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C18orf8 Gene

protein-coding   GIFtS: 49
GCID: GC18P021083

Chromosome 18 Open Reading Frame 8

  See C18orf8-related disease
at  

(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
Chromosome 18 Open Reading Frame 81 2     Mic-12 3
Macrophage Inhibitory Cytokine 11 2     Colon Cancer Associated Protein Mic11
Colon Cancer-Associated Protein Mic12 3     HsT25912
MIC12 3     Uncharacterized Protein C18orf82

External Ids:    HGNC: 243261   Entrez Gene: 299192   Ensembl: ENSG000001414527   UniProtKB: Q96DM33   

Export aliases for C18orf8 gene to outside databases

Previous GC identifers: GC18P019335 GC18P019337 GC18P017938


(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 C18orf8 Gene:
This gene encodes a colon cancer associated protein. (provided by RefSeq, Jan 2013)

GeneCards Summary for C18orf8 Gene:
C18orf8 (chromosome 18 open reading frame 8) is a protein-coding gene. Diseases associated with C18orf8 include colon cancer.




(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_000018.9  NT_010966.15  NC_018929.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the C18orf8 gene promoter:
         USF1   ATF-2   USF2   USF-1:USF-2   POU6F1 (c2)   Roaz   GATA-1   RORalpha1   USF-1   ATF6   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidC18orf8 promoter sequence
   Search Chromatin IP Primers for C18orf8

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat C18orf8


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

Entrez Gene cytogenetic band: 18q11.2   Ensembl cytogenetic band:  18q11.2   HGNC cytogenetic band: 18q11.2

C18orf8 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
C18orf8 gene location

GeneLoc information about chromosome 18         GeneLoc Exon Structure

GeneLoc location for GC18P021083:  view genomic region     (about GC identifiers)

Start:
21,083,462 bp from pter      End:
21,111,746 bp from pter
Size:
28,285 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., 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: MIC1_HUMAN, Q96DM3 (See protein sequence)
Recommended Name: Uncharacterized protein C18orf8  
Size: 657 amino acids; 74975 Da
Sequence caution: Sequence=AAD33909.1; Type=Erroneous initiation;
Secondary accessions: Q9BU17 Q9Y5M0

Explore the universe of human proteins at neXtProt for C18orf8: NX_Q96DM3

Explore proteomics data for C18orf8 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See C18orf8 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (2 alternative transcripts): 
    NP_001263271.1  NP_037458.3  

    ENSEMBL proteins: 
     ENSP00000269221   ENSP00000467852   ENSP00000467007   ENSP00000467692   ENSP00000465956  
     ENSP00000464875   ENSP00000465696  

    C18orf8 Human Recombinant Protein Products:

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    Cloud-Clone Corp. Proteins for C18orf8

     
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    Search eBioscience for ELISAs for C18orf8 


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    3 InterPro protein domains:
     IPR017986 WD40_repeat_dom
     IPR015943 WD40/YVTN_repeat-like_dom
     IPR009755 Mic1

    Graphical View of Domain Structure for InterPro Entry Q96DM3

    ProtoNet protein and cluster: Q96DM3

    UniProtKB/Swiss-Prot: MIC1_HUMAN, Q96DM3
    Similarity: Belongs to the Mic1 family
    Similarity: Contains 1 Mic1 domain


    Find genes that share domains with C18orf8           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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         Gene Ontology (GO): 1 molecular function term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding ----
         
    Find genes that share ontologies with C18orf8           About GenesLikeMe


    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for C18orf8
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for C18orf8
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for C18orf8

    miRNA
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    hsa-miR-1276
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
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    Predesigned siRNA for gene silencing in human, mouse, rat C18orf8

    Gene Editing
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    GenScript: all cDNA clones in your preferred vector: C18orf8 (NM_013326)
    Browse Sino Biological Human cDNA Clones
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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 COMPARTMENTS: 

    CompartmentConfidence
    cytosol2
    nucleus2
    endosome1
    peroxisome1

    Gene Ontology (GO): 1 cellular component term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005765lysosomal membrane IDA17897319

    Find genes that share ontologies with C18orf8           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 C18orf8
    Interactions:

        Search GeneGlobe Interaction Network for C18orf8

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

    5 Interacting proteins for C18orf8 (Q96DM33 ENSP000002692214) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    FYCO1Q9BQS83, ENSP000002961374I2D: score=3 STRING: ENSP00000296137
    ABI1Q8IZP03, ENSP000003653124I2D: score=1 STRING: ENSP00000365312
    HAX1O001653I2D: score=1 
    YWHABP319463I2D: score=1 
    ABI2ENSP000002610174STRING: ENSP00000261017
    About this table

    (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 C18orf8 (MIC1)



