ID   RG-158
AC   CVCL_B582
SY   SI-158; hESC 158; RGIe066-A
DR   hPSCreg; RGIe066-A
DR   ISCR; 381
DR   SKIP; SKIP002165
DR   Wikidata; Q54949907
RX   PubMed=15705304;
CC   From: Reproductive Genetics Institute; Chicago; USA.
CC   Sequence variation: Mutation; HGNC; 4827; HBB; Simple; c.93-21G>A (IVS1,G>A,+110); ClinVar=VCV000015454; Zygosity=Heterozygous (PubMed=15705304).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 29-06-23; Version: 13
//
RX   PubMed=15705304; DOI=10.1016/S1472-6483(10)60810-3;
RA   Verlinsky Y., Strelchenko N., Kukharenko V., Rechitsky S.,
RA   Verlinsky O., Galat V., Kuliev A.;
RT   "Human embryonic stem cell lines with genetic disorders.";
RL   Reprod. BioMed. Online 10:105-110(2005).
//