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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:MAP3K2-IWS1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MAP3K2-IWS1
FusionPDB ID: 51293
FusionGDB2.0 ID: 51293
HgeneTgene
Gene symbol

MAP3K2

IWS1

Gene ID

10746

55677

Gene namemitogen-activated protein kinase kinase kinase 2interacts with SUPT6H, CTD assembly factor 1
SynonymsMEKK2|MEKK2B-
Cytomap

2q14.3

2q14.3

Type of geneprotein-codingprotein-coding
Descriptionmitogen-activated protein kinase kinase kinase 2MAP/ERK kinase kinase 2MAPK/ERK kinase kinase 2MEK kinase 2MEKK 2protein IWS1 homologIWS1 homologIWS1, SUPT6H interacting proteinIWS1-like proteininteracts with Spt6
Modification date2020032920200313
UniProtAcc

Q5TCX8

Main function of 5'-partner protein: FUNCTION: Negative regulator of TLR4 signaling. Does not activate JNK1/MAPK8 pathway, p38/MAPK14, nor ERK2/MAPK1 pathways. {ECO:0000269|PubMed:21602844}.

Q96ST2

Main function of 5'-partner protein: FUNCTION: Transcription factor which plays a key role in defining the composition of the RNA polymerase II (RNAPII) elongation complex and in modulating the production of mature mRNA transcripts. Acts as an assembly factor to recruit various factors to the RNAPII elongation complex and is recruited to the complex via binding to the transcription elongation factor SUPT6H bound to the C-terminal domain (CTD) of the RNAPII subunit RPB1 (POLR2A). The SUPT6H:IWS1:CTD complex recruits mRNA export factors (ALYREF/THOC4, EXOSC10) as well as histone modifying enzymes (such as SETD2) to ensure proper mRNA splicing, efficient mRNA export and elongation-coupled H3K36 methylation, a signature chromatin mark of active transcription. {ECO:0000269|PubMed:17184735, ECO:0000269|PubMed:17234882, ECO:0000269|PubMed:19141475}.
Ensembl transtripts involved in fusion geneENST idsENST00000344908, ENST00000409947, 
ENST00000455721, ENST00000486662, 
ENST00000295321, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 8 X 3=2403 X 4 X 2=24
# samples 94
** MAII scorelog2(9/240*10)=-1.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: MAP3K2 [Title/Abstract] AND IWS1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MAP3K2 [Title/Abstract] AND IWS1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MAP3K2(128093446)-IWS1(128238751), # samples:2
Anticipated loss of major functional domain due to fusion event.MAP3K2-IWS1 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.
MAP3K2-IWS1 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.
MAP3K2-IWS1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MAP3K2-IWS1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
MAP3K2-IWS1 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
MAP3K2-IWS1 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
HgeneMAP3K2

GO:0045893

positive regulation of transcription, DNA-templated

14515274



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/chr2:128093446/chr2:128238751)
- 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 MAP3K2 (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 IWS1 (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)
ENST00000409947MAP3K2chr2128093446-ENST00000295321IWS1chr2128238751-917547271678135

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
ENST00000409947ENST00000295321MAP3K2chr2128093446-IWS1chr2128238751-0.0082617350.99173826

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 MAP3K2-IWS1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MAP3K2chr2128093446IWS1chr212823875154792FGQSMDLHYTNNEFQATSKKGISRLD

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Potential FusionNeoAntigen Information of MAP3K2-IWS1 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.
MAP3K2-IWS1_128093446_128238751.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)
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B15:18LHYTNNEF0.9960.5879614
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B38:02LHYTNNEF0.98720.9194614
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B38:01LHYTNNEF0.9870.9079614
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B15:02DLHYTNNEF0.91590.7638514
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B39:06LHYTNNEFQA0.98880.7805616
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B39:05LHYTNNEF0.98080.8193614
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B15:21DLHYTNNEF0.91920.7382514
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B15:31DLHYTNNEF0.85230.6724514
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B38:05LHYTNNEF0.9870.9079614
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B15:08DLHYTNNEF0.85670.717514
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B35:20DLHYTNNEF0.83280.7521514
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B18:06NEFQATSKK0.74280.91981120
MAP3K2-IWS1chr2128093446chr2128238751547HLA-B18:04DLHYTNNEF0.6210.8755514

