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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: 22449

FusionGeneSummary for MROH8_AGO3

check button Fusion gene summary
Fusion gene informationFusion gene name: MROH8_AGO3
Fusion gene ID: 22449
HgeneTgene
Gene symbol

MROH8

AGO3

Gene ID

140699

192669

Gene namemaestro heat like repeat family member 8argonaute 3, RISC catalytic component
SynonymsC20orf131|C20orf132|dJ621N11.3|dJ621N11.4EIF2C3
Cytomap

20q11.23

1p34.3

Type of geneprotein-codingprotein-coding
Descriptionprotein MROH8maestro heat-like repeat-containing protein family member 8protein argonaute-3argonaute RISC catalytic component 3eukaryotic translation initiation factor 2C, 3hAgo3
Modification date2018051920180522
UniProtAcc

Q9H579

Q9H9G7

Ensembl transtripts involved in fusion geneENST00000441008, ENST00000217333, 
ENST00000400441, ENST00000466091, 
ENST00000324350, ENST00000373191, 
ENST00000397828, ENST00000246314, 
ENST00000471099, 
Fusion gene scores* DoF score1 X 1 X 1=18 X 5 X 8=320
# samples 18
** MAII scorelog2(1/1*10)=3.32192809488736log2(8/320*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MROH8 [Title/Abstract] AND AGO3 [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
TgeneAGO3

GO:0006402

mRNA catabolic process

18771919

TgeneAGO3

GO:0010501

RNA secondary structure unwinding

19966796

TgeneAGO3

GO:0031054

pre-miRNA processing

19966796

TgeneAGO3

GO:0035278

miRNA mediated inhibition of translation

18771919

TgeneAGO3

GO:0035279

mRNA cleavage involved in gene silencing by miRNA

15260970

TgeneAGO3

GO:0035280

miRNA loading onto RISC involved in gene silencing by miRNA

19966796

TgeneAGO3

GO:0090625

mRNA cleavage involved in gene silencing by siRNA

15260970


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
ChiTaRS3.1AI086445MROH8chr20

35759788

-AGO3chr1

36399264

-
* 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-intronENST00000441008ENST00000324350MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000441008ENST00000373191MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000441008ENST00000397828MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000441008ENST00000246314MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000441008ENST00000471099MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000217333ENST00000324350MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000217333ENST00000373191MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000217333ENST00000397828MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000217333ENST00000246314MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000217333ENST00000471099MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000400441ENST00000324350MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000400441ENST00000373191MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000400441ENST00000397828MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000400441ENST00000246314MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000400441ENST00000471099MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000466091ENST00000324350MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000466091ENST00000373191MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000466091ENST00000397828MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000466091ENST00000246314MROH8chr20

35759788

-AGO3chr1

36399264

-
intron-intronENST00000466091ENST00000471099MROH8chr20

35759788

-AGO3chr1

36399264

-

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FusionProtFeatures for MROH8_AGO3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MROH8

Q9H579

AGO3

Q9H9G7

Required for RNA-mediated gene silencing (RNAi). Bindsto short RNAs such as microRNAs (miRNAs) and represses thetranslation of mRNAs which are complementary to them. Proposed tobe involved in stabilization of small RNA derivates (riRNA)derived from processed RNA polymerase III-transcribed Alu repeatscontaining a DR2 retinoic acid response element (RARE) in stemcells and in the subsequent riRNA-dependent degradation of asubset of RNA polymerase II-transcribed coding mRNAs by recruitinga mRNA decapping complex involving EDC4. Possesses RNA sliceractivity but only on select RNAs bearing 5'- and 3'-flankingsequences to the region of guide-target complementarity(PubMed:29040713). {ECO:0000255|HAMAP-Rule:MF_03032,ECO:0000269|PubMed:18771919, ECO:0000269|PubMed:23064648,ECO:0000269|PubMed:29040713}.

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 MROH8_AGO3


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 MROH8_AGO3


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 MROH8_AGO3


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 MROH8_AGO3


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