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NCOA7 Gene

protein-coding   GIFtS: 54
GCID: GC06P126102

Nuclear Receptor Coactivator 7

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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
Nuclear Receptor Coactivator 71 2     Nbla000522
ERAP1402 3 5     Nbla109932
TBC/LysM-Associated Domain Containing 41 2     TLDC42
Estrogen Nuclear Receptor Coactivator 12 3     dJ187J11.32
140 KDa Estrogen Receptor-Associated Protein2 3     Estrogen Receptor Associated Protein 140 KDa2
ESNA12 3     Putative Protein Product Of Nbla000522
NCOA7-AS2     Putative Protein Product Of Nbla109932

External Ids:    HGNC: 210811   Entrez Gene: 1351122   Ensembl: ENSG000001119127   OMIM: 6097525   UniProtKB: Q8NI083   

Export aliases for NCOA7 gene to outside databases

Previous GC identifers: GC06P126037 GC06P126082 GC06P126144 GC06P123687


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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GeneCards Summary for NCOA7 Gene:
NCOA7 (nuclear receptor coactivator 7) is a protein-coding gene. GO annotations related to this gene include nuclear hormone receptor binding and ligand-dependent nuclear receptor transcription coactivator activity. An important paralog of this gene is TLDC1.

UniProtKB/Swiss-Prot: NCOA7_HUMAN, Q8NI08
Function: Enhances the transcriptional activities of several nuclear receptors. Involved in the coactivation of
different nuclear receptors, such as ESR1, THRB, PPARG and RARA

Gene Wiki entry for NCOA7 Gene


(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_000006.11  NT_025741.16  NC_018917.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the NCOA7 gene promoter:
         AhR   AP-1   FOXD1   POU3F2 (N-Oct-5b)   AP-4   Arnt   C/EBPalpha   Egr-2   FOXJ2 (long isoform)   FOXJ2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 3): NCOA7 promoter sequence
   Search Chromatin IP Primers for NCOA7

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat NCOA7


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

Entrez Gene cytogenetic band: 6q22.32   Ensembl cytogenetic band:  6q22.32   HGNC cytogenetic band: 6q22.33

NCOA7 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
NCOA7 gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06P126102:  view genomic region     (about GC identifiers)

Start:
126,102,307 bp from pter      End:
126,253,176 bp from pter
Size:
150,870 bases      Orientation:
plus 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., eBioscience, and/or antibodies-online,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., eBioscience, and/or antibodies-online, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, Cloud-Clone Corp, antibodies-online, and/or others.)
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UniProtKB/Swiss-Prot: NCOA7_HUMAN, Q8NI08 (See protein sequence)
Recommended Name: Nuclear receptor coactivator 7  
Size: 942 amino acids; 106162 Da
Subunit: Interacts with ESR1, ESR2A, ESR2B, THRB, PPARG and RARA in a ligand-inducible manner. Interacts with the
heterodimer AHR-ARNT
Sequence caution: Sequence=CAD89948.1; Type=Frameshift; Positions=782;
Secondary accessions: B2RNS2 B7Z2C4 B9EH71 G8JL91 Q3LID6 Q4G0V1 Q5TF95 Q6IPQ4 Q6NE83 Q86T89
Q8N1W4
Alternative splicing: 7 isoforms:  Q8NI08-1   Q8NI08-2   Q8NI08-3   Q8NI08-4   Q8NI08-5   Q8NI08-6   Q8NI08-7   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for NCOA7: NX_Q8NI08

Explore proteomics data for NCOA7 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See NCOA7 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (6 alternative transcripts): 
    NP_001116314.1  NP_001186548.1  NP_001186549.1  NP_001186550.1  NP_001186551.1  NP_861447.3  

    ENSEMBL proteins: 
     ENSP00000357341   ENSP00000403643   ENSP00000406363   ENSP00000407426   ENSP00000408211  
     ENSP00000389186   ENSP00000411002   ENSP00000402468   ENSP00000398268   ENSP00000407684  
     ENSP00000376269   ENSP00000229634  

    NCOA7 Human Recombinant Protein Products:

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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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    2 InterPro protein domains:
     IPR018392 LysM_dom
     IPR006571 TLDc

