complementing XP-G cells is a protein that in humans is encoded by the ERCC5 gene. Excision repair cross-complementing rodent repair deficiency, complementation...
12 KB (1,408 words) - 15:51, 29 March 2024
corresponding proteins include ERCC1(ERCC1), ERCC2(XPD), ERCC3(XPB), ERCC4(XPF), ERCC5 (XPG), ERCC6(CSB) and ERCC8(CSA). DNA repair-deficient ERCC1 mutant mice...
33 KB (3,623 words) - 18:02, 20 August 2024
during NER at the 3' side of the damaged nucleotide. Mutations in the XPG (ERCC5) gene can lead to XP alone, or in combination with Cockayne syndrome (CS)...
31 KB (3,001 words) - 07:13, 14 August 2024
C12orf57 CC2D2A CHD7 CLDN19 COX7B CRIM1 CRYAA CRYBA4 CRYBB2 DHX38 DPYD ERCC1 ERCC5 FADD FAM111A FNBP4 FOXL2 FRAS1 FREM1 FREM2 FZD5 GDF3 GDF6 GJA1 GRIP1 HCCS...
25 KB (2,173 words) - 09:44, 18 March 2024
HGNC:3434 P18074 5055 ERCC3 HGNC:3435 P19447 5056 ERCC4 HGNC:3436 Q92889 5057 ERCC5 HGNC:3437 P28715 5058 ERCC6 HGNC:3438 P0DP91 Q03468 5059 ERCC6L HGNC:20794...
277 KB (17 words) - 15:46, 9 May 2024
cerebral atrophy ERCC5 (XPG) Nucleotide excision repair, Homologous recombinational repair, Base excision repair mice with deficient ERCC5 show loss of subcutaneous...
96 KB (10,994 words) - 05:19, 16 August 2024
cerebral atrophy ERCC5 (XPG) Nucleotide excision repair, Homologous recombinational repair, Base excision repair mice with deficient ERCC5 show loss of subcutaneous...
42 KB (3,756 words) - 04:23, 25 March 2024
be caused by mutations in any of these genes: DDB2, ERCC2, ERCC3, ERCC4, ERCC5, XPA, XPC. These genes are all involved in the NER repair pathway that repairs...
74 KB (8,726 words) - 06:14, 3 June 2024
proteins are transcribed from the following genes: ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, and ERCC8. Members 1 though 5 are associated with Xeroderma Pigmentosum...
954 bytes (87 words) - 00:25, 24 August 2024
transcription factor 2 (TFIIH) and, thus, functions in class II transcription. XPG (ERCC5) forms a stable complex with TFIIH, which is active in transcription and...
37 KB (4,622 words) - 17:05, 6 April 2024
DNA damage in nerve cells as well. ERCC2 has been shown to interact with: ERCC5, GTF2H1, GTF2H2, and XPB. Click on genes, proteins and metabolites below...
15 KB (1,846 words) - 16:57, 27 August 2024
CHD in smoker mothers who carry genetic variations in them include ERCC1, ERCC5, PARP2, and OSGEP. There are various ways of diagnosing this congenital...
35 KB (3,530 words) - 11:50, 11 June 2024
pigmentosum group F; 278760; ERCC4 Xeroderma pigmentosum group G; 278780; ERCC5 Xeroderma pigmentosum, variant type; 278750; POLH XFE progeroid syndrome;...
234 KB (18,877 words) - 15:43, 9 May 2024