ID   CENSOi053-A
AC   CVCL_WP62
SY   F245R2c2
DR   hPSCreg; CENSOi053-A
DR   Wikidata; Q93446823
WW   Provider; Axol; -; https://axolbio.com/shop/disease-models/huntingtons-disease-censoi053-a/
CC   From: Axol Bioscience, Ltd (Censo Biotechnologies); Cambridge; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[38] (c.52CAG(38)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (Axol).
CC   Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   64Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 10-04-25; Version: 6
//