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Cellosaurus CS1AW (CVCL_M677)

[Text version]
Cell line name CS1AW
Accession CVCL_M677
Resource Identification Initiative To cite this cell line use: CS1AW (RRID:CVCL_M677)
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 (from familial inference of CS2AW).
Disease Cockayne syndrome type A (NCIt: C135725)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZY32 (CS1AW(SV))
Sex of cell Female
Age at sampling 7Y
Category Finite cell line
Publications

DOI=10.11251/ojjscn1969.10.465
Hashimoto T., Hiura K., Kobayashi Y., Kawano N., Takahashi T., Endo S., Fukuda K.
Cockayne's syndrome: report of two sisters and review of literature in Japan.
No To Hattatsu 10:465-472(1978)

PubMed=6481688; DOI=10.1269/jrr.25.150
Watatani M., Ohtani H., Takai S.-i., Ikenaga M.
Host cell reactivation of ultraviolet light irradiated adenovirus 5 in fibroblasts from patients with Cockayne syndrome: a study with six Japanese cases.
J. Radiat. Res. 25:150-159(1984)

Cross-references
Cell line collections (Providers) JCRB; KURB1895
Encyclopedic resources Wikidata; Q54814530
Entry history
Entry creation05-Nov-2013
Last entry update19-Dec-2024
Version number13