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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:FAM162A-GSK3B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: FAM162A-GSK3B
FusionPDB ID: 28633
FusionGDB2.0 ID: 28633
HgeneTgene
Gene symbol

FAM162A

GSK3B

Gene ID

26355

2932

Gene namefamily with sequence similarity 162 member Aglycogen synthase kinase 3 beta
SynonymsC3orf28|E2IG5|HGTD-P-
Cytomap

3q21.1

3q13.33

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM162AE2-induced gene 5 proteinHIF-1 alpha-responsive proapoptotic moleculegrowth and transformation-dependent proteinglycogen synthase kinase-3 betaGSK-3 betaGSK3beta isoformserine/threonine-protein kinase GSK3B
Modification date2020031320200315
UniProtAcc

Q96A26

C14orf129

Ensembl transtripts involved in fusion geneENST idsENST00000469967, ENST00000477892, 
ENST00000232125, 
ENST00000473886, 
ENST00000264235, ENST00000316626, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 5 X 5=1503 X 3 X 3=27
# samples 103
** MAII scorelog2(10/150*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: FAM162A [Title/Abstract] AND GSK3B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)FAM162A(122103146)-GSK3B(119624699), # samples:1
Anticipated loss of major functional domain due to fusion event.FAM162A-GSK3B 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.
FAM162A-GSK3B 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
HgeneFAM162A

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

15082785

HgeneFAM162A

GO:0043065

positive regulation of apoptotic process

15082785

HgeneFAM162A

GO:0071456

cellular response to hypoxia

15082785

HgeneFAM162A

GO:0090200

positive regulation of release of cytochrome c from mitochondria

15082785

TgeneGSK3B

GO:0005977

glycogen metabolic process

8638126

TgeneGSK3B

GO:0006468

protein phosphorylation

11035810|16315267|20937854

TgeneGSK3B

GO:0006983

ER overload response

14744935

TgeneGSK3B

GO:0018105

peptidyl-serine phosphorylation

8638126|11104755|11955436|14744935|17139249

TgeneGSK3B

GO:0018107

peptidyl-threonine phosphorylation

11955436|17139249|25897075

TgeneGSK3B

GO:0031175

neuron projection development

19830702

TgeneGSK3B

GO:0031334

positive regulation of protein complex assembly

8638126

TgeneGSK3B

GO:0032091

negative regulation of protein binding

16890161

TgeneGSK3B

GO:0032436

positive regulation of proteasomal ubiquitin-dependent protein catabolic process

19364825

TgeneGSK3B

GO:0035556

intracellular signal transduction

14749367

TgeneGSK3B

GO:0043066

negative regulation of apoptotic process

14744935

TgeneGSK3B

GO:0046777

protein autophosphorylation

23184662

TgeneGSK3B

GO:0046827

positive regulation of protein export from nucleus

14744935

TgeneGSK3B

GO:1901215

negative regulation of neuron death

19830702

TgeneGSK3B

GO:1901216

positive regulation of neuron death

18508033

TgeneGSK3B

GO:2000300

regulation of synaptic vesicle exocytosis

17989287


check buttonFusion gene breakpoints across FAM162A (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 GSK3B (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
ChimerDB4STADTCGA-CD-5798-01AFAM162Achr3

122103146

+GSK3Bchr3

119624699

-


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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)
ENST00000477892FAM162Achr3122103146+ENST00000264235GSK3Bchr3119624699-613111884665193
ENST00000477892FAM162Achr3122103146+ENST00000316626GSK3Bchr3119624699-80711884704206
ENST00000469967FAM162Achr3122103146+ENST00000264235GSK3Bchr3119624699-611510268649193
ENST00000469967FAM162Achr3122103146+ENST00000316626GSK3Bchr3119624699-79110268688206

