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Cellosaurus GM10649 (CVCL_UR80)

[Text version]
Cell line name GM10649
Accession CVCL_UR80
Resource Identification Initiative To cite this cell line use: GM10649 (RRID:CVCL_UR80)
Comments Cell type: Fibroblast; CL=CL_0000057.
Disease Osteochondrodysplasia (NCIt: C84978)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 3D
Category Finite cell line
Publications

PubMed=1897572; DOI=10.1002/ajmg.1320400212
Faye-Petersen O.M., Ward K., Carey J.C., Knisely A.S.
Osteochondrodysplasia with rhizomelia, platyspondyly, callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension.
Am. J. Med. Genet. 40:183-187(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 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; GM10649 - Discontinued
Encyclopedic resources Wikidata; Q93810070
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number5