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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: 32965

FusionGeneSummary for SDHAF1_TG

check button Fusion gene summary
Fusion gene informationFusion gene name: SDHAF1_TG
Fusion gene ID: 32965
HgeneTgene
Gene symbol

SDHAF1

TG

Gene ID

644096

7038

Gene namesuccinate dehydrogenase complex assembly factor 1thyroglobulin
SynonymsLYRM8AITD3|TGN
Cytomap

19q13.12

8q24.22

Type of geneprotein-codingprotein-coding
Descriptionsuccinate dehydrogenase assembly factor 1, mitochondrialLYR motif containing 8LYR motif-containing protein 8SDH assembly factor 1thyroglobulin
Modification date2018032920180520
UniProtAcc

A6NFY7

P01266

Ensembl transtripts involved in fusion geneENST00000378887, ENST00000377869, 
ENST00000220616, ENST00000542445, 
ENST00000519543, ENST00000522523, 
Fusion gene scores* DoF score2 X 2 X 2=810 X 11 X 5=550
# samples 212
** MAII scorelog2(2/8*10)=1.32192809488736log2(12/550*10)=-2.1963972128035
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SDHAF1 [Title/Abstract] AND TG [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
ChiTaRS3.1BI002377SDHAF1chr19

36486834

-TGchr8

133953700

-
* 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-3CDSENST00000378887ENST00000377869SDHAF1chr19

36486834

-TGchr8

133953700

-
3UTR-3CDSENST00000378887ENST00000220616SDHAF1chr19

36486834

-TGchr8

133953700

-
3UTR-intronENST00000378887ENST00000542445SDHAF1chr19

36486834

-TGchr8

133953700

-
3UTR-intronENST00000378887ENST00000519543SDHAF1chr19

36486834

-TGchr8

133953700

-
3UTR-intronENST00000378887ENST00000522523SDHAF1chr19

36486834

-TGchr8

133953700

-

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FusionProtFeatures for SDHAF1_TG


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

A6NFY7

TG

P01266

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_TG


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_TG


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 SDHAF1_TG


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_TG


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSDHAF1C0011269Dementia, Vascular1CTD_human
HgeneSDHAF1C1855008Mitochondrial Complex II Deficiency1CTD_human;ORPHANET;UNIPROT
TgeneTGC0342194Thyroid Dyshormonogenesis 35CTD_human;UNIPROT
TgeneTGC0018021Goiter2CTD_human;HPO
TgeneTGC0013336Dwarfism1CTD_human