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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 RPSMAP, MSBB, and Mayo

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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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3'-UTR located exon skipping events lost miRNA binding sites

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SNVs in the skipped exons with depth of coverage

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AD stage-associated exon skipping events

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Correlation with RNA binding proteins (RBPs)

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Related drugs with this gene

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Related diseases with this gene

Gene summary for SUPT16H

check button Gene summary
Gene informationGene symbol

SUPT16H

Gene ID

11198

Gene nameSPT16 homolog, facilitates chromatin remodeling subunit
SynonymsCDC68|FACTP140|SPT16|SPT16/CDC68
Cytomap

14q11.2

Type of geneprotein-coding
DescriptionFACT complex subunit SPT16FACT 140 kDa subunitchromatin-specific transcription elongation factor 140 kDa subunitfacilitates chromatin remodeling 140 kDa subunitfacilitates chromatin transcription complex subunit SPT16hSPT16suppressor of Ty 16 homolo
Modification date20200313
UniProtAcc

G3V2X0,

G3V401,

G3V5A4,

Q0VGA3,

Q9Y5B9,

Context

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

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Gene structures and expression levels for SUPT16H

check buttonSkipped exons in the ROSMAP, MSBB, and Mayo 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

ENSG00000092201
check button Differentially expressed gene analysis across multiple brain tissues between AD and control.
Tissue typeDEG directionBase mean exp.log2FC(AD/control)P-valueAdj. p-value

check button Differentially expressed isoform analysis across multiple brain tissues between AD and control.
gencode gene structure
Tissue typeDEG directionENSTTranscript info.Base mean exp.log2FC(AD/control)P-valueAdjc. p-value
HCCUPENST00000557394.5SUPT16H-207:retained_intron:SUPT16H3.611016e+011.386670e+003.487258e-066.569398e-04
PGUPENST00000557652.1SUPT16H-208:nonsense_mediated_decay:SUPT16H5.218012e+001.121811e+001.165138e-031.630125e-02
CBDOWNENST00000557394.5SUPT16H-207:retained_intron:SUPT16H1.419503e+03-9.297805e-013.090578e-112.414334e-09

check button Landscape of isoform expressions across multiple brain tissues between AD and control.
gencode gene structure

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Exon skipping events with PSIs in ROSMAP, MSBB, and Mayo for SUPT16H

check button Landscape of individual exon skipping event across AD tissues and controls (PSI heatmap).
boxplot

check button All exon skipping events in AD cohorts.
Exon skip IDchrExons involved in exon skippingSkipped exon
exon_skip_130835chr1421353703:21353832:21354411:21354540:21357197:2135736621354411:21354540
exon_skip_140855chr1421351479:21352818:21353488:21353565:21353703:2135383221353488:21353565
exon_skip_159923chr1421371874:21372044:21373338:21373430:21383862:2138394621373338:21373430
exon_skip_175591chr1421371874:21372044:21372469:21372717:21373338:2137342621372469:21372717
exon_skip_183176chr1421365070:21365143:21366439:21366529:21368269:2136844121366439:21366529
exon_skip_194189chr1421357927:21358002:21358315:21358427:21359484:2135960921358315:21358427
exon_skip_212029chr1421370336:21370488:21371874:21371970:21373338:2137343021371874:21371970
exon_skip_229248chr1421371874:21372044:21372469:21372717:21373338:2137336121372469:21372717
exon_skip_73139chr1421370336:21370488:21371874:21372044:21373338:2137343021371874:21372044
exon_skip_81072chr1421371874:21372044:21372469:21372717:21373338:2137343021372469:21372717

check button Differentially expressed PSI values of individual exon skipping events in multiple brain tissues between AD and control.
Exon skipping informationTissue typeAvg(PSIs) in ADAvg(PSIs) in controlDifference (PSI)Adj. p-value


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Open reading frame (ORF) annotation in the exon skipping event for SUPT16H

check button Open reading frame (ORF) of individual exon skipping events in ROSMAP based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000002162972136643921366529Frame-shift
ENST000002162972137187421372044In-frame

check button Open reading frame (ORF) of individual exon skipping events in MSBB 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 Mayo based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000002162972135441121354540Frame-shift
ENST000002162972135831521358427Frame-shift
ENST000002162972136643921366529Frame-shift
ENST000002162972135348821353565In-frame
ENST000002162972137187421372044In-frame

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Infer the effects of exon skipping event on protein functional features for SUPT16H

p-ENSG00000092201_img4.png
boxplot

check button Loci of skipped exons in ROSMAP across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST0000021629747011047213718742137204449966853109

check button Loci of skipped exons in MSBB 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 Mayo across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST0000021629747011047213718742137204449966853109
ENST0000021629747011047213534882135356532603336973999

check button Lost protein functional features of individual exon skipping events in ROSMAP.
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
Q9Y5B9531096268Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B9531097377Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B953109103107Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B95310921047ChainID=PRO_0000245169;Note=FACT complex subunit SPT16
Q9Y5B9531094857HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B9531097989HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B9531099599HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B

check button Lost protein functional features of individual exon skipping events in MSBB.
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 Mayo.
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
Q9Y5B9531096268Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B9531097377Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B953109103107Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B95310921047ChainID=PRO_0000245169;Note=FACT complex subunit SPT16
Q9Y5B9531094857HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B9531097989HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B9531099599HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:5E5B
Q9Y5B997399921047ChainID=PRO_0000245169;Note=FACT complex subunit SPT16
Q9Y5B99739999261011Compositional biasNote=Glu-rich (acidic)
Q9Y5B9973999979979Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:21406692;Dbxref=PMID:17081983,PMID:20068231,PMID:21406692
Q9Y5B9973999982982Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:21406692,ECO:0000244|PubMed:23186163;Dbxref=PMID:17081983,PMID:20068231,PMID:21406692,PMID
Q9Y5B9973999986986Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:21406692;Dbxref=PMID:21406692


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3'-UTR located exon skipping events that lost miRNA binding sites in SUPT16H

check button 3'-UTR exon skipping evnets lost miRNA binding.
Tissue typeENSTExon skip startExon skip endmicroRNABinding site by TargetScanBinding type by TargetScanBdinding site by miRandaScore of miRandaEnergy by miRanda

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SNVs in the skipped exons for SUPT16H

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

check button - Depth of Coverage in the skipped exon of the mutated samples.

check button - Sashimi plot in the skipped exon of the mutated samples.

check button - Non-synonymous mutations located in the skipped exons.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange

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AD stage-associated exon skippint events for SUPT16H

check button Associated exon skipping events with Braak staging or Clinical Dementia Rating (CDR).
AD stage infoCohortTissueSE idCoefficient P-valueChromosomeStrandE1 startE1 endSkipped startSkipped endE2 startE2 end

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for SUPT16H

check button sQTL information located at the skipped exons.
Tissue typeExon skip IDSNP idLocationP-valueFDR

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Correlation with RNA binding proteins (RBPs) for SUPT16H

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value

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RelatedDrugs for SUPT16H

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

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RelatedDiseases for SUPT16H

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