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Cellosaurus AG03848 (CVCL_A2MM)

[Text version]
Cell line name AG03848
Synonyms AG 3848; AG3848; SMA2FABE
Accession CVCL_A2MM
Resource Identification Initiative To cite this cell line use: AG03848 (RRID:CVCL_A2MM)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Werdnig-Hoffmann disease (NCIt: C98670)
Proximal spinal muscular atrophy type 1 (ORDO: Orphanet_83330)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 6Y
Category Finite cell line

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) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (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)

PubMed=3941662; DOI=10.1016/0027-5107(86)90121-1
Scudiero D.A., Polinsky R.J., Brumback R.A., Tarone R.E., Nee L.E., Robbins J.H.
Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemical.
Mutat. Res. 159:125-131(1986)

Cell line collections (Providers) Coriell; AG03848 - Discontinued
Encyclopedic resources Wikidata; Q105506266
Entry history
Entry creation12-Jan-2021
Last entry update29-Jun-2023
Version number5