Gene: LAMB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.020 GeneticVariation disease BEFREE No pathogenic NPHS1 or LAMB2 mutations were found in our FSGS cohort. 24856380 2014
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.020 GeneticVariation disease BEFREE The most common mutations are in 4 genes, 3 of which are podocyte genes: NPHS1 (Finnish nephropathy), NPHS2 (podocin-induced focal segmental glomerulosclerosis), WT1 (diffuse mesangial sclerosis), and LAMB2 (Pierson syndrome). 18462046 2008