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Cellosaurus iPSC567-24 MUT (CVCL_C3GP)

[Text version]
Cell line name iPSC567-24 MUT
Synonyms 567.24 MUT; iPSC Patient567 RTT
Accession CVCL_C3GP
Resource Identification Initiative To cite this cell line use: iPSC567-24 MUT (RRID:CVCL_C3GP)
Comments Omics: Transcriptomics; RNAseq.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:6990; MECP2; Simple; p.Ter487Trp (c.1461A>G) (p.Ter499Trp, c.1497A>G); ClinVar=VCV000143490; Zygosity=Unspecified (from parent cell line).
Disease Rett syndrome (NCIt: C75488)
Rett syndrome (ORDO: Orphanet_778)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_4F46 (GM17567)
Sex of cell Female
Age at sampling 5Y
Category Induced pluripotent stem cell
Publications

PubMed=29742391; DOI=10.1016/j.stemcr.2018.04.001; PMCID=PMC5995366
Ohashi M., Korsakova E., Allen D., Lee P., Fu K., Vargas B.S., Cinkornpumin J., Salas C., Park J.C., Germanguz I., Langerman J., Chronis C., Kuoy E., Tran S., Xiao X.-S., Pellegrini M., Plath K., Lowry W.E.
Loss of MECP2 leads to activation of p53 and neuronal senescence.
Stem Cell Reports 10:1453-1463(2018)

Cross-references
Encyclopedic resources Wikidata; Q114311758
Gene expression databases GEO; GSM2866259
GEO; GSM2866261
Entry history
Entry creation22-Sep-2022
Last entry update10-Apr-2025
Version number6