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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: ENSG00000141510

Summary for TP53

check button Gene summary

Gene informationEnsembl ID

ENSG00000141510

Gene symbol

TP53

Gene nametumor protein p53
HGNC

11998

Entrez ID

7157

Gene typeprotein_coding
SynonymsTP53|p53|LFS1
UniProtAcc

P04637


check buttonDrugs associated with this gene(DrugBank).
Gene IDGene SymbolDrug IDDrug NameDrug Type
ENSG00000141510TP53DB00945Acetylsalicylic acidSmallMoleculeDrug
ENSG00000141510TP53DB01593ZincSmallMoleculeDrug
ENSG00000141510TP53DB03347Triethyl phosphateSmallMoleculeDrug
ENSG00000141510TP53DB05404AZD 3355SmallMoleculeDrug
ENSG00000141510TP53DB083631-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamineSmallMoleculeDrug
ENSG00000141510TP53DB14487Zinc acetateSmallMoleculeDrug
ENSG00000141510TP53DB14533Zinc chlorideSmallMoleculeDrug
ENSG00000141510TP53DB14548Zinc sulfate, unspecified formSmallMoleculeDrug

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

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Structure and expression level for TP53

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.
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type

check buttonDifferentially expressed gene analysis between tumor male and normal male samples.
DEG result
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type
TP532.70e+031.08e+003.88e-012.78e+005.43e-031.48e-02CHOL

check buttonDifferentially expressed gene analysis between tumor female and normal female samples.
DEG result
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type
TP533.94e+031.03e+004.02e-012.55e+001.07e-022.62e-02READ

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Sex-biased somatic mutation for TP53

∗For more information on exon skipping events please check the ExonskipDB database.
check buttonTCGA-BRCA
lollipopPlot
check buttonTCGA-LIHC
lollipopPlot
check buttonTCGA-LUSC
lollipopPlot
Gene IDCancer TypeHugo SymbolMaleFemalepvalorci.upci.lowadjPval
ENSG00000141510BRCATP5303281.98e-020.00e+007.58e-010.00e+001.00e+00
ENSG00000141510LIHCTP5381224.25e-032.18e+003.92e+001.25e+006.19e-01
ENSG00000141510LUSCTP53290883.76e-021.74e+002.96e+001.00e+009.90e-01

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DNA methylation with beta values for TP53

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

check buttonDifferentially expressed CpG sites between male tumor and male normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta

check buttonDifferentially expressed CpG sites between female tumor and female normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta

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Exon skipping events with PSI in TCGA for TP53

∗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 TP53

∗Please access CAeditome for RNA editing annotation.
check buttonLandscape of RNA editing events across multiple cancer types.
ED heatmap

check buttonDifferentially expressed RNA editing events between male tumor and female tumor patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre
GBMTP53-018chr17_7666770_-4.66e-013.50e-012.07e+003.88e-024.96e-021.16e-01

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 TP53

check buttonTFs related to TP53.
∗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.
Cancer TypeTFTarget GeneMale Edge ScoreMale Edge ThresholdFemale Edge ScoreFemale Edge ThresholdType

check buttonTP53 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 TP53

check buttonRBPs related to ES in TP53.
∗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.
RBP ES
Cancer TypeRBPTarget ESMale Edge ScoreMale Edge ThresholdFemale Edge ScoreFemale Edge ThresholdType
UVMPCBP2exon_skip_2863846.49e+009.81e-015.94e+005.11e-04Male-biased
THYMPCBP2exon_skip_2863845.92e+004.43e-046.53e+009.82e-01Female-biased
LIHCYBX2exon_skip_2863881.40e+011.86e-031.47e+019.98e-01Female-biased
LUSCYBX2exon_skip_2863881.38e+012.34e-031.43e+019.98e-01Female-biased
LUADYBX2exon_skip_2863881.38e+014.01e-031.42e+019.96e-01Female-biased
KIRPYBX2exon_skip_2863881.38e+011.10e-031.44e+019.99e-01Female-biased
READYBX2exon_skip_2863881.39e+015.65e-041.45e+019.99e-01Female-biased
THCAYBX2exon_skip_2863881.44e+011.00e+001.38e+012.18e-04Male-biased
GBMPCBP2exon_skip_2863846.63e+009.80e-016.18e+002.84e-03Male-biased
KIRCYBX2exon_skip_2863881.39e+011.66e-031.44e+019.98e-01Female-biased
KICHPABPC5exon_skip_2863679.10e+009.42e-039.43e+009.88e-01Female-biased
KICHYBX2exon_skip_2863881.46e+019.99e-011.40e+011.24e-03Male-biased
BLCAYBX2exon_skip_2863881.40e+012.98e-031.45e+019.97e-01Female-biased
HNSCESRP2exon_skip_2863718.38e+002.71e-038.84e+009.92e-01Female-biased
HNSCYBX2exon_skip_2863881.39e+012.93e-031.43e+019.97e-01Female-biased
SARCPCBP2exon_skip_2863846.90e+009.84e-016.27e+001.10e-03Male-biased

check buttonTP53 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
rs9897496chr17:10784575:A:G--0.0616205449147030.0114484671680242LUADFemale-baised eQTL
rs28455468chr17:10868015:G:A-0.05483892314754250.0321586154804776LUADFemale-baised eQTL

check buttonFemale-specific eQTL regulation.
SNP IDSNP InfoPosition to GeneEffect ScoreFDRCancer TypeBiased Type
rs76116797chr17:12836779:A:G-0.06530495702382220.0499338178661313LGGMale-baised eQTL
rs7209078chr17:9428291:T:A--0.04858502749639450.00932059356041898KIRCMale-baised eQTL
rs9904459chr17:9435415:A:G--0.047525976068810.0126995132289115KIRCMale-baised eQTL
rs9908951chr17:9428790:G:A--0.0457313794380560.0189435120755064KIRCMale-baised eQTL
rs9909211chr17:9428890:G:T--0.04316676113653560.0354298890095772KIRCMale-baised eQTL
rs12450050chr17:5535093:A:G--0.04405376114972930.0458328117007087KIRCMale-baised eQTL
rs34081014chr17:3712859:C:G-0.1117728431452620.0464763282076492LUADMale-baised eQTL
rs2013868chr17:12209077:G:A-0.09353072448031840.0399193648679557COADMale-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

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

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
exon_skip_286371chr17:7673534:7673608Frame-shiftrs72841789chr17:8450754:C:TDistant upstream-0.07736938417466550.00113784808462508LUSCFemale-baised sQTL
exon_skip_286371chr17:7673534:7673608Frame-shiftrs72841791chr17:8451003:C:TDistant upstream-0.07736938417466550.00113784808462508LUSCFemale-baised sQTL
exon_skip_286371chr17:7673534:7673608Frame-shiftrs56005127chr17:8451558:C:TDistant upstream-0.07736938417466550.00113784808462508LUSCFemale-baised sQTL
exon_skip_286371chr17:7673534:7673608Frame-shiftrs166563chr17:8498643:T:GDistant upstream-0.07321885463276660.00222310936302541LUSCFemale-baised sQTL
exon_skip_286371chr17:7673534:7673608Frame-shiftrs111981244chr17:8498623:G:ADistant upstream-0.07314359426764140.00229187752414525LUSCFemale-baised sQTL
exon_skip_286371chr17:7673534:7673608Frame-shiftrs4128516chr17:8610945:A:TDistant upstream0.06508083149604940.00784599903214376LUSCFemale-baised sQTL
exon_skip_286371chr17:7673534:7673608Frame-shiftrs166563chr17:8498643:T:CDistant upstream0.05519339772815980.0308809023539419LUSCFemale-baised sQTL
exon_skip_286384chr17:7675993:7676272In-framers17807161chr17:7868478:A:GDistant upstream-0.1545859961507590.0489441031612062BLCAFemale-baised sQTL

