Gene

Golga2

Species
Mus musculus
Symbol
Golga2
Name
golgin A2
Synonyms
  • AW555139
  • expressed sequence AW555139
Biotype
protein coding gene
Automated Description
Enables importin-alpha family protein binding activity. Involved in asymmetric cell division and meiotic spindle assembly. Acts upstream of or within Golgi localization and positive regulation of axonogenesis. Located in Golgi apparatus; perinuclear region of cytoplasm; and spindle pole. Is expressed in several structures, including brain; eye; gonad; musculoskeletal system; and unsegmented mesenchyme. Orthologous to human GOLGA2 (golgin A2).
MGI Description
PHENOTYPE: Homozygotes for a null allele show premature death, developmental delay, ataxia, Purkinje neuron loss, and male infertility with globozoospermia and lack of acrosome formation. Homozygotes for a different null allele show partial prenatal lethality and autophagy-induced liver and lung fibrosis. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR10881
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

          Golga2 molecule type
          Interactor gene
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            Genetic Interactions

            Golga2 role
            Golga2 genetic perturbation
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