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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: 30184

FusionGeneSummary for RAD51B_SMOC1

check button Fusion gene summary
Fusion gene informationFusion gene name: RAD51B_SMOC1
Fusion gene ID: 30184
HgeneTgene
Gene symbol

RAD51B

SMOC1

Gene ID

5890

64093

Gene nameRAD51 paralog BSPARC related modular calcium binding 1
SynonymsR51H2|RAD51L1|REC2OAS
Cytomap

14q24.1

14q24.2

Type of geneprotein-codingprotein-coding
DescriptionDNA repair protein RAD51 homolog 2RAD51 homolog BRecA-like proteinrecombination repair proteinSPARC-related modular calcium-binding protein 1secreted modular calcium-binding protein 1
Modification date2018052320180519
UniProtAcc

O15315

Q9H4F8

Ensembl transtripts involved in fusion geneENST00000487861, ENST00000471583, 
ENST00000487270, ENST00000488612, 
ENST00000390683, ENST00000469165, 
ENST00000555917, ENST00000361956, 
ENST00000381280, 
Fusion gene scores* DoF score13 X 9 X 7=8192 X 2 X 2=8
# samples 152
** MAII scorelog2(15/819*10)=-2.44890095114513
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: RAD51B [Title/Abstract] AND SMOC1 [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-XF-AAMQ-01ARAD51Bchr14

68934967

+SMOC1chr14

70459134

+
* 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-intronENST00000487861ENST00000555917RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000487861ENST00000361956RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000487861ENST00000381280RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000471583ENST00000555917RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000471583ENST00000361956RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000471583ENST00000381280RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000487270ENST00000555917RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000487270ENST00000361956RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000487270ENST00000381280RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000488612ENST00000555917RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000488612ENST00000361956RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000488612ENST00000381280RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000390683ENST00000555917RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000390683ENST00000361956RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
5CDS-intronENST00000390683ENST00000381280RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
3UTR-intronENST00000469165ENST00000555917RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
3UTR-intronENST00000469165ENST00000361956RAD51Bchr14

68934967

+SMOC1chr14

70459134

+
3UTR-intronENST00000469165ENST00000381280RAD51Bchr14

68934967

+SMOC1chr14

70459134

+

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FusionProtFeatures for RAD51B_SMOC1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RAD51B

O15315

SMOC1

Q9H4F8

Plays essential roles in both eye and limb development.Probable regulator of osteoblast differentiation.{ECO:0000269|PubMed:20359165, ECO:0000269|PubMed:21194678,ECO:0000269|PubMed:21194680}.

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 RAD51B_SMOC1


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 RAD51B_SMOC1


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
RAD51BRAD51, RAD51C, RAD51D, XRCC2, SWSAP1, FAM9B, DKKL1, ARL4C, MUC20, ADAMTS4, HELQSMOC1CORO1C, DNAJB11, TCF4, KRTAP10-8, KRTAP10-3, NOTCH2NL, TAZ, GINM1, PON2, NME2, DKK3, DEFA1, EPHA7, TCTN1, NAF1, LRP1, ITGA9, UBR2, PNN, IGFBP1, CISD3, TNFSF8, HSP90AA4P, TRIM25


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 RAD51B_SMOC1


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 RAD51B_SMOC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRAD51BC0236969Substance-Related Disorders1CTD_human
HgeneRAD51BC0242788Breast Neoplasms, Male1CTD_human
HgeneRAD51BC1458155Mammary Neoplasms1CTD_human
TgeneSMOC1C0599973Waardenburg Anophthalmia Syndrome2ORPHANET;UNIPROT
TgeneSMOC1C0023893Liver Cirrhosis, Experimental1CTD_human