PRKG2 (protein kinase cGMP-dependent 2)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5593 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Protein kinase cGMP-dependent 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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PRKG2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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AMD4, PKG2, PRKGR2, SMDP, cGK2, cGKII |
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Chromosome
Chromosome number
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4 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4q21.21 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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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 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| 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
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| Tissue specificity | TISSUE SPECIFICITY: Highly concentrated in brain, lung and intestinal mucosa. | ||||||||||||||||||||
| Sequence |
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| Sequence length | 762 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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