Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease BEFREE Moreover, sedDNA generation was inhibited by treatment of skin explants with spironolactone, which depletes the epidermis of the essential NER protein XPB to mimic the skin of xeroderma pigmentosum patients. 31838380 2020
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease BEFREE TFIIH multi-protein complex with its important helicase-Xeroderma Pigmentosum Protein (XPD) serves as the pivotal factor for opening up of the damaged lesion DNA site and carry out the repair process. 29616226 2018
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE The importance of a fully functional XPB is clearly illustrated by the severe clinical consequences associated with inherited defects in XPB including UV-hypersensitive syndromes xeroderma pigmentosum (XP), Cockayne syndrome (CS), combined XP and CS (XP/CS), and trichothiodystrophy (TTD). 25641424 2015
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE XPB or XPD missense mutations lead to Xeroderma pigmentosum, Cockayne's syndrome, Trichothiodystrophy, or COFS syndrome, suggesting that DNA repair and transcription defects are responsible for clinical heterogeneity. 23276657 2015
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE The subtle transcriptional differences found between various TFIIH variants thus participate in the phenotypic variability observed among XP, XP/CS, and TTD individuals. 25620205 2015
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 AlteredExpression disease BEFREE Mutations in the XPD subunit of the DNA repair/transcription factor TFIIH result in distinct clinical entities, including the cancer-prone xeroderma pigmentosum (XP) and the multisystem disorder trichothiodystrophy (TTD), which share only cutaneous photosensitivity. 25605938 2015
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG). 23623389 2013
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Our results suggested a link between TTD- but not XP-associated XPD mutations, placental maldevelopment and risk of pregnancy complications, possibly due to impairment of TFIIH-mediated functions in placenta. 22234153 2012
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease BEFREE This integration resolves puzzles regarding XP helicase functions and suggests that XP helicase positions and activities within TFIIH detect and verify damage, select the damaged strand for incision, and coordinate repair with transcription and cell cycle through CAK signaling. 21571596 2011
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 AlteredExpression disease BEFREE Xeroderma pigmentosum B (XPB/ERCC3/p89) is an ATP-dependent 3'-->5' directed DNA helicase involved in basal RNA transcription and the nucleotide excision repair (NER) pathway. 19840190 2010
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Mutations in the XPD subunit of the DNA repair/transcription factor TFIIH result in the rare recessive genetic disorder xeroderma pigmentosum (XP). 19934020 2009
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease MGD An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair. 19114557 2009
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 AlteredExpression disease BEFREE Mutations in certain subunits of the DNA repair/transcription factor complex TFIIH are linked to the human syndromes xeroderma pigmentosum (XP), Cockayne's syndrome (CS), and trichothiodystrophy (TTD). 19008953 2008
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease BEFREE Accordingly, defects in specific enzymatic functions typically result in XP, dissociation of the CAK subunit from TFIIH is associated with XP/CS and a more generalized destabilization of TFIIH gives rise to TTD. 18077223 2008
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE The severe xeroderma pigmentosum/Cockayne syndrome (XP/CS) syndrome is caused by mutations in the XPB, XPD and XPG genes that encode the helicase subunits of TFIIH and the 3' endonuclease of nucleotide excision repair (NER). 16167068 2006
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome. 16947863 2006
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE These cell lines result from a stable transfection of the XPB-TTD allele into XP complementation group B fibroblasts, from an XP patient who also have clinical abnormalities corresponding to Cockayne's syndrome (CS). 15608684 2005
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease BEFREE Subtle differences in the effects of these different mutations on the many activities of TFIIH and on its stability determine the clinical outcomes, which can be XP, TTD, XP with CS, XP with TTD or COFS. 14726016 2003
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 Biomarker disease BEFREE Moreover, when XPD mutations prevent interaction with the p44 subunit of TFIIH, transactivation directed by certain nuclear receptors is inhibited, regardless of TTD versus XP phenotype, thus explaining the overlapping symptoms. 12820975 2003
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect. 11955452 2002
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 AlteredExpression disease BEFREE We have also measured TFIIH levels in cells in which different mutations in the XPD gene are associated with clinical symptoms not of TTD but of the highly cancer-prone disorder xeroderma pigmentosum (XP). 12393803 2002
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Mutations in the XPD helicase component of TFIIH can result in the diverse clinical features associated with xeroderma pigmentosum (XP) and trichothiodystrophy (TTD). 11734544 2001
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Inherited mutations of the TFIIH helicase subunits xeroderma pigmentosum (XP) B or XPD yield overlapping DNA repair and transcription syndromes. 11239393 2001
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy. 10660593 2000
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3
0.300 GeneticVariation disease BEFREE We previously reported that p53-mediated apoptosis is attenuated in primary human fibroblasts from individuals with Xeroderma Pigmentosum (XP) that harbor mutations in the TFIIH DNA helicases XPD or XPB. 10467415 1999