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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:SMC5-CDKN2A

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMC5-CDKN2A
FusionPDB ID: 84016
FusionGDB2.0 ID: 84016
HgeneTgene
Gene symbol

SMC5

CDKN2A

Gene ID

23137

1029

Gene namestructural maintenance of chromosomes 5cyclin dependent kinase inhibitor 2A
SynonymsSMC5L1ARF|CDK4I|CDKN2|CMM2|INK4|INK4A|MLM|MTS-1|MTS1|P14|P14ARF|P16|P16-INK4A|P16INK4|P16INK4A|P19|P19ARF|TP16
Cytomap

9q21.12

9p21.3

Type of geneprotein-codingprotein-coding
Descriptionstructural maintenance of chromosomes protein 5SMC protein 5SMC-5SMC5 structural maintenance of chromosomes 5-like 1hSMC5cyclin-dependent kinase inhibitor 2ACDK4 inhibitor p16-INK4alternative reading framecell cycle negative regulator betacyclin-dependent kinase 4 inhibitor Acyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4)multiple tumor suppressor 1
Modification date2020031320200329
UniProtAcc

SLF2,FAM178A

Main function of 5'-partner protein: 1173

Q96HQ2

Main function of 5'-partner protein:
Ensembl transtripts involved in fusion geneENST idsENST00000361138, ENST00000471372, 
ENST00000446177, ENST00000479692, 
ENST00000494262, ENST00000497750, 
ENST00000498124, ENST00000498628, 
ENST00000530628, ENST00000578845, 
ENST00000470819, ENST00000361570, 
ENST00000579755, ENST00000304494, 
ENST00000579122, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 10 X 4=32013 X 5 X 10=650
# samples 916
** MAII scorelog2(9/320*10)=-1.83007499855769
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/650*10)=-2.02236781302845
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SMC5 [Title/Abstract] AND CDKN2A [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SMC5 [Title/Abstract] AND CDKN2A [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMC5(72879361)-CDKN2A(21971207), # samples:1
Anticipated loss of major functional domain due to fusion event.SMC5-CDKN2A 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.
SMC5-CDKN2A 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.
SMC5-CDKN2A seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SMC5-CDKN2A seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
SMC5-CDKN2A seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted 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
HgeneSMC5

GO:0006974

cellular response to DNA damage stimulus

11408570|25931565

TgeneCDKN2A

GO:0000082

G1/S transition of mitotic cell cycle

10208428

TgeneCDKN2A

GO:0007050

cell cycle arrest

15149599

TgeneCDKN2A

GO:0008285

negative regulation of cell proliferation

15149599

TgeneCDKN2A

GO:0030308

negative regulation of cell growth

10208428

TgeneCDKN2A

GO:0032088

negative regulation of NF-kappaB transcription factor activity

10353611

TgeneCDKN2A

GO:0042326

negative regulation of phosphorylation

8259215|10208428

TgeneCDKN2A

GO:0045736

negative regulation of cyclin-dependent protein serine/threonine kinase activity

7739547|8259215



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/chr9:72879361/chr9:21971207)
- 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 SMC5 (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 CDKN2A (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)
ENST00000361138SMC5chr972879361+ENST00000304494CDKN2Achr921971207-11823856950232
ENST00000361138SMC5chr972879361+ENST00000579122CDKN2Achr921971207-87038534651205

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
ENST00000361138ENST00000304494SMC5chr972879361+CDKN2Achr921971207-0.136002590.8639974
ENST00000361138ENST00000579122SMC5chr972879361+CDKN2Achr921971207-0.415678470.58432156

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 SMC5-CDKN2A

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SMC5chr972879361CDKN2Achr921971207385117LAGKPAFMGRADKVMMMGSARVAELL

