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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

HMGN5 Gene

protein-coding   GIFtS: 46
GCID: GC0XM080370

High Mobility Group Nucleosome Binding Domain 5

(Previous names: nucleosomal binding protein 1, high-mobility group nucleosome...)
(Previous symbol: NSBP1)
  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
High Mobility Group Nucleosome Binding Domain 51 2     Nucleosome-Binding Protein 12 3
NSBP11 2 3 5     NBP-452
High-Mobility Group Nucleosome Binding Domain 51 2     High Mobility Group Nucleosome-Binding Domain-Containing Protein 52
Nucleosomal Binding Protein 11 2     

External Ids:    HGNC: 80131   Entrez Gene: 793662   Ensembl: ENSG000001981577   OMIM: 3003855   UniProtKB: P829703   

Export aliases for HMGN5 gene to outside databases

Previous GC identifers: GC0XM080255 GC0XM073949


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for HMGN5 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)

GeneCards Summary for HMGN5 Gene: 
HMGN5 (high mobility group nucleosome binding domain 5) is a protein-coding gene. Diseases associated with HMGN5 include clear cell renal cell carcinoma, and prostatitis. GO annotations related to this gene include chromatin binding and nucleosomal DNA binding.

UniProtKB/Swiss-Prot: HMGN5_HUMAN, P82970
Function: Preferentially binds to euchromatin and modulates cellular transcription by counteracting linker
histone-mediated chromatin compaction (By similarity)




(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000023.10  NC_018934.2  NT_011651.17  
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for HMGN5
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidHMGN5 promoter sequence
   Search SABiosciences Chromatin IP Primers for HMGN5

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat HMGN5


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: Xq13.3   Ensembl cytogenetic band:  Xq21.1   HGNC cytogenetic band: Xq13.3

HMGN5 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
HMGN5 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XM080370:  view genomic region     (about GC identifiers)

Start:
80,369,200 bp from pter      End:
80,457,441 bp from pter
Size:
88,242 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: HMGN5_HUMAN, P82970 (See protein sequence)
Recommended Name: High mobility group nucleosome-binding domain-containing protein 5  
Size: 282 amino acids; 31525 Da
Subcellular location: Nucleus. Note=Associates with nucleosomes in euchromatin and is largely excluded from
constitutive heterochromatin (By similarity)
Sequence caution: Sequence=AK094058; Type=Frameshift; Positions=132;
Secondary accessions: Q5JSL1

Explore the universe of human proteins at neXtProt for HMGN5: NX_P82970

Explore proteomics data for HMGN5 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_P82970

  • HMGN5 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    HMGN5 Protein Expression
    REFSEQ proteins: NP_110390.1  
    ENSEMBL proteins: 
     ENSP00000350848   ENSP00000408060   ENSP00000362347   ENSP00000399626   ENSP00000413402  
     ENSP00000404810  

    Human Recombinant Protein Products for HMGN5: 
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    Novus Biologicals HMGN5 Proteins
    Novus Biologicals HMGN5 Lysate
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Cloud-Clone Corp. Proteins for HMGN5 

    Gene Ontology (GO): 5 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000785chromatin IEA--
    GO:0005634nucleus NAS11161810
    GO:0005654nucleoplasm IEA--
    GO:0005730nucleolus IDA--
    GO:0043231intracellular membrane-bounded organelle IDA--

    HMGN5 for ontologies           About GeneDecksing



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    Cloud-Clone Corp. ELISAs for HMGN5 
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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    HMG: High-mobility group / Canonical

    1 InterPro protein domain:
     IPR000079 HMGN_fam

    Graphical View of Domain Structure for InterPro Entry P82970

    ProtoNet protein and cluster: P82970

    1 Blocks protein domain: IPB000079 High mobility group protein HMG14 and HMG17

    UniProtKB/Swiss-Prot: HMGN5_HUMAN, P82970
    Domain: Specifically targeted by its C-terminus to nucleosomes in euchromatin (By similarity)
    Similarity: Belongs to the HMGN family


    HMGN5 for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: HMGN5_HUMAN, P82970
    Function: Preferentially binds to euchromatin and modulates cellular transcription by counteracting linker
    histone-mediated chromatin compaction (By similarity)

         Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003682chromatin binding NAS11161810
    GO:0031492nucleosomal DNA binding IEA--
         
    HMGN5 for ontologies           About GeneDecksing


    Phenotypes:
         1 MGI mutant phenotype (inferred from 1 allele(MGI details for Hmgn5):
     no phenotypic analysis 

