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Cellosaurus GM02859 (CVCL_M932)

[Text version]
Cell line name GM02859
Synonyms GM-2859; GM 2859; GM2859; GM02859A; GM2859A; GM17312
Accession CVCL_M932
Resource Identification Initiative To cite this cell line use: GM02859 (RRID:CVCL_M932)
Comments Part of: Human variation panel.
Population: South American (Brazil, Guyana, Venezuela).
Karyotypic information: 46,X,t(X;11)(q11.1;p13) (PubMed=10377420).
Omics: CNV analysis.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:2623; CYP2C9; Simple; p.Arg144Cys (c.430C>T) (416C>T); ClinVar=VCV000008409; Zygosity=Heterozygous; Note=CYP2C9*2 allele (Coriell=GM17312).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_1P08 (A9(GM2859)-3)CVCL_1P09 (A9(GM2859)-4)
Originate from same individual CVCL_M933 ! GM03316
Sex of cell Female
Age at sampling 3Y
Category Finite cell line
Publications

PubMed=6947233; DOI=10.1073/pnas.78.10.6339; PMCID=PMC349034
Migeon B.R., Brown T.R., Axelman J., Migeon C.J.
Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse.
Proc. Natl. Acad. Sci. U.S.A. 78:6339-6343(1981)

PubMed=6293786; DOI=10.1002/cyto.990030302
Lebo R.V.
Chromosome sorting and DNA sequence localization.
Cytometry 3:145-154(1982)

PubMed=6617268; DOI=10.1159/000131883
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
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
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
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)

PubMed=2498246; DOI=10.1111/j.1349-7006.1989.tb02278.x; PMCID=PMC5917704
Koi M., Morita H., Shimizu M., Oshimura M.
Construction of mouse A9 clones containing a single human chromosome (X/autosome translocation) via micro-cell fusion.
Jpn. J. Cancer Res. 80:122-125(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)

PubMed=10377420; DOI=10.1073/pnas.96.13.7364; PMCID=PMC22091
Carrel L., Willard H.F.
Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.
Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999)

PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242
Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M., Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.
A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.
G3 (Bethesda) 3:1143-1149(2013)

Cross-references
Cell line collections (Providers) Coriell; GM02859
Coriell; GM17312
Cell line databases/resources CLO; CLO_0012780
CLO; CLO_0013353
Biological sample resources BioSample; SAMN00808154
Encyclopedic resources Wikidata; Q54837734
Entry history
Entry creation05-Nov-2013
Last entry update19-Dec-2024
Version number17