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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:LATS2-CRYL1 (FusionGDB2 ID:44208)

Fusion Gene Summary for LATS2-CRYL1

check button Fusion gene summary
Fusion gene informationFusion gene name: LATS2-CRYL1
Fusion gene ID: 44208
HgeneTgene
Gene symbol

LATS2

CRYL1

Gene ID

26524

51084

Gene namelarge tumor suppressor kinase 2crystallin lambda 1
SynonymsKPMGDH|HEL30|gul3DH|lambda-CRY
Cytomap

13q12.11

13q12.11

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase LATS2LATS (large tumor suppressor, Drosophila) homolog 2LATS, large tumor suppressor, homolog 2kinase phosphorylated during mitosis proteinlarge tumor suppressor homolog 2serine/threonine kinase KPMserine/threonine-prlambda-crystallin homologL-gulonate 3-dehydrogenasecrystallin, lamda 1epididymis luminal protein 30testicular tissue protein Li 44
Modification date2020031320200313
UniProtAcc

Q9NRM7

Q9Y2S2

Ensembl transtripts involved in fusion geneENST00000382592, ENST00000542899, 
ENST00000472754, 
ENST00000480748, 
ENST00000298248, ENST00000382812, 
Fusion gene scores* DoF score4 X 6 X 3=7215 X 9 X 10=1350
# samples 517
** MAII scorelog2(5/72*10)=-0.526068811667588
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1350*10)=-2.98935275580049
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LATS2 [Title/Abstract] AND CRYL1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLATS2(21619824)-CRYL1(21063635), # samples:1
Anticipated loss of major functional domain due to fusion event.LATS2-CRYL1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
LATS2-CRYL1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
LATS2-CRYL1 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
LATS2-CRYL1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
LATS2-CRYL1 seems lost the major protein functional domain in Tgene 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
HgeneLATS2

GO:0000082

G1/S transition of mitotic cell cycle

12853976

HgeneLATS2

GO:0006468

protein phosphorylation

10871863

HgeneLATS2

GO:0009755

hormone-mediated signaling pathway

15131260

HgeneLATS2

GO:0035329

hippo signaling

20412773

HgeneLATS2

GO:0035556

intracellular signal transduction

10871863

HgeneLATS2

GO:0045736

negative regulation of cyclin-dependent protein serine/threonine kinase activity

12853976


check buttonFusion gene breakpoints across LATS2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across CRYL1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4STADTCGA-D7-8570-01ALATS2chr13

21619824

-CRYL1chr13

21063635

-


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Fusion Gene ORF analysis for LATS2-CRYL1

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-intronENST00000382592ENST00000480748LATS2chr13

21619824

-CRYL1chr13

21063635

-
5CDS-intronENST00000542899ENST00000480748LATS2chr13

21619824

-CRYL1chr13

21063635

-
Frame-shiftENST00000542899ENST00000298248LATS2chr13

21619824

-CRYL1chr13

21063635

-
Frame-shiftENST00000542899ENST00000382812LATS2chr13

21619824

-CRYL1chr13

21063635

-
In-frameENST00000382592ENST00000298248LATS2chr13

21619824

-CRYL1chr13

21063635

-
In-frameENST00000382592ENST00000382812LATS2chr13

21619824

-CRYL1chr13

21063635

-
intron-3CDSENST00000472754ENST00000298248LATS2chr13

21619824

-CRYL1chr13

21063635

-
intron-3CDSENST00000472754ENST00000382812LATS2chr13

21619824

-CRYL1chr13

21063635

-
intron-intronENST00000472754ENST00000480748LATS2chr13

21619824

-CRYL1chr13

21063635

-

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)
ENST00000382592LATS2chr1321619824-ENST00000298248CRYL1chr1321063635-20217487551558267
ENST00000382592LATS2chr1321619824-ENST00000382812CRYL1chr1321063635-20177487551558267

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
ENST00000382592ENST00000298248LATS2chr1321619824-CRYL1chr1321063635-0.0066834770.99331653
ENST00000382592ENST00000382812LATS2chr1321619824-CRYL1chr1321063635-0.006685210.9933148

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Fusion Genomic Features for LATS2-CRYL1


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.
genomic feature

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 LATS2-CRYL1


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/chr13:21619824/chr13:21063635)
- 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
LATS2

