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Center for Computational Systems Medicine
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Gene summary

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Gene structure and Gene expression level

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Sex-biased somatic mutation

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DNA methylation with beta values in gene

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Exon skipping events with PSI in TCGA

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RNA A-to-I editing events in TCGA

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Sex-biased TF-Gene network of gene

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Sex-biased RBP-ES network of gene

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Sex-biased CeRNA regulation of gene

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Sex-biased eQTL regulation of gene

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Sex-biased eQTM regulation of gene

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Sex-biased sQTL regulation of gene

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Sex-biased sQTM regulation of gene

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Related disease information of gene

Gene: ENSG00000184937

Summary for WT1

check button Gene summary

Gene informationEnsembl ID

ENSG00000184937

Gene symbol

WT1

Gene nameWT1 transcription factor
HGNC

12796

Entrez ID

7490

Gene typeprotein_coding
SynonymsWT1|WAGR|WIT-2|AWT1|NPHS4|WT-1
UniProtAcc

P19544


check buttonDrugs associated with this gene(DrugBank).
Gene IDGene SymbolDrug IDDrug NameDrug Type

check buttonCancer therapeutic drugs associated with this gene(NCI).
Gene IDGene NameDrug IDDrug NameDrug TypeCancer

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Structure and expression level for WT1

check buttonAS events and RNA A-to-I editing events of the gene in TCGA based on Genvode V22 structure.
∗For more information on exon skipping events please check the ExonskipDB database.
∗For more information on exon skipping events please check the CAeditome database.
UCSC result

check buttonLandscape of gene expressions across multiple cancer types.
gene expression analysis

check buttonDifferentially expressed gene analysis between tumor male and tumor female samples.
DEG result
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type
WT13.34e+02-4.66e+007.52e-01-6.20e+005.57e-101.70e-07BRCA

check buttonDifferentially expressed gene analysis between tumor male and normal male samples.
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type

check buttonDifferentially expressed gene analysis between tumor female and normal female samples.
DEG result
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type
WT12.03e+02-4.70e+008.48e-01-5.54e+002.99e-088.25e-07KIRP
WT13.07e+024.74e+002.56e-011.85e+011.94e-764.10e-75BRCA

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Sex-biased somatic mutation for WT1

∗For more information on exon skipping events please check the ExonskipDB database.
Gene IDCancer TypeHugo SymbolMaleFemalepvalorci.upci.lowadjPval

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DNA methylation with beta values for WT1

check buttonLandscape of DNA methylation across multiple cancer types.
methylation heatmap

check buttonDifferentially expressed CpG sites between male tumor and female tumor patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
BRCAcg14657517chr11:32435364CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.98e-014.17e-01-2.59e+009.71e-032.64e-02-2.19e-01
BRCAcg21548155chr11:32434794CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.94e-015.60e-01-3.04e+002.33e-031.47e-02-2.66e-01
BRCAcg19074340chr11:32435366CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.33e-014.70e-01-2.75e+006.01e-032.19e-02-2.37e-01
BRCAcg07193766chr11:32435581CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.56e-013.40e-01-2.46e+001.38e-023.03e-02-1.83e-01
BRCAcg19570244chr11:32435612CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.50e-015.12e-01-2.99e+002.76e-031.59e-02-2.62e-01
BRCAcg19126300chr11:32435616CGI:chr11:32433328-32435765UTR,promoter,exon,gene body3.20e-015.92e-01-3.03e+002.45e-031.50e-02-2.73e-01
BRCAcg13450005chr11:32435711CGI:chr11:32433328-32435765promoter1.70e-013.76e-01-2.31e+002.08e-023.55e-02-2.06e-01
BRCAcg26232818chr11:32435840CGI:chr11:32433328-32435765promoter2.02e-013.89e-01-2.34e+001.95e-023.46e-02-1.87e-01
BRCAcg16092786chr11:32434189CGI:chr11:32433328-32435765promoter,gene body3.96e-015.67e-01-2.31e+002.11e-023.57e-02-1.70e-01
BRCAcg25563456chr11:32434523CGI:chr11:32433328-32435765promoter,gene body3.20e-015.42e-01-3.18e+001.45e-031.16e-02-2.22e-01
BRCAcg15107670chr11:32435213CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.58e-014.66e-01-2.86e+004.28e-031.91e-02-2.07e-01
BRCAcg13663793chr11:32435578CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.70e-013.56e-01-2.90e+003.74e-031.81e-02-1.86e-01
PAADcg01952234chr11:32435584CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.83e-013.09e-01-3.85e+001.16e-046.44e-04-1.26e-01
PAADcg19074340chr11:32435366CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.85e-014.01e-01-3.41e+006.58e-043.21e-03-1.17e-01
PAADcg07193766chr11:32435581CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.26e-013.58e-01-3.85e+001.20e-046.66e-04-1.32e-01
PAADcg22975913chr11:32436181CGI:chr11:32433328-32435765promoter2.45e-013.73e-01-3.91e+009.24e-055.18e-04-1.28e-01
PAADcg12600018chr11:32436332CGI:chr11:32433328-32435765promoter2.12e-013.12e-01-4.37e+001.22e-057.37e-05-1.00e-01
GBMcg16294566chr11:32437110CGI:chr11:32437876-32438332promoter3.24e-014.67e-01-2.29e+002.19e-023.69e-02-1.43e-01

check buttonDifferentially expressed CpG sites between male tumor and male normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
KIRCcg09257824chr11:32434096CGI:chr11:32433328-32435765promoter,gene body2.41e-011.26e-013.73e+001.89e-043.57e-041.15e-01
KIRCcg16092786chr11:32434189CGI:chr11:32433328-32435765promoter,gene body2.61e-011.37e-014.77e+001.84e-066.17e-061.24e-01
LUSCcg21548155chr11:32434794CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.51e-011.16e-012.38e+001.72e-022.11e-021.36e-01
LUSCcg19074340chr11:32435366CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.47e-011.88e-023.24e+001.19e-032.92e-031.28e-01
LUSCcg19570244chr11:32435612CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.38e-012.00e-022.51e+001.22e-021.62e-021.18e-01
LUSCcg19126300chr11:32435616CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.62e-012.96e-022.11e+003.48e-023.72e-021.32e-01
LUSCcg22511262chr11:32433646CGI:chr11:32433328-32435765promoter,gene body3.58e-011.28e-013.49e+004.74e-041.60e-032.29e-01
LUSCcg18950778chr11:32433816CGI:chr11:32433328-32435765promoter,gene body4.41e-012.09e-014.00e+006.36e-055.92e-042.33e-01
LUSCcg25586361chr11:32433898CGI:chr11:32433328-32435765promoter,gene body5.15e-012.21e-014.14e+003.54e-055.30e-042.94e-01
LUSCcg09257824chr11:32434096CGI:chr11:32433328-32435765promoter,gene body4.38e-011.51e-013.98e+006.89e-056.07e-042.87e-01
LUSCcg16092786chr11:32434189CGI:chr11:32433328-32435765promoter,gene body3.52e-011.38e-013.60e+003.20e-041.26e-032.14e-01
LUSCcg25563456chr11:32434523CGI:chr11:32433328-32435765promoter,gene body2.41e-011.12e-013.17e+001.50e-033.42e-031.29e-01
LUSCcg15107670chr11:32435213CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.45e-011.32e-012.32e+002.05e-022.43e-021.13e-01
LUSCcg12600018chr11:32436332CGI:chr11:32433328-32435765promoter2.56e-011.07e-012.76e+005.78e-039.10e-031.49e-01
LUSCcg16294566chr11:32437110CGI:chr11:32437876-32438332promoter4.76e-019.36e-024.30e+001.70e-055.26e-043.82e-01
BLCAcg14657517chr11:32435364CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.37e-013.96e-022.33e+002.00e-022.45e-021.97e-01
BLCAcg19570244chr11:32435612CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.48e-012.22e-022.25e+002.43e-022.85e-022.25e-01
BLCAcg19126300chr11:32435616CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.88e-013.35e-022.12e+003.39e-023.70e-022.55e-01
BLCAcg26232818chr11:32435840CGI:chr11:32433328-32435765promoter2.19e-012.67e-022.36e+001.83e-022.28e-021.92e-01
BLCAcg22511262chr11:32433646CGI:chr11:32433328-32435765promoter,gene body3.20e-011.67e-012.29e+002.19e-022.62e-021.54e-01
BLCAcg22975913chr11:32436181CGI:chr11:32433328-32435765promoter4.19e-011.32e-012.18e+002.89e-023.26e-022.87e-01
BLCAcg12600018chr11:32436332CGI:chr11:32433328-32435765promoter2.79e-011.24e-011.99e+004.65e-024.72e-021.55e-01
ESCAcg25586361chr11:32433898CGI:chr11:32433328-32435765promoter,gene body5.57e-014.01e-012.41e+001.59e-023.86e-021.55e-01
CHOLcg21548155chr11:32434794CGI:chr11:32433328-32435765promoter,exon,CDS,gene body4.16e-016.38e-022.88e+004.04e-031.47e-023.52e-01
CHOLcg19074340chr11:32435366CGI:chr11:32433328-32435765UTR,promoter,exon,gene body3.73e-012.21e-022.43e+001.50e-022.65e-023.51e-01
CHOLcg07193766chr11:32435581CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.40e-012.64e-022.21e+002.70e-023.50e-022.14e-01
CHOLcg13450005chr11:32435711CGI:chr11:32433328-32435765promoter2.29e-012.15e-022.95e+003.19e-031.32e-022.07e-01
CHOLcg18950778chr11:32433816CGI:chr11:32433328-32435765promoter,gene body4.30e-012.16e-012.65e+007.96e-031.92e-022.14e-01
CHOLcg09257824chr11:32434096CGI:chr11:32433328-32435765promoter,gene body3.54e-011.47e-012.06e+003.90e-024.26e-022.07e-01
CHOLcg16092786chr11:32434189CGI:chr11:32433328-32435765promoter,gene body4.12e-011.59e-012.21e+002.70e-023.50e-022.53e-01
CHOLcg25563456chr11:32434523CGI:chr11:32433328-32435765promoter,gene body3.51e-011.27e-012.51e+001.22e-022.39e-022.24e-01
CHOLcg22975913chr11:32436181CGI:chr11:32433328-32435765promoter3.55e-019.09e-022.51e+001.22e-022.39e-022.64e-01

