Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
CUI: C3888212
Disease: SECKEL SYNDROME 4
SECKEL SYNDROME 4 		0.600 Biomarker GENOMICS_ENGLAND Novel CENPJ mutation causes Seckel syndrome. 20522431

2010
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
CUI: C3888212
Disease: SECKEL SYNDROME 4
SECKEL SYNDROME 4 		0.600 Biomarker 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
CUI: C3888212
Disease: SECKEL SYNDROME 4
SECKEL SYNDROME 4 		0.600 Biomarker GENOMICS_ENGLAND