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Cellosaurus GM01695 (CVCL_V811)

[Text version]
Cell line name GM01695
Synonyms GM-1695; GM1695; GM01695A; GM1695A
Accession CVCL_V811
Resource Identification Initiative To cite this cell line use: GM01695 (RRID:CVCL_V811)
Comments Population: Caucasian.
Karyotypic information: 46,X,t(X;11)(p21;q13) (PubMed=10377420).
Cell type: Fibroblast; CL=CL_0000057.
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_1P05 (A9(GM1695)-3)CVCL_1P06 (A9(GM1695)-4)CVCL_1P07 (A9(GM1695)-5)
Sex of cell Female
Age at sampling 26Y
Category Finite cell line
Publications

PubMed=7438786; DOI=10.1159/000131496
Greenstein R.M., Reardon M.P., Chan T.S., Middleton A.B., Mulivor R.A., Greene A.E., Coriell L.L.
An (X;11) translocation in a girl with Duchenne muscular dystrophy Repository identification No. GM1695.
Cytogenet. Cell Genet. 27:268-268(1980)

PubMed=2498246; DOI=10.1111/j.1349-7006.1989.tb02278.x
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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)

PubMed=10377420; DOI=10.1073/pnas.96.13.7364
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; GM01695
Cell line databases/resources CLO; CLO_0030959
Biological sample resources BioSample; SAMN00807081
Encyclopedic resources Wikidata; Q54837018
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number14