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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: 39458

FusionGeneSummary for TRIB1_SLC25A32

check button Fusion gene summary
Fusion gene informationFusion gene name: TRIB1_SLC25A32
Fusion gene ID: 39458
HgeneTgene
Gene symbol

TRIB1

SLC25A32

Gene ID

10221

81034

Gene nametribbles pseudokinase 1solute carrier family 25 member 32
SynonymsC8FW|GIG-2|GIG2|SKIP1|TRB-1|TRB1MFT|MFTC|RREI
Cytomap

8q24.13

8q22.3

Type of geneprotein-codingprotein-coding
Descriptiontribbles homolog 1G-protein-coupled receptor induced proteinG-protein-coupled receptor-induced gene 2 proteinG-protein-coupled receptor-induced protein 2phosphoprotein regulated by mitogenic pathwaystribbles-like protein 1mitochondrial folate transporter/carriersolute carrier family 25 (mitochondrial folate carrier), member 32
Modification date2018052320180523
UniProtAcc

Q96RU8

Q9H2D1

Ensembl transtripts involved in fusion geneENST00000311922, ENST00000520847, 
ENST00000521778, ENST00000519576, 
ENST00000297578, ENST00000543107, 
ENST00000523701, 
Fusion gene scores* DoF score3 X 2 X 3=183 X 2 X 3=18
# samples 43
** MAII scorelog2(4/18*10)=1.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TRIB1 [Title/Abstract] AND SLC25A32 [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
HgeneTRIB1

GO:0043405

regulation of MAP kinase activity

15299019


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
TCGARVBRCATCGA-E2-A105-01ATRIB1chr8

126445851

+SLC25A32chr8

104420012

-
* 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
Frame-shiftENST00000311922ENST00000297578TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5CDS-5UTRENST00000311922ENST00000543107TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5CDS-intronENST00000311922ENST00000523701TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
Frame-shiftENST00000520847ENST00000297578TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5CDS-5UTRENST00000520847ENST00000543107TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5CDS-intronENST00000520847ENST00000523701TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
intron-3CDSENST00000521778ENST00000297578TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
intron-5UTRENST00000521778ENST00000543107TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
intron-intronENST00000521778ENST00000523701TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5UTR-3CDSENST00000519576ENST00000297578TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5UTR-5UTRENST00000519576ENST00000543107TRIB1chr8

126445851

+SLC25A32chr8

104420012

-
5UTR-intronENST00000519576ENST00000523701TRIB1chr8

126445851

+SLC25A32chr8

104420012

-

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FusionProtFeatures for TRIB1_SLC25A32


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TRIB1

Q96RU8

SLC25A32

Q9H2D1

Adapter protein involved in protein degradation byinteracting with COP1 ubiquitin ligase (PubMed:27041596). TheCOP1-binding motif is masked by autoinhibitory interactions withthe protein kinase domain (PubMed:26455797). Serves to alter COP1substrate specificity by directing the activity of COP1 towardCEBPA (PubMed:27041596). Binds selectively the recognitionsequence of CEBPA (PubMed:26455797). Regulates myeloid celldifferentiation by altering the expression of CEBPA in a COP1-dependent manner (By similarity). Controls macrophage, eosinophiland neutrophil differentiation via the COP1-binding domain (Bysimilarity). Interacts with MAPK kinases and regulates activationof MAP kinases, but has no kinase activity (PubMed:15299019,PubMed:26455797). {ECO:0000250|UniProtKB:Q8K4K4,ECO:0000269|PubMed:15299019, ECO:0000269|PubMed:26455797,ECO:0000305|PubMed:27041596}. Transports folate across the inner membranes ofmitochondria.

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 TRIB1_SLC25A32


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 TRIB1_SLC25A32


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
TRIB1ALOX12, ELAVL1, MYC, RFWD2, STK40, FOSL2, LLGL1, PCDH1, BECN1, STK17B, RASSF8, MORC3, SLAIN2, HNRNPA1L2, FOS, MALT1, PECR, DET1, ISCA1, TRIB2, UBE2E1, JUNBSLC25A32ELAVL1, HNRNPU, PLS1, NEDD8-MDP1, PMVK, LASP1, CCDC25, UBE2T, PICALM, NIPSNAP3A, CTH, TCEA1, DENR, PROSC, CBFB, DBI, PEBP1, SPAG7, PNPO, IRGQ


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 TRIB1_SLC25A32


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 TRIB1_SLC25A32


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTRIB1C1956346Coronary Artery Disease1CTD_human
TgeneSLC25A32C4225187EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE1UNIPROT