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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: 27774

FusionGeneSummary for PLXND1_TMCC1

check button Fusion gene summary
Fusion gene informationFusion gene name: PLXND1_TMCC1
Fusion gene ID: 27774
HgeneTgene
Gene symbol

PLXND1

TMCC1

Gene ID

23129

23023

Gene nameplexin D1transmembrane and coiled-coil domain family 1
SynonymsPLEXD1-
Cytomap

3q22.1

3q22.1

Type of geneprotein-codingprotein-coding
Descriptionplexin-D1transmembrane and coiled-coil domains protein 1
Modification date2018052320180523
UniProtAcc

Q9Y4D7

O94876

Ensembl transtripts involved in fusion geneENST00000324093, ENST00000393239, 
ENST00000504689, 
ENST00000432054, 
ENST00000393238, ENST00000426664, 
ENST00000329333, ENST00000515024, 
Fusion gene scores* DoF score5 X 5 X 3=755 X 5 X 5=125
# samples 57
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/125*10)=-0.836501267717121
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PLXND1 [Title/Abstract] AND TMCC1 [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
TCGARVUCECTCGA-AX-A2H4-01APLXND1chr3

129277271

-TMCC1chr3

129373946

-
* 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-shiftENST00000324093ENST00000432054PLXND1chr3

129277271

-TMCC1chr3

129373946

-
Frame-shiftENST00000324093ENST00000393238PLXND1chr3

129277271

-TMCC1chr3

129373946

-
Frame-shiftENST00000324093ENST00000426664PLXND1chr3

129277271

-TMCC1chr3

129373946

-
Frame-shiftENST00000324093ENST00000329333PLXND1chr3

129277271

-TMCC1chr3

129373946

-
5CDS-intronENST00000324093ENST00000515024PLXND1chr3

129277271

-TMCC1chr3

129373946

-
3UTR-3CDSENST00000393239ENST00000432054PLXND1chr3

129277271

-TMCC1chr3

129373946

-
3UTR-3CDSENST00000393239ENST00000393238PLXND1chr3

129277271

-TMCC1chr3

129373946

-
3UTR-3CDSENST00000393239ENST00000426664PLXND1chr3

129277271

-TMCC1chr3

129373946

-
3UTR-3CDSENST00000393239ENST00000329333PLXND1chr3

129277271

-TMCC1chr3

129373946

-
3UTR-intronENST00000393239ENST00000515024PLXND1chr3

129277271

-TMCC1chr3

129373946

-
intron-3CDSENST00000504689ENST00000432054PLXND1chr3

129277271

-TMCC1chr3

129373946

-
intron-3CDSENST00000504689ENST00000393238PLXND1chr3

129277271

-TMCC1chr3

129373946

-
intron-3CDSENST00000504689ENST00000426664PLXND1chr3

129277271

-TMCC1chr3

129373946

-
intron-3CDSENST00000504689ENST00000329333PLXND1chr3

129277271

-TMCC1chr3

129373946

-
intron-intronENST00000504689ENST00000515024PLXND1chr3

129277271

-TMCC1chr3

129373946

-

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FusionProtFeatures for PLXND1_TMCC1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PLXND1

Q9Y4D7

TMCC1

O94876

Cell surface receptor for SEMA4A and for class 3semaphorins, such as SEMA3A, SEMA3C and SEMA3E. Plays an importantrole in cell-cell signaling, and in regulating the migration of awide spectrum of cell types. Regulates the migration of thymocytesin the medulla. Regulates endothelial cell migration. Plays animportant role in ensuring the specificity of synapse formation.Required for normal development of the heart and vasculature (Bysimilarity). Mediates anti-angiogenic signaling in response toSEMA3E. {ECO:0000250, ECO:0000269|PubMed:20385769}.

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 PLXND1_TMCC1


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 PLXND1_TMCC1


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
PLXND1MACF1, TRIM25TMCC1ZDHHC17, APP, TEX28


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 PLXND1_TMCC1


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 PLXND1_TMCC1


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