ID   GM03900
AC   CVCL_X050
SY   GM 3900; GM3900
DR   CLO; CLO_0015987
DR   Coriell; GM03900
DR   Wikidata; Q54838310
RX   CelloPub=CLPUB00447;
RX   PubMed=3374507;
RX   PubMed=6617268;
CC   Population: African American.
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Arg216Ter (c.646C>T); ClinVar=VCV000127312; Zygosity=Unspecified (Coriell=GM03900).
CC   Derived from site: In situ; Abdomen; UBERON=UBERON_0000916.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C3339; Familial adenomatous polyposis
DI   ORDO; Orphanet_733; Familial adenomatous polyposis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_X334 ! GM03901
SX   Female
AG   15Y
CA   Finite cell line
DT   Created: 17-07-14; Last updated: 30-01-24; Version: 16
//
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).
//
RX   PubMed=3374507; DOI=10.1016/0027-5107(88)90211-4;
RA   Azzarone B., Chaponnier C., Krief P., Mareel M.M., Suarez H.G.,
RA   Macieira-Coelho A.;
RT   "Human fibroblasts from cancer patients: lifespan and transformed
RT   phenotype in vitro and role of mesenchyme in vivo.";
RL   Mutat. Res. 199:313-325(1988).
//
RX   PubMed=6617268; DOI=10.1159/000131883;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Breakpoint map of chromosomal inversion and deletion cell cultures in
RT   the NIGMS Human Genetic Mutant Cell Repository.";
RL   Cytogenet. Cell Genet. 35:298-302(1983).
//