Gene

Sh3glb2

Species
Mus musculus
Symbol
Sh3glb2
Name
SH3-domain GRB2-like endophilin B2
Synonyms
  • mKIAA1848
Biotype
protein coding gene
Automated Description
Predicted to enable identical protein binding activity. Predicted to be involved in membrane organization and postsynaptic neurotransmitter receptor internalization. Predicted to be located in cytosol and nucleoplasm. Predicted to be active in glutamatergic synapse; membrane; and postsynaptic endocytic zone. Is expressed in several structures, including central nervous system; dorsal root ganglion; eye; limb; and skeleton. Orthologous to human SH3GLB2 (SH3 domain containing GRB2 like, endophilin B2).
MGI Description
PHENOTYPE: Mice homozygous for a knock-out allele are born at normal expected Mendelian ratios and appear indistinguishable from wild-type controls. In vitro, mouse embryonic fibroblasts exhibit impaired endosomal trafficking, autophagic flux, and influenza A viral RNA nuclear entry and replication. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR14167
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)
      Allele symbol
      Transgenic construct
      Expressed components
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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

          Sh3glb2 molecule type
          Interactor gene
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            Genetic Interactions

            Sh3glb2 role
            Sh3glb2 genetic perturbation
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