Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 Biomarker disease GENOMICS_ENGLAND Novel compound heterozygous mutation in the POC1B gene underlie peripheral cone dystrophy in a Chinese family. 29377742 2018
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 GeneticVariation disease UNIPROT Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy. 25018096 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 Biomarker disease GENOMICS_ENGLAND Novel recessive cone-rod dystrophy caused by POC1B mutation. 24945461 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 CausalMutation disease CLINVAR Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy. 25018096 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 CausalMutation disease CLINVAR Mutation of POC1B in a severe syndromic retinal ciliopathy. 25044745 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 GeneticVariation disease UNIPROT Novel recessive cone-rod dystrophy caused by POC1B mutation. 24945461 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 GeneticVariation disease UNIPROT Mutation of POC1B in a severe syndromic retinal ciliopathy. 25044745 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 CausalMutation disease CLINVAR Novel recessive cone-rod dystrophy caused by POC1B mutation. 24945461 2014
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 282809
Gene Symbol: POC1B
POC1B 		0.700 Biomarker disease CTD_human