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HMGN1 high mobility group nucleosome binding domain 1 [ Homo sapiens (human) ]

Gene ID: 3150, updated on 11-Apr-2024

Summary

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Official Symbol
HMGN1provided by HGNC
Official Full Name
high mobility group nucleosome binding domain 1provided by HGNC
Primary source
HGNC:HGNC:4984
See related
Ensembl:ENSG00000205581 MIM:163920; AllianceGenome:HGNC:4984
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HMG14
Summary
The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMG17, the encoded protein may help maintain an open chromatin configuration around transcribable genes. [provided by RefSeq, Aug 2011]
Expression
Ubiquitous expression in bone marrow (RPKM 44.3), lymph node (RPKM 41.2) and 25 other tissues See more
Orthologs
mouse all
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Genomic context

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Location:
21q22.2
Exon count:
8
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (39342315..39349088, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (37726869..37733757, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (40714241..40721014, complement)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene bromodomain and WD repeat domain containing 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13326 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:40686351-40687046 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr21:40687047-40687741 Neighboring gene BRWD1 antisense RNA 2 Neighboring gene BRWD1 antisense RNA 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr21:40704110-40704610 Neighboring gene small nucleolar RNA U13 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13327 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 18467 Neighboring gene uncharacterized LOC105372804 Neighboring gene ReSE screen-validated silencer GRCh37_chr21:40723570-40723774 Neighboring gene ReSE screen-validated silencer GRCh37_chr21:40731973-40732197 Neighboring gene ring finger protein 6 pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. Shaking up the silence: consequences of HMGN1 antagonizing PRC2 in the Down syndrome brain. Farley SJ, et al. Epigenetics Chromatin, 2022 Dec 3. PMID 36463299, Free PMC Article
  2. High-mobility group nucleosome binding domain 1 (HMGN1) functions as a Th1-polarizing alarmin. Yang D, et al. Semin Immunol, 2018 Aug. PMID 29503123
  3. High-mobility group nucleosome-binding protein 1 is a novel clinical biomarker in non-small cell lung cancer. Wei F, et al. Tumour Biol, 2015 Dec. PMID 26113410
  4. Genomic profiling of HMGN1 reveals an association with chromatin at regulatory regions. Cuddapah S, et al. Mol Cell Biol, 2011 Feb. PMID 21173166, Free PMC Article
  5. HMGN1 modulates estrogen-mediated transcriptional activation through interactions with specific DNA-binding transcription factors. Zhu N, et al. Mol Cell Biol, 2007 Dec. PMID 17938209, Free PMC Article

See all (92) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Shaking up the silence: consequences of HMGN1 antagonizing PRC2 in the Down syndrome brain.
    Title: Shaking up the silence: consequences of HMGN1 antagonizing PRC2 in the Down syndrome brain.
  2. Spatial and Temporal Expression of High-Mobility-Group Nucleosome-Binding (HMGN) Genes in Brain Areas Associated with Cognition in Individuals with Down Syndrome.
    Title: Spatial and Temporal Expression of High-Mobility-Group Nucleosome-Binding (HMGN) Genes in Brain Areas Associated with Cognition in Individuals with Down Syndrome.
  3. Transcriptional amplification downstream of HMGN1 is enriched for stage-specific programs of B cells and B cell acute lymphoblastic leukemia, dependent on the developmental cellular context.
    Title: Trisomy of a Down Syndrome Critical Region Globally Amplifies Transcription via HMGN1 Overexpression.
  4. Studies indicate that high mobility group nucleosome binding domain 1 (HMGN1) preferentially promotes Th1-type immunity, which makes it relevant for the fields of vaccinology, autoimmunity, and oncoimmunology [Review].
    Title: High-mobility group nucleosome binding domain 1 (HMGN1) functions as a Th1-polarizing alarmin.
  5. HMGN1 and HMGN 2 remodel core and linker histone tail domains within chromatin.
    Title: HMGN1 and 2 remodel core and linker histone tail domains within chromatin.
  6. RNA-seq evidence of biallelic expression of HMGN1 and 10 neighboring genes in at least one primary human tissue tested indicates that the expression of HMGN1 is uncoupled from the control of the maternally inherited 5mCpG imprints at the WRB differentially methylated region (DMR) in disomic controls or trisomy (Down syndrome) individuals.
    Title: Trisomy 21 Alters DNA Methylation in Parent-of-Origin-Dependent and -Independent Manners.
  7. HMGN1 can serve as a useful clinical parameter for evaluating disease progression and predicting the outcomes for early-stage patients with non-small cell lung cancer .
    Title: High-mobility group nucleosome-binding protein 1 is a novel clinical biomarker in non-small cell lung cancer.
  8. nucleosome binding protein HMGN1 as a new PCNA-interacting protein that enhances the binding of PCNA to chromatin
    Title: The nucleosome binding protein HMGN1 interacts with PCNA and facilitates its binding to chromatin.
  9. extracellular HMGN1 acts as a novel alarmin critical for LPS-induced development of innate and adaptive immune responses.
    Title: High-mobility group nucleosome-binding protein 1 acts as an alarmin and is critical for lipopolysaccharide-induced immune responses.
  10. HMGN1 regulates the expression of methyl CpG-binding protein 2 (MECP2) in mouse and human, and affects the behavior of mice
    Title: The chromatin-binding protein HMGN1 regulates the expression of methyl CpG-binding protein 2 (MECP2) and affects the behavior of mice.
Submit: New GeneRIF Correction See all GeneRIFs (18)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

