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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: 19863

FusionGeneSummary for LMAN2_MCC

check button Fusion gene summary
Fusion gene informationFusion gene name: LMAN2_MCC
Fusion gene ID: 19863
HgeneTgene
Gene symbol

LMAN2

MCC

Gene ID

10960

4163

Gene namelectin, mannose binding 2MCC, WNT signaling pathway regulator
SynonymsC5orf8|GP36B|VIP36MCC1
Cytomap

5q35.3

5q22.2

Type of geneprotein-codingprotein-coding
Descriptionvesicular integral-membrane protein VIP36glycoprotein GP36bvesicular integral protein of 36 kDavesicular integral-membrane protein 36colorectal mutant cancer proteinmutated in colorectal cancers
Modification date2018052320180522
UniProtAcc

Q12907

P23508

Ensembl transtripts involved in fusion geneENST00000303127, ENST00000515209, 
ENST00000506310, 
ENST00000302475, 
ENST00000514701, ENST00000515367, 
ENST00000408903, 
Fusion gene scores* DoF score7 X 3 X 7=1477 X 8 X 5=280
# samples 78
** MAII scorelog2(7/147*10)=-1.0703893278914
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: LMAN2 [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
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
TCGALDLIHCTCGA-BC-A10T-01ALMAN2chr5

176761285

-MCCchr5

112783984

-
* 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
5CDS-intronENST00000303127ENST00000302475LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000303127ENST00000514701LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000303127ENST00000515367LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000303127ENST00000408903LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000515209ENST00000302475LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000515209ENST00000514701LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000515209ENST00000515367LMAN2chr5

176761285

-MCCchr5

112783984

-
5CDS-intronENST00000515209ENST00000408903LMAN2chr5

176761285

-MCCchr5

112783984

-
intron-intronENST00000506310ENST00000302475LMAN2chr5

176761285

-MCCchr5

112783984

-
intron-intronENST00000506310ENST00000514701LMAN2chr5

176761285

-MCCchr5

112783984

-
intron-intronENST00000506310ENST00000515367LMAN2chr5

176761285

-MCCchr5

112783984

-
intron-intronENST00000506310ENST00000408903LMAN2chr5

176761285

-MCCchr5

112783984

-

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FusionProtFeatures for LMAN2_MCC


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LMAN2

Q12907

MCC

P23508

Plays a role as an intracellular lectin in the earlysecretory pathway. Interacts with N-acetyl-D-galactosamine andhigh-mannose type glycans and may also bind to O-linked glycans.Involved in the transport and sorting of glycoproteins carryinghigh mannose-type glycans (By similarity). {ECO:0000250}. 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 LMAN2_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 LMAN2_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
LMAN2ISG15, ATP13A2, FLOT1, UBL4A, ATP4A, FRAT1, MAPK9, SUPT5H, RPA3, RPA2, RPA1, MOV10, NXF1, CCDC8, HEATR3, PLXNB2, CENPH, GPC3, TTYH3, CACNA2D1, NDUFS2, PDIA6, TM9SF4, NDUFS3, TMED10, TMED2, NTRK1, SPPL2BMCCCLTC, 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 LMAN2_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 LMAN2_MCC


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