ExonSkipDB: functional annotation of exon skipping event in human

Gene summary for PRMT7

Gene summary

Gene information	Gene symbol	PRMT7
	Gene ID	54496
	Gene name	protein arginine methyltransferase 7
	Synonyms	SBIDDS
	Cytomap	16q22.1
	Type of gene	protein-coding
	Description	protein arginine N-methyltransferase 7[Myelin basic protein]-arginine N-methyltransferase PRMT7histone-arginine N-methyltransferase PRMT7
	Modification date	20180523
	UniProtAcc	Q9NVM4
	Context	PubMed: PRMT7 [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
PRMT7	GO:0016571	histone methylation	15494416
PRMT7	GO:0018216	peptidyl-arginine methylation	15044439

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Exon skipping events across known transcript of Ensembl for PRMT7 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 PRMT7

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 PRMT7

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_138010	16	68344972:68345002:68349799:68349977:68355328:68355365	68349799:68349977	ENSG00000132600.12	ENST00000565356.1,ENST00000449359.3,ENST00000562381.3
exon_skip_138015	16	68344965:68345014:68345944:68346079:68355328:68355365	68345944:68346079	ENSG00000132600.12	ENST00000564441.1
exon_skip_138016	16	68344965:68345014:68349799:68349977:68355328:68355365	68349799:68349977	ENSG00000132600.12	ENST00000569047.3
exon_skip_138018	16	68345036:68345648:68345944:68346079:68349799:68349860	68345944:68346079	ENSG00000132600.12	ENST00000339507.5,ENST00000441236.1,ENST00000348497.4
exon_skip_138022	16	68345944:68346079:68349799:68349977:68355328:68355365	68349799:68349977	ENSG00000132600.12	ENST00000566657.1,ENST00000339507.5,ENST00000441236.1,ENST00000348497.4
exon_skip_138024	16	68345944:68346079:68355328:68355365:68358585:68358669	68355328:68355365	ENSG00000132600.12	ENST00000564441.1
exon_skip_138025	16	68349881:68349977:68355328:68355365:68358585:68358669	68355328:68355365	ENSG00000132600.12	ENST00000566657.1,ENST00000565745.1,ENST00000339507.5,ENST00000568975.1,ENST00000569047.3,ENST00000561806.1,ENST00000563562.1,ENST00000569571.1,ENST00000565356.1,ENST00000348497.4,ENST00000562381.3,ENST00000562456.1
exon_skip_138027	16	68349881:68349977:68358585:68358735:68362968:68363062	68358585:68358735	ENSG00000132600.12	ENST00000562050.1,ENST00000566341.1
exon_skip_138030	16	68355328:68355365:68358585:68358735:68362968:68363062	68358585:68358735	ENSG00000132600.12	ENST00000339507.5,ENST00000568975.1,ENST00000569047.3,ENST00000561806.1,ENST00000569571.1,ENST00000563520.1,ENST00000565356.1,ENST00000562381.3,ENST00000564441.1
exon_skip_138032	16	68358709:68358735:68362968:68363077:68371361:68371424	68362968:68363077	ENSG00000132600.12	ENST00000339507.5,ENST00000568975.1,ENST00000569047.3,ENST00000562050.1,ENST00000569571.1,ENST00000563520.1,ENST00000565356.1,ENST00000566341.1,ENST00000562381.3,ENST00000564441.1
exon_skip_138034	16	68380047:68380183:68381113:68381197:68381533:68381581	68381113:68381197	ENSG00000132600.12	ENST00000339507.5,ENST00000568975.1,ENST00000441236.1,ENST00000566687.1,ENST00000449359.3
exon_skip_138043	16	68381113:68381197:68381533:68381581:68382244:68382334	68381533:68381581	ENSG00000132600.12	ENST00000339507.5,ENST00000568975.1,ENST00000441236.1,ENST00000566687.1,ENST00000449359.3
exon_skip_138046	16	68381533:68381581:68382244:68382334:68386150:68386218	68382244:68382334	ENSG00000132600.12	ENST00000339507.5,ENST00000568975.1,ENST00000441236.1,ENST00000449359.3
exon_skip_138059	16	68389733:68389786:68390603:68390700:68390956:68391105	68390603:68390700	ENSG00000132600.12	ENST00000339507.5,ENST00000568975.1,ENST00000441236.1,ENST00000348497.4,ENST00000449359.3,ENST00000567542.1,ENST00000568463.1

