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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: 21263

FusionGeneSummary for MCCC1_MED10

check button Fusion gene summary
Fusion gene informationFusion gene name: MCCC1_MED10
Fusion gene ID: 21263
HgeneTgene
Gene symbol

MCCC1

MED10

Gene ID

56922

84246

Gene namemethylcrotonoyl-CoA carboxylase 1mediator complex subunit 10
SynonymsMCC-B|MCCAL6|NUT2|TRG20
Cytomap

3q27.1

5p15.31

Type of geneprotein-codingprotein-coding
Descriptionmethylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial3-methylcrotonyl-CoA carboxylase 13-methylcrotonyl-CoA carboxylase biotin-containing subunit3-methylcrotonyl-CoA:carbon dioxide ligase subunit alphaMCCase subunit alphamethylcrotonoyl-CoA camediator of RNA polymerase II transcription subunit 10TRG-17TRG-20mediator of RNA polymerase II transcription, subunit 10transformation-related gene 17 proteintransformation-related gene 20 protein
Modification date2018052220180523
UniProtAcc

Q96RQ3

Q9BTT4

Ensembl transtripts involved in fusion geneENST00000265594, ENST00000492597, 
ENST00000539926, ENST00000489909, 
ENST00000255764, 
Fusion gene scores* DoF score7 X 6 X 5=2104 X 3 X 2=24
# samples 73
** MAII scorelog2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/24*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MCCC1 [Title/Abstract] AND MED10 [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

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
TCGARVBRCATCGA-E2-A1LI-01AMCCC1chr3

182788787

-MED10chr5

6372714

-
* 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
Frame-shiftENST00000265594ENST00000255764MCCC1chr3

182788787

-MED10chr5

6372714

-
Frame-shiftENST00000492597ENST00000255764MCCC1chr3

182788787

-MED10chr5

6372714

-
Frame-shiftENST00000539926ENST00000255764MCCC1chr3

182788787

-MED10chr5

6372714

-
intron-3CDSENST00000489909ENST00000255764MCCC1chr3

182788787

-MED10chr5

6372714

-

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FusionProtFeatures for MCCC1_MED10


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MCCC1

Q96RQ3

MED10

Q9BTT4

Biotin-attachment subunit of the 3-methylcrotonyl-CoAcarboxylase, an enzyme that catalyzes the conversion of 3-methylcrotonyl-CoA to 3-methylglutaconyl-CoA, a critical step forleucine and isovaleric acid catabolism.{ECO:0000269|PubMed:17360195}. Component of the Mediator complex, a coactivatorinvolved in the regulated transcription of nearly all RNApolymerase II-dependent genes. Mediator functions as a bridge toconvey information from gene-specific regulatory proteins to thebasal RNA polymerase II transcription machinery. Mediator isrecruited to promoters by direct interactions with regulatoryproteins and serves as a scaffold for the assembly of a functionalpreinitiation complex with RNA polymerase II and the generaltranscription factors.

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 MCCC1_MED10


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 MCCC1_MED10


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
MCCC1CUL4B, KIF5B, DDX1, EEF1D, DCTN1, DYNC1H1, IFIT1, HUWE1, RNF2, ECH1, RARS2, GCAT, OXCT2, LGALS3, NTRK1, MCCC2, PTEN, ECI2, CHCHD10, C15orf48, C2orf47, ZNF746, TUFM, NPB, FOXRED1, TMEM70, NDUFS7, SUCLA2, ACSM5, METTL2A, FECHMED10MED13L, MED13, MED12, MED14, MED23, MED15, MED16, MED17, MED26, CCNC, CDK8, CDK19, MED27, MED4, MED19, MED6, MED7, MED8, MED18, MED20, MED9, MED29, MED30, MED28, MED21, MED11, MED31, MED1, MED24, MED25, MED22, POLR2A, POLR2B, POLR2C, POLR2E, POLR2F, POLR2G, POLR2H, POLR2I, POLR2L, POLR2K, POLR2D, POLR2J, MOB4, HNF4A, ESR1, ESR2, TRIP4, QKI, NAP1L1, FBXW7, EPAS1, TCL1B, BIRC5


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 MCCC1_MED10


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneMCCC1Q96RQ3DB00121BiotinMethylcrotonoyl-CoA carboxylase subunit alpha, mitochondrialsmall moleculeapproved|investigational|nutraceutical

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RelatedDiseases for MCCC1_MED10


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMCCC1C02686003-methylcrotonyl CoA carboxylase 1 deficiency5CTD_human;ORPHANET;UNIPROT