ID   CS2OS hTERT-1
AC   CVCL_ZY33
DR   JCRB; JCRB3065
DR   JCRB; KURB1904
DR   Wikidata; Q102113721
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=Transduction; Gene=HGNC; HGNC:11730; TERT.
CC   Discontinued: JCRB; JCRB3065; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
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   Telomerase immortalized cell line
DT   Created: 29-10-20; Last updated: 19-12-24; Version: 8
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