IRF4

GENERAL INFORMATION

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Gene name

IRF4

Gene description

Interferon regulatory factor 4

Protein class

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

Predicted localization

Intracellular

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (tonsil)
GTEx:Tissue enhanced (cervix, uterine, spleen)

Protein evidence

Evidence at protein level

Protein localization

Selective nuclear expression in a subset of lymphoid cells.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 3 antibodies.
HPA002038 , HPA002698 , CAB013508
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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

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (tonsil)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cervix, uterine, spleen)

Organ

Expression



GENE INFORMATION

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Gene name

IRF4 (HGNC Symbol)

Synonyms

LSIRF, MUM1

Description

Interferon regulatory factor 4 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene belongs to the IRF (interferon regulatory factor) family of transcription factors, characterized by an unique tryptophan pentad repeat DNA-binding domain. The IRFs are important in the regulation of interferons in response to infection by virus, and in the regulation of interferon-inducible genes. This family member is lymphocyte specific and negatively regulates Toll-like-receptor (TLR) signaling that is central to the activation of innate and adaptive immune systems. A chromosomal translocation involving this gene and the IgH locus, t(6;14)(p25;q32), may be a cause of multiple myeloma. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2010]

Chromosome

6

Cytoband

p25.3

Chromosome location (bp)

391739 - 411447

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000137265 (version 78.38)

Entrez gene

3662

UniProt

Q15306 (UniProt - Evidence at protein level)

neXtProt

NX_Q15306

Antibodypedia

IRF4 antibodies


PROTEIN BROWSER

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ENST00000380956
 
 
 
 


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)

IRF4-001 ENSP00000370343
ENST00000380956
Q15306
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