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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:LASP1-MSL1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: LASP1-MSL1
FusionPDB ID: 44187
FusionGDB2.0 ID: 44187
HgeneTgene
Gene symbol

LASP1

MSL1

Gene ID

3927

339287

Gene nameLIM and SH3 protein 1MSL complex subunit 1
SynonymsLasp-1|MLN50MSL-1
Cytomap

17q12

17q21.1

Type of geneprotein-codingprotein-coding
DescriptionLIM and SH3 domain protein 1metastatic lymph node gene 50 proteinmale-specific lethal 1 homologMSL1-like 1male specific lethal 1 homologmale-specific lethal 1-like 1male-specific lethal-1 homolog 1
Modification date2020031320200313
UniProtAcc

Q14847

Q68DK7

Ensembl transtripts involved in fusion geneENST idsENST00000318008, ENST00000435347, 
ENST00000433206, 
ENST00000577454, 
ENST00000578648, ENST00000579565, 
ENST00000398532, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 17 X 8=244814 X 13 X 6=1092
# samples 2114
** MAII scorelog2(21/2448*10)=-3.54314232502653
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1092*10)=-2.96347412397489
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: LASP1 [Title/Abstract] AND MSL1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)LASP1(37046757)-MSL1(38289295), # samples:1
Anticipated loss of major functional domain due to fusion event.LASP1-MSL1 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.
LASP1-MSL1 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.
LASP1-MSL1 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.
LASP1-MSL1 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.
* 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
TgeneMSL1

GO:0043984

histone H4-K16 acetylation

20018852


check buttonFusion gene breakpoints across LASP1 (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 MSL1 (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
ChimerDB4GBMTCGA-28-2514-01ALASP1chr17

37046757

+MSL1chr17

38289295

+


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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)
ENST00000318008LASP1chr1737046757+ENST00000398532MSL1chr1738289295+3357580331936201
ENST00000435347LASP1chr1737046757+ENST00000398532MSL1chr1738289295+307329647652201

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
ENST00000318008ENST00000398532LASP1chr1737046757+MSL1chr1738289295+0.0016950820.99830484
ENST00000435347ENST00000398532LASP1chr1737046757+MSL1chr1738289295+0.0014520280.998548

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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

>44187_44187_1_LASP1-MSL1_LASP1_chr17_37046757_ENST00000318008_MSL1_chr17_38289295_ENST00000398532_length(amino acids)=201AA_BP=82
MNPNCARCGKIVYPTEKVNCLDKFWHKACFHCETCKMTLNMKNYKGYEKKPYCNAHYPKQSFTMVADTPENLRLKQQSELQSQNLDDSVF
SKRHAKLELDEKRRKRWDIQRIREQRILQRLQLRMYKKKGIQESEPEVTSFFPEPDDVESLMITPFLPVVAFGRPLPKLTPQNFELPWLD

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

>44187_44187_2_LASP1-MSL1_LASP1_chr17_37046757_ENST00000435347_MSL1_chr17_38289295_ENST00000398532_length(amino acids)=201AA_BP=82
MNPNCARCGKIVYPTEKVNCLDKFWHKACFHCETCKMTLNMKNYKGYEKKPYCNAHYPKQSFTMVADTPENLRLKQQSELQSQNLDDSVF
SKRHAKLELDEKRRKRWDIQRIREQRILQRLQLRMYKKKGIQESEPEVTSFFPEPDDVESLMITPFLPVVAFGRPLPKLTPQNFELPWLD

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

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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/chr17:37046757/chr17:38289295)
- 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
LASP1

Q14847

MSL1

Q68DK7

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}.FUNCTION: Component of histone acetyltransferase complex responsible for the majority of histone H4 acetylation at 'Lys-16' (H4K16ac) which is implicated in the formation of higher-order chromatin structure (PubMed:16227571). Greatly enhances MSL2 E3 ubiquitin ligase activity, promoting monoubiquitination of histone H2B at 'Lys-34' (H2BK34Ub) (PubMed:21726816). This modification in turn stimulates histone H3 methylation at 'Lys-4' (H3K4me) and 'Lys-79' (H3K79me) and leads to gene activation, including that of HOXA9 and MEIS1 (PubMed:21726816). In the MSL complex, acts as a scaffold to tether MSL3 and KAT8 together for enzymatic activity regulation (PubMed:22547026). {ECO:0000269|PubMed:16227571, ECO:0000269|PubMed:21726816, ECO:0000269|PubMed:22547026}.

