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Cellosaurus HPSI0616i-eomr_5 (CVCL_LL69)

[Text version]
Cell line name HPSI0616i-eomr_5
Synonyms WTSIi534-A
Accession CVCL_LL69
Resource Identification Initiative To cite this cell line use: HPSI0616i-eomr_5 (RRID:CVCL_LL69)
Comments From: Cambridge BioResource; Cambridge; United Kingdom.
From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
Population: Caucasian; British.
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 Congenital bleeding disorder (NCIt: C103172)
Rare hemorrhagic disorder (ORDO: Orphanet_248308)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 55-59Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650652
Cell line databases/resources HipSci; HPSI0616i-eomr_5
hPSCreg; WTSIi534-A
Biological sample resources BioSamples; SAMEA103884568
Encyclopedic resources Wikidata; Q54891194
Entry history
Entry creation15-Nov-2017
Last entry update29-Jun-2023
Version number10