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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:SMURF1-CDK14

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMURF1-CDK14
FusionPDB ID: 84307
FusionGDB2.0 ID: 84307
HgeneTgene
Gene symbol

SMURF1

CDK14

Gene ID

57154

5218

Gene nameSMAD specific E3 ubiquitin protein ligase 1cyclin dependent kinase 14
Synonyms-PFTAIRE1|PFTK1
Cytomap

7q22.1

7q21.13

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase SMURF1E3 ubiquitin ligase SMURF1HECT-type E3 ubiquitin transferase SMURF1Smad ubiquitination regulatory factor 1Smad-specific E3 ubiquitin ligase 1hSMURF1cyclin-dependent kinase 14PFTAIRE protein kinase 1cell division protein kinase 14serine/threonine-protein kinase PFTAIRE-1
Modification date2020031320200313
UniProtAcc.

O94921

Main function of 5'-partner protein: FUNCTION: Serine/threonine-protein kinase involved in the control of the eukaryotic cell cycle, whose activity is controlled by an associated cyclin. Acts as a cell-cycle regulator of Wnt signaling pathway during G2/M phase by mediating the phosphorylation of LRP6 at 'Ser-1490', leading to the activation of the Wnt signaling pathway. Acts as a regulator of cell cycle progression and cell proliferation via its interaction with CCDN3. Phosphorylates RB1 in vitro, however the relevance of such result remains to be confirmed in vivo. May also play a role in meiosis, neuron differentiation and may indirectly act as a negative regulator of insulin-responsive glucose transport. {ECO:0000269|PubMed:16461467, ECO:0000269|PubMed:17517622, ECO:0000269|PubMed:19524571, ECO:0000269|PubMed:20059949}.
Ensembl transtripts involved in fusion geneENST idsENST00000361125, ENST00000361368, 
ENST00000480055, 
ENST00000496279, 
ENST00000265741, ENST00000380050, 
ENST00000406263, ENST00000436577, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score19 X 8 X 12=182422 X 24 X 12=6336
# samples 2432
** MAII scorelog2(24/1824*10)=-2.92599941855622
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/6336*10)=-4.30742852519225
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SMURF1 [Title/Abstract] AND CDK14 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SMURF1 [Title/Abstract] AND CDK14 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMURF1(98658222)-CDK14(90675212), # samples:3
Anticipated loss of major functional domain due to fusion event.SMURF1-CDK14 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.
SMURF1-CDK14 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.
SMURF1-CDK14 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SMURF1-CDK14 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
SMURF1-CDK14 seems lost the major protein functional domain in Tgene partner, which is a kinase 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
HgeneSMURF1

GO:0000209

protein polyubiquitination

19937093

HgeneSMURF1

GO:0006511

ubiquitin-dependent protein catabolic process

10458166|12151385|19937093

HgeneSMURF1

GO:0006611

protein export from nucleus

11278251

HgeneSMURF1

GO:0016567

protein ubiquitination

11278251

HgeneSMURF1

GO:0030154

cell differentiation

10458166

HgeneSMURF1

GO:0030509

BMP signaling pathway

21572392

HgeneSMURF1

GO:0030512

negative regulation of transforming growth factor beta receptor signaling pathway

