Cellosaurus cell line SBG1-iPSC (CVCL

Cross-references
Cell line name	SBG1-iPSC
Synonyms	SBG1-(8993 T > G)-hiPSC
Accession	CVCL_C6UF
Resource Identification Initiative	To cite this cell line use: SBG1-iPSC (RRID:CVCL_C6UF)
Comments	Cell type: Fibroblast; CL=CL_0000057.
Sequence variations	Mutation; HGNC; HGNC:7414; MT-ATP6; Simple; p.Leu156Arg (m.8993T>G); ClinVar=VCV000009641; Zygosity=Heteroplasmic (PubMed=34662843).
Disease	Leigh disease (NCIt: C84814) Leigh syndrome (ORDO: Orphanet_506)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy	Parent: CVCL_C6UE (SBG1)
Category	Induced pluripotent stem cell
Publications	PubMed=34662843; DOI=10.1016/j.scr.2021.102572; PMCID=PMC10332439 Meshrkey F., Cabrera Ayuso A.R., Rao R.R., Iyer S. Quantitative analysis of mitochondrial morphologies in human induced pluripotent stem cells for Leigh syndrome. Stem Cell Res. 57:102572-102572(2021)
Encyclopedic resources	Wikidata; Q117704835
Entry history
Entry creation	21-Mar-2023
Last entry update	19-Dec-2024
Version number	3