ID   BCNS1KO hTERT
AC   CVCL_F008
DR   JCRB; JCRB3009
DR   JCRB; KURB2738
DR   Wikidata; Q54795704
CC   Population: Japanese.
CC   Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT.
CC   Discontinued: JCRB; KURB2738; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB=JCRB3009
ST   Amelogenin: X,Y
ST   CSF1PO: 11,12
ST   D13S317: 8,9
ST   D16S539: 9,11
ST   D5S818: 11
ST   D7S820: 10,12
ST   TH01: 6
ST   TPOX: 8,11
ST   vWA: 14,17
DI   NCIt; C2892; Nevoid basal cell carcinoma syndrome
DI   ORDO; Orphanet_377; Gorlin syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_2866 ! BCNS1KO
SX   Male
AG   Age unspecified
CA   Telomerase immortalized cell line
DT   Created: 22-10-12; Last updated: 19-12-24; Version: 16
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