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

C18orf32 Gene

protein-coding   GIFtS: 41
GCID: GC18M047008

chromosome 18 open reading frame 32

  Search for C18orf32
in our new
 Human Malady Compendium 
Biological research products
for C18orf32
    

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

Aliases
Chromosome 18 Open Reading Frame 321 2
Putative NF-Kappa-B-Activating Protein 2002 3
FLJ234581
Putative NFkB Activating Protein2
UPF0729 Protein C18orf322

External Ids:    HGNC: 316901   Entrez Gene: 4976612   Ensembl: ENSG000001775767   UniProtKB: Q8TCD13   

Export aliases for C18orf32 gene to outside databases

Previous GC identifers: GC18M045264 GC18M043861


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

UniProtKB/Swiss-Prot: CR032_HUMAN, Q8TCD1
Function: May activate the NF-kappa-B signaling pathway




(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_000018.9  NC_018929.1  NT_010966.14  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the C18orf32 gene promoter:
         POU2F2 (Oct-2.1)   Oct-B1   oct-B3   oct-B2   POU2F2   CREB   POU2F1   deltaCREB   POU2F1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidC18orf32 promoter sequence
   Search SABiosciences Chromatin IP Primers for C18orf32

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat C18orf32


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

Entrez Gene cytogenetic band: 18q21.1   Ensembl cytogenetic band:  18q21.1   HGNC cytogenetic band: 18q21.1

C18orf32 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
C18orf32 gene location

GeneLoc information about chromosome 18         GeneLoc Exon Structure

GeneLoc location for GC18M047008:  view genomic region     (about GC identifiers)

Start:
47,008,028 bp from pter      End:
47,013,622 bp from pter
Size:
5,595 bases      Orientation:
minus 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: CR032_HUMAN, Q8TCD1 (See protein sequence)
Recommended Name: UPF0729 protein C18orf32  
Size: 76 amino acids; 8669 Da

Explore the universe of human proteins at neXtProt for C18orf32: NX_Q8TCD1

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8TCD1

  • C18orf32 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_001030177.1  NP_001186275.1  

    ENSEMBL proteins: 
     ENSP00000464411   ENSP00000323199   ENSP00000462538  

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

    C18orf32 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR026776 UPF0729

    Graphical View of Domain Structure for InterPro Entry Q8TCD1

    ProtoNet protein and cluster: Q8TCD1

    UniProtKB/Swiss-Prot: CR032_HUMAN, Q8TCD1
    Similarity: Belongs to the UPF0729 family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: CR032_HUMAN, Q8TCD1
    Function: May activate the NF-kappa-B signaling pathway

    miRNA
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004871signal transducer activity IMP12761501


    C18orf32 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for C18orf32:
     Increased G1 DNA content 


    (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 C18orf32

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    5/35 Interacting proteins for C18orf32 (Q8TCD13 ENSP000003231994) via UniProtKB, MINT, STRING, and/or I2D (see all 35)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    MAP1LC3AQ9H4923I2D: score=2 
    AMBRA1Q9C0C73I2D: score=1 
    ATG13O751433I2D: score=1 
    ATG14Q6ZNE53I2D: score=1 
    CAMKK2Q96RR43I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007165signal transduction IMP12761501
    GO:0043123positive regulation of I-kappaB kinase/NF-kappaB cascade IMP12761501


    C18orf32 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 C18orf32
    Search CenterWatch for drugs/clinical trials and news about C18orf32 / CR032 

    (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,
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    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 C18orf32 gene (2 alternative transcripts): 
    NM_001035005.3  NM_001199346.1  

    Unigene Cluster for C18orf32:

    Chromosome 18 open reading frame 32
    Hs.603040  [show with all ESTs]
    Unigene Representative Sequence: NM_001199356
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000579820(uc002ldl.3) ENST00000318240(uc002ldk.2) ENST00000582392


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    hsa-miR-374c hsa-miR-122 hsa-miR-655 hsa-miR-934 hsa-miR-3920 hsa-miR-3919 hsa-miR-138-2* hsa-miR-452
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    Inhib. RNA
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    Additional cDNA sequence: 

    AB097012.1 AK027111.1 AK291882.1 BC022357.1 BC093004.1 

    21 DOTS entries:

    DT.100891790  DT.95182723  DT.452028  DT.121105090  DT.100891783  DT.121104983  DT.95182721  DT.100891774 
    DT.95182728  DT.75196436  DT.100809496  DT.121105078  DT.121105088  DT.121105135  DT.95182730  DT.97765301 
    DT.100035658  DT.100891762  DT.121105133  DT.91832582  DT.92471784 

