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

MYNN Gene

protein-coding   GIFtS: 53
GCID: GC03P169490

Myoneurin

  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

This gene clusters with an RNA gene
Subcategory (RNA class): lncRNA

Quality score for the ORGUL clustered with this gene is 3

Aliases
myoneurin1 2
Zinc Finger And BTB Domain-Containing Protein 312 3
OSZF2 3
ZBTB312 3
ZNF9022
Zinc Finger Protein With BTB/POZ Domain2

External Ids:    HGNC: 149551   Entrez Gene: 558922   Ensembl: ENSG000000852747   OMIM: 6060425   UniProtKB: Q9NPC73   
ORGUL members:         
NONCODE14:n409342      

Export aliases for MYNN gene to outside databases

Previous GC identifers: GC03P166758 GC03P170539 GC03P170892 GC03P170812 GC03P170973 GC03P166860


(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 MYNN Gene:
This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in
the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has
been identified on chromosome 14. (provided by RefSeq, Jun 2010)

GeneCards Summary for MYNN Gene: 
MYNN (myoneurin) is a protein-coding gene, and is affiliated with the lncRNA class. Diseases associated with MYNN include celiac disease, and colorectal cancer. GO annotations related to this gene include DNA binding and sequence-specific DNA binding transcription factor activity. An important paralog of this gene is ZBTB18.




(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_000003.11  NT_005612.16  NC_018914.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the MYNN gene promoter:
         HOXA9   AML1a   p53   Sp1   GATA-1   Arnt   AREB6   LyF-1   NF-kappaB1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidMYNN promoter sequence
   Search SABiosciences Chromatin IP Primers for MYNN

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


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

Entrez Gene cytogenetic band: 3q26.2   Ensembl cytogenetic band:  3q26.2   HGNC cytogenetic band: 3q26.31

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

GeneLoc information about chromosome 3         GeneLoc Exon Structure

GeneLoc location for GC03P169490:  view genomic region     (about GC identifiers)

Start:
169,490,619 bp from pter      End:
169,507,504 bp from pter
Size:
16,886 bases      Orientation:
plus 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: MYNN_HUMAN, Q9NPC7 (See protein sequence)
Recommended Name: Myoneurin  
Size: 610 amino acids; 68682 Da
Subcellular location: Nucleus
1 PDB 3D structure from and Proteopedia for MYNN:
2VPK (3D)    
Secondary accessions: B2R6C9 Q6QHA6 Q6QHA7 Q6R3G1 Q6R3G2 Q6R4A0 Q7Z716 Q7Z717 Q86Z11 Q86Z12
Q9NS01 Q9UIW8
Alternative splicing: 4 isoforms:  Q9NPC7-1   Q9NPC7-2   Q9NPC7-3   Q9NPC7-4   

Explore the universe of human proteins at neXtProt for MYNN: NX_Q9NPC7

Explore proteomics data for MYNN at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9NPC7

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

    MYNN Protein Expression
    REFSEQ proteins (3 alternative transcripts): 
    NP_001172047.1  NP_001172048.1  NP_061127.1  

    ENSEMBL proteins: 
     ENSP00000326240   ENSP00000473654   ENSP00000349150   ENSP00000473335   ENSP00000440637  
     ENSP00000376492  

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

    Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--

    MYNN for ontologies           About GeneDecksing



    MYNN Antibody Products: 
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    Cloud-Clone Corp. CLIAs for MYNN


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    BTBD: BTB/POZ domain containing
    ZNF: Zinc fingers, C2H2-type

    5/6 InterPro protein domains (see all 6):
     IPR000210 BTB/POZ-like
     IPR015880 Znf_C2H2-like
     IPR011333 BTB/POZ_fold
     IPR013087 Znf_C2H2/integrase_DNA-bd
     IPR013069 BTB_POZ

    Graphical View of Domain Structure for InterPro Entry Q9NPC7

    ProtoNet protein and cluster: Q9NPC7

    1 Blocks protein domain: IPB000210 BTB/POZ domain

    UniProtKB/Swiss-Prot: MYNN_HUMAN, Q9NPC7
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 1 BTB (POZ) domain
    Similarity: Contains 8 C2H2-type zinc fingers


    MYNN 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

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003677DNA binding IEA--
    GO:0003700sequence-specific DNA binding transcription factor activity TAS10873615
    GO:0005515protein binding ----
    GO:0008270zinc ion binding TAS10873615
    GO:0046872metal ion binding ----
         
    MYNN for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for MYNN:
     Elongated cells 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for MYNN 
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for MYNN 
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    miRNA
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    8/49 QIAGEN miScript miRNA Assays for microRNAs that regulate MYNN (see all 49):
    hsa-miR-607 hsa-miR-106a hsa-miR-519a hsa-miR-766 hsa-miR-764 hsa-miR-502-3p hsa-miR-124 hsa-miR-629*
    SwitchGear 3'UTR luciferase reporter plasmidMYNN 3' UTR sequence
    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for MYNN


    (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 MYNN

    STRING Interaction Network Preview (showing 3 interactants - click image to see more details)

