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Cellosaurus GM06888 (CVCL_CY45)

[Text version]
Cell line name GM06888
Synonyms GM06888A
Accession CVCL_CY45
Resource Identification Initiative To cite this cell line use: GM06888 (RRID:CVCL_CY45)
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.Glu1538Ilefs*5 (c.4612_4613delAG) (P1542X); ClinVar=VCV000000823; Zygosity=Unspecified (Coriell=GM06888).
Disease Familial adenomatous polyposis (NCIt: C3339)
Familial adenomatous polyposis (ORDO: Orphanet_733)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A9Z8 (FAP 6888-1)
Sex of cell Male
Age at sampling 16Y
Category Finite cell line
Publications

CLPUB00447
Mulivor R.A., Suchy S.F.
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)

PubMed=30024920; DOI=10.1371/journal.pone.0200657; PMCID=PMC6053155
Sommer C.A., Capilla A., Molina-Estevez F.J., Gianotti-Sommer A., Skvir N.J., Caballero I., Chowdhury S., Mostoslavsky G.
Modeling APC mutagenesis and familial adenomatous polyposis using human iPS cells.
PLoS ONE 13:E0200657-E0200657(2018)

Cross-references
Cell line collections (Providers) Coriell; GM06888 - Discontinued
Cell line databases/resources CLO; CLO_0036492
Encyclopedic resources Wikidata; Q54842362
Entry history
Entry creation13-Jul-2016
Last entry update19-Dec-2024
Version number14