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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:CABLES1-FTO

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CABLES1-FTO
FusionPDB ID: 12246
FusionGDB2.0 ID: 12246
HgeneTgene
Gene symbol

CABLES1

FTO

Gene ID

91768

79068

Gene nameCdk5 and Abl enzyme substrate 1FTO alpha-ketoglutarate dependent dioxygenase
SynonymsCABL1|CABLES|HsT2563|IK3-1ALKBH9|BMIQ14|GDFD
Cytomap

18q11.2

16q12.2

Type of geneprotein-codingprotein-coding
DescriptionCDK5 and ABL1 enzyme substrate 1interactor with CDK3 1alpha-ketoglutarate-dependent dioxygenase FTOAlkB homolog 9U6 small nuclear RNA (2'-O-methyladenosine-N(6)-)-demethylase FTOU6 small nuclear RNA N(6)-methyladenosine-demethylase FTOfat mass and obesity associatedfat mass and obesity-associated protei
Modification date2020031320200329
UniProtAcc

Q8TDN4

Main function of 5'-partner protein: FUNCTION: Cyclin-dependent kinase binding protein. Enhances cyclin-dependent kinase tyrosine phosphorylation by nonreceptor tyrosine kinases, such as that of CDK5 by activated ABL1, which leads to increased CDK5 activity and is critical for neuronal development, and that of CDK2 by WEE1, which leads to decreased CDK2 activity and growth inhibition. Positively affects neuronal outgrowth. Plays a role as a regulator for p53/p73-induced cell death (By similarity). {ECO:0000250}.

Q9C0B1

Main function of 5'-partner protein: FUNCTION: RNA demethylase that mediates oxidative demethylation of different RNA species, such as mRNAs, tRNAs and snRNAs, and acts as a regulator of fat mass, adipogenesis and energy homeostasis (PubMed:22002720, PubMed:26458103, PubMed:28002401, PubMed:30197295, PubMed:26457839, PubMed:25452335). Specifically demethylates N(6)-methyladenosine (m6A) RNA, the most prevalent internal modification of messenger RNA (mRNA) in higher eukaryotes (PubMed:22002720, PubMed:26458103, PubMed:30197295, PubMed:26457839, PubMed:25452335). M6A demethylation by FTO affects mRNA expression and stability (PubMed:30197295). Also able to demethylate m6A in U6 small nuclear RNA (snRNA) (PubMed:30197295). Mediates demethylation of N(6),2'-O-dimethyladenosine cap (m6A(m)), by demethylating the N(6)-methyladenosine at the second transcribed position of mRNAs and U6 snRNA (PubMed:28002401, PubMed:30197295). Demethylation of m6A(m) in the 5'-cap by FTO affects mRNA stability by promoting susceptibility to decapping (PubMed:28002401). Also acts as a tRNA demethylase by removing N(1)-methyladenine from various tRNAs (PubMed:30197295). Has no activity towards 1-methylguanine (PubMed:20376003). Has no detectable activity towards double-stranded DNA (PubMed:20376003). Also able to repair alkylated DNA and RNA by oxidative demethylation: demethylates single-stranded RNA containing 3-methyluracil, single-stranded DNA containing 3-methylthymine and has low demethylase activity towards single-stranded DNA containing 1-methyladenine or 3-methylcytosine (PubMed:18775698, PubMed:20376003). Ability to repair alkylated DNA and RNA is however unsure in vivo (PubMed:18775698, PubMed:20376003). Involved in the regulation of fat mass, adipogenesis and body weight, thereby contributing to the regulation of body size and body fat accumulation (PubMed:18775698, PubMed:20376003). Involved in the regulation of thermogenesis and the control of adipocyte differentiation into brown or white fat cells (PubMed:26287746). Regulates activity of the dopaminergic midbrain circuitry via its ability to demethylate m6A in mRNAs (By similarity). Plays an oncogenic role in a number of acute myeloid leukemias by enhancing leukemic oncogene-mediated cell transformation: acts by mediating m6A demethylation of target transcripts such as MYC, CEBPA, ASB2 and RARA, leading to promote their expression (PubMed:28017614, PubMed:29249359). {ECO:0000250|UniProtKB:Q8BGW1, ECO:0000269|PubMed:18775698, ECO:0000269|PubMed:20376003, ECO:0000269|PubMed:22002720, ECO:0000269|PubMed:25452335, ECO:0000269|PubMed:26287746, ECO:0000269|PubMed:26457839, ECO:0000269|PubMed:26458103, ECO:0000269|PubMed:28002401, ECO:0000269|PubMed:28017614, ECO:0000269|PubMed:29249359, ECO:0000269|PubMed:30197295}.
Ensembl transtripts involved in fusion geneENST idsENST00000256925, ENST00000400473, 
ENST00000420687, ENST00000585061, 
ENST00000472835, ENST00000471389, 
ENST00000394647, ENST00000431610, 
ENST00000460382, ENST00000463855, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 13 X 3=62412 X 10 X 7=840
# samples 2115
** MAII scorelog2(21/624*10)=-1.57115670119613
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/840*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CABLES1 [Title/Abstract] AND FTO [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CABLES1 [Title/Abstract] AND FTO [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CABLES1(20716571)-FTO(54145674), # samples:3
Anticipated loss of major functional domain due to fusion event.CABLES1-FTO 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.
CABLES1-FTO 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.
CABLES1-FTO 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.
CABLES1-FTO 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.
CABLES1-FTO seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
CABLES1-FTO seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
TgeneFTO

