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MNS1 Gene

protein-coding   GIFtS: 50
GCID: GC15M056720

Meiosis-Specific Nuclear Structural 1

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(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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Aliases
Meiosis-Specific Nuclear Structural 11 2
Spermatogenesis Associated 401 2
SPATA402
Meiosis-Specific Nuclear Structural Protein 12
FLJ112225

External Ids:    HGNC: 296361   Entrez Gene: 553292   Ensembl: ENSG000001385877   OMIM: 6107665   UniProtKB: Q8NEH63   

Export aliases for MNS1 gene to outside databases

Previous GC identifers: GC15M054300 GC15M054437 GC15M054508 GC15M033544


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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Entrez Gene summary for MNS1 Gene:
This gene encodes a protein highly similar to the mouse meiosis-specific nuclear structural 1 protein. The mouse
protein was shown to be expressed at the pachytene stage during spermatogenesis and may function as a nuclear
skeletal protein to regulate nuclear morphology during meiosis. (provided by RefSeq, Oct 2008)

GeneCards Summary for MNS1 Gene:
MNS1 (meiosis-specific nuclear structural 1) is a protein-coding gene. GO annotations related to this gene include identical protein binding.

UniProtKB/Swiss-Prot: MNS1_HUMAN, Q8NEH6
Function: May play a role in the control of meiotic division and germ cell differentiation through regulation of
pairing and recombination during meiosis (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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence at NCBI GenBank:
NC_000015.9  NC_018926.2  NT_010194.18  
Regulatory elements:
   Regulatory transcription factor binding sites in the MNS1 gene promoter:
         MEF-2A   POU2F1   oct-B3   oct-B2   POU2F1a   Cart-1   CUTL1   aMEF-2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidMNS1 promoter sequence
   Search Chromatin IP Primers for MNS1

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat MNS1


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

Entrez Gene cytogenetic band: 15q21.3   Ensembl cytogenetic band:  15q21.3   HGNC cytogenetic band: 15q21.3

MNS1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MNS1 gene location

GeneLoc information about chromosome 15         GeneLoc Exon Structure

GeneLoc location for GC15M056720:  view genomic region     (about GC identifiers)

Start:
56,713,742 bp from pter      End:
56,757,335 bp from pter
Size:
43,594 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, 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, Cloud-Clone Corp., and/or eBioscience,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., and/or eBioscience, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: MNS1_HUMAN, Q8NEH6 (See protein sequence)
Recommended Name: Meiosis-specific nuclear structural protein 1  
Size: 495 amino acids; 60571 Da
Secondary accessions: Q8IYT6 Q9NUP4

Explore the universe of human proteins at neXtProt for MNS1: NX_Q8NEH6

Explore proteomics data for MNS1 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See MNS1 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins: NP_060835.1  
    ENSEMBL proteins: 
     ENSP00000260453  

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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    1 InterPro protein domain:
     IPR026504 MNS1

    Graphical View of Domain Structure for InterPro Entry Q8NEH6

    ProtoNet protein and cluster: Q8NEH6

    UniProtKB/Swiss-Prot: MNS1_HUMAN, Q8NEH6
    Similarity: Belongs to the MNS1 family


    Find genes that share domains with MNS1           About GenesLikeMe


    (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,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: MNS1_HUMAN, Q8NEH6
    Function: May play a role in the control of meiotic division and germ cell differentiation through regulation of
    pairing and recombination during meiosis (By similarity)

         Gene Ontology (GO): 1 molecular function term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0042802identical protein binding IDA--
         
    Find genes that share ontologies with MNS1           About GenesLikeMe


    Phenotypes:
         6 MGI mutant phenotypes (inferred from 1 allele(MGI details for Mns1):
     endocrine/exocrine gland  growth/size/body  mortality/aging  nervous system  reproductive system 
     respiratory system 

    Find genes that share phenotypes with MNS1           About GenesLikeMe

    Animal Models:
         MGI mouse knock-out Mns1tm1Jw for MNS1

       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for MNS1
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       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for MNS1

    miRNA
    Products:
        
    miRTarBase miRNAs that target MNS1:
    hsa-mir-375 (MIRT019835), hsa-mir-192-5p (MIRT026492), hsa-mir-215-5p (MIRT024920)

    Block miRNA regulation of human, mouse, rat MNS1 using miScript Target Protectors
    2 qRT-PCR Assays for microRNAs that regulate MNS1:
    hsa-miR-140-5p hsa-miR-489
    SwitchGear 3'UTR luciferase reporter plasmidMNS1 3' UTR sequence
    Inhib. RNA
    Products:
        
    OriGene RNAi products in human, mouse, rat for MNS1
    Predesigned siRNA for gene silencing in human, mouse, rat MNS1

    Gene Editing
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    Clone
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat MNS1

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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for MNS1


    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from UniProtKB/Swiss-Prot
    MNS1_HUMAN, Q8NEH6: Nucleus (By similarity)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus3
    cytoskeleton2
    cytosol1
    endoplasmic reticulum1

