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Cellosaurus GM01828 (CVCL_JB86)

[Text version]
Cell line name GM01828
Synonyms GM-1828
Accession CVCL_JB86
Resource Identification Initiative To cite this cell line use: GM01828 (RRID:CVCL_JB86)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 6636; LMNA; Simple; p.Thr10Ile (c.29C>T); ClinVar=VCV000066888; Zygosity=Heterozygous (from autologous cell line AG00990).
Disease Progeria (NCIt: C34951)
Hutchinson-Gilford progeria syndrome (ORDO: Orphanet_740)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_W843 ! AG00990
Sex of cell Male
Age at sampling 18Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977)

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

Cross-references
Cell line collections (Providers) Coriell; GM01828 - Discontinued
Encyclopedic resources Wikidata; Q54837108
Entry history
Entry creation15-May-2017
Last entry update29-Jun-2023
Version number11