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for PRMT7

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_138010	16	68344972:68345002:68349799:68349977:68355328:68355365	68349799:68349977	ENSG00000132600.12	ENST00000562381.3,ENST00000449359.3,ENST00000565356.1
exon_skip_138015	16	68344965:68345014:68345944:68346079:68355328:68355365	68345944:68346079	ENSG00000132600.12	ENST00000564441.1
exon_skip_138016	16	68344965:68345014:68349799:68349977:68355328:68355365	68349799:68349977	ENSG00000132600.12	ENST00000569047.3
exon_skip_138018	16	68345036:68345648:68345944:68346079:68349799:68349860	68345944:68346079	ENSG00000132600.12	ENST00000441236.1,ENST00000348497.4,ENST00000339507.5
exon_skip_138022	16	68345944:68346079:68349799:68349977:68355328:68355365	68349799:68349977	ENSG00000132600.12	ENST00000566657.1,ENST00000441236.1,ENST00000348497.4,ENST00000339507.5
exon_skip_138024	16	68345944:68346079:68355328:68355365:68358585:68358669	68355328:68355365	ENSG00000132600.12	ENST00000564441.1
exon_skip_138025	16	68349881:68349977:68355328:68355365:68358585:68358669	68355328:68355365	ENSG00000132600.12	ENST00000566657.1,ENST00000562381.3,ENST00000565745.1,ENST00000569571.1,ENST00000569047.3,ENST00000565356.1,ENST00000348497.4,ENST00000339507.5,ENST00000568975.1,ENST00000563562.1,ENST00000561806.1,ENST00000562456.1
exon_skip_138026	16	68349881:68349977:68355328:68355365:68362968:68363062	68355328:68355365	ENSG00000132600.12	ENST00000449359.3,ENST00000441236.1
exon_skip_138027	16	68349881:68349977:68358585:68358735:68362968:68363062	68358585:68358735	ENSG00000132600.12	ENST00000566341.1,ENST00000562050.1
exon_skip_138030	16	68355328:68355365:68358585:68358735:68362968:68363062	68358585:68358735	ENSG00000132600.12	ENST00000562381.3,ENST00000569571.1,ENST00000569047.3,ENST00000564441.1,ENST00000565356.1,ENST00000563520.1,ENST00000339507.5,ENST00000568975.1,ENST00000561806.1
exon_skip_138032	16	68358709:68358735:68362968:68363077:68371361:68371424	68362968:68363077	ENSG00000132600.12	ENST00000562381.3,ENST00000569571.1,ENST00000566341.1,ENST00000569047.3,ENST00000564441.1,ENST00000565356.1,ENST00000562050.1,ENST00000563520.1,ENST00000339507.5,ENST00000568975.1
exon_skip_138034	16	68380047:68380183:68381113:68381197:68381533:68381581	68381113:68381197	ENSG00000132600.12	ENST00000449359.3,ENST00000441236.1,ENST00000339507.5,ENST00000568975.1,ENST00000566687.1
exon_skip_138043	16	68381113:68381197:68381533:68381581:68382244:68382334	68381533:68381581	ENSG00000132600.12	ENST00000449359.3,ENST00000441236.1,ENST00000339507.5,ENST00000568975.1,ENST00000566687.1
exon_skip_138046	16	68381533:68381581:68382244:68382334:68386150:68386218	68382244:68382334	ENSG00000132600.12	ENST00000449359.3,ENST00000441236.1,ENST00000339507.5,ENST00000568975.1
exon_skip_138059	16	68389733:68389786:68390603:68390700:68390956:68391105	68390603:68390700	ENSG00000132600.12	ENST00000449359.3,ENST00000441236.1,ENST00000348497.4,ENST00000339507.5,ENST00000568975.1,ENST00000567542.1,ENST00000568463.1

