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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: 15749

FusionGeneSummary for H19_NCEH1

check button Fusion gene summary
Fusion gene informationFusion gene name: H19_NCEH1
Fusion gene ID: 15749
HgeneTgene
Gene symbol

H19

NCEH1

Gene ID

283120

57552

Gene nameH19, imprinted maternally expressed transcriptneutral cholesterol ester hydrolase 1
SynonymsASM|ASM1|BWS|D11S813E|LINC00008|NCRNA00008|WT2AADACL1|NCEH
Cytomap

11p15.5

3q26.31

Type of genencRNAprotein-coding
DescriptionH19, imprinted maternally expressed transcript (non-protein coding)H19, imprinted maternally expressed untranslated mRNAlong intergenic non-protein coding RNA 8neutral cholesterol ester hydrolase 1arylacetamide deacetylase-like 1
Modification date2018052720180523
UniProtAcc

Q6PIU2

Ensembl transtripts involved in fusion geneENST00000390168, ENST00000475381, 
ENST00000273512, ENST00000538775, 
ENST00000543711, 
Fusion gene scores* DoF score19 X 23 X 1=4379 X 6 X 6=324
# samples 3012
** MAII scorelog2(30/437*10)=-0.542670779004717
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/324*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: H19 [Title/Abstract] AND NCEH1 [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
ChiTaRS3.1AF074689H19chr11

2018981

+NCEH1chr3

172361111

+
ChiTaRS3.1AI110782H19chr11

2018981

+NCEH1chr3

172361111

+
ChiTaRS3.1AI114579H19chr11

2018981

+NCEH1chr3

172361111

+
ChiTaRS3.1AF116626H19chr11

2018981

+NCEH1chr3

172361111

+
* 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-intronENST00000390168ENST00000475381H19chr11

2018981

+NCEH1chr3

172361111

+
intron-intronENST00000390168ENST00000273512H19chr11

2018981

+NCEH1chr3

172361111

+
intron-intronENST00000390168ENST00000538775H19chr11

2018981

+NCEH1chr3

172361111

+
intron-intronENST00000390168ENST00000543711H19chr11

2018981

+NCEH1chr3

172361111

+

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FusionProtFeatures for H19_NCEH1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
H19

NCEH1

Q6PIU2

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 H19_NCEH1


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 H19_NCEH1


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 H19_NCEH1


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 H19_NCEH1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneH19C0019188Hepatitis, Animal1CTD_human
HgeneH19C0023904Liver Neoplasms, Experimental1CTD_human
HgeneH19C0175693Russell-Silver syndrome1CTD_human