Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
0.020 GeneticVariation disease BEFREE We found missense mutations of AAC (Asn) to AGC (Ser) at DCC codon 176 in one cell line and ACC (Thr) to ATC (Ile) at codon 1105 in one cell line and tumor, respectively; polymorphisms of CGA (Arg) to GGA (Gly) at codon 201 and TTT (Phe) to TTG (Leu) at codon 951 in most of the cell lines and tumors; and a silent mutation of GAG (Glu) to GAA (Glu) at codon 118 in four cell lines and five primary tumors. 9288786 1997
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
0.020 GeneticVariation disease BEFREE In addition, two single base transitions were identified by direct sequencing: [exon 6; codon 95; CGA (Arg) to TGA (stop)] and [exon 7; codon 172; ACC (Thr) to ACT (Thr)] in either transcript. 7479776 1995