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Cellosaurus GM03759 (CVCL_M945)

[Text version]
Cell line name GM03759
Synonyms GM03759A
Accession CVCL_M945
Resource Identification Initiative To cite this cell line use: GM03759 (RRID:CVCL_M945)
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[~2000] (c.*224CTG[(51_?)]); ClinVar=VCV000005049; Zygosity=Unspecified (Coriell=GM03759).
Disease Dystrophia myotonica 1 (NCIt: C84679)
Steinert myotonic dystrophy (ORDO: Orphanet_273)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 33Y
Category Finite cell line
Publications

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM03759
Cell line databases/resources CLO; CLO_0015488
Biological sample resources BioSample; SAMN00808520
Encyclopedic resources Wikidata; Q54838221
Entry history
Entry creation05-Nov-2013
Last entry update19-Dec-2024
Version number17