AC   CVCL_M240
SY   Genea089; SIVF089; GENEAe013-A
DR   BioSamples; SAMEA104012530
DR   hPSCreg; GENEAe013-A
DR   ISCR; 2047
DR   NIHhESC; NIHhESC-14-0247
DR   Wikidata; Q54835661
RX   PubMed=25316320;
RX   PubMed=27346008;
CC   From: Genea Biocells, Ltd; Sydney; Australia.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-14-0247.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-47.
CC   Sequence variation: Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[41] (c.52CAG(41)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Unspecified (Genea).
CC   Donor information: Embryo is sibling to those giving rise to GENEA090 (Cellosaurus=CVCL_M241) and GENEA091 (Cellosaurus=CVCL_M242).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): PubMed=27346008
ST   Amelogenin: X
ST   CSF1PO: 11,15
ST   D13S317: 8,11
ST   D16S539: 12
ST   D18S51: 15
ST   D19S433: 13,14
ST   D21S11: 29,31
ST   D2S1338: 17,19
ST   D3S1358: 17,18
ST   D5S818: 10,12
ST   D7S820: 10
ST   D8S1179: 14,15
ST   FGA: 23,24
ST   TH01: 6,9
ST   TPOX: 8,11
ST   vWA: 18,19
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 05-11-13; Last updated: 29-06-23; Version: 18
RX   PubMed=25316320; DOI=10.1021/pr500649m;
RA   McQuade L.R., Balachandran A., Scott H.A., Khaira S., Baker M.S.,
RA   Schmidt U.;
RT   "Proteomics of Huntington's disease-affected human embryonic stem
RT   cells reveals an evolving pathology involving mitochondrial
RT   dysfunction and metabolic disturbances.";
RL   J. Proteome Res. 13:5648-5659(2014).
RX   PubMed=27346008; DOI=10.1016/j.scr.2016.02.013;
RA   Dumevska B., McKernan R., Hu J., Schmidt U.;
RT   "Derivation of Huntington disease affected Genea089 human embryonic
RT   stem cell line.";
RL   Stem Cell Res. 16:434-436(2016).