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Potential FusionNeoAntigen Information of MAP3K2-IWS1 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.
MAP3K2-IWS1_128093446_128238751.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)
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0478SMDLHYTNNEFQATS318
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0807TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0807NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0807YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0808TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0808NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0811TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0811NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0819TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0819NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0825TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0825NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0834TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-0834NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1153TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1153NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1164TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1168TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-13100TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-13100NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-13100YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1329TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1331TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1331NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1331YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1336TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1338TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1346TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1346NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1346YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1365TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1407TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1407NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1407YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1407NEFQATSKKGISRLD1126
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1414TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1414NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1414YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1422TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1422NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1425TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1425NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1436TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1436NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1436YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1442TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1442NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1442YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1444TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1444NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1444YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1449TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1449NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1451TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1451NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1453TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1453NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1468TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1468NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1468YTNNEFQATSKKGIS823
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1468NEFQATSKKGISRLD1126
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1469TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1469NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1493TNNEFQATSKKGISR924
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1493NNEFQATSKKGISRL1025
MAP3K2-IWS1chr2128093446chr2128238751547DRB1-1493YTNNEFQATSKKGIS823

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Fusion breakpoint peptide structures of MAP3K2-IWS1

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
5081LHYTNNEFQATSKKMAP3K2IWS1chr2128093446chr2128238751547

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MAP3K2-IWS1

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-B14:023BVN5081LHYTNNEFQATSKK-7.9962-8.1096
HLA-B14:023BVN5081LHYTNNEFQATSKK-5.70842-6.74372
HLA-B52:013W395081LHYTNNEFQATSKK-6.83737-6.95077
HLA-B52:013W395081LHYTNNEFQATSKK-4.4836-5.5189
HLA-A11:014UQ25081LHYTNNEFQATSKK-10.0067-10.1201
HLA-A11:014UQ25081LHYTNNEFQATSKK-9.03915-10.0745
HLA-A24:025HGA5081LHYTNNEFQATSKK-6.56204-6.67544
HLA-A24:025HGA5081LHYTNNEFQATSKK-5.42271-6.45801
HLA-B44:053DX85081LHYTNNEFQATSKK-7.85648-8.89178
HLA-B44:053DX85081LHYTNNEFQATSKK-5.3978-5.5112
HLA-A02:016TDR5081LHYTNNEFQATSKK-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of MAP3K2-IWS1

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
MAP3K2-IWS1chr2128093446chr21282387511120NEFQATSKKAACGAGTTTCAGGCGACCTCCAAGAAG
MAP3K2-IWS1chr2128093446chr2128238751514DLHYTNNEFGATCTACATTATACCAATAACGAGTTT
MAP3K2-IWS1chr2128093446chr2128238751614LHYTNNEFCTACATTATACCAATAACGAGTTT
MAP3K2-IWS1chr2128093446chr2128238751616LHYTNNEFQACTACATTATACCAATAACGAGTTTCAGGCG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
MAP3K2-IWS1chr2128093446chr21282387511025NNEFQATSKKGISRLAATAACGAGTTTCAGGCGACCTCCAAGAAGGGTATCAGTCGACTG
MAP3K2-IWS1chr2128093446chr21282387511126NEFQATSKKGISRLDAACGAGTTTCAGGCGACCTCCAAGAAGGGTATCAGTCGACTGGAT
MAP3K2-IWS1chr2128093446chr2128238751318SMDLHYTNNEFQATSTCTATGGATCTACATTATACCAATAACGAGTTTCAGGCGACCTCC
MAP3K2-IWS1chr2128093446chr2128238751823YTNNEFQATSKKGISTATACCAATAACGAGTTTCAGGCGACCTCCAAGAAGGGTATCAGT
MAP3K2-IWS1chr2128093446chr2128238751924TNNEFQATSKKGISRACCAATAACGAGTTTCAGGCGACCTCCAAGAAGGGTATCAGTCGA

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Information of the samples that have these potential fusion neoantigens of MAP3K2-IWS1

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
BRCAMAP3K2-IWS1chr2128093446ENST00000409947chr2128238751ENST00000295321TCGA-AC-A2BM-01A

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Potential target of CAR-T therapy development for MAP3K2-IWS1

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 MAP3K2-IWS1

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 MAP3K2-IWS1

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