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Fusion gene ID: 34335 |
FusionGeneSummary for SLC30A9_XRCC2 |
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Fusion gene information | Fusion gene name: SLC30A9_XRCC2 | Fusion gene ID: 34335 | Hgene | Tgene | Gene symbol | SLC30A9 | XRCC2 | Gene ID | 10463 | 7516 |
Gene name | solute carrier family 30 member 9 | X-ray repair cross complementing 2 | |
Synonyms | BILAPES|C4orf1|GAC63|HUEL|ZNT9 | FANCU | |
Cytomap | 4p13 | 7q36.1 | |
Type of gene | protein-coding | protein-coding | |
Description | zinc transporter 9GRIP1-dependent nuclear receptor coactivatorexpressed in human embryonic lunghuman embryonic lung proteinsolute carrier family 30 (zinc transporter), member 9znT-9 | DNA repair protein XRCC2X-ray repair complementing defective repair in Chinese hamster cells 2X-ray repair cross-complementing protein 2 | |
Modification date | 20180519 | 20180522 | |
UniProtAcc | Q6PML9 | O43543 | |
Ensembl transtripts involved in fusion gene | ENST00000264451, | ENST00000495707, ENST00000359321, | |
Fusion gene scores | * DoF score | 5 X 6 X 2=60 | 2 X 2 X 2=8 |
# samples | 6 | 2 | |
** MAII score | log2(6/60*10)=0 | log2(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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | XRCC2 | GO:0042148 | strand invasion | 11834724 |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | BI060642 | SLC30A9 | chr4 | 42088862 | - | XRCC2 | chr7 | 152372503 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
3UTR-intron | ENST00000264451 | ENST00000495707 | SLC30A9 | chr4 | 42088862 | - | XRCC2 | chr7 | 152372503 | + |
3UTR-intron | ENST00000264451 | ENST00000359321 | SLC30A9 | chr4 | 42088862 | - | XRCC2 | chr7 | 152372503 | + |
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FusionProtFeatures for SLC30A9_XRCC2 |
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Hgene | Tgene |
SLC30A9 | XRCC2 |
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}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for SLC30A9_XRCC2 |
![]() (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 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for SLC30A9_XRCC2 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for SLC30A9_XRCC2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | XRCC2 | C1458155 | Mammary Neoplasms | 1 | CTD_human |