    5 Interacting proteins for MYNN (Q9NPC73 ENSP000003262404) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PAK1Q131533, ENSP000002785684I2D: score=3 STRING: ENSP00000278568
    NRBP1Q9UHY13I2D: score=1 
    RFX2P483783I2D: score=1 
    ELAVL1ENSP000003852694STRING: ENSP00000385269
    UBCENSP000003448184STRING: ENSP00000344818
    About this table

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-dependent IEA--

    MYNN 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 MYNN

    Search CenterWatch for drugs/clinical trials and news about MYNN

    (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 MYNN gene (3 alternative transcripts): 
    NM_001185118.1  NM_001185119.1  NM_018657.4  

    Unigene Cluster for MYNN:

    Myoneurin
    Hs.507025  [show with all ESTs]
    Unigene Representative Sequence: NM_001185118
    6 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000349841(uc011bpm.2 uc003fft.3 uc003ffv.3 uc003ffw.1)
    ENST00000602751 ENST00000356716(uc003ffu.3) ENST00000602391 ENST00000544106(uc010hwo.3)
    ENST00000392733
    miRNA
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    8/49 QIAGEN miScript miRNA Assays for microRNAs that regulate MYNN (see all 49):
    hsa-miR-607 hsa-miR-106a hsa-miR-519a hsa-miR-766 hsa-miR-764 hsa-miR-502-3p hsa-miR-124 hsa-miR-629*
    SwitchGear 3'UTR luciferase reporter plasmidMYNN 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
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    DNA2.0 Custom Codon Optimized Gene Synthesis Service for MYNN
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat MYNN
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat MYNN
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat MYNN

    Additional mRNA sequence: 

    AB079777.1 AB079778.1 AF076249.1 AF148848.2 AF155508.1 AK021646.1 AK056483.1 AK092022.1 
    AK304281.1 AK307916.1 AK312527.1 AL133070.1 AY514901.1 AY515691.1 AY515692.1 AY541760.1 
    AY541761.1 BC020610.1 BC033620.1 BX648128.1 NR_033702.1 NR_033703.1 

    16 DOTS entries:

    DT.452803  DT.97842622  DT.92014447  DT.100789197  DT.120897227  DT.40214826  DT.95250856  DT.95373364 
    DT.95373365  DT.99999445  DT.40109825  DT.100789202  DT.120897211  DT.95201688  DT.102830917  DT.75164117 

    24/159 AceView cDNA sequences (see all 159):

    BM463140 CB069572 AA191075 AK092022 AF148848 BE672025 AA748172 AY514901 
    BC020610 BQ050787 AI655170 CK820838 AA228040 BX371830 AA634199 BC033620 
    AA227869 CA406835 CK820837 Z45694 AK021646 BX648128 NM_018657 AF076249 

    GeneLoc Exon Structure

    5/12 Alternative Splicing Database (ASD) splice patterns (SP) for MYNN (see all 12)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2a · 2b ^ 3 ^ 4a · 4b ^ 5a · 5b · 5c · 5d ^ 6a · 6b ^ 7a · 7b ^ 8 ^ 9 ^ 10a · 10b ^ 11a · 11b ^ 12a · 12b · 12c · 12d ·
    SP1:                          -                 -                                                                 -     -                                       
    SP2:                    -     -                 -                                                                 -     -                                       
    SP3:                    -     -                 -     -                                                           -     -                                       
    SP4:                                            -                                                                 -     -     -     -                           
    SP5:                                                                                                                                                            

    ExUns: 12e
    SP1:      
    SP2:      
    SP3:      
    SP4:      
    SP5:      


    ECgene alternative splicing isoforms for MYNN

    (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

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


    MYNN expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/4 selected tissues (see all 4) fully expand
     
     Cartilage (Muscoskeletal System)    fully expand to see all 2 entries
             Prechondrocytic Mesenchymal Cells Zeugopod
             fetal cartilage   
     
     Limb (Muscoskeletal System)
             Prechondrocytic Mesenchymal Cells Zeugopod
     
     Bone (Muscoskeletal System)
             Prechondrocytic Mesenchymal Cells Zeugopod
     
     Eye (Sensory Organs)
             lens   

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

    SOURCE GeneReport for Unigene cluster: Hs.507025

    UniProtKB/Swiss-Prot: MYNN_HUMAN, Q9NPC7
    Tissue specificity: Mainly expressed in the neuromuscular system. Located in and around synaptic myonuclei in
    adult muscle. Expression is dysregulated after nerve injury. Also found in the testis, ovary and placenta

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

    (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 MYNN gene from 5/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Mynn1 , 5 myoneurin1, 5 87.92(n)1
    91.97(a)1
      3 (14.27 cM)5
    807321  NM_030557.21  NP_085034.21 
     306020875 
    chicken
    (Gallus gallus)
    Aves MYNN1 myoneurin 77.21(n)
    82.13(a)
      771218  XM_001233289.2  XP_001233290.1 
    lizard
    (Anolis carolinensis)
    Reptilia MYNN6
    Uncharacterized protein
    81(a)
    1 ↔ 1
    3(7986430-7992875)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia CF379035.12   -- 81.68(n)    CF379035.1 
    zebrafish
    (Danio rerio)
    Actinopterygii BC045441.12   -- 77.11(n)   327167  BC045441.1 


