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Fusion gene ID: 39160 |
FusionGeneSummary for TP53_ELL |
Fusion gene summary |
Fusion gene information | Fusion gene name: TP53_ELL | Fusion gene ID: 39160 | Hgene | Tgene | Gene symbol | TP53 | ELL | Gene ID | 7158 | 8178 |
Gene name | tumor protein p53 binding protein 1 | elongation factor for RNA polymerase II | |
Synonyms | 53BP1|TDRD30|TP53|p202|p53BP1 | C19orf17|ELL1|MEN|PPP1R68 | |
Cytomap | 15q15.3 | 19p13.11 | |
Type of gene | protein-coding | protein-coding | |
Description | TP53-binding protein 1p53-binding protein 1tumor protein 53-binding protein, 1tumor suppressor p53-binding protein 1 | RNA polymerase II elongation factor ELLELL gene (11-19 lysine-rich leukemia gene)eleven-nineteen lysine-rich leukemia proteinelongation factor RNA polymerase IIprotein phosphatase 1, regulatory subunit 68 | |
Modification date | 20180527 | 20180519 | |
UniProtAcc | P04637 | P55199 | |
Ensembl transtripts involved in fusion gene | ENST00000413465, ENST00000359597, ENST00000269305, ENST00000455263, ENST00000420246, ENST00000445888, ENST00000574684, | ENST00000262809, ENST00000596124, | |
Fusion gene scores | * DoF score | 22 X 7 X 7=1078 | 6 X 10 X 5=300 |
# samples | 21 | 14 | |
** MAII score | log2(21/1078*10)=-2.35989594508638 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(14/300*10)=-1.09953567355091 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: TP53 [Title/Abstract] AND ELL [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | TP53 | GO:0006303 | double-strand break repair via nonhomologous end joining | 23333306|23760478|28241136 |
Hgene | TP53 | GO:0006974 | cellular response to DNA damage stimulus | 17500065|28241136 |
Hgene | TP53 | GO:0045830 | positive regulation of isotype switching | 23345425 |
Hgene | TP53 | GO:0051260 | protein homooligomerization | 23345425 |
Hgene | TP53 | GO:2000042 | negative regulation of double-strand break repair via homologous recombination | 23333306|23345425 |
Tgene | ELL | GO:0010923 | negative regulation of phosphatase activity | 19389623 |
Fusion gene information from three resources (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | LD | SARC | TCGA-K1-A6RU-01A | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
intron-3CDS | ENST00000413465 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
intron-3CDS | ENST00000413465 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
intron-3CDS | ENST00000359597 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
