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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:MYH14-C17orf75 (FusionGDB2 ID:56317)

Fusion Gene Summary for MYH14-C17orf75

check button Fusion gene summary
Fusion gene informationFusion gene name: MYH14-C17orf75
Fusion gene ID: 56317
HgeneTgene
Gene symbol

MYH14

C17orf75

Gene ID

79784

64149

Gene namemyosin heavy chain 14chromosome 17 open reading frame 75
SynonymsDFNA4|DFNA4A|FP17425|MHC16|MYH17|NMHC II-C|NMHC-II-C|PNMHH|myosinNJMU-R1|SRI2
Cytomap

19q13.33

17q11.2

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-Cprotein Njmu-R1sensitization to ricin complex subunit 2spermatogenesis-related protein
Modification date2020031320200313
UniProtAcc

Q7Z406

Q9HAS0

Ensembl transtripts involved in fusion geneENST00000262269, ENST00000376970, 
ENST00000425460, ENST00000440075, 
ENST00000596571, ENST00000598205, 
ENST00000601313, 
ENST00000225805, 
ENST00000577809, 
Fusion gene scores* DoF score30 X 20 X 6=36003 X 4 X 4=48
# samples 314
** MAII scorelog2(31/3600*10)=-3.5376567859428
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYH14 [Title/Abstract] AND C17orf75 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMYH14(50782071)-C17orf75(30658381), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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

TgeneC17orf75

GO:0006886

intracellular protein transport

29426865

TgeneC17orf75

GO:0099041

vesicle tethering to Golgi

29426865


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.

check buttonFusion gene breakpoints across C17orf75 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChiTaRS5.0N/ACB050403MYH14chr19

50782071

-C17orf75chr17

30658381

+


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Fusion Gene ORF analysis for MYH14-C17orf75

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
intron-intronENST00000262269ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000262269ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000376970ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000376970ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000425460ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000425460ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000440075ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000440075ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000596571ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000596571ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000598205ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000598205ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000601313ENST00000225805MYH14chr19

50782071

-C17orf75chr17

30658381

+
intron-intronENST00000601313ENST00000577809MYH14chr19

50782071

-C17orf75chr17

30658381

+

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)

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

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Fusion Genomic Features for MYH14-C17orf75


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.

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 MYH14-C17orf75


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/:50782071/:30658381)
- 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
MYH14

Q7Z406

C17orf75

Q9HAS0

FUNCTION: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. {ECO:0000250}.FUNCTION: As component of the WDR11 complex acts together with TBC1D23 to facilitate the golgin-mediated capture of vesicles generated using AP-1 (PubMed:29426865). May have a role in spermatogenesis. {ECO:0000269|PubMed:29426865}.

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

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for MYH14-C17orf75


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.

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Fusion Gene PPI Analysis for MYH14-C17orf75


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 MYH14-C17orf75


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 MYH14-C17orf75


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