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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: 33560

FusionGeneSummary for SGCG_SGCG

check button Fusion gene summary
Fusion gene informationFusion gene name: SGCG_SGCG
Fusion gene ID: 33560
HgeneTgene
Gene symbol

SGCG

SGCG

Gene ID

6445

6445

Gene namesarcoglycan gammasarcoglycan gamma
Synonyms35DAG|A4|DAGA4|DMDA|DMDA1|LGMD2C|MAM|SCARMD2|SCG3|gamma-SG35DAG|A4|DAGA4|DMDA|DMDA1|LGMD2C|MAM|SCARMD2|SCG3|gamma-SG
Cytomap

13q12.12

13q12.12

Type of geneprotein-codingprotein-coding
Descriptiongamma-sarcoglycan35 kDa dystrophin-associated glycoprotein35kD dystrophin-associated glycoproteinsarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)gamma-sarcoglycan35 kDa dystrophin-associated glycoprotein35kD dystrophin-associated glycoproteinsarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
Modification date2018052320180523
UniProtAcc

Q13326

Q13326

Ensembl transtripts involved in fusion geneENST00000218867, ENST00000537476, 
ENST00000545013, 
ENST00000218867, 
ENST00000537476, ENST00000545013, 
Fusion gene scores* DoF score2 X 2 X 1=41 X 1 X 1=1
# samples 21
** MAII scorelog2(2/4*10)=2.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: SGCG [Title/Abstract] AND SGCG [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
ChiTaRS3.1BQ307129SGCGchr13

23765413

-SGCGchr13

23853508

+
* 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-3CDSENST00000218867ENST00000218867SGCGchr13

23765413

-SGCGchr13

23853508

+
intron-3CDSENST00000218867ENST00000537476SGCGchr13

23765413

-SGCGchr13

23853508

+
intron-3CDSENST00000218867ENST00000545013SGCGchr13

23765413

-SGCGchr13

23853508

+
intron-3CDSENST00000537476ENST00000218867SGCGchr13

23765413

-SGCGchr13

23853508

+
intron-3CDSENST00000537476ENST00000537476SGCGchr13

23765413

-SGCGchr13

23853508

+
intron-3CDSENST00000537476ENST00000545013SGCGchr13

23765413

-SGCGchr13

23853508

+
5UTR-3CDSENST00000545013ENST00000218867SGCGchr13

23765413

-SGCGchr13

23853508

+
5UTR-3CDSENST00000545013ENST00000537476SGCGchr13

23765413

-SGCGchr13

23853508

+
5UTR-3CDSENST00000545013ENST00000545013SGCGchr13

23765413

-SGCGchr13

23853508

+

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FusionProtFeatures for SGCG_SGCG


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

Q13326

SGCG

Q13326

Component of the sarcoglycan complex, a subcomplex ofthe dystrophin-glycoprotein complex which forms a link between theF-actin cytoskeleton and the extracellular matrix. Component of the sarcoglycan complex, a subcomplex ofthe dystrophin-glycoprotein complex which forms a link between theF-actin cytoskeleton and the extracellular matrix.

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 SGCG_SGCG


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 SGCG_SGCG


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 SGCG_SGCG


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 SGCG_SGCG


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSGCGC0410173Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)2CTD_human;ORPHANET;UNIPROT
HgeneSGCGC0029408Degenerative polyarthritis1CTD_human
TgeneSGCGC0410173Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)2CTD_human;ORPHANET;UNIPROT
TgeneSGCGC0029408Degenerative polyarthritis1CTD_human