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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-CD164 (FusionGDB2 ID:56318)

Fusion Gene Summary for MYH14-CD164

check button Fusion gene summary
Fusion gene informationFusion gene name: MYH14-CD164
Fusion gene ID: 56318
HgeneTgene
Gene symbol

MYH14

CD164

Gene ID

79784

8763

Gene namemyosin heavy chain 14CD164 molecule
SynonymsDFNA4|DFNA4A|FP17425|MHC16|MYH17|NMHC II-C|NMHC-II-C|PNMHH|myosinDFNA66|MGC-24|MGC-24v|MUC-24|endolyn
Cytomap

19q13.33

6q21

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-Csialomucin core protein 24CD164 antigen, sialomucinmulti-glycosylated core protein 24
Modification date2020031320200313
UniProtAcc

Q7Z406

Q04900

Ensembl transtripts involved in fusion geneENST00000262269, ENST00000376970, 
ENST00000425460, ENST00000440075, 
ENST00000596571, ENST00000598205, 
ENST00000601313, 
ENST00000275080, 
ENST00000310786, ENST00000324953, 
ENST00000368961, ENST00000413644, 
ENST00000504373, ENST00000506649, 
ENST00000512821, 
Fusion gene scores* DoF score30 X 20 X 6=36008 X 8 X 1=64
# samples 318
** MAII scorelog2(31/3600*10)=-3.5376567859428
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/64*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MYH14 [Title/Abstract] AND CD164 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMYH14(50782069)-CD164(109687717), # 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

TgeneCD164

GO:0007155

cell adhesion

10491205

TgeneCD164

GO:0007157

heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules

10491205


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 CD164 (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/ACB049054MYH14chr19

50782069

-CD164chr6

109687717

+


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Fusion Gene ORF analysis for MYH14-CD164

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-intronENST00000262269ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000262269ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000376970ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000425460ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000440075ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000596571ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000598205ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000275080MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000310786MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000324953MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000368961MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000413644MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000504373MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000506649MYH14chr19

50782069

-CD164chr6

109687717

+
intron-intronENST00000601313ENST00000512821MYH14chr19

50782069

-CD164chr6

109687717

+

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-CD164


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-CD164


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/:50782069/:109687717)
- 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

CD164

Q04900

FUNCTION: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. {ECO:0000250}.FUNCTION: Sialomucin that may play a key role in hematopoiesis by facilitating the adhesion of CD34(+) cells to the stroma and by negatively regulating CD34(+)CD38(lo/-) cell proliferation. Modulates the migration of umbilical cord blood CD133+ cells and this is mediated through the CXCL12/CXCR4 axis. May play an important role in prostate cancer metastasis and the infiltration of bone marrow by cancer cells. Promotes myogenesis by enhancing CXCR4-dependent cell motility. Positively regulates myoblast migration and promotes myoblast fusion into myotubes (By similarity). {ECO:0000250|UniProtKB:Q9R0L9, ECO:0000269|PubMed:16859559, ECO:0000269|PubMed:17077324, ECO:0000269|PubMed:9763543}.

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-CD164


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-CD164


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-CD164


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-CD164


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