Ercc8 - ERCC excision repair 8, CSA ubiquitin ligase complex subunit-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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310071 Ercc8

基因描述

Type	Description
Definition	ERCC excision repair 8, CSA ubiquitin ligase complex subunit

名称对应

Type	IDs
Synonymous	Ckn1
Gene	UniProtKB-ID: G3V7B8_RAT UniprotKB: G3V7B8 UniParc: UPI0000181DA1 EMBL: CH473955, AABR07008024 Ensembl: ENSRNOG00000009968 KO: rno:310071
Nucleutide sequences	EMBL-CDS: EDM10309.1 Gene_ORFName: rCG_44836 Ensembl_TRS: ENSRNOT00000013598
Protein sequencees	Ensembl_PRO: ENSRNOP00000013598 RefSeq: XP_017446311.1, XP_017446310.1, NP_001101120.2
Others	UniRef100: UniRef100_G3V7B8 UniRef90: UniRef90_Q8CFD5 UniRef50: UniRef50_Q13216 UniGene: Rn.107979

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mRNA

Protein

UniprotKB

Description

Refseq

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Location

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Pubmed编号	文献信息	发表日期	相关基因
29545921	CSA and CSB play a role in the response to DNA breaks. Oncotarget Barbara Pascucci , Alessandra Fragale , Veronica Marabitti , Giuseppe Leuzzi , Angelo Salvatore Calcagnile , Eleonora Parlanti , Annapaola Franchitto , Eugenia Dogliotti , Mariarosaria D'Errico	2018-02-20	-
26620705	The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair. J Biol Chem Yooksil Sin , Kiyoji Tanaka , Masafumi Saijo	2016-01-15	-
25762674	Cockayne syndrome group B (Csb) and group a (Csa) deficiencies predispose to hearing loss and cochlear hair cell degeneration in mice. J. Neurosci. A Paul Nagtegaal , Robert N Rainey , Ingrid van der Pluijm , Renata M C Brandt , Gijsbertus T J van der Horst , J Gerard G Borst , Neil Segil	2015-03-11	Cdh23, Ercc6, Ercc8
22900489	Dynamic compartmentalization of DNA repair proteins within spiral ganglion neurons in response to noise stress. Int. J. Neurosci. O'neil W Guthrie	2012-12-01	-
23022597	Noise exposure potentiates the subcellular distribution of nucleotide excision repair proteins within spiral ganglion neurons. Hear. Res. O'neil W Guthrie , Helen Xu	2012-12-01	Xpa, Xpc
22824526	Nucleotide excision repair: new tricks with old bricks. Trends Genet. Irene Kamileri , Ismene Karakasilioti , George A Garinis	2012-11-01	Xab2, Ercc3, Xpa, Ercc5, Ercc4, Ercc6, Ercc2, Ercc8, Xpc, Hmgn1, Gtf2h5, Ddb1
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
21108394	High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel. Am J Med Genet A Morad Khayat , Hagar Hardouf , Joel Zlotogora , Stavit Allon Shalev	2010-12-01	-
19894250	Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. Hum Mutat V Laugel , C Dalloz , M Durand , F Sauvanaud , U Kristensen , M C Vincent , L Pasquier , S Odent , V Cormier-Daire , B Gener , E S Tobias , J L Tolmie , D Martin-Coignard , V Drouin-Garraud , D Heron , H Journel , E Raffo , J Vigneron , S Lyonnet , V Murday , D Gubser-Mercati , B Funalot , L Brueton , J Sanchez Del Pozo , E MuÃ±oz , A R Gennery , M Salih , M Noruzinia , K Prescott , L Ramos , Z Stark , K Fieggen , B Chabrol , P Sarda , P Edery , A Bloch-Zupan , H Fawcett , D Pham , J M Egly , A R Lehmann , A Sarasin , H Dollfus	2010-02-01	-
18166977	Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects. Cell Res. Maria Fousteri , Leon H F Mullenders	2008-01-01	Ercc6, Ercc8

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