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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:ATF7-LYZ (FusionGDB2 ID:7496)

Fusion Gene Summary for ATF7-LYZ

check button Fusion gene summary
Fusion gene informationFusion gene name: ATF7-LYZ
Fusion gene ID: 7496
HgeneTgene
Gene symbol

ATF7

LYZ

Gene ID

11016

4069

Gene nameactivating transcription factor 7lysozyme
SynonymsATFALYZF1|LZM
Cytomap

12q13.13

12q15

Type of geneprotein-codingprotein-coding
Descriptioncyclic AMP-dependent transcription factor ATF-7transcription factor ATF-Alysozyme C1,4-beta-N-acetylmuramidase Cc-type lysozymelysozyme F1
Modification date2020031320200313
UniProtAcc

P17544

P61626

Ensembl transtripts involved in fusion geneENST00000415113, ENST00000420353, 
ENST00000548446, ENST00000591397, 
ENST00000328463, ENST00000456903, 
ENST00000546661, ENST00000548118, 
ENST00000261267, ENST00000548839, 
ENST00000549690, 
Fusion gene scores* DoF score12 X 11 X 10=132051 X 27 X 13=17901
# samples 1860
** MAII scorelog2(18/1320*10)=-2.87446911791614
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(60/17901*10)=-4.89893387178018
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATF7 [Title/Abstract] AND LYZ [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATF7(54020063)-LYZ(69746000), # samples:2
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
HgeneATF7

GO:0006355

regulation of transcription, DNA-templated

8288576

TgeneLYZ

GO:0031640

killing of cells of other organism

9727055

TgeneLYZ

GO:0042742

defense response to bacterium

21093056

TgeneLYZ

GO:0050830

defense response to Gram-positive bacterium

21093056


check buttonFusion gene breakpoints across ATF7 (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 LYZ (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
ChimerDB4SARCTCGA-X6-A8C6-01AATF7chr12

54020063

-LYZchr12

69746000

+


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Fusion Gene ORF analysis for ATF7-LYZ

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-3CDSENST00000415113ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-3CDSENST00000420353ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-3CDSENST00000548446ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-3CDSENST00000591397ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000415113ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000415113ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000420353ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000420353ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000548446ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000548446ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000591397ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
5UTR-intronENST00000591397ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
intron-3CDSENST00000328463ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
intron-3CDSENST00000456903ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
intron-3CDSENST00000546661ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
intron-3CDSENST00000548118ENST00000261267ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000328463ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000328463ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000456903ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000456903ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000546661ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000546661ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000548118ENST00000548839ATF7chr12

54020063

-LYZchr12

69746000

+
intron-intronENST00000548118ENST00000549690ATF7chr12

54020063

-LYZchr12

69746000

+

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 ATF7-LYZ


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)
ATF7chr1254020062-LYZchr1269745999+1.05E-060.9999989
ATF7chr1254020062-LYZchr1269745999+1.05E-060.9999989

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.
genomic feature of top 1%

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Fusion Protein Features for ATF7-LYZ


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/:54020063/:69746000)
- 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
ATF7

P17544

LYZ

P61626

FUNCTION: Stress-responsive chromatin regulator that plays a role in various biological processes including innate immunological memory, adipocyte differentiation or telomerase regulation (PubMed:29490055). In absence of stress, contributes to the formation of heterochromatin and heterochromatin-like structure by recruiting histone H3K9 tri- and di-methyltransferases thus silencing the transcription of target genes such as STAT1 in adipocytes, or genes involved in innate immunity in macrophages and adipocytes (By similarity). Stress induces ATF7 phosphorylation that disrupts interactions with histone methyltransferase and enhances the association with coactivators containing histone acetyltransferase and/or histone demethylase, leading to disruption of the heterochromatin-like structure and subsequently transcriptional activation (By similarity). In response to TNF-alpha, which is induced by various stresses, phosphorylated ATF7 and telomerase are released from telomeres leading to telomere shortening (PubMed:29490055). Plays also a role in maintaining epithelial regenerative capacity and protecting against cell death during intestinal epithelial damage and repair (By similarity). {ECO:0000250|UniProtKB:Q8R0S1, ECO:0000269|PubMed:29490055}.; FUNCTION: [Isoform 4]: Acts as a dominant repressor of the E-selectin/NF-ELAM1/delta-A promoter.; FUNCTION: [Isoform 5]: Acts as a negative regulator, inhibiting both ATF2 and ATF7 transcriptional activities. It may exert these effects by sequestrating in the cytoplasm the Thr-53 phosphorylating kinase, preventing activation. {ECO:0000269|PubMed:21858082}.FUNCTION: Lysozymes have primarily a bacteriolytic function; those in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents.

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 ATF7-LYZ


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 ATF7-LYZ


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 ATF7-LYZ


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 ATF7-LYZ


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