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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: 32532

FusionGeneSummary for SAC3D1_SNX15

check button Fusion gene summary
Fusion gene informationFusion gene name: SAC3D1_SNX15
Fusion gene ID: 32532
HgeneTgene
Gene symbol

SAC3D1

SNX15

Gene ID

29901

29907

Gene nameSAC3 domain containing 1sorting nexin 15
SynonymsHSU79266|SHD1HSAF001435
Cytomap

11q13.1

11q13.1

Type of geneprotein-codingprotein-coding
DescriptionSAC3 domain-containing protein 1SAC3 homology domain-containing protein 1Sac3 homology domain 1sorting nexin-15clone iota unknown protein
Modification date2018051920180519
UniProtAcc

A6NKF1

Q9NRS6

Ensembl transtripts involved in fusion geneENST00000531072, ENST00000398846, 
ENST00000530213, 
ENST00000377244, 
ENST00000352068, 
Fusion gene scores* DoF score1 X 1 X 1=11 X 1 X 1=1
# samples 11
** MAII scorelog2(1/1*10)=3.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: SAC3D1 [Title/Abstract] AND SNX15 [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
TCGARVOVTCGA-13-1511-01ASAC3D1chr11

64809338

+SNX15chr11

64807158

+
* 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
Frame-shiftENST00000531072ENST00000377244SAC3D1chr11

64809338

+SNX15chr11

64807158

+
Frame-shiftENST00000531072ENST00000352068SAC3D1chr11

64809338

+SNX15chr11

64807158

+
Frame-shiftENST00000398846ENST00000377244SAC3D1chr11

64809338

+SNX15chr11

64807158

+
Frame-shiftENST00000398846ENST00000352068SAC3D1chr11

64809338

+SNX15chr11

64807158

+
3UTR-3CDSENST00000530213ENST00000377244SAC3D1chr11

64809338

+SNX15chr11

64807158

+
3UTR-3CDSENST00000530213ENST00000352068SAC3D1chr11

64809338

+SNX15chr11

64807158

+

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FusionProtFeatures for SAC3D1_SNX15


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SAC3D1

A6NKF1

SNX15

Q9NRS6

Involved in centrosome duplication and mitoticprogression. {ECO:0000250}. May be involved in several stages of intracellulartrafficking. Overexpression of SNX15 disrupts the normaltrafficking of proteins from the plasma membrane to recyclingendosomes or the TGN. {ECO:0000269|PubMed:11085978}.

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 SAC3D1_SNX15


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 SAC3D1_SNX15


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
SAC3D1SHFM1, DDX3X, DCUN1D5, HDLBP, TTC4, VPS29, VPS35, VPS26A, WDR5, PRSS33SNX15RABAC1, METTL14, VPS36, FN1, KDM1A, ARL6IP1, RTN4, REEP6, HOXC10, NT5C2


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 SAC3D1_SNX15


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 SAC3D1_SNX15


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSAC3D1C0025202melanoma1CTD_human