Cellosaurus HIHCNi004-A-1 (CVCL_UL60)
| 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; 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 |
| Publications | PubMed=30605842; DOI=10.1016/j.scr.2018.101378 |
| Cross-references | |
| Cell line databases/resources | hPSCreg; HIHCNi004-A-1 |
| Encyclopedic resources | Wikidata; Q94208310 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 19-Dec-2024 |
| Version number | 7 |