Cellosaurus cell line GM01828 (CVCL

Cellosaurus GM01828 (CVCL_JB86)

Cross-references
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; 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 Lewis Lemon Coriell, Arthur E. Greene; 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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977) 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)
Cell line collections (Providers)	Coriell; GM01828 - Discontinued
Encyclopedic resources	Wikidata; Q54837108
Entry history
Entry creation	15-May-2017
Last entry update	19-Dec-2024
Version number	12