Cellosaurus cell line ATLAN1010 fibroblast (CVCL

Cross-references
Cell line name	ATLAN1010 fibroblast
Accession	CVCL_A9F2
Resource Identification Initiative	To cite this cell line use: ATLAN1010 fibroblast (RRID:CVCL_A9F2)
Comments	Population: African American. 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.Arg133Leu (c.398G>T); ClinVar=VCV000014488; Zygosity=Heterozygous (PubMed=12927431).
Disease	Werner syndrome (NCIt: C3447) Atypical Werner syndrome (ORDO: Orphanet_79474)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_A9F3 ! ATLAN1010 LCL
Sex of cell	Female
Age at sampling	18Y
Category	Finite cell line
Publications	PubMed=12927431; DOI=10.1016/S0140-6736(03)14069-X Chen L.-S., Lee L., Kudlow B.A., Dos Santos H.G., Sletvold O., Shafeghati Y., Botha E.G., Garg A., Hanson N.B., Martin G.M., Mian I.S., Kennedy B.K., Oshima J. LMNA mutations in atypical Werner's syndrome. Lancet 362:440-445(2003)
Encyclopedic resources	Wikidata; Q102113575
Entry history
Entry creation	29-Oct-2020
Last entry update	19-Dec-2024
Version number	7