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FLASH GENE
Symbol DYX1C1 contributors: mct/npt - updated : 15-11-2014
HGNC name dyslexia susceptibility 1 candidate 1
HGNC id 21493
ASSOCIATED DISORDERS
corresponding disease(s) ICS26
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation     loss of function
caused a severe ciliary motility defect associated with absent axonemal outer and inner dynein arms (ODAs and IDAs) structures
Susceptibility to dyslexia (DYX1)
Variant & Polymorphism
Candidate gene for susceptibility to dyslexia
Marker
Therapy target
ANIMAL & CELL MODELS