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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 ACSM2B

check button Gene summary
Gene informationGene symbol

ACSM2B

Gene ID

348158

Gene nameacyl-CoA synthetase medium chain family member 2B
SynonymsACSM2|HXMA|HYST1046
Cytomap

16p12.3

Type of geneprotein-coding
Descriptionacyl-coenzyme A synthetase ACSM2B, mitochondrialacyl-CoA synthetase medium-chain family member 2butyrate--CoA ligase 2Bbutyryl-coenzyme A synthetase 2Bmiddle-chain acyl-CoA synthetase 2Bxenobiotic/medium-chain fatty acid-CoA ligase HXM-Axenobiotic/m
Modification date20180523
UniProtAcc

Q68CK6

ContextPubMed: ACSM2B [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

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Exon skipping events across known transcript of Ensembl for ACSM2B 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 ACSM2B

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 ACSM2B

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1427751620551975:20552095:20554235:20554335:20554456:2055458420554235:20554335ENSG00000066813.10ENST00000565232.1,ENST00000566998.1,ENST00000329697.6,ENST00000565322.1,ENST00000567001.1
exon_skip_1427911620557721:20557796:20559383:20559507:20559715:2055979520559383:20559507ENSG00000066813.10ENST00000565232.1,ENST00000329697.6,ENST00000569364.1,ENST00000567288.1,ENST00000563943.1,ENST00000565322.1,ENST00000567001.1
exon_skip_1427981620559383:20559507:20559715:20559795:20563465:2056361920559715:20559795ENSG00000066813.10ENST00000565232.1,ENST00000329697.6,ENST00000569364.1,ENST00000567288.1,ENST00000563943.1,ENST00000565322.1,ENST00000567001.1
exon_skip_1428011620559715:20559795:20563465:20563619:20565098:2056514520563465:20563619ENSG00000066813.10ENST00000565232.1,ENST00000569327.1,ENST00000329697.6,ENST00000569364.1,ENST00000567288.1,ENST00000563943.1,ENST00000565322.1,ENST00000567001.1
exon_skip_1428061620560932:20561200:20563465:20563619:20565098:2056514520563465:20563619ENSG00000066813.10ENST00000569163.1
exon_skip_1428091620563465:20563619:20565098:20565242:20566590:2056661620565098:20565242ENSG00000066813.10ENST00000565232.1,ENST00000329697.6,ENST00000569163.1,ENST00000569364.1,ENST00000563943.1,ENST00000565322.1,ENST00000567001.1
exon_skip_1428111620565098:20565242:20565356:20565499:20566590:2056679820565356:20565499ENSG00000066813.10ENST00000569327.1
exon_skip_1428131620566764:20566798:20570558:20570769:20575990:2057617520570558:20570769ENSG00000066813.10ENST00000565232.1,ENST00000569327.1,ENST00000329697.6,ENST00000569364.1,ENST00000414188.2,ENST00000567001.1
exon_skip_1428141620570629:20570769:20575990:20576175:20586743:2058677820575990:20576175ENSG00000066813.10ENST00000565232.1,ENST00000566384.1,ENST00000569344.1,ENST00000567001.1
exon_skip_1428151620570629:20570769:20575990:20576175:20587528:2058759920575990:20576175ENSG00000066813.10ENST00000569327.1,ENST00000569364.1,ENST00000414188.2
exon_skip_1428171620570629:20570769:20586743:20586822:20587528:2058774920586743:20586822ENSG00000066813.10ENST00000568882.1
exon_skip_1428211620575990:20576175:20586743:20586778:20587528:2058759920586743:20586778ENSG00000066813.10ENST00000567001.1
exon_skip_1428231620575990:20576175:20586743:20586829:20587528:2058759920586743:20586829ENSG00000066813.10ENST00000569344.1
exon_skip_1428241620575990:20576175:20586743:20586871:20587528:2058759920586743:20586871ENSG00000066813.10ENST00000566384.1
exon_skip_1428251620575990:20576175:20586743:20587125:20587528:2058759920586743:20587125ENSG00000066813.10ENST00000565232.1
exon_skip_1428281620585630:20585967:20586743:20586829:20587528:2058759920586743:20586829ENSG00000066813.10ENST00000562026.1

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

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Exon skipping events with PSIs in GTEx for ACSM2B

