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

RNF169 Gene

protein-coding   GIFtS: 41
GCID: GC11P074459

ring finger protein 169

  Search for RNF169
in our new
 Human Malady Compendium 
Biological research products
for RNF169
    

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

Aliases
Ring Finger Protein 1691 2 3
KIAA19911 3
E3 Ubiquitin-Protein Ligase RNF1692
EC 6.3.2.-3
EC 3.1.4.168
EC 3.4.24.578

External Ids:    HGNC: 269611   Entrez Gene: 2542252   Ensembl: ENSG000001664397   UniProtKB: Q8NCN43   

Export aliases for RNF169 gene to outside databases

Previous GC identifers: GC11P074138 GC11P070756


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

UniProtKB/Swiss-Prot: RN169_HUMAN, Q8NCN4
Function: Probable E3 ubiquitin-protein ligase that acts as a negative regulator of double-strand breaks (DSBs) repair
following DNA damage. Recruited to DSB repair sites by recognizing and binding ubiquitin catalyzed by RNF168 and
competes with TP53BP1 and BRCA1 for association with RNF168-modified chromatin, thereby acting as a negative regulator
of DSBs repair. E3 ubiquitin-protein ligase activity is not required for regulation of DSBs repair




(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 RNF169 gene promoter:
         c-Fos   Egr-3   AhR   AP-1   FosB   FOXO3   Roaz   FOXO3b   FOXO3a   c-Jun   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for RNF169

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat RNF169


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

Entrez Gene cytogenetic band: 11q13.4   Ensembl cytogenetic band:  11q13.4   HGNC cytogenetic band: 11q13.4

RNF169 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
RNF169 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P074459:  view genomic region     (about GC identifiers)

Start:
74,459,913 bp from pter      End:
74,553,458 bp from pter
Size:
93,546 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: RN169_HUMAN, Q8NCN4 (See protein sequence)
Recommended Name: E3 ubiquitin-protein ligase RNF169  
Size: 708 amino acids; 77194 Da
Subcellular location: Nucleus, nucleoplasm. Note=Localizes to sites of double-strand breaks (DSBs) following DNA
damage. Recruited to DSBs via recognition of RNF168-dependent ubiquitin products
Sequence caution: Sequence=BAC02700.1; Type=Erroneous initiation;
Secondary accessions: Q6N015

Explore the universe of human proteins at neXtProt for RNF169: NX_Q8NCN4

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8NCN4

  • 2 DME Specific Peptides for RNF169 (Q8NCN4)
     KLQQEEE  CDETAAA 

    RNF169 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_001092108.1  
    ENSEMBL proteins: 
     ENSP00000299563   ENSP00000436339  

    Human Recombinant Protein Products: 
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    Uscn Proteins for RNF169

    Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005654nucleoplasm IDA--
    GO:0035861site of double-strand break IDA--


    RNF169 for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for RNF169


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

    RNF169 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR017907 Znf_RING_CS
     IPR001841 Znf_RING
     IPR013083 Znf_RING/FYVE/PHD

    Graphical View of Domain Structure for InterPro Entry Q8NCN4

    ProtoNet protein and cluster: Q8NCN4

    1 Blocks protein family: IPB001841 Zn-finger

    UniProtKB/Swiss-Prot: RN169_HUMAN, Q8NCN4
    Domain: The MIU motif (motif interacting with ubiquitin) mediates the interaction with both 'Lys-48'- and
    'Lys-63'-linked ubiquitin chains (PubMed:22733822 and PubMed:22492721). The UMI motif also mediates interaction with
    ubiquitin. The specificity for different types of ubiquitin is mediated by juxtaposition of ubiquitin-binding motifs
    (MIU and UMI motifs) with LR motifs (LRMs) (PubMed:22742833)
    Similarity: Belongs to the RNF169 family
    Similarity: Contains 1 RING-type zinc finger


