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

HMGN3 Gene

protein-coding   GIFtS: 49
GCID: GC06M079967

high mobility group nucleosomal binding domain 3

(Previous name: thyroid hormone receptor interactor 7 )
(Previous symbol: TRIP7)
 Explore 4 diseases affiliated with
HMGN3 via our new
 Human Malady Compendium 
Biological research products
for HMGN3
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
High Mobility Group Nucleosomal Binding Domain 31 2     High Mobility Group Nucleosome-Binding Domain-Containing Protein 32
TRIP71 2 3 5     Thyroid Hormone Receptor Interacting Protein 72
TR-Interacting Protein 72 3     TRIP-73
Thyroid Hormone Receptor Interactor 71     Thyroid Receptor-Interacting Protein 73
PNAS-252     

External Ids:    HGNC: 123121   Entrez Gene: 93242   Ensembl: ENSG000001184187   OMIM: 6045025   UniProtKB: Q156513   

Export aliases for HMGN3 gene to outside databases

Previous GC identifers: GC06M079853 GC06M079906 GC06M077104


(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 HMGN3:
Thyroid hormone receptors are hormone-dependent transcription factors that regulate expression of a variety of specific
target genes. The protein encoded by this gene binds thyroid hormone receptor beta, but only in the presence of
thyroid hormone. The encoded protein, 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. Alternatively spliced
transcript variants encoding different isoforms have been found for this gene. (provided by RefSeq, Jan 2011)

UniProtKB/Swiss-Prot: HMGN3_HUMAN, Q15651
Function: Binds to nucleosomes, regulating chromatin structure and consequently, chromatin-dependent processes such as
transcription, DNA replication and DNA repair. Affects both insulin and glucagon levels and modulates the expression
of pancreatic genes involved in insulin secretion. Regulates the expression of the glucose transporter SLC2A2 by
binding specifically to its promoter region and recruiting PDX1 and additional transcription factors. Regulates the
expression of SLC6A9, a glycine transporter which regulates the glycine concentration in synaptic junctions in the
central nervous system, by binding to its transcription start site. May play a role in ocular development and
astrocyte function (By similarity)

Gene Wiki entry for HMGN3


(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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000006.11  NC_018917.1  NT_007299.13  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the HMGN3 gene promoter:
         FOXD1   HNF-3beta   NF-AT   C/EBPalpha   Evi-1   NF-AT4   NF-AT2   NF-AT3   NF-AT1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidHMGN3 promoter sequence
   Search SABiosciences Chromatin IP Primers for HMGN3

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat HMGN3


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

Entrez Gene cytogenetic band: 6q14.1   Ensembl cytogenetic band:  6q14.1   HGNC cytogenetic band: 6q14.3

HMGN3 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
HMGN3 gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06M079967:  view genomic region     (about GC identifiers)

Start:
79,910,962 bp from pter      End:
79,944,455 bp from pter
Size:
33,494 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, 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 Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: HMGN3_HUMAN, Q15651 (See protein sequence)
Recommended Name: High mobility group nucleosome-binding domain-containing protein 3  
Size: 99 amino acids; 10666 Da
Subunit: Interacts with the ligand binding domain of the thyroid receptor (TR) (in vitro). Requires the presence of
thyroid hormone for its interaction. Interacts with nucleosomes
Subcellular location: Nucleus
Sequence caution: Sequence=AAA73877.1; Type=Erroneous initiation;
Secondary accessions: B2RD37 Q5HYD3 Q7RTT0 Q969M5 Q9BZT7
Alternative splicing: 2 isoforms:  Q15651-1   Q15651-2   

Explore the universe of human proteins at neXtProt for HMGN3: NX_Q15651

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q15651

  • HMGN3 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (4 alternative transcripts): 
    NP_001188291.1  NP_001188292.1  NP_004233.1  NP_620058.1  

    ENSEMBL proteins: 
     ENSP00000341267   ENSP00000275036  

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    Uscn Proteins for HMGN3

    Gene Ontology (GO): 4 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000785chromatin IEA--
    GO:0005634nucleus NAS--
    GO:0005730NOT nucleolus IDA--
    GO:0005737cytoplasm IDA--


    HMGN3 for ontologies           About GeneDecksing



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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    HMGN3 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR000079 HMGN_fam

    Graphical View of Domain Structure for InterPro Entry Q15651

    ProtoNet protein and cluster: Q15651

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

    UniProtKB/Swiss-Prot: HMGN3_HUMAN, Q15651
    Similarity: Belongs to the HMGN family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    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, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: HMGN3_HUMAN, Q15651
    Function: Binds to nucleosomes, regulating chromatin structure and consequently, chromatin-dependent processes such as
    transcription, DNA replication and DNA repair. Affects both insulin and glucagon levels and modulates the expression
    of pancreatic genes involved in insulin secretion. Regulates the expression of the glucose transporter SLC2A2 by
    binding specifically to its promoter region and recruiting PDX1 and additional transcription factors. Regulates the
    expression of SLC6A9, a glycine transporter which regulates the glycine concentration in synaptic junctions in the
    central nervous system, by binding to its transcription start site. May play a role in ocular development and
    astrocyte function (By similarity)
    Induction: By estrogen