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Potential FusionNeoAntigen Information of SMC5-CDKN2A 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.
SMC5-CDKN2A_72879361_21971207.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)
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:02GRADKVMMM0.99970.6318817
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:04GRADKVMMM0.99960.822817
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:05GRADKVMMM0.99960.864817
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:07GRADKVMMM0.99920.5088817
SMC5-CDKN2Achr972879361chr921971207385HLA-A74:03KVMMMGSAR0.99310.74641221
SMC5-CDKN2Achr972879361chr921971207385HLA-A74:11KVMMMGSAR0.99310.74641221
SMC5-CDKN2Achr972879361chr921971207385HLA-A74:09KVMMMGSAR0.99310.74641221
SMC5-CDKN2Achr972879361chr921971207385HLA-A31:06KVMMMGSAR0.99280.54881221
SMC5-CDKN2Achr972879361chr921971207385HLA-B14:02GRADKVMMM0.97520.683817
SMC5-CDKN2Achr972879361chr921971207385HLA-B14:01GRADKVMMM0.97520.683817
SMC5-CDKN2Achr972879361chr921971207385HLA-B39:01GRADKVMMM0.96780.7479817
SMC5-CDKN2Achr972879361chr921971207385HLA-A31:02KVMMMGSAR0.95210.77951221
SMC5-CDKN2Achr972879361chr921971207385HLA-B38:02GRADKVMMM0.89110.8652817
SMC5-CDKN2Achr972879361chr921971207385HLA-B15:18GRADKVMMM0.58680.8402817
SMC5-CDKN2Achr972879361chr921971207385HLA-B15:37GRADKVMMM0.51760.6234817
SMC5-CDKN2Achr972879361chr921971207385HLA-C08:15RADKVMMM10.9548917
SMC5-CDKN2Achr972879361chr921971207385HLA-C05:09RADKVMMM10.9248917
SMC5-CDKN2Achr972879361chr921971207385HLA-C04:07RADKVMMM10.73917
SMC5-CDKN2Achr972879361chr921971207385HLA-C04:10RADKVMMM10.6983917
SMC5-CDKN2Achr972879361chr921971207385HLA-C15:06RADKVMMM0.99970.918917
SMC5-CDKN2Achr972879361chr921971207385HLA-C04:06RADKVMMM0.99940.7937917
SMC5-CDKN2Achr972879361chr921971207385HLA-C04:14RADKVMMM0.99870.7119917
SMC5-CDKN2Achr972879361chr921971207385HLA-C08:04RADKVMMM0.99730.9829917
SMC5-CDKN2Achr972879361chr921971207385HLA-C08:13RADKVMMM0.99730.9829917
SMC5-CDKN2Achr972879361chr921971207385HLA-C08:03RADKVMMM0.98880.9822917
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:14GRADKVMMM0.99950.8339817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:95GRADKVMMM0.99710.5451817
SMC5-CDKN2Achr972879361chr921971207385HLA-A31:01KVMMMGSAR0.99350.75891221
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:03GRADKVMMM0.99170.8814817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:27GRADKVMMM0.99010.9538817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:05GRADKVMMM0.98920.9574817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:13GRADKVMMM0.98460.9328817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:46GRADKVMMM0.98360.8668817
SMC5-CDKN2Achr972879361chr921971207385HLA-B39:12GRADKVMMM0.98260.7664817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:29GRADKVMMM0.98210.8821817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:19GRADKVMMM0.97220.6546817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:80GRADKVMMM0.96730.9455817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:67GRADKVMMM0.96730.9455817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:10GRADKVMMM0.95250.9649817
SMC5-CDKN2Achr972879361chr921971207385HLA-B14:03GRADKVMMM0.38790.7249817
SMC5-CDKN2Achr972879361chr921971207385HLA-C12:16GRADKVMMM0.07460.9695817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:95MGRADKVMMM0.94790.7604717
SMC5-CDKN2Achr972879361chr921971207385HLA-C12:16FMGRADKVMMM0.99130.9779617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:19FMGRADKVMMM0.95360.6913617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:10FMGRADKVMMM0.9280.9716617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:05FMGRADKVMMM0.90980.9369617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:95FMGRADKVMMM0.90570.6427617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:27FMGRADKVMMM0.88590.9452617
SMC5-CDKN2Achr972879361chr921971207385HLA-C04:03RADKVMMM10.7772917
SMC5-CDKN2Achr972879361chr921971207385HLA-C04:01RADKVMMM10.73917
SMC5-CDKN2Achr972879361chr921971207385HLA-C18:01RADKVMMM10.7501917
SMC5-CDKN2Achr972879361chr921971207385HLA-C05:01RADKVMMM10.9248917
SMC5-CDKN2Achr972879361chr921971207385HLA-C08:02RADKVMMM10.9548917
SMC5-CDKN2Achr972879361chr921971207385HLA-C15:05RADKVMMM0.99960.9156917
SMC5-CDKN2Achr972879361chr921971207385HLA-C15:02RADKVMMM0.99940.8886917
SMC5-CDKN2Achr972879361chr921971207385HLA-C16:01RADKVMMM0.99920.9776917
SMC5-CDKN2Achr972879361chr921971207385HLA-C16:02RADKVMMM0.99880.9904917
SMC5-CDKN2Achr972879361chr921971207385HLA-C08:01RADKVMMM0.98880.9822917
SMC5-CDKN2Achr972879361chr921971207385HLA-B07:13RADKVMMM0.89620.6831917
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:08GRADKVMMM0.99960.7793817
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:10GRADKVMMM0.99960.8904817
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:06GRADKVMMM0.99950.8222817
SMC5-CDKN2Achr972879361chr921971207385HLA-B27:09GRADKVMMM0.99890.8044817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:01GRADKVMMM0.99740.5273817
SMC5-CDKN2Achr972879361chr921971207385HLA-A74:01KVMMMGSAR0.99310.74641221
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:17GRADKVMMM0.98420.9695817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:02GRADKVMMM0.96730.9455817
SMC5-CDKN2Achr972879361chr921971207385HLA-B39:31GRADKVMMM0.96410.7612817
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:08GRADKVMMM0.95360.9939817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:04GRADKVMMM0.79080.9291817
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:22GRADKVMMM0.77420.6083817
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:06GRADKVMMM0.65220.9895817
SMC5-CDKN2Achr972879361chr921971207385HLA-C03:67GRADKVMMM0.430.9851817
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:17GRADKVMMM0.10810.9929817
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:02GRADKVMMM0.10810.9929817
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:02MGRADKVMMM0.98080.9958717
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:17MGRADKVMMM0.98080.9958717
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:22MGRADKVMMM0.97080.7961717
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:01MGRADKVMMM0.9630.7063717
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:08MGRADKVMMM0.94930.9941717
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:02FMGRADKVMMM0.99320.9952617
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:17FMGRADKVMMM0.99320.9952617
SMC5-CDKN2Achr972879361chr921971207385HLA-C06:08FMGRADKVMMM0.97220.9942617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:22FMGRADKVMMM0.96680.7842617
SMC5-CDKN2Achr972879361chr921971207385HLA-C07:01FMGRADKVMMM0.92420.6248617

