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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:USP22-MYO19 (FusionGDB2 ID:97276)

Fusion Gene Summary for USP22-MYO19

check button Fusion gene summary
Fusion gene informationFusion gene name: USP22-MYO19
Fusion gene ID: 97276
HgeneTgene
Gene symbol

USP22

MYO19

Gene ID

23326

80179

Gene nameubiquitin specific peptidase 22myosin XIX
SynonymsUSP3LMYOHD1
Cytomap

17p11.2

17q12

Type of geneprotein-codingprotein-coding
Descriptionubiquitin carboxyl-terminal hydrolase 22deubiquitinating enzyme 22ubiquitin specific protease 22ubiquitin thioesterase 22ubiquitin thiolesterase 22ubiquitin-specific processing protease 22unconventional myosin-XIXmyosin head domain containing 1myosin head domain-containing protein 1
Modification date2020031320200313
UniProtAcc.

Q96H55

Ensembl transtripts involved in fusion geneENST00000261497, ENST00000455117, 
ENST00000537526, 
ENST00000544606, 
ENST00000586007, ENST00000590081, 
ENST00000268852, ENST00000431794, 
Fusion gene scores* DoF score15 X 14 X 7=14708 X 9 X 5=360
# samples 2210
** MAII scorelog2(22/1470*10)=-2.74024072619907
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/360*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: USP22 [Title/Abstract] AND MYO19 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointUSP22(20945978)-MYO19(34852250), # samples:3
Anticipated loss of major functional domain due to fusion event.USP22-MYO19 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
USP22-MYO19 seems lost the major protein functional domain in Hgene 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
HgeneUSP22

GO:0016574

histone ubiquitination

18469533

HgeneUSP22

GO:0016578

histone deubiquitination

18206972|18206973

HgeneUSP22

GO:0016579

protein deubiquitination

16378762

TgeneMYO19

GO:0034642

mitochondrion migration along actin filament

19932026


check buttonFusion gene breakpoints across USP22 (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 MYO19 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4BRCATCGA-BH-A0DD-01AUSP22chr17

20945978

-MYO19chr17

34852250

-
ChimerDB4BRCATCGA-BH-A0DDUSP22chr17

20945977

-MYO19chr17

34852250

-


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Fusion Gene ORF analysis for USP22-MYO19

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-intronENST00000261497ENST00000544606USP22chr17