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    Gene Ontology (GO): 3 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003682chromatin binding ----
    GO:0031492nucleosomal DNA binding IEA--
    GO:0046966thyroid hormone receptor binding NAS7776974


    HMGN3 for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-out Hmgn3tm1.2Mbus for HMGN3
         2 MGI mutant phenotypes (inferred from 2 alleles(MGI details for Hmgn3):
     homeostasis/metabolism  no phenotypic analysis 

    HMGN3 for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, 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 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for HMGN3

    STRING Interaction Network Preview (showing 5 interactants - click image to see more details)

    5/8 Interacting proteins for HMGN3 (Q156511, 3 ENSP000003412674) via UniProtKB, MINT, STRING, and/or I2D (see all 8)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    GRB2P629931, 3, ENSP000003390074EBI-1758705,EBI-401755 I2D: score=2 STRING: ENSP00000339007
    THRBP108283I2D: score=3 
    VDRP114733I2D: score=3 
    SMAD2Q157963I2D: score=1 
    TERF1ENSP000002766034STRING: ENSP00000276603
    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:0008150biological_process ND--
    GO:0016568chromatin modification IEA--
    GO:0045944positive regulation of transcription from RNA polymerase II promoter IEA--
    GO:0051091positive regulation of sequence-specific DNA binding transcription factor activity IEA--
    GO:0061178regulation of insulin secretion involved in cellular response to glucose stimulus IEA--


    HMGN3 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, 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 HMGN3
    Search CenterWatch for drugs/clinical trials and news about HMGN3 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
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    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for HMGN3 gene (4 alternative transcripts): 
    NM_001201362.1  NM_001201363.1  NM_004242.3  NM_138730.2  

    Unigene Cluster for HMGN3:

    High mobility group nucleosomal binding domain 3
    Hs.77558  [show with all ESTs]
    Unigene Representative Sequence: BX648085
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000344726(uc021zbz.1 uc003pit.3 uc003piu.2) ENST00000275036(uc003pis.3)


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    Additional cDNA sequence: 

    AF274949.1 AF401520.1 AK315391.1 AY043282.1 BC009529.2 BX648085.1 L40357.1 

    15 DOTS entries:

    DT.75146608  DT.95102491  DT.95326107  DT.100789896  DT.100744948  DT.95302036  DT.91646468  DT.95302033 
    DT.95087498  DT.97775329  DT.121305477  DT.448792  DT.92445913  DT.100789892  DT.40201792 

    24/381 AceView cDNA sequences (see all 381):

    CF528375 AA747121 BM927225 BM739279 AI350223 CB069941 AI818698 AJ707560 
    AI290818 BQ950791 CA306359 BM980115 AI348654 CR599808 AA244274 AW026647 
    AV659317 BF933194 Z40802 AA765577 BE894207 AI358625 AA483949 CB068658 

    GeneLoc Exon Structure

    5/8 Alternative Splicing Database (ASD) splice patterns (SP) for HMGN3 (see all 8)    About this scheme

    ExUns: 1a · 1b · 1c · 1d · 1e · 1f ^ 2 ^ 3a · 3b ^ 4 ^ 5 ^ 6a · 6b ^ 7a · 7b · 7c · 7d · 7e ^ 8a · 8b · 8c · 8d
    SP1:                                            -           -                             -     -     -     -                           
    SP2:                                            -           -                             -     -     -     -                           
    SP3:                                            -           -                                   -     -     -                           
    SP4:                                            -           -                       -     -     -     -     -                           
    SP5:                                            -           -                 -     -     -     -     -     -                           


    ECgene alternative splicing isoforms for HMGN3

    (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

    HMGN3 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GATAGTTGTG

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    HMGN3 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    3 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    EyeInner Nuclear LayerMature Horizontal CellsHorizontal, Retina
    EyeInner Nuclear LayerMature Rod Bipolar CellsBipolar, Retina
    OvaryOvigerous CordOvarian Somatic CellsOvary
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See HMGN3 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for HMGN3

    SOURCE GeneReport for Unigene cluster: Hs.77558

    UniProtKB/Swiss-Prot: HMGN3_HUMAN, Q15651
    Tissue specificity: Expressed in kidney, lung, pancreas, testis, skeletal muscle, heart, thyroid gland, pituitary
    gland, prostate and uterus. Low expression in liver, spleen, placenta and ovaries

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for HMGN3

    (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 chordates.

