ID   MCF-10A TP53(-/-)
AC   CVCL_JM25
SY   TP53 (-/-) MCF10A
DR   Horizon_Discovery; HD+101-005
DR   Wikidata; Q54904293
RX   PubMed=20562907;
CC   Knockout cell: Method=Homologous recombination; HGNC; 11998; TP53.
CC   Sequence variation: Gene deletion; HGNC; 1787; CDKN2A; Zygosity=Homozygous (from parent cell line).
CC   Sequence variation: Gene deletion; HGNC; 1788; CDKN2B; Zygosity=Homozygous (from parent cell line).
CC   Derived from site: In situ; Breast, epithelium; UBERON=UBERON_0008359.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0598 ! MCF-10A
SX   Female
AG   36Y
CA   Spontaneously immortalized cell line
DT   Created: 15-05-17; Last updated: 29-06-23; Version: 10
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RX   PubMed=20562907; DOI=10.1038/onc.2010.220;
RA   Weiss M.B., Vitolo M.I., Mohseni M., Rosen D.M., Denmeade S.R.,
RA   Park B.H., Weber D.J., Bachman K.E.;
RT   "Deletion of p53 in human mammary epithelial cells causes chromosomal
RT   instability and altered therapeutic response.";
RL   Oncogene 29:4715-4724(2010).
//