ID   WAe001-A-28
AC   CVCL_XD79
SY   MAPe002-A-28; H1_MECP2_KO4; KO4
DR   hPSCreg; WAe001-A-28
DR   Wikidata; Q98134701
RX   PubMed=31450191;
CC   From: Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research; Singapore; Singapore.
CC   Sequence variation: Mutation; HGNC; 6990; MECP2; Simple_edited; p.Gln110fs; Zygosity=Hemizygous; Note=By CRISPR/Cas9 (PubMed=31450191).
DI   NCIt; C75488; Rett syndrome
DI   ORDO; Orphanet_778; Rett syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
HI   CVCL_9771 ! WA01
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-09-19; Last updated: 20-05-21; Version: 5
//
RX   PubMed=31450191; DOI=10.1016/j.scr.2019.101533;
RA   Zeng R., Sidik H., Robinson K.S., Zhong F.L., Reversade B.,
RA   Pouladi M.A.;
RT   "Generation of four H1 hESC sublines carrying a hemizygous
RT   knock-out/mutant MECP2.";
RL   Stem Cell Res. 40:101533-101533(2019).
//