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Cellosaurus KS-0195 (CVCL_C2A1)

[Text version]
Cell line name KS-0195
Accession CVCL_C2A1
Resource Identification Initiative To cite this cell line use: KS-0195 (RRID:CVCL_C2A1)
Comments From: University of Utah; Salt Lake City; USA.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
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 Age unspecified
Category Finite cell line
STR profile Source(s): PubMed=28284873

Markers:
AmelogeninX,Y
CSF1PO10,11
D5S81811,14
D7S82011,13
D13S3179,10
D16S5399,12
TH017,9
TPOX8
vWA14,15

Run an STR similarity search on this cell line
Publications

PubMed=28284873; DOI=10.1016/j.nmd.2017.02.002; PMCID=PMC5403612
Deborah L. Stabley, Jennifer Holbrook, Ashlee W. Harris, Kathryn J. Swoboda, Thomas Owen Crawford, Katia Sol-Church, Matthew E.R. Butchbach;
Establishing a reference dataset for the authentication of spinal muscular atrophy cell lines using STR profiling and digital PCR.
Neuromuscul. Disord. 27:439-446(2017)

Cross-references
Encyclopedic resources Wikidata; Q114311837
Entry history
Entry creation22-Sep-2022
Last entry update19-Dec-2024
Version number5