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Cellosaurus GM23262 (CVCL_F177)

[Text version]
Cell line name GM23262
Synonyms GM23262*A
Accession CVCL_F177
Resource Identification Initiative To cite this cell line use: GM23262 (RRID:CVCL_F177)
Comments Population: Caucasian.
Omics: Variations; CNV analysis.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex45-53del; Zygosity=Hemizygous (from parent cell line).
Disease Becker's muscular dystrophy (NCIt: C84587)
Becker muscular dystrophy (ORDO: Orphanet_98895)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_8521 (GM04981)
Sex of cell Male
Age at sampling 6Y
Category Induced pluripotent stem cell
Publications

PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242
Zhen-Ya Tang, Dorit S. Berlin, Lorraine H. Toji, Gokce Altay Toruner, Christine M. Beiswanger, Shashikant Kulkarni, Christa Lese Martin, Beverly S. Emanuel, Michael Christman, Norman P. Gerry;
A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.
G3 (Bethesda) 3:1143-1149(2013)

Cross-references
Cell line collections (Providers) Coriell; GM23262
Cell line databases/resources SKIP; SKIP000187
SKIP; SKIP004351
Encyclopedic resources Wikidata; Q54852945
Entry history
Entry creation22-Oct-2012
Last entry update10-Apr-2025
Version number20