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Cellosaurus HPSI0616i-biln_2 (CVCL_LM13)

[Text version]
Cell line name HPSI0616i-biln_2
Synonyms WTSIi498-A
Accession CVCL_LM13
Resource Identification Initiative To cite this cell line use: HPSI0616i-biln_2 (RRID:CVCL_LM13)
Comments From: University College London; London; United Kingdom.
From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
Population: Caucasian.
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_LM12 ! HPSI0616i-biln_1
Sex of cell Female
Age at sampling 45-49Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650632
Cell line databases/resources HipSci; HPSI0616i-biln_2
hPSCreg; WTSIi498-A
Biological sample resources BioSamples; SAMEA103884671
Encyclopedic resources Wikidata; Q54891189
Entry history
Entry creation15-Nov-2017
Last entry update29-Jun-2023
Version number10