Cellosaurus cell line MDCi009-A (CVCL

Cross-references
Cell line name	MDCi009-A
Synonyms	8993-C11; iPSC_C11
Accession	CVCL_C0HF
Resource Identification Initiative	To cite this cell line use: MDCi009-A (RRID:CVCL_C0HF)
Comments	From: Max Delbruck Center Berlin Buch; Berlin; Germany. Population: Caucasian. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:7414; MT-ATP6; Simple; p.Leu156Arg (m.8993T>G); ClinVar=VCV000009641; Zygosity=Homoplasmic (PubMed=35279592).
Disease	Leigh disease (NCIt: C84814) Leigh syndrome (ORDO: Orphanet_506)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Female
Age at sampling	2Y
Category	Induced pluripotent stem cell
Publications	PubMed=35279592; DOI=10.1016/j.scr.2022.102742 Lorenz C., Zink A., Henke M.-T., Staege S., Mlody B., Bunning M., Wanker E.E., Diecke S., Schuelke M., Prigione A. Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6. Stem Cell Res. 61:102742-102742(2022)
Cell line databases/resources	hPSCreg; MDCi009-A
Biological sample resources	BioSamples; SAMEA12276589
Encyclopedic resources	Wikidata; Q112930102
Entry history
Entry creation	23-Jun-2022
Last entry update	19-Dec-2024
Version number	6