ID   HUF6
AC   CVCL_ZY00
SY   HUman Fibroblast 6
DR   Wikidata; Q102114172
RX   PubMed=19774082;
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Homozygous (PubMed=19774082).
CC   Derived from site: In situ; Arm, skin, dermis; UBERON=UBERON_0002427+UBERON_0002067.
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   Female
AG   60Y
CA   Finite cell line
DT   Created: 29-10-20; Last updated: 19-12-24; Version: 7
//
RX   PubMed=19774082; DOI=10.1371/journal.pone.0007118; PMCID=PMC2744017;
RA   Byrne J.A., Nguyen H.N., Reijo Pera R.A.;
RT   "Enhanced generation of induced pluripotent stem cells from a
RT   subpopulation of human fibroblasts.";
RL   PLoS ONE 4:e7118.1-e7118.9(2009).
//