ExonSkipDB: functional annotation of exon skipping event in human

Gene summary for ARPC2

Gene summary

Gene information	Gene symbol	ARPC2
	Gene ID	10109
	Gene name	actin related protein 2/3 complex subunit 2
	Synonyms	ARC34\|PNAS-139\|PRO2446\|p34-Arc
	Cytomap	2q35
	Type of gene	protein-coding
	Description	actin-related protein 2/3 complex subunit 2ARP2/3 protein complex subunit 34actin related protein 2/3 complex, subunit 2, 34kDaarp2/3 complex 34 kDa subunittestis tissue sperm-binding protein Li 53e
	Modification date	20180523
	UniProtAcc	O15144
	Context	PubMed: ARPC2 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract] - Title (PMID)

Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez

Gene	GO ID	GO term	PubMed ID
ARPC2	GO:0034314	Arp2/3 complex-mediated actin nucleation	11741539

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Exon skipping events across known transcript of Ensembl for ARPC2 from UCSC genome browser

Skipped 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.

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Gene isoform structures and expression levels for ARPC2

Expression levels of gene isoforms across TCGA.

Expression levels of gene isoforms across GTEx.

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Exon skipping events with PSIs in TCGA for ARPC2

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENSG00000163466.11	ENST00000420104.1
exon_skip_333425	2	219081924:219081977:219082185:219082267:219090642:219090677	219082185:219082267	ENSG00000163466.11	ENST00000420201.1,ENST00000489598.1,ENST00000414983.1,ENST00000491780.1
exon_skip_333427	2	219082185:219082267:219090642:219090677:219093460:219093519	219090642:219090677	ENSG00000163466.11	ENST00000465395.1,ENST00000420201.1,ENST00000295685.10,ENST00000489598.1,ENST00000315717.5,ENST00000420104.1,ENST00000491780.1
exon_skip_333429	2	219090642:219090677:219091718:219091820:219093460:219093519	219091718:219091820	ENSG00000163466.11	ENST00000414983.1
exon_skip_333433	2	219090642:219090677:219093460:219093573:219099074:219099120	219093460:219093573	ENSG00000163466.11	ENST00000480062.1,ENST00000465395.1,ENST00000420201.1,ENST00000295685.10,ENST00000489598.1,ENST00000315717.5,ENST00000420104.1,ENST00000491780.1
exon_skip_333434	2	219090642:219090677:219093460:219093573:219103386:219103446	219093460:219093573	ENSG00000163466.11	ENST00000472753.1,ENST00000478612.1
exon_skip_333447	2	219093525:219093573:219099074:219099120:219103386:219103446	219099074:219099120	ENSG00000163466.11	ENST00000465395.1,ENST00000295685.10,ENST00000414983.1,ENST00000315717.5
exon_skip_333455	2	219093525:219093573:219103386:219103573:219104113:219104207	219103386:219103573	ENSG00000163466.11	ENST00000478612.1
exon_skip_333460	2	219099074:219099120:219099571:219099767:219103386:219103446	219099571:219099767	ENSG00000163466.11	ENST00000480062.1,ENST00000420201.1
exon_skip_333464	2	219099074:219099120:219103386:219103573:219104113:219104207	219103386:219103573	ENSG00000163466.11	ENST00000295685.10,ENST00000414983.1,ENST00000315717.5,ENST00000470146.1
exon_skip_333471	2	219099582:219099767:219101091:219101456:219103386:219103446	219101091:219101456	ENSG00000163466.11	ENST00000484961.1
exon_skip_333473	2	219103441:219103573:219104113:219104207:219110142:219110180	219104113:219104207	ENSG00000163466.11	ENST00000478612.1,ENST00000477992.1,ENST00000295685.10,ENST00000315717.5,ENST00000470146.1
exon_skip_333475	2	219104113:219104207:219110142:219110269:219114086:219114187	219110142:219110269	ENSG00000163466.11	ENST00000477992.1,ENST00000295685.10,ENST00000315717.5,ENST00000470146.1
exon_skip_333479	2	219114086:219114187:219114543:219114644:219118613:219118831	219114543:219114644	ENSG00000163466.11	ENST00000477992.1,ENST00000295685.10,ENST00000315717.5,ENST00000470146.1
exon_skip_333480	2	219114543:219114644:219117667:219117755:219118613:219118831	219117667:219117755	ENSG00000163466.11	ENST00000456575.1

