| Cell line name | HPSI0616i-kayf_6 |
|---|---|
| Synonyms | WTSIi531-B; WTSIi559-A |
| Accession | CVCL_LM22 |
| Resource Identification Initiative | To cite this cell line use: HPSI0616i-kayf_6 (RRID:CVCL_LM22) |
| Comments | From: University College London; London; United Kingdom. From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom. 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 spastic paraplegia (NCIt: C140267) Hereditary spastic paraplegia (ORDO: Orphanet_685) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_LM21 ! HPSI0616i-kayf_5 |
| Sex of cell | Male |
| Age at sampling | 25-29Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650635 |
| Cell line databases/resources | HipSci; HPSI0616i-kayf_6
hPSCreg; WTSIi531-B |
| Biological sample resources | BioSamples; SAMEA103887530 |
| Encyclopedic resources | Wikidata; Q54891207 |
| Entry history | |
| Entry creation | 15-Nov-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 9 |