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Cellosaurus MUi027-A (CVCL_A6JA)

[Text version]
Cell line name MUi027-A
Synonyms MU013.C2
Accession CVCL_A6JA
Resource Identification Initiative To cite this cell line use: MUi027-A (RRID:CVCL_A6JA)
Comments From: Mahidol University; Bangkok; Thailand.
Population: Southeast Asian; Thai.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:9008; PKD1; Simple; c.7946_7947delCT; Zygosity=Heterozygous (PubMed=35629189).
Disease Autosomal dominant polycystic kidney disease (NCIt: C84578)
Autosomal dominant polycystic kidney disease (ORDO: Orphanet_730)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 42Y
Category Induced pluripotent stem cell
Publications

PubMed=35629189; DOI=10.3390/jpm12050766; PMCID=PMC9145395
Linn A.K., Maneepitasut W., Tubsuwan A., Kitiyanant N., Phakdeekitcharoen B., Borwornpinyo S., Hongeng S., Phanthong P.
Establishment and characterization of MUi027-A: a novel patient-derived cell line of polycystic kidney disease with PKD1 mutation.
J. Pers. Med. 12:766.1-766.10(2022)

Cross-references
Cell line databases/resources hPSCreg; MUi027-A
Biological sample resources BioSamples; SAMEA13864634
Encyclopedic resources Wikidata; Q107116450
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number6