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Cellosaurus ICGi009-B (CVCL_WU28)

[Text version]
Cell line name ICGi009-B
Synonyms iTAF3-37; iTAF3del37; ICGi010-A
Accession CVCL_WU28
Secondary accession CVCL_WP99
Resource Identification Initiative To cite this cell line use: ICGi009-B (RRID:CVCL_WU28)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 2176; CNTN6; Unexplicit; Microdeletion; Zygosity=Unspecified; Note=De novo mutation (PubMed=31678775).
Disease Intellectual disability (NCIt: C97250)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_WP98 ! ICGi009-A
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-B
SKIP; SKIP005568
Biological sample resources BioSamples; SAMEA5859257
BioSamples; SAMEA5843918
Encyclopedic resources Wikidata; Q94313432
Entry history
Entry creation05-Jul-2019
Last entry update29-Jun-2023
Version number8