ID   CS2OS(SVT)
AC   CVCL_2882
DR   JCRB; JCRB1056
DR   JCRB; KURB1902
DR   JCRB; NIHS0305
DR   Wikidata; Q54814547
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:3439; ERCC8; Simple; p.Asp93Leufs*26 (Ex4del); Zygosity=Homozygous (from parent cell line).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=pSVori-).
CC   Discontinued: JCRB; NIHS0305; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB1056
ST   Amelogenin: X,Y
ST   CSF1PO: 11,12
ST   D13S317: 8,9
ST   D16S539: 9
ST   D5S818: 13
ST   D7S820: 11
ST   TH01: 7
ST   TPOX: 11,13
ST   vWA: 16
DI   NCIt; C135725; Cockayne syndrome type A
DI   ORDO; Orphanet_191; Cockayne syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_2881 ! CS2OS
SX   Male
AG   Fetus
CA   Transformed cell line
DT   Created: 04-04-12; Last updated: 19-12-24; Version: 22
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