| Cell line name | HPSI0316i-muwv_3 |
|---|---|
| Synonyms | WTSIi448-A |
| Accession | CVCL_IX77 |
| Resource Identification Initiative | To cite this cell line use: HPSI0316i-muwv_3 (RRID:CVCL_IX77) |
| Comments | From: University College London; London; United Kingdom. From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom. Population: Asian. 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) |
| Originate from same individual | CVCL_IX78 ! HPSI0316i-muwv_6 |
| Sex of cell | Male |
| Age at sampling | 40-44Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650502 |
| Cell line databases/resources | HipSci; HPSI0316i-muwv_3
hPSCreg; WTSIi448-A |
| Biological sample resources | BioSamples; SAMEA4448534 |
| Encyclopedic resources | Wikidata; Q54890639 |
| Entry history | |
| Entry creation | 15-May-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 12 |