ID   GM2096-SV9
AC   CVCL_AD97
SY   GM2096SV9
DR   Wikidata; Q54851496
RX   PubMed=3003928;
RX   PubMed=3413074;
CC   Population: African American.
CC   Sequence variation: Mutation; HGNC; 12816; XPC; Simple; p.Pro334His (c.1001C>A); ClinVar=VCV000000253; Zygosity=Homozygous (from parent cell line).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C114770; Xeroderma pigmentosum, complementation group C
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_7351 ! XP1MI 2
SX   Female
AG   15Y
CA   Transformed cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 10
//
RX   PubMed=3003928; DOI=10.1007/BF01560723;
RA   Canaani D., Naiman T., Teitz T., Berg P.;
RT   "Immortalization of xeroderma pigmentosum cells by simian virus 40 DNA
RT   having a defective origin of DNA replication.";
RL   Somat. Cell Mol. Genet. 12:13-20(1986).
//
RX   PubMed=3413074; DOI=10.1073/pnas.85.16.6042;
RA   Pereira-Smith O.M., Smith J.R.;
RT   "Genetic analysis of indefinite division in human cells:
RT   identification of four complementation groups.";
RL   Proc. Natl. Acad. Sci. U.S.A. 85:6042-6046(1988).
//