check buttonDifferentially expressed CpG sites between female tumor and female normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
BRCAcg14657517chr11:32435364CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.98e-013.97e-027.34e+002.13e-136.88e-131.58e-01
BRCAcg21548155chr11:32434794CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.94e-019.52e-028.63e+005.88e-182.69e-171.98e-01
BRCAcg19074340chr11:32435366CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.33e-013.13e-026.79e+001.15e-113.24e-112.02e-01
BRCAcg07193766chr11:32435581CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.56e-012.90e-025.93e+003.12e-097.27e-091.27e-01
BRCAcg19570244chr11:32435612CGI:chr11:32433328-32435765UTR,promoter,exon,gene body2.50e-014.21e-028.46e+002.72e-171.18e-162.08e-01
BRCAcg19126300chr11:32435616CGI:chr11:32433328-32435765UTR,promoter,exon,gene body3.20e-016.33e-028.64e+005.60e-182.57e-172.56e-01
BRCAcg13450005chr11:32435711CGI:chr11:32433328-32435765promoter1.70e-012.67e-029.35e+008.75e-215.06e-201.43e-01
BRCAcg26232818chr11:32435840CGI:chr11:32433328-32435765promoter2.02e-012.99e-028.48e+002.24e-179.81e-171.72e-01
BRCAcg22511262chr11:32433646CGI:chr11:32433328-32435765promoter,gene body3.49e-011.48e-019.59e+008.50e-225.37e-212.01e-01
BRCAcg18950778chr11:32433816CGI:chr11:32433328-32435765promoter,gene body4.48e-012.19e-011.26e+011.22e-364.77e-352.30e-01
BRCAcg25586361chr11:32433898CGI:chr11:32433328-32435765promoter,gene body4.75e-012.97e-018.93e+004.43e-192.22e-181.78e-01
BRCAcg09257824chr11:32434096CGI:chr11:32433328-32435765promoter,gene body3.74e-011.51e-011.05e+019.90e-269.02e-252.23e-01
BRCAcg16092786chr11:32434189CGI:chr11:32433328-32435765promoter,gene body3.96e-011.30e-011.23e+011.39e-343.82e-332.66e-01
BRCAcg25563456chr11:32434523CGI:chr11:32433328-32435765promoter,gene body3.20e-011.30e-019.30e+001.38e-207.86e-201.90e-01
BRCAcg15107670chr11:32435213CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.58e-011.29e-015.50e+003.82e-088.10e-081.30e-01
BRCAcg13663793chr11:32435578CGI:chr11:32433328-32435765UTR,promoter,exon,gene body1.70e-016.48e-027.57e+003.87e-141.32e-131.05e-01
BRCAcg16294566chr11:32437110CGI:chr11:32437876-32438332promoter4.20e-011.38e-013.15e+001.65e-032.09e-032.82e-01
LUADcg22511262chr11:32433646CGI:chr11:32433328-32435765promoter,gene body2.24e-011.22e-013.21e+001.32e-033.84e-031.02e-01
LIHCcg21548155chr11:32434794CGI:chr11:32433328-32435765promoter,exon,CDS,gene body2.36e-011.03e-012.11e+003.50e-023.77e-021.33e-01
KIRPcg22511262chr11:32433646CGI:chr11:32433328-32435765promoter,gene body3.97e-011.55e-011.98e+004.78e-024.84e-022.42e-01

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Exon skipping events with PSI in TCGA for WT1

∗Please access ExonSkipDB for exon skipping annotation.
check buttonLandscape of exon skipping events across multiple cancer types.
AS event heatmap

check buttonDifferentially expressed exon skipping events between male tumor and female tumor patients.
Cancer TypeExon Skippingave.female_Tave.female_Nwilcoxon.wwilcoxon.ppadjdPSI

check buttonDifferentially expressed exon skipping events between male tumor and male normal patients.
Cancer TypeExon Skippingave.female_Tave.female_Nwilcoxon.wwilcoxon.ppadjdPSI

check buttonDifferentially expressed exon skipping events between female tumor and female normal patients.
Cancer TypeExon Skippingave.female_Tave.female_Nwilcoxon.wwilcoxon.ppadjdPSI

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RNA A-to-I editing events in TCGA for WT1

∗Please access CAeditome for RNA editing annotation.
check buttonDifferentially expressed RNA editing events between male tumor and female tumor patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre

check buttonDifferentially expressed RNA editing events between male tumor and male normal patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre

check buttonDifferentially expressed RNA editing events between female tumor and female normal patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre

check buttonProtein coding RNA editing(s).
Editing PositionVariant TypeGene SymbolTranscript IDNTchangeAAchange

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Sex-biased TF-Gene network for WT1

check buttonTFs related to WT1.
∗The female-biased TF-gene edges were identified if Female_Edge_threshold>0.98 and Male_Edge_threshold<=0.98.
∗The male-biased TF-gene edges were identified if Male_Edge_threshold>0.98 and Female_Edge_threshold<=0.98.
TF Gene
Cancer TypeTFTarget GeneMale Edge ScoreMale Edge ThresholdFemale Edge ScoreFemale Edge ThresholdType
MESOFOXA1WT12.33e+002.90e-033.96e+009.81e-01Female-biased
MESOFOXA3WT12.44e+003.00e-034.06e+009.83e-01Female-biased
MESOFOXR2WT12.08e+001.26e-033.93e+009.83e-01Female-biased
MESOPOU3F3WT12.42e+003.67e-033.98e+009.81e-01Female-biased
MESOZNF25WT12.18e+001.68e-033.95e+009.83e-01Female-biased
MESOZNF79WT12.05e+005.77e-044.10e+009.87e-01Female-biased

check buttonWT1 related gene.
∗Only the gene encode TF might with this result.
∗For more information please check Sex-biased TF-Coding gene network.
related_gene

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Sex-biased RBP-ES network for WT1

check buttonRBPs related to ES in WT1.
∗The female-biased RBP-ES edges were identified if Female_Edge_threshold>0.98 and Male_Edge_threshold<=0.98.
∗The male-biased RBP-ES edges were identified if Male_Edge_threshold>0.98 and Female_Edge_threshold<=0.98.
Cancer TypeRBPTarget ESMale Edge ScoreMale Edge ThresholdFemale Edge ScoreFemale Edge ThresholdType

check buttonWT1 related ES.
∗Only the gene encode RBP might with this result.
∗For more information please check Sex-biased RBP-ES network in cancer.

