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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:TTYH3-ING1 (FusionGDB2 ID:94599)

Fusion Gene Summary for TTYH3-ING1

check button Fusion gene summary
Fusion gene informationFusion gene name: TTYH3-ING1
Fusion gene ID: 94599
HgeneTgene
Gene symbol

TTYH3

ING1

Gene ID

80727

3621

Gene nametweety family member 3inhibitor of growth family member 1
Synonyms-p24ING1c|p33|p33ING1|p33ING1b|p47|p47ING1a
Cytomap

7p22.3

13q34

Type of geneprotein-codingprotein-coding
Descriptionprotein tweety homolog 3hTTY3tweety homolog 3inhibitor of growth protein 1growth inhibitor ING1growth inhibitory protein ING1tumor suppressor ING1
Modification date2020031320200313
UniProtAcc.

Q9UK53

Ensembl transtripts involved in fusion geneENST00000258796, ENST00000407643, 
ENST00000403167, ENST00000477439, 
ENST00000338450, ENST00000333219, 
ENST00000375775, ENST00000375774, 
ENST00000464141, 
Fusion gene scores* DoF score14 X 12 X 7=11767 X 5 X 4=140
# samples 187
** MAII scorelog2(18/1176*10)=-2.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/140*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TTYH3 [Title/Abstract] AND ING1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTTYH3(2688659)-ING1(111372166), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneTTYH3

GO:0006821

chloride transport

16219661


check buttonFusion gene breakpoints across TTYH3 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ING1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABF757166TTYH3chr7

2688659

-ING1chr13

111372166

-


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Fusion Gene ORF analysis for TTYH3-ING1

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-3CDSENST00000258796ENST00000338450TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000258796ENST00000333219TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000258796ENST00000375775TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000258796ENST00000375774TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-intronENST00000258796ENST00000464141TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000407643ENST00000338450TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000407643ENST00000333219TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000407643ENST00000375775TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000407643ENST00000375774TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-intronENST00000407643ENST00000464141TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000403167ENST00000338450TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000403167ENST00000333219TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000403167ENST00000375775TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000403167ENST00000375774TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-intronENST00000403167ENST00000464141TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000477439ENST00000338450TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000477439ENST00000333219TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000477439ENST00000375775TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-3CDSENST00000477439ENST00000375774TTYH3chr7

2688659

-ING1chr13

111372166

-
intron-intronENST00000477439ENST00000464141TTYH3chr7

2688659

-ING1chr13

111372166

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for TTYH3-ING1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for TTYH3-ING1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.ING1

Q9UK53

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Cooperates with p53/TP53 in the negative regulatory pathway of cell growth by modulating p53-dependent transcriptional activation. Implicated as a tumor suppressor gene. {ECO:0000269|PubMed:9440695}.

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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Fusion Gene Sequence for TTYH3-ING1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for TTYH3-ING1


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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Related Drugs for TTYH3-ING1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for TTYH3-ING1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneING1C0011616Contact Dermatitis1CTD_human
TgeneING1C0024623Malignant neoplasm of stomach1CTD_human
TgeneING1C0038356Stomach Neoplasms1CTD_human
TgeneING1C0162351Contact hypersensitivity1CTD_human
TgeneING1C0235874Disease Exacerbation1CTD_human
TgeneING1C0280302Squamous cell carcinoma of lip1ORPHANET
TgeneING1C0280313Squamous cell carcinoma of oropharynx1ORPHANET
TgeneING1C0280321Squamous cell carcinoma of the hypopharynx1ORPHANET
TgeneING1C0280324Laryngeal Squamous Cell Carcinoma1ORPHANET
TgeneING1C0585362Squamous cell carcinoma of mouth1ORPHANET
TgeneING1C1168401Squamous cell carcinoma of the head and neck1CGI;CTD_human;UNIPROT
TgeneING1C1708349Hereditary Diffuse Gastric Cancer1CTD_human