ExonSkipDB Logo

Home

Download

Statistics

Landscape

Help

Contact

Center for Computational Systems Medicine
leaf

Gene summary

leaf

Gene structures and expression levels

leaf

Exon skipping events with PSIs in TCGA

leaf

Exon skipping events with PSIs in GTEx

leaf

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

leaf

Exon skipping events in the canonical protein sequence

leaf

SNVs in the skipped exons with depth of coverage

leaf

Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

leaf

Splicing Quantitative Trait Methylation (sQTM) in the skipped exon

leaf

Related drugs with this gene

leaf

Related diseases with this gene

Gene summary for FOS

check button Gene summary
Gene informationGene symbol

FOS

Gene ID

2353

Gene nameFos proto-oncogene, AP-1 transcription factor subunit
SynonymsAP-1|C-FOS|p55
Cytomap

14q24.3

Type of geneprotein-coding
Descriptionproto-oncogene c-FosFBJ murine osteosarcoma viral (v-fos) oncogene homolog (oncogene FOS)FBJ murine osteosarcoma viral oncogene homologFos proto-oncogene, AP-1 trancription factor subunitG0/G1 switch regulatory protein 7activator protein 1cellular o
Modification date20180523
UniProtAcc

P01100

ContextPubMed: FOS [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
FOS

GO:0007179

transforming growth factor beta receptor signaling pathway

9732876

FOS

GO:0034614

cellular response to reactive oxygen species

17217916

FOS

GO:0045893

positive regulation of transcription, DNA-templated

9732876

FOS

GO:0045944

positive regulation of transcription by RNA polymerase II

10508860

FOS

GO:0060395

SMAD protein signal transduction

9732876


Top

Exon skipping events across known transcript of Ensembl for FOS 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

Top

Gene isoform structures and expression levels for FOS

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

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


Top

Exon skipping events with PSIs in TCGA for FOS

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1082841475745679:75745826:75746579:75746831:75747262:7574731075746579:75746831ENSG00000170345.5ENST00000555242.1
exon_skip_1082851475745530:75745826:75746608:75746831:75747262:7574731075746608:75746831ENSG00000170345.5ENST00000554212.1
exon_skip_1082871475746761:75746831:75747262:75747370:75747485:7574786075747262:75747370ENSG00000170345.5ENST00000555686.1,ENST00000303562.4

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

Top

Exon skipping events with PSIs in GTEx for FOS

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1082841475745679:75745826:75746579:75746831:75747262:7574731075746579:75746831ENSG00000170345.5ENST00000555242.1
exon_skip_1082851475745530:75745826:75746608:75746831:75747262:7574731075746608:75746831ENSG00000170345.5ENST00000554212.1
exon_skip_1082871475746761:75746831:75747262:75747370:75747485:7574786075747262:75747370ENSG00000170345.5ENST00000303562.4,ENST00000555686.1

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

* Skipped exon sequences.

Top

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

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
ENST000003035627574726275747370In-frame

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
ENST000003035627574726275747370In-frame

Top

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

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
ENST0000030356221753807574726275747370603710131167

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
ENST0000030356221753807574726275747370603710131167

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
P01100131167132167Alternative sequenceID=VSP_055561;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
P011001311671380ChainID=PRO_0000076465;Note=Proto-oncogene c-Fos
P01100131167137200DomainNote=bZIP;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00978
P01100131167141191HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1A02
P01100131167139159RegionNote=Basic motif%3B required for the activation of phospholipid synthesis%2C but not for CDS1-binding
P01100131167165193RegionNote=Leucine-zipper;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00978
P01100131167133144Sequence conflictNote=SPEEEEKRRIRR->ISRRRREKENPK;Ontology_term=ECO:0000305;evidence=ECO:0000305


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
P01100131167132167Alternative sequenceID=VSP_055561;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
P011001311671380ChainID=PRO_0000076465;Note=Proto-oncogene c-Fos
P01100131167137200DomainNote=bZIP;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00978
P01100131167141191HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1A02
P01100131167139159RegionNote=Basic motif%3B required for the activation of phospholipid synthesis%2C but not for CDS1-binding
P01100131167165193RegionNote=Leucine-zipper;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00978
P01100131167133144Sequence conflictNote=SPEEEEKRRIRR->ISRRRREKENPK;Ontology_term=ECO:0000305;evidence=ECO:0000305


