Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE We have also shown the association of a novel genetic variant in CDKN2B gene with clinical outcome of patients with ESCC. 30238987 2019
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE Therefore, our findings indicate that genetic variants at 9p21.3 may modulate the expression of MTAP and CDKN2B and contribute to ESCC susceptibility. 27960044 2017
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 AlteredExpression disease BEFREE Furthermore, inhibition of ANRIL was found to increase the expression of p15(INK4b) and transforming growth factor β1 (TGFβ1) and depletion of ANRIL in ESCC cell lines may inhibit cellular proliferation. 24747824 2014
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE We applied TREAT as a multilocus association test on >20 000 genes/regions in a study of esophageal squamous cell carcinoma (ESCC) and detected a highly significant novel association between the gene CDKN2B and ESCC ([Formula: see text]). 24794927 2014
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE At gene level, CDKN2B, CDKN2A and CDKN2B-AS1 were significantly associated with ESCC (P ≤ 4.70 × 10(-) (5)). 25239644 2014
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE In the meta-analyses by ASSET, four SNPs (rs3731239 in CDKN2A, rs615552 and rs573687 in CDKN2B and rs564398 in CDKN2BAS) showed significant associations with ESCC and EC (P<2.46 × 10(-4)). 23361049 2013
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE We performed LOH studies on chromosome bands 9p21-p22 and searched for genetic alterations of CDKN2A and CDKN2B in 56 ESCCs from a high-risk Chinese population. 14732922 2004
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 GeneticVariation disease BEFREE Altogether, 68% of the samples harbor at least one type of alteration in p16INK4a gene and 50% of the samples were altered in p15INK4b gene, indicating that they are the frequent inactivating targets during ESCC development. 9934853 1999
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 Biomarker disease BEFREE Multiple types of aberrations in the p16 (INK4a) and the p15(INK4b) genes in 30 esophageal squamous-cell-carcinoma cell lines. 9033652 1997
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.100 Biomarker disease BEFREE Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma. 8012957 1994