Home  |  Contact

Cellosaurus NIMHi001-A (CVCL_YT35)

[Text version]
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; 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., Sowmithra X., 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)

Cross-references
Cell line databases/resources hPSCreg; NIMHi001-A
SKIP; SKIP005731
Biological sample resources BioSamples; SAMEA6675820
Encyclopedic resources Wikidata; Q98127897
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number7