Cellosaurus cell line SP12.4 (CVCL

Cross-references
Cell line name	SP12.4
Accession	CVCL_RI62
Resource Identification Initiative	To cite this cell line use: SP12.4 (RRID:CVCL_RI62)
Comments	From: Institut de Bioenginyeria de Catalunya (IBEC); Barcelona; Spain. Derived from site: In situ; Skin, epidermis; UBERON=UBERON_0001003. Cell type: Keratinocyte; CL=CL_0000312.
Sequence variations	Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (PubMed=22407749).
Disease	Parkinson disease 8, autosomal dominant (NCIt: C198605) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_RI61 ! SP12.3
Sex of cell	Female
Age at sampling	63Y
Category	Induced pluripotent stem cell
Publications	PubMed=22407749; DOI=10.1002/emmm.201200215; PMCID=PMC3403296 Sanchez-Danes A., Richaud-Patin Y., Carballo-Carbajal I., Jimenez-Delgado S., Caig C., Mora S., Di Guglielmo C., Ezquerra M., Patel B., Giralt A., Canals J.M., Memo M., Alberch J., Lopez-Barneo J., Vila M., Cuervo A.M., Tolosa E., Consiglio A., Raya A. Disease-specific phenotypes in dopamine neurons from human iPS-based models of genetic and sporadic Parkinson's disease. EMBO Mol. Med. 4:380-395(2012)
Cell line databases/resources	SKIP; SKIP000956
Encyclopedic resources	Wikidata; Q54955423
Entry history
Entry creation	05-Mar-2018
Last entry update	19-Dec-2024
Version number	11