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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:NRSN1-FAM120B (FusionGDB2 ID:59991)

Fusion Gene Summary for NRSN1-FAM120B

check button Fusion gene summary
Fusion gene informationFusion gene name: NRSN1-FAM120B
Fusion gene ID: 59991
HgeneTgene
Gene symbol

NRSN1

FAM120B

Gene ID

140767

84498

Gene nameneurensin 1family with sequence similarity 120B
SynonymsVMP|p24CCPG|KIAA1838|PGCC1|SAN1|dJ894D12.1
Cytomap

6p22.3

6q27

Type of geneprotein-codingprotein-coding
Descriptionneurensin-1neuro-p24vesicular membrain protein p24vesicular membrane protein of 24 kDavesicular membrane protein p24constitutive coactivator of peroxisome proliferator-activated receptor gammaPPARG constitutive coactivator 1PPARgamma constitutive coactivator 1constitutive coactivator of PPAR-gammasenataxin-associated nuclease 1
Modification date2020031320200313
UniProtAcc

Q8IZ57

Q96EK7

Ensembl transtripts involved in fusion geneENST00000378478, ENST00000378491, 
ENST00000475830, ENST00000378475, 
ENST00000540480, ENST00000537664, 
ENST00000476287, ENST00000252510, 
ENST00000496635, 
Fusion gene scores* DoF score1 X 1 X 1=110 X 9 X 6=540
# samples 110
** MAII scorelog2(1/1*10)=3.32192809488736log2(10/540*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NRSN1 [Title/Abstract] AND FAM120B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNRSN1(24134744)-FAM120B(170704574), # 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 NRSN1 (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 FAM120B (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
ChimerDB4LGGTCGA-HT-A5R5NRSN1chr6

24134744

+FAM120Bchr6

170704574

+


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Fusion Gene ORF analysis for NRSN1-FAM120B

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-shiftENST00000378478ENST00000540480NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378478ENST00000537664NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378478ENST00000476287NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378478ENST00000252510NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
5CDS-intronENST00000378478ENST00000496635NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378491ENST00000540480NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378491ENST00000537664NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378491ENST00000476287NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378491ENST00000252510NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
5CDS-intronENST00000378491ENST00000496635NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
intron-3CDSENST00000475830ENST00000540480NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
intron-3CDSENST00000475830ENST00000537664NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
intron-3CDSENST00000475830ENST00000476287NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
intron-3CDSENST00000475830ENST00000252510NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
intron-intronENST00000475830ENST00000496635NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378475ENST00000540480NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378475ENST00000537664NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378475ENST00000476287NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
Frame-shiftENST00000378475ENST00000252510NRSN1chr6

24134744

+FAM120Bchr6

170704574

+
5CDS-intronENST00000378475ENST00000496635NRSN1chr6

24134744

+FAM120Bchr6

170704574

+

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 NRSN1-FAM120B


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)
NRSN1chr624134744+FAM120Bchr6170704574+0.799377860.20062213
NRSN1chr624134744+FAM120Bchr6170704574+0.799377860.20062213

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 NRSN1-FAM120B


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
NRSN1

Q8IZ57

FAM120B

Q96EK7

FUNCTION: May play an important role in neural organelle transport, and in transduction of nerve signals or in nerve growth. May play a role in neurite extension. May play a role in memory consolidation (By similarity). {ECO:0000250|UniProtKB:P97799, ECO:0000269|PubMed:12463420}.FUNCTION: Functions as a transactivator of PPARG and ESR1. Functions in adipogenesis through PPARG activation (By similarity). {ECO:0000250}.

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 NRSN1-FAM120B


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 NRSN1-FAM120B


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 NRSN1-FAM120B


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 NRSN1-FAM120B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNRSN1C0005684Malignant neoplasm of urinary bladder1CTD_human
HgeneNRSN1C0005695Bladder Neoplasm1CTD_human
HgeneNRSN1C0017181Gastrointestinal Hemorrhage1GENOMICS_ENGLAND
HgeneNRSN1C0019569Hirschsprung Disease1GENOMICS_ENGLAND
HgeneNRSN1C0019829Hodgkin Disease1GENOMICS_ENGLAND
HgeneNRSN1C0020179Huntington Disease1GENOMICS_ENGLAND