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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 31471

FusionGeneSummary for RNF169_CALCOCO2

check button Fusion gene summary
Fusion gene informationFusion gene name: RNF169_CALCOCO2
Fusion gene ID: 31471
HgeneTgene
Gene symbol

RNF169

CALCOCO2

Gene ID

254225

10241

Gene namering finger protein 169calcium binding and coiled-coil domain 2
Synonyms-NDP52
Cytomap

11q13.4

17q21.32

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase RNF169RING-type E3 ubiquitin transferase RNF169calcium-binding and coiled-coil domain-containing protein 2antigen nuclear dot 52 kDa proteinnuclear domain 10 protein 52nuclear domain 10 protein NDP52nuclear dot protein 52
Modification date2018052020180522
UniProtAcc

Q8NCN4

Q13137

Ensembl transtripts involved in fusion geneENST00000299563, ENST00000258947, 
ENST00000509507, ENST00000448105, 
ENST00000416445, ENST00000508679, 
ENST00000510997, 
Fusion gene scores* DoF score5 X 3 X 4=606 X 5 X 3=90
# samples 76
** MAII scorelog2(7/60*10)=0.222392421336448
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(6/90*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RNF169 [Title/Abstract] AND CALCOCO2 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneRNF169

GO:0006974

cellular response to DNA damage stimulus

22733822

HgeneRNF169

GO:2000780

negative regulation of double-strand break repair

22742833

TgeneCALCOCO2

GO:0034341

response to interferon-gamma

9230084


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVBRCATCGA-EW-A6SC-01ARNF169chr11

74528759

+CALCOCO2chr17

46919060

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-5UTRENST00000299563ENST00000258947RNF169chr11

74528759

+CALCOCO2chr17

46919060

+
5CDS-5UTRENST00000299563ENST00000509507RNF169chr11

74528759

+CALCOCO2chr17

46919060

+
5CDS-5UTRENST00000299563ENST00000448105RNF169chr11

74528759

+CALCOCO2chr17

46919060

+
5CDS-5UTRENST00000299563ENST00000416445RNF169chr11

74528759

+CALCOCO2chr17

46919060

+
5CDS-intronENST00000299563ENST00000508679RNF169chr11

74528759

+CALCOCO2chr17

46919060

+
5CDS-intronENST00000299563ENST00000510997RNF169chr11

74528759

+CALCOCO2chr17

46919060

+

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FusionProtFeatures for RNF169_CALCOCO2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RNF169

Q8NCN4

CALCOCO2

Q13137

Probable E3 ubiquitin-protein ligase that acts as anegative regulator of double-strand breaks (DSBs) repair followingDNA damage. Recruited to DSB repair sites by recognizing andbinding ubiquitin catalyzed by RNF168 and competes with TP53BP1and BRCA1 for association with RNF168-modified chromatin, therebyacting as a negative regulator of DSBs repair. E3 ubiquitin-protein ligase activity is not required for regulation of DSBsrepair. {ECO:0000269|PubMed:22492721, ECO:0000269|PubMed:22733822,ECO:0000269|PubMed:22742833}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

.

* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for RNF169_CALCOCO2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for RNF169_CALCOCO2


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
RNF169UBC, HIST2H2AC, HIST2H2BE, UBE2E1, DYRK1B, DYRK1A, BRCA1, HIST1H2BG, HIST1H3A, USP7, CDC14B, DCAF7, KLHDC2, IL16, CAPZB, CAPZA1, TUBB4B, RPS3, DDB1, C1QBP, HNRNPUCALCOCO2TP53RK, LGALS8, FBF1, ZC2HC1C, CCDC185, LNX1, PIAS4, CCDC33, PSMA1, PTBP1, RABL6, CPNE7, ZNF101, LSM4, SHC1, GABARAPL2, VPS72, ZNF451, DBNDD2, ZNF638, FBXL18, ZNF205, FXR2, MCM10, POLI, PTBP2, AP5B1, KAT7, PCGF1, TCL1A, SMARCD1, TCEB3B, ABLIM1, CALCOCO2, ENKD1, ZNF426, C20orf195, SRI, FASTK, TRAF2, ZNF408, DAZAP2, RHPN1, APEX2, GABARAPL1, FAM107A, KANSL1, TAB3, TBK1, IKBKE, TBKBP1, MAP1LC3A, FMR1, MAVS, PRRC2A, KIAA1407, MTPAP, AZI2, TRAF4, MYO6, TAX1BP1, UBC, GEMIN4, IQCB1, RNF11, MAP1LC3C, DICER1, PARK2, SQSTM1, RPA2, ORC5, TRAF6, IKBKG, GIT2, RB1CC1, ADSL, ARNT2, MVP, NDN, PRKAB2, AES, CCNH, DCX, DDX6, DOCK2, HOXB9, LMO2, SMCP, MOS, MXI1, PFDN5, PHF1, RPL9, RPS27A, SDCBP, SNRPB, UBB, VARS, ARHGEF5, AKAP17A, NAA10, LMO4, STK16, TBRG4, FAM189A2, LITAF, EEF1E1, RIN1, AMMECR1, FARS2, MID2, DUSP12, BAHD1, PEG10, PSME4, FAM168A, PRPF31, ZNF337, NFU1, DCTN4, SLC15A3, ZNF581, HDAC7, CHCHD3, MAGOHB, FAM90A1, TBC1D22B, LIMS2, EXOSC5, CBX8, GATAD2B, KLHL42, FKBPL, TEKT3, METTL17, RBM15, DUSP26, LENG1, FAM161A, BEX2, RTN4IP1, ARHGEF39, LMF2, LONRF1, DDIT4L, GLYCTK, CWF19L2, ZNF564, PAPD4, PPP1R18, SPATA24, BCL6B, RTP5, CEP57L1, UBAC2, PEF1, RNF2, NRBF2, SULT1A2, BBOX1, CDK7, LDLRAD4, TTC23L, HLX, MAP1LC3B, GABARAP, U2AF2, ATG5, C1orf106, CHRDL1, SYNC, CEP55, BCAP29, HDAC11, RAB35, UBE2A


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for RNF169_CALCOCO2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for RNF169_CALCOCO2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource