ID   WS1TKB2
AC   CVCL_J711
DR   CLO; CLO_0050655
DR   RCB; RCB0433
DR   Wikidata; Q54994425
CC   Population: Japanese.
CC   Senescence: Senesces at 12-13 PDL (RCB=RCB0433).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): RCB
ST   Amelogenin: X,Y
ST   CSF1PO: 12
ST   D13S317: 8,9
ST   D16S539: 9,12
ST   D5S818: 11
ST   D7S820: 11
ST   TH01: 9,10
ST   TPOX: 8,11
ST   vWA: 16,18
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_J710 ! WS1TKB
SX   Male
AG   61Y
CA   Finite cell line
DT   Created: 11-02-13; Last updated: 29-06-23; Version: 13
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