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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: 28625

FusionGeneSummary for PRELP_CCDC36

check button Fusion gene summary
Fusion gene informationFusion gene name: PRELP_CCDC36
Fusion gene ID: 28625
HgeneTgene
Gene symbol

PRELP

CCDC36

Gene ID

5549

339834

Gene nameproline and arginine rich end leucine rich repeat proteincoiled-coil domain containing 36
SynonymsMST161|MSTP161|SLRR2ACT74
Cytomap

1q32.1

3p21.31

Type of geneprotein-codingprotein-coding
Descriptionprolargin55 kDa leucine-rich repeat protein of articular cartilageprolargin proteoglycanproline-arginine-rich end leucine-rich repeat proteininteractor of HORMAD1 protein 1cancer/testis antigen 74coiled-coil domain-containing protein 36
Modification date2018052320180522
UniProtAcc

P51888

Q8IYA8

Ensembl transtripts involved in fusion geneENST00000343110, ENST00000296449, 
ENST00000438782, ENST00000452691, 
ENST00000366429, ENST00000451634, 
ENST00000493870, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 1=4
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: PRELP [Title/Abstract] AND CCDC36 [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
ChiTaRS3.1BM686368PRELPchr1

203452459

+CCDC36chr3

49282867

+
* 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-intronENST00000343110ENST00000296449PRELPchr1

203452459

+CCDC36chr3

49282867

+
5CDS-intronENST00000343110ENST00000438782PRELPchr1

203452459

+CCDC36chr3

49282867

+
5CDS-intronENST00000343110ENST00000452691PRELPchr1

203452459

+CCDC36chr3

49282867

+
5CDS-3UTRENST00000343110ENST00000366429PRELPchr1

203452459

+CCDC36chr3

49282867

+
5CDS-3UTRENST00000343110ENST00000451634PRELPchr1

203452459

+CCDC36chr3

49282867

+
5CDS-intronENST00000343110ENST00000493870PRELPchr1

203452459

+CCDC36chr3

49282867

+

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FusionProtFeatures for PRELP_CCDC36


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

P51888

CCDC36

Q8IYA8

May anchor basement membranes to the underlyingconnective tissue. {ECO:0000250}. Required for DNA double-strand breaks (DSBs) formationin unsynapsed regions during meiotic recombination. Probably actsby forming a complex with MEI4 and REC114, which activates DSBsformation in unsynapsed regions, an essential step to ensurecompletion of synapsis. Not required for HORMAD1 functions inpairing-independent synaptonemal complex formation, ATRrecruitment to unsynapsed axes, meiotic silencing of unsynapsedchromatin (MSUC) or meiotic surveillance.{ECO:0000250|UniProtKB:Q6PDM4}.

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 PRELP_CCDC36


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 PRELP_CCDC36


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 PRELP_CCDC36


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 PRELP_CCDC36


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource