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Cellosaurus HPSI0916i-helh_1 (CVCL_LM42)

[Text version]

Cell line name HPSI0916i-helh_1
Synonyms WTSIi717-B; WTSIi719-A
Accession CVCL_LM42
Resource Identification Initiative To cite this cell line use: HPSI0916i-helh_1 (RRID:CVCL_LM42)
Comments From: University College London; London; UK.
From: Wellcome Trust Sanger Institute; Hinxton; UK.
Derived from sampling site: Skin.
Disease Hereditary cerebellar ataxia (NCIt: C140264)
Rare hereditary ataxia (ORDO: Orphanet_183518)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LM43 ! HPSI0916i-helh_6
Sex of cell Male
Age at sampling 45-49Y
Category Induced pluripotent stem cell
Cell line collections ECACC; 77650737
Cell line databases/resources HipSci; HPSI0916i-helh_1
hPSCreg; WTSIi717-B
Biological sample resources BioSamples; SAMEA104012323
Other Wikidata; Q54891524
Entry history
Entry creation15-Nov-2017
Last entry updated12-Mar-2020
Version number5