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Cellosaurus GM00097 (CVCL_V747)

[Text version]
Cell line name GM00097
Synonyms GM-97; GM0097; GM 0097; GM00097A
Accession CVCL_V747
Resource Identification Initiative To cite this cell line use: GM00097 (RRID:CVCL_V747)
Comments Population: Caucasian.
Karyotypic information: 46,X,t(X;1)(q26;q21) (PubMed=10377420).
Cell type: Fibroblast; CL=CL_0000057.
Disease Simpson Golabi Behmel syndrome type 1 (NCIt: C118787)
Simpson-Golabi-Behmel syndrome (ORDO: Orphanet_373)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_1P02 (A9(GM0097)-1)CVCL_1S87 (GM14849)
Sex of cell Female
Age at sampling 1Y
Category Finite cell line
Publications

PubMed=4139001; DOI=10.1159/000130291
Punnett H.H., Kistenmacher M.L., Greene A.E., Coriell L.L.
An (X;1) translocation, balanced, 46 chromosomes. Repository identification No. GM-97.
Cytogenet. Cell Genet. 13:406-407(1974)

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

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)

PubMed=1679663
Bader S.A., Fasching C., Brodeur G.M., Stanbridge E.J.
Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells.
Cell Growth Differ. 2:245-255(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)

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)

Cross-references
Cell line collections (Providers) Coriell; GM00097
Cell line databases/resources CLO; CLO_0025819
Encyclopedic resources Wikidata; Q54836039
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number15