intron-3CDS | ENST00000359597 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000269305 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000269305 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000455263 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000455263 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000420246 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000420246 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000445888 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
5UTR-3CDS | ENST00000445888 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
intron-3CDS | ENST00000574684 | ENST00000262809 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
intron-3CDS | ENST00000574684 | ENST00000596124 | TP53 | chr17 | 7590695 | - | ELL | chr19 | 18561785 | - |
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FusionProtFeatures for TP53_ELL |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
TP53 | ELL |
Elongation factor component of the super elongationcomplex (SEC), a complex required to increase the catalytic rateof RNA polymerase II transcription by suppressing transientpausing by the polymerase at multiple sites along the DNA.Elongation factor component of the little elongation complex(LEC), a complex required to regulate small nuclear RNA (snRNA)gene transcription by RNA polymerase II and III (PubMed:22195968,PubMed:23932780). Specifically required for stimulating theelongation step of RNA polymerase II- and III-dependent snRNA genetranscription (PubMed:23932780). ELL also plays an early rolebefore its assembly into in the SEC complex by stabilizing RNApolymerase II recruitment/initiation and entry into the pausesite. Required to stabilize the pre-initiation complex and earlyelongation. {ECO:0000269|PubMed:16006523,ECO:0000269|PubMed:20159561, ECO:0000269|PubMed:20471948,ECO:0000269|PubMed:22195968, ECO:0000269|PubMed:22252557,ECO:0000269|PubMed:23932780, ECO:0000269|PubMed:8596958}. |
Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at . * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for TP53_ELL |
For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for TP53_ELL |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in . |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
