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Cellosaurus NIMHi015-A (CVCL_D6J5)

[Text version]
Cell line name NIMHi015-A
Synonyms PD06
Accession CVCL_D6J5
Resource Identification Initiative To cite this cell line use: NIMHi015-A (RRID:CVCL_D6J5)
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:8607; PRKN; Simple; c.(171+1_172-1)_(412+1_413-1)del (Ex2i-3i del); Zygosity=Homozygous (PubMed=38739971).
Disease Parkinson disease 2, autosomal recessive juvenile (NCIt: C198603)
Young-onset Parkinson disease (ORDO: Orphanet_2828)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 21Y
Category Induced pluripotent stem cell
Publications

PubMed=38739971; DOI=10.1016/j.scr.2024.103440
Banerjee R., Ghanty R., Jagtap S., Holla V., Kamble N., Yadav R., Pal P.K., Datta I.
Generation of induced pluripotent stem cells (NIMHi015-A) from a Parkinson's disease patient harbouring a homozygous exon 3 deletion in the PRKN gene.
Stem Cell Res. 77:103440-103440(2024)

Cross-references
Cell line databases/resources hPSCreg; NIMHi015-A
Biological sample resources BioSamples; SAMEA115344211
Encyclopedic resources Wikidata; Q127382963
Entry history
Entry creation02-May-2024
Last entry update19-Dec-2024
Version number3