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Protein Coding Gene : Klc2 kinesin light chain 2
Primary Identifier  MGI:107953 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  16594
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables kinesin binding activity. Acts upstream of or within axo-dendritic transport. Located in ciliary rootlet; cytosol; and neuron projection. Part of kinesin complex. Used to study nonsyndromic deafness. Human ortholog(s) of this gene implicated in SPOAN syndrome. Orthologous to human KLC2 (kinesin light chain 2).
PHENOTYPE: Mice homozygous for a null allele display outer hair cell loss and hearing loss with age. [provided by MGI curators]
  • synonyms:
  • MGI:2147719,
  • expressed sequence AW212649,
  • MGI:2447825,
  • 8030455F02Rik,
  • RIKEN cDNA 8030455F02 gene,
  • Klc2,
  • MGD-MRK-36533,
  • AW212649,
  • kinesin light chain 2
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Disease

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