    (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 C18orf8 gene (2 alternative transcripts): 
    NM_001276342.1  NM_013326.4  

    Unigene Cluster for C18orf8:

    Chromosome 18 open reading frame 8
    Hs.464779  [show with all ESTs]
    Unigene Representative Sequence: AK024370
    13 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000269221(uc010xau.1 uc010xav.1 uc010xaw.1 uc021uie.1 uc010xay.2)
    ENST00000589215 ENST00000587153 ENST00000590868 ENST00000587690 ENST00000589860
    ENST00000590870 ENST00000592119 ENST00000590387 ENST00000591367 ENST00000593081
    ENST00000592682 ENST00000589409
    miRNA
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    1 qRT-PCR Assays for microRNA that regulate C18orf8:
    hsa-miR-1276
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
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    Predesigned siRNA for gene silencing in human, mouse, rat C18orf8
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    GenScript: all cDNA clones in your preferred vector: C18orf8 (NM_013326)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for C18orf8
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat C18orf8
    Primer
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    OriGene qPCR primer pairs and template standards for C18orf8
    OriGene qSTAR qPCR primer pairs in human, mouse for C18orf8
    Pre-validated RT2 qPCR Primer Assay in human, mouse, rat C18orf8
      QuantiTect SYBR Green Assays in human, mouse, rat C18orf8
      QuantiFast Probe-based Assays in human, mouse, rat C18orf8

    Additional mRNA sequence: 

    AF143536.1 AK024370.1 AK027106.1 AK057192.1 AK294169.1 AK295246.1 AK296230.1 BC002950.1 
    BC008305.1 NR_075075.1 NR_075076.1 

    Selected DOTS entries (see all 28):

    DT.452148  DT.100813642  DT.121085254  DT.40304003  DT.100816573  DT.100813641  DT.85105210  DT.97847518 
    DT.319097  DT.97847519  DT.100813636  DT.75136867  DT.92427261  DT.100849442  DT.121085292  DT.75129934 
    DT.100046040  DT.100733386  DT.100733427  DT.100813643  DT.101973162  DT.102834494  DT.319093  DT.97847520 

    Selected AceView cDNA sequences (see all 196):

    BQ688572 BC002950 AA424047 Z44352 AI271551 AI275852 F10365 AI086016 
    BU678437 CN481504 AA810829 BP351699 CR626373 AW271613 BM452549 CR592203 
    AA380463 BU145779 BU159289 BU740353 AA402027 BM800143 AL561326 BC008305 

    GeneLoc Exon Structure

    Selected Alternative Splicing Database (ASD) splice patterns (SP) for C18orf8 (see all 13)    About this scheme

    ExUns: 1a · 1b ^ 2a · 2b ^ 3 ^ 4 ^ 5 ^ 6 ^ 7 ^ 8 ^ 9 ^ 10a · 10b ^ 11 ^ 12 ^ 13 ^ 14 ^ 15a · 15b ^ 16a · 16b · 16c ^ 17 ^ 18a · 18b ^ 19a ·
    SP1:                    -                 -           -                                                                                                         
    SP2:                                                                                                        -                                         -         
    SP3:                    -     -           -           -                                                                                                         
    SP4:                                                                                                                                                  -         
    SP5:                    -                                                                                                                                       

    ExUns: 19b ^ 20 ^ 21a · 21b ^ 22
    SP1:                              
    SP2:                              
    SP3:                              
    SP4:                              
    SP5:                              


    ECgene alternative splicing isoforms for C18orf8

    (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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    C18orf8 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TTGCTTTTTT
    C18orf8 Expression
    About this image

    C18orf8 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    C18orf8 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.464779
        Custom PCR Arrays for C18orf8
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for C18orf8

    (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 eukaryotes.

    Orthologs for C18orf8 gene from Selected species (see all 19)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia 3110002H16Rik1 , 5 RIKEN cDNA 3110002H16 gene1, 5 86.96(n)1
    94.98(a)1
      18 (6.15 cM)5
    764821  NM_029623.21  NP_083899.11 
     121687175 
    chicken
    (Gallus gallus)
    Aves C18ORF81 chromosome 2 open reading frame, human C18orf8 79.12(n)
    88.87(a)
      421075  XM_419161.4  XP_419161.2 
    lizard
    (Anolis carolinensis)
    Reptilia C18orf86
    chromosome 18 open reading frame 8
    84(a)
    1 ↔ 1
    4(38261221-38285414)
    African clawed frog
    (Xenopus laevis)
    Amphibia MGC687452 hypothetical protein MGC68745 77.36(n)    BC060357.1 
    zebrafish
    (Danio rerio)
    Actinopterygii Dr.188092 Transcribed sequences 74.34(n)    BQ618494.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG82701 CG8270 48.73(n)
    37.9(a)
      38734  NM_139790.3  NP_648047.2 
    worm
    (Caenorhabditis elegans)
    Secernentea Y50D4A.41 Y50D4A.4 43.35(n)
    32.97(a)
      178616  NM_070991.5  NP_503392.3 
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons AT3G120101 AT3G12010 40.43(n)
    27.82(a)
      820375  NM_112035.4  NP_187808.3 
    rice
    (Oryza sativa)
    Liliopsida Os10g04009001 Os10g0400900 41(n)
    28.24(a)
      4348567  NM_001071081.1  NP_001064546.1 