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1427751620551975:20552095:20554235:20554335:20554456:2055458420554235:20554335ENSG00000066813.10ENST00000329697.6,ENST00000566998.1,ENST00000565322.1,ENST00000565232.1,ENST00000567001.1
exon_skip_1427911620557721:20557796:20559383:20559507:20559715:2055979520559383:20559507ENSG00000066813.10ENST00000329697.6,ENST00000565322.1,ENST00000565232.1,ENST00000567001.1,ENST00000569364.1,ENST00000563943.1,ENST00000567288.1
exon_skip_1427981620559383:20559507:20559715:20559795:20563465:2056361920559715:20559795ENSG00000066813.10ENST00000329697.6,ENST00000565322.1,ENST00000565232.1,ENST00000567001.1,ENST00000569364.1,ENST00000563943.1,ENST00000567288.1
exon_skip_1428011620559715:20559795:20563465:20563619:20565098:2056514520563465:20563619ENSG00000066813.10ENST00000329697.6,ENST00000565322.1,ENST00000565232.1,ENST00000567001.1,ENST00000569364.1,ENST00000563943.1,ENST00000567288.1,ENST00000569327.1
exon_skip_1428091620563465:20563619:20565098:20565242:20566590:2056661620565098:20565242ENSG00000066813.10ENST00000329697.6,ENST00000565322.1,ENST00000565232.1,ENST00000567001.1,ENST00000569364.1,ENST00000563943.1,ENST00000569163.1
exon_skip_1428131620566764:20566798:20570558:20570769:20575990:2057617520570558:20570769ENSG00000066813.10ENST00000329697.6,ENST00000565232.1,ENST00000567001.1,ENST00000569364.1,ENST00000569327.1,ENST00000414188.2
exon_skip_1428151620570629:20570769:20575990:20576175:20587528:2058759920575990:20576175ENSG00000066813.10ENST00000569364.1,ENST00000569327.1,ENST00000414188.2
exon_skip_1428211620575990:20576175:20586743:20586778:20587528:2058759920586743:20586778ENSG00000066813.10ENST00000567001.1
exon_skip_1428231620575990:20576175:20586743:20586829:20587528:2058759920586743:20586829ENSG00000066813.10ENST00000569344.1
exon_skip_1428241620575990:20576175:20586743:20586871:20587528:2058759920586743:20586871ENSG00000066813.10ENST00000566384.1
exon_skip_1428251620575990:20576175:20586743:20587125:20587528:2058759920586743:20587125ENSG00000066813.10ENST00000565232.1
exon_skip_1428281620585630:20585967:20586743:20586829:20587528:2058759920586743:20586829ENSG00000066813.10ENST00000562026.1

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 ACSM2B

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
ENST0000041418820575990205761753UTR-3CDS
ENST0000056523220575990205761753UTR-3CDS
ENST0000056700120575990205761753UTR-3CDS
ENST0000056523220586743205871253UTR-3UTR
ENST0000056700120586743205867783UTR-3UTR
ENST000003296972055423520554335Frame-shift
ENST000005652322055423520554335Frame-shift
ENST000005670012055423520554335Frame-shift
ENST000003296972055938320559507Frame-shift
ENST000005652322055938320559507Frame-shift
ENST000005670012055938320559507Frame-shift
ENST000003296972055971520559795Frame-shift
ENST000005652322055971520559795Frame-shift
ENST000005670012055971520559795Frame-shift
ENST000003296972056346520563619Frame-shift
ENST000005652322056346520563619Frame-shift
ENST000005670012056346520563619Frame-shift
ENST000003296972057055820570769Frame-shift
ENST000004141882057055820570769Frame-shift
ENST000005652322057055820570769Frame-shift
ENST000005670012057055820570769Frame-shift
ENST000003296972056509820565242In-frame
ENST000005652322056509820565242In-frame
ENST000005670012056509820565242In-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
ENST0000041418820575990205761753UTR-3CDS
ENST0000056523220586743205871253UTR-3UTR
ENST0000056700120586743205867783UTR-3UTR
ENST000003296972055423520554335Frame-shift
ENST000005652322055423520554335Frame-shift
ENST000005670012055423520554335Frame-shift
ENST000003296972055938320559507Frame-shift
ENST000005652322055938320559507Frame-shift
ENST000005670012055938320559507Frame-shift
ENST000003296972055971520559795Frame-shift
ENST000005652322055971520559795Frame-shift
ENST000005670012055971520559795Frame-shift
ENST000003296972056346520563619Frame-shift
ENST000005652322056346520563619Frame-shift
ENST000005670012056346520563619Frame-shift
ENST000003296972057055820570769Frame-shift
ENST000004141882057055820570769Frame-shift
ENST000005652322057055820570769Frame-shift
ENST000005670012057055820570769Frame-shift
ENST000003296972056509820565242In-frame
ENST000005652322056509820565242In-frame
ENST000005670012056509820565242In-frame

