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Cellosaurus SP13.4 (CVCL_V203)

[Text version]
Cell line name SP13.4
Synonyms SP13#4; ESi006-A
Accession CVCL_V203
Secondary accession CVCL_RI64
Resource Identification Initiative To cite this cell line use: SP13.4 (RRID:CVCL_V203)
Comments Part of: Spanish Stem Cell Bank (Banco Nacional de Lineas Celulares) collection.
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; 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_RI63 ! SP13.2
Sex of cell Female
Age at sampling 68Y
Category Induced pluripotent stem cell
Web pages https://www.isciii.es/QueHacemos/Servicios/BIOBANCOS/BNLC/Lists/Lneas%20iPS/Attachments/39/Caracteristicas%20-%20pdf_SP_13_4.pdf

PubMed=22407749; DOI=10.1002/emmm.201200215
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 collections (Providers) EBiSC; ESi006-A
ECACC; 66540068 - Discontinued
Cell line databases/resources hPSCreg; ESi006-A
ISCR; 2239
SKIP; SKIP000958
SKIP; SKIP002423
Biological sample resources BioSamples; SAMEA3303225
Encyclopedic resources Wikidata; Q54955440
Entry history
Entry creation16-Apr-2014
Last entry update30-Jan-2024
Version number18