GO:0006307

DNA dealkylation involved in DNA repair

18775698|20376003

TgeneFTO

GO:0035552

oxidative single-stranded DNA demethylation

18775698|20376003

TgeneFTO

GO:0035553

oxidative single-stranded RNA demethylation

18775698|22002720|25452335|26457839|28002401|30197295

TgeneFTO

GO:0042245

RNA repair

18775698

TgeneFTO

GO:0061157

mRNA destabilization

28002401|30197295

TgeneFTO

GO:0070989

oxidative demethylation

18775698

TgeneFTO

GO:0080111

DNA demethylation

18775698



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/chr18:20716571/chr16:54145674)
- 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 CABLES1 (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 FTO (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)
ENST00000256925CABLES1chr1820716571+ENST00000394647FTOchr1654145674+11718450998332
ENST00000256925CABLES1chr1820716571+ENST00000431610FTOchr1654145674+12228450998332
ENST00000256925CABLES1chr1820716571+ENST00000460382FTOchr1654145674+20718450998332
ENST00000256925CABLES1chr1820716571+ENST00000463855FTOchr1654145674+35478450998332
ENST00000256925CABLES1chr1820716571+ENST00000394647FTOchr1654145673+11718450998332
ENST00000256925CABLES1chr1820716571+ENST00000431610FTOchr1654145673+12228450998332
ENST00000256925CABLES1chr1820716571+ENST00000460382FTOchr1654145673+20718450998332
ENST00000256925CABLES1chr1820716571+ENST00000463855FTOchr1654145673+35478450998332
ENST00000256925CABLES1chr1820716570+ENST00000394647FTOchr1654145673+11718450998332
ENST00000256925CABLES1chr1820716570+ENST00000431610FTOchr1654145673+12228450998332
ENST00000256925CABLES1chr1820716570+ENST00000460382FTOchr1654145673+20718450998332
ENST00000256925CABLES1chr1820716570+ENST00000463855FTOchr1654145673+35478450998332

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
ENST00000256925ENST00000394647CABLES1chr1820716571+FTOchr1654145674+0.0175647850.9824353
ENST00000256925ENST00000431610CABLES1chr1820716571+FTOchr1654145674+0.033758830.9662411
ENST00000256925ENST00000460382CABLES1chr1820716571+FTOchr1654145674+0.212011080.78798884
ENST00000256925ENST00000463855CABLES1chr1820716571+FTOchr1654145674+0.161612510.83838755
ENST00000256925ENST00000394647CABLES1chr1820716571+FTOchr1654145673+0.0175647850.9824353
ENST00000256925ENST00000431610CABLES1chr1820716571+FTOchr1654145673+0.033758830.9662411
ENST00000256925ENST00000460382CABLES1chr1820716571+FTOchr1654145673+0.212011080.78798884
ENST00000256925ENST00000463855CABLES1chr1820716571+FTOchr1654145673+0.161612510.83838755
ENST00000256925ENST00000394647CABLES1chr1820716570+FTOchr1654145673+0.0175647850.9824353
ENST00000256925ENST00000431610CABLES1chr1820716570+FTOchr1654145673+0.033758830.9662411
ENST00000256925ENST00000460382CABLES1chr1820716570+FTOchr1654145673+0.212011080.78798884
ENST00000256925ENST00000463855CABLES1chr1820716570+FTOchr1654145673+0.161612510.83838755