Q9NRM7

CRYL1

Q9Y2S2

FUNCTION: Negative regulator of YAP1 in the Hippo signaling pathway that plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. The core of this pathway is composed of a kinase cascade wherein STK3/MST2 and STK4/MST1, in complex with its regulatory protein SAV1, phosphorylates and activates LATS1/2 in complex with its regulatory protein MOB1, which in turn phosphorylates and inactivates YAP1 oncoprotein and WWTR1/TAZ. Phosphorylation of YAP1 by LATS2 inhibits its translocation into the nucleus to regulate cellular genes important for cell proliferation, cell death, and cell migration. Acts as a tumor suppressor which plays a critical role in centrosome duplication, maintenance of mitotic fidelity and genomic stability. Negatively regulates G1/S transition by down-regulating cyclin E/CDK2 kinase activity. Negative regulator of the androgen receptor. Phosphorylates SNAI1 in the nucleus leading to its nuclear retention and stabilization, which enhances its epithelial-mesenchymal transition and tumor cell invasion/migration activities. This tumor-promoting activity is independent of its effects upon YAP1 or WWTR1/TAZ. {ECO:0000269|PubMed:10871863, ECO:0000269|PubMed:12853976, ECO:0000269|PubMed:15131260, ECO:0000269|PubMed:18158288, ECO:0000269|PubMed:21952048}.

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
HgeneLATS2chr13:21619824chr13:21063635ENST00000382592-28668_9731141089.0DomainProtein kinase
HgeneLATS2chr13:21619824chr13:21063635ENST00000382592-28974_10521141089.0DomainAGC-kinase C-terminal
HgeneLATS2chr13:21619824chr13:21063635ENST00000382592-2898_1391141089.0DomainUBA
HgeneLATS2chr13:21619824chr13:21063635ENST00000542899-28668_9731141089.0DomainProtein kinase
HgeneLATS2chr13:21619824chr13:21063635ENST00000542899-28974_10521141089.0DomainAGC-kinase C-terminal
HgeneLATS2chr13:21619824chr13:21063635ENST00000542899-2898_1391141089.0DomainUBA
HgeneLATS2chr13:21619824chr13:21063635ENST00000382592-28515_5181141089.0MotifNote=PPxY motif
HgeneLATS2chr13:21619824chr13:21063635ENST00000542899-28515_5181141089.0MotifNote=PPxY motif
HgeneLATS2chr13:21619824chr13:21063635ENST00000382592-28674_7821141089.0Nucleotide bindingATP
HgeneLATS2chr13:21619824chr13:21063635ENST00000542899-28674_7821141089.0Nucleotide bindingATP
TgeneCRYL1chr13:21619824chr13:21063635ENST000002982481816_1749320.0Nucleotide bindingNAD
TgeneCRYL1chr13:21619824chr13:21063635ENST000003828122916_1727298.0Nucleotide bindingNAD


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Fusion Gene Sequence for LATS2-CRYL1


