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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: 35162

FusionGeneSummary for SNORD104_HNRNPUL1

check button Fusion gene summary
Fusion gene informationFusion gene name: SNORD104_HNRNPUL1
Fusion gene ID: 35162
HgeneTgene
Gene symbol

SNORD104

HNRNPUL1

Gene ID

692227

11100

Gene namesmall nucleolar RNA, C/D box 104heterogeneous nuclear ribonucleoprotein U like 1
SynonymsU104E1B-AP5|E1BAP5|HNRPUL1
Cytomap

17q23.3

19q13.2

Type of genesnoRNAprotein-coding
Description-heterogeneous nuclear ribonucleoprotein U-like protein 1E1B 55kDa associated protein 5E1B-55 kDa-associated protein 5adenovirus early region 1B-associated protein 5
Modification date2018051920180522
UniProtAcc

Q9BUJ2

Ensembl transtripts involved in fusion geneENST00000362883, ENST00000352456, 
ENST00000595018, ENST00000392006, 
ENST00000378215, ENST00000602130, 
ENST00000593587, ENST00000263367, 
ENST00000594207, 
Fusion gene scores* DoF score2 X 1 X 1=213 X 12 X 5=780
# samples 214
** MAII scorelog2(2/2*10)=3.32192809488736log2(14/780*10)=-2.47804729680464
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SNORD104 [Title/Abstract] AND HNRNPUL1 [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
ChiTaRS3.1DB082610SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
* 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-intronENST00000362883ENST00000352456SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-intronENST00000362883ENST00000595018SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-5UTRENST00000362883ENST00000392006SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-5UTRENST00000362883ENST00000378215SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-intronENST00000362883ENST00000602130SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-intronENST00000362883ENST00000593587SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-intronENST00000362883ENST00000263367SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+
5CDS-intronENST00000362883ENST00000594207SNORD104chr17

62223512

+HNRNPUL1chr19

41770276

+

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FusionProtFeatures for SNORD104_HNRNPUL1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SNORD104

HNRNPUL1

Q9BUJ2

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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 SNORD104_HNRNPUL1


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 SNORD104_HNRNPUL1


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


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 SNORD104_HNRNPUL1


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 SNORD104_HNRNPUL1


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