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Cellosaurus FRIMOi005-A (CVCL_WS11)

[Text version]
Cell line name FRIMOi005-A
Synonyms RP3_FiPSC4F11; RP3_FiPS4F11
Accession CVCL_WS11
Resource Identification Initiative To cite this cell line use: FRIMOi005-A (RRID:CVCL_WS11)
Comments Part of: Spanish Stem Cell Bank (Banco Nacional de Lineas Celulares) collection.
From: Fundacio de Recerca de l'Institut de Microcirurgia Ocular; Barcelona; Spain.
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 35Y
Category Induced pluripotent stem cell
STR profile Source(s): BNLC

Markers:
AmelogeninX
CSF1PO10,12
D2S133817,19
D3S135818
D5S81812,13
D7S82012,14
D8S117912,14
D13S31711,13
D16S5398,12
D18S5113,18
D19S43313,15
D21S1128,31.2
FGA21
TH017,9.3
TPOX8
vWA18

Run an STR similarity search on this cell line
Web pages Provider; BNLC; -; https://www.isciii.es/documents/20119/880364/Solicitud%2520deposito_RP3_FiPSC4F11_V2.pdf
Provider; BNLC; -; https://www.isciii.es/documents/20119/880377/ANEXOS%2520RP3_FiPS4F1.pdf
Publications

PubMed=31146251; DOI=10.1016/j.scr.2019.101468
Domingo-Prim J., Riera M., Bures-Jelstrup A., Corcostegui B., Pomares E.
Establishment of an induced pluripotent stem cell line (FRIMOi005-A) derived from a retinitis pigmentosa patient carrying a dominant mutation in RHO gene.
Stem Cell Res. 38:101468-101468(2019)

Cross-references
Cell line databases/resources hPSCreg; FRIMOi005-A
Biological sample resources BioSamples; SAMEA7352797
Encyclopedic resources Wikidata; Q93556550
Entry history
Entry creation05-Jul-2019
Last entry update10-Apr-2025
Version number12