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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:CAMK1D-BNIP3L (FusionGDB2 ID:12634)

Fusion Gene Summary for CAMK1D-BNIP3L

check button Fusion gene summary
Fusion gene informationFusion gene name: CAMK1D-BNIP3L
Fusion gene ID: 12634
HgeneTgene
Gene symbol

CAMK1D

BNIP3L

Gene ID

57118

665

Gene namecalcium/calmodulin dependent protein kinase IDBCL2 interacting protein 3 like
SynonymsCKLiK|CaM-K1|CaMKIDBNIP3a|NIX
Cytomap

10p13

8p21.2

Type of geneprotein-codingprotein-coding
Descriptioncalcium/calmodulin-dependent protein kinase type 1DCAMK1D/ANAPC5 fusionCaM kinase IDCamKI-like protein kinasecaM kinase I deltacaM-KI deltacaMKI deltaBCL2/adenovirus E1B 19 kDa protein-interacting protein 3-likeBCL2/adenovirus E1B 19 kDa protein-interacting protein 3ABCL2/adenovirus E1B 19-kd protein-interacting protein 3aBCL2/adenovirus E1B 19kDa interacting protein 3 likeNIP-3-like protein XNIP3
Modification date2020031320200313
UniProtAcc

Q8IU85

O60238

Ensembl transtripts involved in fusion geneENST00000487696, ENST00000378845, 
ENST00000378847, 
ENST00000380629, 
ENST00000518611, ENST00000520409, 
ENST00000523515, ENST00000521254, 
Fusion gene scores* DoF score24 X 22 X 7=36969 X 8 X 6=432
# samples 2811
** MAII scorelog2(28/3696*10)=-3.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/432*10)=-1.97352778863881
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CAMK1D [Title/Abstract] AND BNIP3L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCAMK1D(12391909)-BNIP3L(26248759), # samples:2
Anticipated loss of major functional domain due to fusion event.CAMK1D-BNIP3L seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CAMK1D-BNIP3L seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CAMK1D-BNIP3L seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
CAMK1D-BNIP3L seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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
HgeneCAMK1D

GO:0032793

positive regulation of CREB transcription factor activity

16324104

TgeneBNIP3L

GO:0043065

positive regulation of apoptotic process

9973195

TgeneBNIP3L

GO:0043066

negative regulation of apoptotic process

10381623

TgeneBNIP3L

GO:0051607

defense response to virus

9973195


check buttonFusion gene breakpoints across CAMK1D (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 BNIP3L (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
ChimerDB4OVTCGA-24-2288-01ACAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+


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Fusion Gene ORF analysis for CAMK1D-BNIP3L

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
3UTR-3CDSENST00000487696ENST00000380629CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
3UTR-5UTRENST00000487696ENST00000518611CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
3UTR-5UTRENST00000487696ENST00000520409CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
3UTR-5UTRENST00000487696ENST00000523515CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
3UTR-intronENST00000487696ENST00000521254CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-5UTRENST00000378845ENST00000518611CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-5UTRENST00000378845ENST00000520409CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-5UTRENST00000378845ENST00000523515CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-5UTRENST00000378847ENST00000518611CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-5UTRENST00000378847ENST00000520409CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-5UTRENST00000378847ENST00000523515CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-intronENST00000378845ENST00000521254CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
5CDS-intronENST00000378847ENST00000521254CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
Frame-shiftENST00000378845ENST00000380629CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+
Frame-shiftENST00000378847ENST00000380629CAMK1Dchr10

12391909

+BNIP3Lchr8

26248759

+

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 CAMK1D-BNIP3L


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)
CAMK1Dchr1012391909+BNIP3Lchr826248758+5.01E-091
CAMK1Dchr1012391909+BNIP3Lchr826248758+5.01E-091

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 CAMK1D-BNIP3L


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/:12391909/:26248759)
- 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
CAMK1D

Q8IU85

BNIP3L

O60238

FUNCTION: Calcium/calmodulin-dependent protein kinase that operates in the calcium-triggered CaMKK-CaMK1 signaling cascade and, upon calcium influx, activates CREB-dependent gene transcription, regulates calcium-mediated granulocyte function and respiratory burst and promotes basal dendritic growth of hippocampal neurons. In neutrophil cells, required for cytokine-induced proliferative responses and activation of the respiratory burst. Activates the transcription factor CREB1 in hippocampal neuron nuclei. May play a role in apoptosis of erythroleukemia cells. In vitro, phosphorylates transcription factor CREM isoform Beta. {ECO:0000269|PubMed:11050006, ECO:0000269|PubMed:15840691, ECO:0000269|PubMed:16324104, ECO:0000269|PubMed:17056143}.FUNCTION: Induces apoptosis. Interacts with viral and cellular anti-apoptosis proteins. Can overcome the suppressors BCL-2 and BCL-XL, although high levels of BCL-XL expression will inhibit apoptosis. Inhibits apoptosis induced by BNIP3. Involved in mitochondrial quality control via its interaction with SPATA18/MIEAP: in response to mitochondrial damage, participates in mitochondrial protein catabolic process (also named MALM) leading to the degradation of damaged proteins inside mitochondria. The physical interaction of SPATA18/MIEAP, BNIP3 and BNIP3L/NIX at the mitochondrial outer membrane regulates the opening of a pore in the mitochondrial double membrane in order to mediate the translocation of lysosomal proteins from the cytoplasm to the mitochondrial matrix. May function as a tumor suppressor. {ECO:0000269|PubMed:10381623, ECO:0000269|PubMed:21264228}.

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 CAMK1D-BNIP3L


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 CAMK1D-BNIP3L


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 CAMK1D-BNIP3L


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 CAMK1D-BNIP3L


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