Gene

PEK

Species
Drosophila melanogaster
Symbol
PEK
Name
pancreatic eIF-2alpha kinase
Synonyms
  • CG2087
  • DmPEK
Biotype
protein coding gene
Automated Description
Enables eukaryotic translation initiation factor 2alpha kinase activity. Involved in several processes, including PERK-mediated unfolded protein response; positive regulation of JNK cascade; and regulation of G2/M transition of mitotic cell cycle. Is active in endoplasmic reticulum. Is expressed in several structures, including adult head; larval muscle cell; larval muscle system; and trunk visceral muscle primordium. Human ortholog(s) of this gene implicated in Wolcott-Rallison syndrome and type 1 diabetes mellitus. Orthologous to human EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3).
FB Description
pancreatic eIF-2alpha kinase (PEK) encodes an endoplasmic reticulum (ER) transmembrane kinase and a component of the integrated stress response. During ER stress the product of PEK phosphorylates the translation initiation factor encoded by eIF2alpha resulting in the inhibition of most cap-dependent translation. This is especially important during the development of secretory tissues and the response to cellular stress.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11042
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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
          R6
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          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

          PEK molecule type
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            Genetic Interactions

            PEK role
            PEK genetic perturbation
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