ID   GM10901
AC   CVCL_F148
DR   CLO; CLO_0023397
DR   BioSample; SAMN00800320
DR   Coriell; GM10901
DR   Wikidata; Q54844723
RX   CelloPub=CLPUB00447;
CC   Population: Mexican.
CC   Sequence variation: Mutation; HGNC; HGNC:3438; ERCC6; Simple; p.Arg735Ter (c.2203C>T) (C2282T); ClinVar=VCV000001701; Zygosity=Heterozygous (from familial inference of GM10903; GM10905).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_F147 ! GM10900
SX   Female
AG   42Y
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 19-12-24; Version: 15
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//