ID   Wilms10M
AC   CVCL_A5SK
DR   CLS; 300418
DR   Wikidata; Q107117464
RX   PubMed=33379206;
CC   Population: Caucasian.
CC   Sequence variation: Gene deletion; HGNC; HGNC:12796; WT1; Zygosity=Homozygous; Note=Nested within a heterozygous 11p13 deletion (PubMed=33379206).
CC   Sequence variation: Mutation; HGNC; HGNC:2514; CTNNB1; Simple; p.Ser45del (c.133_135delTCT); ClinVar=VCV000017576; Zygosity=Homozygous (PubMed=33379206).
CC   Derived from site: Metastatic; Lung; UBERON=UBERON_0002048.
ST   Source(s): PubMed=33379206
ST   Amelogenin: X
ST   CSF1PO: 11,12
ST   D13S317: 12
ST   D16S539: 9,10
ST   D18S51: 14,16
ST   D21S11: 29,30
ST   D3S1358: 17
ST   D5S818: 10,12
ST   D7S820: 11,12
ST   D8S1179: 10,15
ST   FGA: 22,24
ST   Penta D: 10,13
ST   Penta E: 7,10
ST   TH01: 8
ST   TPOX: 8,11
ST   vWA: 15,18
DI   NCIt; C40407; Kidney Wilms tumor
DI   ORDO; Orphanet_654; Nephroblastoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_A5SL ! Wilms10T
SX   Female
AG   2Y
CA   Finite cell line
DT   Created: 20-05-21; Last updated: 19-12-24; Version: 6
//
RX   PubMed=33379206; DOI=10.3390/cancers13010060; PMCID=PMC7801943;
RA   Royer-Pokora B., Busch M.A., Tenbusch S., Schmidt M., Beier M.,
RA   Woods A.D., Thiele H., Mora J.;
RT   "Comprehensive biology and genetics compendium of Wilms tumor cell
RT   lines with different WT1 mutations.";
RL   Cancers (Basel) 13:60.1-60.21(2021).
//