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Cellosaurus NH50164 (CVCL_UX42)

[Text version]
Cell line name NH50164
Accession CVCL_UX42
Resource Identification Initiative To cite this cell line use: NH50164 (RRID:CVCL_UX42)
Comments 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.Ala5Val (c.14C>T) (A4V); ClinVar=VCV000014763; Zygosity=Unspecified (NHCDR=NH50164).
Disease Amyotrophic lateral sclerosis 1 (NCIt: C168749)
Amyotrophic lateral sclerosis (ORDO: Orphanet_803)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) NHCDR; NH50164
Encyclopedic resources Wikidata; Q98127591
Entry history
Entry creation25-Feb-2019
Last entry update19-Dec-2024
Version number10