    HMGN5 for phenotypes           About GeneDecksing

    Animal Models:
         MGI mouse knock-out Hmgn5tm1Mbus for HMGN5

       inGenious Targeting Laboratory - Custom generated mouse model solutions for HMGN5 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for HMGN5

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for HMGN5 
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for HMGN5 

    miRNA
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    SwitchGear 3'UTR luciferase reporter plasmidHMGN5 3' UTR sequence
    Inhib. RNA
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    Gene Editing
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    Clone
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for HMGN5


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for HMGN5

    STRING Interaction Network Preview (showing 2 interactants - click image to see more details)

    2 Interacting proteins for HMGN5 (ENSP000003508484) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    CBX8ENSP000002693854STRING: ENSP00000269385
    SUMO2ENSP000004059654STRING: ENSP00000405965
    About this table

    Gene Ontology (GO): 5 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-dependent IEA--
    GO:0006355regulation of transcription, DNA-dependent NAS11161810
    GO:0006357regulation of transcription from RNA polymerase II promoter IEA--
    GO:0016568chromatin modification IEA--
    GO:0045893positive regulation of transcription, DNA-dependent NAS11161810

    HMGN5 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for HMGN5

    Search CenterWatch for drugs/clinical trials and news about HMGN5

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for HMGN5 gene: 
    NM_030763.2  

    Unigene Cluster for HMGN5:

    High mobility group nucleosome binding domain 5
    Hs.282204  [show with all ESTs]
    Unigene Representative Sequence: NM_030763
    7 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000358130(uc004eee.1) ENST00000447319 ENST00000373250 ENST00000430960
    ENST00000491275 ENST00000436386 ENST00000451455
    miRNA
    Products:
         
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    8/26 QIAGEN miScript miRNA Assays for microRNAs that regulate HMGN5 (see all 26):
    hsa-miR-142-5p hsa-miR-605 hsa-miR-938 hsa-miR-3133 hsa-miR-340 hsa-miR-548a-3p hsa-miR-3161 hsa-miR-3122
    SwitchGear 3'UTR luciferase reporter plasmidHMGN5 3' UTR sequence
    Inhib. RNA
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    Primer
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    Additional mRNA sequence: 

    AF250329.1 AK094058.1 AK315792.1 BC005342.1 

    10 DOTS entries:

    DT.80101740  DT.99956343  DT.40122685  DT.95157733  DT.95210672  DT.97842370  DT.91749233  DT.95157739 
    DT.100751758  DT.95157735 

    24/62 AceView cDNA sequences (see all 62):

    BQ440464 BX280399 BQ432332 AW269166 BM977068 BM761606 NM_030763 BQ232754 
    AF250329 CR602524 BQ432883 BM471235 CA867236 AA669885 BQ438411 BU630790 
    BQ441233 BP371008 BP369740 BQ435553 BG541827 BC005342 CD642349 BI335013 

    GeneLoc Exon Structure


    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    HMGN5 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TAATGTTAAG
    HMGN5 Expression
    About this image


    See HMGN5 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for HMGN5

    SOURCE GeneReport for Unigene cluster: Hs.282204

    UniProtKB/Swiss-Prot: HMGN5_HUMAN, P82970
    Tissue specificity: Ubiquitously expressed

        SABiosciences Custom PCR Arrays for HMGN5
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    In Situ
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for HMGN5

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals and fungi.

    Orthologs for HMGN5 gene from 7/13 species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Hmgn51 , 5 high-mobility group nucleosome binding domain 51, 5 70.14(n)1
    55.02(a)1
      X (47.92 cM)5
    508871  NM_016710.21  NP_057919.21 
     1090045345 
    chicken
    (Gallus gallus)
    Aves HMGN56
    high mobility group nucleosome binding domain 5
    10(a)
    1 ↔ 1
    Z(69478173-69551287)
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    (see all 24)
    Uncharacterized protein
    (see all 24)
    9(a)
    9(a)
    (see all 24)
    possible ortholog
    possible ortholog
    (see all 24)
    GL343260.1(303820-304269)
    GL343328.1(248997-249700)
    zebrafish
    (Danio rerio)
    Actinopterygii 570687682   -- 72.16(n)    57068768 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG437556
    CG317976
    (see all 4)
    --
    5(a)
    2(a)
    (see all 4)
    possible ortholog
    1 ↔ 1
    (see all 4)
    2L(325522-329761)
    2L(19259527-19262893)
    worm
    (Caenorhabditis elegans)
    Secernentea C33G8.36
    T22B11.46
    Protein T22B11.4, isoform a
    9(a)
    5(a)
    1 ↔ 1
    possible ortholog
    V(7007612-7008339)
    IV(4679018-4682595)
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes EAF76
    Subunit of the NuA4 histone acetyltransferase comp...
    5(a)
    1 ↔ 1
    XIV(370368-371645)


