ID   CREM005i-SS2-1GAG
AC   CVCL_YY12
SY   SCD iPSC SS.2-1-GAG; SS2-1GAG
DR   SKIP; SKIP003064
DR   WiCell; crem005i-ss2-1gag
DR   Wikidata; Q98125692
RX   PubMed=28111279;
WW   https://stemcellbank.bu.edu/Catalog/Item/Details/599
CC   Part of: Next Generation Genetic Association studies (Next Gen) program cell lines.
CC   From: Boston University School of Medicine; Boston; USA.
CC   Population: African American.
CC   Sequence variation: Mutation; HGNC; 4827; HBB; Simple_corrected; p.Glu7Val (c.20A>T) (E6V); ClinVar=VCV000015333; Zygosity=Homozygous; Note=By CRISPR/Cas9 (PubMed=28111279).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C34383; Sickle cell disease
DI   ORDO; Orphanet_232; Sickle cell anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_JW27 ! CREM004i-SS2-1
SX   Female
AG   32Y
CA   Induced pluripotent stem cell
DT   Created: 02-07-20; Last updated: 30-01-24; Version: 8
//
RX   PubMed=28111279; DOI=10.1016/j.stemcr.2016.12.017;
RA   Park S., Gianotti-Sommer A., Molina-Estevez F.J., Vanuytsel K.,
RA   Skvir N., Leung A., Rozelle S.S., Shaikho E.M., Weir I., Jiang Z.-H.,
RA   Luo H.-Y., Chui D.H.K., Figueiredo M.S., Alsultan A., Al-Ali A.,
RA   Sebastiani P., Steinberg M.H., Mostoslavsky G., Murphy G.J.;
RT   "A comprehensive, ethnically diverse library of sickle cell
RT   disease-specific induced pluripotent stem cells.";
RL   Stem Cell Reports 8:1076-1085(2017).
//