HMG20A
High mobility group protein 20A
Also known as: FLJ10739, HM20A_HUMAN, HMGX1, HMGXB1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NP66
- Gene
- HMG20A
- Ensembl
- ENSG00000140382
- Chromosome
- 15
- Canonical length
- 347 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables identical protein binding activity. Predicted to be involved in regulation of gene expression. Predicted to act upstream of or within negative regulation of neuron differentiation; negative regulation of protein sumoylation; and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
347 residues, UniProt reviewed canonical sequence.
>Q9NP66|HMG20A
1 MENLMTSSTL PPLFADEDGS KESNDLATTG LNHPEVPYSS GATSSTNNPE FVEDLSQGQL
61 LQSESSNAAE GNEQRHEDEQ RSKRGGWSKG RKRKKPLRDS NAPKSPLTGY VRFMNERREQ
121 LRAKRPEVPF PEITRMLGNE WSKLPPEEKQ RYLDEADRDK ERYMKELEQY QKTEAYKVFS
181 RKTQDRQKGK SHRQDAARQA THDHEKETEV KERSVFDIPI FTEEFLNHSK AREAELRQLR
241 KSNMEFEERN AALQKHVESM RTAVEKLEVD VIQERSRNTV LQQHLETLRQ VLTSSFASMP
301 LPGSGETPTV DTIDSYMNRL HSIILANPQD NENFIATVRE VVNRLDRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HMG20A 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)
- 0.5
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- spleen: 34 nTPM
- thymus: 29 nTPM
- skeletal muscle: 26 nTPM
- tongue: 25 nTPM
- retina: 24 nTPM
- lymph node: 24 nTPM
Single-cell type
- myonuclei: 199 nCPM
- sertoli cells: 139 nCPM
- late spermatids: 129 nCPM
- choroid plexus epithelial cells: 117 nCPM
- cardiomyocytes: 109 nCPM
- adrenal cortex cells: 101 nCPM
Immune cell
- NK-cell: 49 nTPM
- MAIT T-cell: 35 nTPM
- memory B-cell: 31 nTPM
- naive CD4 T-cell: 31 nTPM
- gdT-cell: 29 nTPM
- myeloid DC: 28 nTPM
Brain region
- cerebral cortex: 54 nTPM
- white matter: 52 nTPM
- thalamus: 50 nTPM
- cerebellum: 50 nTPM
- hypothalamus: 50 nTPM
- basal ganglia: 48 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)
- 0.43
- gnomAD pLI
- 0.68
- gnomAD missense Z
- 1.41
- DepMap mean gene effect
- -0.03
- 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
- chromatin organization
- negative regulation of neuron differentiation
- negative regulation of protein sumoylation
- negative regulation of transcription by RNA polymerase II
- regulation of DNA-templated transcription
- regulation of gene expression
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HMG20A 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 HMG20A as an antibody target. Whether an autoantibody or antibody against HMG20A could matter depends on whether native HMG20A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HMG20A 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 HMG20A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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