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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: 4991

FusionGeneSummary for C3orf52_CD86

check button Fusion gene summary
Fusion gene informationFusion gene name: C3orf52_CD86
Fusion gene ID: 4991
HgeneTgene
Gene symbol

C3orf52

CD86

Gene ID

79669

942

Gene namechromosome 3 open reading frame 52CD86 molecule
SynonymsTTMPB7-2|B7.2|B70|CD28LG2|LAB72
Cytomap

3q13.2

3q13.33

Type of geneprotein-codingprotein-coding
DescriptionTPA-induced transmembrane proteinTPA induced trans-membrane proteinnovel endoplasmic reticulum transmembrane proteinT-lymphocyte activation antigen CD86B-lymphocyte activation antigen B7-2BU63CD86 antigen (CD28 antigen ligand 2, B7-2 antigen)CTLA-4 counter-receptor B7.2FUN-1
Modification date2018051920180523
UniProtAcc

P42081

Ensembl transtripts involved in fusion geneENST00000431717, ENST00000430855, 
ENST00000264848, ENST00000467942, 
ENST00000469710, ENST00000493101, 
ENST00000264468, ENST00000330540, 
ENST00000483949, ENST00000393627, 
Fusion gene scores* DoF score2 X 2 X 2=84 X 2 X 4=32
# samples 24
** MAII scorelog2(2/8*10)=1.32192809488736log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: C3orf52 [Title/Abstract] AND CD86 [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
TCGARVLUSCTCGA-58-A46L-01AC3orf52chr3

111821812

+CD86chr3

121836895

+
* 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-shiftENST00000431717ENST00000469710C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000431717ENST00000493101C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000431717ENST00000264468C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000431717ENST00000330540C3orf52chr3

111821812

+CD86chr3

121836895

+
5CDS-intronENST00000431717ENST00000483949C3orf52chr3

111821812

+CD86chr3

121836895

+
5CDS-intronENST00000431717ENST00000393627C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000430855ENST00000469710C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000430855ENST00000493101C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000430855ENST00000264468C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000430855ENST00000330540C3orf52chr3

111821812

+CD86chr3

121836895

+
5CDS-intronENST00000430855ENST00000483949C3orf52chr3

111821812

+CD86chr3

121836895

+
5CDS-intronENST00000430855ENST00000393627C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000264848ENST00000469710C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000264848ENST00000493101C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000264848ENST00000264468C3orf52chr3

111821812

+CD86chr3

121836895

+
Frame-shiftENST00000264848ENST00000330540C3orf52chr3

111821812

+CD86chr3

121836895

+
5CDS-intronENST00000264848ENST00000483949C3orf52chr3

111821812

+CD86chr3

121836895

+
5CDS-intronENST00000264848ENST00000393627C3orf52chr3

111821812

+CD86chr3

121836895

+
intron-3CDSENST00000467942ENST00000469710C3orf52chr3

111821812

+CD86chr3

121836895

+
intron-3CDSENST00000467942ENST00000493101C3orf52chr3

111821812

+CD86chr3

121836895

+
intron-3CDSENST00000467942ENST00000264468C3orf52chr3

111821812

+CD86chr3

121836895

+
intron-3CDSENST00000467942ENST00000330540C3orf52chr3

111821812

+CD86chr3

121836895

+
intron-intronENST00000467942ENST00000483949C3orf52chr3

111821812

+CD86chr3

121836895

+
intron-intronENST00000467942ENST00000393627C3orf52chr3

111821812

+CD86chr3

121836895

+

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FusionProtFeatures for C3orf52_CD86


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
C3orf52

CD86

P42081

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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 C3orf52_CD86


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 C3orf52_CD86


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
C3orf52ELAVL1, SGTA, SYNE4, LIPH, CREB3, TMEM30B, CD79B, CD36, SIGLECL1, FCGRT, TMEM223, LMNACD86CTLA4, MARCH8, MARCH1, PARP1, ECE2, CD80


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 C3orf52_CD86


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneCD86P42081DB00098Antithymocyte immunoglobulin (rabbit)T-lymphocyte activation antigen CD86biotechapproved
TgeneCD86P42081DB01281AbataceptT-lymphocyte activation antigen CD86biotechapproved
TgeneCD86P42081DB06681BelataceptT-lymphocyte activation antigen CD86biotechapproved|investigational

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RelatedDiseases for C3orf52_CD86


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCD86C0011616Contact Dermatitis1CTD_human
TgeneCD86C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneCD86C0023895Liver diseases1CTD_human
TgeneCD86C0026764Multiple Myeloma1CTD_human