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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:CHMP1A-PCM1 (FusionGDB2 ID:16526)

Fusion Gene Summary for CHMP1A-PCM1

check button Fusion gene summary
Fusion gene informationFusion gene name: CHMP1A-PCM1
Fusion gene ID: 16526
HgeneTgene
Gene symbol

CHMP1A

PCM1

Gene ID

5119

5108

Gene namecharged multivesicular body protein 1Apericentriolar material 1
SynonymsCHMP1|PCH8|PCOLN3|PRSM1|VPS46-1|VPS46APTC4|RET/PCM-1
Cytomap

16q24.3

8p22

Type of geneprotein-codingprotein-coding
Descriptioncharged multivesicular body protein 1acharged multivesicular body protein 1/chromatin modifying protein 1chromatin modifying protein 1Aprocollagen (type III) N-endopeptidaseprotease, metallo, 1, 33kDvacuolar protein sorting-associated protein 46-1pericentriolar material 1 proteinPCM-1hPCM-1pericentriolar material 1, PCM1
Modification date2020031320200327
UniProtAcc

Q9HD42

Q15154

Ensembl transtripts involved in fusion geneENST00000253475, ENST00000397901, 
ENST00000535997, ENST00000547614, 
ENST00000550102, 
ENST00000325083, 
ENST00000519253, ENST00000524226, 
ENST00000327578, ENST00000518537, 
ENST00000518936, 
Fusion gene scores* DoF score6 X 9 X 5=27010 X 14 X 6=840
# samples 913
** MAII scorelog2(9/270*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/840*10)=-2.69187770463767
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CHMP1A [Title/Abstract] AND PCM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCHMP1A(89719864)-PCM1(17885267), # 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
HgeneCHMP1A

GO:0007076

mitotic chromosome condensation

11559747

HgeneCHMP1A

GO:0016192

vesicle-mediated transport

11559748

HgeneCHMP1A

GO:0016458

gene silencing

11559747

HgeneCHMP1A

GO:0045892

negative regulation of transcription, DNA-templated

11559747


check buttonFusion gene breakpoints across CHMP1A (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 PCM1 (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/AGW492753CHMP1Achr16

89719864

-PCM1chr8

17885267

-


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Fusion Gene ORF analysis for CHMP1A-PCM1

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-3UTRENST00000253475ENST00000325083CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000253475ENST00000519253CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000253475ENST00000524226CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000397901ENST00000325083CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000397901ENST00000519253CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000397901ENST00000524226CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000535997ENST00000325083CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000535997ENST00000519253CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000535997ENST00000524226CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000547614ENST00000325083CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000547614ENST00000519253CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000547614ENST00000524226CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000550102ENST00000325083CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000550102ENST00000519253CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-3UTRENST00000550102ENST00000524226CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000253475ENST00000327578CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000253475ENST00000518537CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000253475ENST00000518936CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000397901ENST00000327578CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000397901ENST00000518537CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000397901ENST00000518936CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000535997ENST00000327578CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000535997ENST00000518537CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000535997ENST00000518936CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000547614ENST00000327578CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000547614ENST00000518537CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000547614ENST00000518936CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000550102ENST00000327578CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000550102ENST00000518537CHMP1Achr16

89719864

-PCM1chr8

17885267

-
intron-intronENST00000550102ENST00000518936CHMP1Achr16

89719864

-PCM1chr8

17885267

-

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 CHMP1A-PCM1


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 CHMP1A-PCM1


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/:89719864/:17885267)
- 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
CHMP1A

Q9HD42

PCM1

Q15154

FUNCTION: Probable peripherally associated component of the endosomal sorting required for transport complex III (ESCRT-III) which is involved in multivesicular bodies (MVBs) formation and sorting of endosomal cargo proteins into MVBs. MVBs contain intraluminal vesicles (ILVs) that are generated by invagination and scission from the limiting membrane of the endosome and mostly are delivered to lysosomes enabling degradation of membrane proteins, such as stimulated growth factor receptors, lysosomal enzymes and lipids. The MVB pathway appears to require the sequential function of ESCRT-O, -I,-II and -III complexes. ESCRT-III proteins mostly dissociate from the invaginating membrane before the ILV is released. The ESCRT machinery also functions in topologically equivalent membrane fission events, such as the terminal stages of cytokinesis and the budding of enveloped viruses (HIV-1 and other lentiviruses). ESCRT-III proteins are believed to mediate the necessary vesicle extrusion and/or membrane fission activities, possibly in conjunction with the AAA ATPase VPS4. Involved in cytokinesis. Involved in recruiting VPS4A and/or VPS4B to the midbody of dividing cells. May also be involved in chromosome condensation. Targets the Polycomb group (PcG) protein BMI1/PCGF4 to regions of condensed chromatin. May play a role in stable cell cycle progression and in PcG gene silencing. {ECO:0000269|PubMed:11559747, ECO:0000269|PubMed:11559748, ECO:0000269|PubMed:19129479, ECO:0000269|PubMed:23045692}.FUNCTION: Required for centrosome assembly and function (PubMed:12403812, PubMed:15659651, PubMed:16943179). Essential for the correct localization of several centrosomal proteins including CEP250, CETN3, PCNT and NEK2 (PubMed:12403812, PubMed:15659651). Required to anchor microtubules to the centrosome (PubMed:12403812, PubMed:15659651). Also involved in cilium biogenesis by recruiting the BBSome, a ciliary protein complex involved in cilium biogenesis, to the centriolar satellites (PubMed:20551181, PubMed:24121310, PubMed:27979967). {ECO:0000269|PubMed:12403812, ECO:0000269|PubMed:15659651, ECO:0000269|PubMed:16943179, ECO:0000269|PubMed:20551181, ECO:0000269|PubMed:24121310, ECO:0000269|PubMed:27979967}.

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 CHMP1A-PCM1


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 CHMP1A-PCM1


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 CHMP1A-PCM1


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 CHMP1A-PCM1


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