    ENSEMBL Gene Tree for C18orf8 (if available)
    TreeFam Gene Tree for C18orf8 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for C18orf8 gene
    15 SIMAP similar genes for C18orf8 using alignment to 7 protein entries:     MIC1_HUMAN (see all proteins):
    ZNF738    CHID1    FAM210A    RNF217    ZNF585B    DNMT1
    NF2    ZNF212    ZNF737    ZNF461    NSRP1    FKBP3
    DCTN5    EML2    AURA2

    Find genes that share paralogs with C18orf8           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 C18orf8 (see all 729)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 18 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs789055641,2
    C,F--17945849(+) AGAACA/C/GAGAAA 4 -- int13NA 6
    rs1429869541,2
    C--17951630(+) AGAAT-/TTCTTCTT 4 -- int10--------
    rs73597061,2
    C--17956607(+) TCTCTC/TTTTTT 4 -- int1 trp30--------
    rs759915561,2
    C,F--17956607(+) TCTCTC/-TTTTT 4 -- int13Minor allele frequency- -:0.33NA CSA 6
    rs358220601,2
    C,F--17957792(+) CTGGGT/-TGGGC 4 -- int12Minor allele frequency- -:0.50NA CSA 4
    rs1113696761,2
    C--17962567(+) TAAAGTATTGTA 
     TTTCT
    /-
    TAGAG
    4 -- cds1 int11Minor allele frequency- -:0.00CSA 2
    rs792212681,2
    C,F--21076450(+) ACAGAC/AGAATG 4 -- us2k11Minor allele frequency- A:0.13WA 118
    rs1176353211,2
    F--21076511(+) TGAAGG/CAAGGA 4 -- us2k11Minor allele frequency- C:0.02NA 120
    rs777344321,2
    C,F--21076536(+) CTACAT/GGGATG 4 -- us2k11Minor allele frequency- G:0.19EA 120
    rs1857250811,2
    --21076537(+) TACATA/GGATGA 4 -- us2k10--------

    HapMap Linkage Disequilibrium report for C18orf8 (21083462 - 21111746 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 3 variations for C18orf8:    About this table    
    Variant IDTypeSubtypePubMed ID
    nsv509688CNV Insertion20534489
    esv34149CNV Loss18971310
    nsv909458CNV Gain21882294

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing C18orf8
    DNA2.0 Custom Variant and Variant Library Synthesis for C18orf8

    (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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    1 disease for C18orf8:    
    About MalaCards
    colon cancer


    Find genes that share disorders with C18orf8           About GenesLikeMe

    Genetic Association Database (GAD): C18orf8
    Human Genome Epidemiology (HuGE) Navigator: C18orf8 (1 document)

    Export disorders for C18orf8 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 C18orf8 gene, integrated from 10 sources (see all 13):
    (articles sorted by number of sources associating them with C18orf8)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. 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)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    3. 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. (Proc. Natl. Acad. Sci. U.S.A. 2002)
    4. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (Cell 2012)
    5. NOTCH1 nuclear interactome reveals key regulators of its transcriptional activity and oncogenic function. (PubMed id 23022380)1 Yatim A....Benkirane M. (Mol. Cell 2012)
    6. Mass spectrometric analysis of lysine ubiquitylation reveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (amp 2011)
    7. Network organization of the human autophagy system. (PubMed id 20562859)1 Behrends C....Harper J.W. (Nature 2010)
    8. Integral and associated lysosomal membrane proteins. (PubMed id 17897319)1 Schroeder B.... Hasilik A. (Traffic 2007)
    9. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1 Olsen J.V....Mann M. (Cell 2006)
    10. H6D polymorphism in macrophage-inhibitory cytokine-1 gene associated with prostate cancer. (PubMed id 15316060)4 Lindmark F....Xu J. (J. Natl. Cancer Inst. 2004)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 29919 HGNC: 24326 AceView: C18orf8 Ensembl:ENSG00000141452 euGenes: HUgn29919
    ECgene: C18orf8 H-InvDB: C18orf8

    (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 C18orf8 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for C18orf8 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for C18orf8 gene:
    Search GeneIP for patents involving C18orf8

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



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