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GFAP gene

glial fibrillary acidic protein

Key facts

Official symbol
GFAP
Full name
GFAP
Chromosome
17
Map location
17q21.31
Organism
Homo sapiens
NCBI Gene ID
2670
Also known as
ALXDRD

Function summary

This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008].

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Data source: NCBI Gene · alsesAI Gene Library