Gene

Ripk4

Species
Mus musculus
Symbol
Ripk4
Name
receptor-interacting serine-threonine kinase 4
Synonyms
  • 2310069J12Rik
  • AI552420
Biotype
protein coding gene
Automated Description
Enables protein serine kinase activity. Involved in skin development. Located in cytoplasm. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; integumental system; and sensory organ. Used to study popliteal pterygium syndrome. Orthologous to human RIPK4 (receptor interacting serine/threonine kinase 4).
MGI Description
PHENOTYPE: Mutations in this gene result in perinatal lethality, impaired keratinocyte differentiation, impaired skin barrier function, cleft palate and and epithelial fusion phenotypes associated with abnormal periderm development. Homozygous mutant mice lack oral, anal, and nasal openings and display shorter limbs and tail that are partially fused to the body cavity. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24198
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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
          GRCm39
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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

          Ripk4 molecule type
          Interactor gene
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            Genetic Interactions

            Ripk4 role
            Ripk4 genetic perturbation
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