Gene: LRP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.220 Biomarker disease BEFREE Endocytic receptor LRP2/megalin-of holoprosencephaly and renal Fanconi syndrome. 28497274 2017
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.220 Biomarker disease BEFREE Ectopic germinal center and megalin defect in primary Sjogren syndrome with renal Fanconi syndrome. 28577559 2017
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.220 Biomarker disease MGD The soluble intracellular domain of megalin does not affect renal proximal tubular function in vivo. 20531455 2010
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.220 Biomarker disease MGD Megalin knockout mice as an animal model of low molecular weight proteinuria. 10514418 1999
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.220 Biomarker disease MGD Defective forebrain development in mice lacking gp330/megalin. 8710893 1996