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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 MYH10

check button Gene summary
Gene informationGene symbol

MYH10

Gene ID

4628

Gene namemyosin heavy chain 10
SynonymsNMMHC-IIB|NMMHCB
Cytomap

17p13.1

Type of geneprotein-coding
Descriptionmyosin-10cellular myosin heavy chain, type Bmyosin heavy chain, nonmuscle type Bmyosin, heavy chain 10, non-musclemyosin, heavy polypeptide 10, non-musclenonmuscle myosin II heavy chain-Bnonmuscle myosin heavy chain IIB
Modification date20200313
UniProtAcc

A5XEH4,

E7ERA5,

G1UI33,

P35580,

Context

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID
MYH10

GO:0000281

mitotic cytokinesis

15774463

MYH10

GO:0030048

actin filament-based movement

15845534


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Gene structures and expression levels for MYH10

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

ENSG00000133026
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
DLPFCDOWNENST00000476737.1MYH10-209:retained_intron:MYH103.480019e+00-1.441020e+001.595799e-051.987724e-03

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 MYH10

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_130930chr178521092:8521285:8530623:8530685:8535387:85355018530623:8530685
exon_skip_156140chr178622902:8623277:8623424:8623497:8630654:86307178623424:8623497
exon_skip_166433chr178569720:8569812:8576643:8576672:8577236:85773388576643:8576672
exon_skip_282392chr178535387:8535501:8535758:8535931:8542107:85422808535758:8535931
exon_skip_287981chr178577306:8577338:8589081:8589108:8604826:86048938589081:8589108
exon_skip_40531chr178508554:8508677:8509812:8509949:8512451:85126578509812:8509949
exon_skip_58188chr178569720:8569812:8576643:8576672:8577236:85772508576643:8576672
exon_skip_61793chr178569720:8569812:8576643:8576669:8577236:85772508576643:8576669
exon_skip_82295chr178569720:8569812:8576643:8576669:8577236:85773388576643:8576669
exon_skip_8838chr178493733:8493885:8495137:8495241:8499270:84994768495137:8495241

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_166433MSBB_PG7.297015e-018.522642e-01-1.225627e-017.708675e-04
exon_skip_166433Mayo_TC4.592500e-016.005263e-01-1.412763e-012.687869e-06


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Open reading frame (ORF) annotation in the exon skipping event for MYH10

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
ENST0000026924385890818589108Frame-shift
ENST0000026924385098128509949In-frame
ENST0000026924385357588535931In-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
ENST0000026924385890818589108Frame-shift

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
ENST0000026924385890818589108Frame-shift
ENST0000026924384951378495241In-frame
ENST0000026924385357588535931In-frame

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Infer the effects of exon skipping event on protein functional features for MYH10

p-ENSG00000133026_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
ENST00000269243767919768535758853593117151887525582
ENST00000269243767919768509812850994929993135953998

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
ENST00000269243767919768535758853593117151887525582
ENST0000026924376791976849513784952413998410112861320

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
P35580525582567569Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P35580525582572578Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P3558052558211976ChainID=PRO_0000123421;Note=Myosin-10
P3558052558285783DomainNote=Myosin motor;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00782
P35580525582531538HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P35580525582546556HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P3558095399811976ChainID=PRO_0000123421;Note=Myosin-10
P355809539988451976Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
P355809539989081976Natural variantID=VAR_078650;Note=Probable disease-associated mutation found in a patient with intrauterine growth restriction%2C microcephaly%2C developmental delay%2C failure to thrive%2C congenital bilateral hip dysplasia%2C cerebral and cerebellar atrophy%2C hydroce

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
P35580525582567569Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P35580525582572578Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P3558052558211976ChainID=PRO_0000123421;Note=Myosin-10
P3558052558285783DomainNote=Myosin motor;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00782
P35580525582531538HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P35580525582546556HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:4PD3
P355801286132011976ChainID=PRO_0000123421;Note=Myosin-10
P35580128613208451976Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
P355801286132013011301Modified residueNote=N6-acetyllysine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:Q61879
P35580128613209081976Natural variantID=VAR_078650;Note=Probable disease-associated mutation found in a patient with intrauterine growth restriction%2C microcephaly%2C developmental delay%2C failure to thrive%2C congenital bilateral hip dysplasia%2C cerebral and cerebellar atrophy%2C hydroce


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3'-UTR located exon skipping events that lost miRNA binding sites in MYH10

