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Cellosaurus Nalm-6-MSH+ (CVCL_J365)

[Text version]
Cell line name Nalm-6-MSH+
Accession CVCL_J365
Resource Identification Initiative To cite this cell line use: Nalm-6-MSH+ (RRID:CVCL_J365)
Comments Population: Caucasian.
Characteristics: NALM-6 has a partial C-terminal deletion of the MSH2 gene, Nalm-6-MSH+ repairs the gene by transfection of the missing exons.
Transfected with: HGNC; 7325; MSH2 (exons 9 to 16).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Gene fusion; HGNC; 50800; DUX4 + HGNC; 5477; IGH; Name(s)=IGH-DUX4; Note=The translocation occurs in the silenced IGH allele (from parent cell line).
  • Mutation; HGNC; 3236; EGFR; Simple; p.Arg1068Ter (c.3202C>T); Zygosity=Heterozygous (from parent cell line).
  • Mutation; HGNC; 7989; NRAS; Simple; p.Ala146Thr (c.436G>A); Zygosity=Heterozygous (from parent cell line).
  • Mutation; HGNC; 9864; RARA; Simple; p.Gln45Ter (c.133C>T); ClinVar=VCV000393019; Zygosity=Heterozygous (from parent cell line).
Disease Adult B acute lymphoblastic leukemia (NCIt: C9143)
Precursor B-cell acute lymphoblastic leukemia (ORDO: Orphanet_99860)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0092 (NALM-6)
Children:
CVCL_M248 (POLZ KO)
Sex of cell Male
Age at sampling 19Y
Category Cancer cell line
STR profile Source(s): JCRB=JCRB1475

Markers:
AmelogeninX,Y
CSF1PO14
D5S81811,13
D7S8208,12
D13S3179,13
D16S5399,11
TH018,9
TPOX8,10
vWA15,16

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Publications

PubMed=23596518; DOI=10.1371/journal.pone.0061189
Suzuki T., Ukai A., Honma M., Adachi N., Nohmi T.
Restoration of mismatch repair functions in human cell line Nalm-6, which has high efficiency for gene targeting.
PLoS ONE 8:E61189-E61189(2013)

Cross-references
Cell line collections (Providers) JCRB; JCRB1475
Cell line databases/resources cancercelllines; CVCL_J365
Encyclopedic resources Wikidata; Q54907437
Entry history
Entry creation11-Feb-2013
Last entry update02-May-2024
Version number21