    GeneLoc Exon Structure

    4 Alternative Splicing Database (ASD) splice patterns (SP) for C18orf32    About this scheme

    ExUns: 1a · 1b · 1c ^ 2 ^ 3 ^ 4 ^ 5a · 5b · 5c
    SP1:              -     -     -                           
    SP2:                    -     -                           
    SP3:                          -                           
    SP4:                                                      


    ECgene alternative splicing isoforms for C18orf32

    (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

    C18orf32 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AATGGATTAC

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image
    See C18orf32 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for C18orf32

    SOURCE GeneReport for Unigene cluster: Hs.603040
        SABiosciences Custom PCR Arrays for C18orf32
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for C18orf32

    (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 C18orf32 gene from 3/9 species (see all 9)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia BC0311811 , 5 cDNA sequence BC0311811, 5 81.94(n)1
    80.56(a)1
      18 (50.96 cM)5
    4078191  NM_001001181.31  NP_001001181.11 
     750059005 
    chicken
    (Gallus gallus)
    Aves C18orf326
    Uncharacterized protein
    61(a)
    1 ↔ 1
    Z(970546-972146)
    lizard
    (Anolis carolinensis)
    Reptilia C18orf326
    --
    65(a)
    1 ↔ 1
    2(187358-187504)


    ENSEMBL Gene Tree for C18orf32 (if available)
    TreeFam Gene Tree for C18orf32 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for C18orf32 gene

    C18orf32 for paralogs           About GeneDecksing


    5 Pseudogenes.org Pseudogenes for C18orf32
    PGOHUM00000248886 PGOHUM00000245118 PGOHUM00000240961 PGOHUM00000241082 PGOHUM00000237737


    (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

    10/154 NCBI SNPs in C18orf32 are shown (see all 154    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 18 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1419229951,2
    --47007073(+) CAGGTC/TGAGGC 4 -- int1 ds50010--------
    rs21564991,2
    C,F,O,A,H,--47007234(-) GAGTCC/TGCCCC 4 -- ds5001 int123Minor allele frequency- N:0.00NS EA NA WA 2550
    rs360856911,2
    C,F--47007264(+) TTAGCC/TTTGCT 4 -- int1 ds50013Minor allele frequency- T:0.33NA 6
    rs2002058171,2
    --47007324(+) ACCAT-/ACAACAAC 4 -- ds5001 int10--------
    rs560985721,2
    C,F,--47007338(+) AACAAC/AAAAAA 4 -- int1 ds50012Minor allele frequency- A:0.50WA NA 4
    rs2013835081,2
    --47007338(+) AACAA-/CAAAAA 4 -- int1 ds50010--------
    rs606434231,2
    C--47007340(+) AACAACAA/-AAAAA 4 -- int1 ds50011Minor allele frequency- -:0.00NA 2
    rs802811621,2
    --47007341(+) AACAAC/AAAAAC 4 -- int1 ds50011Minor allele frequency- A:0.50CSA 2
    rs789231901,2
    --47007391(+) GTTGAG/TAAAAA 4 -- int1 ds50011Minor allele frequency- T:0.01WA 118
    rs1171178481,2
    --47007409(+) CTTTTC/TATTTA 4 -- ds5001 int11Minor allele frequency- T:0.01NA 120

    HapMap Linkage Disequilibrium report for C18orf32 (47008028 - 47013622 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for C18orf32
         1 CNV: 35573

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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
      --

    (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 C18orf32 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with C18orf32)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways. (PubMed id 12761501)1, 2 Matsuda A....Sugano S. (2003)
    2. Mass spectrometric analysis of lysine ubiquitylation r eveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (2011)
    3. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)
    4. 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)
    5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)
    6. 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. (2002)
    7. Normalization and subtraction: two approaches to facilitate gene discovery. (PubMed id 8889548)1 Bonaldo M.F.... Soares M.B. (1996)

    (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: 497661 HGNC: 31690 Ensembl:ENSG00000177576 euGenes: HUgn497661 ECgene: C18orf32
    H-InvDB: C18orf32

    (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 C18orf32 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for C18orf32 gene:
    Search GeneIP for patents involving C18orf32

    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, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
    In Situ Hybridization Assays from
    Advanced Cell Diagnostics
    About This Section

     
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    GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 27 Apr 2013

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    VWF
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    von Willebrand factor
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    The GeneCards human gene database gene index: 1 3 5 6 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 


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