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.
>44208_44208_1_LATS2-CRYL1_LATS2_chr13_21619824_ENST00000382592_CRYL1_chr13_21063635_ENST00000298248_length(transcript)=2021nt_BP=748nt
TTGGGTCTGCGCTTTGGAACCGCGGCGTGAGCGCCCCGGGAAGATGGAGCAGTCGCCGTCCACGCCACCGCCGCCGCCCGGGGCTCCCCC
GTCCCTGCGGGGCCAGCAGCAGCTCCAGCCACCAGTGCCCGGTCTCCCGGCGCGAGAGGCCCGGGAGCCGCCGGCCAGGACGCCCCCGAG
GGTGTAGACCGCGCCCCTGGAGAGAGTGATAATCTTCAAAATGAAGACTTTGGAAAATTTTAGGTTCTCTATAGGAACTACAAAAATGGA
AGGAAAGAACATTTTCAAAAGGAAATTATTTTGAAAGTATGTTTACAACAAACTGATACTATTGACAGTTTTTTTTTTTAAATAATAAAA
CACTTTAAGAAGATTGTATTTATGGTAAAAGGAAACTGGACTAACAATGAGGCCAAAGACTTTTCCTGCCACGACTTATTCTGGAAATAG
CCGGCAGCGACTGCAAGAGATTCGTGAGGGGTTAAAACAGCCATCCAAGTCTTCGGTTCAGGGGCTACCCGCAGGACCAAACAGTGACAC
TTCCCTGGATGCCAAAGTCCTGGGGAGCAAAGATGCCACCAGGCAGCAGCAGCAGATGAGAGCCACCCCAAAGTTCGGACCTTATCAGAA
AGCCTTGAGGGAAATCAGATATTCCTTGTTGCCTTTTGCTAATGAATCGGGCACCTCTGCAGCTGCAGAAGTGAACCGGCAAATGCTGCA
GGAACTGGTGAACGCAGGATGCGACCAGAAAGGAGATGAAGTTGCTGGAGCAGGCAGGTTCTCTGAAAGGCTCCCTGAGTGTGGAAGAGC
AGCTGTCACTCATCAGTGGTTGTCCCAATATCCAAGAAGCAGTAGAGGGTGCCATGCACATTCAGGAATGTGTTCCAGAAGATCTAGAAC
TGAAGAAGAAGATTTTTGCTCAGTTAGATTCCATCATTGATGATCGAGTGATCTTAAGCAGTTCCACTTCTTGTCTCATGCCTTCCAAGT
TGTTTGCTGGCTTGGTCCATGTGAAGCAATGCATCGTGGCTCATCCTGTGAATCCGCCATACTACATCCCGCTGGTTGAGCTGGTCCCCC
ACCCGGAGACGGCCCCTACGACAGTGGACAGAACCCACGCCCTGATGAAGAAGATTGGACAGTGCCCCATGCGAGTCCAGAAGGAGGTGG
CCGGCTTCGTTCTGAACCGCCTGCAATATGCAATCATCAGCGAGGCCTGGCGGCTAGTGGAGGAAGGAATCGTGTCTCCTAGTGACCTGG
ACCTTGTCATGTCAGAAGGGTTGGGCATGCGGTATGCATTCATTGGACCCCTGGAAACCATGCATCTCAATGCAGAAGGTATGTTAAGCT
ACTGCGACAGATACAGCGAAGGCATAAAACATGTCCTACAGACTTTTGGACCCATTCCAGAGTTTTCCAGGGCCACTGCTGAGAAGGTTA
ACCAGGACATGTGCATGAAGGTCCCTGATGACCCGGAGCACTTAGCTGCCAGGAGGCAGTGGAGGGACGAGTGCCTCATGAGACTCGCCA
AGTTGAAGAGTCAAGTGCAGCCCCAGTGAATTTCTTGTAATGCAGCTTCCACTCCTCTCATTGGAGGCCCTATTTGGGAACACTGCAAGC
CCTTAATCAGCCCTCTGTGACATAGGTAGCAGCCCACGGAGATCCTAAGCTGGCTGTCTTGTGTGCAGCCTGAGTGGGGTGGTGCAGGCC
GGTAGTCTGCCCGTCACTTTGGATCATAGCCCTGGGCCTGGCGGCACAGCAGCACTTGCGTTCTCGGGGCTGTCGATTTCCTGCCACCTG
GGCAGATAACCTGGAGATTTTCACCTTTTCTTTTCAGCTTGATTGCATTTGACTATATTTTACAGCCAGTGATTGTAGTTTCATGTTAAT
ATGTGGCAAAATATTTTTGTAATTATTTTCTAATCCCTTTCTGAGTACTCTGGGGCCCTGCATTTATGAGGCACCTACCTTCATTTTGCT

>44208_44208_1_LATS2-CRYL1_LATS2_chr13_21619824_ENST00000382592_CRYL1_chr13_21063635_ENST00000298248_length(amino acids)=267AA_BP=0
MKLLEQAGSLKGSLSVEEQLSLISGCPNIQEAVEGAMHIQECVPEDLELKKKIFAQLDSIIDDRVILSSSTSCLMPSKLFAGLVHVKQCI
VAHPVNPPYYIPLVELVPHPETAPTTVDRTHALMKKIGQCPMRVQKEVAGFVLNRLQYAIISEAWRLVEEGIVSPSDLDLVMSEGLGMRY

