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Cellosaurus GM24559 (CVCL_Y801)

[Text version]
Cell line name GM24559
Synonyms GM24559*B
Accession CVCL_Y801
Resource Identification Initiative To cite this cell line use: GM24559 (RRID:CVCL_Y801)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:2933; DMPK; Repeat_expansion; c.*224CTG[~1700] (c.*224CTG[(51_?)]); ClinVar=VCV000005049; Zygosity=Heterozygous (from parent cell line).
Disease Dystrophia myotonica 1 (NCIt: C84679)
Steinert myotonic dystrophy (ORDO: Orphanet_273)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_Y794 (GM04602)
Sex of cell Female
Age at sampling 2Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; GM24559
Cell line databases/resources SKIP; SKIP000705
Encyclopedic resources Wikidata; Q54853784
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number10