    Gene Ontology (GO): 4 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005635nuclear envelope IEA--
    GO:0005882intermediate filament IEA--
    GO:0005930axoneme IEA--
    GO:0036126sperm flagellum IEA--

    Find genes that share ontologies with MNS1           About GenesLikeMe


    (SuperPaths according to PathCards, Pathways according to 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 QIAGEN, 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 Apr 2014 via Entrez Gene).
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        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for MNS1
    Interactions:

        Search GeneGlobe Interaction Network for MNS1

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

    Selected Interacting proteins for MNS1 (Q8NEH62, 3 ENSP000002604534) via UniProtKB, MINT, STRING, and/or I2D (see all 6)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    EWSR1Q018443, ENSP000003810314I2D: score=3 STRING: ENSP00000381031
    APCP250543I2D: score=2 
    EIF3HENSP000002766824STRING: ENSP00000276682
    --Q9BWA23, 2MINT-66395 I2D: score=1 
    --Q9BWA23, 2MINT-66395 I2D: score=1 
    About this table

    Gene Ontology (GO): 3 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007126meiotic nuclear division IEA--
    GO:0044782cilium organization IEA--
    GO:0070986left/right axis specification IEA--

    Find genes that share ontologies with MNS1           About GenesLikeMe



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for MNS1



    (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,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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    REFSEQ mRNAs for MNS1 gene: 
    NM_018365.2  

    Unigene Cluster for MNS1:

    Meiosis-specific nuclear structural 1
    Hs.444483  [show with all ESTs]
    Unigene Representative Sequence: NM_018365
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000566386 ENST00000260453(uc010bfo.2 uc002adr.2) ENST00000558694

    miRNA
    Products:
         
    Block miRNA regulation of human, mouse, rat MNS1 using miScript Target Protectors
    2 qRT-PCR Assays for microRNAs that regulate MNS1:
    hsa-miR-140-5p hsa-miR-489
    SwitchGear 3'UTR luciferase reporter plasmidMNS1 3' UTR sequence
    Inhib. RNA
    Products:
         
    OriGene RNAi products in human, mouse, rat for MNS1
    Predesigned siRNA for gene silencing in human, mouse, rat MNS1
    Clone
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    Primer
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    OriGene qPCR primer pairs and template standards for MNS1
    OriGene qSTAR qPCR primer pairs in human, mouse for MNS1
    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat MNS1
      QuantiTect SYBR Green Assays in human, mouse, rat MNS1
      QuantiFast Probe-based Assays in human, mouse, rat MNS1

    Additional mRNA sequence: 

    AK002084.1 AK057542.1 BC012554.1 BC031046.1 BC034991.2 

    7 DOTS entries:

    DT.104221  DT.95106656  DT.100000813  DT.121055886  DT.40203956  DT.75134216  DT.92005376 

    Selected AceView cDNA sequences (see all 63):

    BX332829 BM718474 BM723258 BQ690909 AI263135 AK057542 BI825252 BQ685758 
    AU138250 AA782916 BX350092 AI028266 BC012554 BC031046 BU075701 AK002084 
    AL699110 BM983729 BU674993 AI911786 AI829741 AI968265 BM682262 BM683518 

    GeneLoc Exon Structure

    4 Alternative Splicing Database (ASD) splice patterns (SP) for MNS1    About this scheme

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


    ECgene alternative splicing isoforms for MNS1

    (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™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    MNS1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: CTACAAACTT
    MNS1 Expression
    About this image


    MNS1 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 7) fully expand
     
     Brain (Nervous System)    fully expand to see all 4 entries
             Cerebral Cortex
     
     Testis (Reproductive System)
             Leydig Cells Testis Interstitium
     
     Heart (Cardiovascular System)
             Cardiac Crescent Cells Cardiac Crescent
     
     Trophoblast (Extraembryonic Tissues)
             Trophoblast Cells Trophoblast
     
     Ovary (Reproductive System)
             Oviduct
    MNS1 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    MNS1 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.444483
        Custom PCR Arrays for MNS1
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    In Situ
    Assay Products:
     

     
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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)
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    This gene was present in the common ancestor of animals.

    Orthologs for MNS1 gene from Selected species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Mns11 , 5 meiosis-specific nuclear structural protein 11, 5 76.1(n)1
    77.39(a)1
      9 (40.08 cM)5
    174271  NM_008613.31  NP_032639.11 
     724380115 
    chicken
    (Gallus gallus)
    Aves LOC4262951 meiosis-specific nuclear structural protein 1-like 70(n)
    65.71(a)
      426295  XM_423957.4  XP_423957.4 
    lizard
    (Anolis carolinensis)
    Reptilia MNS16
    meiosis-specific nuclear structural 1
    62(a)
    1 ↔ 1
    GL343573.1(455407-458724)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia Str.70242 Transcribed sequence with weak similarity to protein more 76.2(n)    BX740292.1 
    zebrafish
    (Danio rerio)
    Actinopterygii sbcb4942 sbcb494 72.08(n)   368341  NM_199433.1 
    mosquito
    (Anopheles gambiae)
    Insecta AgaP_AGAP0042081 AgaP_AGAP004208 50(n)
    36.21(a)
      1274046  XM_313110.5  XP_313110.5 


