ID   GM27624
AC   CVCL_C7KW
SY   GM27624*A
DR   Coriell; GM27624
DR   Wikidata; Q117704347
CC   Sequence variation: Gene deletion; HGNC; HGNC:3811; FOXG1; Zygosity=Heterozygous (from parent cell line).
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)
HI   CVCL_A2QS ! GM27615
SX   Male
AG   5Y
CA   Induced pluripotent stem cell
DT   Created: 21-03-23; Last updated: 19-12-24; Version: 3
//