Gene: NFKBIA (nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha)  Homo sapiens

Symbol: NFKBIA
Name: nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
Description: This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: I-kappa-B-alpha; IkappaBalpha; ikB-alpha; IKBA; MAD-3; major histocompatibility complex enhancer-binding protein MAD3; NF-kappa-B inhibitor alpha; NFKBI; nuclear factor of kappa light chain gene enhancer in B-cells; nuclear factor of kappa light chain gene enhancer in b-cells inhibitor, alpha; OTTHUMP00000178842; OTTHUMP00000245015; OTTHUMP00000245885
Orthologs: Mus musculus : Nfkbia (nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha)  MGI
Rattus norvegicus : Nfkbia (nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11416,868,411 - 16,871,655-NCBI
Human Genome Assembly HuRef1415,984,422 - 15,987,685-NCBI
Human Genome Assembly GRCh371435,870,716 - 35,873,960-NCBI
Human Genome Assembly Build 361434,940,468 - 34,943,695-NCBI
Human Cytogenetic Map14q13 NCBI
Human Genome Assembly1434,940,467 - 34,943,695 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on NFKBIA
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 735440
Created: 2004-02-06
Species: Homo sapiens
Last Modified: 2013-05-14
Status: ACTIVE