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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:GALNT7-CHIC2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: GALNT7-CHIC2
FusionPDB ID: 32303
FusionGDB2.0 ID: 32303
HgeneTgene
Gene symbol

GALNT7

CHIC2

Gene ID

117248

26511

Gene namepolypeptide N-acetylgalactosaminyltransferase 15cysteine rich hydrophobic domain 2
SynonymsGALNACT15|GALNT13|GALNT7|GALNTL2|PIH5|pp-GalNAc-T15BTL
Cytomap

3p25.1

4q12

Type of geneprotein-codingprotein-coding
Descriptionpolypeptide N-acetylgalactosaminyltransferase 15UDP-GalNAc transferase T15UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-like protein 2UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 15UDP-N-acetyl-alpha-D-gacysteine-rich hydrophobic domain-containing protein 2BRX-like translocated in leukemiacystein-rich hydrophobic domain 2cysteine-rich hydrophobic domain 2 protein
Modification date2020031320200313
UniProtAcc

Q86SF2

Q9UKJ5

Ensembl transtripts involved in fusion geneENST idsENST00000265000, ENST00000512285, 
ENST00000502407, 
ENST00000263921, 
ENST00000512964, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 6 X 5=2403 X 2 X 2=12
# samples 112
** MAII scorelog2(11/240*10)=-1.12553088208386
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/12*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: GALNT7 [Title/Abstract] AND CHIC2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)GALNT7(174169591)-CHIC2(54915472), # samples:2
Anticipated loss of major functional domain due to fusion event.GALNT7-CHIC2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
GALNT7-CHIC2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
GALNT7-CHIC2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
GALNT7-CHIC2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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

check buttonFusion gene breakpoints across GALNT7 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across CHIC2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4PRADTCGA-EJ-7792GALNT7chr4

174169591

+CHIC2chr4

54915472

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000265000GALNT7chr4174169591+ENST00000263921CHIC2chr454915472-1355670831048321
ENST00000265000GALNT7chr4174169591+ENST00000512964CHIC2chr454915472-126267083991302
ENST00000512285GALNT7chr4174169591+ENST00000263921CHIC2chr454915472-129761225990321
ENST00000512285GALNT7chr4174169591+ENST00000512964CHIC2chr454915472-120461225933302

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
ENST00000265000ENST00000263921GALNT7chr4174169591+CHIC2chr454915472-0.001235630.9987644
ENST00000265000ENST00000512964GALNT7chr4174169591+CHIC2chr454915472-0.0012238390.99877614
ENST00000512285ENST00000263921GALNT7chr4174169591+CHIC2chr454915472-0.0011730940.9988269
ENST00000512285ENST00000512964GALNT7chr4174169591+CHIC2chr454915472-0.0011175780.9988825

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>32303_32303_1_GALNT7-CHIC2_GALNT7_chr4_174169591_ENST00000265000_CHIC2_chr4_54915472_ENST00000263921_length(amino acids)=321AA_BP=196
MRLKIGFILRSLLVVGSFLGLVVLWSSLTPRPDDPSPLSRMREDRDVNDPMPNRGGNGLAPGEDRFKPVVPWPHVEGVEVDLESIRRINK
AKNEQEHHAGGDSQKDIMQRQYLTFKPQTFTYHDPVLRPGILGNFEPKEPEPPGVVGGPGEKAKPLVLGPEFKQAIQASIKEFGFNMVAS
DMISLDRSVNDLRQEEFGLSNKFESEFPSSLTGKVAPEEFKASINRVNSCLKKNLPVNVRWLLCGCLCCCCTLGCSMWPVICLSKRTRRS

--------------------------------------------------------------

>32303_32303_2_GALNT7-CHIC2_GALNT7_chr4_174169591_ENST00000265000_CHIC2_chr4_54915472_ENST00000512964_length(amino acids)=302AA_BP=196
MRLKIGFILRSLLVVGSFLGLVVLWSSLTPRPDDPSPLSRMREDRDVNDPMPNRGGNGLAPGEDRFKPVVPWPHVEGVEVDLESIRRINK
AKNEQEHHAGGDSQKDIMQRQYLTFKPQTFTYHDPVLRPGILGNFEPKEPEPPGVVGGPGEKAKPLVLGPEFKQAIQASIKEFGFNMVAS
DMISLDRSVNDLRQEEFGLSNKFESEFPSSLTGKVAPEEFKASINRVNSCLKKNLPVNVRWLLCGCLCCCCTLGCSMWPVICLSKRLCLH

