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: 17

FusionGeneSummary for A2M_TMEM52B

check button Fusion gene summary
Fusion gene informationFusion gene name: A2M_TMEM52B
Fusion gene ID: 17
HgeneTgene
Gene symbol

A2M

TMEM52B

Gene ID

2

120939

Gene namealpha-2-macroglobulintransmembrane protein 52B
SynonymsA2MD|CPAMD5|FWP007|S863-7C12orf59
Cytomap

12p13.31

12p13.2

Type of geneprotein-codingprotein-coding
Descriptionalpha-2-macroglobulinC3 and PZP-like alpha-2-macroglobulin domain-containing protein 5alpha-2-Mtransmembrane protein 52B
Modification date2018051920180519
UniProtAcc

P01023

Q4KMG9

Ensembl transtripts involved in fusion geneENST00000318602, ENST00000542567, 
ENST00000381923, ENST00000545924, 
ENST00000298530, ENST00000536952, 
Fusion gene scores* DoF score10 X 9 X 4=3602 X 1 X 2=4
# samples 112
** MAII scorelog2(11/360*10)=-1.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: A2M [Title/Abstract] AND TMEM52B [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
HgeneA2M

GO:0001869

negative regulation of complement activation, lectin pathway

12538697


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
TCGALDKIRCTCGA-B0-4714-01AA2Mchr12

9227156

-TMEM52Bchr12

10327881

+
* 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
5CDS-intronENST00000318602ENST00000381923A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
5CDS-3UTRENST00000318602ENST00000545924A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
5CDS-intronENST00000318602ENST00000298530A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
5CDS-intronENST00000318602ENST00000536952A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
intron-intronENST00000542567ENST00000381923A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
intron-3UTRENST00000542567ENST00000545924A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
intron-intronENST00000542567ENST00000298530A2Mchr12

9227156

-TMEM52Bchr12

10327881

+
intron-intronENST00000542567ENST00000536952A2Mchr12

9227156

-TMEM52Bchr12

10327881

+

Top

FusionProtFeatures for A2M_TMEM52B


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
A2M

P01023

TMEM52B

Q4KMG9

Is able to inhibit all four classes of proteinases by aunique 'trapping' mechanism. This protein has a peptide stretch,called the 'bait region' which contains specific cleavage sitesfor different proteinases. When a proteinase cleaves the baitregion, a conformational change is induced in the protein whichtraps the proteinase. The entrapped enzyme remains active againstlow molecular weight substrates (activity against high molecularweight substrates is greatly reduced). Following cleavage in thebait region, a thioester bond is hydrolyzed and mediates thecovalent binding of the protein to the proteinase.

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 A2M_TMEM52B


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 A2M_TMEM52B


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
A2MKLK13, CPB2, ADAMTS1, LRP1, PAEP, LEP, B2M, MMP2, LCAT, AMBP, NGF, KLK3, APOE, HSPA5, IL10, IL4, GRB2, GEM, CDC42, HMOX2, NUDT21, UFD1L, RAP1B, SEPT8, RPP14, H2AFX, TGIF1, TK1, CDKN1A, TNFRSF14, SMN1, TTR, CDK2AP2, ANXA7, TSC22D1, C11orf58, SHBG, MYOC, APP, NOS3, PAXIP1, IFIT5, TRAPPC5, RNF32, PRAM1, FARSA, IFIT3, MGEA5, RHEB, PRDX2, ECSIT, ELAVL3, EXOSC1, GCDH, LONP1, CYP2C8, CYP2C18, RAD23A, MAST1, A2M, AP1M2, SWSAP1, CDC37, DNAJB1, EVI5L, FBXL12, FBXW4, RAB3A, RETN, STAMBPL1, NCDN, UMPS, MLST8, ACTB, ATP1A1, EGLN2, ENO2, FIS1, IGSF8, TUBA1B, TYRO3, TP63, CFTR, TGM2, MAPK6, CDK11A, HIPK1, CDK7, FBXO6, GDPD1, HSPB2, KRAS, MED4, IL1B, PZP, HAPLN3, CRTAC1, METRN, PTX3, PRADC1, LOXL1, EOGT, GALNT12, FKBP14, METRNL, PDF, POGLUT1, EGFL7TMEM52BELAVL1, THAP11, NEDD4L, NEDD4, RHBDF2, ATP2B4, ANKRD13D, FCN1, FLT4, RAB6A, ZDHHC9, CORO2A, LRBA, TAB1, TMEM205, WDR44, PIK3CA, PKP2, SLC26A2, PHLDB3, MYADM, MFAP3, PKP4, BMPR1A, PIK3R3, PTPRD, PIK3CB, PIK3R2, NFRKB, CACHD1, MTMR1, CUEDC1, RHEB, EHD4


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 A2M_TMEM52B


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneA2MP01023DB00515CisplatinAlpha-2-macroglobulinsmall moleculeapproved
HgeneA2MP01023DB08888OcriplasminAlpha-2-macroglobulinbiotechapproved
HgeneA2MP01023DB00102BecaplerminAlpha-2-macroglobulinbiotechapproved|investigational
HgeneA2MP01023DB01593ZincAlpha-2-macroglobulinsmall moleculeapproved|investigational
HgeneA2MP01023DB00626BacitracinAlpha-2-macroglobulinsmall moleculeapproved|vet_approved

Top

RelatedDiseases for A2M_TMEM52B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneA2MC0002395Alzheimer's Disease3CTD_human
HgeneA2MC0011570Mental Depression2PSYGENET
HgeneA2MC0011581Depressive disorder2PSYGENET
HgeneA2MC0024121Lung Neoplasms2CTD_human
HgeneA2MC0009375Colonic Neoplasms1CTD_human
HgeneA2MC0019202Hepatolenticular Degeneration1CTD_human
HgeneA2MC0023890Liver Cirrhosis1CTD_human
HgeneA2MC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneA2MC0024115Lung diseases1CTD_human
HgeneA2MC0027726Nephrotic Syndrome1CTD_human
HgeneA2MC0206669Hepatocellular Adenoma1CTD_human
HgeneA2MC2239176Liver carcinoma1CTD_human
HgeneA2MC2609414Acute kidney injury1CTD_human