ID   Sal Mat
AC   CVCL_3596
DR   CLO; CLO_0008946
DR   ATCC; CRL-1110
DR   BioSample; SAMN03471328
DR   Wikidata; Q54952080
RX   PubMed=503099;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC=CRL-1110
ST   Amelogenin: X,Y
ST   CSF1PO: 7,11
ST   D13S317: 9,12
ST   D16S539: 11,12
ST   D18S51: 13,19
ST   D19S433: 13
ST   D21S11: 29,30
ST   D2S1338: 18,19
ST   D3S1358: 15,17
ST   D5S818: 11,12
ST   D7S820: 8,11
ST   D8S1179: 11,14
ST   FGA: 22,28
ST   Penta D: 2.2,9
ST   Penta E: 7,10
ST   TH01: 7,9
ST   TPOX: 7,8
ST   vWA: 16,18
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   14Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 02-05-24; Version: 15
//
RX   PubMed=503099; DOI=10.1016/0027-5107(79)90089-7;
RA   Myhr, Brian C.
RA   Turnbull, Duncan
RA   DiPaolo, Joseph A.
RT   "Ultraviolet mutagenesis of normal and xeroderma pigmentosum variant
RT   human fibroblasts.";
RL   Mutat. Res. 62:341-353(1979).
//