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Cellosaurus WA21 (CVCL_9782)

[Text version]
Cell line name WA21
Accession CVCL_9782
Resource Identification Initiative To cite this cell line use: WA21 (RRID:CVCL_9782)
Comments From: University of Wisconsin; Madison; USA.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-11-0102.
Omics: Deep exome analysis.
Omics: SNP array analysis.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Blastocyst stage
Category Embryonic stem cell
STR profile Source(s): WiCell=wa21

Markers:
AmelogeninX,Y
CSF1PO12,13
D5S81811
D7S8209
D13S31711,12
D16S53911
TH018,9
TPOX8,12
vWA18

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Publications

PubMed=28445466; DOI=10.1038/nature22312
Merkle F.T., Ghosh S., Kamitaki N., Mitchell J., Avior Y., Mello C., Kashin S., Mekhoubad S., Ilic D., Charlton M., Saphier G., Handsaker R.E., Genovese G., Bar S., Benvenisty N., McCarroll S.A., Eggan K.C.
Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations.
Nature 545:229-233(2017)

Cross-references
Cell line collections (Providers) WiCell; wa21
Cell line databases/resources ISCR; 1835
NIHhESC; NIHhESC-11-0102
Encyclopedic resources Wikidata; Q54993527
Entry history
Entry creation06-Jun-2012
Last entry update02-May-2024
Version number16