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for ARPC2

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENSG00000163466.11	ENST00000420104.1
exon_skip_333425	2	219081924:219081977:219082185:219082267:219090642:219090677	219082185:219082267	ENSG00000163466.11	ENST00000489598.1,ENST00000491780.1,ENST00000420201.1,ENST00000414983.1
exon_skip_333427	2	219082185:219082267:219090642:219090677:219093460:219093519	219090642:219090677	ENSG00000163466.11	ENST00000315717.5,ENST00000420104.1,ENST00000489598.1,ENST00000491780.1,ENST00000420201.1,ENST00000295685.10,ENST00000465395.1
exon_skip_333429	2	219090642:219090677:219091718:219091820:219093460:219093519	219091718:219091820	ENSG00000163466.11	ENST00000414983.1
exon_skip_333433	2	219090642:219090677:219093460:219093573:219099074:219099120	219093460:219093573	ENSG00000163466.11	ENST00000315717.5,ENST00000420104.1,ENST00000489598.1,ENST00000491780.1,ENST00000420201.1,ENST00000480062.1,ENST00000295685.10,ENST00000465395.1
exon_skip_333434	2	219090642:219090677:219093460:219093573:219103386:219103446	219093460:219093573	ENSG00000163466.11	ENST00000478612.1,ENST00000472753.1
exon_skip_333447	2	219093525:219093573:219099074:219099120:219103386:219103446	219099074:219099120	ENSG00000163466.11	ENST00000315717.5,ENST00000414983.1,ENST00000295685.10,ENST00000465395.1
exon_skip_333455	2	219093525:219093573:219103386:219103573:219104113:219104207	219103386:219103573	ENSG00000163466.11	ENST00000478612.1
exon_skip_333460	2	219099074:219099120:219099571:219099767:219103386:219103446	219099571:219099767	ENSG00000163466.11	ENST00000420201.1,ENST00000480062.1
exon_skip_333464	2	219099074:219099120:219103386:219103573:219104113:219104207	219103386:219103573	ENSG00000163466.11	ENST00000315717.5,ENST00000414983.1,ENST00000295685.10,ENST00000470146.1
exon_skip_333471	2	219099582:219099767:219101091:219101456:219103386:219103446	219101091:219101456	ENSG00000163466.11	ENST00000484961.1
exon_skip_333473	2	219103441:219103573:219104113:219104207:219110142:219110180	219104113:219104207	ENSG00000163466.11	ENST00000315717.5,ENST00000478612.1,ENST00000295685.10,ENST00000470146.1,ENST00000477992.1
exon_skip_333475	2	219104113:219104207:219110142:219110269:219114086:219114187	219110142:219110269	ENSG00000163466.11	ENST00000315717.5,ENST00000295685.10,ENST00000470146.1,ENST00000477992.1
exon_skip_333479	2	219114086:219114187:219114543:219114644:219118613:219118831	219114543:219114644	ENSG00000163466.11	ENST00000315717.5,ENST00000295685.10,ENST00000470146.1,ENST00000477992.1
exon_skip_333480	2	219114543:219114644:219117667:219117755:219118613:219118831	219117667:219117755	ENSG00000163466.11	ENST00000456575.1

PSI values of skipped exons in GTEx.

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for ARPC2

Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.

ENST	Start of skipped exon	End of skipped exon	ORF
ENST00000295685	219090642	219090677	Frame-shift
ENST00000315717	219090642	219090677	Frame-shift
ENST00000295685	219093460	219093573	Frame-shift
ENST00000315717	219093460	219093573	Frame-shift
ENST00000295685	219099074	219099120	Frame-shift
ENST00000315717	219099074	219099120	Frame-shift
ENST00000295685	219103386	219103573	Frame-shift
ENST00000315717	219103386	219103573	Frame-shift
ENST00000295685	219104113	219104207	Frame-shift
ENST00000315717	219104113	219104207	Frame-shift
ENST00000295685	219110142	219110269	Frame-shift
ENST00000315717	219110142	219110269	Frame-shift
ENST00000295685	219114543	219114644	Frame-shift
ENST00000315717	219114543	219114644	Frame-shift

Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.

