FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

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

leaf

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

leaf

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

leaf

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

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

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

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:CERK-SCUBE1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CERK-SCUBE1
FusionPDB ID: 15964
FusionGDB2.0 ID: 15964
HgeneTgene
Gene symbol

CERK

SCUBE1

Gene ID

64781

80274

Gene nameceramide kinasesignal peptide, CUB domain and EGF like domain containing 1
SynonymsLK4|dA59H18.2|dA59H18.3|hCERK-
Cytomap

22q13.31

22q13.2

Type of geneprotein-codingprotein-coding
Descriptionceramide kinaseacylsphingosine kinaselipid kinase 4lipid kinase LK4signal peptide, CUB and EGF-like domain-containing protein 1signal peptide, CUB domain, EGF-like 1signal peptide-CUB domain-EGF-related 1
Modification date2020031320200313
UniProtAcc

Q49MI3

Main function of 5'-partner protein: FUNCTION: Has no detectable ceramide-kinase activity. Overexpression of CERKL protects cells from apoptosis in oxidative stress conditions. {ECO:0000269|PubMed:15708351, ECO:0000269|PubMed:19158957}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000216264, ENST00000541677, 
ENST00000471929, 
ENST00000470433, 
ENST00000290460, ENST00000360835, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 11 X 7=13869 X 7 X 9=567
# samples 189
** MAII scorelog2(18/1386*10)=-2.94485844580754
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/567*10)=-2.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CERK [Title/Abstract] AND SCUBE1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CERK [Title/Abstract] AND SCUBE1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CERK(47103740)-SCUBE1(43654341), # samples:1
Anticipated loss of major functional domain due to fusion event.CERK-SCUBE1 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.
CERK-SCUBE1 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.
CERK-SCUBE1 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.
CERK-SCUBE1 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
HgeneCERK

GO:0006672

ceramide metabolic process

19501188



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/chr22:47103740/chr22:43654341)
- 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 CERK (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 SCUBE1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000216264CERKchr2247103740-ENST00000360835SCUBE1chr2243654341-989982811331841023
ENST00000216264CERKchr2247103740-ENST00000290460SCUBE1chr2243654341-24148281131261382
ENST00000541677CERKchr2247103740-ENST00000360835SCUBE1chr2243654341-97817105893066825
ENST00000541677CERKchr2247103740-ENST00000290460SCUBE1chr2243654341-229671059616185

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
ENST00000216264ENST00000360835CERKchr2247103740-SCUBE1chr2243654341-0.0017819290.998218
ENST00000216264ENST00000290460CERKchr2247103740-SCUBE1chr2243654341-0.0224479880.97755194
ENST00000541677ENST00000360835CERKchr2247103740-SCUBE1chr2243654341-0.0030262550.99697375
ENST00000541677ENST00000290460CERKchr2247103740-SCUBE1chr2243654341-0.37035230.6296477

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

Top

Fusion Protein Breakpoint Sequences for CERK-SCUBE1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CERKchr2247103740SCUBE1chr224365434171040LVPSSLRIGIIPAVTCNYGNGGCQHS
CERKchr2247103740SCUBE1chr2243654341828238LVPSSLRIGIIPAVTCNYGNGGCQHS

