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Cellosaurus LCPHi002-A (CVCL_B5G5)

[Text version]
Cell line name LCPHi002-A
Accession CVCL_B5G5
Resource Identification Initiative To cite this cell line use: LCPHi002-A (RRID:CVCL_B5G5)
Comments From: The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital; Liaocheng; China.
Population: Chinese; Han.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:1908; VPS13A; Simple; p.Ala1428fs (c.4282_4289delinsA); Zygosity=Heterozygous (PubMed=35093716).
Disease Parkinson's disease (NCIt: C26845)
Young-onset Parkinson disease (ORDO: Orphanet_2828)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 33Y
Category Induced pluripotent stem cell
Publications

PubMed=35093716; DOI=10.1016/j.scr.2022.102685
Lu X.-J., Wang W., Liu Y.-M., Song N., Li M.-P., Mu X., Zhang N., Chen Q.-F., Jiang L.-C., Kong X.-L., Sun P., Tong J.-B., Zhang Y.-P., Li J.-T., Ma S.-J., Han F.-B.
Establishment and characterization of human induced pluripotent stem cell line from a Parkinson's disease patient harboring VPS13A gene mutation.
Stem Cell Res. 60:102685-102685(2022)

Cross-references
Cell line databases/resources hPSCreg; LCPHi002-A
Biological sample resources BioSamples; SAMEA10558482
Encyclopedic resources Wikidata; Q110433003
Entry history
Entry creation16-Dec-2021
Last entry update19-Dec-2024
Version number5