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FLASH GENE
Symbol KIF21A contributors: mct/npt - updated : 13-12-2017
HGNC name kinesin family member 21A
HGNC id 19349
ASSOCIATED DISORDERS
corresponding disease(s) FEOM1
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
in congenital fibrosis of the extraocular muscles phenotypes 3(FEOM3), rare cause
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS