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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:PSMD3-CDK12

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PSMD3-CDK12
FusionPDB ID: 69692
FusionGDB2.0 ID: 69692
HgeneTgene
Gene symbol

PSMD3

CDK12

Gene ID

5709

51755

Gene nameproteasome 26S subunit, non-ATPase 3cyclin dependent kinase 12
SynonymsP58|RPN3|S3|TSTA2CRK7|CRKR|CRKRS
Cytomap

17q21.1

17q12

Type of geneprotein-codingprotein-coding
Description26S proteasome non-ATPase regulatory subunit 326S proteasome regulatory subunit RPN326S proteasome regulatory subunit S3proteasome (prosome, macropain) 26S subunit, non-ATPase, 3proteasome subunit p58tissue specific transplantation antigen 2cyclin-dependent kinase 12CDC2-related protein kinase 7Cdc2-related kinase, arginine/serine-richcell division cycle 2-related protein kinase 7cell division protein kinase 12
Modification date2020031320200313
UniProtAcc.

Q9NYV4

Main function of 5'-partner protein: FUNCTION: Cyclin-dependent kinase that phosphorylates the C-terminal domain (CTD) of the large subunit of RNA polymerase II (POLR2A), thereby acting as a key regulator of transcription elongation. Regulates the expression of genes involved in DNA repair and is required for the maintenance of genomic stability. Preferentially phosphorylates 'Ser-5' in CTD repeats that are already phosphorylated at 'Ser-7', but can also phosphorylate 'Ser-2'. Required for RNA splicing, possibly by phosphorylating SRSF1/SF2. Involved in regulation of MAP kinase activity, possibly leading to affect the response to estrogen inhibitors. {ECO:0000269|PubMed:11683387, ECO:0000269|PubMed:19651820, ECO:0000269|PubMed:20952539, ECO:0000269|PubMed:22012619, ECO:0000269|PubMed:24662513}.
Ensembl transtripts involved in fusion geneENST idsENST00000264639, ENST00000541736, 
ENST00000559545, ENST00000430627, 
ENST00000447079, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 5 X 7=28036 X 30 X 14=15120
# samples 1255
** MAII scorelog2(12/280*10)=-1.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(55/15120*10)=-4.78088271069641
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PSMD3 [Title/Abstract] AND CDK12 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PSMD3 [Title/Abstract] AND CDK12 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PSMD3(38151321)-CDK12(37657502), # samples:1
PSMD3(38146450)-CDK12(37627132), # samples:1
PSMD3(38151321)-CDK12(37657503), # samples:1
Anticipated loss of major functional domain due to fusion event.PSMD3-CDK12 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.
PSMD3-CDK12 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.
PSMD3-CDK12 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.
PSMD3-CDK12 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.
PSMD3-CDK12 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PSMD3-CDK12 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PSMD3-CDK12 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
PSMD3-CDK12 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PSMD3-CDK12 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PSMD3-CDK12 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
TgeneCDK12

GO:0046777

protein autophosphorylation

11683387



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/chr17:38151321/chr17:37657502)
- 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 PSMD3 (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 CDK12 (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)
ENST00000264639PSMD3chr1738151321+ENST00000430627CDK12chr1737657502+4458127017432961040
ENST00000264639PSMD3chr1738151321+ENST00000447079CDK12chr1737657502+7154127017433231049
ENST00000541736PSMD3chr1738151321+ENST00000430627CDK12chr1737657502+41549662602992910
ENST00000541736PSMD3chr1738151321+ENST00000447079CDK12chr1737657502+68509662603019919
ENST00000264639PSMD3chr1738151321+ENST00000430627CDK12chr1737657503+4458127017432961040
ENST00000264639PSMD3chr1738151321+ENST00000447079CDK12chr1737657503+7154127017433231049
ENST00000541736PSMD3chr1738151321+ENST00000430627CDK12chr1737657503+41549662602992910
ENST00000541736PSMD3chr1738151321+ENST00000447079CDK12chr1737657503+68509662603019919

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
ENST00000264639ENST00000430627PSMD3chr1738151321+CDK12chr1737657502+0.0019411830.99805886
ENST00000264639ENST00000447079PSMD3chr1738151321+CDK12chr1737657502+0.0001339650.999866
ENST00000541736ENST00000430627PSMD3chr1738151321+CDK12chr1737657502+0.0028910630.997109
ENST00000541736ENST00000447079PSMD3chr1738151321+CDK12chr1737657502+0.0003578750.99964213
ENST00000264639ENST00000430627PSMD3chr1738151321+CDK12chr1737657503+0.0019411830.99805886
ENST00000264639ENST00000447079PSMD3chr1738151321+CDK12chr1737657503+0.0001339650.999866
ENST00000541736ENST00000430627PSMD3chr1738151321+CDK12chr1737657503+0.0028910630.997109
ENST00000541736ENST00000447079PSMD3chr1738151321+CDK12chr1737657503+0.0003578750.99964213

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 PSMD3-CDK12

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PSMD3chr1738151321CDK12chr17376575021270360FRQPSLKRSLMPYFLLTQGAFYLVFE
PSMD3chr1738151321CDK12chr1737657502966230FRQPSLKRSLMPYFLLTQGAFYLVFE
PSMD3chr1738151321CDK12chr17376575031270360FRQPSLKRSLMPYFLLTQGAFYLVFE
PSMD3chr1738151321CDK12chr1737657503966230FRQPSLKRSLMPYFLLTQGAFYLVFE

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Potential FusionNeoAntigen Information of PSMD3-CDK12 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.
PSMD3-CDK12_38151321_37657502.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)
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:02KRSLMPYF0.99980.6487614
PSMD3-CDK12chr1738151321chr17376575021270HLA-A02:04SLMPYFLL0.99510.5298816
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:02KRSLMPYFL0.99980.6348615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:05KRSLMPYFL0.99980.8705615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:04KRSLMPYFL0.99970.7022615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B58:02RSLMPYFLL0.99530.8745716
PSMD3-CDK12chr1738151321chr17376575021270HLA-B57:03RSLMPYFLL0.99250.9371716
PSMD3-CDK12chr1738151321chr17376575021270HLA-B15:16RSLMPYFLL0.99210.5889716
PSMD3-CDK12chr1738151321chr17376575021270HLA-B15:17RSLMPYFLL0.98880.8041716
PSMD3-CDK12chr1738151321chr17376575021270HLA-A32:13RSLMPYFLL0.98110.9299716
PSMD3-CDK12chr1738151321chr17376575021270HLA-A02:13SLMPYFLLT0.97870.5084817
PSMD3-CDK12chr1738151321chr17376575021270HLA-A02:38SLMPYFLLT0.96930.5352817
PSMD3-CDK12chr1738151321chr17376575021270HLA-A24:31YFLLTQGAF0.96380.66331221
PSMD3-CDK12chr1738151321chr17376575021270HLA-A30:08RSLMPYFLL0.94590.7516716
PSMD3-CDK12chr1738151321chr17376575021270HLA-B38:01KRSLMPYFL0.80080.9112615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:04KRSLMPYFLL0.99990.6974616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:05KRSLMPYFLL0.99990.8722616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:02KRSLMPYFLL0.99990.6156616
PSMD3-CDK12chr1738151321chr17376575021270HLA-A29:10YFLLTQGAFY0.99860.59181222
PSMD3-CDK12chr1738151321chr17376575021270HLA-A24:31PYFLLTQGAF0.9880.78271121
PSMD3-CDK12chr1738151321chr17376575021270HLA-B56:01MPYFLLTQGA0.98280.62861020
PSMD3-CDK12chr1738151321chr17376575021270HLA-A80:01YFLLTQGAFY0.90150.59031222
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:01MPYFLLTQGAF0.99880.90011021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:05MPYFLLTQGAF0.9980.58941021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:14KRSLMPYFL0.99980.7995615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:95KRSLMPYFL0.99650.8067615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:03KRSLMPYFL0.99450.9005615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:27KRSLMPYFL0.98680.9701615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:05KRSLMPYFL0.98540.9675615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:29KRSLMPYFL0.98140.9376615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:46KRSLMPYFL0.97840.8923615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:19KRSLMPYFL0.97420.7891615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:13KRSLMPYFL0.96940.9213615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:10KRSLMPYFL0.9540.9649615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B39:12KRSLMPYFL0.95280.827615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:80KRSLMPYFL0.95250.9572615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:67KRSLMPYFL0.95250.9572615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B15:21YFLLTQGAF0.75230.96031221
PSMD3-CDK12chr1738151321chr17376575021270HLA-C12:16KRSLMPYFL0.04150.9802615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B54:01MPYFLLTQGA0.99880.79851020
PSMD3-CDK12chr1738151321chr17376575021270HLA-A29:02YFLLTQGAFY0.99860.59181222
PSMD3-CDK12chr1738151321chr17376575021270HLA-A29:01YFLLTQGAFY0.99860.59181222
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:03KRSLMPYFLL0.99840.9008616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B78:01MPYFLLTQGA0.91410.78641020
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:08KRSLMPYFL0.99980.7489615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:06KRSLMPYFL0.99980.6906615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:10KRSLMPYFL0.99970.8517615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:09KRSLMPYFL0.99940.8374615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C15:05RSLMPYFLL0.99840.8801716
PSMD3-CDK12chr1738151321chr17376575021270HLA-C15:02RSLMPYFLL0.99810.7967716
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:01KRSLMPYFL0.99690.7853615
PSMD3-CDK12chr1738151321chr17376575021270HLA-A32:01RSLMPYFLL0.99380.9669716
PSMD3-CDK12chr1738151321chr17376575021270HLA-A02:03SLMPYFLLT0.98280.5355817
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:17KRSLMPYFL0.97630.9702615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:02KRSLMPYFL0.95250.9572615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C06:08KRSLMPYFL0.9120.9721615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:22KRSLMPYFL0.86120.8331615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C07:04KRSLMPYFL0.80730.9389615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B38:05KRSLMPYFL0.80080.9112615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C06:06KRSLMPYFL0.39290.9786615
PSMD3-CDK12chr1738151321chr17376575021270HLA-B15:68LKRSLMPYF0.07860.6513514
PSMD3-CDK12chr1738151321chr17376575021270HLA-C06:17KRSLMPYFL0.07770.9952615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C06:02KRSLMPYFL0.07770.9952615
PSMD3-CDK12chr1738151321chr17376575021270HLA-C14:02YFLLTQGAF0.01620.9881221
PSMD3-CDK12chr1738151321chr17376575021270HLA-C14:03YFLLTQGAF0.01620.9881221
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:08KRSLMPYFLL0.99990.7361616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:10KRSLMPYFLL0.99990.857616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:06KRSLMPYFLL0.99980.6852616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B27:09KRSLMPYFLL0.99950.8376616
PSMD3-CDK12chr1738151321chr17376575021270HLA-B55:02MPYFLLTQGA0.98590.62931020
PSMD3-CDK12chr1738151321chr17376575021270HLA-B56:05MPYFLLTQGA0.94960.5941020
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:23MPYFLLTQGAF0.99890.92081021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:77MPYFLLTQGAF0.99880.90011021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:24MPYFLLTQGAF0.99840.80611021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:17MPYFLLTQGAF0.99760.75551021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:30MPYFLLTQGAF0.99760.75551021
PSMD3-CDK12chr1738151321chr17376575021270HLA-B35:11MPYFLLTQGAF0.99130.89791021

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Potential FusionNeoAntigen Information of PSMD3-CDK12 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 PSMD3-CDK12

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
4581KRSLMPYFLLTQGAPSMD3CDK12chr1738151321chr17376575021270

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PSMD3-CDK12

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-B14:023BVN4581KRSLMPYFLLTQGA-7.15543-7.26883
HLA-B14:023BVN4581KRSLMPYFLLTQGA-4.77435-5.80965
HLA-B52:013W394581KRSLMPYFLLTQGA-6.80875-6.92215
HLA-B52:013W394581KRSLMPYFLLTQGA-4.20386-5.23916
HLA-A11:014UQ24581KRSLMPYFLLTQGA-7.5194-8.5547
HLA-A11:014UQ24581KRSLMPYFLLTQGA-6.9601-7.0735
HLA-A24:025HGA4581KRSLMPYFLLTQGA-7.52403-7.63743
HLA-A24:025HGA4581KRSLMPYFLLTQGA-5.82433-6.85963
HLA-B27:056PYJ4581KRSLMPYFLLTQGA-3.28285-4.31815
HLA-B44:053DX84581KRSLMPYFLLTQGA-5.91172-6.94702
HLA-B44:053DX84581KRSLMPYFLLTQGA-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of PSMD3-CDK12

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
PSMD3-CDK12chr1738151321chr17376575021020MPYFLLTQGATGACTCAAGGTGCCTTTTACCTTGTATTTG
PSMD3-CDK12chr1738151321chr17376575021021MPYFLLTQGAFTGACTCAAGGTGCCTTTTACCTTGTATTTGAGT
PSMD3-CDK12chr1738151321chr17376575021121PYFLLTQGAFCTCAAGGTGCCTTTTACCTTGTATTTGAGT
PSMD3-CDK12chr1738151321chr17376575021221YFLLTQGAFAAGGTGCCTTTTACCTTGTATTTGAGT
PSMD3-CDK12chr1738151321chr17376575021222YFLLTQGAFYAAGGTGCCTTTTACCTTGTATTTGAGTATA
PSMD3-CDK12chr1738151321chr1737657502514LKRSLMPYFTGCCCTATTTCCTTCTGACTCAAGGTG
PSMD3-CDK12chr1738151321chr1737657502614KRSLMPYFCCTATTTCCTTCTGACTCAAGGTG
PSMD3-CDK12chr1738151321chr1737657502615KRSLMPYFLCCTATTTCCTTCTGACTCAAGGTGCCT
PSMD3-CDK12chr1738151321chr1737657502616KRSLMPYFLLCCTATTTCCTTCTGACTCAAGGTGCCTTTT
PSMD3-CDK12chr1738151321chr1737657502716RSLMPYFLLATTTCCTTCTGACTCAAGGTGCCTTTT
PSMD3-CDK12chr1738151321chr1737657502816SLMPYFLLTCCTTCTGACTCAAGGTGCCTTTT
PSMD3-CDK12chr1738151321chr1737657502817SLMPYFLLTTCCTTCTGACTCAAGGTGCCTTTTACC

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 PSMD3-CDK12

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
UCECPSMD3-CDK12chr1738151321ENST00000264639chr1737657502ENST00000430627TCGA-AP-A053

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Potential target of CAR-T therapy development for PSMD3-CDK12

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 PSMD3-CDK12

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 PSMD3-CDK12

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