Symbol
| FRAS1
| contributors: mct/npt/pgu - updated : 16-03-2013
|
HGNC name
| Fraser syndrome 1
|
HGNC id
| 19185
|
corresponding disease(s)
|
FRAS1
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
| germinal mutation
|  
|  
|  
|
in isolated Congenital anomalies of the kidney and urinary tract (CAKUT)  | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| blebbed (Bl)mouse with perturbations of the composition of the extracellular space underlying epithelium is the murine model of human Fraser syndrome |