CTNNB1, catenin beta 1, 1499

N. diseases: 1368; N. variants: 68
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0079218
Disease:
Fibromatosis, Aggressive
0.090 GeneticVariation BEFREE Primary sporadic DTFs harboring a CTNNB1 S45F mutation have a higher risk of recurrence after surgery compared to T41A, S45P, and WT DTF, but this association seems to be mediated by tumor size. 31804402 2019
dbSNP: rs121913412
rs121913412
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0027651
Disease:
Neoplasms
0.070 GeneticVariation BEFREE Additional adjustment for tumor size yielded a P-value of 0.082 with hazard ratio's of 0.83 [95% confidence interval (CI) 0.48-1.42), 0.37 (95% CI 0.12-1.14), and 0.44 (95% CI 0.21-0.92) for T41A, S45P and WT DTF tumors compared to S45F DTF tumors. 31804402 2019
dbSNP: rs121913407
rs121913407
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0027651
Disease:
Neoplasms
0.050 GeneticVariation BEFREE Additional adjustment for tumor size yielded a P-value of 0.082 with hazard ratio's of 0.83 [95% confidence interval (CI) 0.48-1.42), 0.37 (95% CI 0.12-1.14), and 0.44 (95% CI 0.21-0.92) for T41A, S45P and WT DTF tumors compared to S45F DTF tumors. 31804402 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0027651
Disease:
Neoplasms
0.050 GeneticVariation BEFREE Additional adjustment for tumor size yielded a P-value of 0.082 with hazard ratio's of 0.83 [95% confidence interval (CI) 0.48-1.42), 0.37 (95% CI 0.12-1.14), and 0.44 (95% CI 0.21-0.92) for T41A, S45P and WT DTF tumors compared to S45F DTF tumors. 31804402 2019
dbSNP: rs4135385
rs4135385
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0026764
Disease:
Multiple Myeloma
0.010 GeneticVariation BEFREE Our results demonstrate that the polymorphism of β-catenin gene (rs4135385) may be an independent predictive factor in MM. 31506802 2019
dbSNP: rs4533622
rs4533622
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0026764
Disease:
Multiple Myeloma
0.010 GeneticVariation BEFREE The other polymorphism (rs4533622) of β-catenin gene did not markedly influence these clinical parameters, although MM was diagnosed at significantly younger age in subjects with CC genotype compared to AG/AA combined genotypes (59.1 vs. 65.7 years, p = 0.015). 31506802 2019
dbSNP: rs13072632
rs13072632
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167 2019
dbSNP: rs13072632
rs13072632
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167 2019
dbSNP: rs4135385
rs4135385
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167 2019
dbSNP: rs4135385
rs4135385
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167 2019
dbSNP: rs121913407
rs121913407
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0238463
Disease:
Papillary thyroid carcinoma
0.010 GeneticVariation BEFREE SOX11 expression in a case of papillary thyroid carcinoma with fibromatosis/fasciitis-like stroma containing BRAF c.1799_1801delTGA and CTNNB1 c.133T>C mutations. 31327063 2019
dbSNP: rs121913407
rs121913407
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0238463
Disease:
Papillary thyroid carcinoma
0.010 GeneticVariation BEFREE We describe a case of papillary thyroid carcinoma with fibromatosis/fasciitis-like stroma (PTC-FLS) that contained the rare BRAF c.1799_1801delTGA (p.V600_K601delinsE) mutation, which has not previously been reported in this tumour, as well as the CTNNB1 c.133T>C (p.S45P) mutation. 31327063 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0079218
Disease:
Fibromatosis, Aggressive
0.090 GeneticVariation BEFREE Furthermore, the combination of hydroxychloroquine and sorafenib enhances the antiproliferative and proapoptotic effects in S45F-mutated DT cells, suggesting that profiling β-catenin status could guide clinical management of desmoid patients who are considering sorafenib treatment. 30980399 2019
dbSNP: rs121913412
rs121913412
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0079218
Disease:
Fibromatosis, Aggressive
