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MAPT and Alzheimer disease are reported together in 5 articles.

Gene

MAPT

HGNC
HGNC:6893
9articles
9mentions
1variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
455articles
455mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

5 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
geneMAPT“We discuss targeting of critical genes such as APOE4, APP, PSEN1, PSEN2, and MAPT, which play central roles in amyloid processing, tau pathology, lipid metabolism, and neuroinflammatory cascades, and evaluate strategies for allele-specific correction, gene silencing, and transcriptional regulation using CRISPR interference/activation and epigenome editing tools.”0.98hgnc_dict_v1
phenotypeAlzheimer disease“CRISPR-Cas9 and next-generation gene editing strategies for therapeutic intervention of neurodegenerative pathways in Alzheimer's disease: a state-of-the-art review.”0.93phenotype_alias_lexicon_v2
geneAPP“We discuss targeting of critical genes such as APOE4, APP, PSEN1, PSEN2, and MAPT, which play central roles in amyloid processing, tau pathology, lipid metabolism, and neuroinflammatory cascades, and evaluate strategies for allele-specific correction, gene silencing, and transcriptional regulation using CRISPR interference/activation and epigenome editing tools.”0.98hgnc_dict_v1
genePSEN1“We discuss targeting of critical genes such as APOE4, APP, PSEN1, PSEN2, and MAPT, which play central roles in amyloid processing, tau pathology, lipid metabolism, and neuroinflammatory cascades, and evaluate strategies for allele-specific correction, gene silencing, and transcriptional regulation using CRISPR interference/activation and epigenome editing tools.”0.98hgnc_dict_v1

CNV-Finder: Streamlining Copy Number Variation Discovery.

PMID 39605431 | PMCID PMC11601614 | DOI 10.1101/2024.11.22.624040 · bioRxiv : the preprint server for biology · 2025 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMAPT“We incorporate four genes to establish our methods-Parkin (PRKN), Leucine Rich Repeat And Ig Domain Containing 2 (LINGO2), Microtubule Associated Protein Tau (MAPT), and alpha-Synuclein (SNCA)-which may be relevant to neurological diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Progressive Supranuclear Palsy (PSP), or related disorders such as essential tremor (ET).”0.98hgnc_dict_v1
phenotypeAlzheimer disease“We incorporate four genes to establish our methods-Parkin (PRKN), Leucine Rich Repeat And Ig Domain Containing 2 (LINGO2), Microtubule Associated Protein Tau (MAPT), and alpha-Synuclein (SNCA)-which may be relevant to neurological diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Progressive Supranuclear Palsy (PSP), or related disorders such as essential tremor (ET).”0.93phenotype_alias_lexicon_v2
genePRKN“We incorporate four genes to establish our methods-Parkin (PRKN), Leucine Rich Repeat And Ig Domain Containing 2 (LINGO2), Microtubule Associated Protein Tau (MAPT), and alpha-Synuclein (SNCA)-which may be relevant to neurological diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Progressive Supranuclear Palsy (PSP), or related disorders such as essential tremor (ET).”0.98hgnc_dict_v1
geneLINGO2“We incorporate four genes to establish our methods-Parkin (PRKN), Leucine Rich Repeat And Ig Domain Containing 2 (LINGO2), Microtubule Associated Protein Tau (MAPT), and alpha-Synuclein (SNCA)-which may be relevant to neurological diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Progressive Supranuclear Palsy (PSP), or related disorders such as essential tremor (ET).”0.98hgnc_dict_v1

Multiple system atrophy with amyloid-β-predominant Alzheimer's disease neuropathologic change.

PMID 38712319 | PMCID PMC11073746 | DOI 10.1093/braincomms/fcae141 · Brain communications · 2024 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMAPT“We performed genetic testing for APOE, MAPT, PSEN1, PSEN2 and APP.”0.98hgnc_dict_v1
phenotypeAlzheimer disease“Multiple system atrophy with amyloid-β-predominant Alzheimer's disease neuropathologic change.”0.93phenotype_alias_lexicon_v2
geneAPOE“We performed genetic testing for APOE, MAPT, PSEN1, PSEN2 and APP.”0.98hgnc_dict_v1
genePSEN1“We performed genetic testing for APOE, MAPT, PSEN1, PSEN2 and APP.”0.98hgnc_dict_v1
TypeEntitySource evidenceConfidenceExtractor
geneMAPT“According to the NIA-AA (National Institute on Aging-Alzheimer's Association) framework, we selected three AD biomarker genes (APP, NEFL, and MAPT).”0.98hgnc_dict_v1
phenotypeAlzheimer disease“Alzheimer's disease (AD) is a progressive brain disorder that can significantly affect the quality of life.”0.93phenotype_alias_lexicon_v2
geneAPP“According to the NIA-AA (National Institute on Aging-Alzheimer's Association) framework, we selected three AD biomarker genes (APP, NEFL, and MAPT).”0.98hgnc_dict_v1
geneNEFL“According to the NIA-AA (National Institute on Aging-Alzheimer's Association) framework, we selected three AD biomarker genes (APP, NEFL, and MAPT).”0.98hgnc_dict_v1

Developmental exposure to lead (Pb) alters the expression of the human tau gene and its products in a transgenic animal model.

PMID 27293183 | PMCID PMC5738909 | DOI 10.1016/j.neuro.2016.06.001 · Neurotoxicology · 2016 · 3 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneMAPT“The best known of these illnesses is Alzheimer's disease (AD); a disease where the microtubule associated protein tau (MAPT) becomes hyperphosphorylated (lowering its binding affinity to microtubules) and aggregates within neurons in the form of neurofibrillary tangles (NFTs).”0.98hgnc_dict_v1
phenotypeAlzheimer disease“The best known of these illnesses is Alzheimer's disease (AD); a disease where the microtubule associated protein tau (MAPT) becomes hyperphosphorylated (lowering its binding affinity to microtubules) and aggregates within neurons in the form of neurofibrillary tangles (NFTs).”0.93phenotype_alias_lexicon_v2
geneCDK5“Protein and mRNA levels for tau and CDK5 as well as tau phosphorylation at Ser396 were determined.”0.98hgnc_dict_v1