Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ 		0.600 Biomarker disease GENOMICS_ENGLAND Novel CENPJ mutation causes Seckel syndrome. 20522431 2010
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ 		0.600 Biomarker disease GENOMICS_ENGLAND A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly. 16900296 2006
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ 		0.600 Biomarker disease CTD_human
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ 		0.600 CausalMutation disease CLINVAR