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Sex-biased CeRNA regulation of gene

check buttonSex-biased CeRNA regulation of gene.
Gene IDceRNA(lncRNA-miRNA-mRNA)GroupCancer Type

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Sex-biased eQTL regulation of gene

check buttonSex-biased eQTL regulation of gene (The figures only show the pairs with FDR <1e-5. For more information please check the below table).
eQTLDescription

check buttonMale-specific eQTL regulation.
SNP IDSNP InfoPosition to GeneEffect ScoreFDRCancer TypeBiased Type

check buttonFemale-specific eQTL regulation.
SNP IDSNP InfoPosition to GeneEffect ScoreFDRCancer TypeBiased Type
rs71466595chr11:32488555:A:G-0.1366025391545510.0114308455937219SARCMale-baised eQTL
rs12803539chr11:32489246:G:A-0.1366025391545510.0114308455937219SARCMale-baised eQTL
rs12274822chr11:32489465:G:T-0.1366025391545510.0114308455937219SARCMale-baised eQTL
rs7118228chr11:32490882:A:T-0.1366025391545510.0114308455937219SARCMale-baised eQTL
rs9735433chr11:32492498:G:A-0.1366025391545510.0114308455937219SARCMale-baised eQTL

check buttonOpposite sex-biased eQTL regulation.
SNP IDSNP InfoPosition to GeneMale EffectMale FDRFemale EffectFemale FDRSex-biased Gene in CancerCancer Type

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Sex-biased eQTM regulation of gene

check buttonSex-biased eQTM regulation of gene (The figures only show the pairs with FDR<1e-5. For more information please check the below table).
eQTMDescription
eQTM boxplot analysisGene ID: ENSG00000184937
CpG Site: cg15446391
Position to Gene: gene
Male Effect: -
Female Effect: -0.363887400691609

check buttonMale-specific eQTM regulation.
CpG SiteCpG PostionPosition to GeneEffect ScoreFDRCor.rCor.PvalueCancer Type

check buttonFemale-specific eQTM regulation.
CpG SiteCpG PostionPosition to GeneEffect ScoreFDRCor.rCor.PvalueCancer Type
cg15446391chr11:32430824gene-0.3638874006916091.84998441345069e-05-0.473348688988360362.0787407859530013e-09SARC

check buttonOpposite sex-biased eQTM regulation.
CpG SiteCpG PostionCpG IslandPosition to GeneMale EffectMale FDRFemale EffectFemale FDRMale CorMale P-valueFemale CorFemale P-valueSex-biased Coding GeneCancer Type

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Sex-biased sQTL regulation of gene

check buttonSex-biased sQTL regulation of gene (The figures only show the pairs with FDR <1e-5. For more information please check the below table).
sQTLDescription

check buttonMale-specific sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESEffect ScoreFDRCancer TypeBiased Type

check buttonFemale-specific sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESEffect ScoreFDRCancer TypeBiased Type

check buttonOpposite sex-biased sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESMale EffectMale FDRFemale EffectFemale FDRCancer Type

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Sex-biased sQTM regulation of gene

check buttonSex-biased sQTM regulation of gene (The figures only show the pairs with FDR <1e-5. For more information please check the below table).
sQTMDescription

check buttonMale-specific sQTM regulation.
EX IDSkipped ExonCPG SiteCPG PositionPosition to EX EventsEffect ScoreFDRCor.rCor.PvalueORF_annoCancer Type

check buttonFemale-specific sQTM regulation.
EX IDSkipped ExonCPG SiteCPG PositionPosition to EX EventsEffect ScoreFDRCor.rCor.PvalueORF_annoCancer Type

check buttonOpposite sex-biased sQTM regulation.
EX IDEX InfoSkipped ExonCPG SiteCPG PositionCPG IslandPosition to EX EventsMale EffectMale FDRFemale EffectFemale FDRMale CorrelationMale P-valueFemale CorrelationFemale P-valueORF_annoCancer Type

