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Center for Computational Systems Medicine
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Gene summary

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Gene structures and expression levels

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Exon skipping events with PSIs in TCGA

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Exon skipping events with PSIs in GTEx

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Open reading frame (ORF) annotation in the exon skipping event

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Exon skipping events in the canonical protein sequence

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SNVs in the skipped exons with depth of coverage

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon

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Related drugs with this gene

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Related diseases with this gene

Gene summary for VEGFC

check button Gene summary
Gene informationGene symbol

VEGFC

Gene ID

7424

Gene namevascular endothelial growth factor C
SynonymsFlt4-L|LMPH1D|VRP
Cytomap

4q34.3

Type of geneprotein-coding
Descriptionvascular endothelial growth factor CFLT4 ligand DHMvascular endothelial growth factor-related protein
Modification date20180527
UniProtAcc

P49767

ContextPubMed: VEGFC [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract]
- Title (PMID)

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID
VEGFC

GO:0048010

vascular endothelial growth factor receptor signaling pathway

23878260

VEGFC

GO:0050930

induction of positive chemotaxis

19275959

VEGFC

GO:0060754

positive regulation of mast cell chemotaxis

19275959


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Exon skipping events across known transcript of Ensembl for VEGFC from UCSC genome browser

check buttonSkipped exons in TCGA and GTEx based on Ensembl gene isoform structure.
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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Gene isoform structures and expression levels for VEGFC

check button Expression levels of gene isoforms across TCGA.
gencode gene structure

check button Expression levels of gene isoforms across GTEx.
gencode gene structure


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Exon skipping events with PSIs in TCGA for VEGFC

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_4331964177608974:177609081:177632652:177632804:177648931:177649001177632652:177632804ENSG00000150630.2ENST00000280193.2
exon_skip_4332044177632652:177632804:177648931:177649122:177650686:177650746177648931:177649122ENSG00000150630.2ENST00000507638.1,ENST00000280193.2

check button PSI values of skipped exons in TCGA.
psi tcga

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Exon skipping events with PSIs in GTEx for VEGFC

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_4331964177608974:177609081:177632652:177632804:177648931:177649001177632652:177632804ENSG00000150630.2ENST00000280193.2
exon_skip_4332044177632652:177632804:177648931:177649122:177650686:177650746177648931:177649122ENSG00000150630.2ENST00000280193.2,ENST00000507638.1

check button PSI values of skipped exons in GTEx.
psi gtex

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for VEGFC

check button Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF

check button Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF

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Infer the effects of exon skipping event on protein functional features for VEGFC

check button Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.
prot feature distribution

check button Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end

check button Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end

check button Lost protein functional features of individual exon skipping events in TCGA.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature


check button Lost protein functional features of individual exon skipping events in GTEx.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature


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SNVs in the skipped exons for VEGFC

check button - Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.
lollipop

check button - Differential PSIs between mutated versus non-mutated samples.

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
ESCATCGA-L5-A43J-01exon_skip_433196
177632653177632804177632776177632777Frame_Shift_Ins-GAp.Q194fs
ESCATCGA-L5-A43J-01exon_skip_433196
177632653177632804177632776177632777Frame_Shift_Ins-GAp.R194fs
UCECTCGA-AP-A0LM-01exon_skip_433196
177632653177632804177632699177632699Nonsense_MutationGAp.Q220*
KIRCTCGA-B8-A54D-01exon_skip_433196
177632653177632804177632651177632651Splice_SiteAC.
HNSCTCGA-CV-7245-01exon_skip_433204
177648932177649122177649124177649124Splice_SiteTAp.S121_splice

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
SNU175_LARGE_INTESTINE177632653177632804177632669177632669Missense_MutationGAp.P230S
A4FUK_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE177632653177632804177632675177632675Missense_MutationAGp.S228P
NCIH2170_LUNG177632653177632804177632675177632675Missense_MutationAGp.S228P
NCIH460_LUNG177632653177632804177632675177632675Missense_MutationAGp.S228P
NCIH520_LUNG177632653177632804177632675177632675Missense_MutationAGp.S228P
SNU175_LARGE_INTESTINE177632653177632804177632678177632678Missense_MutationGAp.R227C
KYAE1_OESOPHAGUS177632653177632804177632687177632687Missense_MutationTGp.I224L
EMCBAC1_LUNG177632653177632804177632756177632756Missense_MutationTCp.I201V
GCT_SOFT_TISSUE177648932177649122177648954177648954Missense_MutationCTp.S177N
NCIH358_LUNG177648932177649122177648976177648976Missense_MutationCTp.G170R
CP66MEL_SKIN177648932177649122177649021177649021Missense_MutationGAp.P155S
HEC251_ENDOMETRIUM177648932177649122177649031177649031Missense_MutationGTp.F151L
SNU81_LARGE_INTESTINE177648932177649122177649031177649031Missense_MutationGTp.F151L
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE177648932177649122177649046177649047Missense_MutationGATGp.V146A
BICR18_UPPER_AERODIGESTIVE_TRACT177648932177649122177649046177649047Missense_MutationGATGp.V146A
BICR18_UPPER_AERODIGESTIVE_TRACT177648932177649122177649047177649047Missense_MutationAGp.V146A
NCIH1770_LUNG177648932177649122177649057177649057Missense_MutationCTp.E143K
NCIH2106_LUNG177648932177649122177649057177649057Missense_MutationCTp.E143K
HEC6_ENDOMETRIUM177648932177649122177649066177649066Missense_MutationCTp.V140M
SNU1040_LARGE_INTESTINE177648932177649122177649088177649088Missense_MutationCTp.M132I
KATOIII_STOMACH177648932177649122177648933177648933Splice_SiteGAp.T184M

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for VEGFC

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for VEGFC


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for VEGFC


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RelatedDrugs for VEGFC

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for VEGFC

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
VEGFCC1458155Mammary Neoplasms2CTD_human
VEGFCC0018923Hemangiosarcoma1CTD_human
VEGFCC0025202melanoma1CTD_human