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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:ALKBH3-ACTN2 (FusionGDB2 ID:4170)

Fusion Gene Summary for ALKBH3-ACTN2

check button Fusion gene summary
Fusion gene informationFusion gene name: ALKBH3-ACTN2
Fusion gene ID: 4170
HgeneTgene
Gene symbol

ALKBH3

ACTN2

Gene ID

221120

88

Gene namealkB homolog 3, alpha-ketoglutaratedependent dioxygenaseactinin alpha 2
SynonymsABH3|DEPC-1|DEPC1|PCA1|hABH3CMD1AA|CMH23|MPD6|MYOCOZ
Cytomap

11p11.2

1q43

Type of geneprotein-codingprotein-coding
Descriptionalpha-ketoglutarate-dependent dioxygenase alkB homolog 3alkB homolog 3, alpha-ketoglutarate-dependent dioxygenasealkB, alkylation repair homolog 3alkylated DNA repair protein alkB homolog 3prostate cancer antigen-1alpha-actinin-2F-actin cross-linking proteinalpha-actinin skeletal muscle
Modification date2020032720200313
UniProtAcc

Q96Q83

P35609

Ensembl transtripts involved in fusion geneENST00000302708, ENST00000378840, 
ENST00000532410, 
ENST00000542672, 
ENST00000366578, ENST00000492634, 
ENST00000546208, 
Fusion gene scores* DoF score2 X 2 X 2=82 X 2 X 1=4
# samples 22
** MAII scorelog2(2/8*10)=1.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: ALKBH3 [Title/Abstract] AND ACTN2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointALKBH3(43903015)-ACTN2(236891005), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneALKBH3

GO:0006281

DNA repair

16858410

HgeneALKBH3

GO:0006307

DNA dealkylation involved in DNA repair

16858410|22055184

HgeneALKBH3

GO:0035552

oxidative single-stranded DNA demethylation

16858410

HgeneALKBH3

GO:0035553

oxidative single-stranded RNA demethylation

26863196|26863410

TgeneACTN2

GO:0030035

microspike assembly

12356918

TgeneACTN2

GO:0043268

positive regulation of potassium ion transport

17110593

TgeneACTN2

GO:1901018

positive regulation of potassium ion transmembrane transporter activity

17110593


check buttonFusion gene breakpoints across ALKBH3 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ACTN2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABX501306ALKBH3chr11

43903015

+ACTN2chr1

236891005

+


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Fusion Gene ORF analysis for ALKBH3-ACTN2

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-3CDSENST00000302708ENST00000542672ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3CDSENST00000302708ENST00000366578ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3UTRENST00000302708ENST00000492634ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-intronENST00000302708ENST00000546208ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3CDSENST00000378840ENST00000542672ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3CDSENST00000378840ENST00000366578ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3UTRENST00000378840ENST00000492634ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-intronENST00000378840ENST00000546208ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3CDSENST00000532410ENST00000542672ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3CDSENST00000532410ENST00000366578ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-3UTRENST00000532410ENST00000492634ALKBH3chr11

43903015

+ACTN2chr1

236891005

+
intron-intronENST00000532410ENST00000546208ALKBH3chr11

43903015

+ACTN2chr1

236891005

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for ALKBH3-ACTN2


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for ALKBH3-ACTN2


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ALKBH3

Q96Q83

ACTN2

P35609

FUNCTION: Dioxygenase that mediates demethylation of DNA and RNA containing 1-methyladenosine (m1A) (PubMed:12486230, PubMed:12594517, PubMed:16174769, PubMed:26863196, PubMed:26863410). Repairs alkylated DNA containing 1-methyladenosine (m1A) and 3-methylcytosine (m3C) by oxidative demethylation (PubMed:12486230, PubMed:12594517, PubMed:16174769, PubMed:25944111). Has a strong preference for single-stranded DNA (PubMed:12486230, PubMed:12594517, PubMed:16174769). Able to process alkylated m3C within double-stranded regions via its interaction with ASCC3, which promotes DNA unwinding to generate single-stranded substrate needed for ALKBH3 (PubMed:22055184). Also acts on RNA (PubMed:12594517, PubMed:16174769, PubMed:26863196, PubMed:26863410, PubMed:16858410). Demethylates N(1)-methyladenosine (m1A) RNA, an epigenetic internal modification of messenger RNAs (mRNAs) highly enriched within 5'-untranslated regions (UTRs) and in the vicinity of start codons (PubMed:26863196, PubMed:26863410). Requires molecular oxygen, alpha-ketoglutarate and iron (PubMed:22055184, PubMed:16858410). {ECO:0000269|PubMed:12486230, ECO:0000269|PubMed:12594517, ECO:0000269|PubMed:16174769, ECO:0000269|PubMed:16858410, ECO:0000269|PubMed:22055184, ECO:0000269|PubMed:25944111, ECO:0000269|PubMed:26863196, ECO:0000269|PubMed:26863410}.FUNCTION: F-actin cross-linking protein which is thought to anchor actin to a variety of intracellular structures. This is a bundling protein.

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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Fusion Gene Sequence for ALKBH3-ACTN2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for ALKBH3-ACTN2


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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Related Drugs for ALKBH3-ACTN2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneALKBH3Q96Q83DB00126Ascorbic acidActivatorSmall moleculeApproved|Nutraceutical
HgeneALKBH3Q96Q83DB00126Ascorbic acidActivatorSmall moleculeApproved|Nutraceutical
HgeneALKBH3Q96Q83DB00126Ascorbic acidActivatorSmall moleculeApproved|Nutraceutical

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Related Diseases for ALKBH3-ACTN2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneACTN2C2677338Cardiomyopathy, Dilated, 1AA6CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneACTN2C0340427Familial dilated cardiomyopathy2ORPHANET