ID   ND40061
AC   CVCL_EZ41
DR   Coriell; ND40061
DR   NHCDR; ND40061
DR   Wikidata; Q54930144
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:7106; ATXN3; Repeat_expansion; c.892CAG[71]; Zygosity=Heterozygous; Note=The other allele has 23 repeats (NHCDR=ND40061).
CC   Discontinued: Coriell; ND40061; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C26845; Parkinson's disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   56Y
CA   Finite cell line
DT   Created: 26-09-16; Last updated: 19-12-24; Version: 10
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