ID   AG21158
AC   CVCL_2Y81
DR   CLO; CLO_0011294
DR   Coriell; AG21158
DR   Wikidata; Q54748137
RX   PubMed=30699343;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:613; APOE; Simple; p.Arg176Cys (c.526C>T); ClinVar=VCV000017848; Zygosity=Heterozygous; Note=ApoE2 allele (Coriell=AG21158).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C2866; Alzheimer's disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_2Y82 ! AG21159
SX   Female
AG   69Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 19-12-24; Version: 13
//
RX   PubMed=30699343; DOI=10.1016/j.celrep.2019.01.023; PMCID=PMC6386196;
RA   Meyer K., Feldman H.M., Lu T., Drake D., Lim E.T., Ling K.-H.,
RA   Bishop N.A., Pan Y., Seo J., Lin Y.-T., Su S.C., Church G.M.,
RA   Tsai L.-H., Yankner B.A.;
RT   "REST and neural gene network dysregulation in iPSC models of
RT   Alzheimer's disease.";
RL   Cell Rep. 26:1112-1127.e9(2019).
//