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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: 21270

FusionGeneSummary for MCC_PSMD6

check button Fusion gene summary
Fusion gene informationFusion gene name: MCC_PSMD6
Fusion gene ID: 21270
HgeneTgene
Gene symbol

MCC

PSMD6

Gene ID

4163

9861

Gene nameMCC, WNT signaling pathway regulatorproteasome 26S subunit, non-ATPase 6
SynonymsMCC1Rpn7|S10|SGA-113M|p42A|p44S10
Cytomap

5q22.2

3p14.1

Type of geneprotein-codingprotein-coding
Descriptioncolorectal mutant cancer proteinmutated in colorectal cancers26S proteasome non-ATPase regulatory subunit 6breast cancer-associated protein SGA-113Mphosphonoformate immuno-associated protein 4proteasome (prosome, macropain) 26S subunit, non-ATPase, 6proteasome regulatory particle subunit p44S10
Modification date2018052220180523
UniProtAcc

P23508

Q15008

Ensembl transtripts involved in fusion geneENST00000302475, ENST00000514701, 
ENST00000515367, ENST00000408903, 
ENST00000295901, ENST00000492933, 
ENST00000394431, ENST00000482510, 
Fusion gene scores* DoF score5 X 3 X 4=603 X 3 X 3=27
# samples 64
** MAII scorelog2(6/60*10)=0log2(4/27*10)=0.567040592723894
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MCC [Title/Abstract] AND PSMD6 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotationTumor suppressor gene involved fusion gene, retained protein feature but frameshift.
DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain.
* 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
HgeneMCC

GO:0045184

establishment of protein localization

18591935

HgeneMCC

GO:0050680

negative regulation of epithelial cell proliferation

18591935

HgeneMCC

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
TCGARVKIRCTCGA-BP-4968-01AMCCchr5

112630026

-PSMD6chr3

63996631

-
* 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-shiftENST00000302475ENST00000295901MCCchr5

112630026

-PSMD6chr3

63996631

-
Frame-shiftENST00000302475ENST00000492933MCCchr5

112630026

-PSMD6chr3

63996631

-
Frame-shiftENST00000302475ENST00000394431MCCchr5

112630026

-PSMD6chr3

63996631

-
Frame-shiftENST00000302475ENST00000482510MCCchr5

112630026

-PSMD6chr3

63996631

-
5UTR-3CDSENST00000514701ENST00000295901MCCchr5

112630026

-PSMD6chr3

63996631

-
5UTR-3CDSENST00000514701ENST00000492933MCCchr5

112630026

-PSMD6chr3

63996631

-
5UTR-3CDSENST00000514701ENST00000394431MCCchr5

112630026

-PSMD6chr3

63996631

-
5UTR-3CDSENST00000514701ENST00000482510MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000515367ENST00000295901MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000515367ENST00000492933MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000515367ENST00000394431MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000515367ENST00000482510MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000408903ENST00000295901MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000408903ENST00000492933MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000408903ENST00000394431MCCchr5

112630026

-PSMD6chr3

63996631

-
intron-3CDSENST00000408903ENST00000482510MCCchr5

112630026

-PSMD6chr3

63996631

-

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FusionProtFeatures for MCC_PSMD6


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

P23508

PSMD6

Q15008

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}. Component of the 26S proteasome, a multiprotein complexinvolved in the ATP-dependent degradation of ubiquitinatedproteins. This complex plays a key role in the maintenance ofprotein homeostasis by removing misfolded or damaged proteins,which could impair cellular functions, and by removing proteinswhose functions are no longer required. Therefore, the proteasomeparticipates in numerous cellular processes, including cell cycleprogression, apoptosis, or DNA damage repair.{ECO:0000269|PubMed:1317798}.

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 MCC_PSMD6


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 MCC_PSMD6


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
MCCCLTC, 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, MTNR1APSMD6PSMD1, PSMD2, PSMD12, PSMD13, PSMD11, PSMD3, PSMC1, PSMC2, PSMC3, PSMC5, PSMD8, PSMD10, PSMD14, PSMD7, PSMC6, PAAF1, PSMC4, PSMA2, TELO2, PSMB5, PSMD4, UBE3C, UCHL5, USP14, USP20, SLX1B, UBAC1, HDAC5, PCK1, PSMA7, RAD23A, SHFM1, BRCA2, ZFAND5, PSMA6, FKBP8, FBXO25, PSME1, PSME2, PSMA3, PSMB7, PSMA1, PSMA5, PSMB1, PSMB3, PSMB6, PSMB2, PSMB4, PSMA4, PSMB10, PSMA8, PLS3, NUBP2, NOS2, PARK2, RNF11, TP53, HUWE1, UBQLN1, CUL7, AMFR, BUB1B, ZFAND2B, DKK1, CCDC74B, CCDC92, ADRM1, PSMB9, AMBRA1, AHCYL1, PSMB8, ATP1B1, ATP1B3, HNRNPU, MCFD2, PCID2, PEX19, PSMD5, PSMD9, SSRP1, VPS29, SYAP1, NTRK1, MED23, MLH1, TIMM13, PTPN2, UBLCP1, KDELR1, CCDC102B, ATG9A, UBC, RMND5B, DLD, HSD17B10, FAM107A, BRCA1, YAP1


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 MCC_PSMD6


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 MCC_PSMD6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMCCC0004352Autistic Disorder1CTD_human
HgeneMCCC0032580Adenomatous Polyposis Coli1CTD_human
HgeneMCCC0034885Rectal Neoplasms1CTD_human
HgeneMCCC3714756Intellectual Disability1CTD_human
TgenePSMD6C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
TgenePSMD6C0019693HIV Infections1CTD_human