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Cellosaurus L11 (CVCL_JX44)

[Text version]
Cell line name L11
Accession CVCL_JX44
Resource Identification Initiative To cite this cell line use: L11 (RRID:CVCL_JX44)
Comments Population: Japanese.
Sequence variations
  • Mutation; HGNC; HGNC:12796; WT1; Simple; c.895-2A>C; Zygosity=Heterozygous; Note=Splice acceptor mutation (PubMed=10338002).
Disease Childhood acute myeloid leukemia (NCIt: C9160)
Acute myeloid leukemia (ORDO: Orphanet_519)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Sex unspecified
Age at sampling Age unspecified
Category Cancer cell line
Publications

PubMed=10338002; DOI=10.1002/(SICI)1098-2264(199906)25:2<176::AID-GCC14>3.0.CO;2-F
Miyagawa K., Hayashi Y., Fukuda T., Mitani K., Hirai H., Kamiya K.
Mutations of the WT1 gene in childhood nonlymphoid hematological malignancies.
Genes Chromosomes Cancer 25:176-183(1999)

Cross-references
Encyclopedic resources Wikidata; Q54900944
Polymorphism and mutation databases Cosmic; 1017702
Entry history
Entry creation22-Aug-2017
Last entry update19-Dec-2024
Version number8