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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: 39537

FusionGeneSummary for TRIM38_KIAA0232

check button Fusion gene summary
Fusion gene informationFusion gene name: TRIM38_KIAA0232
Fusion gene ID: 39537
HgeneTgene
Gene symbol

TRIM38

KIAA0232

Gene ID

10475

9778

Gene nametripartite motif containing 38KIAA0232
SynonymsRNF15|RORET-
Cytomap

6p22.2

4p16.1

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase TRIM38RING-type E3 ubiquitin transferase TRIM38Ro/SSA ribonucleoprotein homologring finger protein 15tripartite motif-containing protein 38zinc finger protein RoRetuncharacterized protein KIAA0232
Modification date2018052220180519
UniProtAcc

O00635

Q92628

Ensembl transtripts involved in fusion geneENST00000357085, ENST00000349458, 
ENST00000503278, ENST00000425103, 
ENST00000307659, 
Fusion gene scores* DoF score1 X 1 X 1=13 X 3 X 2=18
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TRIM38 [Title/Abstract] AND KIAA0232 [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
HgeneTRIM38

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

23077300

HgeneTRIM38

GO:0046598

positive regulation of viral entry into host cell

18248090

HgeneTRIM38

GO:0051091

positive regulation of DNA binding transcription factor activity

23077300

HgeneTRIM38

GO:0051092

positive regulation of NF-kappaB transcription factor activity

23077300


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
ChiTaRS3.1BF895949TRIM38chr6

25966915

+KIAA0232chr4

6870207

+
* 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-intronENST00000357085ENST00000503278TRIM38chr6

25966915

+KIAA0232chr4

6870207

+
5CDS-intronENST00000357085ENST00000425103TRIM38chr6

25966915

+KIAA0232chr4

6870207

+
5CDS-intronENST00000357085ENST00000307659TRIM38chr6

25966915

+KIAA0232chr4

6870207

+
5CDS-intronENST00000349458ENST00000503278TRIM38chr6

25966915

+KIAA0232chr4

6870207

+
5CDS-intronENST00000349458ENST00000425103TRIM38chr6

25966915

+KIAA0232chr4

6870207

+
5CDS-intronENST00000349458ENST00000307659TRIM38chr6

25966915

+KIAA0232chr4

6870207

+

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FusionProtFeatures for TRIM38_KIAA0232


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TRIM38

O00635

KIAA0232

Q92628

E3 ubiquitin-protein ligase. Mediates 'Lys-48'-linkedpolyubiquitination and proteasomal degradation of the critical TLRadapter TICAM1, inhibiting TLR3-mediated type I interferonsignaling. {ECO:0000269|PubMed:23056470}.

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 TRIM38_KIAA0232


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 TRIM38_KIAA0232


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 TRIM38_KIAA0232


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 TRIM38_KIAA0232


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