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  Domain Name: Kinesin
Kinesin motor domain.
No pairwise interactions found for the domain Kinesin

Total Mutations Found: 81
Total Disease Mutations Found: 26
This domain occurred 42 times on human genes (77 proteins).



  ACROCALLOSAL SYNDROME
  BARDET-BIEDL SYNDROME (BBS)
  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1
  CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 (1 FAMILY)
  CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3
  FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1
  MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
  MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL
  RETARDATION
  SPASTIC PARAPLEGIA 10
  SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY
  SPASTIC PARAPLEGIA 10 WITH PERIPHERAL NEUROPATHY
  SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE
  SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Kinesin





















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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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