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FLASH GENE
Symbol FLG contributors: mct/npt/pgu - updated : 16-05-2018
HGNC name filaggrin
HGNC id 3748
EXPRESSION
Type restricted
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Reproductivefemale systemuterus   
 female systembreastmammary gland  
 male systemtestis   
Skin/Tegumentskin    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Epithelialbarrier/liningepidermisstratum corneum  Homo sapiens
cells
SystemCellPubmedSpeciesStageRna symbol
Skin/Tegumentkeratinocyte Homo sapiens
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
HOMOLOGY
Homologene
FAMILY
  • S100-fused protein family
  • CATEGORY structural protein
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,cytoskeleton,intermed filament
    basic FUNCTION
  • aggregating keratin filaments and promoting disulfite-bonding
  • integral part of the epidermis that plays a key role in engineering and maintaining the barrier function
  • having a key role in maintaining an effective skin barrier against the external environment
  • possible genetic modifier in other genodermatoses
  • FLG and FLG2 display a related structural organization, an identical pattern of expression and localization in epidermis, and proteolytic processing of a large precursor
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
  • constituent of the epidermal differentiation complex (EDC@)
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
    cell & other
  • intermediate filament associated protein (IFAP type I)
  • REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) IVLG
    Susceptibility
  • to atopic dermatis, for the extrinsic subtype of AD, and with concomitant respiratory allergic diseases
  • Variant & Polymorphism other
  • R510X and 2282del4 are very strong predisposing factors for atopic dermatitis
  • four prevalent mutations (R501X, 2282del4, R2447X and S3247X)strongly associated to atopic dermatis
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS