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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: 22697

FusionGeneSummary for MT2A_CDK2

check button Fusion gene summary
Fusion gene informationFusion gene name: MT2A_CDK2
Fusion gene ID: 22697
HgeneTgene
Gene symbol

MT2A

CDK2

Gene ID

4502

1017

Gene namemetallothionein 2Acyclin dependent kinase 2
SynonymsMT-2|MT-II|MT2CDKN2|p33(CDK2)
Cytomap

16q13

12q13.2

Type of geneprotein-codingprotein-coding
Descriptionmetallothionein-2metallothionein-IIcyclin-dependent kinase 2cdc2-related protein kinasecell division protein kinase 2p33 protein kinase
Modification date2018052320180527
UniProtAcc

P02795

P24941

Ensembl transtripts involved in fusion geneENST00000245185, ENST00000563985, 
ENST00000561491, 
ENST00000266970, 
ENST00000553376, ENST00000440311, 
ENST00000354056, ENST00000556656, 
Fusion gene scores* DoF score1 X 1 X 1=11 X 1 X 1=1
# samples 11
** MAII scorelog2(1/1*10)=3.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: MT2A [Title/Abstract] AND CDK2 [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
HgeneMT2A

GO:0035690

cellular response to drug

19536566

TgeneCDK2

GO:0006468

protein phosphorylation

12944431|28666995

TgeneCDK2

GO:0008284

positive regulation of cell proliferation

10767298

TgeneCDK2

GO:0016572

histone phosphorylation

11746698

TgeneCDK2

GO:0018105

peptidyl-serine phosphorylation

23184662

TgeneCDK2

GO:0060968

regulation of gene silencing

20935635


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
ChiTaRS3.1AU125800MT2Achr16

56643384

+CDK2chr12

56360614

+
* 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
3UTR-5UTRENST00000245185ENST00000266970MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000245185ENST00000553376MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000245185ENST00000440311MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000245185ENST00000354056MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-intronENST00000245185ENST00000556656MT2Achr16

56643384

+CDK2chr12

56360614

+
5CDS-5UTRENST00000563985ENST00000266970MT2Achr16

56643384

+CDK2chr12

56360614

+
5CDS-5UTRENST00000563985ENST00000553376MT2Achr16

56643384

+CDK2chr12

56360614

+
5CDS-5UTRENST00000563985ENST00000440311MT2Achr16

56643384

+CDK2chr12

56360614

+
5CDS-5UTRENST00000563985ENST00000354056MT2Achr16

56643384

+CDK2chr12

56360614

+
5CDS-intronENST00000563985ENST00000556656MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000561491ENST00000266970MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000561491ENST00000553376MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000561491ENST00000440311MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-5UTRENST00000561491ENST00000354056MT2Achr16

56643384

+CDK2chr12

56360614

+
3UTR-intronENST00000561491ENST00000556656MT2Achr16

56643384

+CDK2chr12

56360614

+

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FusionProtFeatures for MT2A_CDK2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MT2A

P02795

CDK2

P24941

Metallothioneins have a high content of cysteineresidues that bind various heavy metals; these proteins aretranscriptionally regulated by both heavy metals andglucocorticoids. Serine/threonine-protein kinase involved in the controlof the cell cycle; essential for meiosis, but dispensable formitosis. Phosphorylates CTNNB1, USP37, p53/TP53, NPM1, CDK7, RB1,BRCA2, MYC, NPAT, EZH2. Triggers duplication of centrosomes andDNA. Acts at the G1-S transition to promote the E2Ftranscriptional program and the initiation of DNA synthesis, andmodulates G2 progression; controls the timing of entry intomitosis/meiosis by controlling the subsequent activation of cyclinB/CDK1 by phosphorylation, and coordinates the activation ofcyclin B/CDK1 at the centrosome and in the nucleus. Crucial rolein orchestrating a fine balance between cellular proliferation,cell death, and DNA repair in human embryonic stem cells (hESCs).Activity of CDK2 is maximal during S phase and G2; activated byinteraction with cyclin E during the early stages of DNA synthesisto permit G1-S transition, and subsequently activated by cyclin A2(cyclin A1 in germ cells) during the late stages of DNAreplication to drive the transition from S phase to mitosis, theG2 phase. EZH2 phosphorylation promotes H3K27me3 maintenance andepigenetic gene silencing. Phosphorylates CABLES1 (By similarity).Cyclin E/CDK2 prevents oxidative stress-mediated Ras-inducedsenescence by phosphorylating MYC. Involved in G1-S phase DNAdamage checkpoint that prevents cells with damaged DNA frominitiating mitosis; regulates homologous recombination-dependentrepair by phosphorylating BRCA2, this phosphorylation is low in Sphase when recombination is active, but increases as cellsprogress towards mitosis. In response to DNA damage, double-strandbreak repair by homologous recombination a reduction of CDK2-mediated BRCA2 phosphorylation. Phosphorylation of RB1 disturbsits interaction with E2F1. NPM1 phosphorylation by cyclin E/CDK2promotes its dissociates from unduplicated centrosomes, thusinitiating centrosome duplication. Cyclin E/CDK2-mediatedphosphorylation of NPAT at G1-S transition and until prophasestimulates the NPAT-mediated activation of histone genetranscription during S phase. Required for vitamin D-mediatedgrowth inhibition by being itself inactivated. Involved in thenitric oxide- (NO) mediated signaling in anitrosylation/activation-dependent manner. USP37 is activated byphosphorylation and thus triggers G1-S transition. CTNNB1phosphorylation regulates insulin internalization. PhosphorylatesFOXP3 and negatively regulates its transcriptional activity andprotein stability (By similarity). Phosphorylates CDK2AP2(PubMed:12944431). {ECO:0000250|UniProtKB:P97377,ECO:0000269|PubMed:10499802, ECO:0000269|PubMed:10884347,ECO:0000269|PubMed:10995386, ECO:0000269|PubMed:10995387,ECO:0000269|PubMed:11051553, ECO:0000269|PubMed:11113184,ECO:0000269|PubMed:12944431, ECO:0000269|PubMed:15800615,ECO:0000269|PubMed:17495531, ECO:0000269|PubMed:18372919,ECO:0000269|PubMed:19966300, ECO:0000269|PubMed:20079829,ECO:0000269|PubMed:20147522, ECO:0000269|PubMed:20195506,ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:21262353,ECO:0000269|PubMed:21319273, ECO:0000269|PubMed:21596315,ECO:0000269|PubMed:28666995}.

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 MT2A_CDK2


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 MT2A_CDK2


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 MT2A_CDK2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneMT2AP02795DB01593ZincMetallothionein-2small moleculeapproved|investigational
TgeneCDK2P24941DB06616BosutinibCyclin-dependent kinase 2small moleculeapproved

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RelatedDiseases for MT2A_CDK2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMT2AC0005695Bladder Neoplasm2CTD_human
HgeneMT2AC0033578Prostatic Neoplasms2CTD_human
HgeneMT2AC0011849Diabetes Mellitus1CTD_human
HgeneMT2AC0018799Heart Diseases1CTD_human
HgeneMT2AC0018800Cardiomegaly1CTD_human
HgeneMT2AC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneMT2AC0027626Neoplasm Invasiveness1CTD_human
HgeneMT2AC0035222Respiratory Distress Syndrome, Adult1CTD_human
HgeneMT2AC0038356Stomach Neoplasms1CTD_human
HgeneMT2AC0282612Prostatic Intraepithelial Neoplasias1CTD_human
HgeneMT2AC0349218Recurrent depressive disorder, unspecified1PSYGENET
HgeneMT2AC0403447Chronic Kidney Insufficiency1CTD_human
HgeneMT2AC2239176Liver carcinoma1CTD_human
TgeneCDK2C0025202melanoma1CTD_human