    (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: RN169_HUMAN, Q8NCN4
    Function: Probable E3 ubiquitin-protein ligase that acts as a negative regulator of double-strand breaks (DSBs) repair
    following DNA damage. Recruited to DSB repair sites by recognizing and binding ubiquitin catalyzed by RNF168 and
    competes with TP53BP1 and BRCA1 for association with RNF168-modified chromatin, thereby acting as a negative regulator
    of DSBs repair. E3 ubiquitin-protein ligase activity is not required for regulation of DSBs repair

    Enzyme Numbers (IUBMB): EC 6.3.2.-1 EC 3.4.24.572 EC 3.1.4.162

    miRNA
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    Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0008270zinc ion binding IEA--
    GO:0016874ligase activity IEA--
    GO:0031491nucleosome binding IDA--
    GO:0070530K63-linked polyubiquitin binding IDA--


    RNF169 for ontologies           About GeneDecksing


    2 GenomeRNAi human phenotypes for RNF169:
     Decreased TP53 protein express  Increased S DNA content 

    Animal Models:
         3 MGI mutant phenotypes (inferred from 1 allele(MGI details for Rnf169):
     homeostasis/metabolism  skeleton  vision/eye 

    RNF169 for phenotypes           About GeneDecksing


    (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



    UniProtKB/Swiss-Prot: RN169_HUMAN, Q8NCN4
    Pathway: Protein modification; protein ubiquitination

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for RNF169

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

    5/35 Interacting proteins for RNF169 (Q8NCN42 ENSP000002995634) via UniProtKB, MINT, STRING, and/or I2D (see all 35)

    InteractantInteraction Details
    GeneCardExternal ID(s)
    BEND3Q5T5X72MINT-8173832
    CHAMP1Q96JM32MINT-8173832
    CTPS1P178122MINT-8173832
    CWC22Q9HCG82MINT-8173832
    DHX15O431432MINT-8173832
    About this table

    Gene Ontology (GO): 3 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006974response to DNA damage stimulus IMP--
    GO:0016567protein ubiquitination IEA--
    GO:2000780negative regulation of double-strand break repair IMP--


    RNF169 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 RNF169
    Search CenterWatch for drugs/clinical trials and news about RNF169 / RN169 

    (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, 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 RNF169 gene: 
    NM_001098638.1  

    Unigene Cluster for RNF169:

    Ring finger protein 169
    Hs.370145  [show with all ESTs]
    Unigene Representative Sequence: NM_001098638
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000299563(uc001ovl.4) ENST00000527301

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    8/72 QIAGEN miScript miRNA Assays for microRNAs that regulate RNF169 (see all 72):
    hsa-miR-140-5p hsa-miR-26a-2* hsa-miR-607 hsa-miR-3194-5p hsa-miR-30d hsa-miR-4267 hsa-miR-30a hsa-miR-4325
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    OriGene siRNA: RNF169
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    Clone
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    Additional cDNA sequence: 

    AB082522.1 BX640750.1 

    3 DOTS entries:

    DT.443902  DT.95218489  DT.120758595 

    24/120 AceView cDNA sequences (see all 120):

    BE047843 BE858336 BG679092 AW026154 AI589084 AA748391 AA720793 CB147654 
    BU735651 AI061064 AI082193 BI862829 BX102462 AA437401 BF439964 AI468437 
    BU735906 BU158897 AI911676 AU253596 AA029162 AI369062 BX640750 BX648162 

    GeneLoc Exon Structure


    (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

    RNF169 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: --

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

    About this image
    See RNF169 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for RNF169

    SOURCE GeneReport for Unigene cluster: Hs.370145
        SABiosciences Custom PCR Arrays for RNF169
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for RNF169

    (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 animals.

