ID   L11
AC   CVCL_JX44
DR   Cosmic; 1017702
DR   Wikidata; Q54900944
RX   PubMed=10338002;
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:12796; WT1; Simple; c.895-2A>C; Zygosity=Heterozygous; Note=Splice acceptor mutation (PubMed=10338002).
DI   NCIt; C9160; Childhood acute myeloid leukemia
DI   ORDO; Orphanet_519; Acute myeloid leukemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Cancer cell line
DT   Created: 22-08-17; Last updated: 19-12-24; Version: 8
//
RX   PubMed=10338002; DOI=10.1002/(SICI)1098-2264(199906)25:2<176::AID-GCC14>3.0.CO;2-F;
RA   Miyagawa K., Hayashi Y., Fukuda T., Mitani K., Hirai H., Kamiya K.;
RT   "Mutations of the WT1 gene in childhood nonlymphoid hematological
RT   malignancies.";
RL   Genes Chromosomes Cancer 25:176-183(1999).
//