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 TP53

check buttonDiseases associated with this gene (DisGeNET).
Gene IDGene SymbolDisease IDDisease NameNumber of PMIDSource
ENSG00000141510TP53C0001418Adenocarcinoma3CTD_human
ENSG00000141510TP53C0001430Adenoma1CTD_human
ENSG00000141510TP53C0001624Adrenal Gland Neoplasms1CTD_human
ENSG00000141510TP53C0001969Alcoholic Intoxication2PSYGENET
ENSG00000141510TP53C0001973Alcoholic Intoxication, Chronic2PSYGENET
ENSG00000141510TP53C0002152Alloxan Diabetes1CTD_human
ENSG00000141510TP53C0002736Amyotrophic Lateral Sclerosis1CTD_human
ENSG00000141510TP53C0004698Balkan Nephropathy1CTD_human
ENSG00000141510TP53C0005684Malignant neoplasm of urinary bladder5CTD_human
ENSG00000141510TP53C0005695Bladder Neoplasm5CTD_human
ENSG00000141510TP53C0006142Malignant neoplasm of breast6CTD_human
ENSG00000141510TP53C0006663Calcinosis1CTD_human
ENSG00000141510TP53C0007097Carcinoma2CTD_human
ENSG00000141510TP53C0007102Malignant tumor of colon3CTD_human
ENSG00000141510TP53C0007114Malignant neoplasm of skin1CTD_human
ENSG00000141510TP53C0007131Non-Small Cell Lung Carcinoma4CTD_human
ENSG00000141510TP53C0007134Renal Cell Carcinoma4CTD_human
ENSG00000141510TP53C0007137Squamous cell carcinoma2CTD_human
ENSG00000141510TP53C0007138Carcinoma, Transitional Cell1CTD_human
ENSG00000141510TP53C0007194Hypertrophic Cardiomyopathy1CTD_human
ENSG00000141510TP53C0007273Carotid Artery Diseases1CTD_human
ENSG00000141510TP53C0007621Neoplastic Cell Transformation1CTD_human
ENSG00000141510TP53C0007786Brain Ischemia1CTD_human
ENSG00000141510TP53C0009375Colonic Neoplasms3CTD_human
ENSG00000141510TP53C0009402Colorectal Carcinoma8CTD_human
ENSG00000141510TP53C0009404Colorectal Neoplasms8CTD_human
ENSG00000141510TP53C0010606Adenoid Cystic Carcinoma1CTD_human
ENSG00000141510TP53C0011303Demyelinating Diseases1CTD_human
ENSG00000141510TP53C0011304Demyelination1CTD_human
ENSG00000141510TP53C0011853Diabetes Mellitus, Experimental1CTD_human
ENSG00000141510TP53C0013990Pathological accumulation of air in tissues1CTD_human
ENSG00000141510TP53C0014859Esophageal Neoplasms2CTD_human
ENSG00000141510TP53C0016978gallbladder neoplasm2CTD_human
ENSG00000141510TP53C0017638Glioma3CTD_human
ENSG00000141510TP53C0018923Hemangiosarcoma1CTD_human
ENSG00000141510TP53C0019207Hepatoma, Morris1CTD_human
ENSG00000141510TP53C0019208Hepatoma, Novikoff1CTD_human
ENSG00000141510TP53C0020538Hypertensive disease1CTD_human
ENSG00000141510TP53C0021361Female infertility1CTD_human
ENSG00000141510TP53C0021364Male infertility1CTD_human
ENSG00000141510TP53C0022116Ischemia1CTD_human
ENSG00000141510TP53C0022593Keratosis2CTD_human
ENSG00000141510TP53C0022594Keratosis Blennorrhagica2CTD_human
ENSG00000141510TP53C0022660Kidney Failure, Acute1CTD_human
ENSG00000141510TP53C0022783Vulvar Lichen Sclerosus1CTD_human
ENSG00000141510TP53C0023434Chronic Lymphocytic Leukemia1CTD_human
ENSG00000141510TP53C0023452Childhood Acute Lymphoblastic Leukemia1CTD_human