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Potential FusionNeoAntigen Information of SMC5-CDKN2A 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.
SMC5-CDKN2A_72879361_21971207.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)
SMC5-CDKN2Achr972879361chr921971207385DRB1-0102RADKVMMMGSARVAE924
SMC5-CDKN2Achr972879361chr921971207385DRB1-0102ADKVMMMGSARVAEL1025
SMC5-CDKN2Achr972879361chr921971207385DRB1-0123RADKVMMMGSARVAE924
SMC5-CDKN2Achr972879361chr921971207385DRB1-0123ADKVMMMGSARVAEL1025
SMC5-CDKN2Achr972879361chr921971207385DRB1-1615RADKVMMMGSARVAE924
SMC5-CDKN2Achr972879361chr921971207385DRB1-1615ADKVMMMGSARVAEL1025

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Fusion breakpoint peptide structures of SMC5-CDKN2A

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
2469FMGRADKVMMMGSASMC5CDKN2Achr972879361chr921971207385

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SMC5-CDKN2A

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-B14:023BVN2469FMGRADKVMMMGSA-6.77781-6.89121
HLA-B14:023BVN2469FMGRADKVMMMGSA-3.08719-4.12249
HLA-B52:013W392469FMGRADKVMMMGSA-6.66315-6.77655
HLA-B52:013W392469FMGRADKVMMMGSA-2.65785-3.69315
HLA-A24:025HGA2469FMGRADKVMMMGSA-7.20627-7.31967
HLA-A24:025HGA2469FMGRADKVMMMGSA-6.50211-7.53741
HLA-B44:053DX82469FMGRADKVMMMGSA-7.75024-7.86364
HLA-B44:053DX82469FMGRADKVMMMGSA-6.53073-7.56603
HLA-A02:016TDR2469FMGRADKVMMMGSA-4.4528-5.4881

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Vaccine Design for the FusionNeoAntigens of SMC5-CDKN2A

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
SMC5-CDKN2Achr972879361chr9219712071221KVMMMGSARAAGGTCATGATGATGGGCAGCGCCCGA
SMC5-CDKN2Achr972879361chr921971207617FMGRADKVMMMTTCATGGGACGAGCAGATAAGGTCATGATGATG
SMC5-CDKN2Achr972879361chr921971207717MGRADKVMMMATGGGACGAGCAGATAAGGTCATGATGATG
SMC5-CDKN2Achr972879361chr921971207817GRADKVMMMGGACGAGCAGATAAGGTCATGATGATG
SMC5-CDKN2Achr972879361chr921971207917RADKVMMMCGAGCAGATAAGGTCATGATGATG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SMC5-CDKN2Achr972879361chr9219712071025ADKVMMMGSARVAELGCAGATAAGGTCATGATGATGGGCAGCGCCCGAGTGGCGGAGCTG
SMC5-CDKN2Achr972879361chr921971207924RADKVMMMGSARVAECGAGCAGATAAGGTCATGATGATGGGCAGCGCCCGAGTGGCGGAG

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Information of the samples that have these potential fusion neoantigens of SMC5-CDKN2A

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
OVSMC5-CDKN2Achr972879361ENST00000361138chr921971207ENST00000579122TCGA-13-0725

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Potential target of CAR-T therapy development for SMC5-CDKN2A

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 SMC5-CDKN2A

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 SMC5-CDKN2A

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