HMGN5
High mobility group nucleosome-binding domain-containing protein 5
Also known as: HMGN5_HUMAN, NSBP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P82970
- Gene
- HMGN5
- Ensembl
- ENSG00000198157
- Chromosome
- X
- Canonical length
- 282 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria
OverviewNCBI Gene
This gene encodes a nuclear protein with similarities to the high mobility group proteins, HMG14 and HMG17, which suggests that this protein may function as a nucleosomal binding and transcriptional activating protein. [provided by RefSeq, Sep 2009]
Canonical amino-acid sequenceUniProt
282 residues, UniProt reviewed canonical sequence.
>P82970|HMGN5
1 MPKRKAAGQG DMRQEPKRRS ARLSAMLVPV TPEVKPKRTS SSRKMKTKSD MMEENIDTSA
61 QAVAETKQEA VVEEDYNENA KNGEAKITEA PASEKEIVEV KEENIEDATE KGGEKKEAVA
121 AEVKNEEEDQ KEDEEDQNEE KGEAGKEDKD EKGEEDGKED KNGNEKGEDA KEKEDGKKGE
181 DGKGNGEDGK EKGEDEKEEE DRKETGDGKE NEDGKEKGDK KEGKDVKVKE DEKEREDGKE
241 DEGGNEEEAG KEKEDLKEEE EGKEEDEIKE DDGKKEEPQS IVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HMGN5 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
- 100 nTPM
Expression across tissuesHPA
Tissue
- testis: 100 nTPM
- epididymis: 62 nTPM
- spinal cord: 40 nTPM
- choroid plexus: 38 nTPM
- hypothalamus: 34 nTPM
- midbrain: 33 nTPM
Single-cell type
- sertoli cells: 410 nCPM
- epididymal principal cells: 214 nCPM
- epididymal efferent duct ciliated cells: 168 nCPM
- erythrocyte progenitors: 157 nCPM
- oocytes: 115 nCPM
- respiratory ciliated cells: 108 nCPM
Immune cell
- plasmacytoid DC: 10 nTPM
- naive CD4 T-cell: 8.7 nTPM
- gdT-cell: 7.6 nTPM
- naive CD8 T-cell: 7.6 nTPM
- MAIT T-cell: 6.6 nTPM
- naive B-cell: 6.1 nTPM
Brain region
- medulla oblongata: 36 nTPM
- thalamus: 31 nTPM
- white matter: 31 nTPM
- midbrain: 30 nTPM
- pons: 30 nTPM
- spinal cord: 30 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)
- 1.15
- gnomAD pLI
- 0.31
- gnomAD missense Z
- -0.15
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chromatin organization
- negative regulation of apoptotic process
- positive regulation of cell population proliferation
- positive regulation of DNA-templated transcription
- positive regulation of gene expression
- regulation of DNA-templated transcription
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- High mobility group protein HMGN
- HMG14 and HMG17
- High mobility group nucleosome-binding domain-containing protein 5
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HMGN5 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 HMGN5 as an antibody target. Whether an autoantibody or antibody against HMGN5 could matter depends on whether native HMGN5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HMGN5 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 HMGN5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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