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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: 1901

FusionGeneSummary for ANKS6_STX17

check button Fusion gene summary
Fusion gene informationFusion gene name: ANKS6_STX17
Fusion gene ID: 1901
HgeneTgene
Gene symbol

ANKS6

STX17

Gene ID

203286

55014

Gene nameankyrin repeat and sterile alpha motif domain containing 6syntaxin 17
SynonymsANKRD14|NPHP16|PKDR1|SAMD6-
Cytomap

9q22.33

9q31.1

Type of geneprotein-codingprotein-coding
Descriptionankyrin repeat and SAM domain-containing protein 6SAM domain-containing protein 6ankyrin repeat domain 14samCystinsyntaxin-17
Modification date2018052220180526
UniProtAcc

Q68DC2

P56962

Ensembl transtripts involved in fusion geneENST00000375019, ENST00000375018, 
ENST00000353234, ENST00000540940, 
ENST00000471846, 
ENST00000259400, 
ENST00000525640, ENST00000534052, 
ENST00000525847, 
Fusion gene scores* DoF score2 X 2 X 2=83 X 2 X 3=18
# samples 23
** MAII scorelog2(2/8*10)=1.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: ANKS6 [Title/Abstract] AND STX17 [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
TgeneSTX17

GO:0016240

autophagosome membrane docking

25686604

TgeneSTX17

GO:0034497

protein localization to phagophore assembly site

23455425


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
TCGARVCESCTCGA-JX-A3Q8-01AANKS6chr9

101558415

-STX17chr9

102677460

+
* 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-5UTRENST00000375019ENST00000259400ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-5UTRENST00000375019ENST00000525640ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-5UTRENST00000375019ENST00000534052ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-intronENST00000375019ENST00000525847ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-5UTRENST00000375018ENST00000259400ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-5UTRENST00000375018ENST00000525640ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-5UTRENST00000375018ENST00000534052ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-intronENST00000375018ENST00000525847ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-5UTRENST00000353234ENST00000259400ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-5UTRENST00000353234ENST00000525640ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-5UTRENST00000353234ENST00000534052ANKS6chr9

101558415

-STX17chr9

102677460

+
5CDS-intronENST00000353234ENST00000525847ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-5UTRENST00000540940ENST00000259400ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-5UTRENST00000540940ENST00000525640ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-5UTRENST00000540940ENST00000534052ANKS6chr9

101558415

-STX17chr9

102677460

+
intron-intronENST00000540940ENST00000525847ANKS6chr9

101558415

-STX17chr9

102677460

+
5UTR-5UTRENST00000471846ENST00000259400ANKS6chr9

101558415

-STX17chr9

102677460

+
5UTR-5UTRENST00000471846ENST00000525640ANKS6chr9

101558415

-STX17chr9

102677460

+
5UTR-5UTRENST00000471846ENST00000534052ANKS6chr9

101558415

-STX17chr9

102677460

+
5UTR-intronENST00000471846ENST00000525847ANKS6chr9

101558415

-STX17chr9

102677460

+

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FusionProtFeatures for ANKS6_STX17


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ANKS6

Q68DC2

STX17

P56962

SNAREs, soluble N-ethylmaleimide-sensitive factor-attachment protein receptors, are essential proteins for fusion ofcellular membranes. SNAREs localized on opposing membranesassemble to form a trans-SNARE complex, an extended, parallel fouralpha-helical bundle that drives membrane fusion. STX17 is a SNAREof the autophagosome involved in autophagy through the directcontrol of autophagosome membrane fusion with the lysosomemembrane (PubMed:23217709, PubMed:25686604). May also play a rolein the early secretory pathway where it may maintain thearchitecture of the endoplasmic reticulum-Golgi intermediatecompartment/ERGIC and Golgi and/or regulate transport between theendoplasmic reticulum, the ERGIC and the Golgi (PubMed:21545355).{ECO:0000269|PubMed:21545355, ECO:0000269|PubMed:23217709,ECO:0000269|PubMed:25686604}.

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 ANKS6_STX17


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 ANKS6_STX17


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
ANKS6APP, NEK8, XPO1, ETS2, KIF11, ANKS3, NEK7, DDX1, C19orf52, TIMM10, TIMM9, ATAD1, DCAF7, TRIM25STX17STX5, SNAP29, VPS33A, VPS16, VPS11, VPS18, VPS39, VPS41, PPM1E, EYA3, C5AR2, TMCO3


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 ANKS6_STX17


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 ANKS6_STX17


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneANKS6C0023890Liver Cirrhosis1CTD_human
HgeneANKS6C0037221Situs Inversus1CTD_human
HgeneANKS6C0085413Polycystic Kidney, Autosomal Dominant1CTD_human
HgeneANKS6C0243050Cardiovascular Abnormalities1CTD_human
HgeneANKS6C1691228Cystic Kidney Diseases1CTD_human
HgeneANKS6C3809320NEPHRONOPHTHISIS 161UNIPROT
TgeneSTX17C0002171Alopecia Areata1CTD_human
TgeneSTX17C0025202melanoma1CTD_human