ID   Dch3
AC   CVCL_F011
DR   BioSample; SAMN03472403
DR   JCRB; JCRB3003
DR   JCRB; KURB2100
DR   Wikidata; Q54828676
CC   Population: Japanese.
CC   Discontinued: JCRB; KURB2100; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB3003
ST   Amelogenin: X,Y
ST   CSF1PO: 11,12
ST   D13S317: 8,11
ST   D16S539: 9
ST   D5S818: 9,14
ST   D7S820: 8,11
ST   TH01: 6,9
ST   TPOX: 11,12
ST   vWA: 14,18
DI   NCIt; C118435; Dyschromatosis symmetrica hereditaria
DI   ORDO; Orphanet_41; Dyschromatosis symmetrica hereditaria
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   2Y
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 02-05-24; Version: 14
//