Gene

Kif21b

Species
Mus musculus
Symbol
Kif21b
Name
kinesin family member 21B
Synonyms
  • 2610511N21Rik
  • mKIAA0449
Biotype
protein coding gene
Automated Description
Predicted to enable ATP hydrolysis activity; microtubule binding activity; and microtubule motor activity. Involved in regulation of postsynaptic membrane neurotransmitter receptor levels and retrograde dendritic transport. Acts upstream of or within corpus callosum development. Is active in glutamatergic synapse and postsynaptic endosome. Is expressed in central nervous system; dorsal root ganglion; and neural retina. Orthologous to human KIF21B (kinesin family member 21B).
MGI Description
PHENOTYPE: Homozygous KO reduces dendrite branching and spine density as a result of reduced microtubule growth, resulting in impaired spatial learning and cued conditioning behavior. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24115
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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          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

          Kif21b molecule type
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            Genetic Interactions

            Kif21b role
            Kif21b genetic perturbation
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