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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:MAN1B1-CYP4X1 (FusionGDB2 ID:51079)

Fusion Gene Summary for MAN1B1-CYP4X1

check button Fusion gene summary
Fusion gene informationFusion gene name: MAN1B1-CYP4X1
Fusion gene ID: 51079
HgeneTgene
Gene symbol

MAN1B1

CYP4X1

Gene ID

11253

260293

Gene namemannosidase alpha class 1B member 1cytochrome P450 family 4 subfamily X member 1
SynonymsERMAN1|ERManI|MANA-ER|MRT15CYPIVX1
Cytomap

9q34.3

1p33|1

Type of geneprotein-codingprotein-coding
Descriptionendoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidaseER alpha 1,2-mannosidaseMan9GlcNAc2-specific processing alpha-mannosidaseendoplasmic Reticulum Class I alpha-mannosidaseendoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannoscytochrome P450 4X1cytochrome P450, family 4, subfamily X, polypeptide 1
Modification date2020031320200313
UniProtAcc

Q9UKM7

Q8N118

Ensembl transtripts involved in fusion geneENST00000540391, ENST00000371589, 
ENST00000474902, 
ENST00000371901, 
ENST00000466294, ENST00000538609, 
Fusion gene scores* DoF score2 X 2 X 1=44 X 4 X 3=48
# samples 25
** MAII scorelog2(2/4*10)=2.32192809488736log2(5/48*10)=0.0588936890535686
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MAN1B1 [Title/Abstract] AND CYP4X1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMAN1B1(140001869)-CYP4X1(47483067), # 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
HgeneMAN1B1

GO:0036508

protein alpha-1,2-demannosylation

10521544|22160784

HgeneMAN1B1

GO:0036509

trimming of terminal mannose on B branch

10521544


check buttonFusion gene breakpoints across MAN1B1 (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 CYP4X1 (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/AT20223MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+


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Fusion Gene ORF analysis for MAN1B1-CYP4X1

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
3UTR-intronENST00000540391ENST00000371901MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
3UTR-intronENST00000540391ENST00000466294MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
3UTR-intronENST00000540391ENST00000538609MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
5CDS-intronENST00000371589ENST00000371901MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
5CDS-intronENST00000371589ENST00000466294MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
5CDS-intronENST00000371589ENST00000538609MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
5CDS-intronENST00000474902ENST00000371901MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
5CDS-intronENST00000474902ENST00000466294MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+
5CDS-intronENST00000474902ENST00000538609MAN1B1chr9

140001869

-CYP4X1chr1

47483067

+

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 MAN1B1-CYP4X1


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 MAN1B1-CYP4X1


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/:140001869/:47483067)
- 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
MAN1B1

Q9UKM7

CYP4X1

Q8N118

FUNCTION: Involved in glycoprotein quality control targeting of misfolded glycoproteins for degradation. It primarily trims a single alpha-1,2-linked mannose residue from Man(9)GlcNAc(2) to produce Man(8)GlcNAc(2), but at high enzyme concentrations, as found in the ER quality control compartment (ERQC), it further trims the carbohydrates to Man(5-6)GlcNAc(2). {ECO:0000269|PubMed:12090241, ECO:0000269|PubMed:18003979}.FUNCTION: A cytochrome P450 monooxygenase that selectively catalyzes the epoxidation of the last double bond of the arachidonoyl moiety of anandamide, potentially modulating endocannabinoid signaling. Has no hydroxylase activity toward various fatty acids, steroids and prostaglandins. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase). {ECO:0000269|PubMed:18549450}.

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 MAN1B1-CYP4X1


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 MAN1B1-CYP4X1


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 MAN1B1-CYP4X1


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 MAN1B1-CYP4X1


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