    Graphical View of Domain Structure for InterPro Entry Q8NI08

    ProtoNet protein and cluster: Q8NI08

    2 Blocks protein domains:
    IPB002482 Peptidoglycan-binding LysM
    IPB004182 GRAM domain


    UniProtKB/Swiss-Prot: NCOA7_HUMAN, Q8NI08
    Similarity: Belongs to the OXR1 family
    Similarity: Contains 1 LysM repeat
    Similarity: Contains 1 TLD domain


    Find genes that share domains with NCOA7           About GenesLikeMe


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, 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: NCOA7_HUMAN, Q8NI08
    Function: Enhances the transcriptional activities of several nuclear receptors. Involved in the coactivation of
    different nuclear receptors, such as ESR1, THRB, PPARG and RARA

         Gene Ontology (GO): 3 molecular function terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding IPI10395741
    GO:0030374ligand-dependent nuclear receptor transcription coactivator activity IDA11971969
    GO:0035257nuclear hormone receptor binding IDA11971969
         
    Find genes that share ontologies with NCOA7           About GenesLikeMe


    Animal Models:
       genOway: Develop your customized and physiologically relevant rodent model for NCOA7

    miRNA
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    miRTarBase miRNAs that target NCOA7:
    hsa-mir-375 (MIRT020066)

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    hsa-miR-579 hsa-miR-3938 hsa-miR-520e hsa-miR-4272 hsa-miR-128 hsa-miR-632 hsa-miR-342-3p hsa-miR-519a
    SwitchGear 3'UTR luciferase reporter plasmidNCOA7 3' UTR sequence
    Inhib. RNA
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    (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
    NCOA7_HUMAN, Q8NI08: Nucleus (Probable)
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus4
    cytosol2

    Gene Ontology (GO): 2 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular IDA--
    GO:0005634nucleus IEA--

    Find genes that share ontologies with NCOA7           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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    SuperPaths for NCOA7 About    
    See pathways by source

    SuperPathContained pathways About
    1AHR Pathway (Qiagen)
    AHR Pathway

    1 Downloadable PowerPoint Slide of GeneGlobe Pathway Central Maps for NCOA7
        AHR Pathway


        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for NCOA7
    Interactions:

        GeneGlobe Interaction Network for NCOA7

    STRING Interaction Network Preview (showing 5 interactants - click image to see 18)

    Selected Interacting proteins for NCOA7 (Q8NI081, 3 ENSP000003573414) via UniProtKB, MINT, STRING, and/or I2D (see all 22)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    AHRP358691, 3, ENSP000002420574EBI-80799,EBI-80780 I2D: score=1 STRING: ENSP00000242057
    GABARAPO951661, 3EBI-80799,EBI-712001 I2D: score=3 
    GABARAPL1Q9H0R81, 3EBI-80799,EBI-746969 I2D: score=2 
    ARNTP275401, 3, ENSP000003514074EBI-80799,EBI-80809 I2D: score=1 STRING: ENSP00000351407
    ESR2Q927313, ENSP000003439254I2D: score=1 STRING: ENSP00000343925
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-templated IEA--
    GO:0016998cell wall macromolecule catabolic process IEA--
    GO:0045944positive regulation of transcription from RNA polymerase II promoter IDA11971969

    Find genes that share ontologies with NCOA7           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 NCOA7



    (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 NCOA7 gene (6 alternative transcripts): 
    NM_001122842.2  NM_001199619.1  NM_001199620.1  NM_001199621.1  NM_001199622.1  NM_181782.4  

    Unigene Cluster for NCOA7:

    Nuclear receptor coactivator 7
    Hs.171426  [show with all ESTs]
    Unigene Representative Sequence: NM_001199620
    13 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000368357(uc010kes.3 uc003qae.4) ENST00000453302 ENST00000417494
    ENST00000428318 ENST00000487635(uc003qaj.3) ENST00000419660 ENST00000413085
    ENST00000433571 ENST00000448104 ENST00000438495(uc003qak.3) ENST00000444128
    ENST00000392477(uc003qaf.3 uc003qag.3 uc003qah.3 uc003qai.3 uc010ket.3)
    ENST00000229634
    miRNA
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    hsa-miR-579 hsa-miR-3938 hsa-miR-520e hsa-miR-4272 hsa-miR-128 hsa-miR-632 hsa-miR-342-3p hsa-miR-519a
    SwitchGear 3'UTR luciferase reporter plasmidNCOA7 3' UTR sequence
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      QuantiFast Probe-based Assays in human, mouse, rat NCOA7

