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Cellosaurus ND39026 (CVCL_T862)

[Text version]
Cell line name ND39026
Accession CVCL_T862
Resource Identification Initiative To cite this cell line use: ND39026 (RRID:CVCL_T862)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:11179; SOD1; Simple; p.Glu50Lys (c.148G>A) (E49K); ClinVar=VCV000658902; Zygosity=Unspecified (NHCDR=ND39026).
Disease Amyotrophic lateral sclerosis 1 (NCIt: C168749)
Amyotrophic lateral sclerosis (ORDO: Orphanet_803)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A9SS (CS24iALS-SOD1E50Kn9)CVCL_T861 (ND35668)CVCL_SA25 (ND50079)
Sex of cell Female
Age at sampling 49Y
Category Finite cell line
Publications

PubMed=25760436; DOI=10.1371/journal.pone.0118266; PMCID=PMC4356618
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; ND39026 - Discontinued
NHCDR; ND39026
Encyclopedic resources Wikidata; Q54930098
Entry history
Entry creation03-Feb-2014
Last entry update19-Dec-2024
Version number17