Top

Potential FusionNeoAntigen Information of CERK-SCUBE1 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.
CERK-SCUBE1_47103740_43654341.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)
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:01IPAVTCNY0.99330.80521018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:08IPAVTCNY0.98780.76731018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:02LRIGIIPAV0.99980.8802514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:05LRIGIIPAV0.99980.9648514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:07LRIGIIPAV0.99980.7334514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:04LRIGIIPAV0.99980.8877514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B14:01LRIGIIPAV0.99860.9728514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B14:02LRIGIIPAV0.99860.9728514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B39:06LRIGIIPAV0.99830.9716514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B39:24LRIGIIPAV0.99820.8973514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B39:01LRIGIIPAV0.99620.9788514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:01GIIPAVTCNY0.99870.899818
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:22SLRIGIIPAV0.99410.6325414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:13SLRIGIIPAV0.98930.8044414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:25GIIPAVTCNY0.98690.9165818
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:27SLRIGIIPAV0.97230.7484414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:38SLRIGIIPAV0.95260.7974414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:07SLRIGIIPAV0.940.5247414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:04SLRIGIIPAV0.92090.81414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:21SLRIGIIPAV0.90930.7932414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:16SLRIGIIPAV0.90840.6499414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:11SLRIGIIPAV0.90660.7303414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:60SLRIGIIPAV0.90260.709414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:24SLRIGIIPAV0.90130.7107414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:30SLRIGIIPAV0.90130.7107414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:67SLRIGIIPAV0.90130.7107414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:35SLRIGIIPAV0.8940.7419414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:29SLRIGIIPAV0.86780.7115414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:04SLRIGIIPAV0.85150.8588414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:20SLRIGIIPAV0.83210.7158414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:17SLRIGIIPAV0.81650.7509414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:19SLRIGIIPAV0.73630.7634414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:14LRIGIIPAV0.99980.9379514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B73:01LRIGIIPAV0.9990.9736514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B39:09LRIGIIPAV0.9970.9497514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:05LRIGIIPAV0.99640.9831514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B39:12LRIGIIPAV0.99590.9803514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:27LRIGIIPAV0.99010.9803514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:03LRIGIIPAV0.98660.9686514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:95LRIGIIPAV0.98520.9254514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:13LRIGIIPAV0.96870.9753514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:29LRIGIIPAV0.9280.9773514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:46LRIGIIPAV0.87980.9656514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:10LRIGIIPAV0.85980.9854514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:80LRIGIIPAV0.85920.9816514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:67LRIGIIPAV0.85920.9816514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:19LRIGIIPAV0.83320.9262514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C12:16LRIGIIPAV0.00940.9794514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:07GIIPAVTCNY0.99540.6912818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:14SLRIGIIPAV0.93950.8594414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:01SLRIGIIPAV0.90130.7107414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B73:01SLRIGIIPAV0.87590.874414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:77IPAVTCNY0.99330.80521018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:23IPAVTCNY0.99280.74231018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:24IPAVTCNY0.99030.75891018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:17IPAVTCNY0.98860.61171018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:30IPAVTCNY0.98860.61171018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:11IPAVTCNY0.98220.82711018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:11IPAVTCNY0.94690.69441018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B35:43IPAVTCNY0.93670.70091018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B18:07IPAVTCNY0.80510.69511018
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:09LRIGIIPAV0.99990.9601514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:10LRIGIIPAV0.99980.9483514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:06LRIGIIPAV0.99980.895514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:08LRIGIIPAV0.99980.9319514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B39:31LRIGIIPAV0.9960.9791514
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:27IIPAVTCNY0.99460.7999918
CERK-SCUBE1chr2247103740chr2243654341828HLA-C06:08LRIGIIPAV0.99290.997514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:01LRIGIIPAV0.98780.8783514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:02LRIGIIPAV0.85920.9816514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C07:22LRIGIIPAV0.77540.9163514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C06:06LRIGIIPAV0.33320.994514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C06:02LRIGIIPAV0.07670.9974514
CERK-SCUBE1chr2247103740chr2243654341828HLA-C06:17LRIGIIPAV0.07670.9974514
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:03SLRIGIIPAV0.99890.7855414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:34GIIPAVTCNY0.99870.899818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:125GIIPAVTCNY0.99870.899818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:27GIIPAVTCNY0.99870.9049818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:33GIIPAVTCNY0.99870.899818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:50GIIPAVTCNY0.99830.9186818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:135GIIPAVTCNY0.99820.9159818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:35GIIPAVTCNY0.99530.8952818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B15:39GIIPAVTCNY0.98360.8646818
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:06SLRIGIIPAV0.93520.7925414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:09SLRIGIIPAV0.92490.9316414
CERK-SCUBE1chr2247103740chr2243654341828HLA-B27:08SLRIGIIPAV0.92270.8601414
CERK-SCUBE1chr2247103740chr2243654341828HLA-A02:06SLRIGIIPAV0.90930.7932414

Top

Potential FusionNeoAntigen Information of CERK-SCUBE1 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.

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)

Top

Fusion breakpoint peptide structures of CERK-SCUBE1

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
7934RIGIIPAVTCNYGNCERKSCUBE1chr2247103740chr2243654341828

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CERK-SCUBE1

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-B14:023BVN7934RIGIIPAVTCNYGN-7.9962-8.1096
HLA-B14:023BVN7934RIGIIPAVTCNYGN-5.70842-6.74372
HLA-B52:013W397934RIGIIPAVTCNYGN-6.83737-6.95077
HLA-B52:013W397934RIGIIPAVTCNYGN-4.4836-5.5189
HLA-A11:014UQ27934RIGIIPAVTCNYGN-10.0067-10.1201
HLA-A11:014UQ27934RIGIIPAVTCNYGN-9.03915-10.0745
HLA-A24:025HGA7934RIGIIPAVTCNYGN-6.56204-6.67544
HLA-A24:025HGA7934RIGIIPAVTCNYGN-5.42271-6.45801
HLA-B44:053DX87934RIGIIPAVTCNYGN-7.85648-8.89178
HLA-B44:053DX87934RIGIIPAVTCNYGN-5.3978-5.5112
HLA-A02:016TDR7934RIGIIPAVTCNYGN-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of CERK-SCUBE1

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
CERK-SCUBE1chr2247103740chr22436543411018IPAVTCNYTTCCCGCAGTAACCTGTAATTATG
CERK-SCUBE1chr2247103740chr2243654341414SLRIGIIPAVGCCTCCGGATTGGAATCATTCCCGCAGTAA
CERK-SCUBE1chr2247103740chr2243654341514LRIGIIPAVTCCGGATTGGAATCATTCCCGCAGTAA
CERK-SCUBE1chr2247103740chr2243654341818GIIPAVTCNYGAATCATTCCCGCAGTAACCTGTAATTATG
CERK-SCUBE1chr2247103740chr2243654341918IIPAVTCNYTCATTCCCGCAGTAACCTGTAATTATG

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

Top

Information of the samples that have these potential fusion neoantigens of CERK-SCUBE1

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
PRADCERK-SCUBE1chr2247103740ENST00000216264chr2243654341ENST00000290460TCGA-HC-A8D0-01A

Top

Potential target of CAR-T therapy development for CERK-SCUBE1

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

Top

Related Drugs to CERK-SCUBE1

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

Top

Related Diseases to CERK-SCUBE1

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