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Cellosaurus ESi125-A (CVCL_E3UW)

[Text version]
Cell line name ESi125-A
Synonyms [CORD]-FiPSC1-Ep5F-2
Accession CVCL_E3UW
Resource Identification Initiative To cite this cell line use: ESi125-A (RRID:CVCL_E3UW)
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 Cone-rod dystrophy 12 (NCIt: C212886)
Cone rod dystrophy (ORDO: Orphanet_1872)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 47Y
Category Induced pluripotent stem cell
STR profile Source(s): BNLC

Markers:
AmelogeninX
CSF1PO11
D5S81811
D7S8208,9
D13S31712,13
D16S53912
D21S1128,30
TH019
TPOX8,10
vWA17,18

Run an STR similarity search on this cell line
Web pages https://www.isciii.es/documents/20119/44aefd67-c957-677d-6b56-01023cf0561b
https://www.isciii.es/documents/20119/5363bccf-f83a-f63a-3dfa-d034ed17f6a6
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; ESi125-A
Entry history
Entry creation19-Dec-2024
Last entry update19-Dec-2024
Version number1