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

C11orf82 Gene

protein-coding   GIFtS: 41
GCID: GC11P082612

chromosome 11 open reading frame 82

 Explore 1 disease affiliated with
C11orf82 via our new
 Human Malady Compendium 
Biological research products
for C11orf82
    

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

Aliases
Chromosome 11 Open Reading Frame 821 2
Noxin1
FLJ254161
FLJ388381
Nitric Oxide-Inducible Gene Protein2

External Ids:    HGNC: 263511   Entrez Gene: 2200422   Ensembl: ENSG000001654907   UniProtKB: Q8IXT13   

Export aliases for C11orf82 gene to outside databases

Previous GC identifers: GC11P082291 GC11P078910


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

UniProtKB/Swiss-Prot: NOXIN_HUMAN, Q8IXT1
Function: Acts as an anti-apoptotic factor and its absence increases cell death under normal and stress conditions. Can
induce cell cycle arrest in the G1 or early S phase and this activity is independent of p53/TP53 (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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000011.9  NC_018922.1  NT_167190.1  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the C11orf82 gene promoter:
         GR   Sox5   Tal-1   AML1a   GR-beta   HNF-1A   PPAR-alpha   HNF-1   SEF-1 (1)   GR-alpha   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for C11orf82

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat C11orf82


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

Entrez Gene cytogenetic band: 11q14.1   Ensembl cytogenetic band:  11q14.1   HGNC cytogenetic band: 11q14.1

C11orf82 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
C11orf82 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P082612:  view genomic region     (about GC identifiers)

Start:
82,611,017 bp from pter      End:
82,669,319 bp from pter
Size:
58,303 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: NOXIN_HUMAN, Q8IXT1 (See protein sequence)
Recommended Name: Nitric oxide-inducible gene protein  
Size: 998 amino acids; 111616 Da
Subcellular location: Cytoplasm (By similarity). Nucleus (By similarity). Note=Accumulates in the nucleus in response
to stress (By similarity)
Sequence caution: Sequence=BAB14764.1; Type=Erroneous initiation;
Secondary accessions: Q96LK6 Q9H856
Alternative splicing: 2 isoforms:  Q8IXT1-1   Q8IXT1-2   

Explore the universe of human proteins at neXtProt for C11orf82: NX_Q8IXT1

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8IXT1

  • C11orf82 Protein expression data from MOPED and PaxDb:    About this image 
    C11orf82 Protein Expression
    REFSEQ proteins: NP_659455.3  
    ENSEMBL proteins: 
     ENSP00000433306   ENSP00000436241   ENSP00000431234   ENSP00000435424   ENSP00000435421  
     ENSP00000431206   ENSP00000434427   ENSP00000436611   ENSP00000432871   ENSP00000414687  
     ENSP00000329930  

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    Browse Proteins at Uscn

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IEA--
    GO:0005737cytoplasm IEA--

    C11orf82 for ontologies           About GeneDecksing



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    Browse ELISAs and CLIAs at Uscn


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

    C11orf82 for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR012340 NA-bd_OB-fold
     IPR013955 Rep_factor-A_C

    Graphical View of Domain Structure for InterPro Entry Q8IXT1

    ProtoNet protein and cluster: Q8IXT1


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, 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, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: NOXIN_HUMAN, Q8IXT1
    Function: Acts as an anti-apoptotic factor and its absence increases cell death under normal and stress conditions. Can
    induce cell cycle arrest in the G1 or early S phase and this activity is independent of p53/TP53 (By similarity)

    Phenotypes:
         1 GenomeRNAi human phenotype for C11orf82:

     Decreased influenza A virus in 

    Animal Models:
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    miRNA
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for C11orf82

    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:0006915apoptotic process IEA--
    GO:0007050cell cycle arrest ----
    GO:0007286spermatid development IEA--
    GO:0030097hemopoiesis IEA--
    GO:0033554cellular response to stress IEA--

    C11orf82 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for C11orf82
    Search CenterWatch for drugs/clinical trials and news about C11orf82 / NOXIN 

    (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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, Sirion Biotech, microRNA from QIAGEN,
    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 C11orf82 gene: 
    NM_145018.3  

    Unigene Cluster for C11orf82:

    Chromosome 11 open reading frame 82
    Hs.165607  [show with all ESTs]
    Unigene Representative Sequence: NM_145018
    13 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000532277 ENST00000524921 ENST00000528759(uc010rss.2) ENST00000525361(uc009yvd.2)
    ENST00000533655(uc001ozt.3 uc010rsr.2) ENST00000532764 ENST00000532589
    ENST00000528189 ENST00000525388 ENST00000528262 ENST00000533750 ENST00000430323
    ENST00000329143

    miRNA
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    8/10 QIAGEN miScript miRNA Assays for microRNAs that regulate C11orf82 (see all 10):
    hsa-miR-142-5p hsa-miR-20a hsa-miR-519d hsa-miR-125a-3p hsa-miR-106a hsa-miR-106b hsa-miR-93 hsa-miR-20b
    SwitchGear 3'UTR luciferase reporter plasmidC11orf82 3' UTR sequence
    Inhib. RNA
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    OriGene shRNA RFP: C11orf82
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    Additional cDNA sequence: 

