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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: 39728

FusionGeneSummary for TSC22D2_SDCCAG8

check button Fusion gene summary
Fusion gene informationFusion gene name: TSC22D2_SDCCAG8
Fusion gene ID: 39728
HgeneTgene
Gene symbol

TSC22D2

SDCCAG8

Gene ID

9819

10806

Gene nameTSC22 domain family member 2serologically defined colon cancer antigen 8
SynonymsTILZ4a|TILZ4b|TILZ4cBBS16|CCCAP|CCCAP SLSN7|HSPC085|NPHP10|NY-CO-8|SLSN7|hCCCAP
Cytomap

3q25.1

1q43-q44

Type of geneprotein-codingprotein-coding
DescriptionTSC22 domain family protein 2TSC22 domain family 2TSC22-related-inducible leucine zipper protein 4serologically defined colon cancer antigen 8Bardet-Biedl syndrome 16antigen NY-CO-8centrosomal colon cancer autoantigen proteinnephrocystin 10
Modification date2018051920180523
UniProtAcc

O75157

Q86SQ7

Ensembl transtripts involved in fusion geneENST00000361136, ENST00000361875, 
ENST00000492828, 
ENST00000355875, 
ENST00000366541, ENST00000343783, 
ENST00000391846, ENST00000496361, 
Fusion gene scores* DoF score4 X 3 X 4=4813 X 10 X 7=910
# samples 513
** MAII scorelog2(5/48*10)=0.0588936890535686
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(13/910*10)=-2.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TSC22D2 [Title/Abstract] AND SDCCAG8 [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
TCGARVPRADTCGA-HC-7233-01ATSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
* 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-shiftENST00000361136ENST00000355875TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
Frame-shiftENST00000361136ENST00000366541TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
Frame-shiftENST00000361136ENST00000343783TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
5CDS-intronENST00000361136ENST00000391846TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
5CDS-intronENST00000361136ENST00000496361TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
Frame-shiftENST00000361875ENST00000355875TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
Frame-shiftENST00000361875ENST00000366541TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
Frame-shiftENST00000361875ENST00000343783TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
5CDS-intronENST00000361875ENST00000391846TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
5CDS-intronENST00000361875ENST00000496361TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
intron-3CDSENST00000492828ENST00000355875TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
intron-3CDSENST00000492828ENST00000366541TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
intron-3CDSENST00000492828ENST00000343783TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
intron-intronENST00000492828ENST00000391846TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+
intron-intronENST00000492828ENST00000496361TSC22D2chr3

150129095

+SDCCAG8chr1

243493842

+

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FusionProtFeatures for TSC22D2_SDCCAG8


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TSC22D2

O75157

SDCCAG8

Q86SQ7

Plays a role in the establishment of cell polarity andepithelial lumen formation (By similarity). May play a role inciliogenesis. {ECO:0000250|UniProtKB:Q80UF4}.

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 TSC22D2_SDCCAG8


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 TSC22D2_SDCCAG8


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
TSC22D2KEAP1, TSC22D4, RNF2, WNK3, OSBPL1A, PSMA7, ZNF143, NRBP1, FLNB, LRRC6, MPDZ, REV1, TTN, WDR77, CCDC141, CCDC144A, KIAA0586, PRMT3, SNX3, SPEF2, TMA7, ANAPC10, ANKRD36, ARID2, ATP1B1, CLIP1, ENOPH1, EPCAM, F8, GPBP1, ITGA2, LOXHD1, LPL, MED13, MSH3, MTIF2, NGRN, PSMA8, RBL1, SAP18, SCEL, SEC31A, STK39, UFM1, ZMYM2, ZNF251, TSC22D3, FAM117BSDCCAG8CEP192, SCARA3, KRAS, TENC1, OFD1, IKBKG, CCDC120, LARS, KARS, UBE2N


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 TSC22D2_SDCCAG8


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 TSC22D2_SDCCAG8


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSDCCAG8C0035309Retinal Diseases1CTD_human
TgeneSDCCAG8C0036341Schizophrenia1PSYGENET
TgeneSDCCAG8C1691228Cystic Kidney Diseases1CTD_human