TP53 | WWOX, CDC14A, MAGEB18, DVL2, TP53BP1, BAK1, ATM, BLM, BRCA1, ATR, TFAP2A, EPHA3, BARD1, RAD51, BRCA2, BRE, BRCC3, MDM2, TP53, RPA1, CHEK1, AR, PRKDC, S100B, SFN, TFAP2C, CDKN1A, LINC01194, EP300, PRMT1, CARM1, ANKRD2, YBX1, APTX, PARP1, XRCC1, CABLES2, CABLES1, RPL11, CDKN2A, MDC1, PHB, MTA1, MTA2, PML, EEF2, TP53INP1, ING4, ING5, HIPK1, TP53RK, RCHY1, UBE2A, PTEN, RRM2B, RRM2, HIF1A, HDAC1, CREBBP, SMARCB1, SMARCA4, SMARCC1, SUMO1, UBE2I, CHD3, HIPK3, TDG, TADA3, CREB1, HIPK2, KAT2B, KIAA0087, RAB4A, THAP8, CCDC106, FAM173A, S100A8, ZCCHC10, ANXA3, ARL3, ATF3, BCR, CCT5, COX17, DLEU1, FXYD6, GSTM4, HSPB1, PNP, STX5, WDR33, ARIH2, BTBD2, CCL18, CDC42, EIF2S2, LAMA4, MAD2L1BP, MPHOSPH6, PAFAH1B3, PCDHA4, PPA1, PSMD11, SAT1, SERPINB9, SNRPN, SULT1E1, TK1, CDKN2C, ERH, ZNF24, PLAGL1, THRB, ELL, E4F1, ABL1, GSK3B, HSP90AA1, TOP1, BRF1, ESR1, EIF2AK2, S100A4, HMGB1, APEX1, HNF4A, NDN, PLK3, HTT, PTGS2, AURKA, RFC1, CDK1, CDK2, CCNA2, PIN1, GPS2, CCNG1, YWHAZ, MDM4, TFDP1, NFKBIA, ZNF148, PPP1R13L, MED1, WRN, TBP, CDC14B, STK11, MED17, IFI16, GTF2H1, PIAS1, EFEMP2, ERCC3, ERCC2, ERCC6, MAPK8, MAPK9, MAPK10, CEBPZ, PPP4C, NCL, TSG101, TAF1, BAG1, TOP2A, TOP2B, CDK9, EGR1, PRKRIR, CDK7, MNAT1, GNL3, TAF1B, TAF1A, TAF1C, MAPK3, MAPK1, TOPORS, USP7, HSPA9, ING1, POLA1, SMN1, TEP1, CCNH, TP53BP2, KPNB1, HSPA8, WT1, PTTG1, TAF9, CUL9, NR3C1, FKBP3, RYBP, AIMP2, UCHL1, CFLAR, ITCH, DHFR, CCAR1, PSME3, HSPA4, STUB1, PTK2, NUMB, SERPINH1, COPS5, VRK1, ZMIZ1, ZMIZ2, CDK5, ZMYND11, KAT7, ETHE1, CHD8, DAPK1, TXN, OTUD5, USP11, USP39, WDR48, PADI4, NR4A1, FBXO11, UBE2N, HDAC2, SP1, STAT6, TAF6, RFWD2, ADH5, AGBL2, ASF1A, ASPM, BRD8, NPRL3, TRAPPC11, DAB2IP, DNAJB6, DPH1, AGO1, AGO2, GTPBP4, IGF2BP1, LOC613037, LRPPRC, MTHFSD, MYL9, PIWIL1, RNF38, SMARCD2, SPSB1, TRMT11, TTLL5, CUL7, BANP, RNF20, ZBTB7A, KAT8, PSMD10, SMYD2, SETD7, BACH1, MAFK, NCOR1, KAT6A, XRCC6, CTBP1, MAGEA2, NPM1, KAT5, RPL5, RPL23, YY1, VRK2, SETD2, VHL, RAD23A, HABP4, SERBP1, ZBTB2, ZNF420, KDM1A, H2AFX, SP3, TRRAP, MSH2, ING2, KMT2A, RBBP5, MEN1, WDR5, NFYA, NFYB, HECW2, CHEK2, PHF1, KAT2A, TAF5L, SUPT3H, SUPT7L, TADA1, TADA2A, TAF10, SIRT1, SIN3A, PRAM1, PIAS2, DNMT1, KMT2E, RB1CC1, PRDM2, EHMT1, HMGA1, USP29, VDR, UBE3A, EHMT2, NOC2L, AURKB, SIVA1, MDH1, RNF34, RFFL, HDAC9, G3BP1, G3BP2, KPNA4, TRIM24, L3MBTL1, PSMC5, ZNF668, USP10, UBR5, GNL3L, SETD8, IKBKB, BTRC, MSL2, RYK, UIMC1, NUB1, SKI, SOX4, CDK8, MED21, UBE4B, BAIAP2L1, TTK, DAXX, IGF1R, RFWD3, RPS7, HDAC5, HUWE1, RPS3, PSMC3, PSMD4, UHRF2, FBXO42, USP42, SMURF1, NOTCH4, UTP14A, CSNK1A1, HSPA5, ZNHIT1, SYVN1, OTUB1, PDLIM7, APOH, BMP1, SENP3, UFD1L, RAP1B, BCL2L1, RCC1, ANXA7, GADD45A, TPT1, HSPA1A, USO1, SMAD2, SMAD3, RPL26, TRIM27, BCL2, TRIAP1, TRIM28, PRMT3, AXIN1, SIN3B, AGT, MSH6, SET, ARID1A, ETS1, ETS2, ACTL6A, CSNK2B, MAPK14, MAP9, NR0B2, NCOA1, NCOA3, SIRT7, KDM4D, COPS2, SMARCD1, EWSR1, CCDC8, UBE2B, RANBP2, RPS10, LYN, PPARGC1A, HECW1, GAPDH, SRSF1, CRYAB, FBXO4, CUL4A, DTL, PCNA, RB1, PPP1CC, RNF43, CSNK2A1, PRKD1, GPS1, DHCR24, TP63, PRKCD, NQO1, TFAP4, PIAS4, ZHX1, DMTF1, HEXIM1, MUL1, TSC22D1, UBD, ANG, PDCD5, MIF, ITPK1, TXNRD1, MAP3K1, ERCC8, ARID3A, CSNK1D, VPRBP, ELAVL1, TAF5, ERBB4, PLK1, CASP8, SCAMP1, HRAS, MAGED2, UBE2M, DAPK3, SOCS1, SMAD7, PARK7, SMAD1, BMI1, RING1, RNF2, MUC1, ECT2, TRIM39, HNRNPK, NABP2, TWIST1, PHF20, HECTD3, VCP, EP400, MYC, SNAI1, MTOR, TNFAIP3, MKRN1, PPP1CA, TMED9, RNF39, TRIM8, BHLHE40, RABL6, PAN2, ANXA2, MYBBP1A, GTF2H4, RPS26, ECD, TXNIP, UBE2K, FCAMR, GPX2, SQSTM1, PSMB3, ANK2, NCOA2, CLK3, ICK, CREBZF, C10orf90, RPS27A, XPC, PSMD6, CUL4B, PTTG1IP, HERC2, DNAJB1, ZBTB16, NLK, MCL1, BCL2L2, RUNX2, ATRX, RNF128, TNK2, DNAJC7, ZBTB8A, PATZ1, MVP, MAPK7, ABR, ACSL4, ACTA2, ACTB, AIFM2, AKAP12, ATP5A1, BAG2, PRRC2A, PRRC2C, CAD, CAPN1, CCT2, CCT3, CCT4, CCT6A, CCT7, CCT8, CEP55, CPNE7, CRTC2, TUBB, DDB1, DDX5, DGCR14, DNAJA1, DNAJA2, DOCK7, EBNA1BP2, EEF1A1, EIF4E2, ENAH, MRPS18B, RCN2, RPL24, EXOSC7, EXOSC8, MZT2B, FAU, FBL, FBXO21, FTH1, MOGS, GIGYF2, GPATCH8, GRWD1, GTF3C3, GTF3C4, RPL27AP6, HECTD1, HNRNPA1, HNRNPA2B1, HNRNPF, HNRNPH1, HNRNPM, HNRNPU, HPCA, HSP90AB1, HSPA1L, IDH3B, IGF2BP3, ARHGEF17, IQGAP1, IRS4, ITPKC, RPS15P2, LY6G5B, MFAP4, MRPL24, MRPL38, MRPL39, MRPL41, MRPS14, MRPS2, MRPS22, MRPS23, MRPS25, MRPS27, MRPS28, MRPS5, MRPS9, OBSL1, RPL13, PABPC1, PCBP1, PCMT1, PDCD6, PHKA2, PHKB, PHKG2, POLDIP2, PPFIBP1, PPP3CA, PPP3R1, PTCD3, RAE1, RAVER1, RBBP4, RBBP7, RBX1, RDH13, RFC3, RFC4, TRMT10C, RPL7A, RPL10A, RPL10L, RPL12, RPL14, RPL15, RPL18, RPL18A, RPL19, RPL21, RPL23A, RPL26L1, RPL27, RPL3, RPL30, RPL31, RPL37A, RPL4, RPL6, RPL7, RPL8, RPLP0, RPLP2, RPRD1A, RPS14, RPS15, RPS17, RPS2, RPS24, RPS25, RPS27, RPS3A, RPS6, RPS8, RPS9, RRP1B, SART1, SCO2, SF3B2, SKP1, SLC2A12, SNRPD3, SNW1, SUPT6H, TBC1D4, TCEAL4, TCP1, TFRC, TIMM50, TOR1AIP2, TUBA1A, TUBA1C, TUBA4A, TUBB2A, TUBB4B, TUBG1, UBB, UBR4, VASP, VAT1, DCAF7, YTHDF1, YWHAE, ZWINT, SNAI2, PER2, TRIM59, TSC22D3, UBC, TRIM32, HSPA1B, HSPA2, HSPA6, BAG5, RBM3, RBM39, SRSF6, DDX3X, ACTBL2, TUBA8, MYH9, MYLK, MYO1C, MYO6, TPM1, TPM3, TPM4, CAPZB, GSN, VIM, CKAP4, CORO1C, DBN1, FLNA, LIMA1, LMNA, RPL28, RPS4X, RPS13, RPS16, RPS18, RPS19, HNRNPL, ALYREF, CALD1, CHMP4B, CLTA, CLTB, CLTC, DHRS4, EIF5B, GNB2, GTF2I, HADHB, KCTD17, LSM14A, LYZ, NME4, PPP1R12A, PRMT5, SLC25A5, THRAP3, WDR77, MAP1LC3B, FAM175B, XAF1, FZR1, SENP1, PPP1R13B, RELA, CHUK, CXXC1, ASH2L, SETD1A, WDR82, S100A6, ZNF302, IRF7, RANBP9, CAPG, NMT1, NMT2, BCL6, NABP1, NEIL3, PADI1, TOP1MT, YY2, ZIC3, TCF4, SRPK1, SAFB, SAFB2, MAPKAPK5, KDM6A, ABCE1, CELA2B, TCEAL1, BRD7, HERC5, SRC, ZBTB33, GUCY1A3, COPS4, BIRC6, FBXW11, TFAP2B, KLF5, AAGAB, ACVR1C, ADAM28, ARMCX5, ARPP21, CENPA, CLCA3P, CPA5, CYP20A1, C12orf49, DCLRE1C, DDX50, DKK2, DOT1L, DPP6, DZIP1, EGFR, ELL3, EPG5, ETV1, EXOSC4, RMDN1, FHIT, GABRG3, GFPT2, GK2, GOLGA2P5, GPSM3, GRIN2B, HAUS1, HAUS4, HINT3, HOXA9, HYAL4, IL1A, CXCL8, IMP3, INSIG1, IRX1, JMJD8, KLHL40, KLRF1, LAPTM5, LAP3, LGI4, MCM8, MED8, MED22, MFSD12, MIA2, MORN2, MYBPC1, MYOT, NEUROG2, NT5C3A, PACRG, PDIA5, PHYH, PKIA, PLAC8, POLD3, POLR1D, PRPF6, PSD3, PTX3, PURG, RECQL5, RETNLB, RNASE4, RPL36P14, RPUSD4, SACS, SAMD7, SBF2, SEC63, SLAMF1, SLC7A2, SNX12, SPESP1, STAM2, STT3B, STXBP4, STX2, TBC1D24, THAP1, NELFCD, TMEM200A, TOM1L1, TTC28, UBQLN2, UMPS, USH2A, USP1, ZNF300, ZNF619, ZNF763, TERT, RBBP6, PLCG2, CRK, APPL1, ZBTB17, UBE2Q1, OFD1, SSX2IP, CEP120, CEP152, SPICE1, CEP128, CEP135, NINL, NIN, RPGRIP1L, HINFP, RNF125, FOXO3, PPP2R5C, BAX, PPP2R1A, STK4, CSNK1E, TP73, GLI1, NFATC1, SMARCA5, FBXW8, MOV10, NPAS3, PES1, POLRMT, RNASEL, RPA2, RPL29P11, SMG5, FOXA3, FOXB1, FOXC1, FOXG1, FOXJ3, FOXK1, FOXK2, REV1, HSP90B1, BRINP1, FOXN1, FOXP1, FOXQ1, FOXS1, TFIP11, ERN1, DNMT3L, UHRF1, LAMTOR5, TGM2, NAT10, CCND1, USP24, GMPS, NR1I2, TRIM65, BCL2L12, DGKZ, TSNAX, KIF2A, CDKN1C, HBB, EEA1, GLTSCR2, LRRK2, POLI, ATXN3, USP15, CYLD, USP21, STAMBP, KIT, NGFR, HYPK, TRAF6, SMG7, BECN1, TBPL1, MSI2, OTUD1, FBXW7, FAM111A, GPR156, RORC, HOMER3, HR, OLIG2, KDR, AIPL1, DACH1, DLST, PDHA1, RBPJ, CETP, ACKR3, RAB7A, SLC9A9, STARD10, UBE2V2, ZNF679, ZNF839, HEY1, TRIM45, PARK2, YWHAB | ELL | SIRT2, ZHX1, TP53, EAF1, EAF2, SNF8, USPL1, MLLT3, MLLT1, KMT2A, TFPT, UBC, MED26, ICE2, ICE1, AFF4, CDK9, MCM2, SNRPA1, ELL3, DENND2D, OFD1, DYNLL1, CTR9, HUWE1, NCBP2, FGFR1OP2, SIKE1, VWA9, ASPM, CAMKV, PIP4K2A, TRIM25 |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for TP53_ELL |
Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | TP53 | P04637 | DB01593 | Zinc | Cellular tumor antigen p53 | small molecule | approved|investigational |
Hgene | TP53 | P04637 | DB00945 | Acetylsalicylic acid | Cellular tumor antigen p53 | small molecule | approved|vet_approved |
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RelatedDiseases for TP53_ELL |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | TP53 | C1835398 | LI-FRAUMENI SYNDROME 1 | 19 | CTD_human;UNIPROT |
Hgene | TP53 | C0009404 | Colorectal Neoplasms | 8 | CTD_human |
Hgene | TP53 | C0033578 | Prostatic Neoplasms | 6 | CTD_human;HPO |