--------------------------------------------------------------
>44208_44208_2_LATS2-CRYL1_LATS2_chr13_21619824_ENST00000382592_CRYL1_chr13_21063635_ENST00000382812_length(transcript)=2017nt_BP=748nt
TTGGGTCTGCGCTTTGGAACCGCGGCGTGAGCGCCCCGGGAAGATGGAGCAGTCGCCGTCCACGCCACCGCCGCCGCCCGGGGCTCCCCC
GTCCCTGCGGGGCCAGCAGCAGCTCCAGCCACCAGTGCCCGGTCTCCCGGCGCGAGAGGCCCGGGAGCCGCCGGCCAGGACGCCCCCGAG
GGTGTAGACCGCGCCCCTGGAGAGAGTGATAATCTTCAAAATGAAGACTTTGGAAAATTTTAGGTTCTCTATAGGAACTACAAAAATGGA
AGGAAAGAACATTTTCAAAAGGAAATTATTTTGAAAGTATGTTTACAACAAACTGATACTATTGACAGTTTTTTTTTTTAAATAATAAAA
CACTTTAAGAAGATTGTATTTATGGTAAAAGGAAACTGGACTAACAATGAGGCCAAAGACTTTTCCTGCCACGACTTATTCTGGAAATAG
CCGGCAGCGACTGCAAGAGATTCGTGAGGGGTTAAAACAGCCATCCAAGTCTTCGGTTCAGGGGCTACCCGCAGGACCAAACAGTGACAC
TTCCCTGGATGCCAAAGTCCTGGGGAGCAAAGATGCCACCAGGCAGCAGCAGCAGATGAGAGCCACCCCAAAGTTCGGACCTTATCAGAA
AGCCTTGAGGGAAATCAGATATTCCTTGTTGCCTTTTGCTAATGAATCGGGCACCTCTGCAGCTGCAGAAGTGAACCGGCAAATGCTGCA
GGAACTGGTGAACGCAGGATGCGACCAGAAAGGAGATGAAGTTGCTGGAGCAGGCAGGTTCTCTGAAAGGCTCCCTGAGTGTGGAAGAGC
AGCTGTCACTCATCAGTGGTTGTCCCAATATCCAAGAAGCAGTAGAGGGTGCCATGCACATTCAGGAATGTGTTCCAGAAGATCTAGAAC
TGAAGAAGAAGATTTTTGCTCAGTTAGATTCCATCATTGATGATCGAGTGATCTTAAGCAGTTCCACTTCTTGTCTCATGCCTTCCAAGT
TGTTTGCTGGCTTGGTCCATGTGAAGCAATGCATCGTGGCTCATCCTGTGAATCCGCCATACTACATCCCGCTGGTTGAGCTGGTCCCCC
ACCCGGAGACGGCCCCTACGACAGTGGACAGAACCCACGCCCTGATGAAGAAGATTGGACAGTGCCCCATGCGAGTCCAGAAGGAGGTGG
CCGGCTTCGTTCTGAACCGCCTGCAATATGCAATCATCAGCGAGGCCTGGCGGCTAGTGGAGGAAGGAATCGTGTCTCCTAGTGACCTGG
ACCTTGTCATGTCAGAAGGGTTGGGCATGCGGTATGCATTCATTGGACCCCTGGAAACCATGCATCTCAATGCAGAAGGTATGTTAAGCT
ACTGCGACAGATACAGCGAAGGCATAAAACATGTCCTACAGACTTTTGGACCCATTCCAGAGTTTTCCAGGGCCACTGCTGAGAAGGTTA
ACCAGGACATGTGCATGAAGGTCCCTGATGACCCGGAGCACTTAGCTGCCAGGAGGCAGTGGAGGGACGAGTGCCTCATGAGACTCGCCA
AGTTGAAGAGTCAAGTGCAGCCCCAGTGAATTTCTTGTAATGCAGCTTCCACTCCTCTCATTGGAGGCCCTATTTGGGAACACTGCAAGC
CCTTAATCAGCCCTCTGTGACATAGGTAGCAGCCCACGGAGATCCTAAGCTGGCTGTCTTGTGTGCAGCCTGAGTGGGGTGGTGCAGGCC
GGTAGTCTGCCCGTCACTTTGGATCATAGCCCTGGGCCTGGCGGCACAGCAGCACTTGCGTTCTCGGGGCTGTCGATTTCCTGCCACCTG
GGCAGATAACCTGGAGATTTTCACCTTTTCTTTTCAGCTTGATTGCATTTGACTATATTTTACAGCCAGTGATTGTAGTTTCATGTTAAT
ATGTGGCAAAATATTTTTGTAATTATTTTCTAATCCCTTTCTGAGTACTCTGGGGCCCTGCATTTATGAGGCACCTACCTTCATTTTGCT

>44208_44208_2_LATS2-CRYL1_LATS2_chr13_21619824_ENST00000382592_CRYL1_chr13_21063635_ENST00000382812_length(amino acids)=267AA_BP=0
MKLLEQAGSLKGSLSVEEQLSLISGCPNIQEAVEGAMHIQECVPEDLELKKKIFAQLDSIIDDRVILSSSTSCLMPSKLFAGLVHVKQCI
VAHPVNPPYYIPLVELVPHPETAPTTVDRTHALMKKIGQCPMRVQKEVAGFVLNRLQYAIISEAWRLVEEGIVSPSDLDLVMSEGLGMRY

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Fusion Gene PPI Analysis for LATS2-CRYL1


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 LATS2-CRYL1


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 LATS2-CRYL1


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