ID   CS2AWTERT
AC   CVCL_2880
DR   JCRB; JCRB1059
DR   JCRB; NIHS0309
DR   Wikidata; Q54814545
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:3439; ERCC8; Simple; p.Asp93Leufs*26 (Ex4del); Zygosity=Homozygous (from parent cell line).
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:11730; TERT.
CC   Discontinued: JCRB; NIHS0309; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB1059
ST   Amelogenin: X
ST   CSF1PO: 10,13
ST   D13S317: 10,12
ST   D16S539: 9,10
ST   D5S818: 11,13
ST   D7S820: 11
ST   TH01: 7,10
ST   TPOX: 11
ST   vWA: 14,17
DI   NCIt; C135725; Cockayne syndrome type A
DI   ORDO; Orphanet_191; Cockayne syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_2879 ! CS2AW
SX   Female
AG   4Y
CA   Telomerase immortalized cell line
DT   Created: 04-04-12; Last updated: 19-12-24; Version: 20
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