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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:CHODL-PKM (FusionGDB2 ID:16592)

Fusion Gene Summary for CHODL-PKM

check button Fusion gene summary
Fusion gene informationFusion gene name: CHODL-PKM
Fusion gene ID: 16592
HgeneTgene
Gene symbol

CHODL

PKM

Gene ID

140578

5315

Gene namechondrolectinpyruvate kinase M1/2
SynonymsC21orf68|MT75|PRED12CTHBP|HEL-S-30|OIP3|PK3|PKM2|TCB|THBP1|p58
Cytomap

21q21.1

15q23

Type of geneprotein-codingprotein-coding
Descriptionchondrolectintransmembrane protein MT75pyruvate kinase PKMOPA-interacting protein 3PK, muscle typecytosolic thyroid hormone-binding proteinepididymis secretory protein Li 30pyruvate kinase 2/3pyruvate kinase isozymes M1/M2pyruvate kinase muscle isozymepyruvate kinase, musclethyroid ho
Modification date2020031320200329
UniProtAcc

Q9H9P2

Q99640

Ensembl transtripts involved in fusion geneENST00000299295, ENST00000338326, 
ENST00000400127, ENST00000400128, 
ENST00000400131, ENST00000400135, 
ENST00000543733, 		ENST00000319622, 
ENST00000335181, ENST00000389093, 
ENST00000449901, ENST00000565154, 
ENST00000565184, ENST00000568459, 
ENST00000568883, 
Fusion gene scores* DoF score7 X 7 X 2=9834 X 37 X 9=11322
# samples 741
** MAII scorelog2(7/98*10)=-0.485426827170242
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(41/11322*10)=-4.78736110881616
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CHODL [Title/Abstract] AND PKM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCHODL(19617296)-PKM(72502387), # 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
TgenePKM

GO:0012501

programmed cell death

17308100


check buttonFusion gene breakpoints across CHODL (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 PKM (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/ABU561657CHODLchr21

19617296

+PKMchr15

72502387

+


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Fusion Gene ORF analysis for CHODL-PKM

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-intronENST00000299295ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000299295ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
5UTR-intronENST00000338326ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400127ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400128ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400131ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000400135ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000319622CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000335181CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000389093CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000449901CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000565154CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000565184CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000568459CHODLchr21

19617296

+PKMchr15

72502387

+
intron-intronENST00000543733ENST00000568883CHODLchr21

19617296

+PKMchr15

72502387

+

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 CHODL-PKM


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 CHODL-PKM


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/:19617296/:72502387)
- 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
CHODL

Q9H9P2

PKM

Q99640

FUNCTION: May play a role in the development of the nervous system such as in neurite outgrowth and elongation. May be involved in motor axon growth and guidance. {ECO:0000250|UniProtKB:Q568T5, ECO:0000250|UniProtKB:Q9CXM0}.FUNCTION: Acts as a negative regulator of entry into mitosis (G2 to M transition) by phosphorylation of the CDK1 kinase specifically when CDK1 is complexed to cyclins. Mediates phosphorylation of CDK1 predominantly on 'Thr-14'. Also involved in Golgi fragmentation. May be involved in phosphorylation of CDK1 on 'Tyr-15' to a lesser degree, however tyrosine kinase activity is unclear and may be indirect. May be a downstream target of Notch signaling pathway during eye development. {ECO:0000269|PubMed:10373560, ECO:0000269|PubMed:9001210}.

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 CHODL-PKM


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 CHODL-PKM


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 CHODL-PKM


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 CHODL-PKM


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