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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: 20460

FusionGeneSummary for LYSMD1_MFSD4

check button Fusion gene summary
Fusion gene informationFusion gene name: LYSMD1_MFSD4
Fusion gene ID: 20460
HgeneTgene
Gene symbol

LYSMD1

MFSD4

Gene ID

388695

148808

Gene nameLysM domain containing 1major facilitator superfamily domain containing 4A
SynonymsSB145MFSD4|UNQ3064
Cytomap

1q21.3

1q32.1

Type of geneprotein-codingprotein-coding
DescriptionlysM and putative peptidoglycan-binding domain-containing protein 1LysM, putative peptidoglycan-binding, domain containing 1RP11-68I18.5major facilitator superfamily domain-containing protein 4Amajor facilitator superfamily domain containing 4major facilitator superfamily domain-containing protein 4
Modification date2018051920180523
UniProtAcc

Q96S90

Ensembl transtripts involved in fusion geneENST00000368908, ENST00000440902, 
ENST00000367147, ENST00000539267, 
ENST00000536357, ENST00000478555, 
Fusion gene scores* DoF score1 X 1 X 1=11 X 1 X 1=1
# samples 11
** MAII scorelog2(1/1*10)=3.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: LYSMD1 [Title/Abstract] AND MFSD4 [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

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
TCGARVPRADTCGA-J9-A52C-01ALYSMD1chr1

151138223

-MFSD4chr1

205566908

+
* 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
intron-3CDSENST00000368908ENST00000367147LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
intron-intronENST00000368908ENST00000539267LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
intron-intronENST00000368908ENST00000536357LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
intron-intronENST00000368908ENST00000478555LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
Frame-shiftENST00000440902ENST00000367147LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
5CDS-intronENST00000440902ENST00000539267LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
5CDS-intronENST00000440902ENST00000536357LYSMD1chr1

151138223

-MFSD4chr1

205566908

+
5CDS-intronENST00000440902ENST00000478555LYSMD1chr1

151138223

-MFSD4chr1

205566908

+

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FusionProtFeatures for LYSMD1_MFSD4


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
LYSMD1

Q96S90

MFSD4

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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 LYSMD1_MFSD4


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 LYSMD1_MFSD4


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
LYSMD1GOLGA2, TCF12, MTUS2, TULP3MFSD4SMAP2, CYSTM1, ATP5S, GOLGA7, SLC25A24, ABHD17B, GK, HIP1R, SLC7A2, APOB, LGALS3, ATP11C


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 LYSMD1_MFSD4


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 LYSMD1_MFSD4


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