ENSG00000141510TP53C0023453L2 Acute Lymphoblastic Leukemia1CTD_human
ENSG00000141510TP53C0023897Liver Diseases, Parasitic1CTD_human
ENSG00000141510TP53C0023903Liver neoplasms2CTD_human
ENSG00000141510TP53C0023904Liver Neoplasms, Experimental1CTD_human
ENSG00000141510TP53C0024117Chronic Obstructive Airway Disease1CTD_human
ENSG00000141510TP53C0024121Lung Neoplasms5CTD_human
ENSG00000141510TP53C0024623Malignant neoplasm of stomach2CTD_human
ENSG00000141510TP53C0024809Marijuana Abuse1PSYGENET
ENSG00000141510TP53C0025202melanoma4CTD_human
ENSG00000141510TP53C0026640Mouth Neoplasms1CTD_human
ENSG00000141510TP53C0027022Myeloproliferative disease1CTD_human
ENSG00000141510TP53C0027627Neoplasm Metastasis1CTD_human
ENSG00000141510TP53C0027708Nephroblastoma1CTD_human
ENSG00000141510TP53C0029463Osteosarcoma1CTD_human
ENSG00000141510TP53C0030246Pustulosis of Palms and Soles1CTD_human
ENSG00000141510TP53C0030297Pancreatic Neoplasm1CTD_human
ENSG00000141510TP53C0030849Penile Neoplasms1CTD_human
ENSG00000141510TP53C0032578Polyploidy1CTD_human
ENSG00000141510TP53C0033578Prostatic Neoplasms8CTD_human
ENSG00000141510TP53C0033860Psoriasis1CTD_human
ENSG00000141510TP53C0036341Schizophrenia1CTD_human
ENSG00000141510TP53C0036920Sezary Syndrome2CTD_human
ENSG00000141510TP53C0037286Skin Neoplasms1CTD_human
ENSG00000141510TP53C0038279Sterility, Postpartum1CTD_human
ENSG00000141510TP53C0038356Stomach Neoplasms2CTD_human
ENSG00000141510TP53C0038433Streptozotocin Diabetes1CTD_human
ENSG00000141510TP53C0040100Thymoma1CTD_human
ENSG00000141510TP53C0040136Thyroid Neoplasm1CTD_human
ENSG00000141510TP53C0042065Genitourinary Neoplasms1CTD_human
ENSG00000141510TP53C0042076Urologic Neoplasms1CTD_human
ENSG00000141510TP53C0079772T-Cell Lymphoma1CTD_human
ENSG00000141510TP53C0079773Lymphoma, T-Cell, Cutaneous1CTD_human
ENSG00000141510TP53C0085136Central Nervous System Neoplasms1CTD_human
ENSG00000141510TP53C0085390Li-Fraumeni Syndrome1CTD_human
ENSG00000141510TP53C0086404Experimental Hepatoma1CTD_human
ENSG00000141510TP53C0086501Keratoma2CTD_human
ENSG00000141510TP53C0149925Small cell carcinoma of lung2CTD_human
ENSG00000141510TP53C0151468Thyroid Gland Follicular Adenoma1CTD_human
ENSG00000141510TP53C0153381Malignant neoplasm of mouth1CTD_human
ENSG00000141510TP53C0153452Malignant neoplasm of gallbladder2CTD_human
ENSG00000141510TP53C0153601Malignant neoplasm of penis1CTD_human
ENSG00000141510TP53C0205641Adenocarcinoma, Basal Cell3CTD_human
ENSG00000141510TP53C0205642Adenocarcinoma, Oxyphilic3CTD_human
ENSG00000141510TP53C0205643Carcinoma, Cribriform3CTD_human
ENSG00000141510TP53C0205644Carcinoma, Granular Cell3CTD_human
ENSG00000141510TP53C0205645Adenocarcinoma, Tubular3CTD_human
ENSG00000141510TP53C0205646Adenoma, Basal Cell1CTD_human
ENSG00000141510TP53C0205647Follicular adenoma1CTD_human
ENSG00000141510TP53C0205648Adenoma, Microcystic1CTD_human
ENSG00000141510TP53C0205649Adenoma, Monomorphic1CTD_human
