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Cellosaurus GM10381 (CVCL_N351)

[Text version]
Cell line name GM10381
Accession CVCL_N351
Resource Identification Initiative To cite this cell line use: GM10381 (RRID:CVCL_N351)
Comments Population: African American.
Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
Cell type: Fibroblast; CL=CL_0000057.
Disease Fraser syndrome (NCIt: C118436)
Fraser syndrome (ORDO: Orphanet_2052)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_N350 ! GM10379
Sex of cell Male
Age at sampling 19FW
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; GM10381
Cell line databases/resources CLO; CLO_0028573
Biological sample resources BioSample; SAMN00799969
Encyclopedic resources Wikidata; Q54844423
Entry history
Entry creation05-Nov-2013
Last entry update29-Jun-2023
Version number11