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Cellosaurus THP1-Null2 (CVCL_A8AK)

[Text version]

Cell line name THP1-Null2
Accession CVCL_A8AK
Resource Identification Initiative To cite this cell line use: THP1-Null2 (RRID:CVCL_A8AK)
Comments Population: Japanese.
Transfected with: UniProtKB; P17493; S.hindustanus ble.
Derived from sampling site: Peripheral blood.
Sequence variations Gene fusion; HGNC; 2457; CSNK2A1 + HGNC; 13917; DDX39B; Name(s)=CSNK2A1-DDX39B (from parent cell line).
Gene fusion; HGNC; 7132; KMT2A + HGNC; 7136; MLLT3; Name(s)=KMT2A-MLLT3, MLL-MLLT3, MLL-AF9 (from parent cell line).
Mutation; HGNC; 7989; NRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000039648; Zygosity=Heterozygous (from parent cell line).
Mutation; HGNC; 11998; TP53; Simple; p.Arg174fs*3 (c.520_545del26); Zygosity=Heterozygous (from parent cell line).
Disease Childhood acute monocytic leukemia (NCIt: C9163)
Acute monoblastic/monocytic leukemia (ORDO: Orphanet_514)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0006 (THP-1)
Children:
CVCL_A8AN (THP1-KO-ASC)CVCL_A8AP (THP1-KO-CASP4)CVCL_A8AQ (THP1-KO-GSDMD)
CVCL_A8AR (THP1-KO-NLRC4)CVCL_A8AS (THP1-KO-NLRP3)
Sex of cell Male
Age at sampling 1Y
Category Cancer cell line
Web pages https://www.invivogen.com/thp1-nullz
Cross-references
Other Wikidata; Q107117089
Entry history
Entry creation20-May-2021
Last entry update23-Sep-2021
Version number2