--------------------------------------------------------------

>32303_32303_3_GALNT7-CHIC2_GALNT7_chr4_174169591_ENST00000512285_CHIC2_chr4_54915472_ENST00000263921_length(amino acids)=321AA_BP=196
MRLKIGFILRSLLVVGSFLGLVVLWSSLTPRPDDPSPLSRMREDRDVNDPMPNRGGNGLAPGEDRFKPVVPWPHVEGVEVDLESIRRINK
AKNEQEHHAGGDSQKDIMQRQYLTFKPQTFTYHDPVLRPGILGNFEPKEPEPPGVVGGPGEKAKPLVLGPEFKQAIQASIKEFGFNMVAS
DMISLDRSVNDLRQEEFGLSNKFESEFPSSLTGKVAPEEFKASINRVNSCLKKNLPVNVRWLLCGCLCCCCTLGCSMWPVICLSKRTRRS

--------------------------------------------------------------

>32303_32303_4_GALNT7-CHIC2_GALNT7_chr4_174169591_ENST00000512285_CHIC2_chr4_54915472_ENST00000512964_length(amino acids)=302AA_BP=196
MRLKIGFILRSLLVVGSFLGLVVLWSSLTPRPDDPSPLSRMREDRDVNDPMPNRGGNGLAPGEDRFKPVVPWPHVEGVEVDLESIRRINK
AKNEQEHHAGGDSQKDIMQRQYLTFKPQTFTYHDPVLRPGILGNFEPKEPEPPGVVGGPGEKAKPLVLGPEFKQAIQASIKEFGFNMVAS
DMISLDRSVNDLRQEEFGLSNKFESEFPSSLTGKVAPEEFKASINRVNSCLKKNLPVNVRWLLCGCLCCCCTLGCSMWPVICLSKRLCLH

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Fusion Protein Functional Features


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/chr4:174169591/chr4:54915472)
- 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
GALNT7

Q86SF2

CHIC2

Q9UKJ5

FUNCTION: Glycopeptide transferase involved in O-linked oligosaccharide biosynthesis, which catalyzes the transfer of an N-acetyl-D-galactosamine residue to an already glycosylated peptide. In contrast to other proteins of the family, it does not act as a peptide transferase that transfers GalNAc onto serine or threonine residue on the protein receptor, but instead requires the prior addition of a GalNAc on a peptide before adding additional GalNAc moieties. Some peptide transferase activity is however not excluded, considering that its appropriate peptide substrate may remain unidentified. {ECO:0000269|PubMed:10544240, ECO:0000269|PubMed:11925450}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneGALNT7chr4:174169591chr4:54915472ENST00000265000+2121_6195.66666666666666658.0Topological domainCytoplasmic
HgeneGALNT7chr4:174169591chr4:54915472ENST00000265000+2127_29195.66666666666666658.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneCHIC2chr4:174169591chr4:54915472ENST000002639210688_10639.666666666666664166.0MotifNote=CHIC motif (Cys-rich)

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneGALNT7chr4:174169591chr4:54915472ENST00000265000+212532_652195.66666666666666658.0DomainRicin B-type lectin
HgeneGALNT7chr4:174169591chr4:54915472ENST00000265000+212206_317195.66666666666666658.0RegionNote=Catalytic subdomain A
HgeneGALNT7chr4:174169591chr4:54915472ENST00000265000+212381_443195.66666666666666658.0RegionNote=Catalytic subdomain B
HgeneGALNT7chr4:174169591chr4:54915472ENST00000265000+21230_657195.66666666666666658.0Topological domainLumenal
TgeneCHIC2chr4:174169591chr4:54915472ENST00000263921061_2639.666666666666664166.0Coiled coilOntology_term=ECO:0000255
TgeneCHIC2chr4:174169591chr4:54915472ENST00000263921069_1539.666666666666664166.0Compositional biasNote=Poly-Glu


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
GALNT7
CHIC2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to GALNT7-CHIC2


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to GALNT7-CHIC2


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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