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Cellosaurus ESi126-A (CVCL_E3UX)

[Text version]
Cell line name ESi126-A
Synonyms [RP]-FiPSC1-Ep5F-10
Accession CVCL_E3UX
Resource Identification Initiative To cite this cell line use: ESi126-A (RRID:CVCL_E3UX)
Comments Part of: Spanish Stem Cell Bank (Banco Nacional de Lineas Celulares) collection.
Population: Caucasian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Retinitis pigmentosa (NCIt: C85045)
Retinitis pigmentosa (ORDO: Orphanet_791)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 54Y
Category Induced pluripotent stem cell
STR profile Source(s): BNLC

Markers:
AmelogeninX
CSF1PO10,14
D5S81812,13
D7S8209
D13S31712,14
D16S53912,13
D21S1128,29
TH016,9
TPOX8,11
vWA16,18

Run an STR similarity search on this cell line
Web pages https://www.isciii.es/documents/20119/7711a13a-540e-9dc1-587f-9b4509d24896
https://www.isciii.es/documents/20119/abfec2ea-c819-4b40-7128-944213e41556
Publications

PubMed=38956727; DOI=10.1186/s13287-024-03804-2; PMCID=PMC11218195
Puertas-Neyra K.L., Coco-Martin R.M., Hernandez-Rodriguez L.A., Gobelli D.J., Garcia-Ferrer Y., Palma-Vecino R., Telleria J.J., Simarro-Grande M., de la Fuente M.A., Fernandez-Bueno I.
Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes.
Stem Cell Res. Ther. 15:192.1-192.24(2024)

Cross-references
Cell line databases/resources hPSCreg; ESi126-A
Entry history
Entry creation19-Dec-2024
Last entry update19-Dec-2024
Version number1