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Infer the effects of exon skipping event on protein functional features for ACSM2B

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
ENST0000032969729525772056509820565242766909199246
ENST000005652322339577205650982056524210671210199246
ENST0000056700120055772056509820565242738881199246

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
ENST0000032969729525772056509820565242766909199246
ENST000005652322339577205650982056524210671210199246
ENST0000056700120055772056509820565242738881199246

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
Q68CK619924647577ChainID=PRO_0000306094;Note=Acyl-coenzyme A synthetase ACSM2B%2C mitochondrial
Q68CK619924647577ChainID=PRO_0000306094;Note=Acyl-coenzyme A synthetase ACSM2B%2C mitochondrial
Q68CK619924647577ChainID=PRO_0000306094;Note=Acyl-coenzyme A synthetase ACSM2B%2C mitochondrial
Q68CK6199246221229Nucleotide bindingNote=ATP;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q68CK6199246221229Nucleotide bindingNote=ATP;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q68CK6199246221229Nucleotide bindingNote=ATP;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
Q68CK619924647577ChainID=PRO_0000306094;Note=Acyl-coenzyme A synthetase ACSM2B%2C mitochondrial
Q68CK619924647577ChainID=PRO_0000306094;Note=Acyl-coenzyme A synthetase ACSM2B%2C mitochondrial
Q68CK619924647577ChainID=PRO_0000306094;Note=Acyl-coenzyme A synthetase ACSM2B%2C mitochondrial
Q68CK6199246221229Nucleotide bindingNote=ATP;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q68CK6199246221229Nucleotide bindingNote=ATP;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q68CK6199246221229Nucleotide bindingNote=ATP;Ontology_term=ECO:0000250;evidence=ECO:0000250


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SNVs in the skipped exons for ACSM2B

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.
ACSM2B_KIRP_exon_skip_142791_psi_boxplot.png
boxplot
ACSM2B_LIHC_exon_skip_142791_psi_boxplot.png
boxplot

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
LIHCTCGA-G3-A3CJ-01exon_skip_142791
20559384205595072055940520559405Frame_Shift_DelT-p.E359fs
LIHCTCGA-DD-A39Y-01exon_skip_142813
20570559205707692057057320570573Frame_Shift_DelC-p.G125fs
LIHCTCGA-DD-A39Y-01exon_skip_142813
20570559205707692057060420570604Frame_Shift_DelG-p.R115fs
LIHCTCGA-DD-A1EG-01exon_skip_142813
20570559205707692057071320570713Frame_Shift_DelT-p.E78fs
LIHCTCGA-DD-A3A0-01exon_skip_142813
20570559205707692057071920570719Frame_Shift_DelC-p.G76fs
LIHCTCGA-BC-A112-01exon_skip_142813
20570559205707692057068020570681Frame_Shift_Ins-Tp.K89fs
UCECTCGA-B5-A0JY-01exon_skip_142791
20559384205595072055940720559407Nonsense_MutationCAp.E359*
CESCTCGA-FU-A57G-01exon_skip_142791
20559384205595072055941020559410Nonsense_MutationGAp.R358*
STADTCGA-BR-4369-01exon_skip_142791
20559384205595072055947320559473Nonsense_MutationCAp.G337*
STADTCGA-BR-4369-01exon_skip_142791
20559384205595072055947320559473Nonsense_MutationCAp.G337X
KIRPTCGA-A4-A48D-01exon_skip_142791
20559384205595072055948820559488Nonsense_MutationGAp.Q332*
KIRPTCGA-A4-A48D-01exon_skip_142791
20559384205595072055948820559488Nonsense_MutationGAp.Q332X
SKCMTCGA-D3-A3ML-06exon_skip_142801
exon_skip_142806
20563466205636192056356520563565Nonsense_MutationCTp.W265*
SKCMTCGA-D3-A3ML-06exon_skip_142801
exon_skip_142806
20563466205636192056356520563565Nonsense_MutationCTp.W265X
SKCMTCGA-EE-A183-06exon_skip_142801
exon_skip_142806
20563466205636192056356520563565Nonsense_MutationCTp.W265*
SKCMTCGA-EE-A183-06exon_skip_142801
exon_skip_142806
20563466205636192056356520563565Nonsense_MutationCTp.W265X
SKCMTCGA-EE-A2GC-06exon_skip_142801
exon_skip_142806
20563466205636192056356520563565Nonsense_MutationCTp.W265*
SKCMTCGA-EE-A2GC-06exon_skip_142801
exon_skip_142806
20563466205636192056356520563565Nonsense_MutationCTp.W265X
LUADTCGA-80-5608-01exon_skip_142809
20565099205652422056513220565132Nonsense_MutationGTp.S236*
READTCGA-F5-6814-01exon_skip_142813
20570559205707692057069420570694Nonsense_MutationCAp.E85X
SKCMTCGA-FR-A726-01exon_skip_142813
20570559205707692057070420570704Nonsense_MutationCTp.W81*
UCECTCGA-BS-A0UF-01exon_skip_142815
exon_skip_142814
20575991205761752057600720576007Nonsense_MutationCTp.W54*
SKCMTCGA-D9-A6EC-06exon_skip_142815
exon_skip_142814
20575991205761752057614620576146Nonsense_MutationGAp.Q8*
SKCMTCGA-D9-A6EC-06exon_skip_142815
exon_skip_142814
20575991205761752057614620576146Nonsense_MutationGAp.Q8X
BLCATCGA-ZF-AA5N-01exon_skip_142815
exon_skip_142814
20575991205761752057615520576155Nonsense_MutationGAp.R5*
BRCATCGA-AN-A0XN-01exon_skip_142815
exon_skip_142814
20575991205761752057615520576155Nonsense_MutationGAp.R5*
LGGTCGA-RY-A840-01exon_skip_142815
exon_skip_142814
20575991205761752057615520576155Nonsense_MutationGAp.R5*
SKCMTCGA-ER-A19M-06exon_skip_142815
exon_skip_142814
20575991205761752057617720576177Splice_SiteTA.

