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Cellosaurus CS2OS (CVCL_2881)

[Text version]
Cell line name CS2OS
Synonyms Cockayne Syndrome 2 OSaka
Accession CVCL_2881
Resource Identification Initiative To cite this cell line use: CS2OS (RRID:CVCL_2881)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:3439; ERCC8; Simple; p.Asp93Leufs*26 (Ex4del); Zygosity=Homozygous (PubMed=12655141).
Disease Cockayne syndrome type A (NCIt: C135725)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZY33 (CS2OS hTERT-1)CVCL_ZY34 (CS2OS hTERT-2)CVCL_2882 (CS2OS(SVT))
Sex of cell Male
Age at sampling Fetus
Category Finite cell line
STR profile Source(s): JCRB=JCRB0309

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

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Publications

PubMed=12655141; DOI=10.1266/ggs.78.93
Ren Y., Saijo M., Nakatsu Y., Nakai H., Yamaizumi M., Tanaka K.
Three novel mutations responsible for Cockayne syndrome group A.
Genes Genet. Syst. 78:93-102(2003)

Cross-references
Cell line collections (Providers) JCRB; JCRB0309
JCRB; KURB1900
Biological sample resources BioSample; SAMN03471617
Encyclopedic resources Wikidata; Q54814546
Entry history
Entry creation04-Apr-2012
Last entry update19-Dec-2024
Version number18