INMi004-A

Registration Summary:

A P E C

CRX-LCA-iPSC

The cell line is not submitted yet.

(only basic data is shown)

General

iPSC Line
hPSCreg name	INMi004-A
Cite as:	INMi004-A (RRID:CVCL_WR02)
Alternative name(s)	CRX-LCA-iPSC
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	8th March 2019
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Provider
Generator	Institute for Neurosciences of Montpellier (INM)
External iPSC Databases
Cellosaurus	CVCL_WR02
Wikidata	Q94318004
General iPSC Information
Publications	Erkilic N et al. Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis. Stem cell research. 2019 Jul;38:101476. Erkilic N et al. A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia. Cells. 2019 Sep 11;8(9). Diakatou M et al. Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3. International journal of molecular sciences. 2021 Mar 5;22(5). Bocquet Béatrice et al. TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa. JCI Insight. 2023-11-08. Liang Yuqin et al. Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases. Stem Cell Research & Therapy. 2023-11-27. Chen Yi et al. The occurrence and development of induced pluripotent stem cells. Frontiers in Genetics. 2024-04-18. Mamaeva D et al. Generation of a human iPSC line, INMi007-A, carrying compound heterozygous DCT variants associated with oculocutaneous albinism type 8. Stem cell research. 2025 Oct;88:103810.

iPSC Derivation

General