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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: 10220

FusionGeneSummary for DNAJB6_FTX

check button Fusion gene summary
Fusion gene informationFusion gene name: DNAJB6_FTX
Fusion gene ID: 10220
HgeneTgene
Gene symbol

DNAJB6

FTX

Gene ID

10049

100302692

Gene nameDnaJ heat shock protein family (Hsp40) member B6FTX transcript, XIST regulator
SynonymsDJ4|DnaJ|HHDJ1|HSJ-2|HSJ2|LGMD1D|LGMD1E|MRJ|MSJ-1LINC00182|MIR374AHG|NCRNA00182
Cytomap

7q36.3

Xq13.2

Type of geneprotein-codingncRNA
DescriptiondnaJ homolog subfamily B member 6DnaJ (Hsp40) homolog, subfamily B, member 6DnaJ-like 2 proteinheat shock protein J2FTX transcript, XIST regulator (non-protein coding)five prime to XISTmir-374a-545 cluster host gene (non-protein coding)
Modification date2018052920180517
UniProtAcc

O75190

Ensembl transtripts involved in fusion geneENST00000429029, ENST00000262177, 
ENST00000452797, ENST00000443280, 
ENST00000494267, 
ENST00000429124, 
Fusion gene scores* DoF score3 X 3 X 2=185 X 5 X 2=50
# samples 35
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/50*10)=0
Context

PubMed: DNAJB6 [Title/Abstract] AND FTX [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
HgeneDNAJB6

GO:0006457

protein folding

11896048

HgeneDNAJB6

GO:0043154

negative regulation of cysteine-type endopeptidase activity involved in apoptotic process

11896048

HgeneDNAJB6

GO:0045109

intermediate filament organization

10954706

HgeneDNAJB6

GO:0090084

negative regulation of inclusion body assembly

21231916


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
ChiTaRS3.1AW375983DNAJB6chr7

157155924

+FTXchrX

73470417

-
* 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-intronENST00000429029ENST00000429124DNAJB6chr7

157155924

+FTXchrX

73470417

-
5CDS-intronENST00000262177ENST00000429124DNAJB6chr7

157155924

+FTXchrX

73470417

-
intron-intronENST00000452797ENST00000429124DNAJB6chr7

157155924

+FTXchrX

73470417

-
5CDS-intronENST00000443280ENST00000429124DNAJB6chr7

157155924

+FTXchrX

73470417

-
intron-intronENST00000494267ENST00000429124DNAJB6chr7

157155924

+FTXchrX

73470417

-

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FusionProtFeatures for DNAJB6_FTX


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DNAJB6

O75190

FTX

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 DNAJB6_FTX


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 DNAJB6_FTX


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 DNAJB6_FTX


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 DNAJB6_FTX


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDNAJB6C3148763MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E2ORPHANET;UNIPROT
HgeneDNAJB6C0686353Muscular Dystrophies, Limb-Girdle1CTD_human