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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:HOMER2-BTBD1 (FusionGDB2 ID:37200)

Fusion Gene Summary for HOMER2-BTBD1

check button Fusion gene summary
Fusion gene informationFusion gene name: HOMER2-BTBD1
Fusion gene ID: 37200
HgeneTgene
Gene symbol

HOMER2

BTBD1

Gene ID

9455

53339

Gene namehomer scaffold protein 2BTB domain containing 1
SynonymsACPD|CPD|DFNA68|HOMER-2|VESL-2C15orf1|NS5ATP8
Cytomap

15q25.2

15q25.2

Type of geneprotein-codingprotein-coding
Descriptionhomer protein homolog 2cupidinhomer homolog 2homer homolog 3homer scaffolding protein 2homer, neuronal immediate early gene, 2BTB/POZ domain-containing protein 1BTB (POZ) domain containing 1HCV NS5A-transactivated protein 8hepatitis C virus NS5A-transactivated protein 8
Modification date2020031320200327
UniProtAcc.

B2RXH4

Ensembl transtripts involved in fusion geneENST00000450735, ENST00000304231, 
ENST00000399166, ENST00000426485, 
ENST00000500334, 
ENST00000261721, 
ENST00000379403, ENST00000560015, 
Fusion gene scores* DoF score9 X 5 X 5=2255 X 5 X 4=100
# samples 105
** MAII scorelog2(10/225*10)=-1.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HOMER2 [Title/Abstract] AND BTBD1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHOMER2(83621283)-BTBD1(83686977), # samples:2
BTBD1(83735503)-HOMER2(83561593), # samples:1
Anticipated loss of major functional domain due to fusion event.BTBD1-HOMER2 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
HOMER2-BTBD1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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 HOMER2 (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 BTBD1 (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
ChimerDB4OVTCGA-24-2298-01AHOMER2chr15

83621283

-BTBD1chr15

83686977

-
ChimerDB4OVTCGA-24-2298-01AHOMER2chr15

83621283

-BTBD1chr15

83686977

-


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Fusion Gene ORF analysis for HOMER2-BTBD1

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
Frame-shiftENST00000450735ENST00000261721HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-3UTRENST00000450735ENST00000379403HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-intronENST00000450735ENST00000560015HOMER2chr15

83621283

-BTBD1chr15

83686977

-
Frame-shiftENST00000304231ENST00000261721HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-3UTRENST00000304231ENST00000379403HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-intronENST00000304231ENST00000560015HOMER2chr15

83621283

-BTBD1chr15

83686977

-
Frame-shiftENST00000399166ENST00000261721HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-3UTRENST00000399166ENST00000379403HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-intronENST00000399166ENST00000560015HOMER2chr15

83621283

-BTBD1chr15

83686977

-
Frame-shiftENST00000426485ENST00000261721HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-3UTRENST00000426485ENST00000379403HOMER2chr15

83621283

-BTBD1chr15

83686977

-
5CDS-intronENST00000426485ENST00000560015HOMER2chr15

83621283

-BTBD1chr15

83686977

-
intron-3CDSENST00000500334ENST00000261721HOMER2chr15

83621283

-BTBD1chr15

83686977

-
intron-3UTRENST00000500334ENST00000379403HOMER2chr15

83621283

-BTBD1chr15

83686977

-
intron-intronENST00000500334ENST00000560015HOMER2chr15

83621283

-BTBD1chr15

83686977

-

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 HOMER2-BTBD1


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 HOMER2-BTBD1


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
.BTBD1

B2RXH4

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: Specifically required during spermatogenesis to promote expression of piRNA precursors. The piRNA metabolic process mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins and governs the methylation and subsequent repression of transposons, which is essential for the germline integrity. Acts by facilitating transcription elongation at piRNA loci during pachytene. {ECO:0000250|UniProtKB:A0A0A6YY25}.

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 HOMER2-BTBD1


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 HOMER2-BTBD1


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 HOMER2-BTBD1


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 HOMER2-BTBD1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHOMER2C3711374Nonsyndromic Deafness2CLINGEN
HgeneHOMER2C0009171Cocaine Abuse1CTD_human
HgeneHOMER2C0036341Schizophrenia1PSYGENET
HgeneHOMER2C0236736Cocaine-Related Disorders1CTD_human
HgeneHOMER2C0600427Cocaine Dependence1CTD_human
HgeneHOMER2C4225240DEAFNESS, AUTOSOMAL DOMINANT 681CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneBTBD1C0520757Delayed Emergence from Anesthesia1CTD_human
TgeneBTBD1C4042763Postoperative Residual Curarization1CTD_human