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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:NAA60-MSN (FusionGDB2 ID:57017)

Fusion Gene Summary for NAA60-MSN

check button Fusion gene summary
Fusion gene informationFusion gene name: NAA60-MSN
Fusion gene ID: 57017
HgeneTgene
Gene symbol

NAA60

MSN

Gene ID

79903

4478

Gene nameN-alpha-acetyltransferase 60, NatF catalytic subunitmoesin
SynonymsHAT4|NAT15|NatF|hNaa60HEL70|IMD50
Cytomap

16p13.3

Xq12

Type of geneprotein-codingprotein-coding
DescriptionN-alpha-acetyltransferase 60N-acetyltransferase 15 (GCN5-related, putative)N-alpha-acetyltransferase Fepididymis secretory sperm binding proteinhistone acetyltransferase type B protein 4moesinepididymis luminal protein 70membrane-organizing extension spike protein
Modification date2020031320200327
UniProtAcc

Q9H7X0

P26038

Ensembl transtripts involved in fusion geneENST00000360862, ENST00000407558, 
ENST00000414063, ENST00000421765, 
ENST00000424546, ENST00000570551, 
ENST00000570819, ENST00000572584, 
ENST00000572942, ENST00000573580, 
ENST00000575076, ENST00000576906, 
ENST00000576916, ENST00000577013, 
ENST00000608722, ENST00000608993, 
ENST00000610180, 
ENST00000360270, 
ENST00000609205, 
Fusion gene scores* DoF score10 X 8 X 7=56013 X 16 X 7=1456
# samples 1214
** MAII scorelog2(12/560*10)=-2.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1456*10)=-3.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NAA60 [Title/Abstract] AND MSN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNAA60(3503735)-MSN(64889506), # 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
HgeneNAA60

GO:0006334

nucleosome assembly

21981917

HgeneNAA60

GO:0006474

N-terminal protein amino acid acetylation

25732826|27320834|27550639

HgeneNAA60

GO:0017196

N-terminal peptidyl-methionine acetylation

21750686

HgeneNAA60

GO:0043967

histone H4 acetylation

21981917

TgeneMSN

GO:0001771

immunological synapse formation

27405666

TgeneMSN

GO:0042098

T cell proliferation

27405666

TgeneMSN

GO:0070489

T cell aggregation

27405666

TgeneMSN

GO:0071394

cellular response to testosterone stimulus

24065547

TgeneMSN

GO:0072678

T cell migration

27405666


check buttonFusion gene breakpoints across NAA60 (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 MSN (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/AEF580665NAA60chr16

3503735

-MSNchrX

64889506

-


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Fusion Gene ORF analysis for NAA60-MSN

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-intronENST00000360862ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000360862ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000407558ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000407558ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000414063ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000414063ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000421765ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000421765ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000424546ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000424546ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000570551ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000570551ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000570819ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000570819ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000572584ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000572584ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000572942ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000572942ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000573580ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000573580ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000575076ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000575076ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000576906ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000576906ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000576916ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000576916ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000577013ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000577013ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000608722ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000608722ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000608993ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000608993ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000610180ENST00000360270NAA60chr16

3503735

-MSNchrX

64889506

-
intron-intronENST00000610180ENST00000609205NAA60chr16

3503735

-MSNchrX

64889506

-

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 NAA60-MSN


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 NAA60-MSN


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/:3503735/:64889506)
- 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
NAA60

Q9H7X0

MSN

P26038

FUNCTION: N-alpha-acetyltransferase that specifically mediates the acetylation of N-terminal residues of the transmembrane proteins, with a strong preference for N-termini facing the cytosol (PubMed:25732826). Displays N-terminal acetyltransferase activity towards a range of N-terminal sequences including those starting with Met-Lys, Met-Val, Met-Ala and Met-Met (PubMed:21750686, PubMed:25732826, PubMed:27550639, PubMed:27320834). Required for normal chromosomal segregation during anaphase (PubMed:21750686). May also show histone acetyltransferase activity; such results are however unclear in vivo and would require additional experimental evidences (PubMed:21981917). {ECO:0000269|PubMed:21750686, ECO:0000269|PubMed:25732826, ECO:0000269|PubMed:27320834, ECO:0000269|PubMed:27550639, ECO:0000305|PubMed:21981917}.FUNCTION: Ezrin-radixin-moesin (ERM) family protein that connects the actin cytoskeleton to the plasma membrane and thereby regulates the structure and function of specific domains of the cell cortex. Tethers actin filaments by oscillating between a resting and an activated state providing transient interactions between moesin and the actin cytoskeleton (PubMed:10212266). Once phosphorylated on its C-terminal threonine, moesin is activated leading to interaction with F-actin and cytoskeletal rearrangement (PubMed:10212266). These rearrangements regulate many cellular processes, including cell shape determination, membrane transport, and signal transduction (PubMed:12387735, PubMed:15039356). The role of moesin is particularly important in immunity acting on both T and B-cells homeostasis and self-tolerance, regulating lymphocyte egress from lymphoid organs (PubMed:9298994, PubMed:9616160). Modulates phagolysosomal biogenesis in macrophages (By similarity). Participates also in immunologic synapse formation (PubMed:27405666). {ECO:0000250|UniProtKB:P26041, ECO:0000269|PubMed:10212266, ECO:0000269|PubMed:12387735, ECO:0000269|PubMed:15039356, ECO:0000269|PubMed:27405666, ECO:0000269|PubMed:9298994, ECO:0000269|PubMed:9616160}.

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 NAA60-MSN


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 NAA60-MSN


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 NAA60-MSN


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 NAA60-MSN


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