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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:CWC25-LASP1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CWC25-LASP1
FusionPDB ID: 20771
FusionGDB2.0 ID: 20771
HgeneTgene
Gene symbol

CWC25

LASP1

Gene ID

54883

3927

Gene nameCWC25 spliceosome associated protein homologLIM and SH3 protein 1
SynonymsCCDC49Lasp-1|MLN50
Cytomap

17q12

17q12

Type of geneprotein-codingprotein-coding
Descriptionpre-mRNA-splicing factor CWC25 homologcoiled-coil domain-containing protein 49LIM and SH3 domain protein 1metastatic lymph node gene 50 protein
Modification date2020031320200313
UniProtAcc

Q9NXE8

Q14847

Ensembl transtripts involved in fusion geneENST idsENST00000225428, ENST00000536127, 
ENST00000433206, ENST00000318008, 
ENST00000435347, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 11 X 7=100116 X 20 X 9=2880
# samples 1620
** MAII scorelog2(16/1001*10)=-2.64529816394863
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/2880*10)=-3.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CWC25 [Title/Abstract] AND LASP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CWC25(36971114)-LASP1(37074858), # samples:3
Anticipated loss of major functional domain due to fusion event.CWC25-LASP1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
CWC25-LASP1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
CWC25-LASP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
CWC25-LASP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
CWC25-LASP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CWC25-LASP1 seems lost the major protein functional domain in Tgene partner, which is a CGC 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
HgeneCWC25

GO:0000398

mRNA splicing, via spliceosome

29301961


check buttonFusion gene breakpoints across CWC25 (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 LASP1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4COADTCGA-AA-A02K-01ACWC25chr17

36971114

-LASP1chr17

37074858

+
ChimerDB4COADTCGA-AA-A02KCWC25chr17

36971113

-LASP1chr17

37074857

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000225428CWC25chr1736971114-ENST00000318008LASP1chr1737074858+3892726298993231
ENST00000225428CWC25chr1736971114-ENST00000435347LASP1chr1737074858+3559726298993231
ENST00000225428CWC25chr1736971113-ENST00000318008LASP1chr1737074857+3892726298993231
ENST00000225428CWC25chr1736971113-ENST00000435347LASP1chr1737074857+3559726298993231

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
ENST00000225428ENST00000318008CWC25chr1736971114-LASP1chr1737074858+0.420488150.5795119
ENST00000225428ENST00000435347CWC25chr1736971114-LASP1chr1737074858+0.380674360.61932564
ENST00000225428ENST00000318008CWC25chr1736971113-LASP1chr1737074857+0.420488150.5795119
ENST00000225428ENST00000435347CWC25chr1736971113-LASP1chr1737074857+0.380674360.61932564

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>20771_20771_1_CWC25-LASP1_CWC25_chr17_36971113_ENST00000225428_LASP1_chr17_37074857_ENST00000318008_length(amino acids)=231AA_BP=137
MGGGDLNLKKSWHPQTLRNVEKVWKAEQKHEAERKKIEELQRELREERAREEMQRYAEDVGAVKKKEEKLDWMYQGPGGMVNRDEYLLGR
PIDKYVFEKMEEKEAGCSSETGLLPGSIFAPSGANSLLDMASKIREDPLFIIRSGTARCMTTAPPTRTRSPSRTGTPSSTCSRSTTAGCT

--------------------------------------------------------------

>20771_20771_2_CWC25-LASP1_CWC25_chr17_36971113_ENST00000225428_LASP1_chr17_37074857_ENST00000435347_length(amino acids)=231AA_BP=137
MGGGDLNLKKSWHPQTLRNVEKVWKAEQKHEAERKKIEELQRELREERAREEMQRYAEDVGAVKKKEEKLDWMYQGPGGMVNRDEYLLGR
PIDKYVFEKMEEKEAGCSSETGLLPGSIFAPSGANSLLDMASKIREDPLFIIRSGTARCMTTAPPTRTRSPSRTGTPSSTCSRSTTAGCT

--------------------------------------------------------------

>20771_20771_3_CWC25-LASP1_CWC25_chr17_36971114_ENST00000225428_LASP1_chr17_37074858_ENST00000318008_length(amino acids)=231AA_BP=137
MGGGDLNLKKSWHPQTLRNVEKVWKAEQKHEAERKKIEELQRELREERAREEMQRYAEDVGAVKKKEEKLDWMYQGPGGMVNRDEYLLGR
PIDKYVFEKMEEKEAGCSSETGLLPGSIFAPSGANSLLDMASKIREDPLFIIRSGTARCMTTAPPTRTRSPSRTGTPSSTCSRSTTAGCT

