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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: 11973

FusionGeneSummary for ERCC1_FBRSL1

check button Fusion gene summary
Fusion gene informationFusion gene name: ERCC1_FBRSL1
Fusion gene ID: 11973
HgeneTgene
Gene symbol

ERCC1

FBRSL1

Gene ID

2067

57666

Gene nameERCC excision repair 1, endonuclease non-catalytic subunitfibrosin like 1
SynonymsCOFS4|RAD10|UV20-
Cytomap

19q13.32

12q24.33

Type of geneprotein-codingprotein-coding
DescriptionDNA excision repair protein ERCC-1excision repair cross-complementation group 1excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)fibrosin-1-like proteinAUTS2-like proteinHBV X-transactivated gene 9 proteinHBV XAg-transactivated protein 9
Modification date2018052320180519
UniProtAcc

P07992

Q9HCM7

Ensembl transtripts involved in fusion geneENST00000300853, ENST00000423698, 
ENST00000588738, ENST00000340192, 
ENST00000591636, ENST00000589165, 
ENST00000013807, 
ENST00000434748, 
ENST00000261673, ENST00000542061, 
Fusion gene scores* DoF score5 X 6 X 2=604 X 4 X 4=64
# samples 64
** MAII scorelog2(6/60*10)=0log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ERCC1 [Title/Abstract] AND FBRSL1 [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
HgeneERCC1

GO:0006289

nucleotide-excision repair

3290851


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
ChiTaRS3.1BG983612ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
* 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
intron-intronENST00000300853ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000300853ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000300853ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000423698ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000423698ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000423698ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000588738ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000588738ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000588738ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000340192ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000340192ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000340192ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000591636ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000591636ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000591636ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000589165ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000589165ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000589165ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000013807ENST00000434748ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000013807ENST00000261673ERCC1chr19

45973952

+FBRSL1chr12

133100584

-
intron-intronENST00000013807ENST00000542061ERCC1chr19

45973952

+FBRSL1chr12

133100584

-

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FusionProtFeatures for ERCC1_FBRSL1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ERCC1

P07992

FBRSL1

Q9HCM7

Isoform 1: Non-catalytic component of a structure-specific DNA repair endonuclease responsible for the 5'-incisionduring DNA repair. Responsible, in conjunction with SLX4, for thefirst step in the repair of interstrand cross-links (ICL).Participates in the processing of anaphase bridge-generating DNAstructures, which consist in incompletely processed DNA lesionsarising during S or G2 phase, and can result in cytokinesisfailure. Also required for homology-directed repair (HDR) of DNAdouble-strand breaks, in conjunction with SLX4.

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 ERCC1_FBRSL1


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 ERCC1_FBRSL1


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


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 ERCC1_FBRSL1


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 ERCC1_FBRSL1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneERCC1C0007131Non-Small Cell Lung Carcinoma2CTD_human
HgeneERCC1C0001956alcohol use disorder1PSYGENET
HgeneERCC1C0007873Uterine Cervical Neoplasm1CTD_human
HgeneERCC1C0008625Chromosome Aberrations1CTD_human
HgeneERCC1C0025202melanoma1CTD_human
HgeneERCC1C0027627Neoplasm Metastasis1CTD_human
HgeneERCC1C0027658Neoplasms, Germ Cell and Embryonal1CTD_human
HgeneERCC1C0031117Peripheral Neuropathy1CTD_human
HgeneERCC1C0038356Stomach Neoplasms1CTD_human
HgeneERCC1C0039590Testicular Neoplasms1CTD_human
HgeneERCC1C0152013Adenocarcinoma of lung (disorder)1CTD_human
HgeneERCC1C0311375Arsenic Poisoning1CTD_human
HgeneERCC1C1853100CEREBROOCULOFACIOSKELETAL SYNDROME 41CTD_human;UNIPROT
HgeneERCC1C2931822Nasopharyngeal carcinoma1CTD_human