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Cellosaurus HPSI0916i-vorn_5 (CVCL_LM52)

[Text version]
Cell line name HPSI0916i-vorn_5
Synonyms WTSIi621-A
Accession CVCL_LM52
Resource Identification Initiative To cite this cell line use: HPSI0916i-vorn_5 (RRID:CVCL_LM52)
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 Hereditary cerebellar ataxia (NCIt: C140268)
Rare hereditary ataxia (ORDO: Orphanet_183518)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LM51 ! HPSI0916i-vorn_2
Sex of cell Female
Age at sampling 70-74Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650740
Cell line databases/resources HipSci; HPSI0916i-vorn_5
hPSCreg; WTSIi621-A
Biological sample resources BioSamples; SAMEA104012397
Encyclopedic resources Wikidata; Q54891534
Entry history
Entry creation15-Nov-2017
Last entry update29-Jun-2023
Version number11