ID   WA17
AC   CVCL_9778
DR   NIHhESC; NIHhESC-11-0098
DR   WiCell; wa17
DR   Wikidata; Q54993520
RX   PubMed=28445466;
CC   From: University of Wisconsin; Madison; USA.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-11-0098.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Variations; SNP array analysis.
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): WiCell=wa17
ST   Amelogenin: X,Y
ST   CSF1PO: 12,13
ST   D13S317: 8
ST   D16S539: 11,13
ST   D5S818: 12
ST   D7S820: 8,12
ST   TH01: 6,7
ST   TPOX: 11
ST   vWA: 17,19
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 10-04-25; Version: 18
//
RX   PubMed=28445466; DOI=10.1038/nature22312; PMCID=PMC5427175;
RA   Merkle, Florian T.
RA   Ghosh, Sulagna
RA   Kamitaki, Nolan
RA   Mitchell, Jana
RA   Avior, Yishai
RA   Mello, Curtis
RA   Kashin, Seva
RA   Mekhoubad, Shila
RA   Ilic, Dusko
RA   Charlton, Maura
RA   Saphier, Genevieve
RA   Handsaker, Robert E.
RA   Genovese, Giulio
RA   Bar, Shiran
RA   Benvenisty, Nissim
RA   McCarroll, Steven A.
RA   Eggan, Kevin Carl
RT   "Human pluripotent stem cells recurrently acquire and expand dominant
RT   negative p53 mutations.";
RL   Nature 545:229-233(2017).
//