Fusion Gene Studies
in Kim Lab

FusionBase FusionGDB FusionGDB2 FusionPDB FusionNeoAntigen FusionAI FusionNW FGviewer Publication Contact
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:MCEE-CDC42 (FusionGDB2 ID:HG84693TG998)

Fusion Gene Summary for MCEE-CDC42

check button Fusion gene summary
Fusion gene informationFusion gene name: MCEE-CDC42
Fusion gene ID: hg84693tg998
HgeneTgene
Gene symbol

MCEE

CDC42

Gene ID

84693

998

Gene namemethylmalonyl-CoA epimerasecell division cycle 42
SynonymsGLOD2CDC42Hs|G25K|TKS
Cytomap('MCEE')('CDC42')

2p13.3

1p36.12

Type of geneprotein-codingprotein-coding
Descriptionmethylmalonyl-CoA epimerase, mitochondrialDL-methylmalonyl-CoA racemaseglyoxalase domain containing 2cell division control protein 42 homologG25K GTP-binding proteinGTP binding protein, 25kDadJ224A6.1.1 (cell division cycle 42 (GTP-binding protein, 25kD))dJ224A6.1.2 (cell division cycle 42 (GTP-binding protein, 25kD))growth-regulating proteinsmall
Modification date2020031320200327
UniProtAcc

Q96PE7

P60953

Ensembl transtripts involved in fusion geneENST00000244217, ENST00000462609, 
Fusion gene scores* DoF score7 X 5 X 4=14012 X 6 X 7=504
# samples 712
** MAII scorelog2(7/140*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/504*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MCEE [Title/Abstract] AND CDC42 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMCEE(71357309)-CDC42(22404921), # 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
HgeneMCEE

GO:0046491

L-methylmalonyl-CoA metabolic process

11481338

TgeneCDC42

GO:0030036

actin cytoskeleton organization

11035016

TgeneCDC42

GO:0031274

positive regulation of pseudopodium assembly

11035016

TgeneCDC42

GO:0051489

regulation of filopodium assembly

14978216

TgeneCDC42

GO:1900026

positive regulation of substrate adhesion-dependent cell spreading

11807099



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
ChimerDB4OVTCGA-57-1582MCEEchr2

71357309

-CDC42chr1

22404921

+


Top

Fusion Gene ORF analysis for MCEE-CDC42

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
5CDS-3UTRENST00000244217ENST00000498236MCEEchr2

71357309

-CDC42chr1

22404921

+
5CDS-5UTRENST00000244217ENST00000315554MCEEchr2

71357309

-CDC42chr1

22404921

+
5CDS-5UTRENST00000244217ENST00000344548MCEEchr2

71357309

-CDC42chr1

22404921

+
5CDS-5UTRENST00000244217ENST00000400259MCEEchr2

71357309

-CDC42chr1

22404921

+
5CDS-5UTRENST00000244217ENST00000421089MCEEchr2

71357309

-CDC42chr1

22404921

+
intron-3UTRENST00000462609ENST00000498236MCEEchr2

71357309

-CDC42chr1

22404921

+
intron-5UTRENST00000462609ENST00000315554MCEEchr2

71357309

-CDC42chr1

22404921

+
intron-5UTRENST00000462609ENST00000344548MCEEchr2

71357309

-CDC42chr1

22404921

+
intron-5UTRENST00000462609ENST00000400259MCEEchr2

71357309

-CDC42chr1

22404921

+
intron-5UTRENST00000462609ENST00000421089MCEEchr2

71357309

-CDC42chr1

22404921

+

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

Top

Fusion Genomic Features for MCEE-CDC42


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 that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

Top

Fusion Protein Features for MCEE-CDC42


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/:71357309/:22404921)
- 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
MCEE

Q96PE7

CDC42

P60953

FUNCTION: Methylmalonyl-CoA epimerase involved in propionyl-CoA metabolism. {ECO:0000269|PubMed:11481338}.FUNCTION: Plasma membrane-associated small GTPase which cycles between an active GTP-bound and an inactive GDP-bound state. In active state binds to a variety of effector proteins to regulate cellular responses. Involved in epithelial cell polarization processes. Regulates the bipolar attachment of spindle microtubules to kinetochores before chromosome congression in metaphase (PubMed:15642749). Regulates cell migration (PubMed:17038317). In neurons, plays a role in the extension and maintenance of the formation of filopodia, thin and actin-rich surface projections (PubMed:14978216). Required for DOCK10-mediated spine formation in Purkinje cells and hippocampal neurons. Facilitates filopodia formation upon DOCK11-activation (By similarity). Upon activation by CaMKII, modulates dendritic spine structural plasticity by relaying CaMKII transient activation to synapse-specific, long-term signaling (By similarity). Also plays a role in phagocytosis through organization of the F-actin cytoskeleton associated with forming phagocytic cups (PubMed:26465210). {ECO:0000250|UniProtKB:P60766, ECO:0000250|UniProtKB:Q8CFN2, ECO:0000269|PubMed:14978216, ECO:0000269|PubMed:15642749, ECO:0000269|PubMed:17038317, ECO:0000269|PubMed:26465210}.

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


Top

Fusion Gene Sequence for MCEE-CDC42


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.

Top

Fusion Gene PPI Analysis for MCEE-CDC42


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


Top

Related Drugs for MCEE-CDC42


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for MCEE-CDC42


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMCEEC1855100Methylmalonyl-CoA Epimerase Deficiency3CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneC0036341Schizophrenia4PSYGENET
TgeneC4225222TAKENOUCHI-KOSAKI SYNDROME3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC0001624Adrenal Gland Neoplasms1CTD_human
TgeneC0005818Blood Platelet Disorders1GENOMICS_ENGLAND
TgeneC0007097Carcinoma1CTD_human
TgeneC0019693HIV Infections1CTD_human
TgeneC0024667Animal Mammary Neoplasms1CTD_human
TgeneC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneC0027540Necrosis1CTD_human
TgeneC0205696Anaplastic carcinoma1CTD_human
TgeneC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneC0205698Undifferentiated carcinoma1CTD_human
TgeneC0205699Carcinomatosis1CTD_human
TgeneC0750887Adrenal Cancer1CTD_human
TgeneC1257925Mammary Carcinoma, Animal1CTD_human
TgeneC3714756Intellectual Disability1GENOMICS_ENGLAND
TgeneC4505456HIV Coinfection1CTD_human