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Cellosaurus GM01368 (CVCL_GY15)

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Cell line name GM01368
Synonyms GM-1368
Accession CVCL_GY15
Resource Identification Initiative To cite this cell line use: GM01368 (RRID:CVCL_GY15)
Comments Population: African American.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Gene deletion; HGNC; HGNC:4827; HBB; Zygosity=Homozygous (Coriell=GM01368).
  • Gene deletion; HGNC; HGNC:4829; HBD; Zygosity=Homozygous (Coriell=GM01368).
Disease Hereditary persistence of fetal hemoglobin (NCIt: C129072)
Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome (ORDO: Orphanet_46532)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 15Y
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; GM01368
Cell line databases/resources CLO; CLO_0030847
Biological sample resources BioSample; SAMN00803826
Encyclopedic resources Wikidata; Q54836786
Entry history
Entry creation26-Sep-2016
Last entry update19-Dec-2024
Version number13