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Cellosaurus IOCVi002-A (CVCL_F0SZ)

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Cell line name IOCVi002-A
Synonyms IOCV-FOXE3
Accession CVCL_F0SZ
Resource Identification Initiative To cite this cell line use: IOCVi002-A (RRID:CVCL_F0SZ)
Comments From: Institute of Ophthalmology Conde de Valenciana; Mexico City; Mexico.
Population: Hispanic.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:3808; FOXE3; Simple; p.Tyr98His (c.292T>C); Zygosity=Homozygous (PubMed=40850233).
Disease Anterior segment dysgenesis 2 (NCIt: C222344)
Congenital primary aphakia (ORDO: Orphanet_83461)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 10Y
Category Induced pluripotent stem cell
Publications

PubMed=40850233; DOI=10.1016/j.scr.2025.103816
Jessica Nava, Guillermo Galvez-Romero, German Atzin Mora-Roldan, Oscar Javier Parada-Parra, Arturo Hernandez-Cruz, Juan Carlos Zenteno;
Generation of the induced pluripotent stem cell line IOCVi002-A from a patient with the FOXE3-related sclerocornea-aphakia malformation.
Stem Cell Res. 88:103816-103816(2025)

Cross-references
Cell line databases/resources hPSCreg; IOCVi002-A
Biological sample resources BioSamples; SAMEA115935038
Entry history
Entry creation27-Nov-2025
Last entry update27-Nov-2025
Version number1