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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: 13091

FusionGeneSummary for FBXL20_KRT27

check button Fusion gene summary
Fusion gene informationFusion gene name: FBXL20_KRT27
Fusion gene ID: 13091
HgeneTgene
Gene symbol

FBXL20

KRT27

Gene ID

84961

342574

Gene nameF-box and leucine rich repeat protein 20keratin 27
SynonymsFbl2|Fbl20K25IRS3|KRT25C
Cytomap

17q12

17q21.2

Type of geneprotein-codingprotein-coding
DescriptionF-box/LRR-repeat protein 20F-box protein FBL2keratin, type I cytoskeletal 27CK-27K25CK27cytokeratin-27keratin 27, type Ikeratin-25Ctype I inner root sheath specific keratin 25 irs3type I inner root sheath-specific keratin-K25irs3
Modification date2018052320180519
UniProtAcc

Q96IG2

Q7Z3Y8

Ensembl transtripts involved in fusion geneENST00000583610, ENST00000394294, 
ENST00000264658, ENST00000577399, 
ENST00000540723, ENST00000301656, 
Fusion gene scores* DoF score40 X 12 X 14=67202 X 2 X 2=8
# samples 382
** MAII scorelog2(38/6720*10)=-4.14438990933518
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: FBXL20 [Title/Abstract] AND KRT27 [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
TCGARVBLCATCGA-FD-A62S-01AFBXL20chr17

37437642

-KRT27chr17

38936113

-
* 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-intronENST00000583610ENST00000540723FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000583610ENST00000301656FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000394294ENST00000540723FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000394294ENST00000301656FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000264658ENST00000540723FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000264658ENST00000301656FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000577399ENST00000540723FBXL20chr17

37437642

-KRT27chr17

38936113

-
5CDS-intronENST00000577399ENST00000301656FBXL20chr17

37437642

-KRT27chr17

38936113

-

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FusionProtFeatures for FBXL20_KRT27


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FBXL20

Q96IG2

KRT27

Q7Z3Y8

Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. Role in neuraltransmission (By similarity). {ECO:0000250}. Essential for the proper assembly of type I and type IIkeratin protein complexes and formation of keratin intermediatefilaments in the inner root sheath (irs).{ECO:0000250|UniProtKB:Q9Z320}.

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 FBXL20_KRT27


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 FBXL20_KRT27


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
FBXL20CUL1, KRAS, YPEL3, PVR, YPEL1, RABGGTBKRT27CYLD


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 FBXL20_KRT27


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 FBXL20_KRT27


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