--------------------------------------------------------------

>20771_20771_4_CWC25-LASP1_CWC25_chr17_36971114_ENST00000225428_LASP1_chr17_37074858_ENST00000435347_length(amino acids)=231AA_BP=137
MGGGDLNLKKSWHPQTLRNVEKVWKAEQKHEAERKKIEELQRELREERAREEMQRYAEDVGAVKKKEEKLDWMYQGPGGMVNRDEYLLGR
PIDKYVFEKMEEKEAGCSSETGLLPGSIFAPSGANSLLDMASKIREDPLFIIRSGTARCMTTAPPTRTRSPSRTGTPSSTCSRSTTAGCT

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Fusion Protein Functional Features


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/chr17:36971114/chr17:37074858)
- 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
CWC25

Q9NXE8

LASP1

Q14847

FUNCTION: Involved in pre-mRNA splicing as component of the spliceosome. {ECO:0000269|PubMed:29301961}.FUNCTION: Plays an important role in the regulation of dynamic actin-based, cytoskeletal activities. Agonist-dependent changes in LASP1 phosphorylation may also serve to regulate actin-associated ion transport activities, not only in the parietal cell but also in certain other F-actin-rich secretory epithelial cell types (By similarity). {ECO:0000250}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCWC25chr17:36971113chr17:37074857ENST00000225428-31020_70142.66666666666666426.0Coiled coilOntology_term=ECO:0000255
HgeneCWC25chr17:36971114chr17:37074858ENST00000225428-31020_70142.66666666666666426.0Coiled coilOntology_term=ECO:0000255
TgeneLASP1chr17:36971113chr17:37074857ENST0000031800857201_204204.0262.0Compositional biasNote=Poly-Gly
TgeneLASP1chr17:36971113chr17:37074857ENST0000043534758201_204204.0708.3333333333334Compositional biasNote=Poly-Gly
TgeneLASP1chr17:36971114chr17:37074858ENST0000031800857201_204204.0262.0Compositional biasNote=Poly-Gly
TgeneLASP1chr17:36971114chr17:37074858ENST0000043534758201_204204.0708.3333333333334Compositional biasNote=Poly-Gly
TgeneLASP1chr17:36971113chr17:37074857ENST0000031800857202_261204.0262.0DomainSH3
TgeneLASP1chr17:36971113chr17:37074857ENST0000043534758202_261204.0708.3333333333334DomainSH3
TgeneLASP1chr17:36971114chr17:37074858ENST0000031800857202_261204.0262.0DomainSH3
TgeneLASP1chr17:36971114chr17:37074858ENST0000043534758202_261204.0708.3333333333334DomainSH3

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCWC25chr17:36971113chr17:37074857ENST00000225428-310333_377142.66666666666666426.0Coiled coilOntology_term=ECO:0000255
HgeneCWC25chr17:36971114chr17:37074858ENST00000225428-310333_377142.66666666666666426.0Coiled coilOntology_term=ECO:0000255
HgeneCWC25chr17:36971113chr17:37074857ENST00000225428-310144_190142.66666666666666426.0Compositional biasNote=Lys-rich
HgeneCWC25chr17:36971114chr17:37074858ENST00000225428-310144_190142.66666666666666426.0Compositional biasNote=Lys-rich
TgeneLASP1chr17:36971113chr17:37074857ENST00000318008575_56204.0262.0DomainLIM zinc-binding
TgeneLASP1chr17:36971113chr17:37074857ENST00000435347585_56204.0708.3333333333334DomainLIM zinc-binding
TgeneLASP1chr17:36971114chr17:37074858ENST00000318008575_56204.0262.0DomainLIM zinc-binding
TgeneLASP1chr17:36971114chr17:37074858ENST00000435347585_56204.0708.3333333333334DomainLIM zinc-binding
TgeneLASP1chr17:36971113chr17:37074857ENST000003180085761_95204.0262.0RepeatNote=Nebulin 1
TgeneLASP1chr17:36971113chr17:37074857ENST000003180085797_131204.0262.0RepeatNote=Nebulin 2
TgeneLASP1chr17:36971113chr17:37074857ENST000004353475861_95204.0708.3333333333334RepeatNote=Nebulin 1
TgeneLASP1chr17:36971113chr17:37074857ENST000004353475897_131204.0708.3333333333334RepeatNote=Nebulin 2
TgeneLASP1chr17:36971114chr17:37074858ENST000003180085761_95204.0262.0RepeatNote=Nebulin 1
TgeneLASP1chr17:36971114chr17:37074858ENST000003180085797_131204.0262.0RepeatNote=Nebulin 2
TgeneLASP1chr17:36971114chr17:37074858ENST000004353475861_95204.0708.3333333333334RepeatNote=Nebulin 1
TgeneLASP1chr17:36971114chr17:37074858ENST000004353475897_131204.0708.3333333333334RepeatNote=Nebulin 2