Top

SNVs in the skipped exons for FOS

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
LIHCTCGA-DD-A39Y-01exon_skip_108284
75746580757468317574673775746737Frame_Shift_DelC-p.A100fs
LIHCTCGA-DD-A39Y-01exon_skip_108285
75746609757468317574673775746737Frame_Shift_DelC-p.A100fs
LIHCTCGA-DD-A3A0-01exon_skip_108284
75746580757468317574681575746815Frame_Shift_DelG-p.R126fs
LIHCTCGA-DD-A3A0-01exon_skip_108285
75746609757468317574681575746815Frame_Shift_DelG-p.R126fs
COADTCGA-AZ-6598-01exon_skip_108287
75747263757473707574728475747284Frame_Shift_DelA-p.E138fs
COADTCGA-A6-6781-01exon_skip_108287
75747263757473707574730375747303Frame_Shift_DelA-p.E145fs
LIHCTCGA-DD-A39Y-01exon_skip_108287
75747263757473707574734575747345Frame_Shift_DelG-p.R159fs

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
LS180_LARGE_INTESTINE75746609757468317574673675746737Frame_Shift_Ins-Cp.A100fs
LS180_LARGE_INTESTINE75746580757468317574673675746737Frame_Shift_Ins-Cp.A100fs
HEC251_ENDOMETRIUM75746609757468317574662975746629Missense_MutationTGp.V64G
HEC251_ENDOMETRIUM75746580757468317574662975746629Missense_MutationTGp.V64G
DL40_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE75746609757468317574668075746680Missense_MutationTGp.L81R
DL40_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE75746580757468317574668075746680Missense_MutationTGp.L81R
CAL27_UPPER_AERODIGESTIVE_TRACT75747263757473707574727875747278Missense_MutationGAp.E137K
RCHACV_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE75747263757473707574731875747318Missense_MutationCTp.A150V
HCT116_LARGE_INTESTINE75747263757473707574736975747369Splice_SiteCTp.A167V

Top

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

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

Top

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


Top

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


Top

RelatedDrugs for FOS

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
P01100DB08813NadroparinProto-oncogene c-Fossmall moleculeapproved|investigational

Top

RelatedDiseases for FOS

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
FOSC0036572Seizures4CTD_human
FOSC0038220Status Epilepticus4CTD_human
FOSC0038587Substance Withdrawal Syndrome3CTD_human
FOSC0236736Cocaine-Related Disorders3CTD_human
FOSC0020538Hypertensive disease2CTD_human
FOSC0003469Anxiety Disorders1CTD_human
FOSC0011570Mental Depression1PSYGENET
FOSC0011581Depressive disorder1PSYGENET
FOSC0014175Endometriosis1CTD_human
FOSC0014544Epilepsy1CTD_human
FOSC0016063Osteitis Fibrosa Disseminata1CTD_human
FOSC0018843Heat Stroke1CTD_human
FOSC0019080Hemorrhage1CTD_human
FOSC0020429Hyperalgesia1CTD_human
FOSC0023893Liver Cirrhosis, Experimental1CTD_human
FOSC0024121Lung Neoplasms1CTD_human
FOSC0027765nervous system disorder1CTD_human
FOSC0035126Reperfusion Injury1CTD_human
FOSC0040997Trigeminal Neuralgia1CTD_human
FOSC0041696Unipolar Depression1PSYGENET
FOSC0235032Neurotoxicity Syndromes1CTD_human
FOSC0236733Amphetamine-Related Disorders1CTD_human
FOSC0270458Severe major depression with psychotic features1PSYGENET
FOSC0424295Hyperactive behavior1CTD_human
FOSC0740392Infarction, Middle Cerebral Artery1CTD_human
FOSC0743072Depression, psychotic1PSYGENET
FOSC1269683Major Depressive Disorder1PSYGENET
FOSC1458155Mammary Neoplasms1CTD_human
FOSC1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human
FOSC2239176Liver carcinoma1CTD_human
FOSC3495559Juvenile arthritis1CTD_human