ID   GS-109-V-34
AC   CVCL_2455
DR   CLO; CLO_0003569
DR   CLDB; cl1520
DR   ATCC; CRL-1613
DR   BioSample; SAMN03471405
DR   ECACC; 90110504
DR   Wikidata; Q54871715
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC=CRL-1613; ECACC=90110504
ST   Amelogenin: X
ST   CSF1PO: 10,11
ST   D13S317: 8,11
ST   D16S539: 11,12
ST   D18S51: 12,14
ST   D19S433: 12,14
ST   D21S11: 29,30
ST   D2S1338: 17,23
ST   D3S1358: 16
ST   D5S818: 12
ST   D7S820: 8,12
ST   D8S1179: 8,11
ST   FGA: 21,22
ST   Penta D: 10,12
ST   Penta E: 5,10
ST   TH01: 6,9.3
ST   TPOX: 10,12
ST   vWA: 14,16
DI   NCIt; C6728; Gardner syndrome
DI   ORDO; Orphanet_79665; Gardner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   6Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 02-05-24; Version: 13
//