Cellosaurus MCRIi035-B (CVCL_E6WS)
Cell line name | MCRIi035-B | ||
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Synonyms | MCRIi-UC-cl5; Patient 1-UC-cl5; MCRIi-TC160154-UC-cl5 | ||
Accession | CVCL_E6WS | ||
Resource Identification Initiative | To cite this cell line use: MCRIi035-B (RRID:CVCL_E6WS) | ||
Comments | From: Murdoch Children's Research Institute; Melbourne; Australia. Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | ||
Sequence variations |
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Disease | Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy (NCIt: C215055) | ||
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||
Hierarchy | Children:
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Originate from same individual | CVCL_E6WR ! MCRIi035-A CVCL_E6WT ! MCRIi035-C | ||
Sex of cell | Female | ||
Age at sampling | 14Y | ||
Category | Induced pluripotent stem cell | ||
Publications | PubMed=39787667; DOI=10.1016/j.scr.2024.103640 | ||
Cross-references | |||
Cell line databases/resources | hPSCreg; MCRIi035-B | ||
Entry history | |||
Entry creation | 10-Apr-2025 | ||
Last entry update | 10-Apr-2025 | ||
Version number | 1 |