20945978

-MYO19chr17

34852250

-
5CDS-intronENST00000261497ENST00000544606USP22chr17

20945977

-MYO19chr17

34852250

-
5CDS-intronENST00000261497ENST00000586007USP22chr17

20945978

-MYO19chr17

34852250

-
5CDS-intronENST00000261497ENST00000586007USP22chr17

20945977

-MYO19chr17

34852250

-
5CDS-intronENST00000261497ENST00000590081USP22chr17

20945978

-MYO19chr17

34852250

-
5CDS-intronENST00000261497ENST00000590081USP22chr17

20945977

-MYO19chr17

34852250

-
Frame-shiftENST00000261497ENST00000268852USP22chr17

20945978

-MYO19chr17

34852250

-
Frame-shiftENST00000261497ENST00000268852USP22chr17

20945977

-MYO19chr17

34852250

-
In-frameENST00000261497ENST00000431794USP22chr17

20945978

-MYO19chr17

34852250

-
In-frameENST00000261497ENST00000431794USP22chr17

20945977

-MYO19chr17

34852250

-
intron-3CDSENST00000455117ENST00000268852USP22chr17

20945978

-MYO19chr17

34852250

-
intron-3CDSENST00000455117ENST00000268852USP22chr17

20945977

-MYO19chr17

34852250

-
intron-3CDSENST00000455117ENST00000431794USP22chr17

20945978

-MYO19chr17

34852250

-
intron-3CDSENST00000455117ENST00000431794USP22chr17

20945977

-MYO19chr17

34852250

-
intron-3CDSENST00000537526ENST00000268852USP22chr17

20945978

-MYO19chr17

34852250

-
intron-3CDSENST00000537526ENST00000268852USP22chr17

20945977

-MYO19chr17

34852250

-
intron-3CDSENST00000537526ENST00000431794USP22chr17

20945978

-MYO19chr17

34852250

-
intron-3CDSENST00000537526ENST00000431794USP22chr17

20945977

-MYO19chr17

34852250

-
intron-intronENST00000455117ENST00000544606USP22chr17

20945978

-MYO19chr17

34852250

-
intron-intronENST00000455117ENST00000544606USP22chr17

20945977

-MYO19chr17

34852250

-
intron-intronENST00000455117ENST00000586007USP22chr17

20945978

-MYO19chr17

34852250

-
intron-intronENST00000455117ENST00000586007USP22chr17

20945977

-MYO19chr17

34852250

-
intron-intronENST00000455117ENST00000590081USP22chr17

20945978

-MYO19chr17

34852250

-
intron-intronENST00000455117ENST00000590081USP22chr17

20945977

-MYO19chr17

34852250

-
intron-intronENST00000537526ENST00000544606USP22chr17

20945978

-MYO19chr17

34852250

-
intron-intronENST00000537526ENST00000544606USP22chr17

20945977

-MYO19chr17

34852250

-
intron-intronENST00000537526ENST00000586007USP22chr17

20945978

-MYO19chr17

34852250

-
intron-intronENST00000537526ENST00000586007USP22chr17

20945977

-MYO19chr17

34852250

-
intron-intronENST00000537526ENST00000590081USP22chr17

20945978

-MYO19chr17

34852250

-
intron-intronENST00000537526ENST00000590081USP22chr17

20945977

-MYO19chr17

34852250

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000261497USP22chr1720945978-ENST00000431794MYO19chr1734852250-114937524530168
ENST00000261497USP22chr1720945977-ENST00000431794MYO19chr1734852250-114937524530168

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
ENST00000261497ENST00000431794USP22chr1720945978-MYO19chr1734852250-0.426830230.57316977
ENST00000261497ENST00000431794USP22chr1720945977-MYO19chr1734852250-0.426830230.57316977

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Fusion Genomic Features for USP22-MYO19


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.
genomic feature

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for USP22-MYO19


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/chr17:20945978/chr17:34852250)
- 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 buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.MYO19

Q96H55

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Actin-based motor molecule with ATPase activity that localizes to the mitochondrion outer membrane (PubMed:19932026, PubMed:23568824, PubMed:25447992). Motor protein that moves towards the plus-end of actin filaments (By similarity). Required for mitochondrial inheritance during mitosis (PubMed:25447992). May be involved in mitochondrial transport or positioning (PubMed:23568824). {ECO:0000250|UniProtKB:Q5SV80, ECO:0000269|PubMed:19932026, ECO:0000269|PubMed:25447992, ECO:0000305|PubMed:23568824}.

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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneMYO19chr17:20945977chr17:34852250ENST000002688522022759_779719771.0DomainIQ 1
TgeneMYO19chr17:20945977chr17:34852250ENST000002688522022783_812719771.0DomainIQ 2
TgeneMYO19chr17:20945977chr17:34852250ENST0000058600701135_7580318.0DomainMyosin motor
TgeneMYO19chr17:20945977chr17:34852250ENST00000586007011759_7790318.0DomainIQ 1
TgeneMYO19chr17:20945977chr17:34852250ENST00000586007011783_8120318.0DomainIQ 2
TgeneMYO19chr17:20945978chr17:34852250ENST000002688522022759_779719771.0DomainIQ 1
TgeneMYO19chr17:20945978chr17:34852250ENST000002688522022783_812719771.0DomainIQ 2
TgeneMYO19chr17:20945978chr17:34852250ENST0000058600701135_7580318.0DomainMyosin motor
TgeneMYO19chr17:20945978chr17:34852250ENST00000586007011759_7790318.0DomainIQ 1
TgeneMYO19chr17:20945978chr17:34852250ENST00000586007011783_8120318.0DomainIQ 2
TgeneMYO19chr17:20945977chr17:34852250ENST00000586007011132_1390318.0Nucleotide bindingATP
TgeneMYO19chr17:20945978chr17:34852250ENST00000586007011132_1390318.0Nucleotide bindingATP
TgeneMYO19chr17:20945977chr17:34852250ENST000002688522022824_970719771.0RegionMyMOMA region
TgeneMYO19chr17:20945977chr17:34852250ENST00000586007011602_6240318.0RegionActin-binding
TgeneMYO19chr17:20945977chr17:34852250ENST00000586007011824_9700318.0RegionMyMOMA region
TgeneMYO19chr17:20945978chr17:34852250ENST000002688522022824_970719771.0RegionMyMOMA region
TgeneMYO19chr17:20945978chr17:34852250ENST00000586007011602_6240318.0RegionActin-binding
TgeneMYO19chr17:20945978chr17:34852250ENST00000586007011824_9700318.0RegionMyMOMA region

