Gene: ERCC8-AS1 ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 105378991
Gene Symbol: ERCC8-AS1
ERCC8-AS1 		0.100 CausalMutation disease CLINVAR Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A. 29057985 2017
Entrez Id: 105378991
Gene Symbol: ERCC8-AS1
ERCC8-AS1 		0.100 GeneticVariation disease CLINVAR Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly. 26846091 2016
Entrez Id: 105378991
Gene Symbol: ERCC8-AS1
ERCC8-AS1 		0.100 GeneticVariation disease CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159 2015
Entrez Id: 105378991
Gene Symbol: ERCC8-AS1
ERCC8-AS1 		0.100 GeneticVariation disease CLINVAR Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. 19894250 2010
Entrez Id: 105378991
Gene Symbol: ERCC8-AS1
ERCC8-AS1 		0.100 CausalMutation disease CLINVAR Cockayne syndrome type A: novel mutations in eight typical patients. 16865293 2006
Entrez Id: 105378991
Gene Symbol: ERCC8-AS1
ERCC8-AS1 		0.100 GeneticVariation disease CLINVAR Cockayne syndrome type A: novel mutations in eight typical patients. 16865293 2006