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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: 34288

FusionGeneSummary for SLC2A10_ACSS2

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC2A10_ACSS2
Fusion gene ID: 34288
HgeneTgene
Gene symbol

SLC2A10

ACSS2

Gene ID

81031

55902

Gene namesolute carrier family 2 member 10acyl-CoA synthetase short chain family member 2
SynonymsATS|GLUT10ACAS2|ACECS|ACS|ACSA|dJ1161H23.1
Cytomap

20q13.12

20q11.22

Type of geneprotein-codingprotein-coding
Descriptionsolute carrier family 2, facilitated glucose transporter member 10GLUT-10glucose transporter type 10solute carrier family 2 (facilitated glucose transporter), member 10acetyl-coenzyme A synthetase, cytoplasmicacetate thiokinaseacetate-CoA ligaseacetyl-Coenzyme A synthetase 2 (ADP forming)acyl-activating enzymecytoplasmic acetyl-coenzyme A synthetase
Modification date2018052320180522
UniProtAcc

O95528

Q9NR19

Ensembl transtripts involved in fusion geneENST00000359271, ENST00000486000, 
ENST00000336325, ENST00000360596, 
ENST00000253382, ENST00000476922, 
Fusion gene scores* DoF score3 X 3 X 2=185 X 3 X 3=45
# samples 35
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/45*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SLC2A10 [Title/Abstract] AND ACSS2 [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
TCGARVLUSCTCGA-85-8664-01ASLC2A10chr20

45338379

+ACSS2chr20

33500899

+
* 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
Frame-shiftENST00000359271ENST00000336325SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
Frame-shiftENST00000359271ENST00000360596SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
Frame-shiftENST00000359271ENST00000253382SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
5CDS-intronENST00000359271ENST00000476922SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
3UTR-3CDSENST00000486000ENST00000336325SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
3UTR-3CDSENST00000486000ENST00000360596SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
3UTR-3CDSENST00000486000ENST00000253382SLC2A10chr20

45338379

+ACSS2chr20

33500899

+
3UTR-intronENST00000486000ENST00000476922SLC2A10chr20

45338379

+ACSS2chr20

33500899

+

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FusionProtFeatures for SLC2A10_ACSS2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLC2A10

O95528

ACSS2

Q9NR19

Facilitative glucose transporter. Activates acetate so that it can be used for lipidsynthesis or for energy generation.

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 SLC2A10_ACSS2


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 SLC2A10_ACSS2


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
SLC2A10ACSS2UPF1, MAT2A, CAD, WARS, CTR9


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 SLC2A10_ACSS2


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 SLC2A10_ACSS2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLC2A10C1859726ARTERIAL TORTUOSITY SYNDROME2CTD_human;ORPHANET;UNIPROT
HgeneSLC2A10C1458155Mammary Neoplasms1CTD_human