FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:GALNT14-FHIT (FusionGDB2 ID:32243)

Fusion Gene Summary for GALNT14-FHIT

check button Fusion gene summary
Fusion gene informationFusion gene name: GALNT14-FHIT
Fusion gene ID: 32243
HgeneTgene
Gene symbol

GALNT14

FHIT

Gene ID

79623

2272

Gene namepolypeptide N-acetylgalactosaminyltransferase 14fragile histidine triad diadenosine triphosphatase
SynonymsGALNT15|GalNac-T10|GalNac-T14AP3Aase|FRA3B
Cytomap

2p23.1

3p14.2

Type of geneprotein-codingprotein-coding
Descriptionpolypeptide N-acetylgalactosaminyltransferase 14UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase 14UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase T10UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 (bis(5'-adenosyl)-triphosphataseAP3A hydrolasediadenosine 5',5'''-P1,P3-triphosphate hydrolasedinucleosidetriphosphatase
Modification date2020031320200313
UniProtAcc

Q96FL9

P49789

Ensembl transtripts involved in fusion geneENST00000324589, ENST00000349752, 
ENST00000406653, ENST00000420311, 
ENST00000356174, ENST00000486564, 
ENST00000341848, ENST00000466788, 
ENST00000468189, ENST00000476844, 
ENST00000492590, 
Fusion gene scores* DoF score9 X 7 X 5=31527 X 20 X 11=5940
# samples 932
** MAII scorelog2(9/315*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/5940*10)=-4.21431912080077
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GALNT14 [Title/Abstract] AND FHIT [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGALNT14(31189070)-FHIT(59738047), # samples:1
Anticipated loss of major functional domain due to fusion event.GALNT14-FHIT seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
GALNT14-FHIT seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
GALNT14-FHIT seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
GALNT14-FHIT seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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
TgeneFHIT

GO:0006163

purine nucleotide metabolic process

9323207


check buttonFusion gene breakpoints across GALNT14 (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 FHIT (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
ChimerDB4LIHCTCGA-DD-A116-01AGALNT14chr2

31189070

-FHITchr3

59738047

-


Top

Fusion Gene ORF analysis for GALNT14-FHIT

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-5UTRENST00000324589ENST00000341848GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000324589ENST00000466788GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000324589ENST00000468189GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000349752ENST00000341848GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000349752ENST00000466788GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000349752ENST00000468189GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000406653ENST00000341848GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000406653ENST00000466788GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000406653ENST00000468189GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000420311ENST00000341848GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000420311ENST00000466788GALNT14chr2

31189070

-FHITchr3

59738047

-
5CDS-5UTRENST00000420311ENST00000468189GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000324589ENST00000476844GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000324589ENST00000492590GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000349752ENST00000476844GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000349752ENST00000492590GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000406653ENST00000476844GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000406653ENST00000492590GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000420311ENST00000476844GALNT14chr2

31189070

-FHITchr3

59738047

-
Frame-shiftENST00000420311ENST00000492590GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-3CDSENST00000356174ENST00000476844GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-3CDSENST00000356174ENST00000492590GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-3CDSENST00000486564ENST00000476844GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-3CDSENST00000486564ENST00000492590GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-5UTRENST00000356174ENST00000341848GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-5UTRENST00000356174ENST00000466788GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-5UTRENST00000356174ENST00000468189GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-5UTRENST00000486564ENST00000341848GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-5UTRENST00000486564ENST00000466788GALNT14chr2

31189070

-FHITchr3

59738047

-
intron-5UTRENST00000486564ENST00000468189GALNT14chr2

31189070

-FHITchr3

59738047

-

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

Top

Fusion Genomic Features for GALNT14-FHIT


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.

Top

Fusion Protein Features for GALNT14-FHIT


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:31189070/:59738047)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GALNT14

Q96FL9

FHIT

P49789

FUNCTION: Catalyzes the initial reaction in O-linked oligosaccharide biosynthesis, the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor. Displays activity toward mucin-derived peptide substrates such as Muc2, Muc5AC, Muc7, and Muc13 (-58). May be involved in O-glycosylation in kidney.FUNCTION: Possesses dinucleoside triphosphate hydrolase activity (PubMed:12574506, PubMed:15182206, PubMed:8794732, PubMed:9323207, PubMed:9576908, PubMed:9543008). Cleaves P(1)-P(3)-bis(5'-adenosyl) triphosphate (Ap3A) to yield AMP and ADP (PubMed:12574506, PubMed:15182206, PubMed:8794732, PubMed:9323207, PubMed:9576908, PubMed:9543008). Can also hydrolyze P(1)-P(4)-bis(5'-adenosyl) tetraphosphate (Ap4A), but has extremely low activity with ATP (PubMed:8794732). Exhibits adenylylsulfatase activity, hydrolyzing adenosine 5'-phosphosulfate to yield AMP and sulfate (PubMed:18694747). Exhibits adenosine 5'-monophosphoramidase activity, hydrolyzing purine nucleotide phosphoramidates with a single phosphate group such as adenosine 5'monophosphoramidate (AMP-NH2) to yield AMP and NH2 (PubMed:18694747). Exhibits adenylylsulfate-ammonia adenylyltransferase, catalyzing the ammonolysis of adenosine 5'-phosphosulfate resulting in the formation of adenosine 5'-phosphoramidate (PubMed:26181368). Also catalyzes the ammonolysis of adenosine 5-phosphorofluoridate and diadenosine triphosphate (PubMed:26181368). Modulates transcriptional activation by CTNNB1 and thereby contributes to regulate the expression of genes essential for cell proliferation and survival, such as CCND1 and BIRC5 (PubMed:18077326). Plays a role in the induction of apoptosis via SRC and AKT1 signaling pathways (PubMed:16407838). Inhibits MDM2-mediated proteasomal degradation of p53/TP53 and thereby plays a role in p53/TP53-mediated apoptosis (PubMed:15313915). Induction of apoptosis depends on the ability of FHIT to bind P(1)-P(3)-bis(5'-adenosyl) triphosphate or related compounds, but does not require its catalytic activity, it may in part come from the mitochondrial form, which sensitizes the low-affinity Ca(2+) transporters, enhancing mitochondrial calcium uptake (PubMed:12574506, PubMed:19622739). Functions as tumor suppressor (By similarity). {ECO:0000250|UniProtKB:O89106, ECO:0000269|PubMed:12574506, ECO:0000269|PubMed:15313915, ECO:0000269|PubMed:16407838, ECO:0000269|PubMed:18077326, ECO:0000269|PubMed:18694747, ECO:0000269|PubMed:19622739, ECO:0000269|PubMed:26181368, ECO:0000269|PubMed:8794732, ECO:0000269|PubMed:9323207, ECO:0000269|PubMed:9543008}.

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


Top

Fusion Gene Sequence for GALNT14-FHIT


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.

Top

Fusion Gene PPI Analysis for GALNT14-FHIT


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


Top

Related Drugs for GALNT14-FHIT


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

Top

Related Diseases for GALNT14-FHIT


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