    Orthologs for RNF169 gene from 4/16 species (see all 16)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves RNF1691 ring finger protein 169 66.6(n)
    63.98(a)
      419055  XM_417246.3  XP_417246.3 
    lizard
    (Anolis carolinensis)
    Reptilia RNF1696
    --
    56(a)
    1 ↔ 1
    GL343489.1(504576-511199)
    zebrafish
    (Danio rerio)
    Actinopterygii LOC7957481 RING finger protein 169-like 55.81(n)
    52.9(a)
      795748  XM_001335976.1  XP_001336012.1 
    honey bee
    (Apis mellifera)
    Insecta --
    --
    14(a)
    1 → many
    Group10.9(334179-337316)


    ENSEMBL Gene Tree for RNF169 (if available)
    TreeFam Gene Tree for RNF169 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for RNF169 gene
    RNF1682  

    RNF169 for paralogs           About GeneDecksing



    (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

    10/1467 NCBI SNPs in RNF169 are shown (see all 1467    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1427024201,2
    --74458008(+) TCTGGC/GTCTCT 1 -- us2k10--------
    rs124218991,2
    C,F,H,--74458046(+) CCATTG/AGCCTT 1 -- us2k17Minor allele frequency- A:0.34NA WA EA 366
    rs1505802571,2
    --74458107(+) CATCAC/TCTTTT 1 -- us2k10--------
    rs1871781981,2
    --74458139(+) AATCAA/GTCACT 1 -- us2k10--------
    rs1395812441,2
    --74458147(+) ACTCGG/TCACTG 1 -- us2k10--------
    rs1897348471,2
    --74458164(+) TTTACC/TGCTAG 1 -- us2k10--------
    rs1823478011,2
    --74458178(+) TGGGCA/GATCTC 1 -- us2k10--------
    rs1497136941,2
    --74458198(+) CAGGGC/TTTCTC 1 -- us2k10--------
    rs1478076231,2
    --74458226(+) ATGTTC/GATTTT 1 -- us2k10--------
    rs1877087831,2
    --74458251(+) TGTCTA/CATTCT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for RNF169 (74459913 - 74553458 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 7 variations for RNF169
         4 CNVs: 2932 3858 5634 8692
         3 Indels: 44934 101263 33240

    SABiosciences Cancer Mutation PCR Assays
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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 RNF169 gene, integrated from 9 sources (see all 20):
    (articles sorted by number of sources associating them with RNF169)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Characterization of size-fractionated cDNA libraries generated by the in vitro recombination-assisted method. (PubMed id 12056414)1, 2, 3 Ohara O.... Koseki H. (2002)
    2. Tandem protein interaction modules organize the ubiqui tin-dependent response to DNA double-strand breaks. (PubMed id 22742833)1, 2 Panier S....Durocher D. (2012)
    3. Human RNF169 is a negative regulator of the ubiquitin-dependent response to DNA double-strand breaks. (PubMed id 22492721)1, 2 Poulsen M.... Mailand N. (2012)
    4. Ring finger protein RNF169 antagonizes the ubiquitin-d ependent signaling cascade at sites of DNA damage. (PubMed id 22733822)1, 2 Chen J....Huen M.S. (2012)
    5. Methods for quantification of in vivo changes in prote in ubiquitination following proteasome and deubiquitinase inhibition. (PubMed id 22505724)1 Udeshi N.D....Carr S.A. (2012)
    6. 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)
    7. Ubiquitin ligase substrate identification through qua ntitative proteomics at both the protein and peptide levels. (PubMed id 21987572)1 Lee K.A....Doedens J.R. (2011)
    8. Comparative proteomic analysis identifies a role for S UMO in protein quality control. (PubMed id 21693764)1 Tatham M.H....Hay R.T. (2011)
    9. Purification and identification of endogenous polySUMO conjugates. (PubMed id 21252943)1 Bruderer R....Hay R.T. (2011)
    10. Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis. (PubMed id 20068231)2 Olsen J.V....Mann M. (2010)

    (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: 254225 HGNC: 26961 AceView: KIAA1991 Ensembl:ENSG00000166439 euGenes: HUgn254225
    ECgene: RNF169 H-InvDB: RNF169

    (According to HUGE)
    About This Section
    HUGE: KIAA1991

    (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 RNF169 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 RNF169 gene:
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