Hgene | TP53 | C2239176 | Liver carcinoma | 6 | CTD_human;HPO |
Hgene | TP53 | C0024121 | Lung Neoplasms | 5 | CTD_human |
Hgene | TP53 | C1458155 | Mammary Neoplasms | 5 | CTD_human |
Hgene | TP53 | C0005695 | Bladder Neoplasm | 4 | CTD_human |
Hgene | TP53 | C0007134 | Renal Cell Carcinoma | 4 | CTD_human;HPO |
Hgene | TP53 | C0001418 | Adenocarcinoma | 3 | CTD_human |
Hgene | TP53 | C0007117 | Basal cell carcinoma | 3 | CTD_human |
Hgene | TP53 | C0007131 | Non-Small Cell Lung Carcinoma | 3 | CTD_human |
Hgene | TP53 | C0009375 | Colonic Neoplasms | 3 | CTD_human;HPO |
Hgene | TP53 | C0017638 | Glioma | 3 | CTD_human |
Hgene | TP53 | C0025202 | melanoma | 3 | CTD_human |
Hgene | TP53 | C0206686 | Adrenocortical carcinoma | 3 | CTD_human;HPO;ORPHANET |
Hgene | TP53 | C0001969 | Alcoholic Intoxication | 2 | PSYGENET |
Hgene | TP53 | C0001973 | Alcoholic Intoxication, Chronic | 2 | PSYGENET |
Hgene | TP53 | C0007137 | Squamous cell carcinoma | 2 | CTD_human |
Hgene | TP53 | C0014859 | Esophageal Neoplasms | 2 | CTD_human |
Hgene | TP53 | C0016978 | gallbladder neoplasm | 2 | CTD_human |
Hgene | TP53 | C0023903 | Liver neoplasms | 2 | CTD_human |
Hgene | TP53 | C0036920 | Sezary Syndrome | 2 | CTD_human |
Hgene | TP53 | C0038356 | Stomach Neoplasms | 2 | CTD_human;HPO |
Hgene | TP53 | C0149925 | Small cell carcinoma of lung | 2 | CTD_human;ORPHANET |
Hgene | TP53 | C0311375 | Arsenic Poisoning | 2 | CTD_human |
Hgene | TP53 | C0001430 | Adenoma | 1 | CTD_human |
Hgene | TP53 | C0001624 | Adrenal Gland Neoplasms | 1 | CTD_human |
Hgene | TP53 | C0002736 | Amyotrophic Lateral Sclerosis | 1 | CTD_human |
Hgene | TP53 | C0004698 | Balkan Nephropathy | 1 | CTD_human |
Hgene | TP53 | C0007138 | Carcinoma, Transitional Cell | 1 | CTD_human |
Hgene | TP53 | C0007194 | Hypertrophic Cardiomyopathy | 1 | CTD_human |
Hgene | TP53 | C0007273 | Carotid Artery Diseases | 1 | CTD_human |
Hgene | TP53 | C0007621 | Neoplastic Cell Transformation | 1 | CTD_human |
Hgene | TP53 | C0007786 | Brain Ischemia | 1 | CTD_human |
Hgene | TP53 | C0010606 | Adenoid Cystic Carcinoma | 1 | CTD_human |
Hgene | TP53 | C0011303 | Demyelinating Diseases | 1 | CTD_human |
Hgene | TP53 | C0011853 | Diabetes Mellitus, Experimental | 1 | CTD_human |
Hgene | TP53 | C0013990 | Pathological accumulation of air in tissues | 1 | CTD_human |
Hgene | TP53 | C0018923 | Hemangiosarcoma | 1 | CTD_human |
Hgene | TP53 | C0020538 | Hypertensive disease | 1 | CTD_human |
Hgene | TP53 | C0021361 | Female infertility | 1 | CTD_human |
Hgene | TP53 | C0021364 | Male infertility | 1 | CTD_human |
