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Cellosaurus CS2OS(SVT) (CVCL_2882)

[Text version]
Cell line name CS2OS(SVT)
Accession CVCL_2882
Resource Identification Initiative To cite this cell line use: CS2OS(SVT) (RRID:CVCL_2882)
Comments Population: Japanese.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) [Note=pSVori-].
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_2881 (CS2OS)
Sex of cell Male
Age at sampling Fetus
Category Transformed cell line
STR profile Source(s): JCRB=JCRB1056

Markers:
AmelogeninX,Y
CSF1PO11,12
D5S81813
D7S82011
D13S3178,9
D16S5399
TH017
TPOX11,13
vWA16

Run an STR similarity search on this cell line
Cross-references
Cell line collections (Providers) JCRB; JCRB1056
JCRB; KURB1902
JCRB; NIHS0305 - Discontinued
Encyclopedic resources Wikidata; Q54814547
Entry history
Entry creation04-Apr-2012
Last entry update02-May-2024
Version number20