MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Cognition Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751273
rs63751273
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0009241
Disease:
Cognition Disorders 		0.010 GeneticVariation BEFREE Here, we studied the effects of P301L hTau transduction in the medial EC (MEC) of mice on tau phosphorylation and accumulation, and cognitive deficit. 28634382 2017