Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1031
Gene Symbol: CDKN2C
CDKN2C
0.050 GeneticVariation disease BEFREE Analysis of oligodendrogliomas revealed regions of chromosomal losses syntenic to human 1p involving tumor suppressor genes, such as CDKN2C, as well as genes associated with apoptosis, autophagy, and response to chemotherapy and radiation. 27251041 2016
Entrez Id: 1031
Gene Symbol: CDKN2C
CDKN2C
0.050 GeneticVariation disease BEFREE We have studied these genes and p18(ink4c) using PCR/SSCP methods to detect sequence variations in a series of 40 oligodendrogliomas in which the allelic status at 1p was analyzed. 15711769 2005
Entrez Id: 1031
Gene Symbol: CDKN2C
CDKN2C
0.050 GeneticVariation disease BEFREE These results show that p18 alteration is involved in tumor progression in a subset of oligodendrogliomas. 10994011 2000
Entrez Id: 1031
Gene Symbol: CDKN2C
CDKN2C
0.050 Biomarker disease BEFREE Our data thus provide evidence for more than a single oligodendroglioma-associated tumor suppressor gene on 1p and implicate CDKN2C as a candidate tumor suppressor gene altered in a low fraction of oligodendroglial tumors. 10515227 1999
Entrez Id: 1031
Gene Symbol: CDKN2C
CDKN2C
0.050 AlteredExpression disease BEFREE Coupled with the recent report of rare point mutations of CDKN2C in oligodendrogliomas, these findings suggest that CDKN2C inactivation may be oncogenic in a small percentage of human oligodendrogliomas. 10517502 1999