General

Cell Line
hPSCreg name	NYSCFi008-A-1
Cite as: When citing this cell line, please use the hPSCreg name (see Naming Tool ) and the corresponding Research Resource ID (RRID).	NYSCFi008-A-1
Alternative name(s)	BR0010-01-MCS-421-EDIT0062B
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	8th December 2025
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Provider
Generator	New York Stem Cell Foundation Research Institute (NYSCF)
External Databases
BioSamples	SAMEA120590165
General Information
* Is the cell line readily obtainable for third parties?	Yes Research use: allowed Clinical use: not allowed Commercial use: not allowed
Subclone of	NYSCFi008-A

Donor Information

General Donor Information
Sex	male
Phenotype and Disease related information (Donor)
Diseases	A disease was diagnosed. Ogden Syndrome The donor is a carrier of a disease-associated mutation and affected. Synonyms OGDNS Ogden Syndrome
External Databases (Donor)
BioSamples	SAMEA120590167

Ethics

Also have a look at the ethics information for the parental line NYSCFi008-A .

For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?

hIPSC Derivation

General
The source cell information can be found in the parental cell line NYSCFi008-A.
Reprogramming method
Vector free reprogramming
Other
Derived under xeno-free conditions	Unknown
Derived under GMP?	Unknown
Available as clinical grade?	Unknown

Culture Conditions

Characterisation

No characterisation data could be found for this subclone. Please open parental cell line NYSCFi008-A .

Genotyping

Karyotyping (Cell Line)

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications

Ogden Syndrome Synonyms OGDNS Ogden Syndrome Genetic modifications NAA10 (target) Type of modification Isogenic modification Free text Confirmed Mutation in parental as well as correction/changes in isogenic lines using RT-PCR How has the target locus been modified? Repaired