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
HgeneLASP1chr17:37046757chr17:38289295ENST00000318008+375_5683.0262.0DomainLIM zinc-binding
HgeneLASP1chr17:37046757chr17:38289295ENST00000435347+385_5683.0708.3333333333334DomainLIM zinc-binding
TgeneMSL1chr17:37046757chr17:38289295ENST0000039853249505_519496.0615.0MotifBipartite nuclear localization signal
TgeneMSL1chr17:37046757chr17:38289295ENST00000579565510317_346233.0352.0MotifNuclear localization signal
TgeneMSL1chr17:37046757chr17:38289295ENST00000579565510505_519233.0352.0MotifBipartite nuclear localization signal

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneLASP1chr17:37046757chr17:38289295ENST00000318008+37201_20483.0262.0Compositional biasNote=Poly-Gly
HgeneLASP1chr17:37046757chr17:38289295ENST00000435347+38201_20483.0708.3333333333334Compositional biasNote=Poly-Gly
HgeneLASP1chr17:37046757chr17:38289295ENST00000318008+37202_26183.0262.0DomainSH3
HgeneLASP1chr17:37046757chr17:38289295ENST00000435347+38202_26183.0708.3333333333334DomainSH3
HgeneLASP1chr17:37046757chr17:38289295ENST00000318008+3761_9583.0262.0RepeatNote=Nebulin 1
HgeneLASP1chr17:37046757chr17:38289295ENST00000318008+3797_13183.0262.0RepeatNote=Nebulin 2
HgeneLASP1chr17:37046757chr17:38289295ENST00000435347+3861_9583.0708.3333333333334RepeatNote=Nebulin 1
HgeneLASP1chr17:37046757chr17:38289295ENST00000435347+3897_13183.0708.3333333333334RepeatNote=Nebulin 2
TgeneMSL1chr17:37046757chr17:38289295ENST0000039853249213_282496.0615.0Coiled coilOntology_term=ECO:0000269
TgeneMSL1chr17:37046757chr17:38289295ENST00000579565510213_282233.0352.0Coiled coilOntology_term=ECO:0000269
TgeneMSL1chr17:37046757chr17:38289295ENST000003985324910_15496.0615.0Compositional biasNote=Poly-Ala
TgeneMSL1chr17:37046757chr17:38289295ENST0000039853249208_214496.0615.0Compositional biasNote=Poly-Gly
TgeneMSL1chr17:37046757chr17:38289295ENST000003985324955_185496.0615.0Compositional biasNote=Pro-rich
TgeneMSL1chr17:37046757chr17:38289295ENST0000057956551010_15233.0352.0Compositional biasNote=Poly-Ala
TgeneMSL1chr17:37046757chr17:38289295ENST00000579565510208_214233.0352.0Compositional biasNote=Poly-Gly
TgeneMSL1chr17:37046757chr17:38289295ENST0000057956551055_185233.0352.0Compositional biasNote=Pro-rich
TgeneMSL1chr17:37046757chr17:38289295ENST0000039853249317_346496.0615.0MotifNuclear localization signal


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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
LASP1all structure
MSL1


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
TgeneMSL1chr17:37046757chr17:38289295ENST0000039853249223_237496.0615.0MSL2
TgeneMSL1chr17:37046757chr17:38289295ENST00000579565510223_237233.0352.0MSL2


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Related Drugs to LASP1-MSL1


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 LASP1-MSL1


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
HgeneLASP1C0004352Autistic Disorder1CTD_human
HgeneLASP1C0014170Endometrial Neoplasms1CTD_human
HgeneLASP1C0036341Schizophrenia1PSYGENET
HgeneLASP1C0476089Endometrial Carcinoma1CTD_human