Cellosaurus cell line NIMHi001-A (CVCL

Cross-references
Cell line name	NIMHi001-A
Synonyms	BPPD01
Accession	CVCL_YT35
Resource Identification Initiative	To cite this cell line use: NIMHi001-A (RRID:CVCL_YT35)
Comments	From: National Institute of Mental Health and Neurosciences; Bengaluru; India. Population: Indian. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Ile1371Val (c.4111A>G); ClinVar=VCV000039176; Zygosity=Heterozygous (PubMed=32244201).
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)
Sex of cell	Male
Age at sampling	59Y
Category	Induced pluripotent stem cell
Publications	PubMed=32244201; DOI=10.1016/j.scr.2020.101768 Datta I., No_last_name S., Jagtap S., Potdar C., Yadav R., Pal P.K. Generation of induced pluripotent stem cells (NIMHi001-A) from a Parkinson's disease patient of East Indian ethnicity carrying LRRK2 I1371V variant. Stem Cell Res. 44:101768-101768(2020)
Cell line databases/resources	hPSCreg; NIMHi001-A SKIP; SKIP005731
Biological sample resources	BioSamples; SAMEA6675820
Encyclopedic resources	Wikidata; Q98127897
Entry history
Entry creation	12-Mar-2020
Last entry update	19-Dec-2024
Version number	8