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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: 13565

FusionGeneSummary for FLNA_MGLL

check button Fusion gene summary
Fusion gene informationFusion gene name: FLNA_MGLL
Fusion gene ID: 13565
HgeneTgene
Gene symbol

FLNA

MGLL

Gene ID

2316

11343

Gene namefilamin Amonoglyceride lipase
SynonymsABP-280|ABPX|CSBS|CVD1|FGS2|FLN|FLN-A|FLN1|FMD|MNS|NHBP|OPD|OPD1|OPD2|XLVD|XMVDHU-K5|HUK5|MAGL|MGL
Cytomap

Xq28

3q21.3

Type of geneprotein-codingprotein-coding
Descriptionfilamin-Aactin binding protein 280alpha-filaminendothelial actin-binding proteinfilamin A, alphafilamin-1non-muscle filaminmonoglyceride lipaselysophospholipase homologmonoacylglycerol lipase
Modification date2018052320180523
UniProtAcc

P21333

Q99685

Ensembl transtripts involved in fusion geneENST00000360319, ENST00000422373, 
ENST00000369850, ENST00000369856, 
ENST00000344736, ENST00000498491, 
ENST00000434178, ENST00000265052, 
ENST00000398104, ENST00000453507, 
ENST00000476682, ENST00000398101, 
Fusion gene scores* DoF score18 X 21 X 7=26462 X 2 X 1=4
# samples 252
** MAII scorelog2(25/2646*10)=-3.40381306161659
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(2/4*10)=2.32192809488736
Context

PubMed: FLNA [Title/Abstract] AND MGLL [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
HgeneFLNA

GO:0016479

negative regulation of transcription by RNA polymerase I

22307607

HgeneFLNA

GO:0030334

regulation of cell migration

16291724

HgeneFLNA

GO:0031532

actin cytoskeleton reorganization

10051605

HgeneFLNA

GO:0034394

protein localization to cell surface

18322202

HgeneFLNA

GO:0043113

receptor clustering

10692483

HgeneFLNA

GO:0043433

negative regulation of DNA binding transcription factor activity

15684392

HgeneFLNA

GO:0044319

wound healing, spreading of cells

16291724

HgeneFLNA

GO:0045184

establishment of protein localization

18322202

HgeneFLNA

GO:0051764

actin crosslink formation

10051605

HgeneFLNA

GO:0072659

protein localization to plasma membrane

24951510

HgeneFLNA

GO:0090307

mitotic spindle assembly

18548008

HgeneFLNA

GO:1901381

positive regulation of potassium ion transmembrane transport

24951510

TgeneMGLL

GO:0046464

acylglycerol catabolic process

22969151


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
ChiTaRS3.1BF819641FLNAchrX

153581464

+MGLLchr3

127413933

-
* 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-3CDSENST00000360319ENST00000434178FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000360319ENST00000265052FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000360319ENST00000398104FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000360319ENST00000453507FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000360319ENST00000476682FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000360319ENST00000398101FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000422373ENST00000434178FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000422373ENST00000265052FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000422373ENST00000398104FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000422373ENST00000453507FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000422373ENST00000476682FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000422373ENST00000398101FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369850ENST00000434178FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369850ENST00000265052FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369850ENST00000398104FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369850ENST00000453507FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000369850ENST00000476682FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000369850ENST00000398101FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369856ENST00000434178FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369856ENST00000265052FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369856ENST00000398104FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000369856ENST00000453507FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000369856ENST00000476682FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000369856ENST00000398101FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000344736ENST00000434178FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000344736ENST00000265052FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000344736ENST00000398104FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000344736ENST00000453507FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000344736ENST00000476682FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000344736ENST00000398101FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000498491ENST00000434178FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000498491ENST00000265052FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000498491ENST00000398104FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-3CDSENST00000498491ENST00000453507FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000498491ENST00000476682FLNAchrX

153581464

+MGLLchr3

127413933

-
intron-5UTRENST00000498491ENST00000398101FLNAchrX

153581464

+MGLLchr3

127413933

-

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FusionProtFeatures for FLNA_MGLL


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

P21333

MGLL

Q99685

Promotes orthogonal branching of actin filaments andlinks actin filaments to membrane glycoproteins. Anchors varioustransmembrane proteins to the actin cytoskeleton and serves as ascaffold for a wide range of cytoplasmic signaling proteins.Interaction with FLNA may allow neuroblast migration from theventricular zone into the cortical plate. Tethers cell surface-localized furin, modulates its rate of internalization and directsits intracellular trafficking (By similarity). Involved inciliogenesis. Plays a role in cell-cell contacts and adherensjunctions during the development of blood vessels, heart and brainorgans. Plays a role in platelets morphology through interactionwith SYK that regulates ITAM- and ITAM-like-containing receptorsignaling, resulting in by platelet cytoskeleton organizationmaintenance (By similarity). {ECO:0000250,ECO:0000250|UniProtKB:Q8BTM8, ECO:0000269|PubMed:22121117}. Converts monoacylglycerides to free fatty acids andglycerol. Hydrolyzes the endocannabinoid 2-arachidonoylglycerol,and thereby contributes to the regulation of endocannabinoidsignaling, nociperception and perception of pain (By similarity).Regulates the levels of fatty acids that serve as signalingmolecules and promote cancer cell migration, invasion and tumorgrowth (PubMed:20079333). {ECO:0000250|UniProtKB:O35678,ECO:0000269|PubMed:20079333}.

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 FLNA_MGLL


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 FLNA_MGLL


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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RelatedDrugs for FLNA_MGLL


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneFLNAP21333DB11638ArtenimolFilamin-Asmall moleculeapproved|investigational

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RelatedDiseases for FLNA_MGLL


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFLNAC1848213Periventricular Heterotopia, X-Linked6UNIPROT
HgeneFLNAC0265251Oto-Palato-digital syndrome type 14CTD_human;ORPHANET;UNIPROT
HgeneFLNAC0265293Frontometaphyseal dysplasia4CTD_human;ORPHANET;UNIPROT
HgeneFLNAC1844696OTOPALATODIGITAL SYNDROME, TYPE II4CTD_human;ORPHANET;UNIPROT
HgeneFLNAC0025237Melnick-Needles Syndrome3ORPHANET;UNIPROT
HgeneFLNAC1868720Periventricular Nodular Heterotopia2CTD_human;ORPHANET
HgeneFLNAC0010701Phyllodes Tumor1CTD_human
HgeneFLNAC0014544Epilepsy1CTD_human;HPO
HgeneFLNAC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneFLNAC0029422Osteochondrodysplasias1CTD_human;HPO
HgeneFLNAC0220769FG syndrome1CTD_human
HgeneFLNAC0262436Cardiac valvular dysplasia, X-linked1CTD_human;UNIPROT
HgeneFLNAC1458155Mammary Neoplasms1CTD_human
HgeneFLNAC1845235Heterotopia, Periventricular, Ehlers-Danlos Variant1CTD_human
HgeneFLNAC1845902FG SYNDROME 21UNIPROT
TgeneMGLLC0001973Alcoholic Intoxication, Chronic1PSYGENET
TgeneMGLLC0029456Osteoporosis1CTD_human
TgeneMGLLC0740858Substance abuse problem1PSYGENET