Gene: RELN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5649
Gene Symbol: RELN
RELN 		0.310 GeneticVariation disease BEFREE Heterozygous RELN mutations cause a typical ADLTE syndrome, indistinguishable from that associated with LGI1 mutations. 28142128 2017
Entrez Id: 5649
Gene Symbol: RELN
RELN 		0.310 GermlineCausalMutation disease ORPHANET Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. 26046367 2015