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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: 5009

FusionGeneSummary for C4orf22_MYH13

check button Fusion gene summary
Fusion gene informationFusion gene name: C4orf22_MYH13
Fusion gene ID: 5009
HgeneTgene
Gene symbol

C4orf22

MYH13

Gene ID

8735

Gene namemyosin heavy chain 13
SynonymsMyHC-IIL|MyHC-eo
Cytomap

17p13.1

Type of geneprotein-coding
Descriptionmyosin-13extraocular muscle myosin heavy chainextraocular myosin heavy chainmyosin heavy chain, skeletal muscle, extraocularmyosin heavy chain, skeletal muscle, laryngealmyosin, heavy chain 13, skeletal musclemyosin, heavy polypeptide 13, skeletal m
Modification date20180519
UniProtAcc

Q6V702

Q9UKX3

Ensembl transtripts involved in fusion geneENST00000358105, ENST00000508675, 
ENST00000512931, 
ENST00000418404, 
ENST00000252172, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 1=4
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: C4orf22 [Title/Abstract] AND MYH13 [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

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
ChiTaRS3.1CA335494C4orf22chr4

81580773

+MYH13chr17

10541244

-
* 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
intron-intronENST00000358105ENST00000418404C4orf22chr4

81580773

+MYH13chr17

10541244

-
intron-intronENST00000358105ENST00000252172C4orf22chr4

81580773

+MYH13chr17

10541244

-
intron-intronENST00000508675ENST00000418404C4orf22chr4

81580773

+MYH13chr17

10541244

-
intron-intronENST00000508675ENST00000252172C4orf22chr4

81580773

+MYH13chr17

10541244

-
intron-intronENST00000512931ENST00000418404C4orf22chr4

81580773

+MYH13chr17

10541244

-
intron-intronENST00000512931ENST00000252172C4orf22chr4

81580773

+MYH13chr17

10541244

-

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FusionProtFeatures for C4orf22_MYH13


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
C4orf22

Q6V702

MYH13

Q9UKX3

Fast twitching myosin mediating the high-velocity andlow-tension contractions of specific striated muscles.{ECO:0000269|PubMed:23908353}.

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 C4orf22_MYH13


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 C4orf22_MYH13


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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RelatedDrugs for C4orf22_MYH13


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 C4orf22_MYH13


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMYH13C0029408Degenerative polyarthritis1CTD_human