Mutations

MAPT G86S

Overview

Pathogenicity: Frontotemporal Dementia : Unclear Pathogenicity
Clinical Phenotype: None
Genomic Mutation Name (MET1): g.87825G>A
Genomic Mutation Name (NT1): g.84999G>A
dbSNP ID: rs63751135
Coding/Non-Coding: Coding
Genomic Region: Exon 3
Mutation Type: Point, Missense
Codon Change: GGC to AGC

Findings

This mutation was identified in a woman diagnosed with frontotemporal dementia with onset at age 71.  She presented with decreased concentration and activity, distractibility, perseveration, and personality changes. She later developed frontal release signs and seizures, and became mute and unable to walk without assistance. The proband had a positive family history of neurodegenerative disease, including a mother with unspecified demenita and two siblings with clinical features consistent with Alzheimer's disease. The mutation was not present in either sibling and the mother's DNA was unavailable. The mutation was also absent in 100 control chromosomes, but pathogenicity could not be determined (Stanford et al., 2004).

Neuropathology

Unknown. A PET scan showed frontal hypometabolism (Stanford et al., 2004).

Biological Effect

Exon-trapping experiments indicated that the G86S mutation does not alter the normal splicing of exons 2 or 3. The predicted amino acid substitution results in the creation of a predicted phosphorylation site and a predicted O-glycosylation site (Stanford et al., 2004).

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References

Paper Citations

  1. . Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies. J Neurol. 2004 Sep;251(9):1098-104. PubMed.

Further Reading

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Primary Papers

  1. . Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies. J Neurol. 2004 Sep;251(9):1098-104. PubMed.