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Cellosaurus GM10625 (CVCL_DD85)

[Text version]
Cell line name GM10625
Accession CVCL_DD85
Resource Identification Initiative To cite this cell line use: GM10625 (RRID:CVCL_DD85)
Comments Population: Jewish.
Derived from site: In situ; Buttock, skin; UBERON=UBERON_8480014.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Hereditary optic atrophy (NCIt: C34864)
Hereditary optic neuropathy (ORDO: Orphanet_98671)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_DD84 ! GM10624
Sex of cell Male
Age at sampling 50Y
Category Finite cell line
Publications

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; GM10625
Cell line databases/resources CLO; CLO_0024548
Biological sample resources BioSample; SAMN00800109
Encyclopedic resources Wikidata; Q54844561
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number8