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Cellosaurus ND35669 (CVCL_T863)

[Text version]
Cell line name ND35669
Synonyms ND35669*C
Accession CVCL_T863
Resource Identification Initiative To cite this cell line use: ND35669 (RRID:CVCL_T863)
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:16873; FIG4; Simple; p.Ile9Ile (c.27C>T); ClinVar=VCV000137376; Zygosity=Unspecified (from parent cell line).
Disease Amyotrophic lateral sclerosis 11 (NCIt: C168753)
Amyotrophic lateral sclerosis (ORDO: Orphanet_803)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_T864 (ND39025)
Sex of cell Female
Age at sampling 67Y
Category Induced pluripotent stem cell
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; ND35669 - Discontinued
NHCDR; ND35669
Cell line databases/resources SKIP; SKIP001078
SKIP; SKIP004695
Encyclopedic resources Wikidata; Q54929885
Entry history
Entry creation03-Feb-2014
Last entry update19-Dec-2024
Version number18