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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: 35267

FusionGeneSummary for SNX19_RRP12

check button Fusion gene summary
Fusion gene informationFusion gene name: SNX19_RRP12
Fusion gene ID: 35267
HgeneTgene
Gene symbol

SNX19

RRP12

Gene ID

399979

23223

Gene namesorting nexin 19ribosomal RNA processing 12 homolog
SynonymsCHET8KIAA0690
Cytomap

11q24.3-q25

10q24.1

Type of geneprotein-codingprotein-coding
Descriptionsorting nexin-19RRP12-like protein
Modification date2018051920180519
UniProtAcc

Q92543

Q5JTH9

Ensembl transtripts involved in fusion geneENST00000265909, ENST00000534726, 
ENST00000545537, ENST00000426933, 
ENST00000533318, ENST00000530356, 
ENST00000539184, ENST00000528555, 
ENST00000533214, 
ENST00000479481, 
ENST00000370992, ENST00000536831, 
ENST00000315563, ENST00000414986, 
Fusion gene scores* DoF score5 X 4 X 3=604 X 5 X 4=80
# samples 55
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SNX19 [Title/Abstract] AND RRP12 [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
TCGARVUCECTCGA-A5-A1OH-01ASNX19chr11

130784161

-RRP12chr10

99130553

-
* 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-5UTRENST00000265909ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000265909ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000265909ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000265909ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000265909ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000534726ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000534726ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000534726ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000534726ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000534726ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000545537ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000545537ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000545537ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000545537ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000545537ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000426933ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000426933ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000426933ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000426933ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000426933ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000533318ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000533318ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000533318ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000533318ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000533318ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000530356ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000530356ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000530356ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000530356ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000530356ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000539184ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000539184ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000539184ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000539184ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000539184ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000528555ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000528555ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000528555ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000528555ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
intron-5UTRENST00000528555ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000533214ENST00000479481SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000533214ENST00000370992SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000533214ENST00000536831SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000533214ENST00000315563SNX19chr11

130784161

-RRP12chr10

99130553

-
5CDS-5UTRENST00000533214ENST00000414986SNX19chr11

130784161

-RRP12chr10

99130553

-

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FusionProtFeatures for SNX19_RRP12


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SNX19

Q92543

RRP12

Q5JTH9

Plays a role in intracellular vesicle trafficking andexocytosis (PubMed:24843546). May play a role in maintaininginsulin-containing dense core vesicles in pancreatic beta-cellsand in preventing their degradation. May play a role in insulinsecretion (PubMed:24843546). Interacts with membranes containingphosphatidylinositol 3-phosphate (PtdIns(3P)) (By similarity).{ECO:0000250|UniProtKB:Q6P4T1, ECO:0000269|PubMed:24843546}.

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 SNX19_RRP12


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 SNX19_RRP12


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
SNX19ELAVL1, NOTCH3, TCTN2, PTPRN, PTPRN2, ATP6V0D1, TRIM25RRP12DDX56, AP2M1, SIRT7, CUL3, CUL1, COPS5, COPS6, CAND1, RBM28, RPL5, POLR3F, ESR1, VCP, CSNK2A1, HDAC11, LGR4, LIN28A, TARBP2, CUL7, OBSL1, EED, RNF2, BMI1, ABCE1, HIST1H1A, FMR1NB, RPL6, RPS2, BYSL, PRR11, NTRK1, BRIX1, DDX24, EIF2A, EIF5B, H1FX, NIFK, NOC2L, RBM19, GLTSCR2, NOC3L, NOP58, PRMT5, RPL3, RRP36, SKIV2L2, SRP72, TPR, RSL1D1, TSR1, SCARNA22, IFI16, HNRNPU, NPM1, RPL10, NOP56, KIF2C, PES1, NANOG, POU5F1, ZNF746, CDC14B, TNFRSF1A, RPS14, RRP8, GPATCH4, HIST1H1T, ZNF324B, HIST1H1E, SART3, RPL7, FGF8, FGF3, PDGFB, WDR5B, CHCHD10, SCN3B, TNFRSF13B, INO80B, COX15


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 SNX19_RRP12


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 SNX19_RRP12


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