ID   GENEA015
AC   CVCL_9024
SY   Genea015; SIVF015
DR   NIHhESC; NIHhESC-13-0228
DR   Wikidata; Q54835577
RX   PubMed=27217344;
RX   PubMed=27346028;
RX   PubMed=28445466;
WW   Provider; Genea; -; https://web.archive.org/web/20180912205435/http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
CC   From: Genea Biocells, Ltd; Sydney; Australia.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-13-0228.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-37.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Variations; SNP array analysis.
CC   Donor information: Embryo is sibling to that giving rise to GENEA016 (Cellosaurus=CVCL_9025).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): PubMed=27346028
ST   Amelogenin: X,Y
ST   CSF1PO: 10,12
ST   D13S317: 11,12
ST   D16S539: 10,11
ST   D18S51: 14,15
ST   D19S433: 15,16.2
ST   D21S11: 29,31.2
ST   D2S1338: 18,23
ST   D3S1358: 16,19
ST   D5S818: 11,13
ST   D7S820: 10,11
ST   D8S1179: 13,14
ST   FGA: 21,23
ST   TH01: 6,8
ST   TPOX: 8,12
ST   vWA: 17
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=27217344; DOI=10.5966/sctm.2015-0224; PMCID=PMC4996435;
RA   Caron L., Kher D., Lee K.L., McKernan R., Dumevska B., Hidalgo A.,
RA   Li J., Yang H.H., Main H., Ferri G., Petek L.M., Poellinger L.,
RA   Miller D.G., Gabellini D., Schmidt U.;
RT   "A human pluripotent stem cell model of facioscapulohumeral muscular
RT   dystrophy-affected skeletal muscles.";
RL   Stem Cells Transl. Med. 5:1145-1161(2016).
//
RX   PubMed=27346028; DOI=10.1016/j.scr.2015.11.008;
RA   Dumevska B., Chami O., McKernan R., Goel D., Schmidt U.;
RT   "Derivation of Genea015 human embryonic stem cell line.";
RL   Stem Cell Res. 16:534-536(2016).
//
RX   PubMed=28445466; DOI=10.1038/nature22312; PMCID=PMC5427175;
RA   Merkle F.T., Ghosh S., Kamitaki N., Mitchell J., Avior Y., Mello C.,
RA   Kashin S., Mekhoubad S., Ilic D., Charlton M., Saphier G.,
RA   Handsaker R.E., Genovese G., Bar S., Benvenisty N., McCarroll S.A.,
RA   Eggan K.C.;
RT   "Human pluripotent stem cells recurrently acquire and expand dominant
RT   negative p53 mutations.";
RL   Nature 545:229-233(2017).
//