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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:C1orf21-ANKLE2 (FusionGDB2 ID:11345)

Fusion Gene Summary for C1orf21-ANKLE2

check button Fusion gene summary
Fusion gene informationFusion gene name: C1orf21-ANKLE2
Fusion gene ID: 11345
HgeneTgene
Gene symbol

C1orf21

ANKLE2

Gene ID

81563

23141

Gene namechromosome 1 open reading frame 21ankyrin repeat and LEM domain containing 2
SynonymsPIG13KIAA0692|LEMD7|Lem4|MCPH16
Cytomap

1q25.3

12q24.33

Type of geneprotein-codingprotein-coding
Descriptionuncharacterized protein C1orf21cell proliferation-inducing gene 13 proteinproliferation-inducing protein 13ankyrin repeat and LEM domain-containing protein 2LEM domain containing 7LEM domain-containing protein 4
Modification date2020031320200313
UniProtAcc

Q9H246

Q86XL3

Ensembl transtripts involved in fusion geneENST00000235307, ENST00000367514, 
ENST00000357997, ENST00000539605, 
ENST00000337516, ENST00000542282, 
ENST00000542374, ENST00000542657, 
Fusion gene scores* DoF score6 X 4 X 5=12012 X 6 X 7=504
# samples 612
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/504*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C1orf21 [Title/Abstract] AND ANKLE2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC1orf21(184356466)-ANKLE2(133331505), # 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
TgeneANKLE2

GO:0007417

central nervous system development

25259927

TgeneANKLE2

GO:0035307

positive regulation of protein dephosphorylation

22770216

TgeneANKLE2

GO:0042326

negative regulation of phosphorylation

22770216

TgeneANKLE2

GO:0043066

negative regulation of apoptotic process

25259927


check buttonFusion gene breakpoints across C1orf21 (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 ANKLE2 (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/AAI201468C1orf21chr1

184356466

+ANKLE2chr12

133331505

-


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Fusion Gene ORF analysis for C1orf21-ANKLE2

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
5UTR-3CDSENST00000235307ENST00000357997C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
5UTR-3CDSENST00000235307ENST00000539605C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
5UTR-intronENST00000235307ENST00000337516C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
5UTR-intronENST00000235307ENST00000542282C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
5UTR-intronENST00000235307ENST00000542374C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
5UTR-intronENST00000235307ENST00000542657C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
intron-3CDSENST00000367514ENST00000357997C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
intron-3CDSENST00000367514ENST00000539605C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
intron-intronENST00000367514ENST00000337516C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
intron-intronENST00000367514ENST00000542282C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
intron-intronENST00000367514ENST00000542374C1orf21chr1

184356466

+ANKLE2chr12

133331505

-
intron-intronENST00000367514ENST00000542657C1orf21chr1

184356466

+ANKLE2chr12

133331505

-

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 C1orf21-ANKLE2


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 C1orf21-ANKLE2


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:184356466/:133331505)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
C1orf21

Q9H246

ANKLE2

Q86XL3

FUNCTION: Involved in mitotic nuclear envelope reassembly by promoting dephosphorylation of BAF/BANF1 during mitotic exit (PubMed:22770216). Coordinates the control of BAF/BANF1 dephosphorylation by inhibiting VRK1 kinase and promoting dephosphorylation of BAF/BANF1 by protein phosphatase 2A (PP2A), thereby facilitating nuclear envelope assembly (PubMed:22770216). May regulate nuclear localization of VRK1 in non-dividing cells (PubMed:31735666). It is unclear whether it acts as a real PP2A regulatory subunit or whether it is involved in recruitment of the PP2A complex (PubMed:22770216). Involved in brain development (PubMed:25259927). {ECO:0000269|PubMed:22770216, ECO:0000269|PubMed:25259927, ECO:0000269|PubMed:31735666}.

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 C1orf21-ANKLE2


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 C1orf21-ANKLE2


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 C1orf21-ANKLE2


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 C1orf21-ANKLE2


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