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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:ACTN1-KDM6B (FusionGDB2 ID:1864)

Fusion Gene Summary for ACTN1-KDM6B

check button Fusion gene summary
Fusion gene informationFusion gene name: ACTN1-KDM6B
Fusion gene ID: 1864
HgeneTgene
Gene symbol

ACTN1

KDM6B

Gene ID

87

23135

Gene nameactinin alpha 1lysine demethylase 6B
SynonymsBDPLT15JMJD3|NEDCFSA
Cytomap

14q24.1|14q22-q24

17p13.1

Type of geneprotein-codingprotein-coding
Descriptionalpha-actinin-1F-actin cross-linking proteinactinin 1 smooth musclealpha-actinin cytoskeletal isoformepididymis secretory sperm binding proteinnon-muscle alpha-actinin-1lysine-specific demethylase 6BjmjC domain-containing protein 3jumonji domain containing 3, histone lysine demethylasejumonji domain-containing protein 3lysine (K)-specific demethylase 6B
Modification date2020032720200313
UniProtAcc.

O15054

Ensembl transtripts involved in fusion geneENST00000193403, ENST00000394419, 
ENST00000438964, ENST00000376839, 
ENST00000538545, ENST00000554508, 
ENST00000254846, ENST00000448097, 
ENST00000572030, 
Fusion gene scores* DoF score14 X 14 X 4=7845 X 5 X 4=100
# samples 175
** MAII scorelog2(17/784*10)=-2.20531890797751
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ACTN1 [Title/Abstract] AND KDM6B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointACTN1(69387594)-KDM6B(7752664), # 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

check buttonFusion gene breakpoints across ACTN1 (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 KDM6B (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/ABF810594ACTN1chr14

69387594

-KDM6Bchr17

7752664

-


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Fusion Gene ORF analysis for ACTN1-KDM6B

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-3CDSENST00000193403ENST00000254846ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000193403ENST00000448097ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-intronENST00000193403ENST00000572030ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000394419ENST00000254846ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000394419ENST00000448097ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-intronENST00000394419ENST00000572030ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000438964ENST00000254846ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000438964ENST00000448097ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-intronENST00000438964ENST00000572030ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000376839ENST00000254846ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000376839ENST00000448097ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-intronENST00000376839ENST00000572030ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000538545ENST00000254846ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000538545ENST00000448097ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-intronENST00000538545ENST00000572030ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000554508ENST00000254846ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-3CDSENST00000554508ENST00000448097ACTN1chr14

69387594

-KDM6Bchr17

7752664

-
intron-intronENST00000554508ENST00000572030ACTN1chr14

69387594

-KDM6Bchr17

7752664

-

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 ACTN1-KDM6B


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 ACTN1-KDM6B


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
.KDM6B

O15054

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code (PubMed:17825402, PubMed:17851529, PubMed:17713478, PubMed:18003914). Demethylates trimethylated and dimethylated H3 'Lys-27' (PubMed:17825402, PubMed:17851529, PubMed:17713478, PubMed:18003914). Plays a central role in regulation of posterior development, by regulating HOX gene expression (PubMed:17851529). Involved in inflammatory response by participating in macrophage differentiation in case of inflammation by regulating gene expression and macrophage differentiation (PubMed:17825402). Plays a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression by acting as a link between T-box factors and the SMARCA4-containing SWI/SNF remodeling complex (By similarity). {ECO:0000250|UniProtKB:Q5NCY0, ECO:0000269|PubMed:17713478, ECO:0000269|PubMed:17825402, ECO:0000269|PubMed:17851529, ECO:0000269|PubMed:18003914, ECO:0000269|PubMed:28262558}.

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 ACTN1-KDM6B


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 ACTN1-KDM6B


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 ACTN1-KDM6B


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

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Related Diseases for ACTN1-KDM6B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneACTN1C3554663BLEEDING DISORDER, PLATELET-TYPE, 153CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneACTN1C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneACTN1C4304021Autosomal dominant macrothrombocytopenia1ORPHANET
TgeneKDM6BC0010606Adenoid Cystic Carcinoma1CTD_human
TgeneKDM6BC0020796Profound Mental Retardation1CTD_human
TgeneKDM6BC0025363Mental Retardation, Psychosocial1CTD_human
TgeneKDM6BC0917816Mental deficiency1CTD_human
TgeneKDM6BC3714756Intellectual Disability1CTD_human