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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:EHD2-BLOC1S6 (FusionGDB2 ID:25553)

Fusion Gene Summary for EHD2-BLOC1S6

check button Fusion gene summary
Fusion gene informationFusion gene name: EHD2-BLOC1S6
Fusion gene ID: 25553
HgeneTgene
Gene symbol

EHD2

BLOC1S6

Gene ID

30846

26258

Gene nameEH domain containing 2biogenesis of lysosomal organelles complex 1 subunit 6
SynonymsPAST2BLOS6|HPS9|PA|PALLID|PLDN
Cytomap

19q13.33

15q21.1

Type of geneprotein-codingprotein-coding
DescriptionEH domain-containing protein 2PAST homolog 2biogenesis of lysosome-related organelles complex 1 subunit 6BLOC-1 subunit 6BLOC-1 subunit pallidinbiogenesis of lysosomal organelles complex-1, subunit 5, pallidinbiogenesis of lysosomal organelles complex-1, subunit 6, pallidinpallid protein homol
Modification date2020031520200327
UniProtAcc

Q9NZN4

Q9UL45

Ensembl transtripts involved in fusion geneENST00000263277, ENST00000538399, 
ENST00000540884, 
ENST00000220531, 
ENST00000568816, ENST00000562384, 
ENST00000564765, ENST00000565216, 
ENST00000565323, ENST00000565409, 
ENST00000566753, ENST00000567461, 
ENST00000567740, 
Fusion gene scores* DoF score7 X 7 X 2=981 X 1 X 1=1
# samples 71
** MAII scorelog2(7/98*10)=-0.485426827170242
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: EHD2 [Title/Abstract] AND BLOC1S6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEHD2(48245819)-BLOC1S6(45899668), # 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
TgeneBLOC1S6

GO:0032402

melanosome transport

17182842

TgeneBLOC1S6

GO:0035646

endosome to melanosome transport

17182842

TgeneBLOC1S6

GO:0050942

positive regulation of pigment cell differentiation

17182842


check buttonFusion gene breakpoints across EHD2 (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 BLOC1S6 (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/ACA449248EHD2chr19

48245819

-BLOC1S6chr15

45899668

-


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Fusion Gene ORF analysis for EHD2-BLOC1S6

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-3UTRENST00000263277ENST00000220531EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-3UTRENST00000263277ENST00000568816EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000562384EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000564765EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000565216EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000565323EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000565409EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000566753EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000567461EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
3UTR-intronENST00000263277ENST00000567740EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-3UTRENST00000538399ENST00000220531EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-3UTRENST00000538399ENST00000568816EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-3UTRENST00000540884ENST00000220531EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-3UTRENST00000540884ENST00000568816EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000562384EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000564765EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000565216EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000565323EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000565409EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000566753EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000567461EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000538399ENST00000567740EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000562384EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000564765EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000565216EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000565323EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000565409EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000566753EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000567461EHD2chr19

48245819

-BLOC1S6chr15

45899668

-
intron-intronENST00000540884ENST00000567740EHD2chr19

48245819

-BLOC1S6chr15

45899668

-

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 EHD2-BLOC1S6


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 EHD2-BLOC1S6


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/:48245819/:45899668)
- 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
EHD2

Q9NZN4

BLOC1S6

Q9UL45

FUNCTION: ATP- and membrane-binding protein that controls membrane reorganization/tubulation upon ATP hydrolysis (By similarity). Plays a role in membrane trafficking between the plasma membrane and endosomes (PubMed:17233914). Important for the internalization of GLUT4. Required for fusion of myoblasts to skeletal muscle myotubes. Required for normal translocation of FER1L5 to the plasma membrane (By similarity). Regulates the equilibrium between cell surface-associated and cell surface-dissociated caveolae by constraining caveolae at the cell membrane (PubMed:25588833). {ECO:0000250|UniProtKB:Q8BH64, ECO:0000269|PubMed:17233914, ECO:0000269|PubMed:25588833}.FUNCTION: Component of the BLOC-1 complex, a complex that is required for normal biogenesis of lysosome-related organelles (LRO), such as platelet dense granules and melanosomes. In concert with the AP-3 complex, the BLOC-1 complex is required to target membrane protein cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals. The BLOC-1 complex, in association with SNARE proteins, is also proposed to be involved in neurite extension. May play a role in intracellular vesicle trafficking, particularly in the vesicle-docking and fusion process. {ECO:0000269|PubMed:17182842, ECO:0000269|PubMed:21998198}.

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 EHD2-BLOC1S6


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 EHD2-BLOC1S6


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 EHD2-BLOC1S6


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 EHD2-BLOC1S6


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