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

C17orf58 Gene

protein-coding   GIFtS: 38
GCID: GC17M065987

chromosome 17 open reading frame 58

  Search for C17orf58
in our new
 Human Malady Compendium 
Biological research products
for C17orf58
    

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

Aliases
Chromosome 17 Open Reading Frame 581 2
UPF0450 Protein C17orf582

External Ids:    HGNC: 275681   Entrez Gene: 2840182   Ensembl: ENSG000001866657   UniProtKB: Q2M2W73   

Export aliases for C17orf58 gene to outside databases

Previous GC identifers: GC17M063418 GC17M061371


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

  --

(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_000017.10  NC_018928.1  NT_010783.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the C17orf58 gene promoter:
         POU2F2 (Oct-2.1)   Oct-B1   oct-B3   oct-B2   Pax-2   POU2F2   POU2F2C   POU2F1   POU2F1a   POU2F2B   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for C17orf58

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat C17orf58


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

Entrez Gene cytogenetic band: 17q24.2   Ensembl cytogenetic band:  17q24.2   HGNC cytogenetic band: 17q24.2

C17orf58 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
C17orf58 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17M065987:  view genomic region     (about GC identifiers)

Start:
65,987,217 bp from pter      End:
65,989,765 bp from pter
Size:
2,549 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: CQ058_HUMAN, Q2M2W7 (See protein sequence)
Recommended Name: UPF0450 protein C17orf58  
Size: 97 amino acids; 11219 Da
Secondary accessions: A8MQV2
Alternative splicing: 2 isoforms:  Q2M2W7-1   Q2M2W7-2   (Ref.1 (AL556320) and Ref.2 (AK026583) sequences are in conflict in position: 72:E->G)

Explore the universe of human proteins at neXtProt for C17orf58: NX_Q2M2W7

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q2M2W7

  • C17orf58 Protein expression data from MOPED and PaxDb:    About this image 
    C17orf58 Protein Expression
    REFSEQ proteins (2 alternative transcripts): 
    NP_858041.2  NP_858042.2  

    ENSEMBL proteins: 
     ENSP00000402020   ENSP00000443680   ENSP00000334741  

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

    C17orf58 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR008993 TIMP-like_OB-fold

    Graphical View of Domain Structure for InterPro Entry Q2M2W7

    ProtoNet protein and cluster: Q2M2W7

    UniProtKB/Swiss-Prot: CQ058_HUMAN, Q2M2W7
    Similarity: Belongs to the UPF0450 family


    (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

    Animal Models:
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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 C17orf58

    (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 C17orf58
    Search CenterWatch for drugs/clinical trials and news about C17orf58 / CQ058 

    (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,
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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 C17orf58 gene (2 alternative transcripts): 
    NM_181655.2  NM_181656.3  

    Unigene Cluster for C17orf58:

    Chromosome 17 open reading frame 58
    Hs.90790  [show with all ESTs]
    Unigene Representative Sequence: NM_181656
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000449250 ENST00000536693 ENST00000334461(uc002jgj.4 uc002jgi.4)


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    Additional cDNA sequence: 

    AK026583.1 BC021702.1 BC036760.1 BC105124.1 BC112073.1 

    5 DOTS entries:

    DT.100781627  DT.442873  DT.92423357  DT.95192797  DT.121608847 

    24/69 AceView cDNA sequences (see all 69):

    AA868096 AI492828 CA308257 CR594326 CR592488 CA443532 BF435372 BC036760 
    BX369525 BF511946 AK026583 BX396661 BI224193 NM_181655 R22334 BX369526 
    BM764858 BG529487 BG475090 BM544218 CA443050 BF439607 BC021702 F10593 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for C17orf58    About this scheme

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


    ECgene alternative splicing isoforms for C17orf58

    (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

    C17orf58 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CCTCCCTGCT
    C17orf58 Expression
    About this image
    See C17orf58 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for C17orf58

    SOURCE GeneReport for Unigene cluster: Hs.90790
        SABiosciences Custom PCR Arrays for C17orf58

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    In Situ
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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 C17orf58 gene from 4/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia 1810010H24Rik1 , 5 RIKEN cDNA 1810010H24 gene1, 5 84.54(n)1
    88.66(a)1
      11 (70.10 cM)5
    690661  NM_001163473.11  NP_001156945.11 
     1070281185 
    chicken
    (Gallus gallus)
    Aves C18H17orf581 chromosome 18 open reading frame, human C17orf58 73.33(n)
    74.74(a)
      417421  XM_415673.3  XP_415673.3 
    lizard
    (Anolis carolinensis)
    Reptilia C17orf586
    --
    68(a)
    1 ↔ 1
    GL343250.1(1088080-1089529)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.144042 Xenopus laevis transcribed sequences 72.73(n)    CD255633.1 


    ENSEMBL Gene Tree for C17orf58 (if available)
    TreeFam Gene Tree for C17orf58 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for C17orf58 gene

    C17orf58 for paralogs           About GeneDecksing


    2 Pseudogenes.org Pseudogenes for C17orf58
    PGOHUM00000237415 PGOHUM00000247406


    (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

    10/78 NCBI SNPs in C17orf58 are shown (see all 78    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1453101491,2
    --65986729(+) GTGATC/TAAACC 2 -- int10--------
    rs116577971,2
    C,F,H--65986780(+) CGCTTT/CTGTTG 2 -- int114Minor allele frequency- C:0.09NS EA NA WA CSA 553
    rs1872120821,2
    --65986848(+) TCAAGA/CGATTC 2 -- int10--------
    rs1919265771,2
    --65986902(+) CACCAC/TGCCCG 2 -- int10--------
    rs1449770221,2
    --65987005(+) CCTCCC/GAAAGT 2 -- int10--------
    rs1177268331,2
    F--65987068(+) ACCAAC/TTGAAA 2 -- int11Minor allele frequency- T:0.06EA 120
    rs1490888081,2
    --65987115(+) GTGAAC/TATTGG 2 -- int10--------
    rs1152695841,2
    F--65987395(+) TGGTAC/TGTCAG 2 -- ut311Minor allele frequency- T:0.02WA 118
    rs58214441,2
    C--65987510(-) AAGTATTA/-AAGTT 2 -- ut311Minor allele frequency- -:0.50CSA 2
    rs609564671,2
    C--65987512(+) CTTTA-/ATACTTGT 2 -- ut311Minor allele frequency- ATA:0.00NA 2

    HapMap Linkage Disequilibrium report for C17orf58 (65987217 - 65989765 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 3 variations for C17orf58
         3 CNVs: 73006 73007 22953

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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 C17orf58 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with C17orf58)
        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. (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. DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. (PubMed id 16625196)2 Zody M.C.... Nusbaum C. (2006)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)
    5. Hepatitis C virus core protein interacts with 14-3-3 protein and activates the kinase Raf-1. (PubMed id )2 Aoki H.... Hino O. (2000)

    (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: 284018 HGNC: 27568 AceView: LOC284018 Ensembl:ENSG00000186665 euGenes: HUgn284018
    ECgene: C17orf58 H-InvDB: C17orf58

    (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 C17orf58 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 C17orf58 gene:
    Search GeneIP for patents involving C17orf58

    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 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, LifeMap BioReagents, and Sirion Biotech, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
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    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 , 14 May 2013

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    VWF
    (GIFTS: 73)
    von Willebrand factor
    GIFtS Group
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