ENST	Start of skipped exon	End of skipped exon	ORF
ENST00000295685	219090642	219090677	Frame-shift
ENST00000315717	219090642	219090677	Frame-shift
ENST00000295685	219093460	219093573	Frame-shift
ENST00000315717	219093460	219093573	Frame-shift
ENST00000295685	219099074	219099120	Frame-shift
ENST00000315717	219099074	219099120	Frame-shift
ENST00000295685	219103386	219103573	Frame-shift
ENST00000315717	219103386	219103573	Frame-shift
ENST00000295685	219104113	219104207	Frame-shift
ENST00000315717	219104113	219104207	Frame-shift
ENST00000295685	219110142	219110269	Frame-shift
ENST00000315717	219110142	219110269	Frame-shift
ENST00000295685	219114543	219114644	Frame-shift
ENST00000315717	219114543	219114644	Frame-shift

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Infer the effects of exon skipping event on protein functional features for ARPC2

Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.

Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.

ENST

Length of mRNA

Length of AA seq.

Genomic start

Genomic end

mRNA start

mRNA end

AA start

AA end

Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.

ENST

Length of mRNA

Length of AA seq.

Genomic start

Genomic end

mRNA start

mRNA end

AA start

AA end

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 feature

Description of feature

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 feature

Description of feature

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SNVs in the skipped exons for ARPC2

- Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.

- Differential PSIs between mutated versus non-mutated samples.

- Non-synonymous mutations located in the skipped exons in TCGA.

Cancer type	Sample	ESID	Skipped exon start	Skipped exon end	Mutation start	Mutation end	Mutation type	Reference seq	Mutation seq	AAchange
LIHC	TCGA-DD-A3A0-01	exon_skip_333464 exon_skip_333455	219103387	219103573	219103400	219103400	Frame_Shift_Del	T	-	p.S94fs
GBM	TCGA-32-1979-01	exon_skip_333464 exon_skip_333455	219103387	219103573	219103491	219103492	Frame_Shift_Del	TT	-	p.F125fs
LIHC	TCGA-DD-A1EG-01	exon_skip_333473	219104114	219104207	219104127	219104127	Frame_Shift_Del	A	-	p.K158fs
LIHC	TCGA-DD-A3A0-01	exon_skip_333473	219104114	219104207	219104127	219104127	Frame_Shift_Del	A	-	p.K158fs
ACC	TCGA-OR-A5LD-01	exon_skip_333464 exon_skip_333455	219103387	219103573	219103504	219103505	Frame_Shift_Ins	-	C	p.S129fs
STAD	TCGA-BR-8363-01	exon_skip_333447	219099075	219099120	219099093	219099093	Nonsense_Mutation	G	T	p.E81X
BLCA	TCGA-XF-AAN5-01	exon_skip_333479	219114544	219114644	219114619	219114619	Nonsense_Mutation	G	T	p.E285*

- Depth of coverage in the three exons composing exon skipping event

Depth of coverage in three exons

Mutation description

- Non-synonymous mutations located in the skipped exons in CCLE.

Sample	Skipped exon start	Skipped exon end	Mutation start	Mutation end	Mutation type	Reference seq	Mutation seq	AAchange
LOVO_LARGE_INTESTINE	219090643	219090677	219090651	219090651	Missense_Mutation	C	T	p.P28L
KMS18_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	219103387	219103573	219103393	219103393	Missense_Mutation	A	G	p.N92S
HEC6_ENDOMETRIUM	219103387	219103573	219103419	219103419	Missense_Mutation	A	T	p.N101Y
PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	219103387	219103573	219103447	219103447	Missense_Mutation	T	C	p.V110A
HCC38_BREAST	219103387	219103573	219103535	219103535	Missense_Mutation	G	C	p.E139D
MHHPREB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	219110143	219110269	219110176	219110176	Missense_Mutation	G	A	p.A195T
NUGC2_STOMACH	219110143	219110269	219110224	219110224	Missense_Mutation	G	C	p.D211H
H9_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	219110143	219110269	219110245	219110245	Missense_Mutation	G	A	p.D218N
PACADD137_PANCREAS	219114544	219114644	219114602	219114602	Missense_Mutation	G	A	p.R279H
LS411N_LARGE_INTESTINE	219103387	219103573	219103572	219103572	Splice_Site	A	G	p.M152V
NCIH740_LUNG	219104114	219104207	219104207	219104207	Splice_Site	G	T	p.Q183H

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ARPC2

sQTL information located at the skipped exons.

