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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: 32230

FusionGeneSummary for RRBP1_SNTA1

check button Fusion gene summary
Fusion gene informationFusion gene name: RRBP1_SNTA1
Fusion gene ID: 32230
HgeneTgene
Gene symbol

RRBP1

SNTA1

Gene ID

6238

6640

Gene nameribosome binding protein 1syntrophin alpha 1
SynonymsES/130|ES130|RRp|hESLQT12|SNT1|TACIP1|dJ1187J4.5
Cytomap

20p12.1

20q11.21

Type of geneprotein-codingprotein-coding
Descriptionribosome-binding protein 1180 kDa ribosome receptor homologES/130-related proteinribosome binding protein 1 homolog 180kDa (dog)ribosome receptor proteinalpha-1-syntrophin59 kDa dystrophin-associated protein A1 acidic component 1acidic alpha 1 syntrophindystrophin-associated protein A1, 59kDa, acidic componentpro-TGF-alpha cytoplasmic domain-interacting protein 1syntrophin-1
Modification date2018051920180522
UniProtAcc

Q9P2E9

Q13424

Ensembl transtripts involved in fusion geneENST00000470422, ENST00000246043, 
ENST00000377813, ENST00000377807, 
ENST00000360807, ENST00000455029, 
ENST00000217381, 
Fusion gene scores* DoF score14 X 12 X 7=11763 X 2 X 3=18
# samples 173
** MAII scorelog2(17/1176*10)=-2.79028140869866
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RRBP1 [Title/Abstract] AND SNTA1 [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
TCGALDCOADTCGA-A6-2675-01ARRBP1chr20

17639241

-SNTA1chr20

32026832

-
* 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-3CDSENST00000470422ENST00000217381RRBP1chr20

17639241

-SNTA1chr20

32026832

-
Frame-shiftENST00000246043ENST00000217381RRBP1chr20

17639241

-SNTA1chr20

32026832

-
Frame-shiftENST00000377813ENST00000217381RRBP1chr20

17639241

-SNTA1chr20

32026832

-
intron-3CDSENST00000377807ENST00000217381RRBP1chr20

17639241

-SNTA1chr20

32026832

-
intron-3CDSENST00000360807ENST00000217381RRBP1chr20

17639241

-SNTA1chr20

32026832

-
intron-3CDSENST00000455029ENST00000217381RRBP1chr20

17639241

-SNTA1chr20

32026832

-

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FusionProtFeatures for RRBP1_SNTA1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RRBP1

Q9P2E9

SNTA1

Q13424

Adapter protein that binds to and probably organizes thesubcellular localization of a variety of membrane proteins. Maylink various receptors to the actin cytoskeleton and theextracellular matrix via the dystrophin glycoprotein complex.Plays an important role in synapse formation and in theorganization of UTRN and acetylcholine receptors at theneuromuscular synapse. Binds to phosphatidylinositol 4,5-bisphosphate (By similarity). {ECO:0000250}.

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 RRBP1_SNTA1


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 RRBP1_SNTA1


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
RRBP1DSTN, ZWINT, CUL3, NDUFA7, CDV3, SCP2, RPS19, ILF3, PPIF, HNRNPM, MRPL53, SRPRB, PIN4, RBMS1, KLF5, RAB8A, CHMP2A, PQBP1, RPL38, HSPA1L, HSBP1, IQCB1, SMAD9, PRKD2, MAP1LC3A, KIAA0101, TARDBP, LGR4, VCP, CUL7, NTRK1, MORC2, RBM8A, BUD31, SMNDC1, EWSR1, TMPO, FOXG1, FOXL1, PES1, EMILIN1, EEF1D, KLHL2, TSPYL6, STYX, DLST, PDHA1, TRIM25, YAP1SNTA1KCNJ12, KCNJ4, XRCC6, GLS, DMD, UTRN, DGKZ, GRB2, SCN1A, SCN5A, NOS1, MAPK12, DTNA, MAGEE1, HTR2B, HTR2C, ADRA1D, ADRA2A, ADH5, AGTR2, NAT1, ATP2B2, ADAMTS6, ADRB1, BAI2, BAI3, C3AR1, CD3E, KCNA4, KCNA5, SCN4A, COPB1, FAM189B, GUCY1A2, SLC1A7, F8A1, FABP1, GOLGA2, GLS2, PRLHR, SLC2A3, GDA, LOC100289290, TLX3, IL2RA, IL9, KCNJ10, KCNJ15, ITGB5, PSKH1, MAP4, MAS1, MCM7, SLC16A7, MTMR2, NMU, SLC6A3, PFN2, LMO1, SCTR, SSTR1, TGFA, TRA, TRBV12-3, ATP6V0B, MLC1, BAI1, ABCC4, GNAT3, SLC34A3, NEB, PLCB3, RGS11, RYR2, STAM, SPZ1, SNTG2, HMG20A, NDEL1, TENC1


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 RRBP1_SNTA1


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 RRBP1_SNTA1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSNTA1C2751830Long Qt Syndrome 122CTD_human;UNIPROT
TgeneSNTA1C0038220Status Epilepticus1CTD_human