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FLASH GENE
Symbol FXR1 contributors: mct/npt - updated : 23-06-2015
HGNC name fragile X mental retardation, autosomal homolog 1
HGNC id 4023
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional     --other  
altered expression in FSHMD1A myoblasts may contribute to the physiopathology of this disease (Davidovic 2008)
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS