FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 7557

FusionGeneSummary for CLU_MAP2K2

check button Fusion gene summary
Fusion gene informationFusion gene name: CLU_MAP2K2
Fusion gene ID: 7557
HgeneTgene
Gene symbol

CLU

MAP2K2

Gene ID

1191

5605

Gene nameclusterinmitogen-activated protein kinase kinase 2
SynonymsAAG4|APO-J|APOJ|CLI|CLU1|CLU2|KUB1|NA1/NA2|SGP-2|SGP2|SP-40|TRPM-2|TRPM2CFC4|MAPKK2|MEK2|MKK2|PRKMK2
Cytomap

8p21.1

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionclusterinaging-associated protein 4apolipoprotein Jcomplement cytolysis inhibitorcomplement lysis inhibitorcomplement-associated protein SP-40,40ku70-binding protein 1sulfated glycoprotein 2testosterone-repressed prostate message 2dual specificity mitogen-activated protein kinase kinase 2ERK activator kinase 2MAP kinase kinase 2MAPK/ERK kinase 2mitogen-activated protein kinase kinase 2, p45
Modification date2018052720180523
UniProtAcc

P10909

P36507

Ensembl transtripts involved in fusion geneENST00000316403, ENST00000546343, 
ENST00000560366, ENST00000405140, 
ENST00000523500, 
ENST00000262948, 
ENST00000394867, ENST00000599345, 
Fusion gene scores* DoF score24 X 23 X 8=44163 X 4 X 3=36
# samples 305
** MAII scorelog2(30/4416*10)=-3.87970576628229
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/36*10)=0.473931188332412
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: CLU [Title/Abstract] AND MAP2K2 [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
HgeneCLU

GO:0000902

cell morphogenesis

15857407

HgeneCLU

GO:0001774

microglial cell activation

15857407

HgeneCLU

GO:0017038

protein import

24446231

HgeneCLU

GO:0032463

negative regulation of protein homooligomerization

22179788|23106396

HgeneCLU

GO:0032464

positive regulation of protein homooligomerization

22179788

HgeneCLU

GO:0032760

positive regulation of tumor necrosis factor production

15857407

HgeneCLU

GO:0045429

positive regulation of nitric oxide biosynthetic process

15857407

HgeneCLU

GO:0050821

protein stabilization

11123922

HgeneCLU

GO:0051131

chaperone-mediated protein complex assembly

17412999

HgeneCLU

GO:0051788

response to misfolded protein

19996109

HgeneCLU

GO:0061077

chaperone-mediated protein folding

11123922

HgeneCLU

GO:0061518

microglial cell proliferation

15857407

HgeneCLU

GO:1900221

regulation of amyloid-beta clearance

24446231

HgeneCLU

GO:1901214

regulation of neuron death

17412999

HgeneCLU

GO:1901216

positive regulation of neuron death

15857407

HgeneCLU

GO:1902430

negative regulation of amyloid-beta formation

12047389|17412999

HgeneCLU

GO:1905907

negative regulation of amyloid fibril formation

22179788

TgeneMAP2K2

GO:0036289

peptidyl-serine autophosphorylation

8388392

TgeneMAP2K2

GO:0071902

positive regulation of protein serine/threonine kinase activity

8388392


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
ChiTaRS3.1BF920101CLUchr8

27466480

-MAP2K2chr19

4102492

-
ChiTaRS3.1BF919979CLUchr8

27466480

-MAP2K2chr19

4102495

-
* 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-intronENST00000316403ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000316403ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000316403ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000546343ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000546343ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000546343ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000560366ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000560366ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000560366ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000405140ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000405140ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000405140ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000523500ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000523500ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000523500ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102492

-
intron-intronENST00000316403ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000316403ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000316403ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000546343ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000546343ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000546343ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000560366ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000560366ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000560366ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000405140ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000405140ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000405140ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000523500ENST00000262948CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000523500ENST00000394867CLUchr8

27466480

-MAP2K2chr19

4102495

-
intron-intronENST00000523500ENST00000599345CLUchr8

27466480

-MAP2K2chr19

4102495

-

Top

FusionProtFeatures for CLU_MAP2K2


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

P10909

MAP2K2

P36507

Isoform 1 functions as extracellular chaperone thatprevents aggregation of nonnative proteins. Prevents stress-induced aggregation of blood plasma proteins. Inhibits formationof amyloid fibrils by APP, APOC2, B2M, CALCA, CSN3, SNCA andaggregation-prone LYZ variants (in vitro). Does not require ATP.Maintains partially unfolded proteins in a state appropriate forsubsequent refolding by other chaperones, such as HSPA8/HSC70.Does not refold proteins by itself. Binding to cell surfacereceptors triggers internalization of the chaperone-client complexand subsequent lysosomal or proteasomal degradation. Secretedisoform 1 protects cells against apoptosis and against cytolysisby complement. Intracellular isoforms interact with ubiquitin andSCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligasecomplexes and promote the ubiquitination and subsequentproteasomal degradation of target proteins. Promotes proteasomaldegradation of COMMD1 and IKBKB. Modulates NF-kappa-Btranscriptional activity. Nuclear isoforms promote apoptosis.Mitochondrial isoforms suppress BAX-dependent release ofcytochrome c into the cytoplasm and inhibit apoptosis. Plays arole in the regulation of cell proliferation.{ECO:0000269|PubMed:11123922, ECO:0000269|PubMed:12047389,ECO:0000269|PubMed:12176985, ECO:0000269|PubMed:12551933,ECO:0000269|PubMed:12882985, ECO:0000269|PubMed:16113678,ECO:0000269|PubMed:17260971, ECO:0000269|PubMed:17407782,ECO:0000269|PubMed:17412999, ECO:0000269|PubMed:17689225,ECO:0000269|PubMed:19137541, ECO:0000269|PubMed:19535339,ECO:0000269|PubMed:19996109, ECO:0000269|PubMed:20068069,ECO:0000269|PubMed:21505792}. Catalyzes the concomitant phosphorylation of a threonineand a tyrosine residue in a Thr-Glu-Tyr sequence located in MAPkinases. Activates the ERK1 and ERK2 MAP kinases (By similarity).{ECO:0000250}.

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


Top

FusionGeneSequence for CLU_MAP2K2


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).

Top

FusionGenePPI for CLU_MAP2K2


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


Top

RelatedDrugs for CLU_MAP2K2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneCLUP10909DB01593ZincClusterinsmall moleculeapproved|investigational
TgeneMAP2K2P36507DB06616BosutinibDual specificity mitogen-activated protein kinase kinase 2small moleculeapproved
TgeneMAP2K2P36507DB08911TrametinibDual specificity mitogen-activated protein kinase kinase 2small moleculeapproved

Top

RelatedDiseases for CLU_MAP2K2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCLUC2609414Acute kidney injury5CTD_human
HgeneCLUC0002395Alzheimer's Disease3CTD_human
HgeneCLUC0022658Kidney Diseases3CTD_human
HgeneCLUC0029408Degenerative polyarthritis2CTD_human
HgeneCLUC0024141Lupus Erythematosus, Systemic1CTD_human
HgeneCLUC0025202melanoma1CTD_human
HgeneCLUC0027686Pathologic Neovascularization1CTD_human
HgeneCLUC0033578Prostatic Neoplasms1CTD_human
HgeneCLUC0036341Schizophrenia1PSYGENET
HgeneCLUC0036572Seizures1CTD_human
HgeneCLUC0041755Adverse reaction to drug1CTD_human
HgeneCLUC0333641Atrophic1CTD_human
HgeneCLUC1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human
HgeneCLUC3495559Juvenile arthritis1CTD_human
HgeneCLUC4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneMAP2K2C3809007CARDIOFACIOCUTANEOUS SYNDROME 43UNIPROT
TgeneMAP2K2C1275081Cardio-facio-cutaneous syndrome2CTD_human;ORPHANET
TgeneMAP2K2C0010606Adenoid Cystic Carcinoma1CTD_human
TgeneMAP2K2C0025202melanoma1CTD_human
TgeneMAP2K2C0028326Noonan Syndrome1CTD_human
TgeneMAP2K2C0587248Costello syndrome (disorder)1CTD_human