ID   Dch4F
AC   CVCL_F012
DR   BioSample; SAMN03472404
DR   JCRB; JCRB3004
DR   JCRB; KURB2101
DR   Wikidata; Q54828677
CC   Population: Japanese.
CC   Discontinued: JCRB; KURB2101; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB3004
ST   Amelogenin: X,Y
ST   CSF1PO: 11,12
ST   D13S317: 8,10
ST   D16S539: 9,10
ST   D5S818: 11,12
ST   D7S820: 8,11
ST   TH01: 6
ST   TPOX: 9,11
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   34Y
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 02-05-24; Version: 14
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