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GFAP

glial fibrillary acidic protein
General Information
Name glial fibrillary acidic protein
Alias
  • glial fibrillary acidic protein
Gene_family Intermediate filaments Type III
organism Homo sapiens
entrez_id 2670
location 17q21.31
transcript_count 4
exon_count 10
Location
17p13.3p13.1p11.2q11.1q12q21.2q21.32q23.1q24.1q25.1q25.3
by NCBI GRCh38.p14
Summary
    Entrez 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]
    Stringdb Glial fibrillary acidic protein; GFAP, a class-III intermediate filament, is a cell- specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells
    nextProt GFAP, a class-III intermediate filament, is a cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells.
Interactions
NCBI
StringDB
Ontologies
Pathways
Name DB ID
Signaling by ERBB4 Reactome R-HSA-1236394
Nuclear signaling by ERBB4 Reactome R-HSA-1251985
Signal Transduction Reactome R-HSA-162582
Signaling by Receptor Tyrosine Kinases Reactome R-HSA-9006934
Autophagy Reactome R-HSA-9612973
Chaperone Mediated Autophagy Reactome R-HSA-9613829
Neural crest differentiation (WP2064) WikiPathways WP2064_r117162
Neuroinflammation and glutamatergic signaling (WP5083) WikiPathways WP5083_r120385
Spinal cord injury (WP2431) WikiPathways WP2431_r120812
Transcripts
Accession Version MolecularType Name NCBI Comments
NM_002055 5 mRNA transcript variant 1 NC_000017 Reference
NM_001363846 2 mRNA transcript variant 4 NC_000017 Reference
NM_001131019 3 mRNA transcript variant 2 NC_000017 Reference
NM_001242376 3 mRNA transcript variant 3 NC_000017 Reference