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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:LRR1-CRYZL1 (FusionGDB2 ID:49861)

Fusion Gene Summary for LRR1-CRYZL1

check button Fusion gene summary
Fusion gene informationFusion gene name: LRR1-CRYZL1
Fusion gene ID: 49861
HgeneTgene
Gene symbol

LRR1

CRYZL1

Gene ID

122769

9946

Gene nameleucine rich repeat protein 1crystallin zeta like 1
Synonyms4-1BBLRR|LRR-1|PPIL54P11|QOH-1
Cytomap

14q21.3

21q22.11

Type of geneprotein-codingprotein-coding
Descriptionleucine-rich repeat protein 14-1BB-mediated signaling moleculeLRR-repeat protein 1cyclophilin-like 5epididymis secretory sperm binding proteinpeptidylprolyl isomerase (cyclophilin)-like 5peptidylprolyl isomerase-like 5quinone oxidoreductase-like protein 1crystallin, zeta (quinone reductase)-like 1protein 4P11quinone oxidoreductase homolog 1quinone reductase-like 1zeta-crystallin homolog
Modification date2020031320200313
UniProtAcc

Q96L50

O95825

Ensembl transtripts involved in fusion geneENST00000298288, ENST00000318317, 
ENST00000557531, 
ENST00000290244, 
ENST00000381554, ENST00000361534, 
ENST00000381540, ENST00000399442, 
ENST00000413017, ENST00000445393, 
ENST00000480893, 
Fusion gene scores* DoF score5 X 5 X 2=5015 X 14 X 7=1470
# samples 515
** MAII scorelog2(5/50*10)=0log2(15/1470*10)=-3.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LRR1 [Title/Abstract] AND CRYZL1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLRR1(50075167)-CRYZL1(34961774), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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 buttonFusion gene breakpoints across LRR1 (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 CRYZL1 (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
ChiTaRS5.0N/ABM149608LRR1chr14

50075167

+CRYZL1chr21

34961774

+


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Fusion Gene ORF analysis for LRR1-CRYZL1

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
intron-3UTRENST00000298288ENST00000290244LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-3UTRENST00000298288ENST00000381554LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-3UTRENST00000318317ENST00000290244LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-3UTRENST00000318317ENST00000381554LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-3UTRENST00000557531ENST00000290244LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-3UTRENST00000557531ENST00000381554LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000298288ENST00000361534LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000298288ENST00000381540LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000298288ENST00000399442LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000298288ENST00000413017LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000298288ENST00000445393LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000298288ENST00000480893LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000318317ENST00000361534LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000318317ENST00000381540LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000318317ENST00000399442LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000318317ENST00000413017LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000318317ENST00000445393LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000318317ENST00000480893LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000557531ENST00000361534LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000557531ENST00000381540LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000557531ENST00000399442LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000557531ENST00000413017LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000557531ENST00000445393LRR1chr14

50075167

+CRYZL1chr21

34961774

+
intron-intronENST00000557531ENST00000480893LRR1chr14

50075167

+CRYZL1chr21

34961774

+

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 LRR1-CRYZL1


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 LRR1-CRYZL1


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/:50075167/:34961774)
- 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
LRR1

Q96L50

CRYZL1

O95825

FUNCTION: May negatively regulate the 4-1BB-mediated signaling cascades which result in the activation of NK-kappaB and JNK1. Probable substrate recognition subunit of an ECS (Elongin BC-CUL2/5-SOCS-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. {ECO:0000269|PubMed:15601820}.

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 LRR1-CRYZL1


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 LRR1-CRYZL1


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 LRR1-CRYZL1


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 LRR1-CRYZL1


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