Exon skip ID	Chromosome	Three exons	Skippped exon	ENST	Cancer type	SNP id	Location	DNA change (ref/var)	P-value
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	GBM	rs2271541	chr2:219082119	G/T	3.11e-13
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	GBM	rs2271541	chr2:219082119	G/T	1.73e-06
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	CESC	rs2271541	chr2:219082119	G/T	1.17e-06
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	CESC	rs2271541	chr2:219082119	G/T	7.87e-06
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	COAD	rs2271541	chr2:219082119	G/T	1.78e-19
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	COAD	rs2271541	chr2:219082119	G/T	2.05e-12
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	BLCA	rs2271541	chr2:219082119	G/T	6.50e-22
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	BLCA	rs2271541	chr2:219082119	G/T	9.70e-12
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	ESCA	rs2271541	chr2:219082119	G/T	2.62e-11
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	ESCA	rs2271541	chr2:219082119	G/T	3.07e-07
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	HNSC	rs2271541	chr2:219082119	G/T	2.01e-30
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	HNSC	rs2271541	chr2:219082119	G/T	2.16e-11
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LAML	rs2271541	chr2:219082119	G/T	4.05e-09
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LAML	rs2271541	chr2:219082119	G/T	4.07e-05
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	KIRP	rs2271541	chr2:219082119	G/T	3.84e-13
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	KIRP	rs2271541	chr2:219082119	G/T	8.63e-04
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LGG	rs2271541	chr2:219082119	G/T	5.79e-25
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LGG	rs2271541	chr2:219082119	G/T	5.78e-12
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	KIRC	rs2271541	chr2:219082119	G/T	1.82e-27
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	KIRC	rs2271541	chr2:219082119	G/T	3.51e-07
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LUAD	rs2271541	chr2:219082119	G/T	2.36e-29
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LUAD	rs2271541	chr2:219082119	G/T	1.09e-21
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LIHC	rs2271541	chr2:219082119	G/T	1.32e-09
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LIHC	rs2271541	chr2:219082119	G/T	2.94e-04
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LUSC	rs2271541	chr2:219082119	G/T	3.88e-34
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LUSC	rs2271541	chr2:219082119	G/T	5.23e-14
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	LUSC	rs2271541	chr2:219082119	G/T	2.60e-04
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	OV	rs2271541	chr2:219082119	G/T	1.22e-32
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	OV	rs2271541	chr2:219082119	G/T	8.05e-08
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	READ	rs2271541	chr2:219082119	G/T	6.74e-10
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	READ	rs2271541	chr2:219082119	G/T	3.81e-05
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	PCPG	rs2271541	chr2:219082119	G/T	4.87e-10
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	PAAD	rs2271541	chr2:219082119	G/T	8.02e-09
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	PAAD	rs2271541	chr2:219082119	G/T	4.76e-07
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	PRAD	rs2271541	chr2:219082119	G/T	6.62e-21
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	PRAD	rs2271541	chr2:219082119	G/T	1.46e-07
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	SARC	rs2271541	chr2:219082119	G/T	2.73e-14
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	THYM	rs2271541	chr2:219082119	G/T	5.90e-06
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	TGCT	rs2271541	chr2:219082119	G/T	1.17e-07
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	TGCT	rs2271541	chr2:219082119	G/T	3.93e-05
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	SKCM	rs2271541	chr2:219082119	G/T	7.42e-08
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	STAD	rs2271541	chr2:219082119	G/T	7.96e-29
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	STAD	rs2271541	chr2:219082119	G/T	1.44e-14
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	THCA	rs2271541	chr2:219082119	G/T	3.33e-25
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	THCA	rs2271541	chr2:219082119	G/T	2.39e-12
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	THCA	rs2271541	chr2:219082119	G/T	2.64e-03
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	UVM	rs2271541	chr2:219082119	G/T	6.34e-05
exon_skip_333424	2	219081924:219081977:219082094:219082267:219090642:219090677	219082094:219082267	ENST00000420104.1	UCEC	rs2271541	chr2:219082119	G/T	8.07e-06

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ARPC2

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ARPC2

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RelatedDrugs for ARPC2

Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)

Gene

UniProtAcc

DrugBank ID

Drug name

Drug activity

Drug type

Drug status

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RelatedDiseases for ARPC2

Diseases associated with this gene.
(DisGeNet 4.0)

Gene	Disease ID	Disease name	# pubmeds	Source
ARPC2	C0009324	Ulcerative Colitis	1	CTD_human

	Gene summary
	Gene structures and expression levels
	Exon skipping events with PSIs in TCGA
	Exon skipping events with PSIs in GTEx
	Open reading frame (ORF) annotation in the exon skipping event
	Exon skipping events in the canonical protein sequence
	SNVs in the skipped exons with depth of coverage
	Splicing Quantitative Trait Loci (sQTLs) in the skipped exons
	Splicing Quantitative Trait Methylation (sQTM) in the skipped exon
	Related drugs with this gene
	Related diseases with this gene

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