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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: 35155

FusionGeneSummary for SNIP1_KIF17

check button Fusion gene summary
Fusion gene informationFusion gene name: SNIP1_KIF17
Fusion gene ID: 35155
HgeneTgene
Gene symbol

SNIP1

KIF17

Gene ID

79753

57576

Gene nameSmad nuclear interacting protein 1kinesin family member 17
SynonymsPML1|PMREDKIF17B|KIF3X|KLP-2|OSM-3
Cytomap

1p34.3

1p36.12

Type of geneprotein-codingprotein-coding
Descriptionsmad nuclear-interacting protein 1FHA domain-containing protein SNIP1PML1 homologkinesin-like protein KIF17KIF17 variant proteinKIF3-related motor protein
Modification date2018052320180523
UniProtAcc

Q8TAD8

Q9P2E2

Ensembl transtripts involved in fusion geneENST00000296215, ENST00000468040, 
ENST00000490034, ENST00000375044, 
ENST00000400463, ENST00000247986, 
Fusion gene scores* DoF score4 X 3 X 3=361 X 1 X 1=1
# samples 41
** MAII scorelog2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: SNIP1 [Title/Abstract] AND KIF17 [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
TCGALDLGGTCGA-CS-6188-01ASNIP1chr1

38018246

-KIF17chr1

20992824

-
* 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-5UTRENST00000296215ENST00000490034SNIP1chr1

38018246

-KIF17chr1

20992824

-
5CDS-5UTRENST00000296215ENST00000375044SNIP1chr1

38018246

-KIF17chr1

20992824

-
5CDS-5UTRENST00000296215ENST00000400463SNIP1chr1

38018246

-KIF17chr1

20992824

-
5CDS-5UTRENST00000296215ENST00000247986SNIP1chr1

38018246

-KIF17chr1

20992824

-
5UTR-5UTRENST00000468040ENST00000490034SNIP1chr1

38018246

-KIF17chr1

20992824

-
5UTR-5UTRENST00000468040ENST00000375044SNIP1chr1

38018246

-KIF17chr1

20992824

-
5UTR-5UTRENST00000468040ENST00000400463SNIP1chr1

38018246

-KIF17chr1

20992824

-
5UTR-5UTRENST00000468040ENST00000247986SNIP1chr1

38018246

-KIF17chr1

20992824

-

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FusionProtFeatures for SNIP1_KIF17


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SNIP1

Q8TAD8

KIF17

Q9P2E2

Down-regulates NF-kappa-B signaling by competing withRELA for CREBBP/EP300 binding. Involved in the microRNA (miRNA)biogenesis. May be involved in cyclin-D1/CCND1 mRNA stabilitythrough the SNARP complex which associates with both the 3'end ofthe CCND1 gene and its mRNA. {ECO:0000269|PubMed:11567019,ECO:0000269|PubMed:15378006, ECO:0000269|PubMed:18632581,ECO:0000269|PubMed:18794151}. Transports vesicles containing N-methyl-D-aspartate(NMDA) receptor 2B along microtubules. {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 SNIP1_KIF17


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 SNIP1_KIF17


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
SNIP1DVL2, SMAD1, SMAD2, SMAD4, EP300, CREBBP, RELA, ATR, MYC, MAX, PRPF40A, SF3B1, CHERP, SRRM2, PRPF3, SNW1, MFAP1, IK, C17orf85, TTC14, ZCCHC10, SRPK2, CDK6, CLK2, TNIP1, BCLAF1, THRAP3, ACIN1, ZC3H14, PNN, GPATCH8, NCBP1, CRNKL1, RBM22, AQR, GPALPP1, PPIG, SRSF9, SRSF1, RNPS1, CLASRP, LARP1, CCDC9, CCDC12, SRRT, CDC40, MAGOH, ISY1, EIF4A3, CLK3, CASC3, YTHDC1, NKTR, SRSF6, MKRN1, TRA2A, TRA2B, SRSF8, BUD31, SPTY2D1, SRSF12, SRSF10, DHX8, NKAP, CLCN2, FERMT3, TMEM184B, WSB2, PAIP2B, CDK3, PPIE, RALY, RPL5KIF17MAP3K10, MAP3K11, GFI1B, CDC42


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 SNIP1_KIF17


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 SNIP1_KIF17


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSNIP1C3281055PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM1UNIPROT
TgeneKIF17C0036341Schizophrenia2PSYGENET