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Cellosaurus AIDHC-13010 (CVCL_C1YG)

[Text version]
Cell line name AIDHC-13010
Accession CVCL_C1YG
Resource Identification Initiative To cite this cell line use: AIDHC-13010 (RRID:CVCL_C1YG)
Comments From: Nemours Children's Hospital; Wilmington; USA.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Spinal muscular atrophy type 2 (NCIt: C156310)
Proximal spinal muscular atrophy type 2 (ORDO: Orphanet_83418)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C1YH ! AIDHC-15224
Sex of cell Female
Age at sampling Age unspecified
Category Finite cell line
STR profile Source(s): PubMed=28284873

Markers:
AmelogeninX
CSF1PO10,11
D5S81811,12
D7S82010,11
D13S3179,12
D16S53911,13
TH019.3
TPOX8,11
vWA18

Run an STR similarity search on this cell line
Publications

PubMed=28284873; DOI=10.1016/j.nmd.2017.02.002; PMCID=PMC5403612
Stabley D.L., Holbrook J., Harris A.W., Swoboda K.J., Crawford T.O., Sol-Church K., Butchbach M.E.R.
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; Q114310560
Entry history
Entry creation22-Sep-2022
Last entry update19-Dec-2024
Version number5