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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: 14926

FusionGeneSummary for GNB1_TXN

check button Fusion gene summary
Fusion gene informationFusion gene name: GNB1_TXN
Fusion gene ID: 14926
HgeneTgene
Gene symbol

GNB1

TXN

Gene ID

2782

25828

Gene nameG protein subunit beta 1thioredoxin 2
SynonymsMRD42COXPD29|MT-TRX|MTRX|TRX2|TXN
Cytomap

1p36.33

22q12.3

Type of geneprotein-codingprotein-coding
Descriptionguanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1beta subunit, signal-transducing proteins GS/GIguanine nucleotide binding protein (G protein), beta polypeptide 1testicular tissue protein Li 72transducin beta chain 1thioredoxin, mitochondrialmitochondrial thioredoxin
Modification date2018052220180527
UniProtAcc

P62873

P10599

Ensembl transtripts involved in fusion geneENST00000378609, ENST00000472614, 
ENST00000374515, ENST00000374517, 
ENST00000487892, 
Fusion gene scores* DoF score23 X 23 X 14=74063 X 3 X 3=27
# samples 353
** MAII scorelog2(35/7406*10)=-4.4032677223393
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

PubMed: GNB1 [Title/Abstract] AND TXN [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
TCGALDESCATCGA-LN-A9FR-01AGNB1chr1

1721834

-TXNchr9

113013144

-
* 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
5CDS-intronENST00000378609ENST00000374515GNB1chr1

1721834

-TXNchr9

113013144

-
5CDS-intronENST00000378609ENST00000374517GNB1chr1

1721834

-TXNchr9

113013144

-
5CDS-intronENST00000378609ENST00000487892GNB1chr1

1721834

-TXNchr9

113013144

-
intron-intronENST00000472614ENST00000374515GNB1chr1

1721834

-TXNchr9

113013144

-
intron-intronENST00000472614ENST00000374517GNB1chr1

1721834

-TXNchr9

113013144

-
intron-intronENST00000472614ENST00000487892GNB1chr1

1721834

-TXNchr9

113013144

-

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FusionProtFeatures for GNB1_TXN


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GNB1

P62873

TXN

P10599

Guanine nucleotide-binding proteins (G proteins) areinvolved as a modulator or transducer in various transmembranesignaling systems. The beta and gamma chains are required for theGTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction. Participates in various redox reactions through thereversible oxidation of its active center dithiol to a disulfideand catalyzes dithiol-disulfide exchange reactions. Plays a rolein the reversible S-nitrosylation of cysteine residues in targetproteins, and thereby contributes to the response to intracellularnitric oxide. Nitrosylates the active site Cys of CASP3 inresponse to nitric oxide (NO), and thereby inhibits caspase-3activity. Induces the FOS/JUN AP-1 DNA-binding activity inionizing radiation (IR) cells through its oxidation/reductionstatus and stimulates AP-1 transcriptional activity. ADF augments the expression of the interleukin-2receptor TAC (IL2R/P55).

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 GNB1_TXN


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 GNB1_TXN


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
GNB1ARHGEF18, KCNJ3, GNG13, GNG10, GNG4, GNG11, GNGT1, GNGT2, GNG3, GNG5, GNG7, HDAC5, HDAC4, DISC1, ELAVL1, UBQLN1, PLEKHG2, WDR26, GNB2L1, GNG2, RGS6, GNG12, RADIL, RAP1A, PAK1, ATXN10, RASD1, MCF2, KALRN, MCF2L, ADRBK1, PDCL, CCT5, RASD2, SPAG1, BTK, ADRB2, AVPR2, ADRA2A, MRGPRX1, TBXA2R, GNAS, ARRB1, NR3C1, GNAI1, GNAI2, GNAI3, AKT1, ATP6V1B1, GNA11, ESR1, VCAM1, NCF2, MTNR1A, SVIL, PAN2, NOL11, AFP, EPHA7, CYFIP1, GNG8, MTOR, RICTOR, RPTOR, CCDC8, ABCE1, PIK3R5, PIK3CG, COX4I1, GNAQ, NTRK1, FYN, PTK2, CEP128, XPO1, PDLIM7, SYNPO, CUL4A, GLI1, ESRRB, PIK3R1, PIK3CA, DUSP9, COX15, HSD17B10, SOD1, TRIM25, AKT2, PIK3CBTXNCOL1A1, NCF4, PINX1, VHL, CD40, GAPDH, NR3C1, FST, VIM, TXNIP, MAP3K5, NFKB1, TP53, UCHL5, CUL4B, CUL2, CDK2, CUL1, COPS5, COPS6, DCUN1D1, PTPN6, WDR1, UBQLN4, AHCYL1, UBE2V1, SSSCA1, ATP6V1F, SFPQ, SFXN1, UBL5, UBE2D2, SYNCRIP, ATIC, UBE2K, TAX1BP3, PRDX1, MYC, IFIT3, UBL4A, PAN2, NPM1, MYD88, GPRASP2, DYNLT1, CDKN1A, MLH1, NFE2, SIAH1, ACTN4, PARK2, APEX1, SRP9, GPX1, UNK, NTRK1, AKR7A2, ARHGDIA, CCS, EEF2, EIF4EBP2, GLOD4, GSTO1, HINT1, HSPE1, IMPA2, PDCD6, PRDX2, RAB1A, SOD1, STIP1, TAGLN2, TAGLN3, ASS1, C4orf27, ENO1, ENO2, ENO3, FKBP1A, FKBP2, GLRX5, GSTO2, HSPA5, IMPA1, LGALS3, MAP2K2, PGAM1, PGAM2, PSMD14, RAE1, TMX1, TXN2, TYMS, REV3L, PTEN, EWSR1, SRPK2, GEMIN5, TOR1AIP1, EGFR, CRY1, MCM2, OTUB1, PCGF1, DPPA4, NANOG, POU5F1, CRBN, DUSP13, CDK1, COQ2, COX15, DLD, DNM1L, PARK7, SOAT1, VDAC1, G3BP1


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 GNB1_TXN


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 GNB1_TXN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGNB1C0003469Anxiety Disorders1CTD_human
HgeneGNB1C0011581Depressive disorder1CTD_human
TgeneTXNC0006287Bronchopulmonary Dysplasia1CTD_human
TgeneTXNC0011616Contact Dermatitis1CTD_human
TgeneTXNC0023895Liver diseases1CTD_human
TgeneTXNC0027626Neoplasm Invasiveness1CTD_human
TgeneTXNC0242488Acute Lung Injury1CTD_human
TgeneTXNC0345967Malignant mesothelioma1CTD_human