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Cellosaurus HPSI0316i-beqm_9 (CVCL_WJ61)

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Cell line name HPSI0316i-beqm_9
Accession CVCL_WJ61
Resource Identification Initiative To cite this cell line use: HPSI0316i-beqm_9 (RRID:CVCL_WJ61)
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_WJ60 ! HPSI0316i-beqm_12
Sex of cell Female
Age at sampling 60-64Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650844
Cell line databases/resources HipSci; HPSI0316i-beqm_9
Biological sample resources BioSamples; SAMEA104242350
Encyclopedic resources Wikidata; Q94223236
Entry history
Entry creation24-May-2019
Last entry update29-Jun-2023
Version number8