Cellosaurus HPSI0216i-puxp_1 (CVCL_IX67)
| Cell line name | HPSI0216i-puxp_1 |
|---|---|
| Synonyms | WTSIi449-A |
| Accession | CVCL_IX67 |
| Resource Identification Initiative | To cite this cell line use: HPSI0216i-puxp_1 (RRID:CVCL_IX67) |
| 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 | Congenital hyperinsulinism (NCIt: C131425) Familial hyperinsulinism (ORDO: Orphanet_276525) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 0-4Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650511 |
| Cell line databases/resources | HipSci; HPSI0216i-puxp_1
hPSCreg; WTSIi449-A |
| Biological sample resources | BioSamples; SAMEA4448207 |
| Encyclopedic resources | Wikidata; Q54890585 |
| Entry history | |
| Entry creation | 15-May-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 11 |