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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: 4861

FusionGeneSummary for C1orf174_SNAP47

check button Fusion gene summary
Fusion gene informationFusion gene name: C1orf174_SNAP47
Fusion gene ID: 4861
HgeneTgene
Gene symbol

C1orf174

SNAP47

Gene ID

339448

116841

Gene namechromosome 1 open reading frame 174synaptosome associated protein 47
Synonyms-C1orf142|ESFI5812|HEL-S-290|HEL170|SNAP-47|SVAP1
Cytomap

1p36.32

1q42.13

Type of geneprotein-codingprotein-coding
DescriptionUPF0688 protein C1orf174RP13-531C17.2synaptosomal-associated protein 47epididymis luminal protein 170epididymis secretory protein Li 290synaptosomal-associated 47 kDa proteinsynaptosomal-associated protein, 47kDasynaptosome associated protein 47kDa
Modification date2018051920180523
UniProtAcc

Q8IYL3

Q5SQN1

Ensembl transtripts involved in fusion geneENST00000486765, ENST00000361605, 
ENST00000366760, ENST00000315781, 
ENST00000366759, ENST00000480897, 
Fusion gene scores* DoF score4 X 4 X 3=483 X 4 X 2=24
# samples 45
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/24*10)=1.05889368905357
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: C1orf174 [Title/Abstract] AND SNAP47 [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
TCGARVPRADTCGA-EJ-7321-01AC1orf174chr1

3816736

-SNAP47chr1

227946696

+
* 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
5UTR-5UTRENST00000486765ENST00000366760C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5UTR-5UTRENST00000486765ENST00000315781C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5UTR-5UTRENST00000486765ENST00000366759C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5UTR-intronENST00000486765ENST00000480897C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5CDS-5UTRENST00000361605ENST00000366760C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5CDS-5UTRENST00000361605ENST00000315781C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5CDS-5UTRENST00000361605ENST00000366759C1orf174chr1

3816736

-SNAP47chr1

227946696

+
5CDS-intronENST00000361605ENST00000480897C1orf174chr1

3816736

-SNAP47chr1

227946696

+

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FusionProtFeatures for C1orf174_SNAP47


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
C1orf174

Q8IYL3

SNAP47

Q5SQN1


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 C1orf174_SNAP47


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 C1orf174_SNAP47


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
C1orf174GOLM1, COPS6, EEF1G, KAT5, ELAVL1, TERF2IP, APP, IKZF1, PDIK1L, XPO1, STK35SNAP47GOLGA2, MAGEA6, STX4, SPAG5, MID2, FATE1, KLC3, FAM9B, CEP57L1, OIP5, STX7, STX12, CLEC12A, STX3, STX18, TCTN2, CNTROB, TMEM17, SEC22B, ECHDC1, GGA1


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 C1orf174_SNAP47


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 C1orf174_SNAP47


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