ID   HIHCNi004-A-1
AC   CVCL_UL60
SY   iPSC-STUB1_KO
DR   hPSCreg; HIHCNi004-A-1
DR   Wikidata; Q94208310
RX   PubMed=30605842;
CC   From: Hertie Institute for Clinical Brain Research and German Center for Neurodegenerative Diseases, University of Tubingen; Tubingen; Germany.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:11427; STUB1.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C150250; Spinocerebellar ataxia type 16
DI   ORDO; Orphanet_412057; Autosomal recessive cerebellar ataxia due to STUB1 deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_UL59 ! HIHCNi004-A
SX   Female
AG   37Y
CA   Induced pluripotent stem cell
DT   Created: 25-02-19; Last updated: 19-12-24; Version: 7
//
RX   PubMed=30605842; DOI=10.1016/j.scr.2018.101378;
RA   Schuster, Stefanie
RA   Saravanakumar, Srinethe
RA   Schols, Ludger
RA   Hauser, Stefan
RT   "Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC
RT   line for the STUB1 locus.";
RL   Stem Cell Res. 34:101378-101378(2019).
//