ID   IB PD-R1
AC   CVCL_UM96
SY   FH09-78 C4
DR   Wikidata; Q94312400
WW   Provider; BNLC; -; https://www.isciii.es/documents/20119/880364/IB_PD-R1_FH09-78_C4_Deposito.pdf
WW   Provider; BNLC; -; https://www.isciii.es/documents/20119/880377/Anexo-IB_PD-R1.pdf
CC   Part of: Spanish Stem Cell Bank (Banco Nacional de Lineas Celulares) collection.
CC   From: Inbiomed; Gipuzkoa; Spain.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1441Gly (c.4321C>G); ClinVar=VCV000001936; Zygosity=Unspecified (BNLC).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
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)
SX   Male
AG   Adult
CA   Induced pluripotent stem cell
DT   Created: 25-02-19; Last updated: 10-04-25; Version: 12
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