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Cellosaurus ND39027 (CVCL_T855)

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Cell line name ND39027
Accession CVCL_T855
Resource Identification Initiative To cite this cell line use: ND39027 (RRID:CVCL_T855)
Comments Population: Cape Verdian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:4010; FUS; Simple; p.His517Gln (c.1551C>G); ClinVar=VCV000016221; Zygosity=Homozygous (NHCDR=ND39027).
Disease Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia (NCIt: C168750)
Frontotemporal dementia with motor neuron disease (ORDO: Orphanet_275872)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_T854 (ND35663)CVCL_UX43 (NH50184)CVCL_UX44 (NH50185)
CVCL_YP42 (NH50192)
Originate from same individual CVCL_U113 ! ND10734
Sex of cell Female
Age at sampling 50Y
Category Finite cell line
Publications

PubMed=25760436; DOI=10.1371/journal.pone.0118266; PMCID=PMC4356618
Ying Li, Umamahesw Balasubramanian, Devon Cohen, Ping-Wu Zhang, Elizabeth Mosmiller, Rita Sattler, Nicholas John Maragakis, Jeffrey D. Rothstein;
A comprehensive library of familial human amyotrophic lateral sclerosis induced pluripotent stem cells.
PLoS ONE 10:e0118266.1-e0118266.13(2015)

Cross-references
Cell line collections (Providers) Coriell; ND39027 - Discontinued
NHCDR; ND39027
Encyclopedic resources Wikidata; Q54930099
Entry history
Entry creation03-Feb-2014
Last entry update10-Apr-2025
Version number19