11278251|12151385

HgeneSMURF1

GO:0030514

negative regulation of BMP signaling pathway

27214554

HgeneSMURF1

GO:0030579

ubiquitin-dependent SMAD protein catabolic process

11278251|12151385

HgeneSMURF1

GO:0032801

receptor catabolic process

12151385

HgeneSMURF1

GO:0034394

protein localization to cell surface

12151385

HgeneSMURF1

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

11278251

HgeneSMURF1

GO:1903861

positive regulation of dendrite extension

23999003

TgeneCDK14

GO:0000086

G2/M transition of mitotic cell cycle

20059949

TgeneCDK14

GO:0060828

regulation of canonical Wnt signaling pathway

20059949



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/chr7:98658222/chr7:90675212)
- 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 SMURF1 (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 CDK14 (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)
ENST00000361368SMURF1chr798658221-ENST00000380050CDK14chr790741856+415244220697225
ENST00000361368SMURF1chr798658221-ENST00000265741CDK14chr790741856+415144220697225
ENST00000361368SMURF1chr798658221-ENST00000406263CDK14chr790741856+414744220697225
ENST00000361368SMURF1chr798658221-ENST00000436577CDK14chr790741856+92444220697225
ENST00000361125SMURF1chr798658221-ENST00000380050CDK14chr790741856+4233523101778225
ENST00000361125SMURF1chr798658221-ENST00000265741CDK14chr790741856+4232523101778225
ENST00000361125SMURF1chr798658221-ENST00000406263CDK14chr790741856+4228523101778225
ENST00000361125SMURF1chr798658221-ENST00000436577CDK14chr790741856+1005523101778225

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
ENST00000361368ENST00000380050SMURF1chr798658221-CDK14chr790741856+0.0046270980.99537295
ENST00000361368ENST00000265741SMURF1chr798658221-CDK14chr790741856+0.005862940.99413705
ENST00000361368ENST00000406263SMURF1chr798658221-CDK14chr790741856+0.0062888860.9937111
ENST00000361368ENST00000436577SMURF1chr798658221-CDK14chr790741856+0.0198685420.98013145
ENST00000361125ENST00000380050SMURF1chr798658221-CDK14chr790741856+0.004793340.99520665
ENST00000361125ENST00000265741SMURF1chr798658221-CDK14chr790741856+0.0060739050.9939261
ENST00000361125ENST00000406263SMURF1chr798658221-CDK14chr790741856+0.0065056840.99349433
ENST00000361125ENST00000436577SMURF1chr798658221-CDK14chr790741856+0.0147059690.985294

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 SMURF1-CDK14

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SMURF1chr798658221CDK14chr790741856442141NTLDPKWNQHYDLLSYVNHAEDLASK
SMURF1chr798658221CDK14chr790741856523141NTLDPKWNQHYDLLSYVNHAEDLASK

