IER5
Immediate early response gene 5 protein
Also known as: IER5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VY09
- Gene
- IER5
- Ensembl
- ENSG00000162783
- Chromosome
- 1
- Canonical length
- 327 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein that is similar to other immediate early response proteins. In the mouse, a similar gene may play an important role in mediating the cellular response to mitogenic signals. Studies in rats found the expression of a similar gene to be increased after waking and sleep deprivation. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
327 residues, UniProt reviewed canonical sequence.
>Q5VY09|IER5
1 MEFKLEAHRI VSISLGKIYN SRVQRGGIKL HKNLLVSLVL RSARQVYLSD PCPGLYLAGP
61 AGTPAPPPQQ QPGEPAAGPP AGWGEPPPPA ARASWPETEP QPERSSVSDA PRVGDEVPVA
121 TVTGVGDVFQ GGEADATEAA WSRVEGPRQA AAREAEGTAG GWGVFPEVSR AARRPCGCPL
181 GGEDPPGTPA ATPRAACCCA PQPAEDEPPA PPAVCPRKRC AAGVGGGPAG CPAPGSTPLK
241 KPRRNLEQPP SGGEDDDAEE METGNVANLI SIFGSSFSGL LRKSPGGGRE EEEGEESGPE
301 AAEPGQICCD KPVLRDMNPW STAIVAFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IER5 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.68
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 47 nTPM
- skeletal muscle: 32 nTPM
- spleen: 32 nTPM
- heart muscle: 27 nTPM
- esophagus: 26 nTPM
- lung: 22 nTPM
Single-cell type
- breast hormone-responsive cells: 285 nCPM
- cdc: 283 nCPM
- kupffer cells: 264 nCPM
- monocytes: 254 nCPM
- macrophages: 237 nCPM
- epididymal basal cells: 214 nCPM
Immune cell
- intermediate monocyte: 5.5 nTPM
- non-classical monocyte: 5.3 nTPM
- memory B-cell: 4.1 nTPM
- basophil: 3.6 nTPM
- naive B-cell: 3 nTPM
- eosinophil: 2.7 nTPM
Brain region
- cerebral cortex: 29 nTPM
- white matter: 16 nTPM
- choroid plexus: 13 nTPM
- hypothalamus: 12 nTPM
- hippocampal formation: 11 nTPM
- basal ganglia: 11 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.45
- gnomAD pLI
- 0.87
- gnomAD missense Z
- 0
- DepMap mean gene effect
- 0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to heat
- positive regulation of transcription by RNA polymerase II
- regulation of cell population proliferation
- positive regulation of cellular response to heat
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IER5 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IER5 as an antibody target. Whether an autoantibody or antibody against IER5 could matter depends on whether native IER5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IER5 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label IER5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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