ID   Werner
AC   CVCL_JH28
DR   JCRB; JCRB3041
DR   JCRB; KURB2881
DR   Wikidata; Q54993785
CC   Population: Japanese.
CC   Discontinued: JCRB; KURB2881; probable.
ST   Source(s): JCRB=JCRB3041
ST   Amelogenin: X,Y
ST   CSF1PO: 12,13
ST   D13S317: 8,12
ST   D16S539: 9,12
ST   D5S818: 11,13
ST   D7S820: 8
ST   TH01: 9
ST   TPOX: 8
ST   vWA: 18
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Finite cell line
DT   Created: 15-05-17; Last updated: 02-05-24; Version: 7
//