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FLASH GENE
Symbol FGF13 contributors: mct - updated : 27-10-2018
HGNC name fibroblast growth factor 13
HGNC id 3670
ASSOCIATED DISORDERS
corresponding disease(s) EIEE92
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   deletion    
deletion encompassed only one gene, FGF13, in Wildervanck Syndrome
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
  • 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