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Cellosaurus Cri du Chat (CVCL_4150)

[Text version]
Cell line name Cri du Chat
Synonyms GM00071; GM-0071; GM-71; GM 71; GM71
Accession CVCL_4150
Secondary accession CVCL_X223
Resource Identification Initiative To cite this cell line use: Cri du Chat (RRID:CVCL_4150)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Cri du chat syndrome (NCIt: C34518)
Monosomy 5p (ORDO: Orphanet_281)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 19Y
Category Finite cell line
STR profile Source(s): ATCC=CCL-90

Markers:
AmelogeninX
CSF1PO10,12
D2S133820,23
D3S135816,17
D5S81810,11
D7S8208,11
D8S117913
D13S31711
D16S53911,12
D18S5116,18
D19S43314,15
D21S1130
FGA21,22
Penta D10,11
Penta E7,13
TH019.3
TPOX8
vWA15,16

Run an STR similarity search on this cell line
Publications

DOI=10.1007/BF02618370
Stulberg C.S., Coriell L.L., Kniazeff A.J., Shannon J.E.
The animal cell culture collection.
In Vitro 5:1-16(1970)

PubMed=1001031; DOI=10.1159/000130718
Breg W.R., Aronson M.M., Greene A.E., Coriell L.L.
Deletion of the short arm of chromosome 5 from a subject with cri-du-chat syndrome. Repository identification No. GM-71.
Cytogenet. Cell Genet. 17:239-240(1976)

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=6988327; DOI=10.1007/BF02831503
O'Brien S.J., Shannon J.E., Gail M.H.
A molecular approach to the identification and individualization of human and animal cells in culture: isozyme and allozyme genetic signatures.
In Vitro 16:119-135(1980)

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)

Cross-references
Cell line collections (Providers) ATCC; CCL-90
Coriell; GM00071
ECACC; 90102533 - Discontinued
KCB; KCB 94023YJ
Cell line databases/resources CLO; CLO_0002611
CLO; CLO_0025165
CLDB; cl910
Biological sample resources BioSample; SAMN03471291
Encyclopedic resources Wikidata; Q54814486
Entry history
Entry creation04-Apr-2012
Last entry update02-May-2024
Version number21