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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:DNAH1-PRKCD

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: DNAH1-PRKCD
FusionPDB ID: 23355
FusionGDB2.0 ID: 23355
HgeneTgene
Gene symbol

DNAH1

PRKCD

Gene ID

25981

5580

Gene namedynein axonemal heavy chain 1protein kinase C delta
SynonymsCILD37|DNAHC1|HDHC7|HL-11|HL11|HSRF-1|SPGF18|XLHSRF-1ALPS3|CVID9|MAY1|PKCD|nPKC-delta
Cytomap

3p21.1

3p21.1

Type of geneprotein-codingprotein-coding
Descriptiondynein heavy chain 1, axonemalaxonemal beta dynein heavy chain 1ciliary dynein heavy chain 1dynein, axonemal, heavy polypeptide 1heat shock regulated protein 1testicular tissue protein Li 60protein kinase C delta typeprotein kinase C delta VIIItyrosine-protein kinase PRKCD
Modification date2020032020200313
UniProtAcc

Q9UFH2

Main function of 5'-partner protein: FUNCTION: Force generating protein component of the outer dynein arms (ODAs) in the sperm flagellum. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (Probable). Plays a major role in sperm motility, implicated in sperm flagellar assembly and beating (PubMed:31178125). {ECO:0000269|PubMed:31178125, ECO:0000305|PubMed:31178125}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000420323, ENST00000466628, 
ENST00000477794, ENST00000330452, 
ENST00000394729, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 4=1447 X 7 X 5=245
# samples 67
** MAII scorelog2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/245*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: DNAH1 [Title/Abstract] AND PRKCD [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: DNAH1 [Title/Abstract] AND PRKCD [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DNAH1(52391751)-PRKCD(53221356), # samples:2
Anticipated loss of major functional domain due to fusion event.DNAH1-PRKCD 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.
DNAH1-PRKCD 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.
DNAH1-PRKCD 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.
DNAH1-PRKCD 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
HgeneDNAH1

GO:0036159

inner dynein arm assembly

24360805

TgenePRKCD

GO:0006468

protein phosphorylation

10713049|16611985

TgenePRKCD

GO:0006915

apoptotic process

10770950

TgenePRKCD

GO:0016572

histone phosphorylation

19059439

TgenePRKCD

GO:0018105

peptidyl-serine phosphorylation

18285462

TgenePRKCD

GO:0018107

peptidyl-threonine phosphorylation

10770950

TgenePRKCD

GO:0032147

activation of protein kinase activity

10713049

TgenePRKCD

GO:0042119

neutrophil activation

10770950

TgenePRKCD

GO:0070301

cellular response to hydrogen peroxide

10713049

TgenePRKCD

GO:0071447

cellular response to hydroperoxide

19059439

TgenePRKCD

GO:1904385

cellular response to angiotensin

18285462



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/chr3:52391751/chr3:53221356)
- 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 DNAH1 (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 PRKCD (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)
ENST00000420323DNAH1chr352391751+ENST00000394729PRKCDchr353221356+5371424118649191577
ENST00000420323DNAH1chr352391751+ENST00000330452PRKCDchr353221356+5208424118649191577

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
ENST00000420323ENST00000394729DNAH1chr352391751+PRKCDchr353221356+0.0025835720.9974164
ENST00000420323ENST00000330452DNAH1chr352391751+PRKCDchr353221356+0.0032298340.99677014

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 DNAH1-PRKCD

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
DNAH1chr352391751PRKCDchr35322135642411350GLSEYLETKRSAFPRFYAAEIMCGLQ

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Potential FusionNeoAntigen Information of DNAH1-PRKCD 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.
DNAH1-PRKCD_52391751_53221356.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)
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:02KRSAFPRFY0.99960.8144817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:05KRSAFPRFY0.99950.9588817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:04KRSAFPRFY0.99940.8097817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B14:01SAFPRFYAA0.99710.64631019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B14:02SAFPRFYAA0.99710.64631019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B08:09SAFPRFYAA0.99670.53111019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A30:08RSAFPRFYA0.99050.7501918
DNAH1-PRKCDchr352391751chr3532213564241HLA-A66:01ETKRSAFPR0.98830.6268615
DNAH1-PRKCDchr352391751chr3532213564241HLA-B39:06SAFPRFYAA0.98250.74141019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B52:01SAFPRFYAA0.97950.71471019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A30:08SAFPRFYAA0.97160.71961019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A02:21SAFPRFYAA0.90290.70641019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A26:03ETKRSAFPR0.74180.6392615
DNAH1-PRKCDchr352391751chr3532213564241HLA-B15:03TKRSAFPRF0.24450.7437716
DNAH1-PRKCDchr352391751chr3532213564241HLA-A30:08RSAFPRFYAA0.99310.7711919
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:03FPRFYAAEIM0.98180.84271222
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:04FPRFYAAEIM0.87910.90391222
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:02FPRFYAAEIM0.87910.90391222
DNAH1-PRKCDchr352391751chr3532213564241HLA-C15:04RSAFPRFY0.99460.8324917
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:14KRSAFPRFY0.99850.8474817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C06:03SAFPRFYAA0.99790.99131019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C12:04SAFPRFYAA0.99780.99221019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:03KRSAFPRFY0.9970.9633817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:95KRSAFPRFY0.99670.7633817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C12:12SAFPRFYAA0.99620.92711019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C03:19SAFPRFYAA0.99120.96141019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C03:08SAFPRFYAA0.9890.84071019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B51:07FPRFYAAEI0.98210.61221
DNAH1-PRKCDchr352391751chr3532213564241HLA-C08:13SAFPRFYAA0.98120.93131019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C08:04SAFPRFYAA0.98120.93131019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:27KRSAFPRFY0.97950.9578817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B73:01SAFPRFYAA0.97060.52741019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B51:07SAFPRFYAA0.97050.54961019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:05KRSAFPRFY0.96290.9641817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C08:03SAFPRFYAA0.94880.97071019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A31:01ETKRSAFPR0.93620.5947615
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:19KRSAFPRFY0.88910.732817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B14:03SAFPRFYAA0.86180.73261019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B15:04SAFPRFYAA0.85080.88971019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:80KRSAFPRFY0.80820.9294817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:67KRSAFPRFY0.80820.9294817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:10KRSAFPRFY0.80320.953817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:46KRSAFPRFY0.79480.8725817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B39:10FPRFYAAEI0.75340.79491221
DNAH1-PRKCDchr352391751chr3532213564241HLA-C03:14SAFPRFYAA0.70120.93651019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C12:16KRSAFPRFY0.01510.9455817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:12FPRFYAAEIM0.87910.90391222
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:14KRSAFPRFYAA0.99990.8283819
DNAH1-PRKCDchr352391751chr3532213564241HLA-B73:01KRSAFPRFYAA0.99860.6245819
DNAH1-PRKCDchr352391751chr3532213564241HLA-C15:09RSAFPRFY0.99460.8324917
DNAH1-PRKCDchr352391751chr3532213564241HLA-C16:02RSAFPRFY0.94110.9895917
DNAH1-PRKCDchr352391751chr3532213564241HLA-C16:01RSAFPRFY0.78070.9607917
DNAH1-PRKCDchr352391751chr3532213564241HLA-C15:02SAFPRFYAA0.99950.76941019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:08KRSAFPRFY0.99950.8726817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:10KRSAFPRFY0.99930.9201817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C03:05SAFPRFYAA0.9980.92621019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:01KRSAFPRFY0.99740.7297817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C03:17SAFPRFYAA0.9970.96491019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C16:02SAFPRFYAA0.99660.98981019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C16:04SAFPRFYAA0.99610.98131019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C12:03SAFPRFYAA0.99580.97921019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A30:01RSAFPRFYA0.99150.8497918
DNAH1-PRKCDchr352391751chr3532213564241HLA-A68:02SAFPRFYAA0.98860.52531019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A69:01SAFPRFYAA0.98510.74351019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B27:09KRSAFPRFY0.98380.9468817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C16:01SAFPRFYAA0.98190.97611019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B08:12SAFPRFYAA0.97220.67771019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A30:01SAFPRFYAA0.97130.85511019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C08:01SAFPRFYAA0.94880.97071019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:17KRSAFPRFY0.93740.9436817
DNAH1-PRKCDchr352391751chr3532213564241HLA-A02:06SAFPRFYAA0.90290.70641019
DNAH1-PRKCDchr352391751chr3532213564241HLA-A02:14SAFPRFYAA0.90250.64011019
DNAH1-PRKCDchr352391751chr3532213564241HLA-C12:02SAFPRFYAA0.87730.96821019
DNAH1-PRKCDchr352391751chr3532213564241HLA-B67:01FPRFYAAEI0.85930.68171221
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:22KRSAFPRFY0.81170.7266817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:02KRSAFPRFY0.80820.9294817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C06:08KRSAFPRFY0.41570.9835817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B15:68TKRSAFPRF0.06470.6142716
DNAH1-PRKCDchr352391751chr3532213564241HLA-B15:54TKRSAFPRF0.02990.8395716
DNAH1-PRKCDchr352391751chr3532213564241HLA-C06:06KRSAFPRFY0.02710.9876817
DNAH1-PRKCDchr352391751chr3532213564241HLA-B15:68KRSAFPRFY0.00570.6554817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C06:17KRSAFPRFY0.00220.9917817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C06:02KRSAFPRFY0.00220.9917817
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:01TKRSAFPRFY0.9920.6768717
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:30FPRFYAAEIM0.9750.72411222
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:17FPRFYAAEIM0.9750.72411222
DNAH1-PRKCDchr352391751chr3532213564241HLA-C07:22TKRSAFPRFY0.92610.696717
DNAH1-PRKCDchr352391751chr3532213564241HLA-A25:01ETKRSAFPRF0.90890.9212616
DNAH1-PRKCDchr352391751chr3532213564241HLA-B35:09FPRFYAAEIM0.87910.90391222

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Potential FusionNeoAntigen Information of DNAH1-PRKCD 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.
DNAH1-PRKCD_52391751_53221356.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)
DNAH1-PRKCDchr352391751chr3532213564241DRB1-1407GLSEYLETKRSAFPR015
DNAH1-PRKCDchr352391751chr3532213564241DRB1-1407LSEYLETKRSAFPRF116
DNAH1-PRKCDchr352391751chr3532213564241DRB1-1468GLSEYLETKRSAFPR015
DNAH1-PRKCDchr352391751chr3532213564241DRB1-1468LSEYLETKRSAFPRF116

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Fusion breakpoint peptide structures of DNAH1-PRKCD

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
2173ETKRSAFPRFYAAEDNAH1PRKCDchr352391751chr3532213564241

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of DNAH1-PRKCD

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-B14:023BVN2173ETKRSAFPRFYAAE-7.15543-7.26883
HLA-B14:023BVN2173ETKRSAFPRFYAAE-4.77435-5.80965
HLA-B52:013W392173ETKRSAFPRFYAAE-6.80875-6.92215
HLA-B52:013W392173ETKRSAFPRFYAAE-4.20386-5.23916
HLA-A11:014UQ22173ETKRSAFPRFYAAE-7.5194-8.5547
HLA-A11:014UQ22173ETKRSAFPRFYAAE-6.9601-7.0735
HLA-A24:025HGA2173ETKRSAFPRFYAAE-7.52403-7.63743
HLA-A24:025HGA2173ETKRSAFPRFYAAE-5.82433-6.85963
HLA-B27:056PYJ2173ETKRSAFPRFYAAE-3.28285-4.31815
HLA-B44:053DX82173ETKRSAFPRFYAAE-5.91172-6.94702
HLA-B44:053DX82173ETKRSAFPRFYAAE-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of DNAH1-PRKCD

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
DNAH1-PRKCDchr352391751chr3532213561019SAFPRFYAACTTCCCCAGGTTTTATGCCGCTGAGAT
DNAH1-PRKCDchr352391751chr3532213561221FPRFYAAEICAGGTTTTATGCCGCTGAGATAATGTG
DNAH1-PRKCDchr352391751chr3532213561222FPRFYAAEIMCAGGTTTTATGCCGCTGAGATAATGTGTGG
DNAH1-PRKCDchr352391751chr353221356615ETKRSAFPRCAAGAGGAGCGCCTTCCCCAGGTTTTA
DNAH1-PRKCDchr352391751chr353221356616ETKRSAFPRFCAAGAGGAGCGCCTTCCCCAGGTTTTATGC
DNAH1-PRKCDchr352391751chr353221356716TKRSAFPRFGAGGAGCGCCTTCCCCAGGTTTTATGC
DNAH1-PRKCDchr352391751chr353221356717TKRSAFPRFYGAGGAGCGCCTTCCCCAGGTTTTATGCCGC
DNAH1-PRKCDchr352391751chr353221356817KRSAFPRFYGAGCGCCTTCCCCAGGTTTTATGCCGC
DNAH1-PRKCDchr352391751chr353221356819KRSAFPRFYAAGAGCGCCTTCCCCAGGTTTTATGCCGCTGAGAT
DNAH1-PRKCDchr352391751chr353221356917RSAFPRFYCGCCTTCCCCAGGTTTTATGCCGC
DNAH1-PRKCDchr352391751chr353221356918RSAFPRFYACGCCTTCCCCAGGTTTTATGCCGCTGA
DNAH1-PRKCDchr352391751chr353221356919RSAFPRFYAACGCCTTCCCCAGGTTTTATGCCGCTGAGAT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
DNAH1-PRKCDchr352391751chr353221356015GLSEYLETKRSAFPRCAGCGAGTATCTGGAGACCAAGAGGAGCGCCTTCCCCAGGTTTTA
DNAH1-PRKCDchr352391751chr353221356116LSEYLETKRSAFPRFCGAGTATCTGGAGACCAAGAGGAGCGCCTTCCCCAGGTTTTATGC

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Information of the samples that have these potential fusion neoantigens of DNAH1-PRKCD

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
OVDNAH1-PRKCDchr352391751ENST00000420323chr353221356ENST00000330452TCGA-24-1603-01A

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Potential target of CAR-T therapy development for DNAH1-PRKCD

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 DNAH1-PRKCD

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 DNAH1-PRKCD

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