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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:PICALM-CPQ (FusionGDB2 ID:64737)

Fusion Gene Summary for PICALM-CPQ

check button Fusion gene summary
Fusion gene informationFusion gene name: PICALM-CPQ
Fusion gene ID: 64737
HgeneTgene
Gene symbol

PICALM

CPQ

Gene ID

8301

10404

Gene namephosphatidylinositol binding clathrin assembly proteincarboxypeptidase Q
SynonymsCALM|CLTH|LAPLDP|PGCP
Cytomap

11q14.2

8q22.1

Type of geneprotein-codingprotein-coding
Descriptionphosphatidylinositol-binding clathrin assembly proteinclathrin assembly lymphoid myeloid leukemia proteincarboxypeptidase QSer-Met dipeptidaseaminopeptidaseblood plasma glutamate carboxypeptidaselysosomal dipeptidase
Modification date2020032220200313
UniProtAcc.

Q9Y646

Ensembl transtripts involved in fusion geneENST00000532317, ENST00000526033, 
ENST00000393346, ENST00000528398, 
ENST00000356360, ENST00000528411, 
ENST00000220763, ENST00000529551, 
Fusion gene scores* DoF score24 X 29 X 9=626416 X 14 X 11=2464
# samples 3919
** MAII scorelog2(39/6264*10)=-4.00553818354143
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/2464*10)=-3.69693093236395
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PICALM [Title/Abstract] AND CPQ [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPICALM(85669998)-CPQ(98078317), # 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
HgenePICALM

GO:0006897

endocytosis

22118466

HgenePICALM

GO:0006898

receptor-mediated endocytosis

10436022

HgenePICALM

GO:0032880

regulation of protein localization

10436022

HgenePICALM

GO:0045893

positive regulation of transcription, DNA-templated

11425879

HgenePICALM

GO:0048261

negative regulation of receptor-mediated endocytosis

10436022

HgenePICALM

GO:1905224

clathrin-coated pit assembly

16262731

TgeneCPQ

GO:0006508

proteolysis

10206990

TgeneCPQ

GO:0043171

peptide catabolic process

10206990


check buttonFusion gene breakpoints across PICALM (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 CPQ (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/ACF125182PICALMchr11

85669998

-CPQchr8

98078317

+


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Fusion Gene ORF analysis for PICALM-CPQ

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-3CDSENST00000532317ENST00000220763PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3UTRENST00000532317ENST00000529551PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3CDSENST00000526033ENST00000220763PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3UTRENST00000526033ENST00000529551PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3CDSENST00000393346ENST00000220763PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3UTRENST00000393346ENST00000529551PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3CDSENST00000528398ENST00000220763PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3UTRENST00000528398ENST00000529551PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3CDSENST00000356360ENST00000220763PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3UTRENST00000356360ENST00000529551PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3CDSENST00000528411ENST00000220763PICALMchr11

85669998

-CPQchr8

98078317

+
intron-3UTRENST00000528411ENST00000529551PICALMchr11

85669998

-CPQchr8

98078317

+

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 PICALM-CPQ


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 PICALM-CPQ


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

Q9Y646

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Carboxypeptidase that may play an important role in the hydrolysis of circulating peptides. Catalyzes the hydrolysis of dipeptides with unsubstituted terminals into amino acids. May play a role in the liberation of thyroxine hormone from its thyroglobulin (Tg) precursor.

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 PICALM-CPQ


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 PICALM-CPQ


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 PICALM-CPQ


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneCPQQ9Y646DB00142Glutamic acidSmall moleculeApproved|Nutraceutical
TgeneCPQQ9Y646DB00142Glutamic acidSmall moleculeApproved|Nutraceutical
TgeneCPQQ9Y646DB00142Glutamic acidSmall moleculeApproved|Nutraceutical

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Related Diseases for PICALM-CPQ


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePICALMC0002395Alzheimer's Disease2CTD_human
HgenePICALMC0011265Presenile dementia2CTD_human
HgenePICALMC0276496Familial Alzheimer Disease (FAD)2CTD_human
HgenePICALMC0494463Alzheimer Disease, Late Onset2CTD_human
HgenePICALMC0546126Acute Confusional Senile Dementia2CTD_human
HgenePICALMC0750900Alzheimer's Disease, Focal Onset2CTD_human
HgenePICALMC0750901Alzheimer Disease, Early Onset2CTD_human
HgenePICALMC0234985Mental deterioration1CTD_human
HgenePICALMC0338656Impaired cognition1CTD_human
HgenePICALMC1270972Mild cognitive disorder1CTD_human
TgeneCPQC0007134Renal Cell Carcinoma1CTD_human
TgeneCPQC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneCPQC0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
TgeneCPQC1266042Chromophobe Renal Cell Carcinoma1CTD_human
TgeneCPQC1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
TgeneCPQC1266044Collecting Duct Carcinoma of the Kidney1CTD_human
TgeneCPQC1306837Papillary Renal Cell Carcinoma1CTD_human