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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: 32966

FusionGeneSummary for SDHAF1_TSPAN8

check button Fusion gene summary
Fusion gene informationFusion gene name: SDHAF1_TSPAN8
Fusion gene ID: 32966
HgeneTgene
Gene symbol

SDHAF1

TSPAN8

Gene ID

644096

7103

Gene namesuccinate dehydrogenase complex assembly factor 1tetraspanin 8
SynonymsLYRM8CO-029|TM4SF3
Cytomap

19q13.12

12q21.1

Type of geneprotein-codingprotein-coding
Descriptionsuccinate dehydrogenase assembly factor 1, mitochondrialLYR motif containing 8LYR motif-containing protein 8SDH assembly factor 1tetraspanin-8transmembrane 4 superfamily member 3tspan-8tumor-associated antigen CO-029
Modification date2018032920180523
UniProtAcc

A6NFY7

P19075

Ensembl transtripts involved in fusion geneENST00000378887, ENST00000393330, 
ENST00000247829, ENST00000546561, 
ENST00000552128, ENST00000552786, 
Fusion gene scores* DoF score2 X 2 X 2=827 X 7 X 11=2079
# samples 225
** MAII scorelog2(2/8*10)=1.32192809488736log2(25/2079*10)=-3.05588975819628
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SDHAF1 [Title/Abstract] AND TSPAN8 [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
TCGALDSARCTCGA-DX-A7EI-01ASDHAF1chr19

36486610

+TSPAN8chr12

71526604

-
* 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
3UTR-3CDSENST00000378887ENST00000393330SDHAF1chr19

36486610

+TSPAN8chr12

71526604

-
3UTR-3CDSENST00000378887ENST00000247829SDHAF1chr19

36486610

+TSPAN8chr12

71526604

-
3UTR-3CDSENST00000378887ENST00000546561SDHAF1chr19

36486610

+TSPAN8chr12

71526604

-
3UTR-3CDSENST00000378887ENST00000552128SDHAF1chr19

36486610

+TSPAN8chr12

71526604

-
3UTR-intronENST00000378887ENST00000552786SDHAF1chr19

36486610

+TSPAN8chr12

71526604

-

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FusionProtFeatures for SDHAF1_TSPAN8


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SDHAF1

A6NFY7

TSPAN8

P19075

Plays an essential role in the assembly of succinatedehydrogenase (SDH), an enzyme complex (also referred to asrespiratory complex II) that is a component of both thetricarboxylic acid (TCA) cycle and the mitochondrial electrontransport chain, and which couples the oxidation of succinate tofumarate with the reduction of ubiquinone (coenzyme Q) toubiquinol. Promotes maturation of the iron-sulfur protein subunitSDHB of the SDH catalytic dimer, protecting it from thedeleterious effects of oxidants. May act together with SDHAF3.{ECO:0000269|PubMed:19465911, ECO:0000269|PubMed:24954417}.

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 SDHAF1_TSPAN8


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 SDHAF1_TSPAN8


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
SDHAF1TSPAN8


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 SDHAF1_TSPAN8


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 SDHAF1_TSPAN8


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSDHAF1C0011269Dementia, Vascular1CTD_human
HgeneSDHAF1C1855008Mitochondrial Complex II Deficiency1CTD_human;ORPHANET;UNIPROT
TgeneTSPAN8C0005586Bipolar Disorder1PSYGENET
TgeneTSPAN8C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneTSPAN8C0035222Respiratory Distress Syndrome, Adult1CTD_human
TgeneTSPAN8C0036341Schizophrenia1PSYGENET
TgeneTSPAN8C0525045Mood Disorders1PSYGENET