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Cellosaurus HPSI0816i-daah_1 (CVCL_WJ79)

[Text version]
Cell line name HPSI0816i-daah_1
Accession CVCL_WJ79
Resource Identification Initiative To cite this cell line use: HPSI0816i-daah_1 (RRID:CVCL_WJ79)
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_WJ80 ! HPSI0816i-daah_6
Sex of cell Female
Age at sampling 50-54Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650819
Cell line databases/resources HipSci; HPSI0816i-daah_1
Biological sample resources BioSamples; SAMEA103887431
Encyclopedic resources Wikidata; Q94233027
Entry history
Entry creation24-May-2019
Last entry update29-Jun-2023
Version number8