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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: 15225

FusionGeneSummary for GPM6A_BRWD1

check button Fusion gene summary
Fusion gene informationFusion gene name: GPM6A_BRWD1
Fusion gene ID: 15225
HgeneTgene
Gene symbol

GPM6A

BRWD1

Gene ID

2823

54014

Gene nameglycoprotein M6Abromodomain and WD repeat domain containing 1
SynonymsGPM6|M6AC21orf107|DCAF19|N143|WDR9|WRD9
Cytomap

4q34.2

21q22.2

Type of geneprotein-codingprotein-coding
Descriptionneuronal membrane glycoprotein M6-abromodomain and WD repeat-containing protein 1WD repeat protein WDR9-form2WD repeat-containing protein 9transcriptional unit N143
Modification date2018052320180523
UniProtAcc

P51674

Q9NSI6

Ensembl transtripts involved in fusion geneENST00000280187, ENST00000393658, 
ENST00000506894, ENST00000515090, 
ENST00000506219, 
ENST00000333229, 
ENST00000342449, ENST00000380800, 
ENST00000341322, ENST00000470108, 
Fusion gene scores* DoF score5 X 6 X 1=308 X 8 X 3=192
# samples 68
** MAII scorelog2(6/30*10)=1
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(8/192*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GPM6A [Title/Abstract] AND BRWD1 [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
HgeneGPM6A

GO:0001764

neuron migration

19298174

HgeneGPM6A

GO:0048863

stem cell differentiation

19298174


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
ChiTaRS3.1DA209219GPM6Achr4

176923469

-BRWD1chr21

40669820

-
* 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-intronENST00000280187ENST00000333229GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000280187ENST00000342449GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000280187ENST00000380800GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-3UTRENST00000280187ENST00000341322GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000280187ENST00000470108GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000393658ENST00000333229GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000393658ENST00000342449GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000393658ENST00000380800GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-3UTRENST00000393658ENST00000341322GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000393658ENST00000470108GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506894ENST00000333229GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506894ENST00000342449GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506894ENST00000380800GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-3UTRENST00000506894ENST00000341322GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506894ENST00000470108GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000515090ENST00000333229GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000515090ENST00000342449GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000515090ENST00000380800GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-3UTRENST00000515090ENST00000341322GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000515090ENST00000470108GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506219ENST00000333229GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506219ENST00000342449GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506219ENST00000380800GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-3UTRENST00000506219ENST00000341322GPM6Achr4

176923469

-BRWD1chr21

40669820

-
intron-intronENST00000506219ENST00000470108GPM6Achr4

176923469

-BRWD1chr21

40669820

-

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FusionProtFeatures for GPM6A_BRWD1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GPM6A

P51674

BRWD1

Q9NSI6

Involved in neuronal differentiation, includingdifferentiation and migration of neuronal stem cells. Plays a rolein neuronal plasticity and is involved in neurite and filopodiaoutgrowth, filopodia motility and probably synapse formation.GPM6A-induced filopodia formation involves mitogen-activatedprotein kinase (MAPK) and Src signaling pathways. May be involvedin neuronal NGF-dependent Ca(2+) influx. May be involved inregulation of endocytosis and intracellular trafficking of G-protein-coupled receptors (GPCRs); enhances internalization andrecycling of mu-type opioid receptor.{ECO:0000269|PubMed:19298174}.

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 GPM6A_BRWD1


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 GPM6A_BRWD1


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 GPM6A_BRWD1


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 GPM6A_BRWD1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGPM6AC0036341Schizophrenia1PSYGENET
TgeneBRWD1C0028960Oligospermia1CTD_human