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Cellosaurus GM04025 (CVCL_1N28)

[Text version]

Cell line name GM04025
Synonyms GM4025B; GM04025C; GM04025E
Accession CVCL_1N28
Resource Identification Initiative To cite this cell line use: GM04025 (RRID:CVCL_1N28)
Comments Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from sampling site: Peripheral blood.
Sequence variations Hemizygous for FMR1 645 CGG repeats (PubMed=25776194).
Disease Fragile X syndrome (NCIt: C84717)
Fragile X syndrome (ORDO: Orphanet_908)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_1R91 (GM10330)CVCL_1S11 (GM11010)
Originate from same individual CVCL_1N27 ! GM04024
Sex of cell Male
Age at sampling 29Y
Category Transformed cell line
Publications

PubMed=1672039; DOI=10.1038/349624a0
Vincent A., Heitz D., Petit C., Kretz C., Oberle I., Mandel J.-L.
Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.
Nature 349:624-626(1991)

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)

PubMed=25776194; DOI=10.1016/j.jmoldx.2014.12.005
Lim G.X.Y., Loo Y.L., Mundhofir F.E., Cayami F.K., Faradz S.M.H., Rajan-Babu I.-S., Chong S.S., Koh Y.Y., Guan M.
Validation of a commercially available screening tool for the rapid identification of CGG trinucleotide repeat expansions in FMR1.
J. Mol. Diagn. 17:302-314(2015)

Cross-references
Cell line collections Coriell; GM04025
Ontologies CLO; CLO_0016229
Other Wikidata; Q54838374
Entry history
Entry creation08-Jul-2015
Last entry update12-Mar-2020
Version number10