ExonSkipDB: functional annotation of exon skipping event in human

Gene summary for TRA2B

Gene summary

Gene information	Gene symbol	TRA2B
	Gene ID	6434
	Gene name	transformer 2 beta homolog
	Synonyms	Htra2-beta\|PPP1R156\|SFRS10\|SRFS10\|TRA2-BETA\|TRAN2B
	Cytomap	3q27.2
	Type of gene	protein-coding
	Description	transformer-2 protein homolog betaTRA-2 betaprotein phosphatase 1, regulatory subunit 156splicing factor, arginine/serine-rich 10 (transformer 2 homolog, Drosophila)transformer-2 protein homolog B
	Modification date	20180523
	UniProtAcc	P62995
	Context	PubMed: TRA2B [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
TRA2B	GO:0000381	regulation of alternative mRNA splicing, via spliceosome	12165565\|12761049
TRA2B	GO:0000398	mRNA splicing, via spliceosome	9546399
TRA2B	GO:0048026	positive regulation of mRNA splicing, via spliceosome	15009664
TRA2B	GO:0051259	protein complex oligomerization	10749975

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Exon skipping events across known transcript of Ensembl for TRA2B 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 TRA2B

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 TRA2B

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_390681	3	185635502:185635513:185636152:185636223:185637224:185637284	185636152:185636223	ENSG00000136527.13	ENST00000414862.1
exon_skip_390682	3	185635502:185635513:185636152:185636226:185637224:185637284	185636152:185636226	ENSG00000136527.13	ENST00000382191.4,ENST00000487615.1,ENST00000453386.2,ENST00000492417.1,ENST00000466832.1,ENST00000463328.1,ENST00000456380.1
exon_skip_390683	3	185636152:185636223:185637224:185637284:185638891:185638975	185637224:185637284	ENSG00000136527.13	ENST00000414862.1
exon_skip_390684	3	185636152:185636226:185637224:185637284:185638891:185638969	185637224:185637284	ENSG00000136527.13	ENST00000382191.4,ENST00000487615.1,ENST00000453386.2,ENST00000492417.1,ENST00000466832.1,ENST00000463328.1,ENST00000456380.1
exon_skip_390687	3	185637224:185637284:185638891:185638975:185639798:185639895	185638891:185638975	ENSG00000136527.13	ENST00000382191.4,ENST00000487615.1,ENST00000453386.2,ENST00000492417.1,ENST00000414862.1,ENST00000466832.1,ENST00000463328.1,ENST00000456380.1
exon_skip_390695	3	185639830:185639914:185641583:185641772:185643251:185643414	185641583:185641772	ENSG00000136527.13	ENST00000382191.4,ENST00000487615.1,ENST00000453386.2,ENST00000492417.1,ENST00000456380.1
exon_skip_390697	3	185639830:185639914:185641583:185641796:185643251:185643414	185641583:185641796	ENSG00000136527.13	ENST00000465245.1
exon_skip_390701	3	185641583:185641772:185643251:185643414:185655612:185655775	185643251:185643414	ENSG00000136527.13	ENST00000382191.4
exon_skip_390708	3	185643251:185643414:185644388:185644522:185649364:185649406	185644388:185644522	ENSG00000136527.13	ENST00000487615.1,ENST00000477939.1,ENST00000456380.1
exon_skip_390709	3	185643251:185643414:185644388:185644522:185655612:185655775	185644388:185644522	ENSG00000136527.13	ENST00000485530.1
exon_skip_390718	3	185644514:185644522:185649364:185649640:185655612:185655775	185649364:185649640	ENSG00000136527.13	ENST00000456380.1

