CDX2, caudal type homeobox 2, 1045

N. diseases: 278; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 PosttranslationalModification disease BEFREE The following study was conducted with the main focus on the effect of LINC00518 on the growth and metastasis of BC epithelial cells via the Wnt signaling pathway through regulation of the methylation of CDX2 gene. 30611858 2019
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 Biomarker disease BEFREE SATB2 and CDX2 IHC was performed on 159 primary (n=93) and metastatic (n=66) signet ring cell carcinomas of GI tract origin and 13 metastatic breast carcinomas with signet ring cell features. 30212392 2018
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 GeneticVariation disease BEFREE The recessive polymorphism model with the rs2228570 (FokI) polymorphism seemed to the best predictor of BC in Caucasian patients, whereas the homozygote model with the CDX2 polymorphism appeared to best predict BC in African-American patients. 30059751 2018
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 Biomarker disease BEFREE Cdx2, Bgl1, and Taq1 do not show association with breast cancer. 29072133 2017
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 GeneticVariation disease BEFREE Pearson chi square test was used to assess the association between VDR-Cdx2 genotype and breast cancer while genotype distribution in controls was evaluated by Hardy-Weinberg equilibrium (HWE). 25799416 2015
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 Biomarker disease BEFREE Furthermore, the potential relationship among Cdx2 VDR polymorphism and a number of biomarkers used in clinical management of breast cancer was assessed in an ad hoc set of breast cancer cases. 25849303 2015
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 GeneticVariation disease BEFREE The results of combined analyses indicated that Fok1, Bsm1, Apa1, Cdx2 and Poly-A were not significantly associated with the risk of breast cancer. 24568506 2014
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 GeneticVariation disease BEFREE Therefore, the association between VDR Cdx2 polymorphism and breast cancer susceptibility is only found in Africans. 23821301 2013
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.090 GeneticVariation disease BEFREE Haplotype analysis revealed the haplotype FtCA (FokI F, TaqI t, VDR-5132 C, Cdx2 A), which contains the TaqI t allele, to be associated with a significantly greater breast cancer risk as compared with the most frequent haplotype FTCG (OR = 1.43, 95% CI = 1.00 to 2.05). 18419802 2008