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Protein Coding Gene : Golga1 golgin A1
Primary Identifier  MGI:1924149 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  76899
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Located in perinuclear region of cytoplasm and trans-Golgi network. Is expressed in embryo. Orthologous to human GOLGA1 (golgin A1).
PHENOTYPE: Homozygous mice exhibit tremors and limb grasping behavior at two months of age. A variable severity of hearing loss was also seen. [provided by MGI curators]
  • synonyms:
  • ages with abnormal gait,
  • expressed sequence AW107649,
  • MGI:1919627,
  • golgin-97,
  • 0710001G09Rik,
  • golgin A1,
  • RIKEN cDNA 2210418B03 gene,
  • 2210418B03Rik,
  • awag,
  • AW107649,
  • RIKEN cDNA 0710001G09 gene,
  • MGI:2139296,
  • Golga1,
  • MGI:3510599,
  • Golgi97
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Disease

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