ID   Dch2
AC   CVCL_F010
DR   BioSample; SAMN03472400
DR   JCRB; JCRB3001
DR   JCRB; KURB2099
DR   Wikidata; Q54828675
CC   Population: Japanese.
CC   Discontinued: JCRB; KURB2099; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB3001
ST   Amelogenin: X
ST   CSF1PO: 10,11
ST   D13S317: 8,11
ST   D16S539: 9
ST   D5S818: 11
ST   D7S820: 8
ST   TH01: 6,9
ST   TPOX: 11,12
ST   vWA: 18
DI   NCIt; C118435; Dyschromatosis symmetrica hereditaria
DI   ORDO; Orphanet_41; Dyschromatosis symmetrica hereditaria
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   6Y
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 02-05-24; Version: 15
//