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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: 7840

FusionGeneSummary for COL11A1_DPH5

check button Fusion gene summary
Fusion gene informationFusion gene name: COL11A1_DPH5
Fusion gene ID: 7840
HgeneTgene
Gene symbol

COL11A1

DPH5

Gene ID

1301

51611

Gene namecollagen type XI alpha 1 chaindiphthamide biosynthesis 5
SynonymsCO11A1|COLL6|STL2AD-018|CGI-30|HSPC143|NPD015
Cytomap

1p21.1

1p21.2

Type of geneprotein-codingprotein-coding
Descriptioncollagen alpha-1(XI) chaincollagen XI, alpha-1 polypeptidecollagen, type XI, alpha 1diphthine methyl ester synthaseDPH5 homologdiphthamide biosynthesis methyltransferasediphthine synthaseprotein x 0011
Modification date2018052320180519
UniProtAcc

P12107

Q9H2P9

Ensembl transtripts involved in fusion geneENST00000370096, ENST00000353414, 
ENST00000358392, ENST00000512756, 
ENST00000461720, 
ENST00000370105, 
ENST00000370109, ENST00000427040, 
ENST00000342173, ENST00000488176, 
Fusion gene scores* DoF score2 X 2 X 2=82 X 2 X 2=8
# samples 22
** MAII scorelog2(2/8*10)=1.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: COL11A1 [Title/Abstract] AND DPH5 [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
TCGALDPRADTCGA-EJ-7330-01ACOL11A1chr1

103352466

-DPH5chr1

101491617

-
* 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
intron-intronENST00000370096ENST00000370105COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000370096ENST00000370109COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000370096ENST00000427040COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000370096ENST00000342173COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000370096ENST00000488176COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000353414ENST00000370105COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000353414ENST00000370109COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000353414ENST00000427040COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000353414ENST00000342173COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000353414ENST00000488176COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000358392ENST00000370105COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000358392ENST00000370109COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000358392ENST00000427040COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000358392ENST00000342173COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000358392ENST00000488176COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000512756ENST00000370105COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000512756ENST00000370109COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000512756ENST00000427040COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000512756ENST00000342173COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000512756ENST00000488176COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000461720ENST00000370105COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000461720ENST00000370109COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000461720ENST00000427040COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000461720ENST00000342173COL11A1chr1

103352466

-DPH5chr1

101491617

-
intron-intronENST00000461720ENST00000488176COL11A1chr1

103352466

-DPH5chr1

101491617

-

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FusionProtFeatures for COL11A1_DPH5


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COL11A1

P12107

DPH5

Q9H2P9

S-adenosyl-L-methionine-dependent methyltransferase thatcatalyzes four methylations of the modified target histidineresidue in translation elongation factor 2 (EF-2), to form anintermediate called diphthine methyl ester. The four successivemethylation reactions represent the second step of diphthamidebiosynthesis. {ECO:0000250|UniProtKB:P32469,ECO:0000269|PubMed:23486472}.

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 COL11A1_DPH5


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 COL11A1_DPH5


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
COL11A1FBXL19DPH5ENO1, MOV10, NXF1, C12orf10, CD2AP, HNRNPL, SFPQ, UFD1L, GCLC, NMD3, PARVA, SPG20, ZYX


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 COL11A1_DPH5


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 COL11A1_DPH5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCOL11A1C1858084STICKLER SYNDROME, TYPE II (disorder)3CTD_human;ORPHANET;UNIPROT
HgeneCOL11A1C0017605Angle Closure Glaucoma2CTD_human
HgeneCOL11A1C0021818Intervertebral Disk Displacement1CTD_human
HgeneCOL11A1C0029422Osteochondrodysplasias1CTD_human
HgeneCOL11A1C0029927Ovarian Cysts1CTD_human
HgeneCOL11A1C0265235Marshall syndrome1CTD_human;ORPHANET
HgeneCOL11A1C0376634Craniofacial Abnormalities1CTD_human
HgeneCOL11A1C3278138FIBROCHONDROGENESIS 11UNIPROT