Gene: RCBTB1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55213
Gene Symbol: RCBTB1
RCBTB1 		0.700 Biomarker disease GENOMICS_ENGLAND Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination. 27486781 2016
Entrez Id: 55213
Gene Symbol: RCBTB1
RCBTB1 		0.700 GeneticVariation disease UNIPROT Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination. 27486781 2016
Entrez Id: 55213
Gene Symbol: RCBTB1
RCBTB1 		0.700 Biomarker disease CTD_human
Entrez Id: 55213
Gene Symbol: RCBTB1
RCBTB1 		0.700 CausalMutation disease CLINVAR