGEKLLSSIPMWTTFGELAILYNC
TRTASVKAITNVKTWALDREVFQNIMRRT
AQARDEQYRNFLRSVSLLKNLPEDKLTKIID
CLEVEYYDKGDYIIREGEEGSTFFILAKGKVKVTQSTEGHDQPQLIKTLQKGEYFGEKAL
ISDDVRSANIIAEENDVACLVIDRETFNQTVGT
FEELQKYLEGYVANLNRDDEKRHAKRS
MSNWKLSKALSLEMIQLKEKVARFSSSSPFQNLEIIATLGVGGFGRVELVKVKNENVAFA
MKCIRKKHIVDTKQQEHVYSEKRILEELCSPFIVKLYRTFKDNKYVYMLLEACLGGELWS
ILRDRGSFDEPTSKFCVACVTEAFDYLHRLGIIYRDLKPENLILDAEGYLKLVDFGFAKK
IGSGQKTWTFCGTPEYVAPEVILNKGHDFSVDFWSLGILVYELLTGNPPFSGVDQMMTYN
LILKGIEKMDFPRKITRRPEDLIRRLCRQNPTERLGNLKNGINDIKKHRWL
NGFNWEGLK
ARSLPSPLQRELKGPIDHSYFDKYPPEKGMPPDELSGWDKDF
Sequence length 762
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  cGMP-PKG signaling pathway
Hormone signaling
Gap junction
Platelet activation
Circadian entrainment
Thermogenesis
Long-term depression
Olfactory transduction
Regulation of lipolysis in adipocytes
Renin secretion
Salivary secretion
  Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation
cGMP effects
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Acromesomelic dysplasia acromesomelic dysplasia 4 N/A N/A GenCC
Alopecia Areata Alopecia areata N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acromesomelic dysplasia Associate 33887582
Brain Neoplasms Associate 19543319
Coronary Artery Disease Associate 23233742
Glioma Associate 19543319
Gout Associate 32124961
Mastocytosis Systemic Associate 33663081
Neoplasms Associate 19543319, 33663081, 37522128
Neuroendocrine Tumors Associate 37522128
Osteosarcoma Associate 29617357