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Cellosaurus KOLF2.1J CHCHD10 R15L REV/WT (CVCL_E7JU)

[Text version]
Cell line name KOLF2.1J CHCHD10 R15L REV/WT
Synonyms JIPSC003012
Accession CVCL_E7JU
Resource Identification Initiative To cite this cell line use: KOLF2.1J CHCHD10 R15L REV/WT (RRID:CVCL_E7JU)
Comments From: The Jackson Laboratory; Bar Harbor; USA.
Population: Caucasian; British.
Characteristics: Control cell line which is a CRISPR/Cas9 engineered revertant of the heterozygously edited CHCHD10 p.Arg15Leu (c.44_45delinsTT) cell line (JAX=JIPSC003012).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:18037; ARID2; Simple_corrected; p.Pro197Hisfs*12 (c.590_608delCTAAAATCATCACTTTACT); Zygosity=Heterozygous; Note=By CRISPR/Cas9 (from parent cell line).
  • Mutation; HGNC; HGNC:2201; COL3A1; Simple; c.3526-1G>A; Zygosity=Heterozygous; Note=Splice acceptor mutation (from parent cell line).
  • Mutation; HGNC; HGNC:2201; COL3A1; Simple; p.Gly1176Ser (c.3526G>A); Zygosity=Heterozygous (from parent cell line).
Disease Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 (NCIt: C214862)
Frontotemporal dementia with motor neuron disease (ORDO: Orphanet_275872)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_E7JW (KOLF2.1J CHCHD10 R15L SNV/WT)
Sex of cell Male
Age at sampling 55-59Y
Category Induced pluripotent stem cell
Web pages Provider; JAX; JIPSC003012; https://www.jax.org/jax-mice-and-services/ipsc/cells-collection/JIPSC003012
Entry history
Entry creation10-Apr-2025
Last entry update10-Apr-2025
Version number1