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Cellosaurus Wilms3 (CVCL_A5SF)

[Text version]
Cell line name Wilms3
Accession CVCL_A5SF
Resource Identification Initiative To cite this cell line use: Wilms3 (RRID:CVCL_A5SF)
Comments Population: Caucasian.
Derived from site: In situ; Kidney; UBERON=UBERON_0002113.
Sequence variations
Disease Kidney Wilms tumor (NCIt: C40407)
Nephroblastoma (ORDO: Orphanet_654)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A5SP (imWilms3)
Sex of cell Male
Age at sampling 11-12M
Category Finite cell line
STR profile Source(s): CLS=300414; PubMed=33379206

Markers:
AmelogeninX,Y
CSF1PO11,12
D3S135815,16
D5S8189
D7S82010,11
D8S117910,11
D13S31712,13
D16S5399,11
D18S5113,17
D21S1129,31
FGA22,24
Penta D9,13
Penta E7,10
TH016
TPOX8
vWA16,17

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Publications

PubMed=20106868; DOI=10.1093/hmg/ddq042
Royer-Pokora B., Busch M.A., Beier M., Duhme C., de Torres C., Mora J., Brandt A., Royer H.-D.
Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm.
Hum. Mol. Genet. 19:1651-1668(2010)

PubMed=24619359; DOI=10.1093/hmg/ddu111; PMCID=PMC4082364
Busch M.A., Schwindt H., Brandt A., Beier M., Gorldt N., Romaniuk P., Toska E., Roberts S., Royer H.-D., Royer-Pokora B.
Classification of a frameshift/extended and a stop mutation in WT1 as gain-of-function mutations that activate cell cycle genes and promote Wilms tumour cell proliferation.
Hum. Mol. Genet. 23:3958-3974(2014)

PubMed=33379206; DOI=10.3390/cancers13010060; PMCID=PMC7801943
Royer-Pokora B., Busch M.A., Tenbusch S., Schmidt M., Beier M., Woods A.D., Thiele H., Mora J.
Comprehensive biology and genetics compendium of Wilms tumor cell lines with different WT1 mutations.
Cancers (Basel) 13:60.1-60.21(2021)

Cross-references
Cell line collections (Providers) CLS; 300414
Encyclopedic resources Wikidata; Q107117469
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number7