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Cellosaurus GM04024 (CVCL_1N27)

[Text version]
Cell line name GM04024
Synonyms GM04024B
Accession CVCL_1N27
Resource Identification Initiative To cite this cell line use: GM04024 (RRID:CVCL_1N27)
Comments Population: African American.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 3775; FMR1; Repeat_expansion; CGG[645]; ClinVar=VCV000009972; Zygosity=Hemizygous (from autologous cell line GM04025).
Disease Fragile X syndrome (NCIt: C84717)
Fragile X syndrome (ORDO: Orphanet_908)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_1N28 ! GM04025
Sex of cell Male
Age at sampling 29Y
Category Finite cell line
Publications

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

Cross-references
Cell line collections (Providers) Coriell; GM04024
Cell line databases/resources CLO; CLO_0016245
Encyclopedic resources Wikidata; Q54838373
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number13