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Cellosaurus XP8MY (CVCL_ZQ62)

[Text version]
Cell line name XP8MY
Accession CVCL_ZQ62
Resource Identification Initiative To cite this cell line use: XP8MY (RRID:CVCL_ZQ62)
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:12814; XPA; Simple; c.390-1G>C (IVS3-1G>C); ClinVar=VCV000264684; Zygosity=Homozygous; Note=Splice acceptor mutation (PubMed=7905727).
Disease Xeroderma pigmentosum, complementation group A (NCIt: C3965)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 2Y
Category Finite cell line
Publications

PubMed=7905727; DOI=10.1001/archderm.1994.01690020057009
Nishigori C., Moriwaki S., Takebe H., Tanaka T., Imamura S.
Gene alterations and clinical characteristics of xeroderma pigmentosum group A patients in Japan.
Arch. Dermatol. 130:191-197(1994)

Cross-references
Cell line collections (Providers) JCRB; KURB1307
Encyclopedic resources Wikidata; Q98136191
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number8