PHKB Gene Summary [Human]

Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, encoded by this gene, which is a member of the phosphorylase b kinase regulatory subunit family. The gamma subunit also includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9B, also known as phosphorylase kinase deficiency of liver and muscle. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. Two pseudogenes have been found on chromosomes 14 and 20, respectively.[provided by RefSeq, Feb 2010]

Details

Type
Protein Coding
Official Symbol
PHKB
Official Name
phosphorylase kinase regulatory subunit beta [Source:HGNC Symbol;Acc:HGNC:8927]
Ensembl ID
ENSG00000102893
Bio databases IDs NCBI: 5257 Ensembl: ENSG00000102893
Aliases phosphorylase kinase regulatory subunit beta
Synonyms PHK beta, PHK β, phosphorylase kinase beta, phosphorylase kinase regulatory subunit beta, phosphorylase kinase regulatory subunit β, phosphorylase kinase β
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human PHKB often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • kinase
  • protein binding
  • Phosphorylase b kinase C-terminal domain

Pathways

Biological processes and signaling networks where the PHKB gene in human plays a role, providing insight into its function and relevance in health or disease.

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • glycogen storage disease IXB
  • glycogen storage disease type IX
  • strabismus
  • hereditary pancreatitis
  • preeclampsia
regulated by
regulates

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • Plasma Membrane
  • cytosol

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human PHKB gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • generation of precursor metabolites and energy
  • glycogen metabolic process

Cellular Component

Where in the cell the gene product is active
  • phosphorylase kinase complex
  • cytosol
  • plasma membrane

Molecular Function

What the gene product does at the molecular level
  • calmodulin binding
  • protein binding

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.