ENSG00000141510TP53C0205650Papillary adenoma1CTD_human
ENSG00000141510TP53C0205651Adenoma, Trabecular1CTD_human
ENSG00000141510TP53C0205696Anaplastic carcinoma2CTD_human
ENSG00000141510TP53C0205697Carcinoma, Spindle-Cell2CTD_human
ENSG00000141510TP53C0205698Undifferentiated carcinoma2CTD_human
ENSG00000141510TP53C0205699Carcinomatosis2CTD_human
ENSG00000141510TP53C0205770Choroid Plexus Papilloma1CTD_human
ENSG00000141510TP53C0205944Sarcoma, Epithelioid1CTD_human
ENSG00000141510TP53C0205945Sarcoma, Spindle Cell1CTD_human
ENSG00000141510TP53C0205969Thymic Carcinoma1CTD_human
ENSG00000141510TP53C0206681Adenocarcinoma, Clear Cell1CTD_human
ENSG00000141510TP53C0206686Adrenocortical carcinoma3CTD_human
ENSG00000141510TP53C0206698Cholangiocarcinoma1CTD_human
ENSG00000141510TP53C0235874Disease Exacerbation1CTD_human
ENSG00000141510TP53C0242379Malignant neoplasm of lung5CTD_human
ENSG00000141510TP53C0259783mixed gliomas3CTD_human
ENSG00000141510TP53C0262584Carcinoma, Small Cell1CTD_human
ENSG00000141510TP53C0263628Tumoral calcinosis1CTD_human
ENSG00000141510TP53C0263859Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome1CTD_human
ENSG00000141510TP53C0274861Arsenic Poisoning, Inorganic2CTD_human
ENSG00000141510TP53C0274862Nervous System, Organic Arsenic Poisoning2CTD_human
ENSG00000141510TP53C0279626Squamous cell carcinoma of esophagus1CTD_human
ENSG00000141510TP53C0279628Adenocarcinoma Of Esophagus1CTD_human
ENSG00000141510TP53C0279702Conventional (Clear Cell) Renal Cell Carcinoma4CTD_human
ENSG00000141510TP53C0311375Arsenic Poisoning2CTD_human
ENSG00000141510TP53C0341869Subfertility, Female1CTD_human
ENSG00000141510TP53C0345904Malignant neoplasm of liver2CTD_human
ENSG00000141510TP53C0345905Intrahepatic Cholangiocarcinoma1CTD_human
ENSG00000141510TP53C0345967Malignant mesothelioma1CTD_human
ENSG00000141510TP53C0346647Malignant neoplasm of pancreas1CTD_human
ENSG00000141510TP53C0376358Malignant neoplasm of prostate8CTD_human
ENSG00000141510TP53C0376407Granulomatous Slack Skin1CTD_human
ENSG00000141510TP53C0393554Amyotrophic Lateral Sclerosis With Dementia1CTD_human
ENSG00000141510TP53C0428791Aortic valve calcification1CTD_human
ENSG00000141510TP53C0521174Microcalcification1CTD_human
ENSG00000141510TP53C0543859Amyotrophic Lateral Sclerosis, Guam Form1CTD_human
ENSG00000141510TP53C0546837Malignant neoplasm of esophagus2CTD_human
ENSG00000141510TP53C0549473Thyroid carcinoma1CTD_human
ENSG00000141510TP53C0555198Malignant Glioma3CTD_human
ENSG00000141510TP53C0577631Carotid Atherosclerosis1CTD_human
ENSG00000141510TP53C0600178External Carotid Artery Diseases1CTD_human
ENSG00000141510TP53C0678222Breast Carcinoma6CTD_human
ENSG00000141510TP53C0750887Adrenal Cancer1CTD_human
ENSG00000141510TP53C0750986Internal Carotid Artery Diseases1CTD_human
ENSG00000141510TP53C0750987Arterial Diseases, Common Carotid1CTD_human
ENSG00000141510TP53C0751569Genitourinary Cancer1CTD_human
