ID   GM27615
AC   CVCL_A2QS
DR   Coriell; GM27615
DR   Wikidata; Q105507203
CC   Sequence variation: Gene deletion; HGNC; HGNC:3811; FOXG1; Zygosity=Heterozygous (Coriell=GM27615).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C176903; Rett syndrome, congenital variant
DI   ORDO; Orphanet_3095; Atypical Rett syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   5Y
CA   Finite cell line
DT   Created: 12-01-21; Last updated: 19-12-24; Version: 7
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