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Cellosaurus GM03767 (CVCL_X111)

[Text version]
Cell line name GM03767
Synonyms GM 3767
Accession CVCL_X111
Resource Identification Initiative To cite this cell line use: GM03767 (RRID:CVCL_X111)
Comments Population: Caucasian.
Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Deletion 18p syndrome (NCIt: C84521)
Monosomy 18p (ORDO: Orphanet_1598)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 3Y
Category Finite cell line
Publications

PubMed=6617268; DOI=10.1159/000131883
Margaret M. Aronson, Warren W. Nichols, Richard A. Mulivor, Arthur E. Greene, Lewis Lemon Coriell;
Breakpoint map of chromosomal inversion and deletion cell cultures in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 35:298-302(1983)

PubMed=6661932; DOI=10.1159/000131990
Margaret M. Aronson, Warren W. Nichols, Richard A. Mulivor, Arthur E. Greene, Lewis Lemon Coriell;
Chromosome maps of cell lines with specific monosomic or trisomic portions of the genome in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 36:652-658(1983)

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
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; GM03767
Cell line databases/resources CLO; CLO_0015491
Biological sample resources BioSample; SAMN00808521
Encyclopedic resources Wikidata; Q54838222
Entry history
Entry creation17-Jul-2014
Last entry update29-Jun-2023
Version number10