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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: 4244

FusionGeneSummary for BMPER_ADAM22

check button Fusion gene summary
Fusion gene informationFusion gene name: BMPER_ADAM22
Fusion gene ID: 4244
HgeneTgene
Gene symbol

BMPER

ADAM22

Gene ID

168667

53616

Gene nameBMP binding endothelial regulatorADAM metallopeptidase domain 22
SynonymsCRIM3|CV-2|CV2ADAM 22|EIEE61|MDC2
Cytomap

7p14.3

7q21.12

Type of geneprotein-codingprotein-coding
DescriptionBMP-binding endothelial regulator proteinBMP-binding endothelial regulator precursor proteinbone morphogenetic protein-binding endothelial cell precursor-derived regulatorcrossveinless 2hCV2disintegrin and metalloproteinase domain-containing protein 22a disintegrin and metalloproteinase domain 22metalloproteinase-disintegrin ADAM22-3metalloproteinase-like, disintegrin-like, and cysteine-rich protein 2
Modification date2018052020180519
UniProtAcc

Q8N8U9

Q9P0K1

Ensembl transtripts involved in fusion geneENST00000297161, ENST00000426693, 
ENST00000494786, 
ENST00000398204, 
ENST00000439864, ENST00000398201, 
ENST00000265727, ENST00000315984, 
ENST00000398209, ENST00000476330, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 3 X 4=48
# samples 14
** MAII scorelog2(1/1*10)=3.32192809488736log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BMPER [Title/Abstract] AND ADAM22 [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
HgeneBMPER

GO:0002043

blood vessel endothelial cell proliferation involved in sprouting angiogenesis

18787191

HgeneBMPER

GO:0010594

regulation of endothelial cell migration

18787191

HgeneBMPER

GO:0042118

endothelial cell activation

18787191

HgeneBMPER

GO:0060393

regulation of pathway-restricted SMAD protein phosphorylation

18787191

HgeneBMPER

GO:0070374

positive regulation of ERK1 and ERK2 cascade

18787191


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
ChiTaRS3.1AB009671BMPERchr7

33944715

+ADAM22chr7

87563702

+
* 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
5UTR-5UTRENST00000297161ENST00000398204BMPERchr7

33944715

+ADAM22chr7

87563702

+
5UTR-5UTRENST00000297161ENST00000439864BMPERchr7

33944715

+ADAM22chr7

87563702

+
5UTR-5UTRENST00000297161ENST00000398201BMPERchr7

33944715

+ADAM22chr7

87563702

+
5UTR-5UTRENST00000297161ENST00000265727BMPERchr7

33944715

+ADAM22chr7

87563702

+
5UTR-5UTRENST00000297161ENST00000315984BMPERchr7

33944715

+ADAM22chr7

87563702

+
5UTR-intronENST00000297161ENST00000398209BMPERchr7

33944715

+ADAM22chr7

87563702

+
5UTR-intronENST00000297161ENST00000476330BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000426693ENST00000398204BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000426693ENST00000439864BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000426693ENST00000398201BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000426693ENST00000265727BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000426693ENST00000315984BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-intronENST00000426693ENST00000398209BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-intronENST00000426693ENST00000476330BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000494786ENST00000398204BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000494786ENST00000439864BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000494786ENST00000398201BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000494786ENST00000265727BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-5UTRENST00000494786ENST00000315984BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-intronENST00000494786ENST00000398209BMPERchr7

33944715

+ADAM22chr7

87563702

+
intron-intronENST00000494786ENST00000476330BMPERchr7

33944715

+ADAM22chr7

87563702

+

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FusionProtFeatures for BMPER_ADAM22


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

Q8N8U9

ADAM22

Q9P0K1

Inhibitor of bone morphogenetic protein (BMP) function,it may regulate BMP responsiveness of osteoblasts andchondrocytes. {ECO:0000269|PubMed:14766204}. Probable ligand for integrin in the brain. This is a noncatalytic metalloprotease-like protein (PubMed:19692335). Involvedin regulation of cell adhesion and spreading and in inhibition ofcell proliferation. Neuronal receptor for LGI1.{ECO:0000269|PubMed:12589811, ECO:0000269|PubMed:15882968,ECO:0000269|PubMed:16385342, ECO:0000269|PubMed:19692335}.

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 BMPER_ADAM22


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 BMPER_ADAM22


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 BMPER_ADAM22


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 BMPER_ADAM22


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBMPERC0027412Opioid-Related Disorders1CTD_human
HgeneBMPERC1842691Diaphanospondylodysostosis1ORPHANET;UNIPROT