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for TRA2B

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_390681	3	185635502:185635513:185636152:185636223:185637224:185637284	185636152:185636223	ENSG00000136527.13	ENST00000414862.1
exon_skip_390682	3	185635502:185635513:185636152:185636226:185637224:185637284	185636152:185636226	ENSG00000136527.13	ENST00000453386.2,ENST00000492417.1,ENST00000463328.1,ENST00000466832.1,ENST00000487615.1,ENST00000456380.1,ENST00000382191.4
exon_skip_390683	3	185636152:185636223:185637224:185637284:185638891:185638975	185637224:185637284	ENSG00000136527.13	ENST00000414862.1
exon_skip_390684	3	185636152:185636226:185637224:185637284:185638891:185638969	185637224:185637284	ENSG00000136527.13	ENST00000453386.2,ENST00000492417.1,ENST00000463328.1,ENST00000466832.1,ENST00000487615.1,ENST00000456380.1,ENST00000382191.4
exon_skip_390687	3	185637224:185637284:185638891:185638975:185639798:185639895	185638891:185638975	ENSG00000136527.13	ENST00000453386.2,ENST00000492417.1,ENST00000463328.1,ENST00000414862.1,ENST00000466832.1,ENST00000487615.1,ENST00000456380.1,ENST00000382191.4
exon_skip_390695	3	185639830:185639914:185641583:185641772:185643251:185643414	185641583:185641772	ENSG00000136527.13	ENST00000453386.2,ENST00000492417.1,ENST00000487615.1,ENST00000456380.1,ENST00000382191.4
exon_skip_390697	3	185639830:185639914:185641583:185641796:185643251:185643414	185641583:185641796	ENSG00000136527.13	ENST00000465245.1
exon_skip_390701	3	185641583:185641772:185643251:185643414:185655612:185655775	185643251:185643414	ENSG00000136527.13	ENST00000382191.4
exon_skip_390708	3	185643251:185643414:185644388:185644522:185649364:185649406	185644388:185644522	ENSG00000136527.13	ENST00000487615.1,ENST00000456380.1,ENST00000477939.1
exon_skip_390709	3	185643251:185643414:185644388:185644522:185655612:185655775	185644388:185644522	ENSG00000136527.13	ENST00000485530.1
exon_skip_390718	3	185644514:185644522:185649364:185649640:185655612:185655775	185649364:185649640	ENSG00000136527.13	ENST00000456380.1
exon_skip_390721	3	185649541:185649640:185652216:185652293:185654025:185654388	185652216:185652293	ENSG00000136527.13	ENST00000471134.1

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 TRA2B

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
ENST00000453386	185636152	185636226	Frame-shift
ENST00000453386	185637224	185637284	In-frame
ENST00000453386	185638891	185638975	In-frame
ENST00000453386	185641583	185641772	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
ENST00000453386	185636152	185636226	Frame-shift
ENST00000453386	185637224	185637284	In-frame
ENST00000453386	185638891	185638975	In-frame
ENST00000453386	185641583	185641772	In-frame

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Infer the effects of exon skipping event on protein functional features for TRA2B

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
ENST00000453386	2969	288	185641583	185641772	610	798	111	174
ENST00000453386	2969	288	185638891	185638975	915	998	213	240
ENST00000453386	2969	288	185637224	185637284	999	1058	241	260

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
ENST00000453386	2969	288	185641583	185641772	610	798	111	174
ENST00000453386	2969	288	185638891	185638975	915	998	213	240
ENST00000453386	2969	288	185637224	185637284	999	1058	241	260

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
P62995	111	174	39	288	Alternative sequence	ID=VSP_005899;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:9212162;Dbxref=PMID:9212162
P62995	111	174	120	124	Beta strand	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	144	151	Beta strand	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	153	168	Beta strand	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	2	288	Chain	ID=PRO_0000081983;Note=Transformer-2 protein homolog beta
P62995	111	174	31	113	Compositional bias	Note=Arg/Ser-rich (RS1 domain)
P62995	111	174	118	196	Domain	Note=RRM;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU00176
P62995	111	174	116	118	Helix	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	131	139	Helix	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	169	179	Helix	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	213	240	39	288	Alternative sequence	ID=VSP_005899;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:9212162;Dbxref=PMID:9212162
P62995	213	240	2	288	Chain	ID=PRO_0000081983;Note=Transformer-2 protein homolog beta
P62995	213	240	231	287	Compositional bias	Note=Arg/Ser-rich (RS2 domain)
P62995	213	240	215	215	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
P62995	213	240	237	237	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
P62995	213	240	193	230	Region	Note=Linker
P62995	241	260	39	288	Alternative sequence	ID=VSP_005899;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:9212162;Dbxref=PMID:9212162
P62995	241	260	2	288	Chain	ID=PRO_0000081983;Note=Transformer-2 protein homolog beta
P62995	241	260	231	287	Compositional bias	Note=Arg/Ser-rich (RS2 domain)
P62995	241	260	241	241	Modified residue	Note=Asymmetric dimethylarginine%3B alternate;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:24129315;Dbxref=PMID:24129315
P62995	241	260	241	241	Modified residue	Note=Dimethylated arginine%3B alternate;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244\|PubMed:15782174,ECO:0000269\|Ref.7;Dbxref=PMID:15782174
P62995	241	260	241	241	Modified residue	Note=Omega-N-methylarginine%3B alternate;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:24129315;Dbxref=PMID:24129315

