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Cellosaurus GLNNFi001-A (CVCL_B0PQ)

[Text version]
Cell line name GLNNFi001-A
Synonyms MCD855iclone2
Accession CVCL_B0PQ
Resource Identification Initiative To cite this cell line use: GLNNFi001-A (RRID:CVCL_B0PQ)
Comments From: GROW Laboratory; Bangalore; India.
Population: Indian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:6938; CHST6; Simple; p.Val172Leu; Zygosity=Homozygous (PubMed=35472829).
Disease Macular corneal dystrophy (NCIt: C34793)
Macular corneal dystrophy (ORDO: Orphanet_98969)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 38Y
Category Induced pluripotent stem cell
Publications

PubMed=35472829; DOI=10.1016/j.scr.2022.102789
Chakrabarty K., Prashanthi K.N., Shetty R., Argulwar S., Jeyabalan N., Ghosh A.
Generation of iPSC line (GLNNFi001-A) from peripheral blood mononuclear cells of a patient with macular corneal dystrophy.
Stem Cell Res. 62:102789-102789(2022)

Cross-references
Cell line databases/resources hPSCreg; GLNNFi001-A
Biological sample resources BioSamples; SAMEA9908056
Encyclopedic resources Wikidata; Q108820294
Entry history
Entry creation23-Sep-2021
Last entry update19-Dec-2024
Version number6