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]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
KIF21A-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
KIF21A-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
KIF21A-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
KIF21A-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
KIF21A-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
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]
Gene Symbol : KIF21A
Gene Name : Kinesin family member 21A
Chromosome : CHR 12: 394,434,13-392,932,27
Locus : 12q12
Alt. Genes : KIF20A
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