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 CABLES1-FTO

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CABLES1chr1820716570FTOchr1654145673845280QGGSTSAFEQLQRSRCQSRIARTLPA
CABLES1chr1820716571FTOchr1654145673845280QGGSTSAFEQLQRSRCQSRIARTLPA
CABLES1chr1820716571FTOchr1654145674845280QGGSTSAFEQLQRSRCQSRIARTLPA

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Potential FusionNeoAntigen Information of CABLES1-FTO 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.
CABLES1-FTO_20716570_54145673.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)
CABLES1-FTOchr1820716570chr1654145673845HLA-A30:08RSRCQSRIA0.98670.70411221
CABLES1-FTOchr1820716570chr1654145673845HLA-A30:01RSRCQSRIA0.98720.84831221

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Potential FusionNeoAntigen Information of CABLES1-FTO 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.
CABLES1-FTO_20716570_54145673.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)
CABLES1-FTOchr1820716570chr1654145673845DRB1-1101TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1105TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1108TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1109TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1110TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1112TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1115TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1124TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1127TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1128TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1129TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1132TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1133TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1137TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1139TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1149TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1151TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1161TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1162TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1166TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1172TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1172STSAFEQLQRSRCQS318
CABLES1-FTOchr1820716570chr1654145673845DRB1-1174TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1175TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1180TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1181TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1187TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1190TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1191TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1193TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1194TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1195TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1196TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1305TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1307TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1314TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1326TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1350TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1356TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1360TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1362TSAFEQLQRSRCQSR419
CABLES1-FTOchr1820716570chr1654145673845DRB1-1427TSAFEQLQRSRCQSR419

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Fusion breakpoint peptide structures of CABLES1-FTO

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
188AFEQLQRSRCQSRICABLES1FTOchr1820716570chr1654145673845

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CABLES1-FTO

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-B14:023BVN188AFEQLQRSRCQSRI-7.64441-7.75781
HLA-B14:023BVN188AFEQLQRSRCQSRI-5.94416-6.97946
HLA-B52:013W39188AFEQLQRSRCQSRI-6.36431-6.47771
HLA-B52:013W39188AFEQLQRSRCQSRI-5.79427-6.82957
HLA-A24:025HGA188AFEQLQRSRCQSRI-7.67647-8.71177
HLA-A24:025HGA188AFEQLQRSRCQSRI-6.37962-6.49302
HLA-B44:053DX8188AFEQLQRSRCQSRI-7.31799-7.43139
HLA-B44:053DX8188AFEQLQRSRCQSRI-5.80727-6.84257

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Vaccine Design for the FusionNeoAntigens of CABLES1-FTO

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
CABLES1-FTOchr1820716570chr16541456731221RSRCQSRIACCGGTGCCAGTCACGAATTGCCCGAAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CABLES1-FTOchr1820716570chr1654145673318STSAFEQLQRSRCQSCAGCGCCTTCGAGCAGCTGCAGAGGTCCCGGTGCCAGTCACGAAT
CABLES1-FTOchr1820716570chr1654145673419TSAFEQLQRSRCQSRCGCCTTCGAGCAGCTGCAGAGGTCCCGGTGCCAGTCACGAATTGC

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Information of the samples that have these potential fusion neoantigens of CABLES1-FTO

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
BRCACABLES1-FTOchr1820716570ENST00000256925chr1654145673ENST00000394647TCGA-S3-AA12-01A

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Potential target of CAR-T therapy development for CABLES1-FTO

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 CABLES1-FTO

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 CABLES1-FTO

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