ID   KCL013
AC   CVCL_A247
SY   KCL-013; HD-4; HD4; KCL013_HD4; KCLe010-A
DR   hPSCreg; KCLe010-A
DR   ISCR; 1868
DR   SKIP; SKIP002358
DR   Wikidata; Q54899661
RX   PubMed=27345987;
CC   From: King's College London; London; United Kingdom.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-13-0214.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC10-33.
CC   Sequence variation: Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[42] (c.52CAG(42)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (PubMed=27345987).
CC   Miscellaneous: Sibling to KCL012 (CVCL_A246).
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 16-12-21; Version: 20
RX   PubMed=27345987; DOI=10.1016/j.scr.2016.01.011;
RA   Jacquet L., Hewitson H., Wood V., Kadeva N., Cornwell G.,
RA   Codognotto S., Stephenson E., Ilic D.;
RT   "Generation of KCL013 research grade human embryonic stem cell line
RT   carrying a mutation in the HTT gene.";
RL   Stem Cell Res. 16:293-295(2016).