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 PRMT7

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
ENST00000339507	68349799	68349977	5CDS-5UTR
ENST00000441236	68349799	68349977	5CDS-5UTR
ENST00000339507	68345944	68346079	5UTR-5UTR
ENST00000441236	68345944	68346079	5UTR-5UTR
ENST00000339507	68355328	68355365	Frame-shift
ENST00000339507	68362968	68363077	Frame-shift
ENST00000339507	68390603	68390700	Frame-shift
ENST00000441236	68390603	68390700	Frame-shift
ENST00000339507	68358585	68358735	In-frame
ENST00000339507	68381113	68381197	In-frame
ENST00000441236	68381113	68381197	In-frame
ENST00000339507	68381533	68381581	In-frame
ENST00000441236	68381533	68381581	In-frame
ENST00000339507	68382244	68382334	In-frame
ENST00000441236	68382244	68382334	In-frame

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
ENST00000339507	68349799	68349977	5CDS-5UTR
ENST00000441236	68349799	68349977	5CDS-5UTR
ENST00000339507	68345944	68346079	5UTR-5UTR
ENST00000441236	68345944	68346079	5UTR-5UTR
ENST00000339507	68355328	68355365	Frame-shift
ENST00000441236	68355328	68355365	Frame-shift
ENST00000339507	68362968	68363077	Frame-shift
ENST00000339507	68390603	68390700	Frame-shift
ENST00000441236	68390603	68390700	Frame-shift
ENST00000339507	68358585	68358735	In-frame
ENST00000339507	68381113	68381197	In-frame
ENST00000441236	68381113	68381197	In-frame
ENST00000339507	68381533	68381581	In-frame
ENST00000441236	68381533	68381581	In-frame
ENST00000339507	68382244	68382334	In-frame
ENST00000441236	68382244	68382334	In-frame

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Infer the effects of exon skipping event on protein functional features for PRMT7

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
ENST00000339507	4255	692	68358585	68358735	963	1112	44	94
ENST00000441236	2813	692	68381113	68381197	1874	1957	347	375
ENST00000441236	2813	692	68381533	68381581	1958	2005	375	391
ENST00000441236	2813	692	68382244	68382334	2006	2095	391	421
ENST00000339507	4255	692	68381113	68381197	2022	2105	397	425
ENST00000339507	4255	692	68381533	68381581	2106	2153	425	441
ENST00000339507	4255	692	68382244	68382334	2154	2243	441	471

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
ENST00000339507	4255	692	68358585	68358735	963	1112	44	94
ENST00000441236	2813	692	68381113	68381197	1874	1957	347	375
ENST00000441236	2813	692	68381533	68381581	1958	2005	375	391
ENST00000441236	2813	692	68382244	68382334	2006	2095	391	421
ENST00000339507	4255	692	68381113	68381197	2022	2105	397	425
ENST00000339507	4255	692	68381533	68381581	2106	2153	425	441
ENST00000339507	4255	692	68382244	68382334	2154	2243	441	471

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
Q9NVM4	44	94	45	94	Alternative sequence	ID=VSP_037253;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:14702039;Dbxref=PMID:14702039
Q9NVM4	44	94	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	44	94	14	345	Domain	Note=SAM-dependent MTase PRMT-type 1;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	347	375	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	347	375	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	375	391	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	375	391	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	375	391	387	387	Natural variant	ID=VAR_076330;Note=In SBIDDS. R->G;Ontology_term=ECO:0000269;evidence=ECO:0000269\|PubMed:26437029;Dbxref=dbSNP:rs762515973,PMID:26437029
Q9NVM4	391	421	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	391	421	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	391	421	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	397	425	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	397	425	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	397	425	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	425	441	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	425	441	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	425	441	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	441	471	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	441	471	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	441	471	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015

