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Cellosaurus OGHFUi001-A (CVCL_A8MU)

[Text version]
Cell line name OGHFUi001-A
Synonyms iPS84-1
Accession CVCL_A8MU
Resource Identification Initiative To cite this cell line use: OGHFUi001-A (RRID:CVCL_A8MU)
Comments From: Obstetrics and Gynecology Hospital of Fudan University; Shanghai; China.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:18060; ARX; Simple; p.Arg330Leu (c.989G>T); Zygosity=Hemizygous (PubMed=34087996).
Disease Developmental and epileptic encephalopathy 1 (NCIt: C179866)
Early infantile epileptic encephalopathy (ORDO: Orphanet_1934)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_C0CK (OGHFUi001-A-1)
Sex of cell Male
Age at sampling 7Y
Category Induced pluripotent stem cell
Publications

PubMed=34087996; DOI=10.1016/j.scr.2021.102367
Jia N., Gong X.-H., Chen J., Yang T., Bao C.-X., Shen J., Xiao X.-R.
Generation of an induced pluripotent stem cell line (OGHFUi001-A) from a type 1 early infantile epileptic encephalopathy with ARX mutation.
Stem Cell Res. 53:102367-102367(2021)

PubMed=35121198; DOI=10.1016/j.scr.2022.102693
Gong X.-H., Zheng Z.-Q., Yang T., Zheng H.-Y., Xiao X.-R., Jia N.
Generation of an isogenic gene-corrected iPSC line (OGHFUi001-A-1) from a type 1 early infantile epileptic encephalopathy (EIEE1) patient with a hemizygous R330L mutation in the ARX gene.
Stem Cell Res. 60:102693-102693(2022)

Cross-references
Cell line databases/resources hPSCreg; OGHFUi001-A
Encyclopedic resources Wikidata; Q108821072
Entry history
Entry creation23-Sep-2021
Last entry update19-Dec-2024
Version number7