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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:NCAPD2-MRPL48 (FusionGDB2 ID:57537)

Fusion Gene Summary for NCAPD2-MRPL48

check button Fusion gene summary
Fusion gene informationFusion gene name: NCAPD2-MRPL48
Fusion gene ID: 57537
HgeneTgene
Gene symbol

NCAPD2

MRPL48

Gene ID

9918

51642

Gene namenon-SMC condensin I complex subunit D2mitochondrial ribosomal protein L48
SynonymsCAP-D2|CNAP1|MCPH21|hCAP-D2CGI-118|HSPC290|L48MT|MRP-L48
Cytomap

12p13.31

11q13.4

Type of geneprotein-codingprotein-coding
Descriptioncondensin complex subunit 1XCAP-D2 homologchromosome condensation-related SMC-associated protein 1chromosome-associated protein D239S ribosomal protein L48, mitochondrialmitochondrial large ribosomal subunit protein mL48
Modification date2020031320200313
UniProtAcc

Q15021

Q96GC5

Ensembl transtripts involved in fusion geneENST00000315579, ENST00000545962, 
ENST00000542492, 
ENST00000310614, 
ENST00000398483, ENST00000411840, 
ENST00000535529, ENST00000542303, 
ENST00000314282, 
Fusion gene scores* DoF score4 X 2 X 4=3213 X 10 X 8=1040
# samples 416
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(16/1040*10)=-2.70043971814109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NCAPD2 [Title/Abstract] AND MRPL48 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNCAPD2(6603320)-MRPL48(73516072), # samples:2
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
HgeneNCAPD2

GO:0007076

mitotic chromosome condensation

11136719


check buttonFusion gene breakpoints across NCAPD2 (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 MRPL48 (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
ChimerDB4ACCTCGA-OR-A5J1-01ANCAPD2chr12

6603320

+MRPL48chr11

73516072

+


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Fusion Gene ORF analysis for NCAPD2-MRPL48

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-3CDSENST00000315579ENST00000310614NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-3CDSENST00000545962ENST00000310614NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000315579ENST00000398483NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000315579ENST00000411840NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000315579ENST00000535529NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000315579ENST00000542303NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000545962ENST00000398483NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000545962ENST00000411840NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000545962ENST00000535529NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-5UTRENST00000545962ENST00000542303NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-intronENST00000315579ENST00000314282NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
5UTR-intronENST00000545962ENST00000314282NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
intron-3CDSENST00000542492ENST00000310614NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
intron-5UTRENST00000542492ENST00000398483NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
intron-5UTRENST00000542492ENST00000411840NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
intron-5UTRENST00000542492ENST00000535529NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
intron-5UTRENST00000542492ENST00000542303NCAPD2chr12

6603320

+MRPL48chr11

73516072

+
intron-intronENST00000542492ENST00000314282NCAPD2chr12

6603320

+MRPL48chr11

73516072

+

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 NCAPD2-MRPL48


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)
NCAPD2chr126603320+MRPL48chr1173516071+1.84E-081
NCAPD2chr126603320+MRPL48chr1173516071+1.84E-081

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.
genomic feature of top 1%

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Fusion Protein Features for NCAPD2-MRPL48


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/:6603320/:73516072)
- 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
NCAPD2

Q15021

MRPL48

Q96GC5

FUNCTION: Regulatory subunit of the condensin complex, a complex required for conversion of interphase chromatin into mitotic-like condense chromosomes. The condensin complex probably introduces positive supercoils into relaxed DNA in the presence of type I topoisomerases and converts nicked DNA into positive knotted forms in the presence of type II topoisomerases. May target the condensin complex to DNA via its C-terminal domain (PubMed:11136719). May promote the resolution of double-strand DNA catenanes (intertwines) between sister chromatids. Condensin-mediated compaction likely increases tension in catenated sister chromatids, providing directionality for type II topoisomerase-mediated strand exchanges toward chromatid decatenation. Required for decatenation of non-centromeric ultrafine DNA bridges during anaphase. Early in neurogenesis, may play an essential role to ensure accurate mitotic chromosome condensation in neuron stem cells, ultimately affecting neuron pool and cortex size (PubMed:27737959). {ECO:0000269|PubMed:11136719, ECO:0000269|PubMed:27737959}.

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 NCAPD2-MRPL48


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 NCAPD2-MRPL48


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 NCAPD2-MRPL48


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 NCAPD2-MRPL48


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