Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 404672
Gene Symbol: GTF2H5
GTF2H5
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.040 Biomarker BEFREE MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation. 20797633

2010
Entrez Id: 404672
Gene Symbol: GTF2H5
GTF2H5
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.040 Biomarker BEFREE The xeroderma pigmentosum group D (XPD) helicase subunit of TFIIH functions in DNA repair and transcription initiation. 11242112

2001
Entrez Id: 404672
Gene Symbol: GTF2H5
GTF2H5
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.040 Biomarker BEFREE We consider the possible consequences of the reduced cellular content of TFIIH for the clinical symptoms in XP-B or XP-D patients, and discuss a 'conditional phenotype' that may involve an impairment of cellular function only under certain growth conditions. 9427533

1997
Entrez Id: 404672
Gene Symbol: GTF2H5
GTF2H5
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.040 GeneticVariation BEFREE To study the relationships between mutagenesis and carcinogenesis, we compared the mutations and their frequency induced by ultraviolet irradiation at 254 nm (UV-C) in XP-D (GM-08207B/XP6BE), TTD/XP-D (TTD1VI-LAS-KMT11) and wild-type (MRC-5V1) human cells. 7563073

1995