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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:ASGR2-ASGR2 (FusionGDB2 ID:7079)

Fusion Gene Summary for ASGR2-ASGR2

check button Fusion gene summary
Fusion gene informationFusion gene name: ASGR2-ASGR2
Fusion gene ID: 7079
HgeneTgene
Gene symbol

ASGR2

ASGR2

Gene ID

433

433

Gene nameasialoglycoprotein receptor 2asialoglycoprotein receptor 2
SynonymsASGP-R2|ASGPR2|CLEC4H2|HBXBP|HL-2ASGP-R2|ASGPR2|CLEC4H2|HBXBP|HL-2
Cytomap

17p13.1

17p13.1

Type of geneprotein-codingprotein-coding
Descriptionasialoglycoprotein receptor 2C-type lectin domain family 4 member H2HBxAg-binding proteinhepatic lectin H2asialoglycoprotein receptor 2C-type lectin domain family 4 member H2HBxAg-binding proteinhepatic lectin H2
Modification date2020031320200313
UniProtAcc

P07307

P07307

Ensembl transtripts involved in fusion geneENST00000254850, ENST00000355035, 
ENST00000380952, ENST00000446679, 
ENST00000254850, ENST00000355035, 
ENST00000380952, ENST00000446679, 
Fusion gene scores* DoF score1 X 1 X 1=13 X 3 X 3=27
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: ASGR2 [Title/Abstract] AND ASGR2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointASGR2(7012176)-ASGR2(7004782), # 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

check buttonFusion gene breakpoints across ASGR2 (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 ASGR2 (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/ACB162748ASGR2chr17

7012176

+ASGR2chr17

7004782

-


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Fusion Gene ORF analysis for ASGR2-ASGR2

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-3UTRENST00000254850ENST00000254850ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000254850ENST00000355035ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000254850ENST00000380952ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000355035ENST00000254850ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000355035ENST00000355035ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000355035ENST00000380952ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000380952ENST00000254850ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000380952ENST00000355035ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000380952ENST00000380952ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000446679ENST00000254850ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000446679ENST00000355035ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-3UTRENST00000446679ENST00000380952ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-intronENST00000254850ENST00000446679ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-intronENST00000355035ENST00000446679ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-intronENST00000380952ENST00000446679ASGR2chr17

7012176

+ASGR2chr17

7004782

-
intron-intronENST00000446679ENST00000446679ASGR2chr17

7012176

+ASGR2chr17

7004782

-

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 ASGR2-ASGR2


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 ASGR2-ASGR2


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/:7012176/:7004782)
- 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
ASGR2

P07307

ASGR2

P07307

FUNCTION: Mediates the endocytosis of plasma glycoproteins to which the terminal sialic acid residue on their complex carbohydrate moieties has been removed. The receptor recognizes terminal galactose and N-acetylgalactosamine units. After ligand binding to the receptor, the resulting complex is internalized and transported to a sorting organelle, where receptor and ligand are disassociated. The receptor then returns to the cell membrane surface.FUNCTION: Mediates the endocytosis of plasma glycoproteins to which the terminal sialic acid residue on their complex carbohydrate moieties has been removed. The receptor recognizes terminal galactose and N-acetylgalactosamine units. After ligand binding to the receptor, the resulting complex is internalized and transported to a sorting organelle, where receptor and ligand are disassociated. The receptor then returns to the cell membrane surface.

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 ASGR2-ASGR2


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 ASGR2-ASGR2


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 ASGR2-ASGR2


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 ASGR2-ASGR2


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