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Cellosaurus HPSI0216i-feht_1 (CVCL_LF21)

[Text version]
Cell line name HPSI0216i-feht_1
Synonyms WTSIi576-A
Accession CVCL_LF21
Resource Identification Initiative To cite this cell line use: HPSI0216i-feht_1 (RRID:CVCL_LF21)
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 Usher syndrome (NCIt: C85217)
Usher syndrome (ORDO: Orphanet_886)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 30-34Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650630
Cell line databases/resources HipSci; HPSI0216i-feht_1
hPSCreg; WTSIi576-A
Biological sample resources BioSamples; SAMEA4453879
Encyclopedic resources Wikidata; Q54890580
Entry history
Entry creation22-Aug-2017
Last entry update29-Jun-2023
Version number10