Cellosaurus HPSI0916i-moyn_4 (CVCL_LM48)
Cell line name | HPSI0916i-moyn_4 |
---|---|
Synonyms | WTSIi657-A |
Accession | CVCL_LM48 |
Resource Identification Initiative | To cite this cell line use: HPSI0916i-moyn_4 (RRID:CVCL_LM48) |
Comments | From: University College London; London; United Kingdom. From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom. Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Disease | Genetic macular dystrophy (NCIt: C140264) Rare genetic macular disorder (ORDO: Orphanet_522574) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Originate from same individual | CVCL_LM47 ! HPSI0916i-moyn_1 |
Sex of cell | Male |
Age at sampling | 55-59Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | ECACC; 77650762 |
Cell line databases/resources | HipSci; HPSI0916i-moyn_4
hPSCreg; WTSIi657-A |
Biological sample resources | BioSamples; SAMEA104130574 |
Encyclopedic resources | Wikidata; Q54891530 |
Entry history | |
Entry creation | 15-Nov-2017 |
Last entry update | 29-Jun-2023 |
Version number | 11 |