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Cellosaurus GM28029 (CVCL_A5MG)

[Text version]
Cell line name GM28029
Accession CVCL_A5MG
Resource Identification Initiative To cite this cell line use: GM28029 (RRID:CVCL_A5MG)
Comments Population: Native North American; Cherokee, Caucasian and Mexican.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:11474; SURF1; Simple; p.Leu105Ter (c.312_321del10insAT) (p.Pro104_Leu105insTer); ClinVar=VCV000215237; Zygosity=Heterozygous (Coriell=GM28029).
  • Mutation; HGNC; HGNC:11474; SURF1; Simple; p.Arg230Ter (c.688C>T); ClinVar=VCV000280010; Zygosity=Heterozygous (Coriell=GM28029).
Disease Leigh disease (NCIt: C84814)
Mitochondrial complex IV deficiency, nuclear type 1 (NCIt: C176895)
Leigh syndrome (ORDO: Orphanet_506)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 4Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM28029
Encyclopedic resources Wikidata; Q107115202
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number7