Cellosaurus cell line MiPSC5-T3 (CVCL

Cross-references
Cell line name	MiPSC5-T3
Accession	CVCL_A4RG
Resource Identification Initiative	To cite this cell line use: MiPSC5-T3 (RRID:CVCL_A4RG)
Comments	Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:7490; MT-TL1; Simple_corrected; m.3243A>G; ClinVar=VCV000009589; Zygosity=Heteroplasmic; Note=By TALEN (PubMed=29318513).
Disease	MELAS syndrome (NCIt: C84885) MELAS (ORDO: Orphanet_550)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy	Parent: CVCL_A4RE (MiPSC5)
Sex of cell	Male
Age at sampling	Age unspecified
Category	Induced pluripotent stem cell
Publications	PubMed=29318513; DOI=10.1007/s13238-017-0499-y; PMCID=PMC5829275 Yang Y., Wu H., Kang X.-J., Liang Y.-H., Lan T., Li T.-J., Tan T., Peng J.-Y., Zhang Q.-J., An G., Liu Y.-L., Yu Q., Ma Z.-L., Lian Y., Soh B.S., Chen Q.-F., Liu P., Chen Y.-Y., Sun X.-F., Li R., Zhen X.-M., Liu P., Yu Y., Li X.-P., Fan Y. Targeted elimination of mutant mitochondrial DNA in MELAS-iPSCs by mitoTALENs. Protein Cell 9:283-297(2018)
Cell line databases/resources	SKIP; SKIP002970
Encyclopedic resources	Wikidata; Q105510149
Entry history
Entry creation	12-Jan-2021
Last entry update	19-Dec-2024
Version number	6