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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:BANP-SLC7A5 (FusionGDB2 ID:8963)

Fusion Gene Summary for BANP-SLC7A5

check button Fusion gene summary
Fusion gene informationFusion gene name: BANP-SLC7A5
Fusion gene ID: 8963
HgeneTgene
Gene symbol

BANP

SLC7A5

Gene ID

54971

8140

Gene nameBTG3 associated nuclear proteinsolute carrier family 7 member 5
SynonymsBEND1|SMAR1|SMARBP14F2LC|CD98|D16S469E|E16|LAT1|MPE16
Cytomap

16q24.2

16q24.2

Type of geneprotein-codingprotein-coding
Descriptionprotein BANPBEN domain-containing protein 1scaffold/matrix-associated region-1-binding proteinlarge neutral amino acids transporter small subunit 14F2 light chainCD98 light chainL-type amino acid transporter 1integral membrane protein E16sodium-independent neutral amino acid transporter LAT1solute carrier family 7 (amino acid transporter lig
Modification date2020031520200313
UniProtAcc

Q8N9N5

Q9GIP4

Ensembl transtripts involved in fusion geneENST00000286122, ENST00000355022, 
ENST00000355163, ENST00000393208, 
ENST00000479780, ENST00000393207, 
ENST00000481948, ENST00000538234, 
ENST00000261622, ENST00000565644, 
Fusion gene scores* DoF score8 X 7 X 8=4487 X 4 X 6=168
# samples 87
** MAII scorelog2(8/448*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BANP [Title/Abstract] AND SLC7A5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBANP(87985121)-SLC7A5(87874761), # 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
TgeneSLC7A5

GO:1904556

L-tryptophan transmembrane transport

30867591


check buttonFusion gene breakpoints across BANP (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 SLC7A5 (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
ChimerDB4LUADTCGA-38-4630BANPchr16

87985121

+SLC7A5chr16

87874761

-


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Fusion Gene ORF analysis for BANP-SLC7A5

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
5UTR-5UTRENST00000286122ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000286122ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000355022ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000355022ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000355163ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000355163ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000393208ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000393208ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000479780ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
5UTR-5UTRENST00000479780ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
intron-5UTRENST00000393207ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
intron-5UTRENST00000393207ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
intron-5UTRENST00000481948ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
intron-5UTRENST00000481948ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-
intron-5UTRENST00000538234ENST00000261622BANPchr16

87985121

+SLC7A5chr16

87874761

-
intron-5UTRENST00000538234ENST00000565644BANPchr16

87985121

+SLC7A5chr16

87874761

-

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 BANP-SLC7A5


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 BANP-SLC7A5


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/:87985121/:87874761)
- 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
BANP

Q8N9N5

SLC7A5

Q9GIP4

FUNCTION: Controls V(D)J recombination during T-cell development by repressing T-cell receptor (TCR) beta enhancer function. Binds to scaffold/matrix attachment region beta (S/MARbeta), an ATC-rich DNA sequence located upstream of the TCR beta enhancer. Represses cyclin D1 transcription by recruiting HDAC1 to its promoter, thereby diminishing H3K9ac, H3S10ph and H4K8ac levels. Promotes TP53 'Ser-15' phosphorylation and nuclear accumulation, which causes cell cycle arrest (By similarity). {ECO:0000250, ECO:0000269|PubMed:16166625}.

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 BANP-SLC7A5


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 BANP-SLC7A5


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 BANP-SLC7A5


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 BANP-SLC7A5


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