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
Q9NVM4	44	94	45	94	Alternative sequence	ID=VSP_037253;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:14702039;Dbxref=PMID:14702039
Q9NVM4	44	94	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	44	94	14	345	Domain	Note=SAM-dependent MTase PRMT-type 1;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	347	375	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	347	375	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	375	391	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	375	391	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	375	391	387	387	Natural variant	ID=VAR_076330;Note=In SBIDDS. R->G;Ontology_term=ECO:0000269;evidence=ECO:0000269\|PubMed:26437029;Dbxref=dbSNP:rs762515973,PMID:26437029
Q9NVM4	391	421	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	391	421	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	391	421	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	397	425	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	397	425	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	397	425	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	425	441	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	425	441	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	425	441	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015
Q9NVM4	441	471	399	472	Alternative sequence	ID=VSP_005214;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:11572484;Dbxref=PMID:11572484
Q9NVM4	441	471	1	692	Chain	ID=PRO_0000212335;Note=Protein arginine N-methyltransferase 7
Q9NVM4	441	471	358	684	Domain	Note=SAM-dependent MTase PRMT-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU01015

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SNVs in the skipped exons for PRMT7

- 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-G3-A3CJ-01	exon_skip_138030 exon_skip_138027	68358586	68358735	68358656	68358656	Frame_Shift_Del	T	-	p.V68fs
LIHC	TCGA-DD-A1EG-01	exon_skip_138046	68382245	68382334	68382290	68382290	Frame_Shift_Del	A	-	p.K457fs
THYM	TCGA-XM-A8R8-01	exon_skip_138032	68362969	68363077	68363008	68363008	Nonsense_Mutation	G	T	p.E108X
CHOL	TCGA-3X-AAV9-01	exon_skip_138025 exon_skip_138024	68355329	68355365	68355328	68355328	Splice_Site	G	T	.
UCEC	TCGA-AX-A05Z-01	exon_skip_138030 exon_skip_138027	68358586	68358735	68358585	68358585	Splice_Site	G	T	e3-1
SKCM	TCGA-D9-A6EC-06	exon_skip_138046	68382245	68382334	68382243	68382243	Splice_Site	A	G	.

- 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
DB_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	68358586	68358735	68358703	68358703	Missense_Mutation	A	T	p.T84S
LN443_CENTRAL_NERVOUS_SYSTEM	68362969	68363077	68363004	68363004	Missense_Mutation	T	G	p.I106M
CW2_LARGE_INTESTINE	68362969	68363077	68363026	68363026	Missense_Mutation	G	A	p.D114N
SKMEL2_SKIN	68382245	68382334	68382300	68382300	Missense_Mutation	A	T	p.E460V
OE21_OESOPHAGUS	68390604	68390700	68390620	68390620	Missense_Mutation	G	A	p.A610T
JHH1_LIVER	68390604	68390700	68390696	68390696	Missense_Mutation	C	T	p.P635L
HCC2998_LARGE_INTESTINE	68349800	68349977	68349976	68349976	Splice_Site	A	C	p.R32R
EFO27_OVARY	68381534	68381581	68381580	68381583	Splice_Site	AAGT	-	p.K441fs
J82_URINARY_TRACT	68390604	68390700	68390688	68390730	Splice_Site	TGCAGACCCCGAGGTAGTGCCTGCGCACCGGGCCCAGTGTGCG	-	p.PADPE632fs

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for PRMT7

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

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for PRMT7

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for PRMT7

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RelatedDrugs for PRMT7

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 PRMT7

Diseases associated with this gene.
(DisGeNet 4.0)

Gene

Disease ID

Disease name

# pubmeds

Source

	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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