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Cellosaurus AG03819 (CVCL_A2ML)

[Text version]
Cell line name AG03819
Synonyms AG3819
Accession CVCL_A2ML
Resource Identification Initiative To cite this cell line use: AG03819 (RRID:CVCL_A2ML)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Spinocerebellar ataxia (NCIt: C82341)
Rare hereditary ataxia (ORDO: Orphanet_183518)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 29Y
Category Finite cell line
Publications

CLPUB00387
Coriell L.L., Greene A.E., Mulivor R.A.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 7th edition. October 1980.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda; USA (1980)

PubMed=7253718; DOI=10.1016/0047-6374(81)90027-0
Das N.K., Murphy D.G.
The National Institute on Aging repository cell cultures.
Mech. Ageing Dev. 16:1-17(1981)

Cross-references
Cell line collections (Providers) Coriell; AG03819 - Discontinued
Encyclopedic resources Wikidata; Q105506261
Entry history
Entry creation12-Jan-2021
Last entry update29-Jun-2023
Version number5