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Cellosaurus HPSI0516i-yist_1 (CVCL_LF15)

[Text version]
Cell line name HPSI0516i-yist_1
Synonyms WTSIi623-B; WTSIi639-A
Accession CVCL_LF15
Resource Identification Initiative To cite this cell line use: HPSI0516i-yist_1 (RRID:CVCL_LF15)
Comments From: University College London; London; United Kingdom.
From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
Population: Caucasian and Chinese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 2206; COL4A4; Simple; p.Pro1096Ser (c.3286C>T); Zygosity=Heterozygous (from autologous cell line HPSI0516i-yist_3).
  • Mutation; HGNC; 2207; COL4A5; Simple; p.Gly1232Asp (c.3695G>A); Zygosity=Hemizygous (from autologous cell line HPSI0516i-yist_3).
Disease Alport syndrome (NCIt: C34842)
Alport syndrome (ORDO: Orphanet_63)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LF16 ! HPSI0516i-yist_3
Sex of cell Male
Age at sampling 22Y
Category Induced pluripotent stem cell
Cell line collections (Providers) ECACC; 77650675
Cell line databases/resources HipSci; HPSI0516i-yist_1
hPSCreg; WTSIi623-B
Biological sample resources BioSamples; SAMEA4675918
Encyclopedic resources Wikidata; Q54890983
Entry history
Entry creation22-Aug-2017
Last entry update29-Jun-2023
Version number11