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
P62995	111	174	39	288	Alternative sequence	ID=VSP_005899;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:9212162;Dbxref=PMID:9212162
P62995	111	174	120	124	Beta strand	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	144	151	Beta strand	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	153	168	Beta strand	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	2	288	Chain	ID=PRO_0000081983;Note=Transformer-2 protein homolog beta
P62995	111	174	31	113	Compositional bias	Note=Arg/Ser-rich (RS1 domain)
P62995	111	174	118	196	Domain	Note=RRM;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU00176
P62995	111	174	116	118	Helix	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	131	139	Helix	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	111	174	169	179	Helix	Ontology_term=ECO:0000244;evidence=ECO:0000244\|PDB:2CQC
P62995	213	240	39	288	Alternative sequence	ID=VSP_005899;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:9212162;Dbxref=PMID:9212162
P62995	213	240	2	288	Chain	ID=PRO_0000081983;Note=Transformer-2 protein homolog beta
P62995	213	240	231	287	Compositional bias	Note=Arg/Ser-rich (RS2 domain)
P62995	213	240	215	215	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
P62995	213	240	237	237	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
P62995	213	240	193	230	Region	Note=Linker
P62995	241	260	39	288	Alternative sequence	ID=VSP_005899;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:9212162;Dbxref=PMID:9212162
P62995	241	260	2	288	Chain	ID=PRO_0000081983;Note=Transformer-2 protein homolog beta
P62995	241	260	231	287	Compositional bias	Note=Arg/Ser-rich (RS2 domain)
P62995	241	260	241	241	Modified residue	Note=Asymmetric dimethylarginine%3B alternate;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:24129315;Dbxref=PMID:24129315
P62995	241	260	241	241	Modified residue	Note=Dimethylated arginine%3B alternate;Ontology_term=ECO:0000244,ECO:0000269;evidence=ECO:0000244\|PubMed:15782174,ECO:0000269\|Ref.7;Dbxref=PMID:15782174
P62995	241	260	241	241	Modified residue	Note=Omega-N-methylarginine%3B alternate;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:24129315;Dbxref=PMID:24129315

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SNVs in the skipped exons for TRA2B

- 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.

TRA2B_BRCA_exon_skip_390695_psi_boxplot.png
boxplot

TRA2B_LIHC_exon_skip_390695_psi_boxplot.png
boxplot

TRA2B_OV_exon_skip_390695_psi_boxplot.png
boxplot

- 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
OV	TCGA-24-1422-01	exon_skip_390695	185641584	185641772	185641608	185641608	Frame_Shift_Del	A	-	p.F166fs
OV	TCGA-24-1422-01	exon_skip_390697	185641584	185641796	185641608	185641608	Frame_Shift_Del	A	-	p.F166fs
LIHC	TCGA-DD-A39Y-01	exon_skip_390695	185641584	185641772	185641759	185641759	Frame_Shift_Del	G	-	p.P116fs
LIHC	TCGA-DD-A39Y-01	exon_skip_390697	185641584	185641796	185641759	185641759	Frame_Shift_Del	G	-	p.P116fs
LIHC	TCGA-DD-A1EG-01	exon_skip_390708 exon_skip_390709	185644389	185644522	185644458	185644458	Frame_Shift_Del	G	-	p.P34fs
LIHC	TCGA-DD-A3A0-01	exon_skip_390708 exon_skip_390709	185644389	185644522	185644475	185644475	Frame_Shift_Del	T	-	p.K28fs
UCEC	TCGA-D1-A17B-01	exon_skip_390683 exon_skip_390684	185637225	185637284	185637275	185637276	Frame_Shift_Ins	-	T	p.G244fs
BRCA	TCGA-AO-A03O-01	exon_skip_390695	185641584	185641772	185641773	185641773	Splice_Site	C	G	e4-1

