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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 12365

FusionGeneSummary for EZH2_ATP2A2

check button Fusion gene summary
Fusion gene informationFusion gene name: EZH2_ATP2A2
Fusion gene ID: 12365
HgeneTgene
Gene symbol

EZH2

ATP2A2

Gene ID

2146

488

Gene nameenhancer of zeste 2 polycomb repressive complex 2 subunitATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2
SynonymsENX-1|ENX1|EZH2b|KMT6|KMT6A|WVS|WVS2ATP2B|DAR|DD|SERCA2
Cytomap

7q36.1

12q24.11

Type of geneprotein-codingprotein-coding
Descriptionhistone-lysine N-methyltransferase EZH2enhancer of zeste homolog 2lysine N-methyltransferase 6sarcoplasmic/endoplasmic reticulum calcium ATPase 2ATPase Ca++ transporting cardiac muscle slow twitch 2ATPase, Ca++ dependent, slow-twitch, cardiac muscle-2SR Ca(2+)-ATPase 2calcium pump 2calcium-transporting ATPase sarcoplasmic reticulum type, slow
Modification date2018052720180523
UniProtAcc

Q15910

P16615

Ensembl transtripts involved in fusion geneENST00000478654, ENST00000460911, 
ENST00000350995, ENST00000320356, 
ENST00000541220, ENST00000476773, 
ENST00000483967, ENST00000536783, 
ENST00000308664, ENST00000395494, 
ENST00000539276, ENST00000550248, 
ENST00000552636, 
Fusion gene scores* DoF score6 X 7 X 3=1268 X 11 X 2=176
# samples 612
** MAII scorelog2(6/126*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/176*10)=-0.552541023028779
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EZH2 [Title/Abstract] AND ATP2A2 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneEZH2

GO:0000122

negative regulation of transcription by RNA polymerase II

20154697

HgeneEZH2

GO:0010718

positive regulation of epithelial to mesenchymal transition

20154697

HgeneEZH2

GO:0043406

positive regulation of MAP kinase activity

20154697

HgeneEZH2

GO:0043547

positive regulation of GTPase activity

20154697

HgeneEZH2

GO:0045814

negative regulation of gene expression, epigenetic

20154697

HgeneEZH2

GO:0070734

histone H3-K27 methylation

24474760

HgeneEZH2

GO:0071902

positive regulation of protein serine/threonine kinase activity

20154697

TgeneATP2A2

GO:0032469

endoplasmic reticulum calcium ion homeostasis

16402920

TgeneATP2A2

GO:0032470

positive regulation of endoplasmic reticulum calcium ion concentration

16402920

TgeneATP2A2

GO:0070588

calcium ion transmembrane transport

16402920

TgeneATP2A2

GO:1903515

calcium ion transport from cytosol to endoplasmic reticulum

16402920


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1AI207549EZH2chr7

148579372

+ATP2A2chr12

110788015

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000478654ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000478654ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000478654ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000478654ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000478654ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000460911ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000460911ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000460911ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000460911ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000460911ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000350995ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000350995ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000350995ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000350995ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000350995ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000320356ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000320356ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000320356ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000320356ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000320356ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000541220ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000541220ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000541220ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000541220ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000541220ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000476773ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000476773ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000476773ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000476773ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000476773ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000483967ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000483967ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000483967ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000483967ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000483967ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000536783ENST00000308664EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-3UTRENST00000536783ENST00000395494EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000536783ENST00000539276EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000536783ENST00000550248EZH2chr7

148579372

+ATP2A2chr12

110788015

+
intron-intronENST00000536783ENST00000552636EZH2chr7

148579372

+ATP2A2chr12

110788015

+

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FusionProtFeatures for EZH2_ATP2A2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EZH2

Q15910

ATP2A2

P16615

This magnesium-dependent enzyme catalyzes the hydrolysisof ATP coupled with the translocation of calcium from the cytosolto the sarcoplasmic reticulum lumen. Isoform 2 is involved in theregulation of the contraction/relaxation cycle (PubMed:16402920).Acts as a regulator of TNFSF11-mediated Ca(2+) signaling pathwaysvia its interaction with TMEM64 which is critical for the TNFSF11-induced CREB1 activation and mitochondrial ROS generationnecessary for proper osteoclast generation. Association betweenTMEM64 and SERCA2 in the ER leads to cytosolic Ca (2+) spiking foractivation of NFATC1 and production of mitochondrial ROS, therebytriggering Ca (2+) signaling cascades that promote osteoclastdifferentiation and activation (By similarity).{ECO:0000250|UniProtKB:O55143, ECO:0000269|PubMed:16402920}.

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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FusionGeneSequence for EZH2_ATP2A2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for EZH2_ATP2A2


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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RelatedDrugs for EZH2_ATP2A2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for EZH2_ATP2A2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneEZH2C0033578Prostatic Neoplasms3CTD_human
HgeneEZH2C0001815Primary Myelofibrosis1CTD_human
HgeneEZH2C0010278Craniosynostosis1CTD_human
HgeneEZH2C0014170Endometrial Neoplasms1CTD_human
HgeneEZH2C0024301Lymphoma, Follicular1CTD_human
HgeneEZH2C0029463Osteosarcoma1CTD_human
HgeneEZH2C0079744Diffuse Large B-Cell Lymphoma1CTD_human
HgeneEZH2C0265210Weaver syndrome1ORPHANET;UNIPROT
HgeneEZH2C0349639Juvenile Myelomonocytic Leukemia1CTD_human
HgeneEZH2C0749794Upper Extremity Deformities, Congenital1CTD_human
HgeneEZH2C1301355Myelodysplastic-Myeloproliferative Diseases1CTD_human
HgeneEZH2C1458155Mammary Neoplasms1CTD_human
HgeneEZH2C1860789Leukemia, Megakaryoblastic, of Down Syndrome1CTD_human
HgeneEZH2C3463824MYELODYSPLASTIC SYNDROME1CTD_human
TgeneATP2A2C0022595Keratosis Follicularis4CTD_human;ORPHANET;UNIPROT
TgeneATP2A2C0011570Mental Depression2PSYGENET
TgeneATP2A2C0011581Depressive disorder2PSYGENET
TgeneATP2A2C0525045Mood Disorders2PSYGENET
TgeneATP2A2C0005586Bipolar Disorder1HPO;PSYGENET
TgeneATP2A2C0011853Diabetes Mellitus, Experimental1CTD_human
TgeneATP2A2C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
TgeneATP2A2C0018799Heart Diseases1CTD_human
TgeneATP2A2C0018800Cardiomegaly1CTD_human
TgeneATP2A2C0018801Heart failure1CTD_human
TgeneATP2A2C0027055Myocardial Reperfusion Injury1CTD_human
TgeneATP2A2C0036341Schizophrenia1HPO;PSYGENET
TgeneATP2A2C0038220Status Epilepticus1CTD_human
TgeneATP2A2C0206146Myocardial Stunning1CTD_human
TgeneATP2A2C0242698Ventricular Dysfunction, Left1CTD_human
TgeneATP2A2C0265971Acrokeratosis Verruciformis of Hopf1ORPHANET;UNIPROT
TgeneATP2A2C0853897Diabetic Cardiomyopathies1CTD_human