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors
LASP1TRIP13, PLSCR1, FHL3, MDFI, ZYX, Fancc, TERF1, TINF2, ACD, POT1, ATXN1, FN1, DAZAP2, Prkg1, Prkaca, CD81, GOLGA2, PSMA3, REL, TRIM27, TCF4, FXR2, SPRY2, ARHGEF15, ZC2HC1A, THAP1, SEPT3, LZTS2, RHOXF2, KRTAP4-2, ZBTB9, ZDHHC17, CCDC8, ILK, HAX1, DNAAF2, THAP8, FYTTD1, NFYA, OR10H3, RDH12, SLC25A32, SLC25A44, C11orf65, TAS2R41, AHNAK, ARFGAP1, DDB1, EIF4B, HSPB1, HSPE1, LGALS1, MAP4, NXF1, CRK, STAT3, SH2D2A, CEP170, FBF1, SCLT1, DCTN1, Prkcz, U2AF2, CDH1, ZNF764, SNRNP27, PGK1, EZR, SPTAN1, NCL, UHRF1, NAT10, PDIA5, API5, KRT18, KRT2, G3BP2, AP3M1, NCOR2, CDK12, MYO1C, ACTR3, CLTC, DNMT1, EHMT2, SNAI1, HIST1H3A, TRIM25, TES, PPP6C, EFTUD2, TNIP2, RBPMS, DPF2, COPS5, SFN, MYC, CDK9, CANX, ATG16L1, DCAF15, BICD1, BICD2, BMH1, BMH2, TRIM28, FAM168A, POLD1, DMRT3, POU1F1, ANKS1A, PITX1, CAMK2A, RBFOX1, CHERP, DTX2, NUTF2, VAC14, MED25, HOXA1, CRYBA1, TENC1, TFG, OTX1, GCM2, TEKT3, CPSF3L, ARHGEF16, BHLHE40, ZC3H10, VEZF1, RNF38, SPAG8, GUCD1, BAHD1, GAS8, LMO4, YTHDF1, FAM168B, TEKT5, BAG4, FOXH1, PRR35, PPP1R32, OXER1, TEKT4, CRYBA2, TLX3, RBPMS2, CERCAM, LENG8, MGAT5B, VPS37C, HNRNPF, EVX2, CATSPER1, YES1, UFSP1, CSTF2T, MKRN3, C14orf119, CTNNA3, HGS, WWOX, KRTAP19-6, KRTAP6-2, KRTAP19-4, KRTAP10-8, UBQLN2, C19orf54, NOXA1, ARID5A, CYSRT1, KRTAP26-1, QRICH1, PRR20B, PRR20A, DOK6, VGLL3, KRTAP3-3, KRTAP3-2, KRTAP12-4, PRR20D, PRR20C, PRR20E, KRTAP19-3, FBXO17, PLEKHA4, HCVgp1, PRNP, NUPR1, BRD4, USP15, RIN3, ACTB, PFN1, PRPH, RDX, TJP2, VASP, VIM, NAA40, FAM24B, RPL35A, HSPA1A, BTF3, EP300, STAT1,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CWC25
LASP1all structure


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to CWC25-LASP1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to CWC25-LASP1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneLASP1C0004352Autistic Disorder1CTD_human
TgeneLASP1C0014170Endometrial Neoplasms1CTD_human
TgeneLASP1C0036341Schizophrenia1PSYGENET
TgeneLASP1C0476089Endometrial Carcinoma1CTD_human