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Cellosaurus HIHCNi004-A-1 (CVCL_UL60)

[Text version]
Cell line name HIHCNi004-A-1
Synonyms iPSC-STUB1_KO
Accession CVCL_UL60
Resource Identification Initiative To cite this cell line use: HIHCNi004-A-1 (RRID:CVCL_UL60)
Comments From: Hertie Institute for Clinical Brain Research and German Center for Neurodegenerative Diseases, University of Tubingen; Tubingen; Germany.
Knockout cell: Method=CRISPR/Cas9; HGNC; 11427; STUB1.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Spinocerebellar ataxia type 16 (NCIt: C150250)
Autosomal recessive cerebellar ataxia due to STUB1 deficiency (ORDO: Orphanet_412057)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_UL59 (HIHCNi004-A)
Sex of cell Female
Age at sampling 37Y
Category Induced pluripotent stem cell

PubMed=30605842; DOI=10.1016/j.scr.2018.101378
Schuster S., Saravanakumar S., Schols L., Hauser S.
Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for the STUB1 locus.
Stem Cell Res. 34:101378-101378(2019)

Cell line databases/resources hPSCreg; HIHCNi004-A-1
Encyclopedic resources Wikidata; Q94208310
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number6