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Cellosaurus ICGi009-A (CVCL_WP98)

[Text version]

Cell line name ICGi009-A
Synonyms iTAF3-17; iTAF3del17
Accession CVCL_WP98
Resource Identification Initiative To cite this cell line use: ICGi009-A (RRID:CVCL_WP98)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Population: Caucasian.
Derived from sampling site: Skin.
Sequence variations CNTN6 microdeletion; de novo mutation (PubMed=31678775).
Disease Intellectual disability (NCIt: C97250)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_WU28 ! ICGi009-B
Sex of cell Male
Age at sampling 20Y
Category Induced pluripotent stem cell
Publications

PubMed=31678775; DOI=10.1016/j.scr.2019.101591
Shnaider T.A., Pristyazhnyuk I.E., Menzorov A.G., Matveeva N.M., Nikitina T.V., Khabarova A.A., Skryabin N.A., Kashevarova A.A., Lopatkina M.E., Nazarenko L.P., Lebedev I.N., Serov O.L.
Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability.
Stem Cell Res. 41:101591-101591(2019)

Cross-references
Cell line databases/resources hPSCreg; ICGi009-A
Biological sample resources BioSamples; SAMEA5780089
Entry history
Entry creation05-Jul-2019
Last entry updated19-Dec-2019
Version number2