PKIA (cAMP-dependent protein kinase inhibitor alpha)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 5569 |
| Gene name | CAMP-dependent protein kinase inhibitor alpha |
| Gene symbol | PKIA |
| Synonyms (NCBI Gene) |
PRKACN1
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| Chromosome | 8 |
| Chromosome location | 8q21.13 |
| Summary | The protein encoded by this gene is a member of the cAMP-dependent protein kinase (PKA) inhibitor family. This protein was demonstrated to interact with and inhibit the activities of both C alpha and C beta catalytic subunits of the PKA. Alternatively spl |
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miRNA
miRNA information provided by mirtarbase database.
259
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P61925 | ||||||||||
| Protein name | cAMP-dependent protein kinase inhibitor alpha (PKI-alpha) (cAMP-dependent protein kinase inhibitor, muscle/brain isoform) | ||||||||||
| Protein function | Extremely potent competitive inhibitor of cAMP-dependent protein kinase activity, this protein interacts with the catalytic subunit of the enzyme after the cAMP-induced dissociation of its regulatory chains. | ||||||||||
| PDB | 1CMK , 1JLU , 1Q8T , 1VEB , 1XH4 , 1XH5 , 1XH6 , 1XH7 , 1XH8 , 1XH9 , 1XHA , 1YDR , 2C1A , 2C1B , 2F7E , 2GNI , 2JDS , 2JDT , 2JDV , 2L1L , 2UVX , 2UVY , 2UVZ , 2UW0 , 2UW3 , 2UW4 , 2UW5 , 2UW6 , 2UW7 , 2UW8 , 2VNW , 2VNY , 2VO0 , 2VO3 , 2VO6 , 2VO7 , 3AMA , 3AMB , 3L9L , 3L9M , 3L9N , 3MVJ , 3NX8 , 3OOG , 3OVV , 3OWP , 3OXT , 3P0M , 3POO , 3VQH , 3WYG | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 76 | ||||||||||
| 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 from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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