HIV-1 interactions

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Protein interactions

Protein Gene Interaction Pubs
Tat tat HIV-1 Tat specifically associates with HMGN1 promoter to upregulate HMGN1 expression in T cells PubMed

Go to the HIV-1, Human Interaction Database

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • FLJ27265, FLJ31471, MGC104230, MGC117425

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables DNA binding TAS
Traceable Author Statement
more info
 PubMed 
enables chromatin binding IBA
Inferred from Biological aspect of Ancestor
more info
  
enables nucleosomal DNA binding IEA
Inferred from Electronic Annotation
more info
  
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
Process Evidence Code Pubs
involved_in chromatin organization IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in positive regulation of DNA-templated transcription, elongation TAS
Traceable Author Statement
more info
 PubMed 
involved_in post-embryonic camera-type eye morphogenesis IEA
Inferred from Electronic Annotation
more info
  
involved_in pyrimidine dimer repair by nucleotide-excision repair IEA
Inferred from Electronic Annotation
more info
  
involved_in regulation of development, heterochronic IEA
Inferred from Electronic Annotation
more info
  
involved_in regulation of epithelial cell proliferation IEA
Inferred from Electronic Annotation
more info
  
involved_in regulation of transcription by RNA polymerase II IEA
Inferred from Electronic Annotation
more info
  
involved_in response to UV-B IEA
Inferred from Electronic Annotation
more info
  
involved_in response to UV-C IEA
Inferred from Electronic Annotation
more info
  
involved_in transcription-coupled nucleotide-excision repair IEA
Inferred from Electronic Annotation
more info
  
Component Evidence Code Pubs
part_of chromatin IEA
Inferred from Electronic Annotation
more info
  
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
  
located_in female germ cell nucleus IEA
Inferred from Electronic Annotation
more info
  
located_in nucleoplasm IDA
Inferred from Direct Assay
more info
  
located_in nucleoplasm TAS
Traceable Author Statement
more info
  
located_in nucleus HDA PubMed 
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
  

General protein information

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Preferred Names
non-histone chromosomal protein HMG-14
Names
high mobility group nucleosome-binding domain-containing protein 1
high-mobility group (nonhistone chromosomal) protein 14
high-mobility group nucleosome binding 1
nonhistone chromosomal protein HMG-14

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_004965.7 → NP_004956.5  non-histone chromosomal protein HMG-14

    See identical proteins and their annotated locations for NP_004956.5

    Status: REVIEWED

    Source sequence(s)
    AL582106, BC070154, BE779939
    Consensus CDS
    CCDS33559.1
    UniProtKB/Swiss-Prot
    P05114, Q3KQR8
    UniProtKB/TrEMBL
    Q6NSG7
    Related
    ENSP00000370125.5, ENST00000380749.10
    Conserved Domains (1) summary
    pfam01101
    Location:1 → 94
    HMG14_17; HMG14 and HMG17

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000021.9 Reference GRCh38.p14 Primary Assembly

    Range
    39342315..39349088 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_047440757.1 → XP_047296713.1  non-histone chromosomal protein HMG-14 isoform X1

  2. XM_047440758.1 → XP_047296714.1  non-histone chromosomal protein HMG-14 isoform X1

    Related
    ENST00000492280.5

  3. XM_024452071.2 → XP_024307839.1  non-histone chromosomal protein HMG-14 isoform X1

    UniProtKB/TrEMBL
    Q96N32

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    37726869..37733757 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054324457.1 → XP_054180432.1  non-histone chromosomal protein HMG-14 isoform X2

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
P05114.3 GenPept UniProtKB/Swiss-Prot:P05114

Gene LinkOut

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