Cellosaurus logo
expasy logo

Cellosaurus XP1CH [XP-V Caucasian] (CVCL_ZP88)

[Text version]
Cell line name XP1CH [XP-V Caucasian]
Accession CVCL_ZP88
Resource Identification Initiative To cite this cell line use: XP1CH [XP-V Caucasian] (RRID:CVCL_ZP88)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:9181; POLH; Simple; p.Phe247fs (c.738delC); Zygosity=Heterozygous (PubMed=26884178).
  • Mutation; HGNC; HGNC:9181; POLH; Simple; p.Arg356Ter (c.1066C>T); ClinVar=VCV001459259; Zygosity=Heterozygous (PubMed=26884178).
Disease Xeroderma pigmentosum variant type (NCIt: C141367)
Xeroderma pigmentosum variant (ORDO: Orphanet_90342)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Sex unspecified
Age at sampling 26Y
Category Finite cell line
Publications

PubMed=26884178; DOI=10.1073/pnas.1519444113; PMCID=PMC4780618
Fassihi H., Sethi M., Fawcett H., Wing J.F., Chandler N., Mohammed S., Craythorne E., Morley A.M.S., Lim R.-X., Turner S., Henshaw T., Garrood I., Giunti P., Hedderly T., Abiona A., Naik H., Harrop G., McGibbon D., Jaspers N.G.J., Botta E., Nardo T., Stefanini M., Young A.R., Sarkany R.P.E., Lehmann A.R.
Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect.
Proc. Natl. Acad. Sci. U.S.A. 113:E1236-E1245(2016)

Cross-references
Encyclopedic resources Wikidata; Q98135407
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number10