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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: 22994

FusionGeneSummary for MYH7_CLCN1

check button Fusion gene summary
Fusion gene informationFusion gene name: MYH7_CLCN1
Fusion gene ID: 22994
HgeneTgene
Gene symbol

MYH7

CLCN1

Gene ID

4625

1180

Gene namemyosin heavy chain 7chloride voltage-gated channel 1
SynonymsCMD1S|CMH1|MPD1|MYHCB|SPMD|SPMMCLC1
Cytomap

14q11.2

7q34

Type of geneprotein-codingprotein-coding
Descriptionmyosin-7cardiac muscle myosin heavy chain 7 betamyHC-betamyhc-slowmyopathy, distal 1myosin 7myosin heavy chain beta-subunitmyosin heavy chain slow isoformmyosin heavy chain, cardiac muscle beta isoformmyosin, heavy chain 7, cardiac muscle, betamchloride channel protein 1chloride channel 1, skeletal musclechloride channel protein, skeletal musclechloride channel, voltage-sensitive 1clC-1
Modification date2018051920180523
UniProtAcc

P12883

P35523

Ensembl transtripts involved in fusion geneENST00000355349, ENST00000343257, 
ENST00000495612, 
Fusion gene scores* DoF score3 X 3 X 1=91 X 1 X 1=1
# samples 41
** MAII scorelog2(4/9*10)=2.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: MYH7 [Title/Abstract] AND CLCN1 [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
HgeneMYH7

GO:0002026

regulation of the force of heart contraction

15621050

HgeneMYH7

GO:0002027

regulation of heart rate

15621050

HgeneMYH7

GO:0006936

muscle contraction

15621050

HgeneMYH7

GO:0006941

striated muscle contraction

15621050

HgeneMYH7

GO:0046034

ATP metabolic process

15621050


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
ChiTaRS3.1AA211487MYH7chr14

23883034

+CLCN1chr7

143022954

-
* 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-intronENST00000355349ENST00000343257MYH7chr14

23883034

+CLCN1chr7

143022954

-
intron-intronENST00000355349ENST00000495612MYH7chr14

23883034

+CLCN1chr7

143022954

-

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FusionProtFeatures for MYH7_CLCN1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYH7

P12883

CLCN1

P35523

Voltage-gated chloride channel. Chloride channels haveseveral functions including the regulation of cell volume;membrane potential stabilization, signal transduction andtransepithelial transport. {ECO:0000269|PubMed:12456816,ECO:0000269|PubMed:22521272, ECO:0000269|PubMed:26007199,ECO:0000269|PubMed:26502825, ECO:0000269|PubMed:26510092,ECO:0000269|PubMed:7951242, ECO:0000269|PubMed:8112288,ECO:0000269|PubMed:9122265, ECO:0000269|PubMed:9736777}.

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 MYH7_CLCN1


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 MYH7_CLCN1


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 MYH7_CLCN1


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 MYH7_CLCN1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMYH7C3495498Cardiomyopathy, Familial Hypertrophic, 1 (disorder)58CTD_human;UNIPROT
HgeneMYH7C1834481CARDIOMYOPATHY, DILATED, 1S6CTD_human;UNIPROT
HgeneMYH7C1842160MYOPATHY, MYOSIN STORAGE (disorder)4CTD_human;UNIPROT
HgeneMYH7C0221054Welander Distal Myopathy2ORPHANET;UNIPROT
HgeneMYH7C0007193Cardiomyopathy, Dilated1CTD_human;HPO
HgeneMYH7C0027051Myocardial Infarction1CTD_human
HgeneMYH7C0242231Coronary Stenosis1CTD_human
HgeneMYH7C0949658Cardiomyopathy, Hypertrophic, Familial1CTD_human
HgeneMYH7C1850709Myopathy, Hyaline Body, Autosomal Recessive1UNIPROT
TgeneCLCN1C0751360Becker Generalized Myotonia24UNIPROT
TgeneCLCN1C2936781Generalized Myotonia of Thomsen14CTD_human;ORPHANET;UNIPROT
TgeneCLCN1C0027127Myotonia Congenita1CTD_human;ORPHANET