Cellosaurus HPSI0216i-feht_1 (CVCL_LF21)
Cell line name | HPSI0216i-feht_1 |
---|---|
Synonyms | WTSIi576-A |
Accession | CVCL_LF21 |
Resource Identification Initiative | To cite this cell line use: HPSI0216i-feht_1 (RRID:CVCL_LF21) |
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 | Usher syndrome (NCIt: C85217) Usher syndrome (ORDO: Orphanet_886) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Sex of cell | Male |
Age at sampling | 30-34Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | ECACC; 77650630 |
Cell line databases/resources | HipSci; HPSI0216i-feht_1
hPSCreg; WTSIi576-A |
Biological sample resources | BioSamples; SAMEA4453879 |
Encyclopedic resources | Wikidata; Q54890580 |
Entry history | |
Entry creation | 22-Aug-2017 |
Last entry update | 29-Jun-2023 |
Version number | 10 |