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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:PRDM6-NIPAL4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PRDM6-NIPAL4
FusionPDB ID: 68453
FusionGDB2.0 ID: 68453
HgeneTgene
Gene symbol

PRDM6

NIPAL4

Gene ID

93166

348938

Gene namePR/SET domain 6NIPA like domain containing 4
SynonymsKMT8C|PDA3|PRISMARCI6|ICHTHYIN|ICHYN
Cytomap

5q23.2

5q33.3

Type of geneprotein-codingprotein-coding
Descriptionputative histone-lysine N-methyltransferase PRDM6PR domain 6PR domain containing 6PR domain-containing protein 6PR-domain zinc finger protein 6magnesium transporter NIPA4NIPA-like protein 4non-imprinted in Prader-Willi/Angelman syndrome region protein 4
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000407847, ENST00000464424, 
ENST00000521390, ENST00000311946, 
ENST00000435489, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score1 X 1 X 1=12 X 1 X 1=2
# samples 11
** MAII scorelog2(1/1*10)=3.32192809488736log2(1/2*10)=2.32192809488736
Fusion gene context

PubMed: PRDM6 [Title/Abstract] AND NIPAL4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PRDM6 [Title/Abstract] AND NIPAL4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PRDM6(122495332)-NIPAL4(156890102), # samples:3
Anticipated loss of major functional domain due to fusion event.PRDM6-NIPAL4 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.
PRDM6-NIPAL4 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.
PRDM6-NIPAL4 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.
PRDM6-NIPAL4 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


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/chr5:122495332/chr5:156890102)
- 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 PRDM6 (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 NIPAL4 (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)
ENST00000407847PRDM6chr5122495332+ENST00000435489NIPAL4chr5156890102+282815672462687813
ENST00000407847PRDM6chr5122495332+ENST00000311946NIPAL4chr5156890102+450215672462744832

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
ENST00000407847ENST00000435489PRDM6chr5122495332+NIPAL4chr5156890102+0.0139648740.9860351
ENST00000407847ENST00000311946PRDM6chr5122495332+NIPAL4chr5156890102+0.0093528640.99064714

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 PRDM6-NIPAL4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PRDM6chr5122495332NIPAL4chr51568901021567441GIPLQCIAQDENCSLLHLYCSSQEVL

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Potential FusionNeoAntigen Information of PRDM6-NIPAL4 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.
PRDM6-NIPAL4_122495332_156890102.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)
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:13AQDENCSL0.83420.9064715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B35:03IAQDENCSL0.860.7843615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-A02:21AQDENCSLL0.69910.535716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:13AQDENCSLL0.65010.9288716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B35:04IAQDENCSL0.63270.8264615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B35:02IAQDENCSL0.63270.8264615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B38:01AQDENCSLL0.60470.925716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B38:02AQDENCSLL0.58020.9364716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B13:01AQDENCSLL0.37170.8555716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B47:01AQDENCSLL0.24760.5376716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B44:03DENCSLLHLY0.99670.8471919
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B13:01AQDENCSLLHL0.98680.7532718
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C05:09AQDENCSL10.9346715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:15AQDENCSL0.99990.9474715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:08AQDENCSL0.94350.8009715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C05:09AQDENCSLL0.99970.9261716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:10AQDENCSLL0.99950.7339716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:07AQDENCSLL0.99950.7524716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:15AQDENCSLL0.99930.9437716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:19IAQDENCSL0.99920.9798615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:07IAQDENCSL0.99870.9458615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:08IAQDENCSL0.99850.84615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:15IAQDENCSL0.99550.9733615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:06IAQDENCSL0.98850.829615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:04IAQDENCSL0.97350.9628615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:13IAQDENCSL0.97350.9628615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:06AQDENCSLL0.95830.7738716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:14AQDENCSLL0.90080.7847716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:03AQDENCSLL0.84490.969716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:04AQDENCSLL0.840.9372716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:13AQDENCSLL0.840.9372716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:03IAQDENCSL0.76740.9818615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:09AQDENCSLL0.73790.594716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B35:12IAQDENCSL0.63270.8264615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:08AQDENCSLL0.61560.7923716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:05AQDENCSLL0.58850.8821716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C05:09IAQDENCSLL0.99960.9427616
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:15IAQDENCSLL0.99870.9694616
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:03IAQDENCSLL0.77450.9849616
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:08AQDENCSLLHL0.98020.7801718
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C05:01AQDENCSL10.9346715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:02AQDENCSL0.99990.9474715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:02AQDENCSL0.94890.9025715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:11AQDENCSL0.9090.7328715
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C05:01AQDENCSLL0.99970.9261716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:03AQDENCSLL0.99960.8061716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:01AQDENCSLL0.99950.7524716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:02AQDENCSLL0.99930.9437716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:03IAQDENCSL0.99920.9797615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:04IAQDENCSL0.99920.9797615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C01:03AQDENCSLL0.99920.9212716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C18:01AQDENCSLL0.99920.771716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:05IAQDENCSL0.99820.9079615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:17IAQDENCSL0.99820.9516615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:03IAQDENCSL0.9980.8521615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:02IAQDENCSL0.99550.9733615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C03:06IAQDENCSL0.98740.9802615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B35:13IAQDENCSL0.84930.7923615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:01AQDENCSLL0.84490.969716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C16:01IAQDENCSL0.84250.965615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:01IAQDENCSL0.76740.9818615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:02AQDENCSLL0.76440.9254716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B07:13IAQDENCSL0.70290.74615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-A02:06AQDENCSLL0.69910.535716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B35:09IAQDENCSL0.63270.8264615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B18:04ENCSLLHLY0.62170.56671019
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B38:05AQDENCSLL0.60470.925716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B39:11AQDENCSLL0.58410.7285716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C07:04AQDENCSLL0.53840.9214716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B18:11DENCSLLHL0.52040.5161918
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B15:73AQDENCSLL0.40090.9031716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C17:01IAQDENCSL0.34560.8656615
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B15:30AQDENCSLL0.33940.8331716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B15:09AQDENCSLL0.18130.6766716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B07:13AQDENCSLL0.02880.7753716
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C04:03IAQDENCSLL0.99960.8511616
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C05:01IAQDENCSLL0.99960.9427616
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:02IAQDENCSLL0.99870.9694616
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B44:26DENCSLLHLY0.99670.8471919
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B44:13DENCSLLHLY0.99670.8471919
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-B44:07DENCSLLHLY0.99670.8471919
PRDM6-NIPAL4chr5122495332chr51568901021567HLA-C08:01IAQDENCSLL0.77450.9849616

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Potential FusionNeoAntigen Information of PRDM6-NIPAL4 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)

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Fusion breakpoint peptide structures of PRDM6-NIPAL4

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
3597IAQDENCSLLHLYCPRDM6NIPAL4chr5122495332chr51568901021567

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PRDM6-NIPAL4

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-B14:023BVN3597IAQDENCSLLHLYC-6.18902-6.30242
HLA-B14:023BVN3597IAQDENCSLLHLYC-5.51674-6.55204
HLA-B52:013W393597IAQDENCSLLHLYC-6.26372-6.37712
HLA-B52:013W393597IAQDENCSLLHLYC-2.88933-3.92463
HLA-A11:014UQ23597IAQDENCSLLHLYC-8.95966-9.99496
HLA-A24:025HGA3597IAQDENCSLLHLYC-7.97421-8.08761
HLA-A24:025HGA3597IAQDENCSLLHLYC-4.46014-5.49544
HLA-B44:053DX83597IAQDENCSLLHLYC-4.21738-4.33078
HLA-B44:053DX83597IAQDENCSLLHLYC-3.79801-4.83331
HLA-A02:016TDR3597IAQDENCSLLHLYC-6.07498-7.11028

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Vaccine Design for the FusionNeoAntigens of PRDM6-NIPAL4

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
PRDM6-NIPAL4chr5122495332chr51568901021019ENCSLLHLYATGAAAACTGTTCCCTGCTCCACCTCT
PRDM6-NIPAL4chr5122495332chr5156890102615IAQDENCSLGCATTGCCCAGGATGAAAACTGTTCCC
PRDM6-NIPAL4chr5122495332chr5156890102616IAQDENCSLLGCATTGCCCAGGATGAAAACTGTTCCCTGC
PRDM6-NIPAL4chr5122495332chr5156890102715AQDENCSLTTGCCCAGGATGAAAACTGTTCCC
PRDM6-NIPAL4chr5122495332chr5156890102716AQDENCSLLTTGCCCAGGATGAAAACTGTTCCCTGC
PRDM6-NIPAL4chr5122495332chr5156890102718AQDENCSLLHLTTGCCCAGGATGAAAACTGTTCCCTGCTCCACC
PRDM6-NIPAL4chr5122495332chr5156890102918DENCSLLHLAGGATGAAAACTGTTCCCTGCTCCACC
PRDM6-NIPAL4chr5122495332chr5156890102919DENCSLLHLYAGGATGAAAACTGTTCCCTGCTCCACCTCT

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

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Information of the samples that have these potential fusion neoantigens of PRDM6-NIPAL4

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
KIRCPRDM6-NIPAL4chr5122495332ENST00000407847chr5156890102ENST00000311946TCGA-BP-4986-01A

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Potential target of CAR-T therapy development for PRDM6-NIPAL4

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
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606118_1380467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606165_1850467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606187_2070467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606216_2360467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606258_2780467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606286_3060467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606324_3440467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606356_3760467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000031194606387_4070467.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905118_1380448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905165_1850448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905187_2070448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905216_2360448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905258_2780448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905286_3060448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905324_3440448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905356_3760448.0TransmembraneHelical
TgeneNIPAL4chr5:122495332chr5:156890102ENST0000043548905387_4070448.0TransmembraneHelical

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 PRDM6-NIPAL4

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 PRDM6-NIPAL4

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