Hgene | TP53 | C0022116 | Ischemia | 1 | CTD_human |
Hgene | TP53 | C0022593 | Keratosis | 1 | CTD_human |
Hgene | TP53 | C0022783 | Vulvar Lichen Sclerosus | 1 | CTD_human |
Hgene | TP53 | C0023434 | Chronic Lymphocytic Leukemia | 1 | CTD_human;ORPHANET |
Hgene | TP53 | C0023897 | Liver Diseases, Parasitic | 1 | CTD_human |
Hgene | TP53 | C0023904 | Liver Neoplasms, Experimental | 1 | CTD_human |
Hgene | TP53 | C0024117 | Chronic Obstructive Airway Disease | 1 | CTD_human |
Hgene | TP53 | C0024809 | Marijuana Abuse | 1 | PSYGENET |
Hgene | TP53 | C0026640 | Mouth Neoplasms | 1 | CTD_human |
Hgene | TP53 | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Hgene | TP53 | C0029463 | Osteosarcoma | 1 | CTD_human;HPO |
Hgene | TP53 | C0030849 | Penile Neoplasms | 1 | CTD_human |
Hgene | TP53 | C0032578 | Polyploidy | 1 | CTD_human |
Hgene | TP53 | C0033860 | Psoriasis | 1 | CTD_human |
Hgene | TP53 | C0036341 | Schizophrenia | 1 | CTD_human |
Hgene | TP53 | C0037286 | Skin Neoplasms | 1 | CTD_human;HPO |
Hgene | TP53 | C0040100 | Thymoma | 1 | CTD_human |
Hgene | TP53 | C0040136 | Thyroid Neoplasm | 1 | CTD_human |
Hgene | TP53 | C0042065 | Genitourinary Neoplasms | 1 | CTD_human |
Hgene | TP53 | C0042076 | Urologic Neoplasms | 1 | CTD_human |
Hgene | TP53 | C0079772 | T-Cell Lymphoma | 1 | CTD_human |
Hgene | TP53 | C0079773 | Lymphoma, T-Cell, Cutaneous | 1 | CTD_human |
Hgene | TP53 | C0085136 | Central Nervous System Neoplasms | 1 | CTD_human |
Hgene | TP53 | C0085390 | Li-Fraumeni Syndrome | 1 | CTD_human;ORPHANET |
Hgene | TP53 | C0206681 | Adenocarcinoma, Clear Cell | 1 | CTD_human |
Hgene | TP53 | C0206698 | Cholangiocarcinoma | 1 | CTD_human |
Hgene | TP53 | C0262584 | Carcinoma, Small Cell | 1 | CTD_human |
Hgene | TP53 | C0279626 | Squamous cell carcinoma of esophagus | 1 | CTD_human |
Hgene | TP53 | C0279628 | Adenocarcinoma Of Esophagus | 1 | CTD_human |
Hgene | TP53 | C0345967 | Malignant mesothelioma | 1 | CTD_human |
Hgene | TP53 | C0677886 | Epithelial ovarian cancer | 1 | CTD_human |
Hgene | TP53 | C1168401 | Squamous cell carcinoma of the head and neck | 1 | CTD_human |
Hgene | TP53 | C1261473 | Sarcoma | 1 | CTD_human;HPO |
Hgene | TP53 | C1860789 | Leukemia, Megakaryoblastic, of Down Syndrome | 1 | CTD_human |
Hgene | TP53 | C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | 1 | CTD_human |
Hgene | TP53 | C2609414 | Acute kidney injury | 1 | CTD_human |
Hgene | TP53 | C2931713 | Chromosome 17 deletion | 1 | CTD_human |
Hgene | TP53 | C2931822 | Nasopharyngeal carcinoma | 1 | CTD_human |