ID   GS-109-V-21
AC   CVCL_2454
DR   CLO; CLO_0003568
DR   ATCC; CRL-1643
DR   BioSample; SAMN03471411
DR   Wikidata; Q54871714
CC   Population: Caucasian.
CC   Karyotypic information: 46,XX,-2,2q+ (ATCC=CRL-1643).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC=CRL-1643
ST   Amelogenin: X
ST   CSF1PO: 10,12
ST   D13S317: 12,14
ST   D16S539: 12,13
ST   D18S51: 12,14
ST   D19S433: 14.2,16.2
ST   D21S11: 29,32.2
ST   D2S1338: 16,17
ST   D3S1358: 15,18
ST   D5S818: 11,12
ST   D7S820: 8,13
ST   D8S1179: 11,14
ST   FGA: 20,22
ST   Penta D: 10
ST   Penta E: 12,15
ST   TH01: 6,9
ST   TPOX: 8
ST   vWA: 14,17
DI   NCIt; C6728; Gardner syndrome
DI   ORDO; Orphanet_79665; Gardner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   17Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 02-05-24; Version: 13
//