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 MYH10

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 MYH10

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 MYH10

check button sQTL information located at the skipped exons.
Tissue typeExon skip IDSNP idLocationP-valueFDR
TCexon_skip_156140rs8079726chr17:85318878.709034e-051.461436e-02

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Correlation with RNA binding proteins (RBPs) for MYH10

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value
CBHNRNPDLexon_skip_1309304.344660e-012.776358e-08
CBPUF60exon_skip_1309304.507369e-017.124628e-09
CBHNRNPKexon_skip_822954.337511e-017.460946e-07
FLRALYLexon_skip_1309305.855153e-014.674298e-19
FLNOVA1exon_skip_1309305.121972e-013.107531e-14
HCCTRNAU1APexon_skip_130930-4.627919e-011.247924e-15
HCCPTBP1exon_skip_130930-6.097612e-011.115484e-28
HCCSRSF5exon_skip_130930-4.012792e-018.633640e-12
HCCHNRNPFexon_skip_82295-5.546407e-012.248786e-22
HCCHNRNPA2B1exon_skip_166433-4.551577e-017.448036e-15
HCCSRSF1exon_skip_166433-4.003837e-011.514234e-11
HCCHNRNPFexon_skip_166433-6.217355e-011.591230e-29
IFGNOVA1exon_skip_1309304.358731e-012.041792e-02
IFGILF2exon_skip_822954.576838e-013.695589e-02
IFGHNRNPH2exon_skip_822954.895850e-012.427901e-02
IFGESRP1exon_skip_822954.813730e-012.714943e-02
IFGRBM25exon_skip_166433-4.130861e-012.890185e-02
IFGTRA2Aexon_skip_166433-4.317753e-012.177065e-02
PCCRALYLexon_skip_1309304.845299e-014.728434e-13
PCCPTBP1exon_skip_130930-5.626330e-016.328639e-18
PCCHNRNPFexon_skip_82295-4.791695e-011.572520e-12
PCCHNRNPFexon_skip_166433-5.578826e-012.405685e-17
PGHNRNPDLexon_skip_1309304.100310e-011.062378e-07
PGRALYLexon_skip_1309307.164666e-017.364269e-26
PGPTBP1exon_skip_130930-5.774906e-012.974237e-15
PGNOVA1exon_skip_1309305.556974e-015.082994e-14
PGILF2exon_skip_1664335.090153e-011.017598e-13
PGHNRNPKexon_skip_1664334.913903e-019.270425e-13
PGHNRNPLexon_skip_1664334.820877e-012.830195e-12
PGHNRNPH2exon_skip_1664335.894557e-016.987742e-19
STGRALYLexon_skip_1309305.884115e-016.122263e-09
STGNOVA1exon_skip_1309304.140061e-011.104404e-04
STGILF2exon_skip_1664335.107032e-015.065141e-07
STGHNRNPKexon_skip_1664334.789781e-013.082825e-06
STGHNRNPLexon_skip_1664335.362510e-011.029682e-07
STGHNRNPH2exon_skip_1664335.741034e-017.515388e-09
TCHNRNPDLexon_skip_1309305.295508e-018.833632e-12
TCRALYLexon_skip_1309308.227718e-011.164502e-36
TCPTBP1exon_skip_130930-4.036212e-015.266843e-07
TCPTBP3exon_skip_1309304.786102e-011.298902e-09
TCSRSF5exon_skip_1309304.863652e-016.400284e-10
TCNOVA1exon_skip_1309307.351897e-019.508566e-26
TCILF2exon_skip_822955.155435e-014.367523e-09
TCHNRNPKexon_skip_822954.172643e-013.864480e-06
TCHNRNPLexon_skip_822954.013737e-019.606548e-06
TCSRSF1exon_skip_822954.128182e-015.009378e-06
TCHNRNPH2exon_skip_822956.926277e-011.381945e-17
TCESRP1exon_skip_822956.051060e-019.983549e-13
TCRBM25exon_skip_1664334.363404e-019.819272e-08
TCILF2exon_skip_1664335.445422e-016.052693e-12
TCHNRNPKexon_skip_1664334.156649e-014.392260e-07
TCHNRNPLexon_skip_1664334.619552e-011.329435e-08
TCHNRNPH2exon_skip_1664337.351974e-011.479826e-24
TCESRP1exon_skip_1664335.969476e-011.375628e-14

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RelatedDrugs for MYH10

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 MYH10

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