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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: 34205

FusionGeneSummary for SLC25A23_SLC2A9

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC25A23_SLC2A9
Fusion gene ID: 34205
HgeneTgene
Gene symbol

SLC25A23

SLC2A9

Gene ID

79085

56606

Gene namesolute carrier family 25 member 23solute carrier family 2 member 9
SynonymsAPC2|MCSC2|SCaMC-3GLUT9|GLUTX|UAQTL2|URATv1
Cytomap

19p13.3

4p16.1

Type of geneprotein-codingprotein-coding
Descriptioncalcium-binding mitochondrial carrier protein SCaMC-3mitochondrial ATP-Mg/Pi carrier protein 2mitochondrial Ca(2+)-dependent solute carrier protein 2mitochondrial Ca2+-dependent solute carrier protein 2short calcium-binding mitochondrial carrier 3smasolute carrier family 2, facilitated glucose transporter member 9GLUT-9glucose transporter type 9human glucose transporter-like protein-9solute carrier family 2 (facilitated glucose transporter), member 9urate voltage-driven efflux transporter 1
Modification date2018052320180527
UniProtAcc

Q9BV35

Q9NRM0

Ensembl transtripts involved in fusion geneENST00000601760, ENST00000301454, 
ENST00000414491, ENST00000334510, 
ENST00000264784, ENST00000506583, 
ENST00000309065, ENST00000481042, 
Fusion gene scores* DoF score1 X 1 X 1=13 X 3 X 2=18
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SLC25A23 [Title/Abstract] AND SLC2A9 [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
TCGALDBRCATCGA-B6-A0RT-01ASLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
* 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-intronENST00000601760ENST00000264784SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000601760ENST00000506583SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000601760ENST00000309065SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000601760ENST00000481042SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000301454ENST00000264784SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000301454ENST00000506583SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000301454ENST00000309065SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000301454ENST00000481042SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000414491ENST00000264784SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000414491ENST00000506583SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000414491ENST00000309065SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
intron-intronENST00000414491ENST00000481042SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000334510ENST00000264784SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000334510ENST00000506583SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000334510ENST00000309065SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-
5CDS-intronENST00000334510ENST00000481042SLC25A23chr19

6456431

-SLC2A9chr4

9772993

-

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FusionProtFeatures for SLC25A23_SLC2A9


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLC25A23

Q9BV35

SLC2A9

Q9NRM0

Calcium-dependent mitochondrial solute carrier.Mitochondrial solute carriers shuttle metabolites, nucleotides,and cofactors through the mitochondrial inner membrane(PubMed:15123600). May act as a ATP-Mg/Pi exchanger that mediatesthe transport of Mg-ATP in exchange for phosphate, catalyzing thenet uptake or efflux of adenine nucleotides into or from themitochondria (PubMed:15123600). Acts as a regulator ofmitochondrial calcium uptake via interaction with MCU and MICU1(PubMed:24430870). {ECO:0000269|PubMed:15123600,ECO:0000269|PubMed:24430870}. Transport urate and fructose. May have a role in theurate reabsorption by proximal tubules. Also transports glucose atlow rate. {ECO:0000269|PubMed:14739288,ECO:0000269|PubMed:18327257}.

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 SLC25A23_SLC2A9


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 SLC25A23_SLC2A9


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
SLC25A23ELAVL1, CUL3, TARDBP, APPBP2, NRG1, SLC25A25, IL13RA2, SYP, CD79B, PDCD1, SLC22A6, SLC2A12, AIFM1, APLNR, VSIG4, TMEM108, SLC5A8, LRP1SLC2A9TKT


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 SLC25A23_SLC2A9


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 SLC25A23_SLC2A9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSLC2A9C2677549Hypouricemia, Renal, 23CTD_human;UNIPROT
TgeneSLC2A9C0018099Gout2CTD_human
TgeneSLC2A9C0473219Renal hypouricemia2CTD_human;ORPHANET
TgeneSLC2A9C0740394Hyperuricemia1CTD_human