Gene: CEP152 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.310 GeneticVariation disease BEFREE Exomes of patients with PM showed a significant burden of variants in 75 PM genes, that persisted after removing monogenic causes of PM (e.g., biallelic pathogenic variants in CEP152). 31696992 2019
Entrez Id: 22995
Gene Symbol: CEP152
CEP152 		0.310 Biomarker disease GENOMICS_ENGLAND