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Results for the Protein: P52732
116242604

KIF11_HUMAN RecName: Full=Kinesin-like protein KIF11; AltName: Full=Kinesin-like protein 1; AltName: Full=Kinesin-like spindle protein HKSP; AltName: Full=Kinesin-related motor protein Eg5; AltName: Full=Thyroid receptor-interacting protein 5; Short=TR-interacting protein 5; Short=TRIP-5

Known Diseases associated with this Protein:
  MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL
  MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION (MCLMR)
  RETARDATION
7
1
3
0
5
Tips:
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Default View:

KIP1 - COG5059
KISc_C_terminal - cd01366
KISc_KHC_KIF5 - cd01369
KISc_BimC_Eg5 - cd01364
KISc_KLP2_like - cd01373
KISc_KIF3 - cd01371
KISc_KIF4 - cd01372
KISc_KIF1A_KIF1B - cd01365
KISc_KIF23_like - cd01368
KISc_KIF2_like - cd01367
KISc_KIF9_like - cd01375
KISc - smart00129
KISc_KID_like - cd01376
KISc - cd00106
KISc_KIP3_like - cd01370
KISc_CENP_E - cd01374
Motor_domain - cd01363
Kinesin - pfam00225


Swiss-Prot Protein: P52732
Identical to: NP_004514
   Default View:




















Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
KISc_C_terminalcd013661e-10315362
KISc_BimC_Eg5cd013641.3e-27416368
KISc_KHC_KIF5cd013699.4e-11316359
KISc_KIF1A_KIF1Bcd013651.3e-9717366
KISc_KIF2_likecd013673.3e-7317357
KISc_KIF23_likecd013682.2e-2017357
KISc_KIF3cd013713.4e-13417359
KISc_KLP2_likecd013738.4e-9317359
KISc_KIF4cd013727.5e-10117360
KISccd001061.7e-16418357
KISc_CENP_Ecd013741.5e-10818359
KISc_KIP3_likecd013704.2e-9118359
KISc_KID_likecd013761.1e-7018357
KISc_KIF9_likecd013752.9e-7618357
Motor_domaincd013631.8e-17121338
KIP1COG50599e-1061586
Kinesinpfam002257.7e-17524359
KIScsmart001291.8e-18418366

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
Swiss-ProtVAR_067830Diseasep.ARG234CYSMicrocephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)
Swiss-ProtVAR_067832Diseasep.ARG944CYSMicrocephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)
Swiss-ProtVAR_049682Polymorphismp.LEU1042PHEN/A
Swiss-ProtVAR_067829Diseasep.PHE144LEUMicrocephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)
Swiss-ProtVAR_067831Diseasep.SER235CYSMicrocephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)
OMIM148760.0003 Diseasep.ARG944CYSMICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL||RETARDATION
OMIM148760.0001 Diseasep.ARG387TERMICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL||RETARDATION
OMIM148760.0006 Diseasep.SER235CYSMICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL||RETARDATION



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