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Cellosaurus GM05131 (CVCL_AX78)

[Text version]
Cell line name GM05131
Accession CVCL_AX78
Resource Identification Initiative To cite this cell line use: GM05131 (RRID:CVCL_AX78)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Fragile X syndrome (NCIt: C84717)
Fragile X syndrome (ORDO: Orphanet_908)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_E7VR (UNIPDi008-A)CVCL_E7VS (UNIPDi008-B)CVCL_IU03 (WISi006-A)
Sex of cell Male
Age at sampling 3Y
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 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; GM05131
Cell line databases/resources CLO; CLO_0025352
Encyclopedic resources Wikidata; Q54838877
Entry history
Entry creation02-May-2016
Last entry update10-Apr-2025
Version number10