Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Finnish congenital nephrotic syndrome
0.010 Biomarker disease BEFREE Because of its location and the proposed interference of amyloid with basement membrane assembly, APLP1 has been considered a candidate gene for CNF. 9521588 1998
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
0.010 Biomarker group BEFREE Based on these data, a mechanism is proposed whereby p53-dependent induction of APLP1 is involved in neural cell death, and which may exacerbate neuronal cell loss in some acute or chronic neurodegenerative disorders. 17533371 2007
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.010 Biomarker disease BEFREE Methods APLP1 and NPTXR concentrations were measured in the CSF of patients with mild cognitive impairment (MCI) (n = 14), mild AD (n = 21), moderate AD (n = 43) and severe AD (n = 30) using enzyme-linked immunosorbent assays (ELISAs). 31415236 2019
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 AlteredExpression group BEFREE Quantitative real-time PCR and western blot analysis demonstrated higher expression of APLP1 in carcinoid metastases relative to primary tumours indicating a role of APLP1 in tumour dissemination. 18430897 2008
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital
0.010 GeneticVariation disease BEFREE We have previously mapped the gene for congenital nephrotic syndrome (CNF) to the APLP1 region, to the vicinity of marker D19S610 located between markers D19S191 and DS19608. 9521588 1998
Influenza due to Influenza A virus subtype H1N1
0.100 GeneticVariation disease GWASCAT No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. 26379185 2015