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
ENST00000477892ENST00000264235FAM162Achr3122103146+GSK3Bchr3119624699-0.0051969110.994803
ENST00000477892ENST00000316626FAM162Achr3122103146+GSK3Bchr3119624699-0.0253078170.97469217
ENST00000469967ENST00000264235FAM162Achr3122103146+GSK3Bchr3119624699-0.0051454120.99485457
ENST00000469967ENST00000316626FAM162Achr3122103146+GSK3Bchr3119624699-0.0241958870.9758041

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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

>28633_28633_1_FAM162A-GSK3B_FAM162A_chr3_122103146_ENST00000469967_GSK3B_chr3_119624699_ENST00000264235_length(amino acids)=193AA_BP=11
MGSLSGLRLAADVWSAGCVLAELLLGQPIFPGDSGVDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHPWTKVFRPRTPPEAIALC
SRLLEYTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALFNFTTQELSSNPPLATILIPPHARIQAAASTPTNATAASDANTGDRGQ

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

>28633_28633_2_FAM162A-GSK3B_FAM162A_chr3_122103146_ENST00000469967_GSK3B_chr3_119624699_ENST00000316626_length(amino acids)=206AA_BP=11
MGSLSGLRLAADVWSAGCVLAELLLGQPIFPGDSGVDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHPWTKDSSGTGHFTSGVRV
FRPRTPPEAIALCSRLLEYTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALFNFTTQELSSNPPLATILIPPHARIQAAASTPTNA

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

>28633_28633_3_FAM162A-GSK3B_FAM162A_chr3_122103146_ENST00000477892_GSK3B_chr3_119624699_ENST00000264235_length(amino acids)=193AA_BP=11
MGSLSGLRLAADVWSAGCVLAELLLGQPIFPGDSGVDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHPWTKVFRPRTPPEAIALC
SRLLEYTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALFNFTTQELSSNPPLATILIPPHARIQAAASTPTNATAASDANTGDRGQ

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

>28633_28633_4_FAM162A-GSK3B_FAM162A_chr3_122103146_ENST00000477892_GSK3B_chr3_119624699_ENST00000316626_length(amino acids)=206AA_BP=11
MGSLSGLRLAADVWSAGCVLAELLLGQPIFPGDSGVDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHPWTKDSSGTGHFTSGVRV
FRPRTPPEAIALCSRLLEYTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALFNFTTQELSSNPPLATILIPPHARIQAAASTPTNA

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

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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/chr3:122103146/chr3:119624699)
- 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
FAM162A

Q96A26

GSK3B

C14orf129

FUNCTION: Proposed to be involved in regulation of apoptosis; the exact mechanism may differ between cell types/tissues (PubMed:15082785). May be involved in hypoxia-induced cell death of transformed cells implicating cytochrome C release and caspase activation (such as CASP9) and inducing mitochondrial permeability transition (PubMed:15082785). May be involved in hypoxia-induced cell death of neuronal cells probably by promoting release of AIFM1 from mitochondria to cytoplasm and its translocation to the nucleus; however, the involvement of caspases has been reported conflictingly (By similarity). {ECO:0000250|UniProtKB:Q9D6U8, ECO:0000269|PubMed:15082785}.139

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

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneFAM162Achr3:122103146chr3:119624699ENST00000477892+1576_10211.333333333333334155.0RegionRequired for proapoptotic activity
HgeneFAM162Achr3:122103146chr3:119624699ENST00000477892+15103_12011.333333333333334155.0TransmembraneHelical
TgeneGSK3Bchr3:122103146chr3:119624699ENST0000026423551156_340238.33333333333334421.0DomainProtein kinase
TgeneGSK3Bchr3:122103146chr3:119624699ENST0000031662651256_340238.33333333333334434.0DomainProtein kinase
TgeneGSK3Bchr3:122103146chr3:119624699ENST0000026423551162_70238.33333333333334421.0Nucleotide bindingATP
TgeneGSK3Bchr3:122103146chr3:119624699ENST0000031662651262_70238.33333333333334434.0Nucleotide bindingATP


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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
FAM162A
GSK3B


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 FAM162A-GSK3B


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 FAM162A-GSK3B


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