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FLASH GENE
Symbol NFKBIL1 contributors: mct/npt - updated : 27-08-2013
HGNC name nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1
HGNC id 7800
EXPRESSION
Type widely
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Digestiveintestinesmall intestine   
Endocrineneuroendocrinepituitary   
 pancreas   highly
Reproductivemale systemprostate   
Respiratoryrespiratory tractlarynx  highly
Urinarykidney    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Connective    
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
HOMOLOGY
Homologene
FAMILY nuclear I&
954;appaB family
CATEGORY transcription factor
SUBCELLULAR LOCALIZATION     intracellular
intracellular,cytoplasm,cytosolic
intracellular,nucleus
basic FUNCTION
  • nuclear transcription factor of kappa light chain gene enhancer in B cells
  • inhibitor of REL/NFKB transcription factors
  • (NF-kappa B) inhibitor, sequestering it in the cytoplasm, also inhibiting NF-kappa B DNA binding
  • influences the risk of developing systemic lupus erythematosus and primary Sjögren's syndrome
  • affected the pathogenesis of rheumatoid arthritis at least in part through the regulation of dendritic cells functions
  • functions in the nucleus and controls various inflammatory responses including autoimmune arthritis
  • CELLULAR PROCESS nucleotide, transcription
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • may interact with members of the NF-kappaB/Rel family (Castiblanco 2008)
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Susceptibility
  • rheumatoid arthritis
  • to systemic lupus erythematosus (SLE)and Sjögren's syndrome (SS)
  • to the development of chronic Chagas' cardiomyopathy among Trypanosoma cruzi-infected individuals (CCC)
  • Variant & Polymorphism SNP
  • 96452(T/A) increase the risk of rheumatoid arthritis
  • +738C allele was associated with a more than twofold and threefold increase in the risk of SLE and SS respectively, relative to the +738T allele (Castiblanco 2008)
  • -262A -62A was prevalent in patients with CCC (Ramasawmy 2008)
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS