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Cellosaurus HPSI0216i-vieg_3 (CVCL_IX75)

[Text version]
Cell line name HPSI0216i-vieg_3
Synonyms WTSIi472-B; WTSIi547-A
Accession CVCL_IX75
Resource Identification Initiative To cite this cell line use: HPSI0216i-vieg_3 (RRID:CVCL_IX75)
Comments From: University College London; London; United Kingdom.
From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
Population: Caucasian.
Omics: Deep exome analysis.
Omics: Deep proteome analysis.
Omics: Transcriptome analysis by RNAseq.
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_IX76 ! HPSI0216i-vieg_5
Sex of cell Male
Age at sampling 40-44Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650491
Cell line databases/resources HipSci; HPSI0216i-vieg_3
hPSCreg; WTSIi472-B
Biological sample resources BioSamples; SAMEA4453872
Encyclopedic resources Wikidata; Q54890588
Entry history
Entry creation15-May-2017
Last entry update29-Jun-2023
Version number12