Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7376
Gene Symbol: NR1H2
NR1H2
0.030 Biomarker disease BEFREE In this perspective, we outline recent data on how lesion-stalled Pol II initiates TC-NER and we discuss new mechanistic insights in the TC-NER reaction, which have resulted in a better understanding of the causative-linked Cockayne syndrome and UV-sensitive syndrome. 30195642 2018
Entrez Id: 7376
Gene Symbol: NR1H2
NR1H2
0.030 Biomarker disease BEFREE Inherited defects in NER are manifested in different diseases including xeroderma pigmentosum (XP), Cockayne syndrome (CS), UV sensitive syndrome (UVsS) and the photosensitive form of trichothiodystrophy (TTD). 30065996 2018
Entrez Id: 7376
Gene Symbol: NR1H2
NR1H2
0.030 Biomarker disease BEFREE Defective TC-NER gives rise to the human disorders Cockayne syndrome and UV-sensitive syndrome (UV(S)S). 22466611 2012