ID   NYSCF-PD-1040-10001.198.01-Skin-SV-iPSC4
AC   CVCL_AD55
DR   SKIP; SKIP004919
DR   Wikidata; Q54931465
CC   From: New York Stem Cell Foundation; New York; USA.
CC   Sequence variation: Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Unspecified (NYSCF).
CC   Donor information: Established from monozygotic twin of NYSCF-PD-1039-10001.197.01-Skin-SV-iPSC2 (Cellosaurus=CVCL_AD53) and NYSCF-PD-1039-10001.197.01-Skin-SV-iPSC5 (Cellosaurus=CVCL_AD54).
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
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_AD56 ! NYSCF-PD-1040-10001.198.01-Skin-SV-iPSC5
SX   Male
AG   66Y
CA   Induced pluripotent stem cell
DT   Created: 23-02-16; Last updated: 19-12-24; Version: 14
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