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Cellosaurus GM03809 (CVCL_JE58)

[Text version]
Cell line name GM03809
Synonyms GM3809
Accession CVCL_JE58
Resource Identification Initiative To cite this cell line use: GM03809 (RRID:CVCL_JE58)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome (NCIt: C3718)
WAGR syndrome (ORDO: Orphanet_893)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 2Y
Category Finite cell line
Publications

PubMed=2570029; DOI=10.1016/0888-7543(89)90084-0
Gessler M., Bruns G.A.P.
A physical map around the WAGR complex on the short arm of chromosome 11.
Genomics 5:43-55(1989)

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; GM03809
Cell line databases/resources CLO; CLO_0015559
Biological sample resources BioSample; SAMN00808542
Encyclopedic resources Wikidata; Q54838246
Entry history
Entry creation15-May-2017
Last entry update29-Jun-2023
Version number10