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description
ACSM2B_20557721_20557796_20559383_20559507_20559715_20559795_TCGA-A4-A48D-01Sample: TCGA-A4-A48D-01
Cancer type: KIRP
ESID: exon_skip_142791
Skipped exon start: 20559384
Skipped exon end: 20559507
Mutation start: 20559488
Mutation end: 20559488
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: A
AAchange: p.Q332X
ACSM2B_20557721_20557796_20559383_20559507_20559715_20559795_TCGA-A4-A48D-01Sample: TCGA-A4-A48D-01
Cancer type: KIRP
ESID: exon_skip_142791
Skipped exon start: 20559384
Skipped exon end: 20559507
Mutation start: 20559488
Mutation end: 20559488
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: A
AAchange: p.Q332*
exon_skip_142791_KIRP_TCGA-A4-A48D-01.png
boxplot
exon_skip_484457_KIRP_TCGA-A4-A48D-01.png
boxplot
exon_skip_489149_KIRP_TCGA-A4-A48D-01.png
boxplot
exon_skip_75089_KIRP_TCGA-A4-A48D-01.png
boxplot

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
SW1088_CENTRAL_NERVOUS_SYSTEM20554236205543352055424720554247Missense_MutationCTp.V500I
NCIH847_LUNG20554236205543352055425820554258Missense_MutationCAp.S496I
SUPB15_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE20559384205595072055943820559438Missense_MutationGTp.N348K
SNU81_LARGE_INTESTINE20559384205595072055945020559450Missense_MutationTAp.E344D
MM383_SKIN20559384205595072055945520559455Missense_MutationGAp.P343S
NCIH1793_LUNG20559384205595072055947220559472Missense_MutationCAp.G337V
MEWO_SKIN20559384205595072055949620559496Missense_MutationGAp.P329L
NCIH2286_LUNG20559384205595072055949720559497Missense_MutationGCp.P329A
SNU1105_CENTRAL_NERVOUS_SYSTEM20559716205597952055974320559743Missense_MutationCTp.R316Q
NCIH345_LUNG20563466205636192056355020563550Missense_MutationCAp.L270F
HS939T_SKIN20563466205636192056357020563570Missense_MutationCTp.G264S
DAOY_CENTRAL_NERVOUS_SYSTEM20563466205636192056359720563597Missense_MutationCAp.D255Y
T84_LARGE_INTESTINE20565099205652422056510220565102Missense_MutationGAp.A246V
COLO794_SKIN20565099205652422056519920565199Missense_MutationCTp.E214K
COLO741_SKIN20565099205652422056519920565199Missense_MutationCTp.E214K
COLO800_SKIN20565099205652422056519920565199Missense_MutationCTp.E214K
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE20565099205652422056522020565220Missense_MutationAGp.C207R
VMRCLCD_LUNG20565099205652422056523420565234Missense_MutationGCp.S202C
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE20570559205707692057056420570564Missense_MutationCTp.R128Q
ESO26_OESOPHAGUS20570559205707692057061320570613Missense_MutationTCp.M112V
HUTU80_SMALL_INTESTINE20570559205707692057061320570613Missense_MutationTCp.M112V
LAMA84_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE20570559205707692057061320570613Missense_MutationTCp.M112V
NCIH838_LUNG20570559205707692057061320570613Missense_MutationTCp.M112V
SNU119_OVARY20570559205707692057061320570613Missense_MutationTCp.M112V
CCRFCEM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE20570559205707692057062420570624Missense_MutationCTp.R108H
CORL303_LUNG20570559205707692057071520570715Missense_MutationCTp.E78K
