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Cellosaurus XP4PA (CVCL_ZP32)

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Cell line name XP4PA
Accession CVCL_ZP32
Resource Identification Initiative To cite this cell line use: XP4PA (RRID:CVCL_ZP32)
Comments Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Sequence variations
  • Mutation; HGNC; HGNC:12816; XPC; Simple; p.Val548Alafs*25 (c.1639_1640TG[2]) (c.1643_1644delTG) (1744_1745delTG); ClinVar=VCV000000262; Zygosity=Heterozygous (from child cell line XP4PA(SV)).
Disease Xeroderma pigmentosum, complementation group C (NCIt: C114770)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Fetus
Category Finite cell line
Publications

PubMed=3029584; DOI=10.1016/0167-8817(87)90061-7
Leela Daya-Grosjean, Michael R. James, Christiane Drougard, Alain Sarasin;
An immortalized xeroderma pigmentosum, group C, cell line which replicates SV40 shuttle vectors.
Mutat. Res. 183:185-196(1987)

Cross-references
Encyclopedic resources Wikidata; Q98135894
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number7