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneUSP22chr17:20945977chr17:34852250ENST00000261497-113176_52057526.0DomainNote=USP
HgeneUSP22chr17:20945977chr17:34852250ENST00000537526-113176_5200514.0DomainNote=USP
HgeneUSP22chr17:20945978chr17:34852250ENST00000261497-113176_52057526.0DomainNote=USP
HgeneUSP22chr17:20945978chr17:34852250ENST00000537526-113176_5200514.0DomainNote=USP
HgeneUSP22chr17:20945977chr17:34852250ENST00000261497-11361_12157526.0Zinc fingerUBP-type
HgeneUSP22chr17:20945977chr17:34852250ENST00000537526-11361_1210514.0Zinc fingerUBP-type
HgeneUSP22chr17:20945978chr17:34852250ENST00000261497-11361_12157526.0Zinc fingerUBP-type
HgeneUSP22chr17:20945978chr17:34852250ENST00000537526-11361_1210514.0Zinc fingerUBP-type
TgeneMYO19chr17:20945977chr17:34852250ENST00000268852202235_758719771.0DomainMyosin motor
TgeneMYO19chr17:20945977chr17:34852250ENST00000431794242635_758919971.0DomainMyosin motor
TgeneMYO19chr17:20945977chr17:34852250ENST000004317942426759_779919971.0DomainIQ 1
TgeneMYO19chr17:20945977chr17:34852250ENST000004317942426783_812919971.0DomainIQ 2
TgeneMYO19chr17:20945978chr17:34852250ENST00000268852202235_758719771.0DomainMyosin motor
TgeneMYO19chr17:20945978chr17:34852250ENST00000431794242635_758919971.0DomainMyosin motor
TgeneMYO19chr17:20945978chr17:34852250ENST000004317942426759_779919971.0DomainIQ 1
TgeneMYO19chr17:20945978chr17:34852250ENST000004317942426783_812919971.0DomainIQ 2
TgeneMYO19chr17:20945977chr17:34852250ENST000002688522022132_139719771.0Nucleotide bindingATP
TgeneMYO19chr17:20945977chr17:34852250ENST000004317942426132_139919971.0Nucleotide bindingATP
TgeneMYO19chr17:20945978chr17:34852250ENST000002688522022132_139719771.0Nucleotide bindingATP
TgeneMYO19chr17:20945978chr17:34852250ENST000004317942426132_139919971.0Nucleotide bindingATP
TgeneMYO19chr17:20945977chr17:34852250ENST000002688522022602_624719771.0RegionActin-binding
TgeneMYO19chr17:20945977chr17:34852250ENST000004317942426602_624919971.0RegionActin-binding
TgeneMYO19chr17:20945977chr17:34852250ENST000004317942426824_970919971.0RegionMyMOMA region
TgeneMYO19chr17:20945978chr17:34852250ENST000002688522022602_624719771.0RegionActin-binding
TgeneMYO19chr17:20945978chr17:34852250ENST000004317942426602_624919971.0RegionActin-binding
TgeneMYO19chr17:20945978chr17:34852250ENST000004317942426824_970919971.0RegionMyMOMA region


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Fusion Gene Sequence for USP22-MYO19


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>97276_97276_1_USP22-MYO19_USP22_chr17_20945977_ENST00000261497_MYO19_chr17_34852250_ENST00000431794_length(transcript)=1149nt_BP=375nt
GCAGCCGCAGCTCGGGGGCGGTGCCTGCCTTGCAGCCTCCCCTCGGCGATCGCGCAGCCCCATCTTTGTCCGGCCTCCGCGCTTTGTTCT
CGGCGCCCGGGCCTTGGCCAGCCTGGCCAGCCGCCGAGCAGCCCCCACGCCGCGCTGGCGTCGTCCTCGCCTCCCTCGCCGCCGCCCCCC
GCGCGCGGCCGGGCCTTGCCCCCCATGGTGTCCCGGCCAGAGCCCGAGGGCGAGGCCATGGACGCCGAGCTGGCGGTAGCGCCGCCGGGC
TGCTCGCACCTGGGCAGCTTCAAGGTGGACAACTGGAAGCAGAACCTGCGGGCCATCTACCAGTGCTTCGTGTGGAGCGGCACGGCTGAG
GCCCGCAAGCGCAAGGGATCGATAAAGTTTCACTGCAGAAAGTCTCCACTGCGGTATGCTGACATCTGCCCTGAACCTTCACCCTACAGC
ATTACAGGCTTTAATCAGATTCTGCTGGAAAGACACAGGCTGATCCACGTGACCTCTTCTGCCTTCACTGGGCTGGGGTGATCCTTGGTG
CCTTTGTTTCCACAAGGCCTTTTCCTGCCCCCTGCCTTGCCAAAGACATTTAATCAGCACACAGCTGCCAGACTATTCCCACAGTGCTCC
AAATGCACATGAACAACAGTGACGGCTCCAGCCTTCGACCCAGAGCCCCGTGCCCAGTGCGTCAGTGGGCCTGGGGTTCCAGGCTACATC
AAGCACTGATGGTGTCAGGGCTGGTAGTTACCAAATCAGGGTTAAGAAACATCAGGGCCACATTTCACTACCTTCACAGATCAAACTCAG
CAGCAGTCATGACTGTCTGTCACTACACTGGGGATCCCAATTCCACATAAGCACTTTTGGAAGAAAACAGCCAAAGTTGGCCTAAAATTG
GCGCTGGAATTTGGGCTGGGAAAAATCTTGTGGTTATTTCCTTTAAAAAGGAACAAAACTTTAGTATTTAATTAGTTGATTTATTTAATG
TAATTTCAAACAATTAAATTATGAATAATGCAATGTACAGTAGAATCACGTTTTGATTTTATTAACACTGACCAAGTTTAACTCCATATG

