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

MNDA Gene

protein-coding   GIFtS: 53
GCID: GC01P158801

myeloid cell nuclear differentiation antigen

 Explore 21 diseases affiliated with
MNDA via our new
 Human Malady Compendium 
Biological research products
for MNDA
    

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

Aliases
Myeloid Cell Nuclear Differentiation Antigen1 2
PYHIN31 2

External Ids:    HGNC: 71831   Entrez Gene: 43322   Ensembl: ENSG000001635637   OMIM: 1595535   UniProtKB: P412183   

Export aliases for MNDA gene to outside databases

Previous GC identifers: GC01P156593 GC01P154533 GC01P155579 GC01P156017 GC01P155614 GC01P157067 GC01P130158


(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 MNDA:
The myeloid cell nuclear differentiation antigen (MNDA) is detected only in nuclei of cells of the granulocyte-monocyte
lineage. A 200-amino acid region of human MNDA is strikingly similar to a region in the proteins encoded by a family
of interferon-inducible mouse genes, designated Ifi-201, Ifi-202, and Ifi-203, that are not regulated in a cell- or
tissue-specific fashion. The 1.8-kb MNDA mRNA, which contains an interferon-stimulated response element in the 5-prime
untranslated region, was significantly upregulated in human monocytes exposed to interferon alpha. MNDA is located
within 2,200 kb of FCER1A, APCS, CRP, and SPTA1. In its pattern of expression and/or regulation, MNDA resembles IFI16,
suggesting that these genes participate in blood cell-specific responses to interferons. (provided by RefSeq, Jul
2008)

UniProtKB/Swiss-Prot: MNDA_HUMAN, P41218
Function: May act as a transcriptional activator/repressor in the myeloid lineage. Plays a role in the
granulocyte/monocyte cell-specific response to interferon. Stimulates the DNA binding of the transcriptional repressor
protein YY1

Gene Wiki entry for MNDA


(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_000001.10  NC_018912.1  NT_004487.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the MNDA gene promoter:
         S8   FOXJ2 (long isoform)   ATF-2   Chx10   Cart-1   FOXJ2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidMNDA promoter sequence
   Search SABiosciences Chromatin IP Primers for MNDA

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


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

Entrez Gene cytogenetic band: 1q22   Ensembl cytogenetic band:  1q23.1   HGNC cytogenetic band: 1q22

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

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01P158801:  view genomic region     (about GC identifiers)

Start:
158,801,107 bp from pter      End:
158,819,296 bp from pter
Size:
18,190 bases      Orientation:
plus 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: MNDA_HUMAN, P41218 (See protein sequence)
Recommended Name: Myeloid cell nuclear differentiation antigen  
Size: 407 amino acids; 45836 Da
Subunit: Participates in a ternary complex with YY1 and the YY1 target DNA element. Binds nucleolin and
nucleophosmin/NPM/B23
Subcellular location: Nucleus. Cytoplasm. Note=Uniformly distributed throughout the interphase cell nucleus. Associates
with chromatin
1 PDB 3D structure from and Proteopedia for MNDA:
2DBG (3D)    

Explore the universe of human proteins at neXtProt for MNDA: NX_P41218

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P41218

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

    REFSEQ proteins: NP_002423.1  
    ENSEMBL proteins: 
     ENSP00000357123   ENSP00000406800  

    Human Recombinant Protein Products: 
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    OriGene Protein Over-expression Lysate: MNDA
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    Novus Biologicals MNDA Proteins
    Novus Biologicals MNDA Lysates
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    ProSpec Recombinant Protein for MNDA
    Uscn Proteins for MNDA

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005730NOT nucleolus IDA--
    GO:0005737cytoplasm IDA--
    GO:0043231intracellular membrane-bounded organelle IDA--


    MNDA for ontologies           About GeneDecksing



    MNDA Antibody Products: 
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    Uscn ELISAs and CLIAs for MNDA


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

    MNDA for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR004021 HIN200/IF120x
     IPR012340 NA-bd_OB-fold
     IPR004020 DAPIN

    Graphical View of Domain Structure for InterPro Entry P41218

    ProtoNet protein and cluster: P41218

    1 Blocks protein family: IPB004021 HIN-200/IF120x domain

    UniProtKB/Swiss-Prot: MNDA_HUMAN, P41218
    Domain: Its N-terminal half (200 amino acids) is sufficient for maximum enhancement of YY1 DNA binding and a portion of
    this sequence is responsible for binding YY1
    Similarity: Contains 1 DAPIN domain
    Similarity: Contains 1 HIN-200 domain


    (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: MNDA_HUMAN, P41218
    Function: May act as a transcriptional activator/repressor in the myeloid lineage. Plays a role in the
    granulocyte/monocyte cell-specific response to interferon. Stimulates the DNA binding of the transcriptional repressor
    protein YY1
    Induction: Strongly induced by alpha interferon which selectively affects expression in late stage cells in the
    monocytic but not the granulocytic lineage. Induced in vitro by dimethylsulfoxide and 1,25 dihydroxyvitamin D3

