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Cellosaurus XP69TMA LCL (CVCL_1F35)

[Text version]
Cell line name XP69TMA LCL
Synonyms Xeroderma Pigmentosum Turkey MAlatya 69 LCL; GM14870; GM14870A
Accession CVCL_1F35
Resource Identification Initiative To cite this cell line use: XP69TMA LCL (RRID:CVCL_1F35)
Comments Population: Turkish.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 12816; XPC; Simple; p.Tyr430Ter (c.1290_1295delTAAAGA) (p.Tyr430_Glu432delinsTer) (1395_1400delTAAAGA); ClinVar=VCV000940041; Zygosity=Homozygous (Coriell=GM14870).
Disease Xeroderma pigmentosum, complementation group C (NCIt: C114770)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_1F36 ! XP69TMA
Sex of cell Male
Age at sampling 10Y
Category Transformed cell line
Publications

PubMed=16081512; DOI=10.1093/carcin/bgi204
Khan S.G., Oh K.-S., Shahlavi T., Ueda T., Busch D.B., Inui H., Emmert S., Imoto K., Muniz-Medina V., Baker C.C., DiGiovanna J.J., Schmidt D., Khadavi A., Metin A., Gozukara E.M., Slor H., Sarasin A., Kraemer K.H.
Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.
Carcinogenesis 27:84-94(2006)

Cross-references
Cell line collections (Providers) Coriell; GM14870
Cell line databases/resources CLO; CLO_0031925
Encyclopedic resources Wikidata; Q54847485
Entry history
Entry creation08-Jul-2015
Last entry update30-Jan-2024
Version number15