PHKG1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

PHKG1

Phosphorylase b kinase gamma catalytic chain, skeletal muscle isoform is an enzyme that in humans is encoded by the PHKG1 gene.[5][6]

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PHKG1
Identifiers
AliasesPHKG1, PHKG, phosphorylase kinase catalytic subunit gamma 1
External IDsOMIM: 172470; MGI: 97579; HomoloGene: 68508; GeneCards: PHKG1; OMA:PHKG1 - orthologs
EC number2.7.11.26
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001258459
NM_001258460
NM_006213

NM_011079

RefSeq (protein)

NP_001245388
NP_001245389
NP_006204

NP_035209

Location (UCSC)Chr 7: 56.08 – 56.09 MbChr 5: 129.89 – 129.93 Mb
PubMed search[3][4]
Wikidata
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This gene is a member of the Ser/Thr protein kinase family and encodes a protein with one protein kinase domain and two calmodulin-binding domains. This protein is the catalytic member of a 16 subunit protein kinase complex which contains equimolar ratios of 4 subunit types. The complex is a crucial glycogenolytic regulatory enzyme. This gene has two pseudogenes at chromosome 7q11.21 and one at chromosome 11p11.12.[6]

References

Further reading

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