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Cellosaurus HPSI0816i-neow_7 (CVCL_LF18)

[Text version]
Cell line name HPSI0816i-neow_7
Synonyms WTSIi611-B; WTSIi631-A
Accession CVCL_LF18
Resource Identification Initiative To cite this cell line use: HPSI0816i-neow_7 (RRID:CVCL_LF18)
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 Alport syndrome (NCIt: C34842)
Alport syndrome (ORDO: Orphanet_63)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LF17 ! HPSI0816i-neow_5
Sex of cell Male
Age at sampling 55-59Y
Category Induced pluripotent stem cell
Cell line collections (Providers) ECACC; 77650706
Cell line databases/resources HipSci; HPSI0816i-neow_7
hPSCreg; WTSIi611-B
Biological sample resources BioSamples; SAMEA104011453
Encyclopedic resources Wikidata; Q54891433
Entry history
Entry creation22-Aug-2017
Last entry update29-Jun-2023
Version number10