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Protein Coding Gene : Camsap2 calmodulin regulated spectrin-associated protein family, member 2
Primary Identifier  MGI:1922434 Organism  mouse, laboratory
Chromosome  1 NCBI Gene Number  67886
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables microtubule minus-end binding activity. Involved in regulation of organelle organization. Located in ciliary basal body and microtubule minus-end. Is expressed in jaw bone; liver; lung; nervous system; and neural retina. Orthologous to human CAMSAP2 (calmodulin regulated spectrin associated protein family member 2).
PHENOTYPE: Mice homozygous for a knockout allele exhibit postnatal growth retardation, decreased body and brain size, and abnormal dendrite morphology. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 4930541M15 gene,
  • RIKEN cDNA 1600013L13 gene,
  • calmodulin regulated spectrin-associated protein 1-like 1,
  • 1600013L13Rik,
  • Camsap2,
  • calmodulin regulated spectrin-associated protein family, member 2,
  • 4930541M15Rik,
  • Camsap1l1,
  • mKIAA1078,
  • MGI:1915136
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3 Involved In Mutations

Trail: ProteinCodingGene

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