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FLASH GENE
Symbol KIF1B contributors: mct/pgu - updated : 13-04-2017
HGNC name kinesin family member 1B
HGNC id 16636
ASSOCIATED DISORDERS
corresponding disease(s) CMT2A1
related resource Mutation Database of Inherited Peripheral Neuropathies
KinMutBase: A registry of disease causing mutations in tyrosine kinase domains
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
tumoral     --over  
in favorable subset of primary neuroblastoma
tumoral     --low  
in unfavorable subset of primary neuroblastoma
Susceptibility
  • to multiple sclerosis
  • to hepatitis B virus (HBV)-related hepatocellular carcinoma
  • Variant & Polymorphism SNP
  • variant rs10492972 (SNP located in intron 5) associated to multiple sclerosis
  • intronic SNP (rs17401966) highly associated with HBV-related HCC (
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS