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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:RAB31-ZEB1 (FusionGDB2 ID:70862)

Fusion Gene Summary for RAB31-ZEB1

check button Fusion gene summary
Fusion gene informationFusion gene name: RAB31-ZEB1
Fusion gene ID: 70862
HgeneTgene
Gene symbol

RAB31

ZEB1

Gene ID

11031

6935

Gene nameRAB31, member RAS oncogene familyzinc finger E-box binding homeobox 1
SynonymsRab22BAREB6|BZP|DELTAEF1|FECD6|NIL2A|PPCD3|TCF8|ZFHEP|ZFHX1A
Cytomap

18p11.22

10p11.22

Type of geneprotein-codingprotein-coding
Descriptionras-related protein Rab-31ras-related protein Rab-22Bzinc finger E-box-binding homeobox 1delta-crystallin enhancer binding factor 1negative regulator of IL2posterior polymorphous corneal dystrophy 3transcription factor 8 (represses interleukin 2 expression)zinc finger homeodomain enhancer-binding prote
Modification date2020031320200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000578921, ENST00000577284, 
ENST00000320985, ENST00000361642, 
ENST00000559858, ENST00000560721, 
ENST00000542815, ENST00000446923, 
Fusion gene scores* DoF score6 X 7 X 2=847 X 8 X 3=168
# samples 78
** MAII scorelog2(7/84*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RAB31 [Title/Abstract] AND ZEB1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRAB31(9722157)-ZEB1(31608180), # 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
TgeneZEB1

GO:0000122

negative regulation of transcription by RNA polymerase II

23765923|23814079

TgeneZEB1

GO:0045892

negative regulation of transcription, DNA-templated

20418909


check buttonFusion gene breakpoints across RAB31 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ZEB1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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/AU19969RAB31chr18

9722157

+ZEB1chr10

31608180

+


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Fusion Gene ORF analysis for RAB31-ZEB1

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-3CDSENST00000578921ENST00000320985RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3CDSENST00000578921ENST00000361642RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3UTRENST00000578921ENST00000559858RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3UTRENST00000578921ENST00000560721RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3UTRENST00000578921ENST00000542815RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-intronENST00000578921ENST00000446923RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3CDSENST00000577284ENST00000320985RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3CDSENST00000577284ENST00000361642RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3UTRENST00000577284ENST00000559858RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3UTRENST00000577284ENST00000560721RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-3UTRENST00000577284ENST00000542815RAB31chr18

9722157

+ZEB1chr10

31608180

+
intron-intronENST00000577284ENST00000446923RAB31chr18

9722157

+ZEB1chr10

31608180

+

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 RAB31-ZEB1


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)

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.

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.

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Fusion Protein Features for RAB31-ZEB1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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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Fusion Gene Sequence for RAB31-ZEB1


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 RAB31-ZEB1


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 RAB31-ZEB1


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 RAB31-ZEB1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRAB31C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneZEB1C2750448CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 64CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneZEB1C0006142Malignant neoplasm of breast2CTD_human
TgeneZEB1C0339284Polymorphous corneal dystrophy2ORPHANET
TgeneZEB1C0678222Breast Carcinoma2CTD_human
TgeneZEB1C1257931Mammary Neoplasms, Human2CTD_human
TgeneZEB1C1458155Mammary Neoplasms2CTD_human
TgeneZEB1C1836724CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)2CTD_human;GENOMICS_ENGLAND
TgeneZEB1C4704874Mammary Carcinoma, Human2CTD_human
TgeneZEB1C0007621Neoplastic Cell Transformation1CTD_human
TgeneZEB1C0014170Endometrial Neoplasms1CTD_human
TgeneZEB1C0016781Fuchs Endothelial Dystrophy1GENOMICS_ENGLAND;ORPHANET
TgeneZEB1C0027626Neoplasm Invasiveness1CTD_human
TgeneZEB1C0029172Oral Submucous Fibrosis1CTD_human
TgeneZEB1C0036920Sezary Syndrome1CTD_human
TgeneZEB1C0079773Lymphoma, T-Cell, Cutaneous1CTD_human
TgeneZEB1C0151744Myocardial Ischemia1CTD_human
TgeneZEB1C0235874Disease Exacerbation1CTD_human
TgeneZEB1C0238463Papillary thyroid carcinoma1CTD_human
TgeneZEB1C0376407Granulomatous Slack Skin1CTD_human
TgeneZEB1C0476089Endometrial Carcinoma1CTD_human
TgeneZEB1C0919267ovarian neoplasm1CTD_human
TgeneZEB1C1140680Malignant neoplasm of ovary1CTD_human
TgeneZEB1C3501843Nonmedullary Thyroid Carcinoma1CTD_human
TgeneZEB1C3501844Familial Nonmedullary Thyroid Cancer1CTD_human