FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 34733

FusionGeneSummary for SMAD2_ZBTB7C

check button Fusion gene summary
Fusion gene informationFusion gene name: SMAD2_ZBTB7C
Fusion gene ID: 34733
HgeneTgene
Gene symbol

SMAD2

ZBTB7C

Gene ID

4087

201501

Gene nameSMAD family member 2zinc finger and BTB domain containing 7C
SynonymsJV18|JV18-1|MADH2|MADR2|hMAD-2|hSMAD2APM-1|APM1|ZBTB36|ZNF857C
Cytomap

18q21.1

18q21.1

Type of geneprotein-codingprotein-coding
Descriptionmothers against decapentaplegic homolog 2MAD homolog 2SMAD, mothers against DPP homolog 2Sma- and Mad-related protein 2mother against DPP homolog 2zinc finger and BTB domain-containing protein 7CB230208J24Rikaffected by papillomavirus DNA integration in ME180 cells protein 1zinc finger and BTB domain containing 36zinc finger and BTB domain-containing protein 36zinc finger protein 857C
Modification date2018052220180519
UniProtAcc

Q15796

A1YPR0

Ensembl transtripts involved in fusion geneENST00000262160, ENST00000402690, 
ENST00000356825, ENST00000586040, 
ENST00000591214, ENST00000587353, 
ENST00000535628, ENST00000588982, 
ENST00000586438, ENST00000590800, 
ENST00000332053, 
Fusion gene scores* DoF score6 X 4 X 6=1447 X 6 X 5=210
# samples 78
** MAII scorelog2(7/144*10)=-1.04064198449735
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SMAD2 [Title/Abstract] AND ZBTB7C [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
HgeneSMAD2

GO:0007179

transforming growth factor beta receptor signaling pathway

8752209|9389648|9732876|18548003

HgeneSMAD2

GO:0007182

common-partner SMAD protein phosphorylation

16806156

HgeneSMAD2

GO:0007183

SMAD protein complex assembly

9111321

HgeneSMAD2

GO:0045893

positive regulation of transcription, DNA-templated

9311995|9389648|9732876

HgeneSMAD2

GO:0045944

positive regulation of transcription by RNA polymerase II

9389648

HgeneSMAD2

GO:0070723

response to cholesterol

17878231

TgeneZBTB7C

GO:0008285

negative regulation of cell proliferation

9427755


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
TCGARVACCTCGA-OU-A5PI-01ASMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
TCGARVBRCATCGA-A8-A092-01ASMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
* 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
5UTR-5UTRENST00000262160ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
5UTR-5UTRENST00000262160ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
5UTR-5UTRENST00000262160ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
5UTR-5UTRENST00000262160ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
5UTR-5UTRENST00000262160ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000402690ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000402690ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000402690ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000402690ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000402690ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000356825ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000356825ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000356825ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000356825ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000356825ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000586040ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000586040ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000586040ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000586040ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000586040ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000591214ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000591214ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000591214ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000591214ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000591214ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000587353ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000587353ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000587353ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000587353ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
intron-5UTRENST00000587353ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45567494

-
5UTR-intronENST00000262160ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
5UTR-intronENST00000262160ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
5UTR-intronENST00000262160ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
5UTR-5UTRENST00000262160ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
5UTR-intronENST00000262160ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000402690ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000402690ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000402690ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-5UTRENST00000402690ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000402690ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000356825ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000356825ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000356825ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-5UTRENST00000356825ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000356825ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000586040ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000586040ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000586040ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-5UTRENST00000586040ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000586040ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000591214ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000591214ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000591214ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-5UTRENST00000591214ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000591214ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000587353ENST00000535628SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000587353ENST00000588982SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000587353ENST00000586438SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-5UTRENST00000587353ENST00000590800SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-
intron-intronENST00000587353ENST00000332053SMAD2chr18

45456732

-ZBTB7Cchr18

45864769

-

Top

FusionProtFeatures for SMAD2_ZBTB7C


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SMAD2

Q15796

ZBTB7C

A1YPR0

Receptor-regulated SMAD (R-SMAD) that is anintracellular signal transducer and transcriptional modulatoractivated by TGF-beta (transforming growth factor) and activintype 1 receptor kinases. Binds the TRE element in the promoterregion of many genes that are regulated by TGF-beta and, onformation of the SMAD2/SMAD4 complex, activates transcription. Mayact as a tumor suppressor in colorectal carcinoma. Positivelyregulates PDPK1 kinase activity by stimulating its dissociationfrom the 14-3-3 protein YWHAQ which acts as a negative regulator.{ECO:0000269|PubMed:16751101, ECO:0000269|PubMed:16862174,ECO:0000269|PubMed:17327236, ECO:0000269|PubMed:19289081,ECO:0000269|PubMed:9892009}. May be a tumor suppressor gene.{ECO:0000269|PubMed:9427755}.

