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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:MYH14-MYH9

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MYH14-MYH9
FusionPDB ID: 56331
FusionGDB2.0 ID: 56331
HgeneTgene
Gene symbol

MYH14

MYH9

Gene ID

79784

4627

Gene namemyosin heavy chain 14myosin heavy chain 9
SynonymsDFNA4|DFNA4A|FP17425|MHC16|MYH17|NMHC II-C|NMHC-II-C|PNMHH|myosinBDPLT6|DFNA17|EPSTS|FTNS|MATINS|MHA|NMHC-II-A|NMMHC-IIA|NMMHCA
Cytomap

19q13.33

22q12.3

Type of geneprotein-codingprotein-coding
Descriptionmyosin-14MYH14 variant proteinmyosin heavy chain, non-muscle IIcmyosin, heavy chain 14, non-musclemyosin, heavy polypeptide 14non-muscle myosin heavy chain IIcnonmuscle myosin heavy chain II-Cmyosin-9cellular myosin heavy chain, type Amyosin, heavy chain 9, non-musclenon-muscle myosin heavy chain 9non-muscle myosin heavy chain Anon-muscle myosin heavy chain IIanon-muscle myosin heavy polypeptide 9nonmuscle myosin heavy chain II-A
Modification date2020031320200315
UniProtAcc

Q7Z406

Main function of 5'-partner protein: FUNCTION: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. {ECO:0000250}.

P35579

Main function of 5'-partner protein: FUNCTION: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. Promotes also cell motility together with S100A4 (PubMed:16707441). During cell spreading, plays an important role in cytoskeleton reorganization, focal contacts formation (in the margins but not the central part of spreading cells), and lamellipodial retraction; this function is mechanically antagonized by MYH10 (PubMed:20052411). {ECO:0000250|UniProtKB:Q8VDD5, ECO:0000269|PubMed:16707441, ECO:0000269|PubMed:20052411}.
Ensembl transtripts involved in fusion geneENST idsENST00000262269, ENST00000376970, 
ENST00000425460, ENST00000440075, 
ENST00000596571, ENST00000598205, 
ENST00000601313, 
ENST00000401701, 
ENST00000475726, ENST00000216181, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score30 X 20 X 6=360044 X 46 X 15=30360
# samples 3156
** MAII scorelog2(31/3600*10)=-3.5376567859428
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(56/30360*10)=-5.76060115335786
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: MYH14 [Title/Abstract] AND MYH9 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MYH14 [Title/Abstract] AND MYH9 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MYH14(50783398)-MYH9(36689527), # samples:1
MYH9(36689804)-MYH14(50783487), # samples:1
Anticipated loss of major functional domain due to fusion event.MYH14-MYH9 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.
MYH14-MYH9 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.
MYH14-MYH9 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.
MYH14-MYH9 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.
MYH9-MYH14 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
MYH9-MYH14 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
MYH9-MYH14 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
HgeneMYH14

GO:0031032

actomyosin structure organization

24072716

TgeneMYH9

GO:0001525

angiogenesis

16403913

TgeneMYH9

GO:0001778

plasma membrane repair

27325790

TgeneMYH9

GO:0006509

membrane protein ectodomain proteolysis

16186248

TgeneMYH9

GO:0030048

actin filament-based movement

12237319|15845534

TgeneMYH9

GO:0031032

actomyosin structure organization

24072716



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/chr19:50783398/chr22:36689527)
- 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 MYH14 (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 MYH9 (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)
ENST00000598205MYH14chr1950783398+ENST00000216181MYH9chr2236689527-74914163561032032
ENST00000376970MYH14chr1950783398+ENST00000216181MYH9chr2236689527-748841604761002017
ENST00000425460MYH14chr1950783398+ENST00000216181MYH9chr2236689527-741340854760251992
ENST00000440075MYH14chr1950783398+ENST00000216181MYH9chr2236689527-751241844761242025
ENST00000601313MYH14chr1950783398+ENST00000216181MYH9chr2236689527-749541673061072025
ENST00000262269MYH14chr1950783398+ENST00000216181MYH9chr2236689527-74724144760842025
ENST00000596571MYH14chr1950783398+ENST00000216181MYH9chr2236689527-73424014059541984

