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Cellosaurus DMDCl2 (CVCL_6B26)

[Text version]
Cell line name DMDCl2
Accession CVCL_6B26
Resource Identification Initiative To cite this cell line use: DMDCl2 (RRID:CVCL_6B26)
Comments Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT.
Genetic integration: Method=Transduction; Gene=MGI; MGI:88357; Cdk4.
Genetic integration: Method=Transduction; Gene=UniProtKB; P13249; S.alboniger pac (PuroR).
Genetic integration: Method=Transduction; Gene=UniProtKB; P00552; Transposon Tn5 neo.
Derived from site: In situ; Thigh, quadriceps skeletal muscle; UBERON=UBERON_0004498.
Cell type: Myoblast; CL=CL_0000056.
Sequence variations
  • Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex48-50del; Zygosity=Hemizygous (PubMed=22040608).
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 1Y8M
Category Telomerase immortalized cell line
Publications

PubMed=22040608; DOI=10.1186/2044-5040-1-34; PMCID=PMC3235972
Mamchaoui K., Trollet C., Bigot A., Negroni E., Chaouch S., Wolff A., Kandalla P.K., Marie S., Di Santo J.P., St Guily J.L., Muntoni F., Kim J., Philippi S., Spuler S., Levy N., Blumen S.C., Voit T., Wright W.E., Aamiri A., Butler-Browne G.S., Mouly V.
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders.
Skelet. Muscle 1:34.1-34.11(2011)

Cross-references
Encyclopedic resources Wikidata; Q54831289
Entry history
Entry creation23-Feb-2016
Last entry update10-Apr-2025
Version number13