Gene

Phkb

Species
Mus musculus
Symbol
Phkb
Name
phosphorylase kinase beta
Synonyms
  • AI463271
  • expressed sequence AI463271
Biotype
protein coding gene
Automated Description
Predicted to enable calmodulin binding activity. Involved in glucose homeostasis and positive regulation of glycogen catabolic process. Predicted to be located in plasma membrane. Predicted to be part of phosphorylase kinase complex. Is expressed in cerebral cortex; gut; heart; and liver. Used to study glycogen storage disease IXb. Human ortholog(s) of this gene implicated in glycogen storage disease IXb. Orthologous to human PHKB (phosphorylase kinase regulatory subunit beta).
MGI Description
PHENOTYPE: Homozygous null mice exhibit hepatomegaly, lower fasting blood glucose levels, decreased glycogen phosphorylase activity and increased sensitivity to pyruvate indicating partial glycogenolytic activity, and increased gluconeogenesis and lipid metabolism. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR10749
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

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    Disease Associations

    Cases where the expected disease association was NOT found
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    Alleles and Variants

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      Transgenic Alleles

      Species
      (carrying the transgene)
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCm39
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          Data currently unavailable; sequence viewer under construction

          Sequence Details

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          Expression

          Primary Sources
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          Phkb molecule type
          Interactor gene
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            Genetic Interactions

            Phkb role
            Phkb genetic perturbation
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