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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: 20242

FusionGeneSummary for LRRC56_DEAF1

check button Fusion gene summary
Fusion gene informationFusion gene name: LRRC56_DEAF1
Fusion gene ID: 20242
HgeneTgene
Gene symbol

LRRC56

DEAF1

Gene ID

115399

10522

Gene nameleucine rich repeat containing 56DEAF1, transcription factor
Synonyms-MRD24|NUDR|SPN|ZMYND5
Cytomap

11p15.5

11p15.5

Type of geneprotein-codingprotein-coding
Descriptionleucine-rich repeat-containing protein 56deformed epidermal autoregulatory factor 1 homolognuclear DEAF-1-related transcriptional regulatorsuppressinzinc finger MYND domain-containing protein 5
Modification date2018051920180523
UniProtAcc

Q8IYG6

O75398

Ensembl transtripts involved in fusion geneENST00000270115, ENST00000338675, 
ENST00000382409, ENST00000525904, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 3 X 6=126
# samples 17
** MAII scorelog2(1/1*10)=3.32192809488736log2(7/126*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LRRC56 [Title/Abstract] AND DEAF1 [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
TgeneDEAF1

GO:0000122

negative regulation of transcription by RNA polymerase II

24726472

TgeneDEAF1

GO:0033599

regulation of mammary gland epithelial cell proliferation

18826651

TgeneDEAF1

GO:0045892

negative regulation of transcription, DNA-templated

24726472

TgeneDEAF1

GO:0045893

positive regulation of transcription, DNA-templated

24726472


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
TCGARVTGCTTCGA-2G-AAM3-01ALRRC56chr11

549998

+DEAF1chr11

679816

-
* 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
Frame-shiftENST00000270115ENST00000338675LRRC56chr11

549998

+DEAF1chr11

679816

-
Frame-shiftENST00000270115ENST00000382409LRRC56chr11

549998

+DEAF1chr11

679816

-
5CDS-5UTRENST00000270115ENST00000525904LRRC56chr11

549998

+DEAF1chr11

679816

-

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FusionProtFeatures for LRRC56_DEAF1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LRRC56

Q8IYG6

DEAF1

O75398


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 LRRC56_DEAF1


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 LRRC56_DEAF1


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
LRRC56RANGRF, METAP1D, MAPK9, PPP2CA, EEF1A2, HSPA8DEAF1LMO4, ASCC2, RAD23B, AIMP2, TK1, FHL1, CDKN1A, CDC37, PIN1, HRAS, PPP1CA, PPP1CC, GSK3A, GSK3B, PELI1, IRF3, IRF7, CREB1, CDKN2A, HRSP12, PELI2, BSPRY, SP1, SUB1, SP3


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 LRRC56_DEAF1


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 LRRC56_DEAF1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDEAF1C0041696Unipolar Depression5PSYGENET
TgeneDEAF1C1269683Major Depressive Disorder5PSYGENET
TgeneDEAF1C0011570Mental Depression4PSYGENET
TgeneDEAF1C0011581Depressive disorder4PSYGENET
TgeneDEAF1C4014414MENTAL RETARDATION, AUTOSOMAL DOMINANT 242UNIPROT
TgeneDEAF1C3714756Intellectual Disability1CTD_human;HPO