Gene Gene information from NCBI Gene database.
Entrez ID 5593
Gene name Protein kinase cGMP-dependent 2
Gene symbol PRKG2
Synonyms (NCBI Gene)
AMD4PKG2PRKGR2SMDPcGK2cGKII
Chromosome 4
Chromosome location 4q21.21
Summary 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.
122
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601591 9416 ENSG00000138669
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
19
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acromesomelic dysplasia 4 Pathogenic; Likely pathogenic rs1291510415, rs2110087773, rs2546101657, rs995285513 RCV001786318
RCV001786319
RCV003228231
RCV003228694
Spondylometaphyseal dysplasia, pagnamenta type Pathogenic rs2109933573 RCV001786320
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Likely benign rs201667781 RCV005931722
Colorectal cancer Likely benign rs201667781 RCV005931723
Familial cancer of breast Likely benign rs201667781 RCV005931721
PRKG2-related disorder Likely benign; Benign rs201667781, rs139565161, rs17005080, rs9992933, rs748041886, rs56210303, rs145769252, rs569602525, rs140694607, rs778024870, rs17484474 RCV003926366
RCV003907141
RCV003979760
RCV003984672
RCV003933868
RCV003951412
RCV003917358
RCV003934233
RCV003954483
RCV003978975
RCV003978983
Associations from Text MiningDisease 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