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Cellosaurus GM27255 (CVCL_UT86)

[Text version]
Cell line name GM27255
Accession CVCL_UT86
Resource Identification Initiative To cite this cell line use: GM27255 (RRID:CVCL_UT86)
Comments Population: Caucasian; Dutch.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:3811; FOXG1; Simple; p.Tyr208Cys (c.623A>G); Zygosity=Heterozygous (Coriell=GM27255).
Disease Rett syndrome, congenital variant (NCIt: C176903)
Atypical Rett syndrome (ORDO: Orphanet_3095)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A1UW ! GM27379
Sex of cell Male
Age at sampling 2Y2M
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM27255
Encyclopedic resources Wikidata; Q93933132
Entry history
Entry creation25-Feb-2019
Last entry update19-Dec-2024
Version number10