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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: 23150

FusionGeneSummary for MYO1E_GPR176

check button Fusion gene summary
Fusion gene informationFusion gene name: MYO1E_GPR176
Fusion gene ID: 23150
HgeneTgene
Gene symbol

MYO1E

GPR176

Gene ID

4643

11245

Gene namemyosin IEG protein-coupled receptor 176
SynonymsFSGS6|HuncM-IC|MYO1CHB-954
Cytomap

15q22.2

15q14-q15.1

Type of geneprotein-codingprotein-coding
Descriptionunconventional myosin-IeMYO1E variant proteinmyosin-ICunconventional myosin 1EG-protein coupled receptor 176probable G-protein coupled receptor 176
Modification date2018051920180517
UniProtAcc

Q12965

Q14439

Ensembl transtripts involved in fusion geneENST00000288235, ENST00000558814, 
ENST00000299092, ENST00000561100, 
ENST00000543580, ENST00000560729, 
Fusion gene scores* DoF score11 X 8 X 8=7044 X 1 X 4=16
# samples 124
** MAII scorelog2(12/704*10)=-2.55254102302878
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MYO1E [Title/Abstract] AND GPR176 [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
TCGARVSTADTCGA-CG-4444-01AMYO1Echr15

59510090

-GPR176chr15

40099459

-
* 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
5CDS-intronENST00000288235ENST00000299092MYO1Echr15

59510090

-GPR176chr15

40099459

-
5CDS-intronENST00000288235ENST00000561100MYO1Echr15

59510090

-GPR176chr15

40099459

-
5CDS-intronENST00000288235ENST00000543580MYO1Echr15

59510090

-GPR176chr15

40099459

-
5CDS-5UTRENST00000288235ENST00000560729MYO1Echr15

59510090

-GPR176chr15

40099459

-
intron-intronENST00000558814ENST00000299092MYO1Echr15

59510090

-GPR176chr15

40099459

-
intron-intronENST00000558814ENST00000561100MYO1Echr15

59510090

-GPR176chr15

40099459

-
intron-intronENST00000558814ENST00000543580MYO1Echr15

59510090

-GPR176chr15

40099459

-
intron-5UTRENST00000558814ENST00000560729MYO1Echr15

59510090

-GPR176chr15

40099459

-

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FusionProtFeatures for MYO1E_GPR176


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYO1E

Q12965

GPR176

Q14439

Myosins are actin-based motor molecules with ATPaseactivity. Unconventional myosins serve in intracellular movements.Their highly divergent tails bind to membranous compartments,which are then moved relative to actin filaments. Binds tomembranes containing anionic phospholipids via its tail domain.Required for normal morphology of the glomerular basementmembrane, normal development of foot processes by kidney podocytesand normal kidney function. In dendritic cells, may control themovement of class II-containing cytoplasmic vesicles along theactin cytoskeleton by connecting them with the actin network viaARL14EP and ARL14. {ECO:0000269|PubMed:11940582,ECO:0000269|PubMed:17257598, ECO:0000269|PubMed:20860408}. Orphan receptor involved in normal circadian rhythmbehavior. Acts through the G-protein subclass G(z)-alpha and hasan agonist-independent basal activity to repress cAMP production.{ECO:0000250|UniProtKB:Q80WT4}.

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 MYO1E_GPR176


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 MYO1E_GPR176


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
MYO1EEMD, SP1, CUL1, DIAPH1, MOV10, DTNA, ILF3, MYH11, RNF20, PAN2, ASNS, ATIC, CAPNS1, ISOC1, MCTS1, STK26, OGFOD1, PAFAH1B1, PDIA4, PROSC, SNRPF, TBCB, YWHAH, RPA1, RPA2, RPA3, ENO1, SHMT2, NXF1, ARPC4-TTLL3, ARPC4, CAND1, MYH9, CTTN, FNBP1, LGALS3, STMN1, MYO5A, PPA1, SRPK2, CAPZA2, DBN1, FLNA, PDGFRB, PPP1CB, IQGAP1, SLC33A1, PDLIM7, SYNPO, MAPRE1, LIMA1, ANLN, MYO5C, MYO19, MYO18A, ZNF764, OSTF1, UNC45A, RAC1, TRIM25GPR176


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 MYO1E_GPR176


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 MYO1E_GPR176


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMYO1EC3279905FOCAL SEGMENTAL GLOMERULOSCLEROSIS 61UNIPROT