    AK023998.1 AK058145.1 AK096157.1 AK292399.1 AK297366.1 AK299581.1 BC039268.1 

    7 DOTS entries:

    DT.91846921  DT.442170  DT.95191334  DT.100777136  DT.95149443  DT.120742517  DT.120742542 

    24/53 AceView cDNA sequences (see all 53):

    AK058145 AW664845 BU431639 AW872975 BF478106 CR613676 AA946869 AA781175 
    AA992090 AA477171 CA441300 AI766808 AI654796 BX365621 BX370517 AW515075 
    BG743904 BM829262 NM_145018 BF343258 AU253903 AL705883 AI376202 AU142737 

    GeneLoc Exon Structure

    5/6 Alternative Splicing Database (ASD) splice patterns (SP) for C11orf82 (see all 6)    About this scheme

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


    ECgene alternative splicing isoforms for C11orf82

    (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

    C11orf82 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: --
    C11orf82 Expression
    About this image

    C11orf82 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table

    Stem Cell Differentiation: 2 LifeMap Cells 
    NameCategory
    PureStem™ progenitor E44 (Embryonic Progenitor Cell)
    PureStem™ progenitor F15 (Embryonic Progenitor Cell)
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See C11orf82 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for C11orf82

    SOURCE GeneReport for Unigene cluster: Hs.165607
        SABiosciences Custom PCR Arrays for C11orf82
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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)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for C11orf82 gene from 4/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia 4632434I11Rik1 , 5 RIKEN cDNA 4632434I11 gene1, 5 73.55(n)1
    55.19(a)1
      7 (51.64 cM)5
    740411  NM_001080995.11  NP_001074464.11 
     928575295 
    chicken
    (Gallus gallus)
    Aves C11orf826
    Uncharacterized protein
    38(a)
    1 ↔ 1
    1(193403817-193409109)
    lizard
    (Anolis carolinensis)
    Reptilia C11orf826
    --
    58(a)
    1 ↔ 1
    3(202240803-202241881)
    zebrafish
    (Danio rerio)
    Actinopterygii si:ch73-115d3.46
    si:ch73-115d3.4
    24(a)
    1 ↔ 1
    21(21987708-21992855)


    ENSEMBL Gene Tree for C11orf82 (if available)
    TreeFam Gene Tree for C11orf82 (if available) 

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

    (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

    10/558 NCBI SNPs in C11orf82 are shown (see all 558    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1817828801,2
    --82613597(+) TCTTTA/TACATG 1 -- int10--------
    rs1850842841,2
    --82613707(+) GCACTA/GTCCTC 1 -- int10--------
    rs1510320771,2
    --82613897(+) TGCTAA/GGTACT 1 -- int10--------
    rs1895487971,2
    C--82613989(+) AAACTA/GTGTGA 1 -- int10--------
    rs1831688581,2
    --82614008(+) GGTCTA/GAGAAG 1 -- int10--------
    rs1411060361,2
    --82614242(+) AGACCA/GGATCA 1 -- int10--------
    rs1448982121,2
    --82614385(+) GTGTGA/TTGTGG 1 -- int10--------
    rs1865258811,2
    --82614465(+) GTACCA/GTTTAC 1 -- int10--------
    rs761477751,2
    F--82614538(+) GTATCG/ATACTA 1 -- int12Minor allele frequency- A:0.07WA NA 238
    rs1479327491,2
    --82614746(+) AGTATC/GTGCCA 1 -- int10--------

    HapMap Linkage Disequilibrium report for C11orf82 (82611017 - 82669319 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for C11orf82
         1 CNV: 6945

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

    C11orf82 for disorders           About GeneDecksing

    1 disease for C11orf82:    About MalaCards
    carcinoma


    Export disorders for C11orf82 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 C11orf82 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with C11orf82)
        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. (2004)
    2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1, 3 Strausberg R.L....Marra M.A. (2002)
    3. noxin, a novel stress-induced gene involved in cell cycle and apoptosis. (PubMed id 17515607)1 Nakaya N....Enikolopov G. (2007)
    4. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
    5. Human chromosome 11 DNA sequence and analysis including novel gene identification. (PubMed id 16554811)2 Taylor T.D....Sakaki Y. (2006)
    6. 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. (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: 220042 HGNC: 26351 AceView: FLJ25416 Ensembl:ENSG00000165490 euGenes: HUgn220042
    ECgene: C11orf82 H-InvDB: C11orf82

    (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 C11orf82 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
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    VWF
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    von Willebrand factor
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