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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: 10644

FusionGeneSummary for DTL_INTS7

check button Fusion gene summary
Fusion gene informationFusion gene name: DTL_INTS7
Fusion gene ID: 10644
HgeneTgene
Gene symbol

DTL

INTS7

Gene ID

51514

25896

Gene namedenticleless E3 ubiquitin protein ligase homologintegrator complex subunit 7
SynonymsCDT2|DCAF2|L2DTL|RAMPC1orf73|INT7
Cytomap

1q32.3

1q32.3

Type of geneprotein-codingprotein-coding
Descriptiondenticleless protein homologDDB1- and CUL4-associated factor 2RA-regulated nuclear matrix-associated proteinlethal(2) denticleless protein homologretinoic acid-regulated nuclear matrix-associated proteinintegrator complex subunit 7
Modification date2018051920180523
UniProtAcc

Q9NZJ0

Q9NVH2

Ensembl transtripts involved in fusion geneENST00000366991, ENST00000542077, 
ENST00000475419, 
ENST00000469606, 
ENST00000366994, ENST00000366993, 
ENST00000366992, ENST00000440600, 
Fusion gene scores* DoF score2 X 1 X 3=65 X 5 X 5=125
# samples 36
** MAII scorelog2(3/6*10)=2.32192809488736log2(6/125*10)=-1.05889368905357
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DTL [Title/Abstract] AND INTS7 [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
HgeneDTL

GO:0000209

protein polyubiquitination

18794347

HgeneDTL

GO:0006511

ubiquitin-dependent protein catabolic process

18794347

HgeneDTL

GO:0006513

protein monoubiquitination

20129063

HgeneDTL

GO:0006974

cellular response to DNA damage stimulus

20129063

HgeneDTL

GO:0009411

response to UV

18794347

HgeneDTL

GO:0019985

translesion synthesis

20129063

TgeneINTS7

GO:0016180

snRNA processing

16239144

TgeneINTS7

GO:0071479

cellular response to ionizing radiation

21659603


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
TCGARVPRADTCGA-CH-5752-01ADTLchr1

212220759

+INTS7chr1

212194554

-
TCGARVSTADTCGA-BR-8362-01ADTLchr1

212220759

+INTS7chr1

212194554

-
* 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-5UTRENST00000366991ENST00000469606DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000366991ENST00000366994DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000366991ENST00000366993DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000366991ENST00000366992DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000366991ENST00000440600DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000542077ENST00000469606DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000542077ENST00000366994DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000542077ENST00000366993DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000542077ENST00000366992DTLchr1

212220759

+INTS7chr1

212194554

-
5CDS-5UTRENST00000542077ENST00000440600DTLchr1

212220759

+INTS7chr1

212194554

-
3UTR-5UTRENST00000475419ENST00000469606DTLchr1

212220759

+INTS7chr1

212194554

-
3UTR-5UTRENST00000475419ENST00000366994DTLchr1

212220759

+INTS7chr1

212194554

-
3UTR-5UTRENST00000475419ENST00000366993DTLchr1

212220759

+INTS7chr1

212194554

-
3UTR-5UTRENST00000475419ENST00000366992DTLchr1

212220759

+INTS7chr1

212194554

-
3UTR-5UTRENST00000475419ENST00000440600DTLchr1

212220759

+INTS7chr1

212194554

-

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FusionProtFeatures for DTL_INTS7


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

Q9NZJ0

INTS7

Q9NVH2

Substrate-specific adapter of a DCX (DDB1-CUL4-X-box) E3ubiquitin-protein ligase complex required for cell cycle control,DNA damage response and translesion DNA synthesis. The DCX(DTL)complex, also named CRL4(CDT2) complex, mediates thepolyubiquitination and subsequent degradation of CDT1,CDKN1A/p21(CIP1), FBH1, KMT5A and SDE2 (PubMed:16861906,PubMed:16949367, PubMed:16964240, PubMed:17085480,PubMed:18703516, PubMed:18794347, PubMed:18794348,PubMed:19332548, PubMed:20129063, PubMed:23478441,PubMed:23478445, PubMed:23677613, PubMed:27906959). CDT1degradation in response to DNA damage is necessary to ensureproper cell cycle regulation of DNA replication (PubMed:16861906,PubMed:16949367, PubMed:17085480). CDKN1A/p21(CIP1) degradationduring S phase or following UV irradiation is essential to controlreplication licensing (PubMed:18794348, PubMed:19332548). KMT5Adegradation is also important for a proper regulation ofmechanisms such as TGF-beta signaling, cell cycle progression, DNArepair and cell migration (PubMed:23478445). Most substratesrequire their interaction with PCNA for their polyubiquitination:substrates interact with PCNA via their PIP-box, and thosecontaining the 'K+4' motif in the PIP box, recruit the DCX(DTL)complex, leading to their degradation. In undamaged proliferatingcells, the DCX(DTL) complex also promotes the 'Lys-164'monoubiquitination of PCNA, thereby being involved in PCNA-dependent translesion DNA synthesis (PubMed:20129063,PubMed:23478441, PubMed:23478445, PubMed:23677613).{ECO:0000269|PubMed:16861906, ECO:0000269|PubMed:16949367,ECO:0000269|PubMed:16964240, ECO:0000269|PubMed:17085480,ECO:0000269|PubMed:18703516, ECO:0000269|PubMed:18794347,ECO:0000269|PubMed:18794348, ECO:0000269|PubMed:19332548,ECO:0000269|PubMed:20129063, ECO:0000269|PubMed:23478441,ECO:0000269|PubMed:23478445, ECO:0000269|PubMed:23677613,ECO:0000269|PubMed:27906959}.

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 DTL_INTS7


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 DTL_INTS7


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
DTLCDKN1A, COPS6, DDB1, CUL4B, CUL4A, WDR5, SETD8, KAT2A, PCNA, MSH6, MSH2, TP53, MDM2, COPS5, AURKB, TOB1, ATR, TUBG1, DDA1, COPS3, COPS4, CHEK1, CFTR, SHPRH, HLTF, RAD18, FBXO11, LYN, CDT1, FBXO18, TDG, YWHAE, YWHAQ, YWHAZ, YWHAB, YWHAG, YWHAH, SFN, UBE2D1, UBE2N, TCEAL1, C9orf41, ERCC5, UBE2I, COPS7A, WHSC1, RBX1, UBE2E2, UBE2E3, UBE2E1, POLD4, CCT3, PFDN2, CCT7, SSSCA1, COPS8, GLMN, PDDC1, CAMK2D, DEF8INTS7RPAP2, INTS1, INTS3, INTS5, INTS6, SHFM1, INTS10, CTDP1, INTS2, INTS8, PAXIP1, SOX2, DCP2, SSBP1, HLA-DPA1, SPACA1, NRG1, SLAMF1, DLK1, TMEFF1, PRKCSH, VSIG4, FNDC4, FAF2, C7orf26, CPSF3L, ASUN, FGD1, HNRNPD, PML, RALA, BUB3, VPS26A, CKAP5, SYNCRIP, KIF1C, GOLT1B, ANLN, ACTR5, SCN3B, VSIG1, CD79B, PDCD1, TOR1AIP2, CLEC14A, PMEL, NTRK3, MGRN1, TNFRSF17, IL13RA2, TRIM25


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 DTL_INTS7


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 DTL_INTS7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDTLC0010606Adenoid Cystic Carcinoma1CTD_human
HgeneDTLC0036095Salivary Gland Neoplasms1CTD_human