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Protein Coding Gene : Stard9 StAR related lipid transfer domain containing 9
Primary Identifier  MGI:3045258 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  668880
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable microtubule binding activity and microtubule motor activity. Predicted to be involved in spindle assembly. Predicted to be located in cytoskeleton. Predicted to be active in centriole; cytoplasm; and nucleus. Orthologous to human STARD9 (StAR related lipid transfer domain containing 9).
PHENOTYPE: Mice homozygous for a null allele exhibit Purkinje cell degeneration associated with tremors, ataxia, loss of grip strength, and abnormal gait. [provided by MGI curators]
  • synonyms:
  • kinesin family member 16A,
  • 4831403C07Rik,
  • E230025N21Rik,
  • Stard9,
  • MGI:2444446,
  • Kif16a,
  • mKIAA1300,
  • RIKEN cDNA E230025N21 gene,
  • StAR related lipid transfer domain containing 9,
  • N-3 kinesin,
  • MGI:1098241,
  • RIKEN cDNA 4831403C07 gene
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2 Involved In Mutations

Trail: ProteinCodingGene

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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