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- NCIT_C75636 IAO_0000115 "Human MAPT wild-type allele is located in the vicinity of 17q21.1 and is approximately 134 kb in length. This allele, which encodes microtubule-associated protein tau, may play a role in the development and maintenance of neuronal polarity. Mutations in the gene are associated with a large number of neurodegenerative diseases." @default.
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- NCIT_C75636 NCIT_P102 "J03778" @default.
- NCIT_C75636 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75636 NCIT_P108 "MAPT wt Allele" @default.
- NCIT_C75636 NCIT_P207 "C2697954" @default.
- NCIT_C75636 NCIT_P321 "4137" @default.
- NCIT_C75636 NCIT_P366 "MAPT_wt_Allele" @default.
- NCIT_C75636 NCIT_P98 "17q21 microdeletion syndrome is associated with deletions in both the MAPT gene and the CRHR1 gene. (OMIM)" @default.
- NCIT_C75636 NCIT_P98 "Mutations and variations in the MAPT gene are associated with Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. (Entrez Gene)" @default.
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- NCIT_C75636 hasExactSynonym "DDPAC" @default.
- NCIT_C75636 hasExactSynonym "FLJ31424" @default.
- NCIT_C75636 hasExactSynonym "FTDP-17" @default.
- NCIT_C75636 hasExactSynonym "MAPT wt Allele" @default.
- NCIT_C75636 hasExactSynonym "MAPTL" @default.
- NCIT_C75636 hasExactSynonym "MGC138549" @default.
- NCIT_C75636 hasExactSynonym "MSTD" @default.
- NCIT_C75636 hasExactSynonym "MTBT1" @default.
- NCIT_C75636 hasExactSynonym "MTBT2" @default.
- NCIT_C75636 hasExactSynonym "Microtubule-Associated Protein Tau wt Allele" @default.
- NCIT_C75636 hasExactSynonym "PPND" @default.
- NCIT_C75636 hasExactSynonym "TAU" @default.
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- NCIT_C75636 label "MAPT wt Allele" @default.
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