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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:MSH2-CCDC57 (FusionGDB2 ID:54938)

Fusion Gene Summary for MSH2-CCDC57

check button Fusion gene summary
Fusion gene informationFusion gene name: MSH2-CCDC57
Fusion gene ID: 54938
HgeneTgene
Gene symbol

MSH2

CCDC57

Gene ID

4436

284001

Gene namemutS homolog 2coiled-coil domain containing 57
SynonymsCOCA1|FCC1|HNPCC|HNPCC1|LCFS2|hMSH2-
Cytomap

2p21-p16.3

17q25.3

Type of geneprotein-codingprotein-coding
DescriptionDNA mismatch repair protein Msh2DNA mismatch repair protein Msh2 transcriptmutS homolog 2, colon cancer, nonpolyposis type 1coiled-coil domain-containing protein 57
Modification date2020032220200313
UniProtAcc.

Q2TAC2

Ensembl transtripts involved in fusion geneENST00000233146, ENST00000543555, 
ENST00000406134, ENST00000461394, 
ENST00000392347, ENST00000389641, 
ENST00000392346, ENST00000327026, 
ENST00000392343, 
Fusion gene scores* DoF score15 X 12 X 10=180019 X 12 X 13=2964
# samples 2322
** MAII scorelog2(23/1800*10)=-2.96829114027266
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(22/2964*10)=-3.75197001878117
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MSH2 [Title/Abstract] AND CCDC57 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMSH2(47637511)-CCDC57(80121233), # samples:3
Anticipated loss of major functional domain due to fusion event.MSH2-CCDC57 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
MSH2-CCDC57 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
HgeneMSH2

GO:0006281

DNA repair

8942985

HgeneMSH2

GO:0006298

mismatch repair

7923193|11555625

HgeneMSH2

GO:0006301

postreplication repair

7923193

HgeneMSH2

GO:0045910

negative regulation of DNA recombination

17715146

HgeneMSH2

GO:0051096

positive regulation of helicase activity

17715146


check buttonFusion gene breakpoints across MSH2 (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 CCDC57 (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
ChimerDB4CESCTCGA-ZJ-AB0I-01AMSH2chr2

47637511

+CCDC57chr17

80121233

-
ChimerDB4CESCTCGA-ZJ-AB0IMSH2chr2

47637511

+CCDC57chr17

80121233

-
ChimerDB4CESCTCGA-ZJ-AB0I-01AMSH2chr2

47637511

-CCDC57chr17

80121233

-


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Fusion Gene ORF analysis for MSH2-CCDC57

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-shiftENST00000233146ENST00000392347MSH2chr2

47637511

+CCDC57chr17

80121233

-
Frame-shiftENST00000233146ENST00000389641MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-intronENST00000233146ENST00000392346MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-5UTRENST00000233146ENST00000327026MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-5UTRENST00000233146ENST00000392343MSH2chr2

47637511

+CCDC57chr17

80121233

-
Frame-shiftENST00000543555ENST00000392347MSH2chr2

47637511

+CCDC57chr17

80121233

-
Frame-shiftENST00000543555ENST00000389641MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-intronENST00000543555ENST00000392346MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-5UTRENST00000543555ENST00000327026MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-5UTRENST00000543555ENST00000392343MSH2chr2

47637511

+CCDC57chr17

80121233

-
Frame-shiftENST00000406134ENST00000392347MSH2chr2

47637511

+CCDC57chr17

80121233

-
Frame-shiftENST00000406134ENST00000389641MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-intronENST00000406134ENST00000392346MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-5UTRENST00000406134ENST00000327026MSH2chr2

47637511

+CCDC57chr17

80121233

-
5CDS-5UTRENST00000406134ENST00000392343MSH2chr2

47637511

+CCDC57chr17

80121233

-
intron-3CDSENST00000461394ENST00000392347MSH2chr2

47637511

+CCDC57chr17

80121233

-
intron-3CDSENST00000461394ENST00000389641MSH2chr2

47637511

+CCDC57chr17

80121233

-
intron-intronENST00000461394ENST00000392346MSH2chr2

47637511

+CCDC57chr17

80121233

-
intron-5UTRENST00000461394ENST00000327026MSH2chr2

47637511

+CCDC57chr17

80121233

-
intron-5UTRENST00000461394ENST00000392343MSH2chr2

47637511

+CCDC57chr17

80121233

-

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 MSH2-CCDC57


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 MSH2-CCDC57


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
.CCDC57

Q2TAC2

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: Pleiotropic regulator of centriole duplication, mitosis, and ciliogenesis. Critical interface between centrosome and microtubule-mediated cellular processes. Centriole duplication protein required for recruitment of CEP63, CEP152, and PLK4 to the centrosome. Independent of its centrosomal targeting, localizes to and interacts with microtubules and regulates microtubule nucleation, stability, and mitotic progression. {ECO:0000269|PubMed:32402286}.

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 MSH2-CCDC57


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 MSH2-CCDC57


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 MSH2-CCDC57


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 MSH2-CCDC57


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMSH2C2936783Colorectal cancer, hereditary nonpolyposis, type 155GENOMICS_ENGLAND;UNIPROT
HgeneMSH2C0265325Turcot syndrome (disorder)14CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneMSH2C1333990Hereditary Nonpolyposis Colorectal Cancer11CLINGEN;CTD_human;ORPHANET
HgeneMSH2C4321324Constitutional Mismatch Repair Deficiency Syndrome10CLINGEN
HgeneMSH2C4552100Lynch Syndrome10CLINGEN;CTD_human;GENOMICS_ENGLAND
HgeneMSH2C0009405Hereditary Nonpolyposis Colorectal Neoplasms9CLINGEN;CTD_human
HgeneMSH2C1112155Hereditary non-polyposis colorectal cancer syndrome7CLINGEN;ORPHANET
HgeneMSH2C0009402Colorectal Carcinoma5CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneMSH2C1321489Torre-Muir syndrome4CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneMSH2C0346153Breast Cancer, Familial2CLINGEN
HgeneMSH2C0009404Colorectal Neoplasms1CTD_human
HgeneMSH2C0919267ovarian neoplasm1CGI;CTD_human
HgeneMSH2C1140680Malignant neoplasm of ovary1CGI;CTD_human;GENOMICS_ENGLAND
HgeneMSH2C2931459Lynch syndrome I (site-specific colonic cancer)1CTD_human
HgeneMSH2C4733333familial non-medullary thyroid cancer1GENOMICS_ENGLAND