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FLASH GENE
Symbol FRAS1 contributors: mct/npt/pgu - updated : 16-03-2013
HGNC name Fraser syndrome 1
HGNC id 19185
ASSOCIATED DISORDERS
corresponding disease(s) FRAS1
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
in isolated Congenital anomalies of the kidney and urinary tract (CAKUT)
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
blebbed (Bl)mouse with perturbations of the composition of the extracellular space underlying epithelium is the murine model of human Fraser syndrome