KYSE270_OESOPHAGUS20575991205761752057602320576023Missense_MutationCTp.D49N
NCIH345_LUNG20575991205761752057604320576043Missense_MutationGTp.A42D
A2058_SKIN20575991205761752057610120576101Missense_MutationGAp.L23F
CORL24_LUNG20575991205761752057612620576127Missense_MutationCCAAp.W14F
CORL24_LUNG20575991205761752057612620576126Missense_MutationCAp.W14C
CORL24_LUNG20575991205761752057612720576127Missense_MutationCAp.W14L
MCC13_SKIN20575991205761752057614320576143Missense_MutationCTp.G9R
NCIBL1395_MATCHED_NORMAL_TISSUE20559384205595072055942820559428Nonsense_MutationGAp.Q352*
NCIH1395_LUNG20559384205595072055942820559428Nonsense_MutationGAp.Q352*
ZR751_BREAST20575991205761752057606320576063Nonsense_MutationCTp.W35*
LN215_CENTRAL_NERVOUS_SYSTEM20563466205636192056346620563466Splice_SiteCAp.K298N

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ACSM2B

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value
exon_skip_1428251620575990:20576175:20586743:20587125:20587528:2058759920586743:20587125ENST00000565232.1KIRCrs76447095chr16:20586919C/G2.72e-03
exon_skip_1428251620575990:20576175:20586743:20587125:20587528:2058759920586743:20587125ENST00000565232.1PCPGrs76447095chr16:20586919C/G5.18e-04
exon_skip_1428111620565098:20565242:20565356:20565499:20566590:2056679820565356:20565499ENST00000569327.1KIRCrs6497500chr16:20565396C/T1.29e-03
exon_skip_1428111620565098:20565242:20565356:20565499:20566590:2056679820565356:20565499ENST00000569327.1KIRCrs6497500chr16:20565396C/T2.99e-03
exon_skip_1428111620565098:20565242:20565356:20565499:20566590:2056679820565356:20565499ENST00000569327.1PCPGrs6497500chr16:20565396C/T2.62e-04
exon_skip_1428151620570629:20570769:20575990:20576175:20587528:2058759920575990:20576175ENST00000569327.1,ENST00000569364.1,ENST00000414188.2KIRCrs112352583chr16:20576048C/A3.14e-04
exon_skip_1428151620570629:20570769:20575990:20576175:20587528:2058759920575990:20576175ENST00000569327.1,ENST00000569364.1,ENST00000414188.2KIRCrs112352583chr16:20576048C/A2.15e-03
exon_skip_1428151620570629:20570769:20575990:20576175:20587528:2058759920575990:20576175ENST00000569327.1,ENST00000569364.1,ENST00000414188.2PCPGrs112352583chr16:20576048C/A7.33e-04
exon_skip_1428141620570629:20570769:20575990:20576175:20586743:2058677820575990:20576175ENST00000565232.1,ENST00000566384.1,ENST00000569344.1,ENST00000567001.1KIRCrs112352583chr16:20576048C/A3.14e-04
exon_skip_1428141620570629:20570769:20575990:20576175:20586743:2058677820575990:20576175ENST00000565232.1,ENST00000566384.1,ENST00000569344.1,ENST00000567001.1KIRCrs112352583chr16:20576048C/A2.15e-03
exon_skip_1428141620570629:20570769:20575990:20576175:20586743:2058677820575990:20576175ENST00000565232.1,ENST00000566384.1,ENST00000569344.1,ENST00000567001.1PCPGrs112352583chr16:20576048C/A7.33e-04

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ACSM2B


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ACSM2B


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RelatedDrugs for ACSM2B

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 ACSM2B

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