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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ITGAV-SMAD2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ITGAV-SMAD2
FusionPDB ID: 40495
FusionGDB2.0 ID: 40495
HgeneTgene
Gene symbol

ITGAV

SMAD2

Gene ID

3685

4087

Gene nameintegrin subunit alpha VSMAD family member 2
SynonymsCD51|MSK8|VNRA|VTNRJV18|JV18-1|MADH2|MADR2|hMAD-2|hSMAD2
Cytomap

2q32.1

18q21.1

Type of geneprotein-codingprotein-coding
Descriptionintegrin alpha-Vantigen identified by monoclonal antibody L230integrin alphaVbeta3integrin, alpha V (vitronectin receptor, alpha polypeptide, antigen CD51)vitronectin receptor subunit alphamothers against decapentaplegic homolog 2MAD homolog 2SMAD, mothers against DPP homolog 2Sma- and Mad-related protein 2mother against DPP homolog 2
Modification date2020031320200322
UniProtAcc

P06756

Main function of 5'-partner protein: FUNCTION: The alpha-V (ITGAV) integrins are receptors for vitronectin, cytotactin, fibronectin, fibrinogen, laminin, matrix metalloproteinase-2, osteopontin, osteomodulin, prothrombin, thrombospondin and vWF. They recognize the sequence R-G-D in a wide array of ligands. ITGAV:ITGB3 binds to fractalkine (CX3CL1) and may act as its coreceptor in CX3CR1-dependent fractalkine signaling (PubMed:23125415). ITGAV:ITGB3 binds to NRG1 (via EGF domain) and this binding is essential for NRG1-ERBB signaling (PubMed:20682778). ITGAV:ITGB3 binds to FGF1 and this binding is essential for FGF1 signaling (PubMed:18441324). ITGAV:ITGB3 binds to FGF2 and this binding is essential for FGF2 signaling (PubMed:28302677). ITGAV:ITGB3 binds to IGF1 and this binding is essential for IGF1 signaling (PubMed:19578119). ITGAV:ITGB3 binds to IGF2 and this binding is essential for IGF2 signaling (PubMed:28873464). ITGAV:ITGB3 binds to IL1B and this binding is essential for IL1B signaling (PubMed:29030430). ITGAV:ITGB3 binds to PLA2G2A via a site (site 2) which is distinct from the classical ligand-binding site (site 1) and this induces integrin conformational changes and enhanced ligand binding to site 1 (PubMed:18635536, PubMed:25398877). ITGAV:ITGB3 and ITGAV:ITGB6 act as a receptor for fibrillin-1 (FBN1) and mediate R-G-D-dependent cell adhesion to FBN1 (PubMed:12807887, PubMed:17158881). Integrin alpha-V/beta-6 or alpha-V/beta-8 (ITGAV:ITGB6 or ITGAV:ITGB8) mediates R-G-D-dependent release of transforming growth factor beta-1 (TGF-beta-1) from regulatory Latency-associated peptide (LAP), thereby playing a key role in TGF-beta-1 activation (PubMed:15184403, PubMed:22278742, PubMed:28117447). ITGAV:ITGB3 act as a receptor for CD40LG (PubMed:31331973). {ECO:0000269|PubMed:12807887, ECO:0000269|PubMed:15184403, ECO:0000269|PubMed:17158881, ECO:0000269|PubMed:18441324, ECO:0000269|PubMed:18635536, ECO:0000269|PubMed:19578119, ECO:0000269|PubMed:20682778, ECO:0000269|PubMed:22278742, ECO:0000269|PubMed:23125415, ECO:0000269|PubMed:25398877, ECO:0000269|PubMed:28117447, ECO:0000269|PubMed:28302677, ECO:0000269|PubMed:28873464, ECO:0000269|PubMed:29030430, ECO:0000269|PubMed:31331973}.; FUNCTION: (Microbial infection) Integrin ITGAV:ITGB5 acts as a receptor for Adenovirus type C. {ECO:0000269|PubMed:20615244}.; FUNCTION: (Microbial infection) Integrin ITGAV:ITGB5 and ITGAV:ITGB3 act as receptors for Coxsackievirus A9 and B1. {ECO:0000269|PubMed:15194773, ECO:0000269|PubMed:7519807, ECO:0000269|PubMed:9426447}.; FUNCTION: (Microbial infection) Integrin ITGAV:ITGB3 acts as a receptor for Herpes virus 8/HHV-8. {ECO:0000269|PubMed:18045938}.; FUNCTION: (Microbial infection) Integrin ITGAV:ITGB6 acts as a receptor for herpes simplex 1/HHV-1. {ECO:0000269|PubMed:24367260}.; FUNCTION: (Microbial infection) Integrin ITGAV:ITGB3 acts as a receptor for Human parechovirus 1. {ECO:0000269|PubMed:11160695}.; FUNCTION: (Microbial infection) Integrin ITGAV:ITGB3 acts as a receptor for West nile virus. {ECO:0000269|PubMed:23658209}.; FUNCTION: (Microbial infection) In case of HIV-1 infection, the interaction with extracellular viral Tat protein seems to enhance angiogenesis in Kaposi's sarcoma lesions. {ECO:0000269|PubMed:10397733}.
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Ensembl transtripts involved in fusion geneENST idsENST00000261023, ENST00000374907, 
ENST00000433736, ENST00000474571, 
ENST00000587353, ENST00000262160, 
ENST00000356825, ENST00000402690, 
ENST00000586040, ENST00000591214, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 9 X 8=79212 X 9 X 5=540
# samples 1312
** MAII scorelog2(13/792*10)=-2.60698880705116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/540*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ITGAV [Title/Abstract] AND SMAD2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ITGAV [Title/Abstract] AND SMAD2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ITGAV(187490314)-SMAD2(45377698), # samples:1
Anticipated loss of major functional domain due to fusion event.ITGAV-SMAD2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ITGAV-SMAD2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ITGAV-SMAD2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
ITGAV-SMAD2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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
HgeneITGAV

