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  Domain Name: KIP1
Kinesin-like protein [Cytoskeleton]
No pairwise interactions found for the domain KIP1

Total Mutations Found: 146
Total Disease Mutations Found: 51
This domain occurred 39 times on human genes (73 proteins).



  ACROCALLOSAL SYNDROME
  ACROCALLOSAL SYNDROME (ACLS)
  BARDET-BIEDL SYNDROME (BBS)
  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1
  CONGENITAL FIBROSIS OF EXTRAOCULAR MUSCLES 1 (CFEOM1)
  CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 (1 FAMILY)
  CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3
  FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1
  HYDROLETHALUS SYNDROME 2 (HLS2)
  MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
  MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL
  MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION (MCLMR)
  PALLISTER-HALL SYNDROME (PHS)
  RETARDATION
  SPASTIC PARAPLEGIA 10
  SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY
  SPASTIC PARAPLEGIA 10 WITH PERIPHERAL NEUROPATHY
  SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT (SPG10)
  SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE
  SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (SPG30)
  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 KIP1




























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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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