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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: 8795

FusionGeneSummary for CTIF_GLTSCR1

check button Fusion gene summary
Fusion gene informationFusion gene name: CTIF_GLTSCR1
Fusion gene ID: 8795
HgeneTgene
Gene symbol

CTIF

GLTSCR1

Gene ID

9811

Gene namecap binding complex dependent translation initiation factor
SynonymsGm672|KIAA0427
Cytomap

18q21.1

Type of geneprotein-coding
DescriptionCBP80/20-dependent translation initiation factor
Modification date20180523
UniProtAcc

O43310

Ensembl transtripts involved in fusion geneENST00000256413, ENST00000382998, 
ENST00000592658, 
ENST00000396720, 
Fusion gene scores* DoF score12 X 7 X 8=6724 X 4 X 3=48
# samples 124
** MAII scorelog2(12/672*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CTIF [Title/Abstract] AND GLTSCR1 [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
ChiTaRS3.1BF931044CTIFchr18

46353821

-GLTSCR1chr19

48118644

-
* 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
intron-intronENST00000256413ENST00000396720CTIFchr18

46353821

-GLTSCR1chr19

48118644

-
intron-intronENST00000382998ENST00000396720CTIFchr18

46353821

-GLTSCR1chr19

48118644

-
intron-intronENST00000592658ENST00000396720CTIFchr18

46353821

-GLTSCR1chr19

48118644

-

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FusionProtFeatures for CTIF_GLTSCR1


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

O43310

GLTSCR1

Specifically required for the pioneer round of mRNAtranslation mediated by the cap-binding complex (CBC), that takesplace during or right after mRNA export via the nuclear porecomplex (NPC). Acts via its interaction with the NCBP1/CBP80component of the CBC complex and recruits the 40S small subunit ofthe ribosome via eIF3. In contrast, it is not involved in steadystate translation, that takes place when the CBC complex isreplaced by cytoplasmic cap-binding protein eIF4E. Also requiredfor nonsense-mediated mRNA decay (NMD), the pioneer round of mRNAtranslation mediated by the cap-binding complex playing a centralrole in nonsense-mediated mRNA decay (NMD).{ECO:0000269|PubMed:19648179}. Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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 CTIF_GLTSCR1


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 CTIF_GLTSCR1


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


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RelatedDrugs for CTIF_GLTSCR1


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 CTIF_GLTSCR1


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