Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol LGI4 contributors: mct/npt - updated : 10-05-2017
HGNC name leucine-rich repeat LGI family, member 4
HGNC id 18712
ASSOCIATED DISORDERS
corresponding disease(s) LCCS12
Susceptibility
  • to benign familial infantile convulsions (BFIC) and idiopathic generalized epilepsy
  • Variant & Polymorphism other
  • c.1914GC --> AT polymorphism, associated to benign familial infantile convulsions (BFIC) and idiopathic generalized epilepsy (Gu 2004)
  • c.1722G/A polymorphism might contribute to the susceptibility to BFIC
  • Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    neurologyleukoencephalopathy 
    may be regarded as a novel therapeutic target to stimulate myelination
    ANIMAL & CELL MODELS
  • Lgi4-deficient mice exhibited a more severe phenotype than claw paw mice and had gliogenic defects in sensory, sympathetic, and enteric ganglia