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Cellosaurus Wilms4 (CVCL_A5SG)

[Text version]
Cell line name Wilms4
Accession CVCL_A5SG
Resource Identification Initiative To cite this cell line use: Wilms4 (RRID:CVCL_A5SG)
Comments Population: Caucasian.
Derived from site: In situ; Kidney; UBERON=UBERON_0002113.
Sequence variations
Disease Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome (NCIt: C3718)
WAGR syndrome (ORDO: Orphanet_893)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 11M
Category Finite cell line
STR profile Source(s): PubMed=33379206

Markers:
AmelogeninX,Y
CSF1PO10,11
D3S135816,17
D5S81810,12
D7S82010,11
D8S117913
D13S3178
D16S5399,12
D18S5116,17
D21S1127,31.2
FGA20
Penta D10,12
Penta E11,15
TH017,8
TPOX8,11
vWA15,17

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Publications

PubMed=20106868; DOI=10.1093/hmg/ddq042
Brigitte Royer-Pokora, Maike Anna Busch, Manfred Beier, Constanze Duhme, Carmen de Torres, Jaume Mora, Artur Brandt, Hans-Dieter Royer;
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=33379206; DOI=10.3390/cancers13010060; PMCID=PMC7801943
Brigitte Royer-Pokora, Maike Anna Busch, Sarah Tenbusch, Mathias Schmidt, Manfred Beier, Andrew D. Woods, Holger Thiele, Jaume Mora;
Comprehensive biology and genetics compendium of Wilms tumor cell lines with different WT1 mutations.
Cancers (Basel) 13:60.1-60.21(2021)

Cross-references
Encyclopedic resources Wikidata; Q107117471
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number5