ID   THP-1/IL15
AC   CVCL_XD94
DR   cancercelllines; CVCL_XD94
DR   Wikidata; Q98133248
CC   Population: Japanese.
CC   Sequence variation: Gene fusion; HGNC; 2457; CSNK2A1 + HGNC; 13917; DDX39B; Name(s)=CSNK2A1-DDX39B (from parent cell line).
CC   Sequence variation: Gene fusion; HGNC; 7132; KMT2A + HGNC; 7136; MLLT3; Name(s)=KMT2A-MLLT3, MLL-MLLT3, MLL-AF9 (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 7989; NRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000039648; Zygosity=Heterozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Arg174fs*3 (c.520_545del26); Zygosity=Heterozygous (from parent cell line).
CC   Transfected with: HGNC; 5977; IL15.
CC   Miscellaneous: Formerly the CCRID database had an entry describing this cell line (3111C0001CCC000462). It was the sole source of information for this entry.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
ST   Source(s): CCRID
ST   Amelogenin: X
ST   CSF1PO: 11,13
ST   D12S391: 19
ST   D13S317: 13
ST   D16S539: 11,12
ST   D18S51: 13,14
ST   D19S433: 12.2,13
ST   D21S11: 30,32.2
ST   D2S1338: 17,18
ST   D3S1358: 15,17
ST   D5S818: 11,12
ST   D6S1043: 14
ST   D7S820: 10
ST   D8S1179: 10,14
ST   FGA: 24,25
ST   Penta E: 11,15
ST   TH01: 8,9.3
ST   TPOX: 8,11
ST   vWA: 16
DI   NCIt; C9163; Childhood acute monocytic leukemia
DI   ORDO; Orphanet_514; Acute monoblastic/monocytic leukemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0006 ! THP-1
SX   Male
AG   1Y
CA   Cancer cell line
DT   Created: 06-09-19; Last updated: 05-10-23; Version: 9
//