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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 43462

FusionGeneSummary for ZNF578_MYH14

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF578_MYH14
Fusion gene ID: 43462
HgeneTgene
Gene symbol

ZNF578

MYH14

Gene ID

147660

79784

Gene namezinc finger protein 578myosin heavy chain 14
Synonyms-DFNA4|DFNA4A|FP17425|MHC16|MYH17|NMHC II-C|NMHC-II-C|PNMHH|myosin
Cytomap

19q13.41

19q13.33

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 578myosin-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-C
Modification date2018052320180519
UniProtAcc

Q96N58

Q7Z406

Ensembl transtripts involved in fusion geneENST00000421239, ENST00000596382, 
ENST00000598205, ENST00000376970, 
ENST00000425460, ENST00000440075, 
ENST00000601313, ENST00000262269, 
ENST00000596571, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 8 X 6=336
# samples 18
** MAII scorelog2(1/1*10)=3.32192809488736log2(8/336*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZNF578 [Title/Abstract] AND MYH14 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
TgeneMYH14

GO:0031032

actomyosin structure organization

24072716


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDMESOTCGA-TS-A7P7-01AZNF578chr19

52960211

+MYH14chr19

50766569

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
5UTR-3CDSENST00000421239ENST00000598205ZNF578chr19

52960211

+MYH14chr19

50766569

+
5UTR-3CDSENST00000421239ENST00000376970ZNF578chr19

52960211

+MYH14chr19

50766569

+
5UTR-3CDSENST00000421239ENST00000425460ZNF578chr19

52960211

+MYH14chr19

50766569

+
5UTR-3CDSENST00000421239ENST00000440075ZNF578chr19

52960211

+MYH14chr19

50766569

+
5UTR-3CDSENST00000421239ENST00000601313ZNF578chr19

52960211

+MYH14chr19

50766569

+
5UTR-3CDSENST00000421239ENST00000262269ZNF578chr19

52960211

+MYH14chr19

50766569

+
5UTR-3CDSENST00000421239ENST00000596571ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000598205ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000376970ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000425460ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000440075ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000601313ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000262269ZNF578chr19

52960211

+MYH14chr19

50766569

+
3UTR-3CDSENST00000596382ENST00000596571ZNF578chr19

52960211

+MYH14chr19

50766569

+

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FusionProtFeatures for ZNF578_MYH14


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF578

Q96N58

MYH14

Q7Z406

May be involved in transcriptional regulation.

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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FusionGeneSequence for ZNF578_MYH14


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for ZNF578_MYH14


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
ZNF578MDFI, CEP70, KRTAP10-7, KRTAP10-9, KRTAP10-8, KRTAP10-3MYH14SIRT7, SP1, FBXO25, GFI1B, PIK3R2, SHC1, ESR1, MDC1, PAN2, CDC73, CHUK, COG3, CTR9, MYH9, MYL12A, MYL6, MYL9, OTUD6B, PAF1, RABL6, LGR4, CCDC8, SUZ12, C7orf25, MGC39584, SGK1, ZBTB44, ETV5, FAM58A, MED20, DNMT1, ECH1, ABCD3, SRI, SSR3, NUP155, CEPT1, CHMP2B, GAN, MCM2, ZNF746, MYL3, UNC45A, FCF1, DLST, BRCA1


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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RelatedDrugs for ZNF578_MYH14


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for ZNF578_MYH14


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMYH14C1833503Deafness, Autosomal Dominant 42CTD_human;UNIPROT
TgeneMYH14C0033578Prostatic Neoplasms1CTD_human
TgeneMYH14C3280556PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS1ORPHANET;UNIPROT