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Cellosaurus GM03913 (CVCL_1K35)

[Text version]
Cell line name GM03913
Synonyms GM03913A
Accession CVCL_1K35
Resource Identification Initiative To cite this cell line use: GM03913 (RRID:CVCL_1K35)
Comments Population: Caucasian; French Canadian.
Karyotypic information: 46,XY [46%]; 47,XY,+7 [54%] (Coriell=GM03913).
Cell type: Fibroblast; CL=CL_0000057.
Disease Roberts-SC phocomelia syndrome (NCIt: C4681)
Roberts syndrome (ORDO: Orphanet_3103)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_HE60 (hTERT-RBS)
Sex of cell Male
Age at sampling 1Y8M
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)

PubMed=10655550; DOI=10.1093/hmg/9.3.403
Ouellette M.M., McDaniel L.D., Wright W.E., Shay J.W., Schultz R.A.
The establishment of telomerase-immortalized cell lines representing human chromosome instability syndromes.
Hum. Mol. Genet. 9:403-411(2000)

Cross-references
Cell line collections (Providers) Coriell; GM03913
Cell line databases/resources CLO; CLO_0016129
Encyclopedic resources Wikidata; Q54838320
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number10