ID   ND34394
AC   CVCL_T844
SY   ND34394*C
DR   Coriell; ND34394
DR   NHCDR; ND34394
DR   SKIP; SKIP001368
DR   SKIP; SKIP004682
DR   Wikidata; Q54929777
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1441Cys (c.4321C>T); ClinVar=VCV000001938; Zygosity=Unspecified (from parent cell line).
CC   Discontinued: Coriell; ND34394; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198605; Parkinson disease 8, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_EY28 ! ND32944
SX   Male
AG   58Y
CA   Induced pluripotent stem cell
DT   Created: 03-02-14; Last updated: 19-12-24; Version: 16
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