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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 HMGN1

check button Gene summary
Gene informationGene symbol

HMGN1

Gene ID

3150

Gene namehigh mobility group nucleosome binding domain 1
SynonymsHMG14
Cytomap

21q22.2

Type of geneprotein-coding
Descriptionnon-histone chromosomal protein HMG-14high mobility group nucleosome-binding domain-containing protein 1high-mobility group (nonhistone chromosomal) protein 14high-mobility group nucleosome binding 1nonhistone chromosomal protein HMG-14
Modification date20200320
UniProtAcc

A0A494C035,

A6NEL0,

A6NL93,

F2Z2W6,

F2Z2Y5,

H7BXJ5,

P05114,

Q3B790,

Q6NSG7,

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 HMGN1

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

ENSG00000205581
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
DLPFCDOWNENST00000471260.1HMGN1-211:lncRNA:HMGN11.795566e+00-1.139202e+001.753934e-034.853034e-02
CBDOWNENST00000288344.14HMGN1-201:nonsense_mediated_decay:HMGN12.936962e+02-2.139525e+007.932487e-115.200878e-09
CBDOWNENST00000492280.5HMGN1-220:retained_intron:HMGN16.685372e+02-9.226937e-013.096001e-075.526144e-06
CBDOWNENST00000479586.5HMGN1-212:lncRNA:HMGN12.768540e+01-9.207053e-011.451124e-024.697330e-02
TCDOWNENST00000288344.14HMGN1-201:nonsense_mediated_decay:HMGN11.322124e+02-1.627207e+001.256902e-081.092195e-06
TCUPENST00000490032.5HMGN1-218:lncRNA:HMGN11.905467e+019.058845e-012.756903e-032.139392e-02
TCDOWNENST00000479586.5HMGN1-212:lncRNA:HMGN12.345159e+01-8.841277e-013.145271e-032.365376e-02

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 HMGN1

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_113422chr2139347247:39347292:39347379:39347483:39347916:3934795239347379:39347483
exon_skip_12354chr2139347447:39347483:39347916:39347952:39348292:3934833939347916:39347952
exon_skip_136884chr2139345217:39345274:39347379:39347478:39348292:3934833939347379:39347478
exon_skip_158112chr2139345146:39345274:39345830:39345958:39348292:3934833939345830:39345958
exon_skip_182630chr2139347247:39347292:39347379:39347483:39348292:3934833939347379:39347483
exon_skip_189515chr2139345217:39345274:39347247:39347292:39347379:3934747839347247:39347292
exon_skip_190757chr2139345146:39345274:39345830:39345958:39347379:3934747439345830:39345958
exon_skip_231172chr2139345146:39345274:39347379:39347478:39348292:3934833939347379:39347478
exon_skip_245503chr2139345217:39345274:39347247:39347292:39348292:3934833939347247:39347292
exon_skip_24815chr2139345217:39345274:39345830:39345958:39347379:3934747839345830:39345958
exon_skip_249751chr2139345217:39345274:39345830:39345958:39347247:3934729239345830:39345958
exon_skip_255556chr2139345146:39345274:39347247:39347292:39348292:3934833939347247:39347292
exon_skip_260691chr2139345217:39345274:39345830:39347292:39347379:3934747839345830:39347292
exon_skip_264600chr2139345146:39345274:39345830:39347292:39347379:3934747839345830:39347292
exon_skip_270380chr2139345146:39345274:39345830:39345958:39347379:3934747839345830:39345958
exon_skip_276545chr2139345217:39345274:39345830:39345958:39348292:3934833939345830:39345958
exon_skip_284245chr2139345217:39345274:39347379:39347483:39348292:3934833939347379:39347483
exon_skip_29530chr2139348292:39348339:39348422:39348451:39348545:3934857739348422:39348451
exon_skip_31855chr2139345830:39345958:39347247:39347292:39347379:3934747839347247:39347292
exon_skip_35998chr2139345830:39345958:39347114:39347292:39347379:3934747839347114:39347292
exon_skip_56500chr2139347379:39347483:39347916:39347952:39348292:3934833939347916:39347952
exon_skip_58361chr2139345146:39345274:39345830:39345958:39347247:3934729239345830:39345958
exon_skip_61162chr2139345830:39345958:39347379:39347483:39348292:3934833939347379:39347483
exon_skip_82122chr2139345830:39345958:39347379:39347478:39348292:3934833939347379:39347478
exon_skip_82555chr2139345146:39345274:39347247:39347292:39347379:3934747839347247:39347292
exon_skip_98560chr2139345146:39345274:39348292:39348339:39348422:3934845139348292:39348339
exon_skip_99566chr2139345146:39345274:39347379:39347483:39348292:3934833939347379:39347483