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
ENST00000598205ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.0145147610.98548526
ENST00000376970ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.0151591480.9848408
ENST00000425460ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.015191360.9848087
ENST00000440075ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.0151237670.98487616
ENST00000601313ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.0150739030.9849261
ENST00000262269ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.0150663590.9849337
ENST00000596571ENST00000216181MYH14chr1950783398+MYH9chr2236689527-0.0149396320.9850604

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 MYH14-MYH9

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MYH14chr1950783398MYH9chr2236689527401449GGGPGSGTSPQVEWTARRLVWVPSEL
MYH14chr1950783398MYH9chr2236689527408549GGGPGSGTSPQVEWTARRLVWVPSEL
MYH14chr1950783398MYH9chr2236689527414449GGGPGSGTSPQVEWTARRLVWVPSEL
MYH14chr1950783398MYH9chr2236689527416049GGGPGSGTSPQVEWTARRLVWVPSEL
MYH14chr1950783398MYH9chr2236689527416389GGGPGSGTSPQVEWTARRLVWVPSEL
MYH14chr1950783398MYH9chr2236689527416749GGGPGSGTSPQVEWTARRLVWVPSEL
MYH14chr1950783398MYH9chr2236689527418449GGGPGSGTSPQVEWTARRLVWVPSEL

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Potential FusionNeoAntigen Information of MYH14-MYH9 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.
MYH14-MYH9_50783398_36689527.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)
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:01GTSPQVEW0.99960.9848614
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:01GTSPQVEW0.99850.9734614
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:02GTSPQVEW0.99850.9742614
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:03GTSPQVEW0.9950.9905614
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:01SGTSPQVEW0.99210.953514
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:01SGTSPQVEW0.99020.9736514
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:02SGTSPQVEW0.97070.9681514
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:03SGTSPQVEW0.81570.99514
MYH14-MYH9chr1950783398chr22366895274144HLA-B53:01SGTSPQVEW0.78590.5795514
MYH14-MYH9chr1950783398chr22366895274144HLA-B41:01VEWTARRLV0.31460.92071120
MYH14-MYH9chr1950783398chr22366895274144HLA-B50:01VEWTARRLV0.07450.83311120
MYH14-MYH9chr1950783398chr22366895274144HLA-B52:01VEWTARRLV0.01660.98821120
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:01GSGTSPQVEW0.99770.9579414
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:02GSGTSPQVEW0.99350.9475414
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:01GSGTSPQVEW0.99310.9402414
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:03VEWTARRLVW0.98820.971121
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:02VEWTARRLVW0.98080.56131121
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:03GSGTSPQVEW0.9030.9851414
MYH14-MYH9chr1950783398chr22366895274144HLA-A31:06GTSPQVEWTAR0.98810.7785617
MYH14-MYH9chr1950783398chr22366895274144HLA-B40:03VEWTARRL0.99610.51691119
MYH14-MYH9chr1950783398chr22366895274144HLA-B54:01SPQVEWTA0.7430.8688816
MYH14-MYH9chr1950783398chr22366895274144HLA-B40:06VEWTARRLV0.99360.87771120
MYH14-MYH9chr1950783398chr22366895274144HLA-B40:03VEWTARRLV0.68320.51011120
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:08VEWTARRLVW0.9790.67271121
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:10GTSPQVEW0.99960.9848614
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:04GTSPQVEW0.99930.7722614
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:06GTSPQVEW0.99830.9517614
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:02GTSPQVEW0.99810.9503614
MYH14-MYH9chr1950783398chr22366895274144HLA-B55:02SPQVEWTA0.71740.7371816
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:10SGTSPQVEW0.99020.9736514
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:04SGTSPQVEW0.98250.7912514
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:06SGTSPQVEW0.95080.9321514
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:02SGTSPQVEW0.78770.9583514
MYH14-MYH9chr1950783398chr22366895274144HLA-B50:04VEWTARRLV0.07450.83311120
MYH14-MYH9chr1950783398chr22366895274144HLA-B50:05VEWTARRLV0.07450.83311120
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:10GSGTSPQVEW0.99770.9579414
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:04GSGTSPQVEW0.99630.7334414
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:13VEWTARRLVW0.98820.971121
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:07VEWTARRLVW0.98820.971121
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:26VEWTARRLVW0.98820.971121
MYH14-MYH9chr1950783398chr22366895274144HLA-B58:06GSGTSPQVEW0.9840.9346414
MYH14-MYH9chr1950783398chr22366895274144HLA-B44:22VEWTARRLVW0.98080.56131121
MYH14-MYH9chr1950783398chr22366895274144HLA-B57:02GSGTSPQVEW0.9050.9401414

