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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: 34304

FusionGeneSummary for SLC2A13_ZNF329

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC2A13_ZNF329
Fusion gene ID: 34304
HgeneTgene
Gene symbol

SLC2A13

ZNF329

Gene ID

114134

79673

Gene namesolute carrier family 2 member 13zinc finger protein 329
SynonymsHMIT-
Cytomap

12q12

19q13.43

Type of geneprotein-codingprotein-coding
Descriptionproton myo-inositol cotransporterH(+)-myo-inositol symporterh(+)-myo-inositol cotransporterproton (H+) myo-inositol symportersolute carrier family 2 (facilitated glucose transporter), member 13zinc finger protein 329
Modification date2018052320180523
UniProtAcc

Q96QE2

Q86UD4

Ensembl transtripts involved in fusion geneENST00000280871, ENST00000380858, 
ENST00000598312, ENST00000358067, 
Fusion gene scores* DoF score9 X 5 X 7=3152 X 2 X 2=8
# samples 72
** MAII scorelog2(7/315*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: SLC2A13 [Title/Abstract] AND ZNF329 [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
TCGALDBLCATCGA-CU-A0YN-01ASLC2A13chr12

40422103

-ZNF329chr19

58654028

-
* 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
5CDS-5UTRENST00000280871ENST00000598312SLC2A13chr12

40422103

-ZNF329chr19

58654028

-
5CDS-5UTRENST00000280871ENST00000358067SLC2A13chr12

40422103

-ZNF329chr19

58654028

-
5CDS-5UTRENST00000380858ENST00000598312SLC2A13chr12

40422103

-ZNF329chr19

58654028

-
5CDS-5UTRENST00000380858ENST00000358067SLC2A13chr12

40422103

-ZNF329chr19

58654028

-

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FusionProtFeatures for SLC2A13_ZNF329


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLC2A13

Q96QE2

ZNF329

Q86UD4

H(+)-myo-inositol cotransporter. Can also transportrelated stereoisomers. {ECO:0000269|PubMed:11500374}. May be involved in transcriptional regulation.

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 SLC2A13_ZNF329


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 SLC2A13_ZNF329


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
SLC2A13ZNF329SMAD3, MEOX2, TRIM37, OPTN, MTUS2, CEP70, TRIM41, KRT40, KRTAP10-7, KRTAP10-1, KRTAP10-5


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 SLC2A13_ZNF329


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 SLC2A13_ZNF329


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLC2A13C0236969Substance-Related Disorders1CTD_human