Cellosaurus cell line SBG9 (CVCL

Cross-references
Cell line name	SBG9
Accession	CVCL_C6US
Resource Identification Initiative	To cite this cell line use: SBG9 (RRID:CVCL_C6US)
Comments	Cell type: Fibroblast; CL=CL_0000057.
Sequence variations	Mutation; HGNC; HGNC:Group_1972; MT-@; Unexplicit; m.7342_9916del; Zygosity=Heteroplasmic (PubMed=34200828).
Disease	Kearns-Sayre syndrome (NCIt: C84798) Pearson syndrome (NCIt: C115326) Kearns-Sayre syndrome (ORDO: Orphanet_480) Pearson syndrome (ORDO: Orphanet_699)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category	Finite cell line
Publications	PubMed=34200828; DOI=10.3390/ijms22126263; PMCID=PMC8230542 Bakare A.B., Daniel J., Stabach J., Rojas A., Bell A., Henry B., Iyer S. Quantifying mitochondrial dynamics in patient fibroblasts with multiple developmental defects and mitochondrial disorders. Int. J. Mol. Sci. 22:6263.1-6263.26(2021)
Encyclopedic resources	Wikidata; Q117704848
Entry history
Entry creation	21-Mar-2023
Last entry update	19-Dec-2024
Version number	3