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Open reading frame (ORF) annotation in the exon skipping event | |
3'-UTR located exon skipping events lost miRNA binding sites | |
Splicing Quantitative Trait Loci (sQTLs) in the skipped exons | |
Gene summary for WNT10B |
Gene summary |
Gene information | Gene symbol | WNT10B | Gene ID | 7480 |
Gene name | Wnt family member 10B | |
Synonyms | SHFM6|STHAG8|WNT-12 | |
Cytomap | 12q13.12 | |
Type of gene | protein-coding | |
Description | protein Wnt-10bWNT-10B proteinwingless-type MMTV integration site family, member 10B | |
Modification date | 20200313 | |
UniProtAcc | ||
Context |
Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Gene | GO ID | GO term | PubMed ID |
WNT10B | GO:0045599 | negative regulation of fat cell differentiation | 10937998 |
WNT10B | GO:0050821 | protein stabilization | 10937998 |
WNT10B | GO:0060070 | canonical Wnt signaling pathway | 17761539 |
WNT10B | GO:0071425 | hematopoietic stem cell proliferation | 9787155 |
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Gene structures and expression levels for WNT10B |
Skipped 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. |
Differentially expressed gene analysis across multiple brain tissues between AD and control. |
Tissue type | DEG direction | Base mean exp. | log2FC(AD/control) | P-value | Adj. p-value |
Differentially expressed isoform analysis across multiple brain tissues between AD and control. |
Tissue type | DEG direction | ENST | Transcript info. | Base mean exp. | log2FC(AD/control) | P-value | Adjc. p-value |
Landscape of isoform expressions across multiple brain tissues between AD and control. |
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Exon skipping events with PSIs in ROSMAP, MSBB, and Mayo for WNT10B |
Landscape of individual exon skipping event across AD tissues and controls (PSI heatmap). |
All exon skipping events in AD cohorts. |
Exon skip ID | chr | Exons involved in exon skipping | Skipped exon |
exon_skip_1344 | chr12 | 48966313:48966553:48967946:48968006:48968149:48968319 | 48967946:48968006 |
exon_skip_22423 | chr12 | 48965556:48966553:48967946:48968006:48968149:48968319 | 48967946:48968006 |
exon_skip_260539 | chr12 | 48968296:48968319:48969110:48969144:48970089:48970342 | 48969110:48969144 |
exon_skip_266634 | chr12 | 48967946:48968006:48968203:48968319:48970089:48970351 | 48968203:48968319 |
exon_skip_276879 | chr12 | 48966313:48966553:48967946:48968319:48970089:48970351 | 48967946:48968319 |
exon_skip_43512 | chr12 | 48965556:48966553:48967946:48968319:48970089:48970351 | 48967946:48968319 |
exon_skip_53112 | chr12 | 48968296:48968319:48969110:48969144:48970089:48970351 | 48969110:48969144 |
exon_skip_83736 | chr12 | 48967946:48968006:48968149:48968319:48970089:48970351 | 48968149:48968319 |
Differentially expressed PSI values of individual exon skipping events in multiple brain tissues between AD and control. |
Exon skipping information | Tissue type | Avg(PSIs) in AD | Avg(PSIs) in control | Difference (PSI) | Adj. p-value |
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Open reading frame (ORF) annotation in the exon skipping event for WNT10B |
Open reading frame (ORF) of individual exon skipping events in ROSMAP based on the Ensembl gene structure combined from isoforms. |
ENST | Start of skipped exon | End of skipped exon | ORF |
ENST00000301061 | 48967946 | 48968319 | Frame-shift |
Open reading frame (ORF) of individual exon skipping events in MSBB based on the Ensembl gene structure combined from isoforms. |
ENST | Start of skipped exon | End of skipped exon | ORF |
ENST00000301061 | 48967946 | 48968319 | Frame-shift |
Open reading frame (ORF) of individual exon skipping events in Mayo based on the Ensembl gene structure combined from isoforms. |
ENST | Start of skipped exon | End of skipped exon | ORF |
ENST00000301061 | 48967946 | 48968319 | Frame-shift |
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Infer the effects of exon skipping event on protein functional features for WNT10B |
p-ENSG00000169884_img4.png |
Loci of skipped exons in ROSMAP 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 MSBB 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 Mayo 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 ROSMAP. |
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 MSBB. |
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 Mayo. |
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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3'-UTR located exon skipping events that lost miRNA binding sites in WNT10B |
3'-UTR exon skipping evnets lost miRNA binding. |
Tissue type | ENST | Exon skip start | Exon skip end | microRNA | Binding site by TargetScan | Binding type by TargetScan | Bdinding site by miRanda | Score of miRanda | Energy by miRanda |
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SNVs in the skipped exons for WNT10B |
- Differential PSIs between mutated versus non-mutated samples. |
- Depth of Coverage in the skipped exon of the mutated samples. |
- Sashimi plot in the skipped exon of the mutated samples. |
- Non-synonymous mutations located in the skipped exons. |
Cancer type | Sample | ESID | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
- 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 |
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AD stage-associated exon skippint events for WNT10B |
Associated exon skipping events with Braak staging or Clinical Dementia Rating (CDR). |
AD stage info | Cohort | Tissue | SE id | Coefficient | P-value | Chromosome | Strand | E1 start | E1 end | Skipped start | Skipped end | E2 start | E2 end |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for WNT10B |
sQTL information located at the skipped exons. |
Tissue type | Exon skip ID | SNP id | Location | P-value | FDR |
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Correlation with RNA binding proteins (RBPs) for WNT10B |
Correlated RBP and related information. |
Tissue type | RBP name | Exon skip ID | Correlation coeifficient | P-value |
DLPFC | RBM25 | exon_skip_43512 | 4.692918e-01 | 2.922882e-15 |
DLPFC | RBM5 | exon_skip_43512 | 4.115040e-01 | 9.271781e-12 |
DLPFC | SRSF5 | exon_skip_43512 | 4.242171e-01 | 1.790059e-12 |
DLPFC | NOVA1 | exon_skip_43512 | 4.600047e-01 | 1.186121e-14 |
IFG | SRSF2 | exon_skip_43512 | -4.650358e-01 | 3.882447e-02 |
IFG | RBM25 | exon_skip_43512 | -4.869644e-01 | 2.943902e-02 |
IFG | MBNL1 | exon_skip_43512 | -5.724100e-01 | 8.351352e-03 |
IFG | ILF2 | exon_skip_43512 | -5.777031e-01 | 7.639570e-03 |
IFG | HNRNPK | exon_skip_43512 | -5.383829e-01 | 1.432745e-02 |
IFG | PUM1 | exon_skip_43512 | -4.778905e-01 | 3.307815e-02 |
IFG | HNRNPA2B1 | exon_skip_43512 | -4.809151e-01 | 3.182808e-02 |
IFG | RALYL | exon_skip_43512 | -6.518063e-01 | 1.846353e-03 |
IFG | SRSF9 | exon_skip_43512 | -5.885105e-01 | 6.339790e-03 |
IFG | SRSF5 | exon_skip_43512 | -4.506689e-01 | 4.613193e-02 |
IFG | HNRNPH2 | exon_skip_43512 | -5.421637e-01 | 1.352957e-02 |
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RelatedDrugs for WNT10B |
Approved drugs targeting this gene. (DrugBank Version 5.1.0 2018-04-02) |
UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for WNT10B |
Diseases associated with this gene. (DisGeNet 4.0) |
Gene | Disease ID | Disease name | # pubmeds | Source |