    Orthologs for HMGN3 gene from 5/8 species (see all 8)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Hmgn35 high mobility group nucleosomal binding domain 3   --   9 (45.29 cM) 83109948 
    chicken
    (Gallus gallus)
    Aves HMGN36
    high mobility group nucleosomal binding domain 3
    57(a)
    1 ↔ 1
    3(82198928-82223271)
    lizard
    (Anolis carolinensis)
    Reptilia HMGN36
    --
    71(a)
    1 ↔ 1
    1(199635815-199649360)
    African clawed frog
    (Xenopus laevis)
    Amphibia MGC642522 hypothetical protein MGC64252 87.3(n)    BC041718.1 
    zebrafish
    (Danio rerio)
    Actinopterygii 570367902   -- 80.18(n)   334804  57036790 


    ENSEMBL Gene Tree for HMGN3 (if available)
    TreeFam Gene Tree for HMGN3 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for HMGN3 gene
    HMGN22  HMGN12  HMGN42  
    2 SIMAP similar genes for HMGN3 using alignment to 1 protein entry:     HMGN3_HUMAN:
    HMGN1    HMGN5

    HMGN3 for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for HMGN3
    PGOHUM00000245004


    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, 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

    10/547 NCBI SNPs in HMGN3 are shown (see all 547    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1872373821,2
    --79910868(+) AGATAC/TCGCTA 4 -- ds50010--------
    rs1511428681,2
    --79910902(+) TATATC/TTTCTG 4 -- ds50010--------
    rs1921686351,2
    --79910967(+) TTCTGC/TAGACA 4 -- ut310--------
    rs1451156671,2
    --79911143(+) AGGACC/TAAATT 4 -- ut310--------
    rs340437891,2
    C,F,--79911190(+) ACACAG/ACTTCC 4 -- ut316Minor allele frequency- A:0.14NA CSA WA 248
    rs1475963211,2
    --79911277(+) CCATCC/TTTATA 4 -- ut310--------
    rs94486571,2
    C,F,H,--79911290(+) TTTTCG/ATATGC 4 -- ut31 ese319Minor allele frequency- A:0.13NA NS EA CSA WA 2032
    rs1826810161,2
    C,--79911414(+) TCTCCC/TTCGTT 6 E syn1 ut310--------
    rs715477441,2
    C,--79911460(+) AAAGG-/AAAAAA 4 -- int1 ut311Minor allele frequency- A:0.50NA 2
    rs94486581,2
    C,--79911481(+) TTACTA/GCTGAA 4 -- int1 ut311Minor allele frequency- G:0.00EU 1099

    HapMap Linkage Disequilibrium report for HMGN3 (79910962 - 79944455 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for HMGN3: --

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    HMGN3 for disorders           About GeneDecksing

    OMIM gene information: 604502    OMIM disorders: --

    4 diseases for HMGN3:    About MalaCards
    thyroiditis    rhabdomyosarcoma    pancreatitis    prostatitis


    Export disorders for HMGN3 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 HMGN3 gene, integrated from 9 sources (see all 21):
    (articles sorted by number of sources associating them with HMGN3)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. HMGN3a and HMGN3b, two protein isoforms with a tissue-specific expression pattern, expand the cellular repertoire of nucleosome- binding proteins. (PubMed id 11356838)1, 2, 3, 9 West K.L.... Bustin M. (2001)
    2. Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor. (PubMed id 7776974)1, 2, 3 Lee J.W....Moore D.D. (1995)
    3. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1, 2 Olsen J.V....Mann M. (2006)
    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. The DNA sequence and analysis of human chromosome 6. (PubMed id 14574404)1, 2 Mungall A.J.... Beck S. (2003)
    7. Differential display RT-PCR analysis of enterovirus-71-infected rhabdomyosarcoma cells reveals mRNA expression responses of multiple human genes with known and novel functions. (PubMed id 12033773)1, 2 Leong P.W.... Chow V.T.K. (2002)
    8. Genome-wide association study identifies HMGN3 locus f or spine bone size variation in Chinese. (PubMed id 21947420)1 Lei S.F....Deng H.W. (2012)
    9. Initial characterization of the human central proteome. (PubMed id 21269460)2 Burkard T.R.... Colinge J. (2011)
    10. Systematic and quantitative assessment of the ubiquiti n-modified proteome. (PubMed id 21906983)1 Kim W....Gygi S.P. (2011)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 9324 HGNC: 12312 AceView: HMGN3 Ensembl:ENSG00000118418 euGenes: HUgn9324
    ECgene: HMGN3 H-InvDB: HMGN3

    (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 HMGN3 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 HMGN3 gene:
    Search GeneIP for patents involving HMGN3

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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    GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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