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

Depth of coverage in three exons	Mutation description
	Sample: TCGA-24-1422-01
	Cancer type: OV
	ESID: exon_skip_390695
	Skipped exon start: 185641584
	Skipped exon end: 185641772
	Mutation start: 185641608
	Mutation end: 185641608
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.F166fs
	Sample: TCGA-24-1422-01
	Cancer type: OV
	ESID: exon_skip_390697
	Skipped exon start: 185641584
	Skipped exon end: 185641796
	Mutation start: 185641608
	Mutation end: 185641608
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.F166fs
exon_skip_390697_OV_TCGA-24-1422-01.png
	Sample: TCGA-AO-A03O-01
	Cancer type: BRCA
	ESID: exon_skip_390695
	Skipped exon start: 185641584
	Skipped exon end: 185641772
	Mutation start: 185641773
	Mutation end: 185641773
	Mutation type: Splice_Site
	Reference seq: C
	Mutation seq: G
	AAchange: e4-1
exon_skip_361771_BRCA_TCGA-AO-A03O-01.png
exon_skip_390695_BRCA_TCGA-AO-A03O-01.png
	Sample: TCGA-24-1422-01
	Cancer type: OV
	ESID: exon_skip_390695
	Skipped exon start: 185641584
	Skipped exon end: 185641772
	Mutation start: 185641608
	Mutation end: 185641608
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.F166fs
	Sample: TCGA-24-1422-01
	Cancer type: OV
	ESID: exon_skip_390697
	Skipped exon start: 185641584
	Skipped exon end: 185641796
	Mutation start: 185641608
	Mutation end: 185641608
	Mutation type: Frame_Shift_Del
	Reference seq: A
	Mutation seq: -
	AAchange: p.F166fs
exon_skip_390697_OV_TCGA-24-1422-01.png

- 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
UMUC3_URINARY_TRACT	185638892	185638975	185638965	185638965	Frame_Shift_Del	G	-	p.R219fs
CP67MEL_SKIN	185643252	185643414	185643352	185643353	In_Frame_Ins	-	GGGAGC	p.77_78insRS
SLR26_KIDNEY	185643252	185643414	185643352	185643353	In_Frame_Ins	-	GGGAGC	p.77_78insRS
KYSE180_OESOPHAGUS	185636153	185636226	185636180	185636180	Missense_Mutation	G	A	p.R277C
KYSE180_OESOPHAGUS	185636153	185636223	185636180	185636180	Missense_Mutation	G	A	p.R277C
NCIH1944_LUNG	185636153	185636226	185636210	185636210	Missense_Mutation	G	A	p.P267S
NCIH1944_LUNG	185636153	185636223	185636210	185636210	Missense_Mutation	G	A	p.P267S
SNU175_LARGE_INTESTINE	185636153	185636226	185636222	185636222	Missense_Mutation	G	A	p.R263W
SNU175_LARGE_INTESTINE	185636153	185636223	185636222	185636222	Missense_Mutation	G	A	p.R263W
HA7EBV_MATCHED_NORMAL_TISSUE	185636153	185636226	185636222	185636222	Missense_Mutation	G	A	p.R263W
HA7EBV_MATCHED_NORMAL_TISSUE	185636153	185636223	185636222	185636222	Missense_Mutation	G	A	p.R263W
HO1N1_UPPER_AERODIGESTIVE_TRACT	185637225	185637284	185637238	185637238	Missense_Mutation	C	T	p.D257N
LU165_LUNG	185638892	185638975	185638901	185638901	Missense_Mutation	C	A	p.R238I
MM415_SKIN	185638892	185638975	185638932	185638932	Missense_Mutation	G	A	p.R228W
PEDS005TPFAD_KIDNEY	185638892	185638975	185638935	185638935	Missense_Mutation	C	A	p.D227Y
ISTMES2_PLEURA	185641584	185641772	185641637	185641637	Missense_Mutation	G	T	p.R157S
ISTMES2_PLEURA	185641584	185641796	185641637	185641637	Missense_Mutation	G	T	p.R157S
SNU1040_LARGE_INTESTINE	185641584	185641772	185641660	185641660	Missense_Mutation	A	G	p.I149T
SNU1040_LARGE_INTESTINE	185641584	185641796	185641660	185641660	Missense_Mutation	A	G	p.I149T
HT115_LARGE_INTESTINE	185641584	185641772	185641670	185641670	Missense_Mutation	C	T	p.D146N
HT115_LARGE_INTESTINE	185641584	185641796	185641670	185641670	Missense_Mutation	C	T	p.D146N
HEC251_ENDOMETRIUM	185641584	185641772	185641692	185641692	Missense_Mutation	G	T	p.F138L
HEC251_ENDOMETRIUM	185641584	185641796	185641692	185641692	Missense_Mutation	G	T	p.F138L
HEC251_ENDOMETRIUM	185643252	185643414	185643359	185643359	Missense_Mutation	G	A	p.R76C
KYSE140_OESOPHAGUS	185643252	185643414	185643394	185643394	Missense_Mutation	G	A	p.S64F
SNU1040_LARGE_INTESTINE	185644389	185644522	185644518	185644518	Missense_Mutation	G	A	p.S14F
CORL279_LUNG	185638892	185638975	185638892	185638892	Splice_Site	C	G	p.R241T

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for TRA2B

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 TRA2B

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for TRA2B

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RelatedDrugs for TRA2B

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 TRA2B

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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