ID   GM02694
AC   CVCL_4N28
SY   GM02694A
DR   CLO; CLO_0014911
DR   BioSample; SAMN00808024
DR   Coriell; GM02694
DR   Wikidata; Q54837637
RX   CelloPub=CLPUB00447;
RX   PubMed=3374507;
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Gln215Ter (c.643C>T); ClinVar=VCV000000814; Zygosity=Unspecified (Coriell=GM02694).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3339; Familial adenomatous polyposis
DI   NCIt; C3938; Turcot syndrome
DI   ORDO; Orphanet_733; Familial adenomatous polyposis
DI   ORDO; Orphanet_99818; Turcot syndrome with polyposis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   40Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 30-01-24; Version: 14
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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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (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).
//