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Cellosaurus GM02063 (CVCL_F127)

[Text version]
Cell line name GM02063
Synonyms LN; GM-2063; GM 2063; GM-02063; GM00177; GM 177; GM-177; GM177
Accession CVCL_F127
Resource Identification Initiative To cite this cell line use: GM02063 (RRID:CVCL_F127)
Comments Population: African American.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Lesch-Nyhan syndrome (NCIt: C61255)
Lesch-Nyhan syndrome (ORDO: Orphanet_510)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_7908 (GM00847)
Sex of cell Male
Age at sampling 5Y6M
Category Finite cell line
Publications

PubMed=180603; DOI=10.1126/science.180603
Martin D.W. Jr., Maler B.A.
Phosphoribosylpyrophosphate synthetase is elevated in fibroblasts from patients with the Lesch-Nyhan syndrome.
Science 193:408-411(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)

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) Coriell; GM00177 - Discontinued
Coriell; GM02063 - Discontinued
Encyclopedic resources Wikidata; Q54837280
Entry history
Entry creation22-Oct-2012
Last entry update29-Jun-2023
Version number15