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Cellosaurus GM08889 (CVCL_0N09)

[Text version]
Cell line name GM08889
Accession CVCL_0N09
Resource Identification Initiative To cite this cell line use: GM08889 (RRID:CVCL_0N09)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Phe508del (c.1521_1523delCTT); ClinVar=VCV000007105; Zygosity=Heterozygous (Coriell=GM08889).
  • Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Arg1162Ter (c.3484C>T); ClinVar=VCV000007137; Zygosity=Heterozygous (Coriell=GM08889).
Disease Cystic fibrosis (NCIt: C2975)
Cystic fibrosis (ORDO: Orphanet_586)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 19FW
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)

Cross-references
Cell line collections (Providers) Coriell; GM08889
Cell line databases/resources CLO; CLO_0011197
Biological sample resources BioSample; SAMN00798260
Encyclopedic resources Wikidata; Q54843388
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number14