    ENSEMBL Gene Tree for MNS1 (if available)
    TreeFam Gene Tree for MNS1 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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      --

    (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), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for MNS1 (see all 850)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 15 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1807336691,2
    --33543596(+) TATTAC/TCCACA 1 -- ds50010--------
    rs746659281,2
    F--33543604(+) ACACAT/GTTTTA 1 -- ds50011Minor allele frequency- G:0.12WA 118
    rs1999495521,2
    C--33543633(+) GTGGCC/GTACTC 1 -- ds50010--------
    rs1863135601,2
    C--33543637(+) CCTACA/TCTTAA 1 -- ds50010--------
    rs3680012961,2
    C--33543638(+) CTACTC/GTTAAT 1 -- ds50010--------
    rs1427053021,2
    F--33543705(+) ATGCTA/GTCTTT 1 -- ds50011Minor allele frequency- G:0.00NA 4524
    rs1423955201,2
    C--33543762(+) GTGATC/GTACTT 1 -- ds50010--------
    rs770315911,2
    C,F--33543818(+) TTGTAG/CTGGTT 1 -- ds50011Minor allele frequency- C:0.07NA 120
    rs15544101,2
    C,F,A--33543829(-) AAAATA/CATTCA 1 -- ds50017Minor allele frequency- C:0.36MN NA WA EA 548
    rs286228881,2
    C,F--33543951(+) TTAGCG/ATGACA 1 -- ds500112Minor allele frequency- A:0.27NA WA CSA EA 378

    HapMap Linkage Disequilibrium report for MNS1 (56713742 - 56757335 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 10 variations for MNS1:    About this table    
    Variant IDTypeSubtypePubMed ID
    dgv10n31CNV Deletion19718026
    esv2525559CNV Loss19546169
    nsv9270CNV Loss18304495
    nsv433294CNV Loss18776910
    nsv498847CNV Loss21111241
    nsv510662CNV Loss20534489
    nsv1545CNV Loss18451855
    nsv904246CNV Loss21882294
    esv35150CNV Loss17911159
    dgv749e1CNV Complex17122850

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing MNS1
    DNA2.0 Custom Variant and Variant Library Synthesis for MNS1

    (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.)
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    OMIM gene information: 610766    OMIM disorders: --

    1 disease from the University of Copenhagen DISEASES database for MNS1:
    Situs inversus

    Find genes that share disorders with MNS1           About GenesLikeMe

    Genetic Association Database (GAD): MNS1

    Export disorders for MNS1 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)
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    PubMed articles for MNS1 gene integrated from 10 sources:
    (articles sorted by number of sources associating them with MNS1)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    2. Meiosis specific transcription and functional proteins. (PubMed id 7625268)1, 3 Hotta Y....Tabata S. (Adv. Biophys. 1995)
    3. cDNA cloning and functional characterization of a meiosis-specific protein (MNS1) with apparent nuclear association. (PubMed id 8032679)1, 3 Furukawa K....Hotta Y. (Chromosome Res. 1994)
    4. Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. (PubMed id 24068947)1 Brandler W.M....Paracchini S. (PLoS Genet. 2013)
    5. A Y2H-seq approach defines the human protein methyltransferase interactome. (PubMed id 23455924)1 Weimann M.... Stelzl U. (Nat. Methods 2013)
    6. Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. (PubMed id 17903303)4 O'Donnell C.J....Demissie S. (BMC Med. Genet. 2007)
    7. Towards a proteome-scale map of the human protein-protein interaction network. (PubMed id 16189514)1 Rual J.F....Vidal M. (Nature 2005)
    8. Proteomics profiling of nuclear proteins for kidney fibroblasts suggests hypoxia, meiosis, and cancer may meet in the nucleus. (PubMed id 15942958)1 Shakib K....Godovac-Zimmermann J. (Proteomics 2005)
    9. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S.... Malek J. (Genome Res. 2004)
    10. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (Proc. Natl. Acad. Sci. U.S.A. 2002)

    (in PubMed, OMIM, and NCBI Bookshelf)
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     ANDOR
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      Query String
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    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)
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    Entrez Gene: 55329 HGNC: 29636 AceView: MNS1 Ensembl:ENSG00000138587 euGenes: HUgn55329
    ECgene: MNS1 H-InvDB: MNS1

    (According to HUGE)
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    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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    NameDescription
    PharmGKB entry for MNS1 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for MNS1 gene:
    Search GeneIP for patents involving MNS1

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, eBioscience, and/or others, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Addgene, Cell lines from GenScript, and ESI BIO, Flow cytometery from eBioscience, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
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