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Cellosaurus CS2AWTERT (CVCL_2880)

[Text version]
Cell line name CS2AWTERT
Accession CVCL_2880
Resource Identification Initiative To cite this cell line use: CS2AWTERT (RRID:CVCL_2880)
Comments Population: Japanese.
Transfected with: HGNC; 11730; TERT.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 3439; ERCC8; Simple; p.Asp93Leufs*26 (Ex4del); Zygosity=Homozygous (from parent cell line).
Disease Cockayne syndrome type A (NCIt: C135725)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_2879 (CS2AW)
Sex of cell Female
Age at sampling 4Y
Category Telomerase immortalized cell line
STR profile Source(s): JCRB=JCRB1059

Markers:
AmelogeninX
CSF1PO10,13
D5S81811,13
D7S82011
D13S31710,12
D16S5399,10
TH017,10
TPOX11
vWA14,17

Run an STR similarity search on this cell line
Cross-references
Cell line collections (Providers) JCRB; JCRB1059
JCRB; NIHS0309 - Discontinued
Encyclopedic resources Wikidata; Q54814545
Entry history
Entry creation04-Apr-2012
Last entry update02-May-2024
Version number18