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Cellosaurus GM02694 (CVCL_4N28)

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Cell line name GM02694
Synonyms GM02694A
Accession CVCL_4N28
Resource Identification Initiative To cite this cell line use: GM02694 (RRID:CVCL_4N28)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:583; APC; Simple; p.Gln215Ter (c.643C>T); ClinVar=VCV000000814; Zygosity=Unspecified (Coriell=GM02694).
Disease Familial adenomatous polyposis (NCIt: C3339)
Turcot syndrome (NCIt: C3938)
Familial adenomatous polyposis (ORDO: Orphanet_733)
Turcot syndrome with polyposis (ORDO: Orphanet_99818)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 40Y
Category Finite cell line
Publications

PubMed=3374507; DOI=10.1016/0027-5107(88)90211-4
Bruno Azzarone, Christine Chaponnier, Patricia Krief, Marc M. Mareel, Horacio Guillermo Suarez, Alvaro Macieira-Coelho;
Human fibroblasts from cancer patients: lifespan and transformed phenotype in vitro and role of mesenchyme in vivo.
Mutat. Res. 199:313-325(1988)

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM02694
Cell line databases/resources CLO; CLO_0014911
Biological sample resources BioSample; SAMN00808024
Encyclopedic resources Wikidata; Q54837637
Entry history
Entry creation22-Sep-2015
Last entry update19-Dec-2024
Version number15