ID   Dch1
AC   CVCL_F009
DR   BioSample; SAMN03472401
DR   JCRB; JCRB3002
DR   JCRB; KURB2098
DR   Wikidata; Q54828674
CC   Population: Japanese.
CC   Discontinued: JCRB; KURB2098; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB3002
ST   Amelogenin: X,Y
ST   CSF1PO: 10,12
ST   D13S317: 11,13
ST   D16S539: 9,13
ST   D5S818: 12,13
ST   D7S820: 10,12
ST   TH01: 6,9
ST   TPOX: 8,11
ST   vWA: 17,18
DI   NCIt; C118435; Dyschromatosis symmetrica hereditaria
DI   ORDO; Orphanet_41; Dyschromatosis symmetrica hereditaria
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 02-05-24; Version: 14
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