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Related disease information of WT1

check buttonDiseases associated with this gene (DisGeNET).
Gene IDGene SymbolDisease IDDisease NameNumber of PMIDSource
ENSG00000184937WT1C0003076Aniridia1CTD_human
ENSG00000184937WT1C0006142Malignant neoplasm of breast1CTD_human
ENSG00000184937WT1C0007102Malignant tumor of colon1CTD_human
ENSG00000184937WT1C0009375Colonic Neoplasms1CTD_human
ENSG00000184937WT1C0017636Glioblastoma1CTD_human
ENSG00000184937WT1C0017658Glomerulonephritis1CTD_human
ENSG00000184937WT1C0019284Diaphragmatic Hernia1CTD_human
ENSG00000184937WT1C0023418leukemia1CTD_human
ENSG00000184937WT1C0023467Leukemia, Myelocytic, Acute2CTD_human
ENSG00000184937WT1C0023473Myeloid Leukemia, Chronic1CTD_human
ENSG00000184937WT1C0023487Acute Promyelocytic Leukemia1CTD_human
ENSG00000184937WT1C0024121Lung Neoplasms1CTD_human
ENSG00000184937WT1C0026998Acute Myeloid Leukemia, M12CTD_human
ENSG00000184937WT1C0027708Nephroblastoma2CTD_human
ENSG00000184937WT1C0027809Neurilemmoma1CTD_human
ENSG00000184937WT1C0029463Osteosarcoma1CTD_human
ENSG00000184937WT1C0030297Pancreatic Neoplasm1CTD_human
ENSG00000184937WT1C0031149Peritoneal Neoplasms1CTD_human
ENSG00000184937WT1C0085215Ovarian Failure, Premature1CTD_human
ENSG00000184937WT1C0086367Gonadotropin-Resistant Ovary Syndrome1CTD_human
ENSG00000184937WT1C0206115WAGR Syndrome1CTD_human
ENSG00000184937WT1C0235833Congenital diaphragmatic hernia1CTD_human
ENSG00000184937WT1C0242379Malignant neoplasm of lung1CTD_human
ENSG00000184937WT1C0265699Congenital hernia of foramen of Morgagni1CTD_human
ENSG00000184937WT1C0265700Congenital hernia of foramen of Bochdalek1CTD_human
ENSG00000184937WT1C0334588Giant Cell Glioblastoma1CTD_human
ENSG00000184937WT1C0345967Malignant mesothelioma1CTD_human
ENSG00000184937WT1C0346647Malignant neoplasm of pancreas1CTD_human
ENSG00000184937WT1C0346990Carcinomatosis of peritoneal cavity1CTD_human
ENSG00000184937WT1C0678222Breast Carcinoma1CTD_human
ENSG00000184937WT1C0751374Schwannomatosis, Plexiform1CTD_human
ENSG00000184937WT1C0950121Denys-Drash Syndrome1CTD_human
ENSG00000184937WT1C0950122Frasier Syndrome1CTD_human
ENSG00000184937WT1C1257931Mammary Neoplasms, Human1CTD_human
ENSG00000184937WT1C1458155Mammary Neoplasms1CTD_human
ENSG00000184937WT1C1621958Glioblastoma Multiforme1CTD_human
ENSG00000184937WT1C1704377Bright Disease1CTD_human
ENSG00000184937WT1C1837026MEACHAM SYNDROME (disorder)1CTD_human
ENSG00000184937WT1C1879321Acute Myeloid Leukemia (AML-M2)2CTD_human
ENSG00000184937WT1C2930471Bilateral Wilms Tumor2CTD_human
ENSG00000184937WT1C3151568NEPHROTIC SYNDROME, TYPE 41CTD_human
ENSG00000184937WT1C3494522Hypergonadotropic Ovarian Failure, X-Linked1CTD_human
ENSG00000184937WT1C4552079Premature Ovarian Failure 11CTD_human
ENSG00000184937WT1C4704874Mammary Carcinoma, Human1CTD_human