FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 34160

FusionGeneSummary for SLC23A2_NDUFS2

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC23A2_NDUFS2
Fusion gene ID: 34160
HgeneTgene
Gene symbol

SLC23A2

NDUFS2

Gene ID

9963

4720

Gene namesolute carrier family 23 member 1NADH:ubiquinone oxidoreductase core subunit S2
SynonymsSLC23A2|SVCT1|YSPL3CI-49
Cytomap

5q31.2

1q23.3

Type of geneprotein-codingprotein-coding
Descriptionsolute carrier family 23 member 1Na(+)/L-ascorbic acid transporter 1hSVCT1sodium-dependent vitamin C transporter-1solute carrier family 23 (ascorbic acid transporter), member 1solute carrier family 23 (nucleobase transporters), member 1solute carrieNADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrialCI-49kDNADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase)NADH-ubiquinone oxidoreductase 49 kDa subunitNADH-ubiquinone oxidoreductase NDUFS2 subunitcomp
Modification date2018052320180522
UniProtAcc

Q9UGH3

O75306

Ensembl transtripts involved in fusion geneENST00000338244, ENST00000379333, 
ENST00000424750, ENST00000468355, 
ENST00000367993, ENST00000392179, 
ENST00000476409, ENST00000465923, 
Fusion gene scores* DoF score7 X 7 X 6=2945 X 5 X 3=75
# samples 95
** MAII scorelog2(9/294*10)=-1.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLC23A2 [Title/Abstract] AND NDUFS2 [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
HgeneSLC23A2

GO:0006814

sodium ion transport

18094143

HgeneSLC23A2

GO:0009636

response to toxic substance

17575980

HgeneSLC23A2

GO:0015882

L-ascorbic acid transmembrane transport

10631088|11895172|18247577|18417304|19216494

HgeneSLC23A2

GO:0070904

transepithelial L-ascorbic acid transport

18417304

TgeneNDUFS2

GO:0006979

response to oxidative stress

12857734


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
ChiTaRS3.1BM708210SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
* 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-3UTRENST00000338244ENST00000367993SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000338244ENST00000392179SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-intronENST00000338244ENST00000476409SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000338244ENST00000465923SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000379333ENST00000367993SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000379333ENST00000392179SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-intronENST00000379333ENST00000476409SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000379333ENST00000465923SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000424750ENST00000367993SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000424750ENST00000392179SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-intronENST00000424750ENST00000476409SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000424750ENST00000465923SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000468355ENST00000367993SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000468355ENST00000392179SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-intronENST00000468355ENST00000476409SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+
intron-3UTRENST00000468355ENST00000465923SLC23A2chr20

4835006

-NDUFS2chr1

161184136

+

Top

FusionProtFeatures for SLC23A2_NDUFS2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLC23A2

Q9UGH3

NDUFS2

O75306

Sodium/ascorbate cotransporter. Mediates electrogenicuptake of vitamin C, with a stoichiometry of 2 Na(+) for eachascorbate. Core subunit of the mitochondrial membrane respiratorychain NADH dehydrogenase (Complex I) that is believed to belong tothe minimal assembly required for catalysis. Complex I functionsin the transfer of electrons from NADH to the respiratory chain.The immediate electron acceptor for the enzyme is believed to beubiquinone (PubMed:12611891). {ECO:0000269|PubMed:12611891}.

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


Top

FusionGeneSequence for SLC23A2_NDUFS2


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).

Top

FusionGenePPI for SLC23A2_NDUFS2


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


Top

RelatedDrugs for SLC23A2_NDUFS2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

RelatedDiseases for SLC23A2_NDUFS2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLC23A2C0008370Cholestasis1CTD_human
TgeneNDUFS2C0162666Mitochondrial Encephalomyopathies1CTD_human
TgeneNDUFS2C0878544Cardiomyopathies1CTD_human
TgeneNDUFS2C1838979MITOCHONDRIAL COMPLEX I DEFICIENCY1CTD_human;UNIPROT