GO:0007155

cell adhesion

10218736

HgeneITGAV

GO:0008284

positive regulation of cell proliferation

19578119

HgeneITGAV

GO:0033627

cell adhesion mediated by integrin

12807887|17158881

HgeneITGAV

GO:0034446

substrate adhesion-dependent cell spreading

24658351

HgeneITGAV

GO:0045785

positive regulation of cell adhesion

10708943

HgeneITGAV

GO:0050764

regulation of phagocytosis

10570297

HgeneITGAV

GO:0070588

calcium ion transmembrane transport

18395422

HgeneITGAV

GO:1901388

regulation of transforming growth factor beta activation

22278742

HgeneITGAV

GO:2000536

negative regulation of entry of bacterium into host cell

10570297

TgeneSMAD2

GO:0007179

transforming growth factor beta receptor signaling pathway

8752209|9389648|9732876|18548003

TgeneSMAD2

GO:0007182

common-partner SMAD protein phosphorylation

16806156

TgeneSMAD2

GO:0007183

SMAD protein complex assembly

9111321

TgeneSMAD2

GO:0045893

positive regulation of transcription, DNA-templated

9311995|9389648|9732876

TgeneSMAD2

GO:0045944

positive regulation of transcription by RNA polymerase II

9389648

TgeneSMAD2

GO:0070723

response to cholesterol

17878231



check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr2:187490314/chr18:45377698)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across ITGAV (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across SMAD2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Amino Acid Sequences


