Gene data
IRF4- Name
- interferon regulatory factor 4
- Type
- protein-coding
- Position
- 391,739–411,443 (+)
- Aliases
- IMD131, LSIRF, MUM1, NF-EM5, SHEP8
- Ensembl
- ENSG00000137265
- RefSeq RNA
- NM_001195286.2, NM_002460.4, NR_036585.1, NR_046000.3, XM_006715090.3
- RefSeq protein
- NP_001182215.1, NP_002451.2, XP_006715153.1, XP_047274686.1, XP_054211324.1
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].
Gene Ontology
Biological process
Molecular function
Cellular component
Pathways
via MyGene.info
Gene · Ensembl
interferon regulatory factor 4
- Symbol
- IRF4
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 6:391,739-411,443
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Protein IRF4 PDB 2dll.png
Show 9 more facts
- HomoloGene ID
- 1842
- found in taxon
- Homo sapiens
- genetic association
- progressive supranuclear palsy
- exact match
- identifiers.org/ncbigene/3662
- genomic end
- 411443
- genomic start
- 391739
- chromosome
- human chromosome 6
- cytogenetic location
- 6p25.3
- expressed in
- superficial temporal artery
Sources (8)
via Wikidata · CC0