NFKBIA

GENERAL INFORMATION

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Gene name

NFKBIA

Gene description

Nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha

Protein class

Cancer-related genes
Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in essentially all cells except in squamous epithelial cells, liver and stroma cells.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA029207 , CAB003815
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Urinary bladder

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

NFKBIA (HGNC Symbol)

Synonyms

IkappaBalpha, IKBA, MAD-3, NFKBI

Description

Nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (HGNC Symbol)

Entrez gene summary

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]

Chromosome

14

Cytoband

q13.2

Chromosome location (bp)

35401511 - 35404749

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000100906 (version 78.38)

Entrez gene

4792

UniProt

P25963 (UniProt - Evidence at protein level)

neXtProt

NX_P25963

Antibodypedia

NFKBIA antibodies


PROTEIN BROWSER

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ENST00000216797
 
ENST00000553342
 
ENST00000557140
 
ENST00000557389
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

NFKBIA-001 ENSP00000216797
ENST00000216797
P25963
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Show » Show » 317 35.6 No 0
NFKBIA-002 ENSP00000451257
ENST00000557140
G3V3I4
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Show » Show » 274 30.9 No 0
NFKBIA-004 ENSP00000450514
ENST00000557389
G3V286
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Show » Show » 227 25 No 0
NFKBIA-011 ENSP00000451281
ENST00000553342
G3V3K1
Show all »
Show » 69 8.1 No 0