ID   ND41007
AC   CVCL_EZ67
DR   NHCDR; ND41007
DR   Wikidata; Q54930188
CC   Population: Asian.
CC   Sequence variation: Mutation; HGNC; HGNC:16812; COQ8A; Simple; p.Ser616Leufs*114 (c.1844dupG) (p.Gly615fs) (c.1844_1845insG); ClinVar=VCV000214046; Zygosity=Unspecified (NHCDR=ND41007).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C26845; Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Age unspecified
CA   Finite cell line
DT   Created: 26-09-16; Last updated: 10-04-25; Version: 11
//