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Potential FusionNeoAntigen Information of SMURF1-CDK14 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.
SMURF1-CDK14_98658221_90741856.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)
SMURF1-CDK14chr798658221chr790741856523HLA-B15:01NQHYDLLSY0.99980.5571716
SMURF1-CDK14chr798658221chr790741856523HLA-B39:01QHYDLLSYV0.99770.6083817
SMURF1-CDK14chr798658221chr790741856523HLA-B38:01QHYDLLSYV0.99710.725817
SMURF1-CDK14chr798658221chr790741856523HLA-B38:02QHYDLLSYV0.99690.7235817
SMURF1-CDK14chr798658221chr790741856523HLA-B15:25NQHYDLLSY0.98720.6267716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:02NQHYDLLSY0.96540.6532716
SMURF1-CDK14chr798658221chr790741856523HLA-B18:01NQHYDLLSY0.92760.5344716
SMURF1-CDK14chr798658221chr790741856523HLA-B52:01QHYDLLSYV0.21090.611817
SMURF1-CDK14chr798658221chr790741856523HLA-B15:01KWNQHYDLLSY0.98940.6011516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:25KWNQHYDLLSY0.97630.6632516
SMURF1-CDK14chr798658221chr790741856523HLA-C04:07HYDLLSYV10.5734917
SMURF1-CDK14chr798658221chr790741856523HLA-C04:10HYDLLSYV10.5639917
SMURF1-CDK14chr798658221chr790741856523HLA-C04:14HYDLLSYV0.97850.5115917
SMURF1-CDK14chr798658221chr790741856523HLA-B15:21QHYDLLSY0.97540.6738816
SMURF1-CDK14chr798658221chr790741856523HLA-B39:12QHYDLLSYV0.99740.6142817
SMURF1-CDK14chr798658221chr790741856523HLA-B39:05QHYDLLSYV0.99660.5808817
SMURF1-CDK14chr798658221chr790741856523HLA-B15:21NQHYDLLSY0.96530.6362716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:04NQHYDLLSY0.94940.5518716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:31NQHYDLLSY0.94230.5009716
SMURF1-CDK14chr798658221chr790741856523HLA-C04:14KWNQHYDLL0.14070.7472514
SMURF1-CDK14chr798658221chr790741856523HLA-C12:16QHYDLLSYV0.00830.8505817
SMURF1-CDK14chr798658221chr790741856523HLA-B15:05KWNQHYDLLSY0.96950.5409516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:04KWNQHYDLLSY0.91260.6323516
SMURF1-CDK14chr798658221chr790741856523HLA-C04:01HYDLLSYV10.5734917
SMURF1-CDK14chr798658221chr790741856523HLA-C18:01HYDLLSYV0.99990.6099917
SMURF1-CDK14chr798658221chr790741856523HLA-C04:04HYDLLSYV0.99460.6395917
SMURF1-CDK14chr798658221chr790741856523HLA-B48:02QHYDLLSY0.97150.6889816
SMURF1-CDK14chr798658221chr790741856523HLA-B18:04QHYDLLSY0.91320.6269816
SMURF1-CDK14chr798658221chr790741856523HLA-B18:06QHYDLLSY0.90780.6003816
SMURF1-CDK14chr798658221chr790741856523HLA-B15:34NQHYDLLSY0.99980.5571716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:135NQHYDLLSY0.99980.5379716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:125NQHYDLLSY0.99980.5571716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:27NQHYDLLSY0.99980.6083716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:33NQHYDLLSY0.99980.5571716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:50NQHYDLLSY0.99970.6133716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:12NQHYDLLSY0.99820.6182716
SMURF1-CDK14chr798658221chr790741856523HLA-B39:31QHYDLLSYV0.99770.6094817
SMURF1-CDK14chr798658221chr790741856523HLA-B38:05QHYDLLSYV0.99710.725817
SMURF1-CDK14chr798658221chr790741856523HLA-B18:04NQHYDLLSY0.97170.5665716
SMURF1-CDK14chr798658221chr790741856523HLA-B15:20NQHYDLLSY0.96250.6013716
SMURF1-CDK14chr798658221chr790741856523HLA-B35:28NQHYDLLSY0.95270.6072716
SMURF1-CDK14chr798658221chr790741856523HLA-B35:20NQHYDLLSY0.94150.6331716
SMURF1-CDK14chr798658221chr790741856523HLA-B18:05NQHYDLLSY0.92760.5344716
SMURF1-CDK14chr798658221chr790741856523HLA-B18:06NQHYDLLSY0.90110.5479716
SMURF1-CDK14chr798658221chr790741856523HLA-B18:03NQHYDLLSY0.90030.5307716
SMURF1-CDK14chr798658221chr790741856523HLA-B35:24NQHYDLLSY0.86450.5825716
SMURF1-CDK14chr798658221chr790741856523HLA-B39:11QHYDLLSYV0.83550.6055817
SMURF1-CDK14chr798658221chr790741856523HLA-B48:02NQHYDLLSY0.61320.5612716
SMURF1-CDK14chr798658221chr790741856523HLA-C07:04QHYDLLSYV0.52990.8668817
SMURF1-CDK14chr798658221chr790741856523HLA-C06:06QHYDLLSYV0.13540.9574817
SMURF1-CDK14chr798658221chr790741856523HLA-C06:08QHYDLLSYV0.10520.9189817
SMURF1-CDK14chr798658221chr790741856523HLA-C06:02QHYDLLSYV0.05630.9495817
SMURF1-CDK14chr798658221chr790741856523HLA-C06:17QHYDLLSYV0.05630.9495817
SMURF1-CDK14chr798658221chr790741856523HLA-B15:50WNQHYDLLSY0.94070.5386616
SMURF1-CDK14chr798658221chr790741856523HLA-B15:20WNQHYDLLSY0.92360.5605616
SMURF1-CDK14chr798658221chr790741856523HLA-B35:28WNQHYDLLSY0.91130.586616
SMURF1-CDK14chr798658221chr790741856523HLA-B15:27KWNQHYDLLSY0.99020.6375516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:50KWNQHYDLLSY0.98990.6115516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:33KWNQHYDLLSY0.98940.6011516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:34KWNQHYDLLSY0.98940.6011516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:125KWNQHYDLLSY0.98940.6011516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:135KWNQHYDLLSY0.98680.6058516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:35KWNQHYDLLSY0.98480.5578516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:53KWNQHYDLLSY0.97310.5442516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:54KWNQHYDLLSY0.97180.5178516
SMURF1-CDK14chr798658221chr790741856523HLA-B15:20KWNQHYDLLSY0.97120.6522516
SMURF1-CDK14chr798658221chr790741856523HLA-B35:28KWNQHYDLLSY0.96470.6647516

