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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 TIMELESS

check button Gene summary
Gene informationGene symbol

TIMELESS

Gene ID

8914

Gene nametimeless circadian regulator
SynonymsTIM|TIM1|hTIM
Cytomap

12q13.3

Type of geneprotein-coding
Descriptionprotein timeless homologTof1 homologtimeless circadian clock 1timeless homolog
Modification date20180523
UniProtAcc

Q9UNS1

ContextPubMed: TIMELESS [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
TIMELESS

GO:0045892

negative regulation of transcription, DNA-templated

9856465


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Exon skipping events across known transcript of Ensembl for TIMELESS 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 TIMELESS

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 TIMELESS

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_936841256811690:56811792:56811917:56812143:56814352:5681447156811917:56812143ENSG00000111602.7ENST00000553532.1,ENST00000557589.1,ENST00000229201.4,ENST00000554616.1
exon_skip_936871256814746:56814918:56815134:56815277:56815510:5681559356815134:56815277ENSG00000111602.7ENST00000553532.1,ENST00000229201.4,ENST00000554616.1
exon_skip_936891256815889:56815975:56816630:56816776:56817057:5681725956816630:56816776ENSG00000111602.7ENST00000553532.1,ENST00000557589.1,ENST00000229201.4
exon_skip_936921256822019:56822189:56822332:56822436:56822666:5682288456822332:56822436ENSG00000111602.7ENST00000553532.1,ENST00000229201.4
exon_skip_936941256822666:56822884:56823888:56824065:56824664:5682475256823888:56824065ENSG00000111602.7ENST00000553532.1,ENST00000229201.4
exon_skip_936951256825254:56825388:56826152:56826305:56826809:5682691156826152:56826305ENSG00000111602.7ENST00000229201.4
exon_skip_936961256825254:56825388:56826152:56826308:56826809:5682691156826152:56826308ENSG00000111602.7ENST00000553532.1,ENST00000554616.1
exon_skip_936971256826152:56826308:56826809:56826911:56827164:5682722756826809:56826911ENSG00000111602.7ENST00000553532.1,ENST00000554616.1

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

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Exon skipping events with PSIs in GTEx for TIMELESS

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_936841256811690:56811792:56811917:56812143:56814352:5681447156811917:56812143ENSG00000111602.7ENST00000229201.4,ENST00000553532.1,ENST00000557589.1,ENST00000554616.1
exon_skip_936871256814746:56814918:56815134:56815277:56815510:5681559356815134:56815277ENSG00000111602.7ENST00000229201.4,ENST00000553532.1,ENST00000554616.1
exon_skip_936891256815889:56815975:56816630:56816776:56817057:5681725956816630:56816776ENSG00000111602.7ENST00000229201.4,ENST00000553532.1,ENST00000557589.1
exon_skip_936921256822019:56822189:56822332:56822436:56822666:5682288456822332:56822436ENSG00000111602.7ENST00000229201.4,ENST00000553532.1
exon_skip_936941256822666:56822884:56823888:56824065:56824664:5682475256823888:56824065ENSG00000111602.7ENST00000229201.4,ENST00000553532.1
exon_skip_936951256825254:56825388:56826152:56826305:56826809:5682691156826152:56826305ENSG00000111602.7ENST00000229201.4
exon_skip_936961256825254:56825388:56826152:56826308:56826809:5682691156826152:56826308ENSG00000111602.7ENST00000553532.1,ENST00000554616.1
exon_skip_936971256826152:56826308:56826809:56826911:56827164:5682722756826809:56826911ENSG00000111602.7ENST00000553532.1,ENST00000554616.1

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 TIMELESS

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
ENST000005535325681191756812143Frame-shift
ENST000005535325681513456815277Frame-shift
ENST000005535325681663056816776Frame-shift
ENST000005535325682233256822436Frame-shift
ENST000005535325682388856824065In-frame
ENST000005535325682615256826308In-frame
ENST000005535325682680956826911In-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
ENST000005535325681191756812143Frame-shift
ENST000005535325681513456815277Frame-shift
ENST000005535325681663056816776Frame-shift
ENST000005535325682233256822436Frame-shift
ENST000005535325682388856824065In-frame
ENST000005535325682615256826308In-frame
ENST000005535325682680956826911In-frame

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

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
ENST00000553532438812085682680956826911581682143177
ENST00000553532438812085682615256826308683838177229
ENST0000055353243881208568238885682406510611237303362

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
ENST00000553532438812085682680956826911581682143177
ENST00000553532438812085682615256826308683838177229
ENST0000055353243881208568238885682406510611237303362

