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Cellosaurus WA17 (CVCL_9778)

[Text version]
Cell line name WA17
Accession CVCL_9778
Resource Identification Initiative To cite this cell line use: WA17 (RRID:CVCL_9778)
Comments From: University of Wisconsin; Madison; USA.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-11-0098.
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=wa17

Markers:
AmelogeninX,Y
CSF1PO12,13
D5S81812
D7S8208,12
D13S3178
D16S53911,13
TH016,7
TPOX11
vWA17,19

Run an STR similarity search on this cell line
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; wa17
Cell line databases/resources ISCR; 1831
NIHhESC; NIHhESC-11-0098
Encyclopedic resources Wikidata; Q54993520
Entry history
Entry creation06-Jun-2012
Last entry update02-May-2024
Version number16