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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: 7890

FusionGeneSummary for COL1A2_C1orf159

check button Fusion gene summary
Fusion gene informationFusion gene name: COL1A2_C1orf159
Fusion gene ID: 7890
HgeneTgene
Gene symbol

COL1A2

C1orf159

Gene ID

1278

54991

Gene namecollagen type I alpha 2 chainchromosome 1 open reading frame 159
SynonymsEDSARTH2|EDSCV|OI4-
Cytomap

7q21.3

1p36.33

Type of geneprotein-codingprotein-coding
Descriptioncollagen alpha-2(I) chainalpha 2 type I procollagenalpha 2(I) procollagenalpha 2(I)-collagenalpha-2 type I collagencollagen I, alpha-2 polypeptidecollagen of skin, tendon and bone, alpha-2 chaincollagen, type I, alpha 2type I procollagenuncharacterized protein C1orf159
Modification date2018052720180524
UniProtAcc

P08123

Q96HA4

Ensembl transtripts involved in fusion geneENST00000297268, ENST00000379339, 
ENST00000448924, ENST00000294576, 
ENST00000421241, ENST00000482816, 
ENST00000437760, ENST00000379320, 
ENST00000379319, 
Fusion gene scores* DoF score15 X 20 X 5=15005 X 4 X 4=80
# samples 215
** MAII scorelog2(21/1500*10)=-2.83650126771712
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COL1A2 [Title/Abstract] AND C1orf159 [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
HgeneCOL1A2

GO:0007179

transforming growth factor beta receptor signaling pathway

17217948

HgeneCOL1A2

GO:0007266

Rho protein signal transduction

17217948


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
ChiTaRS3.1BE928186COL1A2chr7

94056572

+C1orf159chr1

1044385

-
* 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-intronENST00000297268ENST00000379339COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000448924COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000294576COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000421241COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000482816COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000437760COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000379320COL1A2chr7

94056572

+C1orf159chr1

1044385

-
5CDS-intronENST00000297268ENST00000379319COL1A2chr7

94056572

+C1orf159chr1

1044385

-

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FusionProtFeatures for COL1A2_C1orf159


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COL1A2

P08123

C1orf159

Q96HA4


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 COL1A2_C1orf159


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 COL1A2_C1orf159


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 COL1A2_C1orf159


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneCOL1A2P08123DB00048Collagenase clostridium histolyticumCollagen alpha-2(I) chainbiotechapproved|investigational

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RelatedDiseases for COL1A2_C1orf159


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCOL1A2C0268362Osteogenesis imperfecta type III (disorder)17CTD_human;ORPHANET;UNIPROT
HgeneCOL1A2C0268358Osteogenesis imperfecta, dominant perinatal lethal14CTD_human;ORPHANET;UNIPROT
HgeneCOL1A2C0268363Osteogenesis imperfecta type IV (disorder)11CTD_human;ORPHANET;UNIPROT
HgeneCOL1A2C0023931Lobstein's Disease6ORPHANET;UNIPROT
HgeneCOL1A2C0000786Spontaneous abortion1CTD_human
HgeneCOL1A2C0016059Fibrosis1CTD_human
HgeneCOL1A2C0018824Heart valve disease1CTD_human
HgeneCOL1A2C0023890Liver Cirrhosis1CTD_human
HgeneCOL1A2C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneCOL1A2C0029172Oral Submucous Fibrosis1CTD_human
HgeneCOL1A2C0029408Degenerative polyarthritis1CTD_human
HgeneCOL1A2C0036421Systemic Scleroderma1CTD_human
HgeneCOL1A2C1857034Ehlers-Danlos syndrome, cardiac valvular form1CTD_human;ORPHANET