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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:FERMT1-CDRT4 (FusionGDB2 ID:30103)

Fusion Gene Summary for FERMT1-CDRT4

check button Fusion gene summary
Fusion gene informationFusion gene name: FERMT1-CDRT4
Fusion gene ID: 30103
HgeneTgene
Gene symbol

FERMT1

CDRT4

Gene ID

55612

284040

Gene namefermitin family member 1CMT1A duplicated region transcript 4
SynonymsC20orf42|DTGCU2|KIND1|UNC112A|URP1-
Cytomap

20p12.3

17p12

Type of geneprotein-codingprotein-coding
Descriptionfermitin family homolog 1UNC112 related protein 1kindlerinkindlin 1kindlin syndrome proteinunc-112-related protein 1CMT1A duplicated region transcript 4 protein
Modification date2020031320200327
UniProtAcc

Q9BQL6

Q8N9R6

Ensembl transtripts involved in fusion geneENST00000217289, ENST00000536936, 
ENST00000478194, 
ENST00000312177, 
ENST00000519354, 
Fusion gene scores* DoF score8 X 8 X 3=1925 X 2 X 5=50
# samples 86
** MAII scorelog2(8/192*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/50*10)=0.263034405833794
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FERMT1 [Title/Abstract] AND CDRT4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFERMT1(6096458)-CDRT4(15341517), # samples:2
Anticipated loss of major functional domain due to fusion event.FERMT1-CDRT4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
* 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
HgeneFERMT1

GO:0007155

cell adhesion

17012746

HgeneFERMT1

GO:0043616

keratinocyte proliferation

17012746

HgeneFERMT1

GO:0051546

keratinocyte migration

17012746

HgeneFERMT1

GO:0090162

establishment of epithelial cell polarity

17012746


check buttonFusion gene breakpoints across FERMT1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across CDRT4 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4BRCATCGA-E2-A109-01AFERMT1chr20

6096458

-CDRT4chr17

15341517

-
ChimerDB4BRCATCGA-E2-A109-01AFERMT1chr20

6096458

-CDRT4chr17

15343599

-


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Fusion Gene ORF analysis for FERMT1-CDRT4

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-5UTRENST00000217289ENST00000312177FERMT1chr20

6096458

-CDRT4chr17

15343599

-
5CDS-5UTRENST00000217289ENST00000519354FERMT1chr20

6096458

-CDRT4chr17

15341517

-
5CDS-intronENST00000217289ENST00000519354FERMT1chr20

6096458

-CDRT4chr17

15343599

-
5UTR-3CDSENST00000536936ENST00000312177FERMT1chr20

6096458

-CDRT4chr17

15341517

-
5UTR-5UTRENST00000536936ENST00000312177FERMT1chr20

6096458

-CDRT4chr17

15343599

-
5UTR-5UTRENST00000536936ENST00000519354FERMT1chr20

6096458

-CDRT4chr17

15341517

-
5UTR-intronENST00000536936ENST00000519354FERMT1chr20

6096458

-CDRT4chr17

15343599

-
Frame-shiftENST00000217289ENST00000312177FERMT1chr20

6096458

-CDRT4chr17

15341517

-
intron-3CDSENST00000478194ENST00000312177FERMT1chr20

6096458

-CDRT4chr17

15341517

-
intron-5UTRENST00000478194ENST00000312177FERMT1chr20

6096458

-CDRT4chr17

15343599

-
intron-5UTRENST00000478194ENST00000519354FERMT1chr20

6096458

-CDRT4chr17

15341517

-
intron-intronENST00000478194ENST00000519354FERMT1chr20

6096458

-CDRT4chr17

15343599

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for FERMT1-CDRT4


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for FERMT1-CDRT4


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:6096458/:15341517)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FERMT1

Q9BQL6

CDRT4

Q8N9R6

FUNCTION: Involved in cell adhesion. Contributes to integrin activation. When coexpressed with talin, potentiates activation of ITGA2B. Required for normal keratinocyte proliferation. Required for normal polarization of basal keratinocytes in skin, and for normal cell shape. Required for normal adhesion of keratinocytes to fibronectin and laminin, and for normal keratinocyte migration to wound sites. May mediate TGF-beta 1 signaling in tumor progression. {ECO:0000269|PubMed:14634021, ECO:0000269|PubMed:17012746, ECO:0000269|PubMed:19804783}.

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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Fusion Gene Sequence for FERMT1-CDRT4


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for FERMT1-CDRT4


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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Related Drugs for FERMT1-CDRT4


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for FERMT1-CDRT4


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