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Cellosaurus GM02214 (CVCL_H179)

[Text version]
Cell line name GM02214
Synonyms GM-2214
Accession CVCL_H179
Resource Identification Initiative To cite this cell line use: GM02214 (RRID:CVCL_H179)
Comments Population: Caucasian.
Donor information: At sampling donor was not affected with metachromatic leukodystrophy but at risk for disease.
Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Disease Metachromatic leukodystrophy (NCIt: C61251)
Metachromatic leukodystrophy (ORDO: Orphanet_512)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 20FW
Category Finite cell line
Publications

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)

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)

Cross-references
Cell line collections (Providers) Coriell; GM02214
Cell line databases/resources CLO; CLO_0032259
Biological sample resources BioSample; SAMN00807610
Encyclopedic resources Wikidata; Q54837376
Entry history
Entry creation11-Feb-2013
Last entry update29-Jun-2023
Version number12