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KIF1B

HGNC:16636 1p36.22 MIM.605995

Tuesday 20 December 2011

Pathology

- KIF1B germline mutations in

  • Charcot-Marie-Tooth disease, type 2A1 (CMT2A1) (MIM.118210)
  • predispositon to pheochromocytoma (MIM.171300)

- KIF1B variants in

  • susceptibility to neuroblastoma, type 1 (MIM.256700)