0.060 GeneticVariation BEFREE Our findings suggest that the response to sorafenib differs when comparing S45F-mutated DTs and T41A-mutated or wild-type DTs. 30980399 2019
dbSNP: rs121913412
rs121913412
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C1269955
Disease:
Tumor Cell Invasion
0.010 GeneticVariation BEFREE Our results revealed that a lower dose of sorafenib was able to inhibit cell viability, migration, and invasion of wild-type and T41A-mutated DTs. 30980399 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0027651
Disease:
Neoplasms
0.050 GeneticVariation BEFREE Finally, using a previously reported 16-gene signature, it was shown that YAP1-ΔN90-β-catenin HB tumors exhibited genetic similarities with more proliferative, less differentiated, GS-negative HB patient tumors, whereas YAP1-S33Y/S45Y-β-catenin HB exhibited heterogeneity and clustered with both well-differentiated GS-positive and proliferative GS-negative patient tumors. 30794807 2019
dbSNP: rs121913400
rs121913400
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0027651
Disease:
Neoplasms
0.030 GeneticVariation BEFREE Because heterogeneity in downstream signaling is being identified owing to mutational differences even in the β-catenin gene alone, we investigated if co-expression of point mutants of β-catenin (S33Y or S45Y) with S127A-YAP1 led to similar tumors as YAP1-ΔN90-β-catenin. 30794807 2019
dbSNP: rs121913400
rs121913400
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0206624
Disease:
Hepatoblastoma
0.010 GeneticVariation BEFREE Co-expression of S33Y/S45Y-β-catenin and S127A-YAP1 led to activation of Yap and Wnt signaling and development of HB, with 100% mortality by 13 to 14 weeks. 30794807 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0206624
Disease:
Hepatoblastoma
0.010 GeneticVariation BEFREE Finally, using a previously reported 16-gene signature, it was shown that YAP1-ΔN90-β-catenin HB tumors exhibited genetic similarities with more proliferative, less differentiated, GS-negative HB patient tumors, whereas YAP1-S33Y/S45Y-β-catenin HB exhibited heterogeneity and clustered with both well-differentiated GS-positive and proliferative GS-negative patient tumors. 30794807 2019
dbSNP: rs1722845
rs1722845
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0079218
Disease:
Fibromatosis, Aggressive
0.090 GeneticVariation BEFREE This study examines whether the different CTNNB1 mutants (T41A, S45F) occurring in DTF tumors differentially affect Wnt signaling activity, which might explain the different disease course between DTF patients harboring different CTNNB1 mutations. 30528042 2019
dbSNP: rs121913412
rs121913412
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0079218
Disease:
Fibromatosis, Aggressive
0.060 GeneticVariation BEFREE No statistically significant difference in relative expression levels of Wnt target genes AXIN2, DKK1 and CCND1 was identified between either CTNNB1 wild-type, S45F or T41A mutated DTF samples. 30528042 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0027651
Disease:
Neoplasms
0.050 GeneticVariation BEFREE This study examines whether the different CTNNB1 mutants (T41A, S45F) occurring in DTF tumors differentially affect Wnt signaling activity, which might explain the different disease course between DTF patients harboring different CTNNB1 mutations. 30528042 2019
dbSNP: rs121913409
rs121913409
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C2239176
Disease:
Liver carcinoma
0.820 GeneticVariation BEFREE Oncogenic potential of N-terminal deletion and S45Y mutant β-catenin in promoting hepatocellular carcinoma development in mice. 30419856 2018
dbSNP: rs1131692181
rs1131692181
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C0267026
Disease:
Actinic cheilitis
0.010 GeneticVariation BEFREE We generated transgenic mice with cardiomyocyte-specific overexpression of a FLAG-tagged human desmoglein-2 harbouring the Q558* nonsense mutation found in an AC patient. 30304392 2019