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Cellosaurus ND35661 (CVCL_T852)

[Text version]
Cell line name ND35661
Synonyms ND35661*E
Accession CVCL_T852
Resource Identification Initiative To cite this cell line use: ND35661 (RRID:CVCL_T852)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 11179; SOD1; Simple; p.Ile114Thr (c.341T>C) (I113T); ClinVar=VCV000197145; Zygosity=Unspecified (Coriell=ND35661).
Disease Amyotrophic lateral sclerosis 1 (NCIt: C168749)
Amyotrophic lateral sclerosis (ORDO: Orphanet_803)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_T851 (ND29422)
Sex of cell Male
Age at sampling 55Y
Category Induced pluripotent stem cell
Publications

PubMed=25760436; DOI=10.1371/journal.pone.0118266
Li Y., Balasubramanian U., Cohen D., Zhang P.-W., Mosmiller E., Sattler R., Maragakis N.J., Rothstein J.D.
A comprehensive library of familial human amyotrophic lateral sclerosis induced pluripotent stem cells.
PLoS ONE 10:E0118266-E0118266(2015)

Cross-references
Cell line collections (Providers) Coriell; ND35661 - Discontinued
NHCDR; ND35661
Cell line databases/resources SKIP; SKIP001072
SKIP; SKIP004689
Encyclopedic resources Wikidata; Q54929878
Entry history
Entry creation03-Feb-2014
Last entry update30-Jan-2024
Version number20