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FLASH GENE
Symbol CEP170 contributors: mct - updated : 27-04-2014
HGNC name centrosomal protein 170kDa
HGNC id 28920
EXPRESSION
Type widely
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Cardiovascularheart    
Nervousbrain    
Respiratorylung    
Urinarykidney    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Muscularstriatumskeletal  
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
one LISH domain
conjugated PhosphoP
HOMOLOGY
interspecies homolog to Xenopus APC
ortholog to murine Cep170
Homologene
FAMILY forkhead-associated (FHA) family
CATEGORY DNA associated
SUBCELLULAR LOCALIZATION     intracellular
intracellular,cytoplasm,cytoskeleton,microtubule,centrosome
intracellular,cytoplasm,cytoskeleton,microtubule,mitotic spindle
text
  • associates with centrosomes during interphase and with spindle microtubules during mitosis
  • basic FUNCTION
  • may be playing a role in the maintenance of the fundamental structure of the fibrillar center and dense fibrillar component in the nucleolus
  • ZBTB18 is implicated with CEP170 as novel genes causative for corpus callosal abnormalities in patients with a terminal 1q deletion
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • DKC1
  • fibrillarin
  • physiological substrate of PLK1 )
  • binding partner of WDR62, which is of interest given the involvement of other centrosomal proteins in microcephaly
  • CEP170 and CEP170B (KIAA0284) are specifically associating with KIF2B
  • TBK1 binds to the centrosomal protein CEP170 and to the mitotic apparatus protein NUMA1, and both CEP170 and NUMA1 are TBK1 substrates
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
  • marker for maternal centrioles important to elucidate the pathogenesis of numerical centriole aberrations in tumor cells
  • Therapy target
    ANIMAL & CELL MODELS