ID   XP81TO
AC   CVCL_DE30
SY   Xeroderma Pigmentosum 81 TOkyo
DR   JCRB; KURB1085
DR   Wikidata; Q54994969
RX   PubMed=1376435;
RX   PubMed=12812979;
CC   Population: Japanese.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C114771; Xeroderma pigmentosum, complementation group E
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 7
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RX   PubMed=1376435; DOI=10.1016/0921-8777(92)90049-9;
RA   Keeney S.N., Wein H., Linn S.M.;
RT   "Biochemical heterogeneity in xeroderma pigmentosum complementation
RT   group E.";
RL   Mutat. Res. 273:49-56(1992).
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RX   PubMed=12812979; DOI=10.1093/hmg/ddg174;
RA   Rapic-Otrin V., Navazza V., Nardo T., Botta E., McLenigan M.,
RA   Bisi D.C., Levine A.S., Stefanini M.;
RT   "True XP group E patients have a defective UV-damaged DNA binding
RT   protein complex and mutations in DDB2 which reveal the functional
RT   domains of its p48 product.";
RL   Hum. Mol. Genet. 12:1507-1522(2003).
//