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000261023ITGAVchr2187490314+ENST00000262160SMAD2chr1845377698-11747797491470473
ENST00000261023ITGAVchr2187490314+ENST00000402690SMAD2chr1845377698-11747797491470473
ENST00000261023ITGAVchr2187490314+ENST00000356825SMAD2chr1845377698-10203797491470473
ENST00000261023ITGAVchr2187490314+ENST00000586040SMAD2chr1845377698-2073797491470473
ENST00000261023ITGAVchr2187490314+ENST00000591214SMAD2chr1845377698-1775797491452467
ENST00000374907ITGAVchr2187490314+ENST00000262160SMAD2chr1845377698-11732782341455473
ENST00000374907ITGAVchr2187490314+ENST00000402690SMAD2chr1845377698-11732782341455473
ENST00000374907ITGAVchr2187490314+ENST00000356825SMAD2chr1845377698-10188782341455473
ENST00000374907ITGAVchr2187490314+ENST00000586040SMAD2chr1845377698-2058782341455473
ENST00000374907ITGAVchr2187490314+ENST00000591214SMAD2chr1845377698-1760782341437467
ENST00000433736ITGAVchr2187490314+ENST00000262160SMAD2chr1845377698-114655151301188352
ENST00000433736ITGAVchr2187490314+ENST00000402690SMAD2chr1845377698-114655151301188352
ENST00000433736ITGAVchr2187490314+ENST00000356825SMAD2chr1845377698-99215151301188352
ENST00000433736ITGAVchr2187490314+ENST00000586040SMAD2chr1845377698-17915151301188352
ENST00000433736ITGAVchr2187490314+ENST00000591214SMAD2chr1845377698-14935151301170346

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000261023ENST00000262160ITGAVchr2187490314+SMAD2chr1845377698-0.0011716280.99882835
ENST00000261023ENST00000402690ITGAVchr2187490314+SMAD2chr1845377698-0.0011716280.99882835
ENST00000261023ENST00000356825ITGAVchr2187490314+SMAD2chr1845377698-0.0011733710.99882656
ENST00000261023ENST00000586040ITGAVchr2187490314+SMAD2chr1845377698-0.0054496030.9945504
ENST00000261023ENST00000591214ITGAVchr2187490314+SMAD2chr1845377698-0.0032023330.99679774
ENST00000374907ENST00000262160ITGAVchr2187490314+SMAD2chr1845377698-0.0011684660.99883157
ENST00000374907ENST00000402690ITGAVchr2187490314+SMAD2chr1845377698-0.0011684660.99883157
ENST00000374907ENST00000356825ITGAVchr2187490314+SMAD2chr1845377698-0.0011700560.9988299
ENST00000374907ENST00000586040ITGAVchr2187490314+SMAD2chr1845377698-0.0052394560.9947606
ENST00000374907ENST00000591214ITGAVchr2187490314+SMAD2chr1845377698-0.0030787430.9969213
ENST00000433736ENST00000262160ITGAVchr2187490314+SMAD2chr1845377698-0.0002985680.99970144
ENST00000433736ENST00000402690ITGAVchr2187490314+SMAD2chr1845377698-0.0002985680.99970144
ENST00000433736ENST00000356825ITGAVchr2187490314+SMAD2chr1845377698-0.0003095270.99969053
ENST00000433736ENST00000586040ITGAVchr2187490314+SMAD2chr1845377698-0.0006693630.99933064
ENST00000433736ENST00000591214ITGAVchr2187490314+SMAD2chr1845377698-0.0006943150.9993057

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for ITGAV-SMAD2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ITGAVchr2187490314SMAD2chr1845377698515129GTKTVEYAPCRSRSPAELSPTTLSPV
ITGAVchr2187490314SMAD2chr1845377698782250GTKTVEYAPCRSRSPAELSPTTLSPV
ITGAVchr2187490314SMAD2chr1845377698797250GTKTVEYAPCRSRSPAELSPTTLSPV

