ID   GS-109-V-63
AC   CVCL_2456
SY   G96
DR   CLO; CLO_0003570
DR   CLDB; cl1521
DR   ATCC; CRL-1614
DR   BioSample; SAMN03471406
DR   ECACC; 90110503
DR   Wikidata; Q54871733
CC   Population: Caucasian.
CC   Karyotypic information: Diploid karyotype (ATCC=CRL-1614).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC=CRL-1614; ECACC=90110503
ST   Amelogenin: X,Y
ST   CSF1PO: 11
ST   D13S317: 11,12
ST   D16S539: 12,13
ST   D18S51: 12,17
ST   D19S433: 13,13.2
ST   D21S11: 29,33.2
ST   D2S1338: 22,23
ST   D3S1358: 15,16
ST   D5S818: 11,12
ST   D7S820: 9,10
ST   D8S1179: 13,15
ST   FGA: 20,21
ST   Penta D: 9
ST   Penta E: 10,12
ST   TH01: 7,8
ST   TPOX: 8,11
ST   vWA: 14,17
DI   NCIt; C6728; Gardner syndrome
DI   ORDO; Orphanet_79665; Gardner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   13Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 02-05-24; Version: 14
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