| Cell line name | HPSI0616i-biln_2 |
|---|---|
| Synonyms | WTSIi498-A |
| Accession | CVCL_LM13 |
| Resource Identification Initiative | To cite this cell line use: HPSI0616i-biln_2 (RRID:CVCL_LM13) |
| 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 spastic paraplegia (NCIt: C140267) Hereditary spastic paraplegia (ORDO: Orphanet_685) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_LM12 ! HPSI0616i-biln_1 |
| Sex of cell | Female |
| Age at sampling | 45-49Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650632 |
| Cell line databases/resources | HipSci; HPSI0616i-biln_2
hPSCreg; WTSIi498-A |
| Biological sample resources | BioSamples; SAMEA103884671 |
| Encyclopedic resources | Wikidata; Q54891189 |
| Entry history | |
| Entry creation | 15-Nov-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 10 |