ID   GM06855
AC   CVCL_F297
SY   GM6855
DR   CLO; CLO_0036519
DR   Coriell; GM06855
DR   Wikidata; Q54842348
RX   CelloPub=CLPUB00447;
RX   PubMed=3374507;
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Glu1538Ilefs*5 (c.4612_4613delAG) (P1542X); ClinVar=VCV000000823; Zygosity=Unspecified (Coriell=GM06855).
CC   Derived from site: In situ; Skin; Note=From a fibroma; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3339; Familial adenomatous polyposis
DI   ORDO; Orphanet_733; Familial adenomatous polyposis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_F309 ! GM07500
SX   Male
AG   19Y
CA   Finite cell line
DT   Created: 11-02-13; Last updated: 30-01-24; Version: 14
//
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).
//