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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: 34335

FusionGeneSummary for SLC30A9_XRCC2

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC30A9_XRCC2
Fusion gene ID: 34335
HgeneTgene
Gene symbol

SLC30A9

XRCC2

Gene ID

10463

7516

Gene namesolute carrier family 30 member 9X-ray repair cross complementing 2
SynonymsBILAPES|C4orf1|GAC63|HUEL|ZNT9FANCU
Cytomap

4p13

7q36.1

Type of geneprotein-codingprotein-coding
Descriptionzinc transporter 9GRIP1-dependent nuclear receptor coactivatorexpressed in human embryonic lunghuman embryonic lung proteinsolute carrier family 30 (zinc transporter), member 9znT-9DNA repair protein XRCC2X-ray repair complementing defective repair in Chinese hamster cells 2X-ray repair cross-complementing protein 2
Modification date2018051920180522
UniProtAcc

Q6PML9

O43543

Ensembl transtripts involved in fusion geneENST00000264451, ENST00000495707, 
ENST00000359321, 
Fusion gene scores* DoF score5 X 6 X 2=602 X 2 X 2=8
# samples 62
** MAII scorelog2(6/60*10)=0log2(2/8*10)=1.32192809488736
Context

PubMed: SLC30A9 [Title/Abstract] AND XRCC2 [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
TgeneXRCC2

GO:0042148

strand invasion

11834724


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
ChiTaRS3.1BI060642SLC30A9chr4

42088862

-XRCC2chr7

152372503

+
* 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-intronENST00000264451ENST00000495707SLC30A9chr4

42088862

-XRCC2chr7

152372503

+
3UTR-intronENST00000264451ENST00000359321SLC30A9chr4

42088862

-XRCC2chr7

152372503

+

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FusionProtFeatures for SLC30A9_XRCC2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLC30A9

Q6PML9

XRCC2

O43543

Acts as a zinc transporter involved in intracellularzinc homeostasis (PubMed:28334855). Functions as a secondarycoactivator for nuclear receptors by cooperating with p160coactivators subtypes. Plays a role in transcriptional activationof Wnt-responsive genes (By similarity).{ECO:0000250|UniProtKB:Q5IRJ6, ECO:0000269|PubMed:28334855}. Involved in the homologous recombination repair (HRR)pathway of double-stranded DNA, thought to repair chromosomalfragmentation, translocations and deletions. Part of the Rad21paralog protein complex BCDX2 which acts in the BRCA1-BRCA2-dependent HR pathway. Upon DNA damage, BCDX2 acts downstream ofBRCA2 recruitment and upstream of RAD51 recruitment. BCDX2 bindspredominantly to the intersection of the four duplex arms of theHolliday junction and to junction of replication forks. The BCDX2complex was originally reported to bind single-stranded DNA,single-stranded gaps in duplex DNA and specifically to nicks induplex DNA. {ECO:0000269|PubMed:11751635,ECO:0000269|PubMed:11834724, ECO:0000269|PubMed:21276791,ECO:0000269|PubMed:23149936, ECO:0000269|PubMed:27233470}.

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 SLC30A9_XRCC2


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 SLC30A9_XRCC2


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 SLC30A9_XRCC2


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 SLC30A9_XRCC2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneXRCC2C1458155Mammary Neoplasms1CTD_human