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Potential FusionNeoAntigen Information of SMURF1-CDK14 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.
SMURF1-CDK14_98658221_90741856.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)
SMURF1-CDK14chr798658221chr790741856523DRB1-1457HYDLLSYVNHAEDLA924
SMURF1-CDK14chr798658221chr790741856523DRB1-1457QHYDLLSYVNHAEDL823
SMURF1-CDK14chr798658221chr790741856523DRB1-1512HYDLLSYVNHAEDLA924
SMURF1-CDK14chr798658221chr790741856523DRB1-1512QHYDLLSYVNHAEDL823
SMURF1-CDK14chr798658221chr790741856523DRB1-1512NQHYDLLSYVNHAED722
SMURF1-CDK14chr798658221chr790741856523DRB1-1518HYDLLSYVNHAEDLA924
SMURF1-CDK14chr798658221chr790741856523DRB1-1536HYDLLSYVNHAEDLA924

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Fusion breakpoint peptide structures of SMURF1-CDK14

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
10516WNQHYDLLSYVNHASMURF1CDK14chr798658221chr790741856523

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SMURF1-CDK14

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-B14:023BVN10516WNQHYDLLSYVNHA-5.61094-5.61094
HLA-A24:025HGA10516WNQHYDLLSYVNHA-8.4661-8.4661

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Vaccine Design for the FusionNeoAntigens of SMURF1-CDK14

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
SMURF1-CDK14chr798658221chr790741856514KWNQHYDLLAAAGTGGAACCAGCACTATGATCTGCT
SMURF1-CDK14chr798658221chr790741856516KWNQHYDLLSYAAAGTGGAACCAGCACTATGATCTGCTCAGCTA
SMURF1-CDK14chr798658221chr790741856616WNQHYDLLSYGTGGAACCAGCACTATGATCTGCTCAGCTA
SMURF1-CDK14chr798658221chr790741856716NQHYDLLSYGAACCAGCACTATGATCTGCTCAGCTA
SMURF1-CDK14chr798658221chr790741856816QHYDLLSYCCAGCACTATGATCTGCTCAGCTA
SMURF1-CDK14chr798658221chr790741856817QHYDLLSYVCCAGCACTATGATCTGCTCAGCTATGT
SMURF1-CDK14chr798658221chr790741856917HYDLLSYVGCACTATGATCTGCTCAGCTATGT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SMURF1-CDK14chr798658221chr790741856722NQHYDLLSYVNHAEDGAACCAGCACTATGATCTGCTCAGCTATGTGAACCATGCAGAGGA
SMURF1-CDK14chr798658221chr790741856823QHYDLLSYVNHAEDLCCAGCACTATGATCTGCTCAGCTATGTGAACCATGCAGAGGACCT
SMURF1-CDK14chr798658221chr790741856924HYDLLSYVNHAEDLAGCACTATGATCTGCTCAGCTATGTGAACCATGCAGAGGACCTGGC

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Information of the samples that have these potential fusion neoantigens of SMURF1-CDK14

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
STADSMURF1-CDK14chr798658221ENST00000361125chr790741856ENST00000265741TCGA-BR-8484

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Potential target of CAR-T therapy development for SMURF1-CDK14

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 SMURF1-CDK14

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 SMURF1-CDK14

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