         Genatlas biochemistry entry for MNDA:
    myeloid nuclear differentiation antigen,interferon alpha-inducible protein

    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat MNDA
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    SwitchGear 3'UTR luciferase reporter plasmidMNDA 3' UTR sequence
    Inhib. RNA
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003677DNA binding IEA--


    MNDA for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for MNDA:
     Synthetic lethal with Ras 


    (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

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Apoptosis and Autophagy
    Apoptosis and Autophagy1.00
    2Lymphocyte Signaling
    Lymphocyte Signaling1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    2 Cell Signaling Technology (CST) Pathways for MNDA
        Apoptosis and Autophagy
    Lymphocyte Signaling



    MNDA for pathways           About GeneDecksing

    Interactions:

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

    STRING Interaction Network Preview (showing 5 interactants - click image to see 6)

    5/19 Interacting proteins for MNDA (P412182, 3 ENSP000003571234) via UniProtKB, MINT, STRING, and/or I2D (see all 19)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    CDK2P249413, ENSP000002669704I2D: score=2 STRING: ENSP00000266970
    RBL2Q089993, ENSP000002621334I2D: score=2 STRING: ENSP00000262133
    TP53P046373, ENSP000002693054I2D: score=2 STRING: ENSP00000269305
    RB1P064003, ENSP000002671634I2D: score=2 STRING: ENSP00000267163
    HOXB2P146523, ENSP000003317414I2D: score=2 STRING: ENSP00000331741
    About this table

    Gene Ontology (GO): 5/7 biological process terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-dependent IEA--
    GO:0006355regulation of transcription, DNA-dependent IEA--
    GO:0006968cellular defense response TAS1644857
    GO:0006974response to DNA damage stimulus IMP17875758
    GO:0030889negative regulation of B cell proliferation IMP17875758


    MNDA 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

    MNDA for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for MNDA
    5 Novoseek chemical compound relationships for MNDA gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    mnda 99.6 217 15778972 (12), 7890814 (11), 10492038 (9), 8175894 (9) (see all 38)
    p202 93.9 3 17981573 (1), 9642285 (1)
    physostigmine 70 4 11215814 (1), 17981573 (1), 9642285 (1)
    endotoxin 13.2 2 7890814 (1), 8175894 (1)
    lipid 0 1 15778972 (1)

    Search CenterWatch for drugs/clinical trials and news about MNDA 

    (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 MNDA gene: 
    NM_002432.1  

    Unigene Cluster for MNDA:

    Myeloid cell nuclear differentiation antigen
    Hs.153837  [show with all ESTs]
    Unigene Representative Sequence: BC032319
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000368141(uc001fsz.1) ENST00000491210 ENST00000438394

    miRNA
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    Inhib. RNA
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    Additional cDNA sequence: 

    AK290392.1 AK313210.1 BC020715.1 BC032319.1 M81750.1 

    6 DOTS entries:

    DT.101986484  DT.210891  DT.95265764  DT.95265765  DT.100709149  DT.92426782 

    24/57 AceView cDNA sequences (see all 57):

    AV715791 AU140092 BX952054 BI821232 AU135562 BC020715 BC032319 AV718301 
    CA412436 M81750 NM_002432 BM903669 BP432041 N47924 AV714775 BG540480 
    BI760503 BX111714 AV717567 BG506590 BI836969 R77431 AV713616 BX366163 

    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

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

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

    About this image
    See MNDA Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for MNDA

    SOURCE GeneReport for Unigene cluster: Hs.153837

    UniProtKB/Swiss-Prot: MNDA_HUMAN, P41218
    Tissue specificity: Expressed constitutively in cells of the myeloid lineage. Found in promyelocyte stage cells as well
    as in all other stage cells including peripheral blood monocytes and granulocytes. Also appear in myeloblast cells in
    some cases of acute myeloid Leukemia

        SABiosciences Expression via Pathway-Focused PCR Arrays including MNDA: 
              Interferons & Receptors in human mouse rat
              Type I Interferon Response in human mouse rat

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    In Situ
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    (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
      --

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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for MNDA gene
    AIM22  IFI162  PYHIN12  
    3 SIMAP similar genes for MNDA using alignment to 4 protein entries:     MNDA_HUMAN (see all proteins):
    PYHIN1    IFI16    AIM2

    MNDA for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for MNDA
    PGOHUM00000245030


