| Cell line name | HPSI0216i-rihx_4 |
|---|---|
| Synonyms | WTSIi568-A |
| Accession | CVCL_IX74 |
| Resource Identification Initiative | To cite this cell line use: HPSI0216i-rihx_4 (RRID:CVCL_IX74) |
| Comments | From: University College London; London; United Kingdom. From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom. Population: Caucasian. Omics: Deep exome analysis. Omics: Transcriptome analysis by RNAseq. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Hereditary cerebellar ataxia (NCIt: C140268) Rare hereditary ataxia (ORDO: Orphanet_183518) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 30-34Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650545 |
| Cell line databases/resources | HipSci; HPSI0216i-rihx_4
hPSCreg; WTSIi568-A |
| Biological sample resources | BioSamples; SAMEA4447136 |
| Encyclopedic resources | Wikidata; Q54890586 |
| Entry history | |
| Entry creation | 15-May-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 12 |