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Cellosaurus HPSI0616i-kayf_6 (CVCL_LM22)

[Text version]
Cell line name HPSI0616i-kayf_6
Synonyms WTSIi531-B; WTSIi559-A
Accession CVCL_LM22
Resource Identification Initiative To cite this cell line use: HPSI0616i-kayf_6 (RRID:CVCL_LM22)
Comments From: University College London; London; United Kingdom.
From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
Omics: Deep exome 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 spastic paraplegia (NCIt: C140267)
Hereditary spastic paraplegia (ORDO: Orphanet_685)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LM21 ! HPSI0616i-kayf_5
Sex of cell Male
Age at sampling 25-29Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650635
Cell line databases/resources HipSci; HPSI0616i-kayf_6
hPSCreg; WTSIi531-B
Biological sample resources BioSamples; SAMEA103887530
Encyclopedic resources Wikidata; Q54891207
Entry history
Entry creation15-Nov-2017
Last entry update29-Jun-2023
Version number9