Fusion Gene Studies
in Kim Lab

FusionBase FusionGDB FusionGDB2 FusionPDB FusionNeoAntigen FusionAI FusionNW FGviewer Publication Contact
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:COL5A2-EML5 (FusionGDB2 ID:HG1290TG161436)

Fusion Gene Summary for COL5A2-EML5

check button Fusion gene summary
Fusion gene informationFusion gene name: COL5A2-EML5
Fusion gene ID: hg1290tg161436
HgeneTgene
Gene symbol

COL5A2

EML5

Gene ID

1290

161436

Gene namecollagen type V alpha 2 chainEMAP like 5
SynonymsEDSC|EDSCL2EMAP-2|EMAP-5|FAP16
Cytomap('COL5A2')('EML5')

2q32.2

14q31.3

Type of geneprotein-codingprotein-coding
Descriptioncollagen alpha-2(V) chainAB collagencollagen, fetal membrane, A polypeptidetype V preprocollagen alpha 2 chainechinoderm microtubule-associated protein-like 5echinoderm microtubule associated protein like 5
Modification date2020031320200313
UniProtAcc

P05997

Q05BV3

Ensembl transtripts involved in fusion geneENST00000374866, 
Fusion gene scores* DoF score12 X 11 X 5=6606 X 6 X 2=72
# samples 126
** MAII scorelog2(12/660*10)=-2.4594316186373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/72*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COL5A2 [Title/Abstract] AND EML5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOL5A2(189897245)-EML5(89096700), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneCOL5A2

GO:1903225

negative regulation of endodermal cell differentiation

23154389



check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABI493711COL5A2chr2

189897245

-EML5chr14

89096700

-


Top

Fusion Gene ORF analysis for COL5A2-EML5

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-intronENST00000374866ENST00000352093COL5A2chr2

189897245

-EML5chr14

89096700

-
intron-intronENST00000374866ENST00000380664COL5A2chr2

189897245

-EML5chr14

89096700

-
intron-intronENST00000374866ENST00000553320COL5A2chr2

189897245

-EML5chr14

89096700

-
intron-intronENST00000374866ENST00000554922COL5A2chr2

189897245

-EML5chr14

89096700

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

Top

Fusion Genomic Features for COL5A2-EML5


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)


Top

Fusion Protein Features for COL5A2-EML5


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:189897245/:89096700)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COL5A2

P05997

EML5

Q05BV3

FUNCTION: Type V collagen is a member of group I collagen (fibrillar forming collagen). It is a minor connective tissue component of nearly ubiquitous distribution. Type V collagen binds to DNA, heparan sulfate, thrombospondin, heparin, and insulin. Type V collagen is a key determinant in the assembly of tissue-specific matrices (By similarity). {ECO:0000250}.FUNCTION: May modify the assembly dynamics of microtubules, such that microtubules are slightly longer, but more dynamic. {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

Fusion Gene Sequence for COL5A2-EML5


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

Top

Fusion Gene PPI Analysis for COL5A2-EML5


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

Related Drugs for COL5A2-EML5


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for COL5A2-EML5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCOL5A2C4538407EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 24GENOMICS_ENGLAND;UNIPROT
HgeneCOL5A2C4552122EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 13GENOMICS_ENGLAND
HgeneCOL5A2C0220679Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified2ORPHANET
HgeneCOL5A2C3151201MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME2GENOMICS_ENGLAND
HgeneCOL5A2C0000786Spontaneous abortion1CTD_human
HgeneCOL5A2C0000822Abortion, Tubal1CTD_human
HgeneCOL5A2C0005779Blood Coagulation Disorders1GENOMICS_ENGLAND
HgeneCOL5A2C0023890Liver Cirrhosis1CTD_human
HgeneCOL5A2C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneCOL5A2C0239946Fibrosis, Liver1CTD_human
HgeneCOL5A2C0268335Ehlers-Danlos syndrome type 11GENOMICS_ENGLAND
HgeneCOL5A2C0268336Ehlers-Danlos syndrome type 21GENOMICS_ENGLAND
HgeneCOL5A2C1458140Bleeding tendency1GENOMICS_ENGLAND
HgeneCOL5A2C1846545Autoimmune Lymphoproliferative Syndrome Type 2B1GENOMICS_ENGLAND
HgeneCOL5A2C3830362Early Pregnancy Loss1CTD_human
HgeneCOL5A2C4225429Ehlers-Danlos syndrome classic type1GENOMICS_ENGLAND
HgeneCOL5A2C4552766Miscarriage1CTD_human
TgeneC0036341Schizophrenia1PSYGENET