ID   GM27880
AC   CVCL_A2TB
SY   GM27880*C; 1123-FOXG1-LOF-Hom#A8
DR   Coriell; GM27880
DR   Wikidata; Q105507379
RX   PubMed=37071670;
CC   Sequence variation: Mutation; HGNC; HGNC:3811; FOXG1; Simple_edited; p.Ser19Glnfs*120 (c.53_54insT); Zygosity=Homozygous; Note=By CRISPR/Cas9 (Coriell=GM27880).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
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_A2TY ! S1123-01 iPS #3
SX   Male
AG   52Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 19-12-24; Version: 7
//
RX   PubMed=37071670; DOI=10.1089/crispr.2022.0050; PMCID=PMC10123805;
RA   Panda A., Suvakov M., Mariani J., Drucker K.L., Park Y., Jang Y.,
RA   Kollmeyer T.M., Sarkar G., Bae T., Kim J.J., Yoon W.H., Jenkins R.B.,
RA   Vaccarino F.M., Abyzov A.;
RT   "Clonally selected lines after CRISPR-Cas editing are not isogenic.";
RL   CRISPR J. 6:176-182(2023).
//