ID   GM27462
AC   CVCL_YE51
DR   Coriell; GM27462
DR   Wikidata; Q93933249
CC   Population: Caucasian; French.
CC   Sequence variation: Mutation; HGNC; HGNC:3811; FOXG1; Simple; p.Ser326Glufs*129 (c.974_975insA); Zygosity=Heterozygous (Coriell=GM27462).
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)
OI   CVCL_VV63 ! GM27335
SX   Male
AG   7Y
CA   Finite cell line
DT   Created: 19-12-19; Last updated: 19-12-24; Version: 11
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