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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 11329

FusionGeneSummary for EIF4G1_MCC

check button Fusion gene summary
Fusion gene informationFusion gene name: EIF4G1_MCC
Fusion gene ID: 11329
HgeneTgene
Gene symbol

EIF4G1

MCC

Gene ID

1981

4163

Gene nameeukaryotic translation initiation factor 4 gamma 1MCC, WNT signaling pathway regulator
SynonymsEIF-4G1|EIF4F|EIF4G|EIF4GI|P220|PARK18MCC1
Cytomap

3q27.1

5q22.2

Type of geneprotein-codingprotein-coding
Descriptioneukaryotic translation initiation factor 4 gamma 1EIF4-gammaeIF-4-gamma 1eucaryotic translation initiation factor 4Gcolorectal mutant cancer proteinmutated in colorectal cancers
Modification date2018052320180522
UniProtAcc

Q04637

P23508

Ensembl transtripts involved in fusion geneENST00000346169, ENST00000414031, 
ENST00000392537, ENST00000382330, 
ENST00000350481, ENST00000352767, 
ENST00000427845, ENST00000342981, 
ENST00000319274, ENST00000424196, 
ENST00000411531, ENST00000441154, 
ENST00000434061, ENST00000435046, 
ENST00000302475, ENST00000514701, 
ENST00000515367, ENST00000408903, 
Fusion gene scores* DoF score9 X 11 X 6=5947 X 8 X 5=280
# samples 148
** MAII scorelog2(14/594*10)=-2.0850361038558
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/280*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EIF4G1 [Title/Abstract] AND MCC [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneEIF4G1

GO:1905612

positive regulation of mRNA cap binding

23409027

HgeneEIF4G1

GO:1905618

positive regulation of miRNA mediated inhibition of translation

23409027

TgeneMCC

GO:0045184

establishment of protein localization

18591935

TgeneMCC

GO:0050680

negative regulation of epithelial cell proliferation

18591935

TgeneMCC

GO:0090090

negative regulation of canonical Wnt signaling pathway

18591935


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BQ009628EIF4G1chr3

184052945

-MCCchr5

112389659

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
3UTR-3CDSENST00000346169ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000346169ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000346169ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000346169ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000414031ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000414031ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000414031ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000414031ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000392537ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000392537ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000392537ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000392537ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-3CDSENST00000382330ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000382330ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000382330ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000382330ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000350481ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000350481ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000350481ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000350481ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-3CDSENST00000352767ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000352767ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000352767ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000352767ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-3CDSENST00000427845ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000427845ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000427845ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000427845ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000342981ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000342981ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000342981ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000342981ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000319274ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000319274ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000319274ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000319274ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000424196ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000424196ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000424196ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000424196ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-3CDSENST00000411531ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000411531ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000411531ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000411531ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-3CDSENST00000441154ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000441154ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000441154ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
intron-5UTRENST00000441154ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000434061ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000434061ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000434061ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000434061ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-3CDSENST00000435046ENST00000302475EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000435046ENST00000514701EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000435046ENST00000515367EIF4G1chr3

184052945

-MCCchr5

112389659

-
3UTR-5UTRENST00000435046ENST00000408903EIF4G1chr3

184052945

-MCCchr5

112389659

-

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FusionProtFeatures for EIF4G1_MCC


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EIF4G1

Q04637

MCC

P23508

Candidate for the putative colorectal tumor suppressorgene located at 5q21. Suppresses cell proliferation and the Wnt/b-catenin pathway in colorectal cancer cells. Inhibits DNA bindingof b-catenin/TCF/LEF transcription factors. Involved in cellmigration independently of RAC1, CDC42 and p21-activated kinase(PAK) activation (PubMed:18591935, PubMed:19555689,PubMed:22480440). Represses the beta-catenin pathway (canonicalWnt signaling pathway) in a CCAR2-dependent manner by sequesteringCCAR2 to the cytoplasm, thereby impairing its ability to inhibitSIRT1 which is involved in the deacetylation and negativeregulation of beta-catenin (CTNB1) transcriptional activity(PubMed:24824780). {ECO:0000269|PubMed:18591935,ECO:0000269|PubMed:19555689, ECO:0000269|PubMed:22480440,ECO:0000269|PubMed:24824780}.

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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FusionGeneSequence for EIF4G1_MCC


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for EIF4G1_MCC


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
EIF4G1EIF4A2, NELFCD, EIF4A1, GABARAPL2, MAGEA6, MKNK2, PDCD4, EIF4E, EIF3B, EIF3A, EIF3I, MKNK1, NCBP1, PABPC1, HNRNPD, USP10, EIF3H, EIF3F, USP3, G3BP1, UBE3A, CENPU, RAD21, SIRT7, ISG15, CUL3, TRAF2, EIF4G2, EIF4B, EIF4G3, SF3A3, FTL, RAB31, ESR1, FN1, VCAM1, HTRA2, ZFYVE9, ITGA4, BRCA1, GK, TARDBP, AIMP1, AIMP2, EEF1E1, IQGAP1, PSMB8, PTBP1, QARS, LGR4, POLDIP3, CUL7, CCDC8, MAMDC2, PSMC3, UNK, DCTN4, KIAA0020, NAT10, PUS7, SF3A1, SF3A2, SKIV2L2, FBL, NUP50, PABPC4, POLE, SF3B3, TNKS1BP1, NTRK1, HERC2, SRPK2, CLCN2, HSPA5, TOR1AIP1, SGTB, MRPL9, ACTR5, CNTROB, FOXB1, FOXL1, MCM2, RC3H1, SLBP, CDH1, GCHFR, NFATC2IP, EMILIN1, CYLD, DLD, DLST, PDHA1, TRIM25MCCCLTC, STRN, STK24, STRN3, STRN4, EPRS, PPP2R1A, VCP, CSNK1D, MYH10, KRT18, TPM3, CSNK1E, EIF3A, PFAS, IARS, TARS, PFKP, SNRNP200, MTHFD1, PDCD10, DFFA, PSME3, MARS, CBR1, VDAC1, STRIP1, HPRT1, PSMD2, CCNA1, EZR, VHL, PAICS, VPS35, LTA4H, DYNC1I1, NEK2, APP, ERBB2IP, GTF2E2, CBX5, CCAR2, NFKBIB, MAGEE1, SYNC, CCDC83, DAB2IP, DFNB31, MTNR1A


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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RelatedDrugs for EIF4G1_MCC


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for EIF4G1_MCC


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneEIF4G1C3280271PARKINSON DISEASE 181UNIPROT
TgeneMCCC0004352Autistic Disorder1CTD_human
TgeneMCCC0032580Adenomatous Polyposis Coli1CTD_human
TgeneMCCC0034885Rectal Neoplasms1CTD_human
TgeneMCCC3714756Intellectual Disability1CTD_human