    Additional mRNA sequence: 

    AB074156.1 AF493978.1 AJ420542.1 AK094706.1 AK127512.1 AK294558.1 AK307395.1 AL832621.2 
    AL832628.2 AL834442.1 AY364254.1 BC009399.2 BC033612.1 BC039853.1 BC071782.1 BC137094.1 
    BC137095.1 BX537385.1 

    16 DOTS entries:

    DT.443898  DT.100818615  DT.101984130  DT.95159186  DT.95159187  DT.95100047  DT.100818616  DT.40193940 
    DT.95323840  DT.121338514  DT.121338542  DT.100818614  DT.40229034  DT.40313541  DT.91785426  DT.99999305 

    Selected AceView cDNA sequences (see all 180):

    BC039853 F02660 AI273202 Z40903 BQ774052 AI745670 BM980857 BC071782 
    AA588025 AK127512 AW593500 AW004797 BF002319 BQ003857 BM194579 AW778883 
    AI621035 BM788863 BM264079 BU674846 CD677634 BF594619 BQ227562 BC036461 

    GeneLoc Exon Structure

    Selected Alternative Splicing Database (ASD) splice patterns (SP) for NCOA7 (see all 9)    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3a · 3b · 3c ^ 4 ^ 5 ^ 6a · 6b ^ 7 ^ 8 ^ 9 ^ 10 ^ 11a · 11b ^ 12a · 12b ^ 13 ^ 14 ^ 15a · 15b ^ 16 ^ 17a · 17b ^ 18a ·
    SP1:                    -     -     -     -                                                     -                             -     -                 -         
    SP2:                                      -                                                     -     -                       -     -                 -         
    SP3:                                      -                                                     -                             -     -                 -         
    SP4:                                      -                                                                                                                     
    SP5:                                      -           -     -                                   -     -                                                         

    ExUns: 18b ^ 19 ^ 20a · 20b · 20c
    SP1:                              
    SP2:                              
    SP3:                              
    SP4:                              
    SP5:                              


    ECgene alternative splicing isoforms for NCOA7

    (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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    NCOA7 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: --
    NCOA7 Expression
    About this image


    NCOA7 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 5) fully expand
     
     Blood (Hematopoietic System)
             Proerythroblasts Hematopoietic Bone Marrow
     
     Brain (Nervous System)
             Cerebral Cortex
     
     Adrenal Gland (Endocrine System)
     
     Kidney (Urinary System)
     
     Gall Bladder (Hepatobiliary System)
    NCOA7 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    NCOA7 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.171426

    UniProtKB/Swiss-Prot: NCOA7_HUMAN, Q8NI08
    Tissue specificity: Highly expressed in brain. Weakly expressed in mammary gland, ovary, uterus, prostate,
    stomach, bladder, spinal cord and pancreas. Expressed in cancer cell line

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    In Situ
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for NCOA7

    (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 chordates.

    Orthologs for NCOA7 gene from Selected species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Ncoa71 , 5 nuclear receptor coactivator 71, 5 83.78(n)1
    83.17(a)1
      10 (17.11 cM)5
    2113291  NM_172495.51  NP_766083.31 
     306455845 
    chicken
    (Gallus gallus)
    Aves NCOA71 nuclear receptor coactivator 7 70.85(n)
    69(a)
      421717  NM_001012878.1  NP_001012896.1 
    lizard
    (Anolis carolinensis)
    Reptilia NCOA76
    nuclear receptor coactivator 7
    65(a)
    1 ↔ 1
    1(180399509-180442908)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia LOC1004874481 nuclear receptor coactivator 7-like 67.55(n)
    68.17(a)
      100487448  XM_002933215.2  XP_002933261.2 
    zebrafish
    (Danio rerio)
    Actinopterygii Dr.198162 Transcribed sequence with weak similarity to protein more 76.35(n)    57051357 


    ENSEMBL Gene Tree for NCOA7 (if available)
    TreeFam Gene Tree for NCOA7 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for NCOA7 gene
    TLDC12  OXR12  TLDC22  
    6 SIMAP similar genes for NCOA7 using alignment to 12 protein entries:     NCOA7_HUMAN (see all proteins):
    Nbla00052    DKFZp451P0217    DKFZp761B2210    C20orf118    OXR1    TLDC2

