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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
Hope Handler Punnett, Mildred Lever Kistenmacher, Arthur E. Greene, Lewis Lemon Coriell;
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
Lewis Lemon Coriell, Arthur E. Greene;
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
Minoru Koi, Hiroyuki Morita, Motoyuki Shimizu, Mitsuo Oshimura;
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
Scott A. Bader, Clare Fasching, Garrett M. Brodeur, Eric John Stanbridge;
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
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)

PubMed=10377420; DOI=10.1073/pnas.96.13.7364; PMCID=PMC22091
Laura Carrel, Huntington Faxon Willard;
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