ENSG00000141510TP53C0751571Cancer of Urinary Tract1CTD_human
ENSG00000141510TP53C0751620Central Nervous System Neoplasms, Primary1CTD_human
ENSG00000141510TP53C0751851Arsenic Encephalopathy2CTD_human
ENSG00000141510TP53C0751852Arsenic Induced Polyneuropathy2CTD_human
ENSG00000141510TP53C0848676Subfertility, Male1CTD_human
ENSG00000141510TP53C0876994Cardiotoxicity1CTD_human
ENSG00000141510TP53C0917730Female sterility1CTD_human
ENSG00000141510TP53C0917731Male sterility1CTD_human
ENSG00000141510TP53C0917798Cerebral Ischemia1CTD_human
ENSG00000141510TP53C0919267ovarian neoplasm1CTD_human
ENSG00000141510TP53C1140680Malignant neoplasm of ovary1CTD_human
ENSG00000141510TP53C1168401Squamous cell carcinoma of the head and neck2CTD_human
ENSG00000141510TP53C1176475Ductal Carcinoma1CTD_human
ENSG00000141510TP53C1257931Mammary Neoplasms, Human6CTD_human
ENSG00000141510TP53C1261473Sarcoma1CTD_human
ENSG00000141510TP53C1266042Chromophobe Renal Cell Carcinoma4CTD_human
ENSG00000141510TP53C1266043Sarcomatoid Renal Cell Carcinoma4CTD_human
ENSG00000141510TP53C1266044Collecting Duct Carcinoma of the Kidney4CTD_human
ENSG00000141510TP53C1306837Papillary Renal Cell Carcinoma4CTD_human
ENSG00000141510TP53C1368275Pigmented Basal Cell Carcinoma3CTD_human
ENSG00000141510TP53C1458155Mammary Neoplasms6CTD_human
ENSG00000141510TP53C1527303Chronic Airflow Obstruction1CTD_human
ENSG00000141510TP53C1565662Acute Kidney Insufficiency1CTD_human
ENSG00000141510TP53C1708349Hereditary Diffuse Gastric Cancer2CTD_human
ENSG00000141510TP53C1859972ADRENOCORTICAL CARCINOMA, HEREDITARY1CTD_human
ENSG00000141510TP53C1860789Leukemia, Megakaryoblastic, of Down Syndrome1CTD_human
ENSG00000141510TP53C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human
ENSG00000141510TP53C2239176Liver carcinoma6CTD_human
ENSG00000141510TP53C2350037Clinically Isolated Syndrome, CNS Demyelinating1CTD_human
ENSG00000141510TP53C2609414Acute kidney injury1CTD_human
ENSG00000141510TP53C2713368Hematopoetic Myelodysplasia1CTD_human
ENSG00000141510TP53C2930471Bilateral Wilms Tumor1CTD_human
ENSG00000141510TP53C2930974Acute erythroleukemia1CTD_human
ENSG00000141510TP53C2930975Acute erythroleukemia - M6a subtype1CTD_human
ENSG00000141510TP53C2930976Acute myeloid leukemia FAB-M61CTD_human
ENSG00000141510TP53C2930977Acute erythroleukemia - M6b subtype1CTD_human
ENSG00000141510TP53C2931713Chromosome 17 deletion1CTD_human
ENSG00000141510TP53C2931822Nasopharyngeal carcinoma1CTD_human
ENSG00000141510TP53C3463824MYELODYSPLASTIC SYNDROME1CTD_human
ENSG00000141510TP53C3683846Chromosome 17p Deletion Syndrome1CTD_human
ENSG00000141510TP53C3805278Extrahepatic Cholangiocarcinoma1CTD_human
ENSG00000141510TP53C4551472Hypertrophic obstructive cardiomyopathy1CTD_human
ENSG00000141510TP53C4704874Mammary Carcinoma, Human6CTD_human
ENSG00000141510TP53C4721610Carcinoma, Ovarian Epithelial1CTD_human
ENSG00000141510TP53C4721806Carcinoma, Basal Cell3CTD_human