KEGG   VARIANT: 388698v1
Entry
388698v1                      Variant                              
Name
FLG2 mutation
Type
Loss of function
Gene
FLG2  filaggrin-2 [KO:K10384]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 616284
Network
nt06545  Cornified envelope formation
Disease
H00737  Peeling skin syndrome
Reference
  Authors
Alfares A, Al-Khenaizan S, Al Mutairi F
  Title
Peeling skin syndrome associated with novel variant in FLG2 gene.
  Journal
Am J Med Genet A 173:3201-3204 (2017)
DOI:10.1002/ajmg.a.38468
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