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Cellosaurus WC010i-CMT2A-1.1 (CVCL_UB79)

[Text version]
Cell line name WC010i-CMT2A-1.1
Accession CVCL_UB79
Resource Identification Initiative To cite this cell line use: WC010i-CMT2A-1.1 (RRID:CVCL_UB79)
Comments Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 16877; MFN2; Unexplicit; Not described; Zygosity=Unspecified (WiCell=wc010i-cmt2a-1.1).
Disease Charcot-Marie-Tooth disease type 2A2A (NCIt: C150646)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (ORDO: Orphanet_99947)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UB80 ! WC011i-CMT2A-1.2
CVCL_UB81 ! WC012i-CMT2A-1.3
Sex of cell Male
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) WiCell; wc010i-cmt2a-1.1
Encyclopedic resources Wikidata; Q98134781
Entry history
Entry creation13-Nov-2018
Last entry update05-Oct-2023
Version number9