HMGN4
High mobility group nucleosome-binding domain-containing protein 4
Also known as: HMG17L3, HMGN4_HUMAN, NHC
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00479
- Gene
- HMGN4
- Ensembl
- ENSG00000182952
- Chromosome
- 6
- Canonical length
- 90 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]
Canonical amino-acid sequenceUniProt
90 residues, UniProt reviewed canonical sequence.
>O00479|HMGN4
1 MPKRKAKGDA KGDKAKVKDE PQRRSARLSA KPAPPKPEPR PKKASAKKGE KLPKGRKGKA
61 DAGKDGNNPA KNRDASTLQS QKAEGTGDAKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HMGN4 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)
- 0.74
- Highest tissue expression
- 67 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 67 nTPM
- thymus: 66 nTPM
- lymph node: 64 nTPM
- smooth muscle: 62 nTPM
- parathyroid gland: 55 nTPM
- blood vessel: 55 nTPM
Single-cell type
- extravillous trophoblasts: 154 nCPM
- megakaryocytes: 142 nCPM
- decidual stromal cells: 114 nCPM
- syncytiotrophoblasts: 113 nCPM
- migrating cytotrophoblasts: 102 nCPM
- melanocytes: 93 nCPM
Immune cell
- basophil: 182 nTPM
- T-reg: 94 nTPM
- total PBMC: 92 nTPM
- memory CD8 T-cell: 86 nTPM
- memory CD4 T-cell: 85 nTPM
- eosinophil: 82 nTPM
Brain region
- choroid plexus: 40 nTPM
- hypothalamus: 27 nTPM
- white matter: 26 nTPM
- midbrain: 24 nTPM
- spinal cord: 24 nTPM
- medulla oblongata: 23 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)
- 1.86
- gnomAD pLI
- 0.32
- gnomAD missense Z
- 0.27
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HMGN4 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 HMGN4 as an antibody target. Whether an autoantibody or antibody against HMGN4 could matter depends on whether native HMGN4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HMGN4 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 HMGN4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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