>97276_97276_1_USP22-MYO19_USP22_chr17_20945977_ENST00000261497_MYO19_chr17_34852250_ENST00000431794_length(amino acids)=168AA_BP=117
MPCSLPSAIAQPHLCPASALCSRRPGLGQPGQPPSSPHAALASSSPPSPPPPARGRALPPMVSRPEPEGEAMDAELAVAPPGCSHLGSFK

--------------------------------------------------------------
>97276_97276_2_USP22-MYO19_USP22_chr17_20945978_ENST00000261497_MYO19_chr17_34852250_ENST00000431794_length(transcript)=1149nt_BP=375nt
GCAGCCGCAGCTCGGGGGCGGTGCCTGCCTTGCAGCCTCCCCTCGGCGATCGCGCAGCCCCATCTTTGTCCGGCCTCCGCGCTTTGTTCT
CGGCGCCCGGGCCTTGGCCAGCCTGGCCAGCCGCCGAGCAGCCCCCACGCCGCGCTGGCGTCGTCCTCGCCTCCCTCGCCGCCGCCCCCC
GCGCGCGGCCGGGCCTTGCCCCCCATGGTGTCCCGGCCAGAGCCCGAGGGCGAGGCCATGGACGCCGAGCTGGCGGTAGCGCCGCCGGGC
TGCTCGCACCTGGGCAGCTTCAAGGTGGACAACTGGAAGCAGAACCTGCGGGCCATCTACCAGTGCTTCGTGTGGAGCGGCACGGCTGAG
GCCCGCAAGCGCAAGGGATCGATAAAGTTTCACTGCAGAAAGTCTCCACTGCGGTATGCTGACATCTGCCCTGAACCTTCACCCTACAGC
ATTACAGGCTTTAATCAGATTCTGCTGGAAAGACACAGGCTGATCCACGTGACCTCTTCTGCCTTCACTGGGCTGGGGTGATCCTTGGTG
CCTTTGTTTCCACAAGGCCTTTTCCTGCCCCCTGCCTTGCCAAAGACATTTAATCAGCACACAGCTGCCAGACTATTCCCACAGTGCTCC
AAATGCACATGAACAACAGTGACGGCTCCAGCCTTCGACCCAGAGCCCCGTGCCCAGTGCGTCAGTGGGCCTGGGGTTCCAGGCTACATC
AAGCACTGATGGTGTCAGGGCTGGTAGTTACCAAATCAGGGTTAAGAAACATCAGGGCCACATTTCACTACCTTCACAGATCAAACTCAG
CAGCAGTCATGACTGTCTGTCACTACACTGGGGATCCCAATTCCACATAAGCACTTTTGGAAGAAAACAGCCAAAGTTGGCCTAAAATTG
GCGCTGGAATTTGGGCTGGGAAAAATCTTGTGGTTATTTCCTTTAAAAAGGAACAAAACTTTAGTATTTAATTAGTTGATTTATTTAATG
TAATTTCAAACAATTAAATTATGAATAATGCAATGTACAGTAGAATCACGTTTTGATTTTATTAACACTGACCAAGTTTAACTCCATATG

>97276_97276_2_USP22-MYO19_USP22_chr17_20945978_ENST00000261497_MYO19_chr17_34852250_ENST00000431794_length(amino acids)=168AA_BP=117
MPCSLPSAIAQPHLCPASALCSRRPGLGQPGQPPSSPHAALASSSPPSPPPPARGRALPPMVSRPEPEGEAMDAELAVAPPGCSHLGSFK

--------------------------------------------------------------

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Fusion Gene PPI Analysis for USP22-MYO19


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for USP22-MYO19


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for USP22-MYO19


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource