Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0302142
Disease: Deformity
Deformity 		0.030 Biomarker BEFREE Further, we found that reelin signaling is important for the normal migration of rostral, but not caudal hindbrain raphe nuclei and that reelin deficiency results in the malformation of the paramedian raphe nucleus and the lateral wings of the dorsal raphe nuclei. 30001399

2018
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0302142
Disease: Deformity
Deformity 		0.030 GeneticVariation BEFREE In humans, loss of Reelin results in a type of lissencephaly with severe cortical and cerebellar malformation. 16266828

2006
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0302142
Disease: Deformity
Deformity 		0.030 GeneticVariation BEFREE To our knowledge, this syndrome represents the first human lipoprotein receptor malformation syndrome and the second human disease associated with a reelin pathway defect. 16080122

2005