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Protein-coding gene in the species Homo sapiens

PRKCG

PRKCG
All data from the card 19
Aliases
PRKCG, PKC-gamma, PKCC, PKCG, SCA14, protein kinase C gamma, PKCI(3), PKCgamma
External IDs
OMIM: 176980; MGI: 97597; GeneCards: PRKCG
PDB
Ortholog search: PDBe RCSB
2.7.11.13
↗
Chr.
Chromosome 19 (human)
Band
19q13.42
End
53,907,652 bp
Chr.
Chromosome 7 (mouse)
Band
7 A1|7 1.93 cM
End
3,379,615 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
5582
Ensembl
ENSG00000126583
UniProt
P05129
RefSeq (mRNA)
NM_002739NM_001316329
RefSeq (protein)
NP_001303258NP_002730
Location (UCSC)
Chr 19: 53.88 – 53.91 Mb

Protein kinase C gamma type is an enzyme that in humans is encoded by the PRKCG gene.

Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC also serves as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells. The protein encoded by this gene is one of the PKC family members. This protein kinase is expressed solely in the brain and spinal cord and its localization is restricted to neurons. It has been demonstrated that several neuronal functions, including long term potentiation (LTP) and long term depression (LTD), specifically require this kinase. Knockout studies in mice also suggest that this kinase may be involved in neuropathic pain development. Defects in this protein have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14).

Interactions

PRKCG has been shown to interact with GRIA4.

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Text from Wikipedia, CC BY-SA 4.0 · Source article