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KIF21A

Official Full Name
kinesin family member 21A
Organism
Homo sapiens
GeneID
55605
Background
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]
Synonyms
FEOM1; CFEOM1; FEOM3A;

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