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: 12489

FusionGeneSummary for FAM114A2_FBN2

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM114A2_FBN2
Fusion gene ID: 12489
HgeneTgene
Gene symbol

FAM114A2

FBN2

Gene ID

10827

2201

Gene namefamily with sequence similarity 114 member A2fibrillin 2
Synonyms133K02|C5orf3CCA|DA9|EOMD
Cytomap

5q33.2

5q23.3

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM114A2testis tissue sperm-binding protein Li 81Pfibrillin-2fibrillin 5
Modification date2018051920180523
UniProtAcc

Q9NRY5

P35556

Ensembl transtripts involved in fusion geneENST00000351797, ENST00000522858, 
ENST00000520667, ENST00000518946, 
ENST00000520313, 
ENST00000508053, 
ENST00000262464, ENST00000507835, 
ENST00000508989, ENST00000511489, 
Fusion gene scores* DoF score3 X 3 X 3=271 X 1 X 1=1
# samples 31
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: FAM114A2 [Title/Abstract] AND FBN2 [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

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
TCGARVSKCMTCGA-D3-A51N-06AFAM114A2chr5

153413351

-FBN2chr5

127609660

-
* 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
Frame-shiftENST00000351797ENST00000508053FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000351797ENST00000262464FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000351797ENST00000507835FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000351797ENST00000508989FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000351797ENST00000511489FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000522858ENST00000508053FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000522858ENST00000262464FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000522858ENST00000507835FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000522858ENST00000508989FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000522858ENST00000511489FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000520667ENST00000508053FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000520667ENST00000262464FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000520667ENST00000507835FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000520667ENST00000508989FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000520667ENST00000511489FAM114A2chr5

153413351

-FBN2chr5

127609660

-
intron-3CDSENST00000518946ENST00000508053FAM114A2chr5

153413351

-FBN2chr5

127609660

-
intron-3CDSENST00000518946ENST00000262464FAM114A2chr5

153413351

-FBN2chr5

127609660

-
intron-intronENST00000518946ENST00000507835FAM114A2chr5

153413351

-FBN2chr5

127609660

-
intron-intronENST00000518946ENST00000508989FAM114A2chr5

153413351

-FBN2chr5

127609660

-
intron-intronENST00000518946ENST00000511489FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000520313ENST00000508053FAM114A2chr5

153413351

-FBN2chr5

127609660

-
Frame-shiftENST00000520313ENST00000262464FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000520313ENST00000507835FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000520313ENST00000508989FAM114A2chr5

153413351

-FBN2chr5

127609660

-
5CDS-intronENST00000520313ENST00000511489FAM114A2chr5

153413351

-FBN2chr5

127609660

-

Top

FusionProtFeatures for FAM114A2_FBN2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM114A2

Q9NRY5

FBN2

P35556

Fibrillin-2: Fibrillins are structural components of 10-12 nm extracellular calcium-binding microfibrils, which occureither in association with elastin or in elastin-free bundles.Fibrillin-2-containing microfibrils regulate the early process ofelastic fiber assembly. Regulates osteoblast maturation bycontrolling TGF-beta bioavailability and calibrating TGF-beta andBMP levels, respectively. {ECO:0000250|UniProtKB:Q61555}.

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 FAM114A2_FBN2


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 FAM114A2_FBN2


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
FAM114A2ELAVL1, COPS5, APP, TMEM51, CD274, KIR3DL1, SCN2B, EWSR1, KIR3DL2, EPHA1, LRRC4, CPNE5, TMEM206, SIGLECL1FBN2ELN, MATN2, PTEN, FBXO6, SFRP4, FOXD4L6, ZFP41, AURKA, PRG2, ZNF408, LYPD4, ADAMTSL1, FAM19A3, VWCE, PRG3


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 FAM114A2_FBN2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneFBN2P35556DB11093Calcium CitrateFibrillin-2small moleculeapproved
TgeneFBN2P35556DB11348Calcium PhosphateFibrillin-2small moleculeapproved

Top

RelatedDiseases for FAM114A2_FBN2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneFBN2C0220668Congenital contractural arachnodactyly9CTD_human;ORPHANET;UNIPROT
TgeneFBN2C0009404Colorectal Neoplasms1CTD_human
TgeneFBN2C4015286MACULAR DEGENERATION, EARLY-ONSET1UNIPROT