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
Q9UNS1143177177177Alternative sequenceID=VSP_051693;Note=In isoform 2. Missing;Ontology_term=ECO:0000303,ECO:0000303;evidence=ECO:0000303|PubMed:15489334,ECO:0000303|PubMed:9856465;Dbxref=PMID:15489334,PMID:9856465
Q9UNS114317711208ChainID=PRO_0000072538;Note=Protein timeless homolog
Q9UNS1143177145147HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1143177150168HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS11431771309RegionNote=Required for homodimerization and for interaction with CRY1 and CHEK1;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q9UNS1177229177177Alternative sequenceID=VSP_051693;Note=In isoform 2. Missing;Ontology_term=ECO:0000303,ECO:0000303;evidence=ECO:0000303|PubMed:15489334,ECO:0000303|PubMed:9856465;Dbxref=PMID:15489334,PMID:9856465
Q9UNS117722911208ChainID=PRO_0000072538;Note=Protein timeless homolog
Q9UNS1177229184195HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1177229198207HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1177229209214HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1177229215225HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS11772291309RegionNote=Required for homodimerization and for interaction with CRY1 and CHEK1;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q9UNS1177229226228TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS130336211208ChainID=PRO_0000072538;Note=Protein timeless homolog
Q9UNS1303362336352HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1303362354367HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS13033621309RegionNote=Required for homodimerization and for interaction with CRY1 and CHEK1;Ontology_term=ECO:0000250;evidence=ECO:0000250


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
Q9UNS1143177177177Alternative sequenceID=VSP_051693;Note=In isoform 2. Missing;Ontology_term=ECO:0000303,ECO:0000303;evidence=ECO:0000303|PubMed:15489334,ECO:0000303|PubMed:9856465;Dbxref=PMID:15489334,PMID:9856465
Q9UNS114317711208ChainID=PRO_0000072538;Note=Protein timeless homolog
Q9UNS1143177145147HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1143177150168HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS11431771309RegionNote=Required for homodimerization and for interaction with CRY1 and CHEK1;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q9UNS1177229177177Alternative sequenceID=VSP_051693;Note=In isoform 2. Missing;Ontology_term=ECO:0000303,ECO:0000303;evidence=ECO:0000303|PubMed:15489334,ECO:0000303|PubMed:9856465;Dbxref=PMID:15489334,PMID:9856465
Q9UNS117722911208ChainID=PRO_0000072538;Note=Protein timeless homolog
Q9UNS1177229184195HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1177229198207HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1177229209214HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1177229215225HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS11772291309RegionNote=Required for homodimerization and for interaction with CRY1 and CHEK1;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q9UNS1177229226228TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS130336211208ChainID=PRO_0000072538;Note=Protein timeless homolog
Q9UNS1303362336352HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS1303362354367HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5MQI
Q9UNS13033621309RegionNote=Required for homodimerization and for interaction with CRY1 and CHEK1;Ontology_term=ECO:0000250;evidence=ECO:0000250


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SNVs in the skipped exons for TIMELESS

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-A3A0-01exon_skip_93687
56815135568152775681515456815154Frame_Shift_DelT-p.K949fs
LIHCTCGA-DD-A3A0-01exon_skip_93689
56816631568167765681673556816735Frame_Shift_DelA-p.F777fs
LUADTCGA-44-2656-01exon_skip_93684
56811918568121435681191856811918Nonsense_MutationCAp.E1152*
HNSCTCGA-CN-4728-01exon_skip_93687
56815135568152775681518856815188Nonsense_MutationCAp.E938*
HNSCTCGA-CN-4728-01exon_skip_93687
56815135568152775681518856815188Nonsense_MutationCAp.E939*
CESCTCGA-DR-A0ZM-01exon_skip_93687
56815135568152775681523556815235Nonsense_MutationGCp.S922*
CESCTCGA-DR-A0ZM-01exon_skip_93687
56815135568152775681523556815235Nonsense_MutationGCp.S923*
BLCATCGA-GV-A6ZA-01exon_skip_93697
56826810568269115682681856826818Nonsense_MutationGAp.Q175*
STADTCGA-BR-6452-01exon_skip_93692
56822333568224365682233256822332Splice_SiteCT.
STADTCGA-BR-6452-01exon_skip_93692
56822333568224365682233256822332Splice_SiteCTp.N470_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
IGR1_SKIN56811918568121435681197556811975Missense_MutationCGp.A1133P
OVCA433_OVARY56811918568121435681197556811975Missense_MutationCGp.A1133P
AMO1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56811918568121435681197756811977Missense_MutationTCp.Q1132R
SW1463_LARGE_INTESTINE56811918568121435681200556812005Missense_MutationCTp.E1123K
HEC151_ENDOMETRIUM56811918568121435681202556812025Missense_MutationGTp.P1116H
TT_OESOPHAGUS56815135568152775681518256815182Missense_MutationGAp.R941W
ALLSIL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56816631568167765681664056816640Missense_MutationAGp.L810P
SNU1076_UPPER_AERODIGESTIVE_TRACT56823889568240655682389656823896Missense_MutationGAp.S360L
HCC2998_LARGE_INTESTINE56823889568240655682404456824044Missense_MutationACp.L311V
QIMRWIL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56826153568263055682628956826289Missense_MutationCGp.S184T
QIMRWIL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56826153568263085682628956826289Missense_MutationCGp.S184T
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE56823889568240655682388956823890Splice_Site-Tp.K362fs

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

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 TIMELESS


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


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RelatedDrugs for TIMELESS

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 TIMELESS

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
TIMELESSC0005586Bipolar Disorder5PSYGENET
TIMELESSC0011570Mental Depression2PSYGENET
TIMELESSC0011581Depressive disorder2PSYGENET
TIMELESSC0525045Mood Disorders2PSYGENET