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Cellosaurus FMCPGHi003-A (CVCL_D0F1)

[Text version]
Cell line name FMCPGHi003-A
Synonyms 301-iPSC-FHM-001A
Accession CVCL_D0F1
Resource Identification Initiative To cite this cell line use: FMCPGHi003-A (RRID:CVCL_D0F1)
Comments From: The First Medical Center of PLA General Hospital; Beijing; China.
Population: Chinese; Han.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:10585; SCN1A; Simple; p.Phe1774Cys (c.5321A>C); Zygosity=Heterozygous (PubMed=38880015).
Disease Familial hemiplegic migraine-3 (NCIt: C205634)
Familial or sporadic hemiplegic migraine (ORDO: Orphanet_569)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 38Y
Category Induced pluripotent stem cell
Publications

PubMed=38880015; DOI=10.1016/j.scr.2024.103465
Tao Wang, Ya-Nan Li, Chun-Xiao Yang, Hui-Juan Yuan, Wei-Nan Na, Sheng-Yuan Yu;
Generation of iPSC line (FMCPGHi003-A) from human PBMCs of a patient with familial hemiplegic migraine type 3.
Stem Cell Res. 79:103465-103465(2024)

Cross-references
Cell line databases/resources hPSCreg; FMCPGHi003-A
Biological sample resources BioSamples; SAMEA115171192
Encyclopedic resources Wikidata; Q123031296
Entry history
Entry creation05-Oct-2023
Last entry update19-Dec-2024
Version number5