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Cellosaurus ICGi016-A (CVCL_UF64)

[Text version]

Cell line name ICGi016-A
Synonyms iTAF9-11; iTaf9-11; ICAGi001-A
Accession CVCL_UF64
Resource Identification Initiative To cite this cell line use: ICGi016-A (RRID:CVCL_UF64)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Derived from sampling site: Skin.
Disease Mental retardation, autosomal dominant 39 (NCIt: C156309)
Autosomal dominant non-syndromic intellectual disability (ORDO: Orphanet_178469)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 3Y
Category Induced pluripotent stem cell
Publications

PubMed=30616144; DOI=10.1016/j.scr.2018.101377
Khabarova A.A., Pristyazhnyuk I.E., Nikitina T.V., Gayner T.A., Torkhova N.B., Skryabin N.A., Kashevarova A.A., Babushkina N.P., Markova Z.G., Minzhenkova M.E., Nazarenko L.P., Shilova N.V., Shorina A.R., Lebedev I.N., Serov O.L.
Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication.
Stem Cell Res. 34:101377-101377(2019)

Cross-references
Cell line databases/resources hPSCreg; ICGi016-A
Biological sample resources BioSamples; SAMEA5230331
Other Wikidata; Q94313458
Entry history
Entry creation13-Nov-2018
Last entry update02-Jul-2020
Version number5