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


Top

FusionGeneSequence for SMAD2_ZBTB7C


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).

Top

FusionGenePPI for SMAD2_ZBTB7C


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
SMAD2BRCA2, PML, ZFYVE9, ANAPC10, PIAS3, EID2, HIPK2, SKI, PIAS4, SMAD4, ZEB1, DVL1, ERBB2IP, TGIF1, HDAC1, FOXH1, EP300, SNIP1, JUN, SKIL, CDC27, CDC16, DAB2, CTNNB1, MEF2A, MEF2C, SMURF2, AKT1, SMAD3, NFYC, CAMK2G, MYC, INSR, RUNX1, RUNX2, RUNX3, SNW1, STRAP, ACVR1B, SMAD7, NEDD9, SP1, ESR1, TGFBR1, CAV1, LEF1, SMAD6, PIN1, RNF111, UCHL5, PRDM16, BPTF, POU2AF1, NEDD4, CITED2, WWP1, SMURF1, MYOCD, YY1, MED15, MED24, MED6, GTF2I, GTF2IRD1, MECOM, SMAD2, SOX9, ING2, KAT2B, KAT2A, CREBBP, SMARCC2, ARID1A, SMARCC1, SMARCA4, TRIM33, NCOA3, KDM6B, ATF3, ARID1B, STUB1, WWP2, USP9X, TP53, NUP214, USP15, CDK8, CDK9, ITCH, ELAVL1, RGCC, TCF12, ETV4, NEDD4L, HGS, ACVR2B, CSNK1D, DDX3Y, HSPA4, LEMD3, OPA1, DCAF7, SLC25A5, SLC25A6, SQRDL, BUB3, RIN1, KLF5, SMAD5, SMAD1, SLC25A3, ITGB4, CCT6A, C1orf116, DHX8, U2AF2, SIK3, DNAJA2, ATAD3B, PCID2, WRNIP1, PSPC1, DOCK9, EPB41L5, CAD, DGKA, FAM83G, CPSF7, S100A4, CHUK, CDK4, CDK2, ELAC2, NOTCH4, SMAD9, PSMD11, LAMA5, ZEB2, RANBP6, PLIN3, UBR5, SNAPIN, CSH1, CSH2, CYP11A1, PSAP, SNRNP70, PRKAR1A, RARB, RXRA, TGM2, PPP2R1A, SRI, PEX19, PSMD8, ST13, PAPOLA, ZNF41, MLLT4, ANTXR2, RPS14, UBA52, EEF1A1, ST5, KHDRBS1, PAPPA, OS9, ROCK1, ANK3, NCOA6, KPNB1, PSG9, ZMYND11, KIAA1033, RPS27A, RNF123, PAXIP1, TBC1D1, DOCK8, GATAD2B, COPS5, CUL5, ABTB1, DCUN1D1, RNPC3, FAM161B, RANBP9, DNAJC7, TRIM62, BTBD2, C22orf46, DYNC1H1, BAZ1A, CISH, ZNHIT6, NAGK, ANAPC2, EIF3L, SPTBN1, SH2D2A, LCK, PIK3CA, IRF7, IRF3, TSC2, FHL1, FHL2, FHL3, GFER, OTUB1, PPARG, NEFM, ANP32E, ANP32B, TUBA1B, PTMS, SOD1, SYT1, ATP5I, HDAC2, RHOA, GLI1, LDLRAD4, NFIA, PARD3, CAMK2A, YAP1, MAPTZBTB7CSREBF1, CDC5L, JUN, ZBTB17


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


Top

RelatedDrugs for SMAD2_ZBTB7C


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

RelatedDiseases for SMAD2_ZBTB7C


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSMAD2C0376634Craniofacial Abnormalities2CTD_human
HgeneSMAD2C0019189Hepatitis, Chronic1CTD_human
HgeneSMAD2C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneSMAD2C0265287Acromicric Dysplasia1CTD_human
HgeneSMAD2C0600519Ventricular Remodeling1CTD_human
HgeneSMAD2C1876165Copper-Overload Cirrhosis1CTD_human