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Cellosaurus ICGi013-A (CVCL_WU29)

[Text version]
Cell line name ICGi013-A
Synonyms iTAF13-26; iTAF13del26
Accession CVCL_WU29
Resource Identification Initiative To cite this cell line use: ICGi013-A (RRID:CVCL_WU29)
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; 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_WU30 ! ICGi013-B
Sex of cell Female
Age at sampling 18Y
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; ICGi013-A
SKIP; SKIP005570
Biological sample resources BioSamples; SAMEA5859254
Encyclopedic resources Wikidata; Q94313435
Entry history
Entry creation05-Jul-2019
Last entry update19-Dec-2024
Version number9