Symbol
| FGF13
| contributors: mct - updated : 27-10-2018
|
HGNC name
| fibroblast growth factor 13
|
HGNC id
| 3670
|
corresponding disease(s)
|
EIEE92
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
| deletion
|  
|  
|
deletion encompassed only one gene, FGF13, in Wildervanck Syndrome | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| deletion of Fgf13 in mice results in neuronal migration defects in both the neocortex and the hippocampus, and Fgf13-deficient mice also exhibit weakened learning and memory |