Your search for "kif21a" returned 354 TaqMan® SNP Genotyping Assays
kinesin family member 21A
This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
CFEOM1, FEOM1, FEOM3A, KIF21A
(Human) Q7Z4S6, (Human) A8MX28, (Human) B0I1R9, (Human) B9EGE4, (Human) F5H0C3, (Human) F5H219, (Human) Q2UVF1, (Human) Q6UKL9, (Human) Q7Z668, (Human) Q86WZ5, (Human) Q8IVZ8, (Human) Q9C0F5, (Human) Q9NXU4, (Human) Q9Y590, (Mouse) Q9QXL2, (Mouse) Q6P5H1, (Mouse) Q6ZPJ8, (Mouse) Q8BWZ9, (Mouse) Q8BXF1
Please enter the information below and press OK to send your cart to Core Services for purchase.