ID   L14 [Human leukemia]
AC   CVCL_JX45
DR   Cosmic; 1017703
DR   Wikidata; Q54900974
RX   PubMed=10338002;
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:12796; WT1; Simple; p.His397Gln (c.1191C>A); Zygosity=Heterozygous (PubMed=10338002).
DI   NCIt; C2993; Down syndrome
DI   NCIt; C43223; Myeloid leukemia associated with Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
DI   ORDO; Orphanet_99887; Acute megakaryoblastic leukemia in Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Age unspecified
CA   Cancer cell line
DT   Created: 22-08-17; Last updated: 19-12-24; Version: 9
//
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).
//