check button Differentially expressed PSI values of individual exon skipping events in multiple brain tissues between AD and control.
psi tcga
Exon skipping informationTissue typeAvg(PSIs) in ADAvg(PSIs) in controlDifference (PSI)Adj. p-value
exon_skip_264600Mayo_CB5.479710e-016.711864e-01-1.232154e-013.275222e-04
exon_skip_56500Mayo_TC4.109375e-015.271186e-01-1.161811e-018.820143e-03


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Open reading frame (ORF) annotation in the exon skipping event for HMGN1

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
ENST000003807493934842239348451In-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
ENST000003807493934829239348339In-frame
ENST000003807493934842239348451In-frame

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Infer the effects of exon skipping event on protein functional features for HMGN1

p-ENSG00000205581_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
ENST00000380749140010039348422393484513323601625

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
ENST00000380749140010039348422393484513323601625
ENST00000380749140010039348292393483393624082641

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
P0511416251100ChainID=PRO_0000206691;Note=Non-histone chromosomal protein HMG-14
P0511416252121Modified residueNote=Phosphoserine%3B by RPS6KA5;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244|PubMed:23186163,ECO:0000269|PubMed:10739259;Dbxref=PMID:23186163,PMID:10739259
P0511416252525Modified residueNote=ADP-ribosylserine%3B alternate;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:28190768;Dbxref=PMID:28190768
P0511416252525Modified residueNote=Phosphoserine%3B alternate%3B by RPS6KA5;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244|PubMed:23186163,ECO:0000269|PubMed:10739259;Dbxref=PMID:23186163,PMID:10739259

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
P0511416251100ChainID=PRO_0000206691;Note=Non-histone chromosomal protein HMG-14
P0511416252121Modified residueNote=Phosphoserine%3B by RPS6KA5;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244|PubMed:23186163,ECO:0000269|PubMed:10739259;Dbxref=PMID:23186163,PMID:10739259
P0511416252525Modified residueNote=ADP-ribosylserine%3B alternate;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:28190768;Dbxref=PMID:28190768
P0511416252525Modified residueNote=Phosphoserine%3B alternate%3B by RPS6KA5;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244|PubMed:23186163,ECO:0000269|PubMed:10739259;Dbxref=PMID:23186163,PMID:10739259
P0511426411100ChainID=PRO_0000206691;Note=Non-histone chromosomal protein HMG-14
P0511426412727Modified residueNote=N6-acetyllysine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:P18608


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3'-UTR located exon skipping events that lost miRNA binding sites in HMGN1

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 HMGN1

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 HMGN1

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 HMGN1

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 HMGN1

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value
CBU2AF2exon_skip_264600-4.285394e-014.500692e-07
CBRBM3exon_skip_2646004.314056e-013.697090e-07
CBRBM45exon_skip_2646004.278342e-014.722511e-07
CBZNF638exon_skip_253477-4.215879e-013.125674e-08
CBRBM6exon_skip_253477-4.235781e-012.649815e-08
CBU2AF2exon_skip_253477-5.248471e-011.233212e-12
CBPCBP4exon_skip_2534775.123803e-015.059514e-12
CBSNRPAexon_skip_253477-4.340562e-011.091019e-08
CBRBM45exon_skip_2534775.889499e-013.207070e-16
CBRBM4exon_skip_253477-6.173935e-014.431007e-18
TCPCBP4exon_skip_2359545.221293e-011.433428e-12

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RelatedDrugs for HMGN1

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 HMGN1

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