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Cellosaurus DS-2-iPSC (CVCL_A3ZC)

[Text version]
Cell line name DS-2-iPSC
Accession CVCL_A3ZC
Resource Identification Initiative To cite this cell line use: DS-2-iPSC (RRID:CVCL_A3ZC)
Comments Population: Korean.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:10585; SCN1A; Simple; p.Ile1183Cysfs*21 (c.3576_3580delTCAAA); Zygosity=Heterozygous (PubMed=29295803).
Disease Developmental and epileptic encephalopathy 6A (NCIt: C147071)
Dravet syndrome (ORDO: Orphanet_33069)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=29295803; DOI=10.1016/j.braindev.2017.12.002
Hyun Woo Kim, Zhe-Jiu Quan, Young-Beom Kim, Eunji Cheong, Heung Dong Kim, Min-Jung Cho, Jiho Jang, Young Rang Yoo, Joon Soo Lee, Ji Hun Kim, Yang In Kim ...Show all 13 authors... , Dae-Sung Kim, Hoon-Chul Kang; Show fewer authors
Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patients.
Brain Dev. 40:287-298(2018)

Cross-references
Cell line databases/resources SKIP; SKIP003050
Encyclopedic resources Wikidata; Q105506776
Entry history
Entry creation12-Jan-2021
Last entry update19-Dec-2024
Version number7