| Cell line name | HPSI0616i-giql_1 |
|---|---|
| Synonyms | WTSIi506-B; WTSIi577-A |
| Accession | CVCL_LL72 |
| Resource Identification Initiative | To cite this cell line use: HPSI0616i-giql_1 (RRID:CVCL_LL72) |
| Comments | From: Cambridge BioResource; Cambridge; 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 | Congenital bleeding disorder (NCIt: C103172) Rare hemorrhagic disorder (ORDO: Orphanet_248308) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_LL73 ! HPSI0616i-giql_5 |
| Sex of cell | Female |
| Age at sampling | 55-59Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650653 |
| Cell line databases/resources | HipSci; HPSI0616i-giql_1
hPSCreg; WTSIi506-B |
| Biological sample resources | BioSamples; SAMEA103884210 |
| Encyclopedic resources | Wikidata; Q54891198 |
| Entry history | |
| Entry creation | 15-Nov-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 9 |