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for MYNN gene
    ZBTB182  ZBTB212  ZBTB32  ZBTB142  ZBTB7B2  ENSG000002545532  ZBTB462  ZBTB7C2  
    ZBTB8B2  ZBTB102  ZBTB8A2  ZBTB7A2  ZBTB52  ZBTB442  ZBTB492  ZBTB242  
    ZBTB422  
    18/375 SIMAP similar genes for MYNN using alignment to 3 protein entries:     MYNN_HUMAN (see all proteins) (see all similar genes):
    ZBTB32    kr-znf3    ZNF500    ZNF516    ZNF891    ZNF585B
    DKFZp434J0650    ZBTB4    ZNF233    ZNF35    ZBTB49    ZFP3
    DKFZp686O111    HKR1    ZFS-5    ZNF214    ZNF251    ZNF268

    MYNN for paralogs           About GeneDecksing


    2 Pseudogenes.org Pseudogenes for MYNN
    PGOHUM00000247734 PGOHUM00000241227


    (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

    10/363 SNPs in MYNN are shown (see all 363)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 3 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1149560601,2
    C,F--169489728(+) TGTAAT/CAAAAC 4 -- us2k11Minor allele frequency- C:0.02NA 120
    rs112936181,2
    C--169489750(+) GAGAC-/AAAAAA 4 -- us2k1 trp30--------
    rs359439601,2
    C--169489761(+) AAAAA-/A/AA  
            
    GGCCA
    4 -- us2k11NA 2
    rs790004711,2
    --169489761(+) AAAAAA/GGGCCA 4 -- us2k10--------
    rs1831671861,2
    --169489840(+) CGTGCA/TGATTC 4 -- us2k10--------
    rs351006731,2
    C,F,H--169489937(+) TTCCTC/TTCAAT 4 -- us2k115Minor allele frequency- T:0.04EA NS NA 1770
    rs38213831,2
    C,F,A,H--169489946(-) TATTAA/C/G/
            
    CAAAT
    4 -- us2k122NA EA NS WA CSA 2241
    rs1874580321,2
    --169489960(+) ACTTGA/GGAATT 4 -- us2k10--------
    rs1918684291,2
    --169490002(+) CAAAAC/TCCTCT 4 -- us2k10--------
    rs1145475981,2
    F--169490003(+) AAAACC/TCTCTC 4 -- us2k11Minor allele frequency- T:0.01WA 118

    HapMap Linkage Disequilibrium report for MYNN (169490619 - 169507504 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for MYNN:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2422204CNV Deletion17116639
    nsv7356OTHER Inversion18451855

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    (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: 606042    OMIM disorders: --

    5 diseases for MYNN:    About MalaCards
    celiac disease    colorectal cancer    ovarian cancer    multiple sclerosis
    lung cancer


    MYNN for disorders           About GeneDecksing

    Genetic Association Database (GAD): MYNN
    Human Genome Epidemiology (HuGE) Navigator: MYNN (4 documents)

    Export disorders for MYNN 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 MYNN gene, integrated from 9 sources (see all 26):
    (articles sorted by number of sources associating them with MYNN)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Myoneurin, a novel member of the BTB/POZ-zinc finger family highly expressed in human muscle. (PubMed id 10873615)1, 2, 3, 9 Alliel P.M.... Perin J.-P. (2000)
    2. Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin. (PubMed id 14694499)1, 2, 9 Cifuentes-Diaz C.... Alliel P.M. (2004)
    3. Genetic risk and a primary role for cell-mediated immu ne mechanisms in multiple sclerosis. (PubMed id 21833088)1, 4  ....Compston A. (2011)
    4. Genetic susceptibility to distinct bladder cancer sub phenotypes. (PubMed id 19692168)1, 4 Guey L.T....Malats N. (2010)
    5. Multiple common variants for celiac disease influenci ng immune gene expression. (PubMed id 20190752)1, 4 Dubois P.C....van Heel D.A. (2010)
    6. Meta-analysis of three genome-wide association studie s identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.1 3 and 20q13.33. (PubMed id 20972440)1, 4 Houlston R.S....Tomlinson I.P. (2010)
    7. PTEN identified as important risk factor of chronic o bstructive pulmonary disease. (PubMed id 19625176)1, 4 Hosgood H.D....Lan Q. (2009)
    8. Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China. (PubMed id 19170196)1, 4 Shen M....Lan Q. (2009)
    9. Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway. (PubMed id 18676680)1, 4 Hosgood H.D....Lan Q. (2008)
    10. 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)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (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: 55892 HGNC: 14955 AceView: MYNN Ensembl:ENSG00000085274 euGenes: HUgn55892
    ECgene: MYNN H-InvDB: MYNN

    (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 MYNN 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 MYNN gene:
    Search GeneIP for patents involving MYNN

    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: 23 Oct 2013 - Incrementals: 4 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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