ID   AG11368
AC   CVCL_4M66
DR   CLO; CLO_0021588
DR   Coriell; AG11368
DR   Wikidata; Q54743900
RX   CelloPub=CLPUB00597;
CC   Sequence variation: Mutation; HGNC; HGNC:613; APOE; Simple; p.Cys130Arg (c.388T>C); ClinVar=VCV000017864; Zygosity=Homozygous; Note=ApoE4 allele (Coriell=AG11368).
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
DI   ORDO; Orphanet_1020; Early-onset autosomal dominant Alzheimer disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_4M06 ! AG09952
SX   Male
AG   77Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 19-12-24; Version: 13
//
RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994).
//