    Find genes that share paralogs with NCOA7           About GenesLikeMe



    (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 NCOA7 (see all 2776)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1872944101,2
    --126100328(+) ATAGCA/CGGGCC 2 -- us2k10--------
    rs1157486251,2
    F--126100521(+) CAAAGG/ATTAGG 2 -- us2k11Minor allele frequency- A:0.01WA 118
    rs17393861,2
    C,F,H--126100556(+) AAAAAC/ACCTTA 2 -- us2k19Minor allele frequency- A:0.14NS EA WA CSA 646
    rs1918680251,2
    --126100589(+) CTTTTC/TTTGAC 2 -- us2k10--------
    rs1497175291,2
    --126100625(+) AGGAAC/TTCCCA 2 -- us2k10--------
    rs1839505071,2
    --126100782(+) GTTAGA/CCAAAA 2 -- us2k10--------
    rs1894039311,2
    --126100908(+) AATAAA/TCTCCA 2 -- us2k10--------
    rs775230441,2
    F--126100927(+) AATCTT/CAATGT 2 -- us2k11Minor allele frequency- C:0.02EA 120
    rs1927166521,2
    C--126101026(+) AATCAA/GGGTTA 2 -- us2k10--------
    rs1445673191,2
    C--126101103(+) TTAGAA/GTCACA 2 -- us2k10--------

    HapMap Linkage Disequilibrium report for NCOA7 (126102307 - 126253176 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for NCOA7 (see all 16):    About this table    
    Variant IDTypeSubtypePubMed ID
    dgv1150e199CNV Deletion23128226
    esv2732680CNV Deletion23290073
    esv2677863CNV Deletion23128226
    esv2670095CNV Deletion23128226
    esv2425031CNV Deletion19546169
    nsv820882CNV Deletion20802225
    esv2421628CNV Deletion20811451
    nsv436509CNV Deletion17901297
    nsv830796CNV Loss17160897
    nsv499628CNV Loss21111241

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing NCOA7
    DNA2.0 Custom Variant and Variant Library Synthesis for NCOA7

    (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: 609752    OMIM disorders: --


    Find genes that share disorders with NCOA7           About GenesLikeMe

    Genetic Association Database (GAD): NCOA7
    Human Genome Epidemiology (HuGE) Navigator: NCOA7 (2 documents)

    Export disorders for NCOA7 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 NCOA7 gene, integrated from 10 sources (see all 31):
    (articles sorted by number of sources associating them with NCOA7)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. ERAP140, a conserved tissue-specific nuclear receptor coactivator. (PubMed id 11971969)1, 2, 3 Shao W.... Brown M. (Mol. Cell. Biol. 2002)
    2. No association between the Nuclear Receptor Coactivator 7 gene and schizophrenia in the Chinese Han population. (PubMed id 17079118)1, 4, 9 Liu Y....He L. (Schizophr. Res. 2007)
    3. 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. (Genome Res. 2004)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    5. Neuroblastoma oligo-capping cDNA project: toward the understanding of the genesis and biology of neuroblastoma. (PubMed id 12880961)1, 2 Ohira M.... Nakagawara A. (Cancer Lett. 2003)
    6. The DNA sequence and analysis of human chromosome 6. (PubMed id 14574404)1, 2 Mungall A.J.... Beck S. (Nature 2003)
    7. Interactions of nuclear receptor coactivator/corepressor proteins with the aryl hydrocarbon receptor complex. (PubMed id 10395741)1, 2 Nguyen T.A.... Safe S. (Arch. Biochem. Biophys. 1999)
    8. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. (PubMed id 23872634)1 Bezzina C.R....Redon R. (Nat. Genet. 2013)
    9. A high-throughput approach for measuring temporal changes in the interactome. (PubMed id 22863883)1 Kristensen A.R....Foster L.J. (Nat. Methods 2012)
    10. N-terminal acetylome analyses and functional insights of the N- terminal acetyltransferase NatB. (PubMed id 22814378)2 Van Damme P....Aldabe R. (Proc. Natl. Acad. Sci. U.S.A. 2012)

    (in PubMed, OMIM, and NCBI Bookshelf)
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     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)
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    Entrez Gene: 135112 HGNC: 21081 AceView: NCOA7 Ensembl:ENSG00000111912 euGenes: HUgn135112
    ECgene: NCOA7 H-InvDB: NCOA7

    (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 NCOA7 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 NCOA7 gene:
    Search GeneIP for patents involving NCOA7

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



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