Cellosaurus cell line ULUNDi008-A (CVCL

Cross-references
Cell line name	ULUNDi008-A
Synonyms	CSC-32B; CSC-32
Accession	CVCL_YC61
Resource Identification Initiative	To cite this cell line use: ULUNDi008-A (RRID:CVCL_YC61)
Comments	From: University of Lund; Lund; Sweden. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (PubMed=31954327).
Disease	Parkinson disease 1, autosomal dominant (NCIt: C198602) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	45Y
Category	Induced pluripotent stem cell
Publications	PubMed=31954327; DOI=10.1016/j.scr.2019.101694 Azevedo C., Chumarina M., Serafimova E., Goldwurm S., Collin A., Roybon L., Savchenko E., Pomeshchik Y. Generation of an induced pluripotent stem cell line (CSC-32) from a patient with Parkinson's disease carrying a heterozygous variation p.A53T in the SNCA gene. Stem Cell Res. 43:101694-101694(2020)
Cell line databases/resources	hPSCreg; ULUNDi008-A
Encyclopedic resources	Wikidata; Q98134025
Entry history
Entry creation	19-Dec-2019
Last entry update	19-Dec-2024
Version number	9