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Cellosaurus GM00084 (CVCL_V547)

[Text version]
Cell line name GM00084
Synonyms GM-84; GM-0084; GM 84; GM84; GM00084A; Der(22) fibroblast
Accession CVCL_V547
Resource Identification Initiative To cite this cell line use: GM00084 (RRID:CVCL_V547)
Comments Population: Caucasian.
Karyotypic information: 47,XY,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM00084).
Cell type: Fibroblast; CL=CL_0000057.
Disease Trisomy 22 (NCIt: C114765)
Total autosomal trisomy (ORDO: Orphanet_98131)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_UG56 (Der(22)-iPS-C2)CVCL_UG57 (Der(22)-iPS-C4)
Sex of cell Male
Age at sampling 1M
Category Finite cell line
STR profile Source(s): PubMed=21949351

Markers:
AmelogeninX,Y
CSF1PO10,12
D3S135816,17
D5S81812
D7S8209
D8S117912
D13S31712
D16S53912
D18S5113,16
D21S1128,29
FGA21,22.2
Penta D13
Penta E12,15
TH019.3,10
TPOX8,12
vWA16

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Publications

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=7471105
Weichselbaum R.R., Nove J., Little J.B.
X-ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders.
Cancer Res. 40:920-925(1980)

PubMed=7329430; DOI=10.1016/0027-5107(81)90059-2
Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.
Abnormalities of human chromosome 13 and in vitro radiosensitivity; a study of 19 fibroblast strains.
Mutat. Res. 84:157-167(1981)

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)

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=21949351; DOI=10.1093/hmg/ddr435
Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S., Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J., Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D., Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y., Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes.
Hum. Mol. Genet. 21:32-45(2012)

Cross-references
Cell line collections (Providers) Coriell; GM00084
Cell line databases/resources CLO; CLO_0025153
Encyclopedic resources Wikidata; Q54836026
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number13