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Potential FusionNeoAntigen Information of MYH14-MYH9 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.
MYH14-MYH9_50783398_36689527.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)
MYH14-MYH9chr1950783398chr22366895274144DRB1-1401SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1426SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1435SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1454SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1458SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1460SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1462SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1486SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1487SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1488SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1490SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1497SPQVEWTARRLVWVP823
MYH14-MYH9chr1950783398chr22366895274144DRB1-1499SPQVEWTARRLVWVP823

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Fusion breakpoint peptide structures of MYH14-MYH9

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
3180GTSPQVEWTARRLVMYH14MYH9chr1950783398chr22366895274144

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MYH14-MYH9

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-B14:023BVN3180GTSPQVEWTARRLV-7.15543-7.26883
HLA-B14:023BVN3180GTSPQVEWTARRLV-4.77435-5.80965
HLA-B52:013W393180GTSPQVEWTARRLV-6.80875-6.92215
HLA-B52:013W393180GTSPQVEWTARRLV-4.20386-5.23916
HLA-A11:014UQ23180GTSPQVEWTARRLV-7.5194-8.5547
HLA-A11:014UQ23180GTSPQVEWTARRLV-6.9601-7.0735
HLA-A24:025HGA3180GTSPQVEWTARRLV-7.52403-7.63743
HLA-A24:025HGA3180GTSPQVEWTARRLV-5.82433-6.85963
HLA-B27:056PYJ3180GTSPQVEWTARRLV-3.28285-4.31815
HLA-B44:053DX83180GTSPQVEWTARRLV-5.91172-6.94702
HLA-B44:053DX83180GTSPQVEWTARRLV-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of MYH14-MYH9

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
MYH14-MYH9chr1950783398chr22366895271119VEWTARRLGCCCAGGAGCTGCTGCAGGAGGAG
MYH14-MYH9chr1950783398chr22366895271120VEWTARRLVGCCCAGGAGCTGCTGCAGGAGGAGAAC
MYH14-MYH9chr1950783398chr22366895271121VEWTARRLVWGCCCAGGAGCTGCTGCAGGAGGAGAACCGG
MYH14-MYH9chr1950783398chr2236689527414GSGTSPQVEWACAGAAGCCCAGCTGCACGATGCCCAGGAG
MYH14-MYH9chr1950783398chr2236689527514SGTSPQVEWGAAGCCCAGCTGCACGATGCCCAGGAG
MYH14-MYH9chr1950783398chr2236689527614GTSPQVEWGCCCAGCTGCACGATGCCCAGGAG
MYH14-MYH9chr1950783398chr2236689527617GTSPQVEWTARGCCCAGCTGCACGATGCCCAGGAGCTGCTGCAG
MYH14-MYH9chr1950783398chr2236689527816SPQVEWTACTGCACGATGCCCAGGAGCTGCTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
MYH14-MYH9chr1950783398chr2236689527823SPQVEWTARRLVWVPCTGCACGATGCCCAGGAGCTGCTGCAGGAGGAGAACCGGCAGAAG

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Information of the samples that have these potential fusion neoantigens of MYH14-MYH9

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
Non-CancerMYH14-MYH9chr1950783398ENST00000262269chr2236689527ENST000002161812397N

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Potential target of CAR-T therapy development for MYH14-MYH9

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 MYH14-MYH9

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 MYH14-MYH9

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