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Cellosaurus GM16825 (CVCL_U890)

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Cell line name GM16825
Synonyms ALX-2
Accession CVCL_U890
Resource Identification Initiative To cite this cell line use: GM16825 (RRID:CVCL_U890)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:4235; GFAP; Simple; p.Arg239Cys (c.729C>T); ClinVar=VCV000016167; Zygosity=Heterozygous (Coriell=GM16825).
Disease Alexander disease (NCIt: C84545)
Alexander disease (ORDO: Orphanet_58)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_C6VY (Alex1)
Sex of cell Male
Age at sampling 6Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM16825
Cell line databases/resources CLO; CLO_0018411
Encyclopedic resources Wikidata; Q54848761
Entry history
Entry creation16-Apr-2014
Last entry update19-Dec-2024
Version number16