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Potential FusionNeoAntigen Information of ITGAV-SMAD2 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
ITGAV-SMAD2_187490314_45377698.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B39:06SRSPAELSP0.9890.84031120
ITGAV-SMAD2chr2187490314chr1845377698797HLA-A30:08RSRSPAELS0.97740.73231019
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B07:10CRSRSPAEL0.02190.5172918
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B50:02VEYAPCRSRSP0.94360.5116415
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B50:01VEYAPCRSRSP0.92720.6476415
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B73:01SRSPAELSP0.96680.72261120
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B07:12APCRSRSPAEL0.99970.5633718
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C01:17RSPAELSPTTL0.99920.95581223
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C01:30RSPAELSPTTL0.99740.95691223
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B07:13RSRSPAEL0.93030.87671018
ITGAV-SMAD2chr2187490314chr1845377698797HLA-A30:01RSRSPAELS0.98050.8661019
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C06:08CRSRSPAEL0.90130.9889918
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C07:22CRSRSPAEL0.76080.7817918
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C06:17CRSRSPAEL0.12850.9899918
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C06:02CRSRSPAEL0.12850.9899918
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C01:03RSPAELSPTTL0.99960.94411223
ITGAV-SMAD2chr2187490314chr1845377698797HLA-C01:02RSPAELSPTTL0.99860.95461223
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B50:05VEYAPCRSRSP0.92720.6476415
ITGAV-SMAD2chr2187490314chr1845377698797HLA-B50:04VEYAPCRSRSP0.92720.6476415

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Potential FusionNeoAntigen Information of ITGAV-SMAD2 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
ITGAV-SMAD2_187490314_45377698.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
ITGAV-SMAD2chr2187490314chr1845377698797DRB5-0106TKTVEYAPCRSRSPA116

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Fusion breakpoint peptide structures of ITGAV-SMAD2

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
10578YAPCRSRSPAELSPITGAVSMAD2chr2187490314chr1845377698797

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ITGAV-SMAD2

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN10578YAPCRSRSPAELSP-7.15543-7.26883
HLA-B14:023BVN10578YAPCRSRSPAELSP-4.77435-5.80965
HLA-B52:013W3910578YAPCRSRSPAELSP-6.80875-6.92215
HLA-B52:013W3910578YAPCRSRSPAELSP-4.20386-5.23916
HLA-A11:014UQ210578YAPCRSRSPAELSP-7.5194-8.5547
HLA-A11:014UQ210578YAPCRSRSPAELSP-6.9601-7.0735
HLA-A24:025HGA10578YAPCRSRSPAELSP-7.52403-7.63743
HLA-A24:025HGA10578YAPCRSRSPAELSP-5.82433-6.85963
HLA-B27:056PYJ10578YAPCRSRSPAELSP-3.28285-4.31815
HLA-B44:053DX810578YAPCRSRSPAELSP-5.91172-6.94702
HLA-B44:053DX810578YAPCRSRSPAELSP-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of ITGAV-SMAD2

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
ITGAV-SMAD2chr2187490314chr18453776981018RSRSPAELGTAGATCACGCTCTCCAGCAGAAC
ITGAV-SMAD2chr2187490314chr18453776981019RSRSPAELSGTAGATCACGCTCTCCAGCAGAACTAT
ITGAV-SMAD2chr2187490314chr18453776981120SRSPAELSPGATCACGCTCTCCAGCAGAACTATCTC
ITGAV-SMAD2chr2187490314chr18453776981223RSPAELSPTTLCACGCTCTCCAGCAGAACTATCTCCTACTACTC
ITGAV-SMAD2chr2187490314chr1845377698415VEYAPCRSRSPCTGTTGAGTATGCTCCATGTAGATCACGCTCTC
ITGAV-SMAD2chr2187490314chr1845377698718APCRSRSPAELATGCTCCATGTAGATCACGCTCTCCAGCAGAAC
ITGAV-SMAD2chr2187490314chr1845377698918CRSRSPAELCATGTAGATCACGCTCTCCAGCAGAAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ITGAV-SMAD2chr2187490314chr1845377698116TKTVEYAPCRSRSPAGAACAAAGACTGTTGAGTATGCTCCATGTAGATCACGCTCTCCAG

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Information of the samples that have these potential fusion neoantigens of ITGAV-SMAD2

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
STADITGAV-SMAD2chr2187490314ENST00000261023chr1845377698ENST00000262160TCGA-BR-A4QI-01A

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Potential target of CAR-T therapy development for ITGAV-SMAD2

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to ITGAV-SMAD2

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to ITGAV-SMAD2

check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource