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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:FANCL-FANCL (FusionGDB2 ID:29344)

Fusion Gene Summary for FANCL-FANCL

check button Fusion gene summary
Fusion gene informationFusion gene name: FANCL-FANCL
Fusion gene ID: 29344
HgeneTgene
Gene symbol

FANCL

FANCL

Gene ID

55120

55120

Gene nameFA complementation group LFA complementation group L
SynonymsFAAP43|PHF9|POGFAAP43|PHF9|POG
Cytomap

2p16.1

2p16.1

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase FANCLFanconi anemia complementation group LPHD finger protein 9RING-type E3 ubiquitin transferase FANCLfanconi anemia group L proteinfanconi anemia-associated polypeptide of 43 kDaE3 ubiquitin-protein ligase FANCLFanconi anemia complementation group LPHD finger protein 9RING-type E3 ubiquitin transferase FANCLfanconi anemia group L proteinfanconi anemia-associated polypeptide of 43 kDa
Modification date2020031320200313
UniProtAcc

Q9NW38

Q9NW38

Ensembl transtripts involved in fusion geneENST00000233741, ENST00000403295, 
ENST00000403676, ENST00000402135, 
ENST00000481670, ENST00000540646, 
ENST00000403676, ENST00000481670, 
ENST00000540646, ENST00000233741, 
ENST00000402135, ENST00000403295, 
Fusion gene scores* DoF score5 X 6 X 2=602 X 5 X 2=20
# samples 64
** MAII scorelog2(6/60*10)=0log2(4/20*10)=1
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FANCL [Title/Abstract] AND FANCL [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFANCL(58459250)-FANCL(58425728), # samples:1
FANCL(58425728)-FANCL(58459250), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneFANCL

GO:0006513

protein monoubiquitination

16916645|24389026

TgeneFANCL

GO:0006513

protein monoubiquitination

16916645|24389026


check buttonFusion gene breakpoints across FANCL (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across FANCL (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABE694274FANCLchr2

58459250

+FANCLchr2

58425728

+
ChiTaRS5.0N/ABE694283FANCLchr2

58425728

-FANCLchr2

58459250

-


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Fusion Gene ORF analysis for FANCL-FANCL

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-intronENST00000233741ENST00000403676FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000233741ENST00000481670FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000233741ENST00000540646FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000403295ENST00000403676FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000403295ENST00000481670FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000403295ENST00000540646FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000403676ENST00000403676FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000403676ENST00000481670FANCLchr2

58425728

-FANCLchr2

58459250

-
5CDS-intronENST00000403676ENST00000540646FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000233741ENST00000233741FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000233741ENST00000402135FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000233741ENST00000403295FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000403295ENST00000233741FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000403295ENST00000402135FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000403295ENST00000403295FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000403676ENST00000233741FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000403676ENST00000402135FANCLchr2

58425728

-FANCLchr2

58459250

-
In-frameENST00000403676ENST00000403295FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000402135ENST00000233741FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000402135ENST00000402135FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000402135ENST00000403295FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000481670ENST00000233741FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000481670ENST00000402135FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000481670ENST00000403295FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000540646ENST00000233741FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000540646ENST00000402135FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-3CDSENST00000540646ENST00000403295FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000233741ENST00000233741FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000233741ENST00000402135FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000233741ENST00000403295FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000233741ENST00000403676FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000233741ENST00000481670FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000233741ENST00000540646FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000233741FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000402135FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000403295FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000403676FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000403676FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000402135ENST00000481670FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000481670FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000402135ENST00000540646FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000402135ENST00000540646FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000403295ENST00000233741FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403295ENST00000402135FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403295ENST00000403295FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403295ENST00000403676FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403295ENST00000481670FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403295ENST00000540646FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403676ENST00000233741FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403676ENST00000402135FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403676ENST00000403295FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403676ENST00000403676FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403676ENST00000481670FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000403676ENST00000540646FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000233741FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000402135FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000403295FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000403676FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000403676FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000481670ENST00000481670FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000481670FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000481670ENST00000540646FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000481670ENST00000540646FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000540646ENST00000233741FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000540646ENST00000402135FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000540646ENST00000403295FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000540646ENST00000403676FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000540646ENST00000403676FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000540646ENST00000481670FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000540646ENST00000481670FANCLchr2

58425728

-FANCLchr2

58459250

-
intron-intronENST00000540646ENST00000540646FANCLchr2

58459250

+FANCLchr2

58425728

+
intron-intronENST00000540646ENST00000540646FANCLchr2

58425728

-FANCLchr2

58459250

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for FANCL-FANCL


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
FANCLchr258459247+FANCLchr258425728+0.997213070.002786911
FANCLchr258459247+FANCLchr258425728+0.997213070.002786911

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.
genomic feature

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

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Fusion Protein Features for FANCL-FANCL


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr2:58459250/chr2:58425728)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

Q9NW38

FANCL

Q9NW38

FUNCTION: Ubiquitin ligase protein that mediates monoubiquitination of FANCD2 in the presence of UBE2T, a key step in the DNA damage pathway (PubMed:12973351, PubMed:16916645, PubMed:17938197, PubMed:19111657, PubMed:24389026). Also mediates monoubiquitination of FANCI (PubMed:19589784). May stimulate the ubiquitin release from UBE2W. May be required for proper primordial germ cell proliferation in the embryonic stage, whereas it is probably not needed for spermatogonial proliferation after birth. {ECO:0000269|PubMed:12973351, ECO:0000269|PubMed:16916645, ECO:0000269|PubMed:17938197, ECO:0000269|PubMed:19111657, ECO:0000269|PubMed:19589784, ECO:0000269|PubMed:24389026}.FUNCTION: Ubiquitin ligase protein that mediates monoubiquitination of FANCD2 in the presence of UBE2T, a key step in the DNA damage pathway (PubMed:12973351, PubMed:16916645, PubMed:17938197, PubMed:19111657, PubMed:24389026). Also mediates monoubiquitination of FANCI (PubMed:19589784). May stimulate the ubiquitin release from UBE2W. May be required for proper primordial germ cell proliferation in the embryonic stage, whereas it is probably not needed for spermatogonial proliferation after birth. {ECO:0000269|PubMed:12973351, ECO:0000269|PubMed:16916645, ECO:0000269|PubMed:17938197, ECO:0000269|PubMed:19111657, ECO:0000269|PubMed:19589784, ECO:0000269|PubMed:24389026}.

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
TgeneFANCLchr2:58425728chr2:58459250ENST00000233741014104_29432376.0RegionNote=UBC-RWD region (URD)
TgeneFANCLchr2:58425728chr2:58459250ENST00000402135014104_29432381.0RegionNote=UBC-RWD region (URD)
TgeneFANCLchr2:58425728chr2:58459250ENST00000233741014307_36532376.0Zinc fingerNote=RING-type
TgeneFANCLchr2:58425728chr2:58459250ENST00000402135014307_36532381.0Zinc fingerNote=RING-type

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneFANCLchr2:58425728chr2:58459250ENST00000233741-714104_294180376.0RegionNote=UBC-RWD region (URD)
HgeneFANCLchr2:58425728chr2:58459250ENST00000402135-114104_2940381.0RegionNote=UBC-RWD region (URD)
HgeneFANCLchr2:58425728chr2:58459250ENST00000233741-714307_365180376.0Zinc fingerNote=RING-type
HgeneFANCLchr2:58425728chr2:58459250ENST00000402135-114307_3650381.0Zinc fingerNote=RING-type


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Fusion Gene Sequence for FANCL-FANCL


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for FANCL-FANCL


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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Related Drugs for FANCL-FANCL


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for FANCL-FANCL


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