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Cellosaurus HPSI1013i-mijn_2 (CVCL_AH71)

[Text version]
Cell line name HPSI1013i-mijn_2
Synonyms WTSIi147-A
Accession CVCL_AH71
Resource Identification Initiative To cite this cell line use: HPSI1013i-mijn_2 (RRID:CVCL_AH71)
Comments From: University College London; London; United Kingdom.
From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
Population: Caucasian; British.
Omics: Deep exome analysis.
Omics: Deep proteome analysis.
Omics: DNA methylation analysis.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Bardet-Biedl syndrome (NCIt: C118632)
Bardet-Biedl syndrome (ORDO: Orphanet_110)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 35-39Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; WTSIi147-A
ECACC; 66540301 - Discontinued
ECACC; 77650266
Cell line databases/resources HipSci; HPSI1013i-mijn_2
hPSCreg; WTSIi147-A
SKIP; SKIP002800
Biological sample resources BioSamples; SAMEA2398395
Encyclopedic resources Wikidata; Q54891562
Entry history
Entry creation23-Feb-2016
Last entry update30-Jan-2024
Version number14