    ENSEMBL Gene Tree for HMGN5 (if available)
    TreeFam Gene Tree for HMGN5 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for HMGN5 gene
    2 SIMAP similar genes for HMGN5 using alignment to 6 protein entries:     HMGN5_HUMAN (see all proteins):
    HMGN1    HMGN3

    HMGN5 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/1062 SNPs in HMGN5 are shown (see all 1062)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs23370021,2
    C,F,A,H--80340674(-) taattC/Gtatgc 1 -- ds500123Minor allele frequency- G:0.37NS EA NA WA 2537
    rs1836760441,2
    --80340738(+) GGATCA/GCTGCA 1 -- ds50010--------
    rs1888945861,2
    --80340773(+) AAGGCA/GGGAAC 1 -- ds50010--------
    rs19372921,2
    C--80340784(-) gtctaG/Agatgg 1 -- ds50012Minor allele frequency- A:0.00NA 4
    rs736317181,2
    C,F--80340867(+) GATCAC/TTTAGG 1 -- ds50011Minor allele frequency- T:0.00WA 2
    rs19372911,2
    C--80340886(-) ttttaG/Agttaa 1 -- ds50011Minor allele frequency- A:0.00NA 2
    rs19372901,2
    C--80341046(-) cAGCAG/AGTCTC 1 -- ds50012Minor allele frequency- A:0.00NA 4
    rs1996721931,2
    --80341226(+) GGGGG-/ATAAGT 1 -- ut310--------
    rs1482287551,2
    --80341229(+) GGATAA/CGTTGG 1 -- ut310--------
    rs681837771,2
    C--80341564(+) TCAAA-/ACTGCC 1 -- ut310--------

    HapMap Linkage Disequilibrium report for HMGN5 (80369200 - 80457441 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 4 variations for HMGN5:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2671958CNV Deletion23128226
    esv271671CNV Insertion20981092
    esv24043CNV Loss19812545
    esv33127CNV Loss17666407


    Locus Specific Mutation Databases (LSDB): HMGN5
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing HMGN5
    DNA2.0 Custom Variant and Variant Library Synthesis for HMGN5

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 300385    OMIM disorders: --

    4 diseases for HMGN5:    About MalaCards
    clear cell renal cell carcinoma    prostatitis    renal cell carcinoma    prostate cancer


    HMGN5 for disorders           About GeneDecksing


    Export disorders for HMGN5 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for HMGN5 gene, integrated from 9 sources (see all 28):
    (articles sorted by number of sources associating them with HMGN5)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Characterization of a human gene encoding nucleosomal binding protein NSBP1. (PubMed id 11161810)1, 2, 3 King L.M. and Francomano C.A. (2001)
    2. The interaction of NSBP1/HMGN5 with nucleosomes in eu chromatin counteracts linker histone-mediated chromatin compaction and modulate s transcription. (PubMed id 19748358)1, 3 Rochman M....Bustin M. (2009)
    3. Immunoaffinity profiling of tyrosine phosphorylation in cancer cells. (PubMed id 15592455)1, 2 Rush J.... Comb M.J. (2005)
    4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    6. High mobility group protein N5 (HMGN5) and lamina-asso ciated polypeptide 2a (LAP2a) interact and reciprocally affect their genome-wide chromatin organization. (PubMed id 23673662)1 Zhang S....Bustin M. (2013)
    7. Small interfering RNA targeting HMGN5 induces apoptosi s via modulation of a mitochondrial pathway and Bcl-2 family proteins in prostat e cancer cells. (PubMed id 22504871)1 Zhang X.Y....Zhou L.Q. (2012)
    8. Knockdown of HMGN5 expression by RNA interference indu ces cell cycle arrest in human lung cancer cells. (PubMed id 22994738)1 Chen P....Yang J.L. (2012)
    9. Knockdown of the nucleosome binding protein 1 inhibits the growth and invasion of clear cell renal cell carcinoma cells in vitro and i n vivo. (PubMed id 22420896)1 Ji S.Q....Zhou L.Q. (2012)
    10. Distinct properties of human HMGN5 reveal a rapidly e volving but functionally conserved nucleosome binding protein. (PubMed id 21518955)1 Malicet C....Bustin M. (2011)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 79366 HGNC: 8013 AceView: NSBP1 Ensembl:ENSG00000198157 euGenes: HUgn79366
    ECgene: HMGN5 H-InvDB: HMGN5

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for HMGN5 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for HMGN5 gene:
    Search GeneIP for patents involving HMGN5

    GeneCards and IP:
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