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Cellosaurus GM15876 (CVCL_F509)

[Text version]
Cell line name GM15876
Synonyms XP2OS-pCAH19WS; XP20S-pCAH19WS; XP20S(pCAH19WS); GM15876A
Accession CVCL_F509
Resource Identification Initiative To cite this cell line use: GM15876 (RRID:CVCL_F509)
Comments Population: Japanese.
Characteristics: Transfection of wildtype XPA corrects the c.390-1G>C mutation of this gene in the cell line.
Genetic integration: Method=Transfection/transduction; Gene=HGNC; 12814; XPA.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 12814; XPA; Simple; c.390-1G>C (IVS3-1G>C); ClinVar=VCV000264684; Zygosity=Homozygous; Note=Splice acceptor mutation (from parent cell line).
Disease Xeroderma pigmentosum, complementation group A (NCIt: C3965)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_ZN80 (XP2OS SV40-transformed)
Sex of cell Female
Age at sampling 7Y
Category Transformed cell line
Cross-references
Cell line collections (Providers) Coriell; GM15876
Cell line databases/resources CLO; CLO_0018536
Encyclopedic resources Wikidata; Q54848248
Entry history
Entry creation11-Feb-2013
Last entry update10-Sep-2024
Version number17