    (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

    10/393 NCBI SNPs in MNDA are shown (see all 393    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1178355441,2
    F,--158799193(+) TCAAAC/TTCTAA 1 -- us2k11Minor allele frequency- T:0.12EA 120
    rs1461211441,2
    C,--158799215(+) CTAGGC/TCAGGG 1 -- us2k10--------
    rs1921147831,2
    --158799336(+) TTCTGC/TCACTA 1 -- us2k10--------
    rs66794121,2
    C,--158799367(+) attcaA/Tcaagt 1 -- us2k10--------
    rs8577951,2
    C,F,A,H,--158799391(-) GGGAAC/TGTTTG 1 -- us2k15Minor allele frequency- T:0.25NA CSA 8
    rs120923471,2
    C,--158799418(+) TTCTGA/CGCCTT 1 -- us2k13Minor allele frequency- C:0.15NA EA 242
    rs66904461,2
    C,F,H,--158799453(+) ACCCAG/ATTTTA 1 -- us2k110Minor allele frequency- A:0.08NS EA NA 1080
    rs66846291,2
    C,F,--158799603(+) CTTAAT/CGTTCC 1 -- us2k13Minor allele frequency- C:0.07WA NA EA 358
    rs1508945981,2
    --158799670(+) CTTACA/GTAGAT 1 -- us2k10--------
    rs23256981,2
    C,F,A,H,--158799738(+) taaaaC/Tgatca 1 -- us2k1 tfbs310Minor allele frequency- T:0.08NS EA NA WA 766

    HapMap Linkage Disequilibrium report for MNDA (158801107 - 158819296 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for MNDA: --

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing MNDA
    DNA2.0 Custom Variant and Variant Library Synthesis for MNDA

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

    MNDA for disorders           About GeneDecksing

    OMIM gene information: 159553    OMIM disorders: --

    20/21 diseases for MNDA (see all 21):    About MalaCards
    abdominal aortic aneurysm    familial combined hyperlipidemia    aortic aneurysm    burkitt's lymphoma
    myeloid leukemia    systemic lupus erythematosus    lupus erythematosus    myelodysplastic syndrome
    acute lymphoblastic leukemia    chronic lymphocytic leukemia    acute myeloid leukemia    lymphoblastic leukemia
    lymphocytic leukemia    hyperlipidemia    kaposi's sarcoma    leukemia
    lymphoblastic lymphoma    acute leukemia    atherosclerosis    sarcoma

    10 Novoseek disease relationships for MNDA gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    myeloid leukemia 37 2 2259228 (1), 8175894 (1)
    myelodysplastic syndromes 36.1 3 16651415 (2), 9328447 (1)
    burkitt lymphoma 34.7 1 11215814 (1)
    myeloid leukemia chronic 32.8 3 10492038 (1), 2259228 (1), 7890814 (1)
    melanoma 26.2 5 9642285 (1), 14757431 (1), 20187706 (1)
    lymphoma 24.3 8 19474799 (2), 10492038 (1), 7890814 (1)
    leukemia 23.2 2 2259228 (1), 7890814 (1)
    inflammation 16.4 5 15778972 (2), 10492038 (1), 16651415 (1)
    atherosclerosis 0 1 15778972 (1)
    tumors 0 2 1377701 (1), 18681780 (1)

    Human Genome Epidemiology (HuGE) Navigator: MNDA (2 documents)

    Export disorders for MNDA 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 MNDA gene, integrated from 9 sources (see all 51):
    (articles sorted by number of sources associating them with MNDA)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Cloning and expression of the human myeloid cell nuclear differentiation antigen: regulation by interferon alpha. (PubMed id 1644857)1, 2, 3, 9 Briggs J.A.... Briggs R.C. (1992)
    2. The human myeloid cell nuclear differentiation antigen gene is one of at least two related interferon-inducible genes located on chromosome 1q that are expressed specifically in hematopoietic cells. (PubMed id 7512843)1, 2, 3, 9 Briggs R.C.... Dessypris E.N. (1994)
    3. Interferon alpha selectively affects expression of the human myeloid cell nuclear differentiation antigen in late stage cells in the monocytic but not the granulocytic lineage. (PubMed id 8175894)1, 2, 9 Briggs R....Lian J. (1994)
    4. Human hematopoietic cell specific nuclear protein MNDA interacts with the multifunctional transcription factor YY1 and stimulates YY1 DNA binding. (PubMed id 9712147)1, 2, 9 Xie J.... Briggs R.C. (1998)
    5. Characterization of the human myeloid cell nuclear differentiation antigen: relationship to interferon-inducible proteins. (PubMed id 1377701)1, 2, 9 Burrus G.R.... Briggs R.C. (1992)
    6. The closely linked genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expression. (PubMed id 7806273)1, 2, 9 Dawson M.J....Baker E. (1995)
    7. 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)
    8. Variable expression of human myeloid specific nuclear antigen MNDA in monocyte lineage cells in atherosclerosis. (PubMed id 15778972)1, 9 Briggs R.C....Miranda R.N. (2005)
    9. Identification of MNDA as a new marker for nodal marg inal zone lymphoma. (PubMed id 19474799)1, 9 Kanellis G....Piris M.A. (2009)
    10. Dysregulated human myeloid nuclear differentiation antigen expression in myelodysplastic syndromes: evidence for a role in apoptosis. (PubMed id 16651415)1, 9 Briggs R.C....Head D.R. (2006)

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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 4332 HGNC: 7183 AceView: MNDA Ensembl:ENSG00000163563 euGenes: HUgn4332
    ECgene: MNDA H-InvDB: MNDA

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

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    Patent Information for MNDA gene:
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