ID   HIHCNi008-A-4
AC   CVCL_D5HA
SY   iPSC-REEP1_hetKO
DR   hPSCreg; HIHCNi008-A-4
DR   Wikidata; Q127381755
RX   PubMed=38479332;
CC   From: Hertie Institute for Clinical Brain Research and German Center for Neurodegenerative Diseases, University of Tubingen; Tubingen; Germany.
CC   Population: Caucasian.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 25786; REEP1 (Note=1 of 2 alleles).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C189921; Spastic paraplegia 31
DI   ORDO; Orphanet_101011; Autosomal dominant spastic paraplegia type 31
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_B7BQ ! HIHCNi006-A
SX   Male
AG   47Y
CA   Induced pluripotent stem cell
DT   Created: 02-05-24; Last updated: 10-09-24; Version: 2
//
RX   PubMed=38479332; DOI=10.1016/j.scr.2024.103378;
RA   Korneck M., Leonhardt A., Schols L., Hauser S.;
RT   "Generation of homozygous and heterozygous REEP1 knockout induced
RT   pluripotent stem cell lines by CRISPR/Cas9 gene editing.";
RL   Stem Cell Res. 77:103378-103378(2024).
//