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Cellosaurus IMGTi001-B (CVCL_VQ14)

[Text version]
Cell line name IMGTi001-B
Synonyms iPSC-r(22)-2; iTAF5-32
Accession CVCL_VQ14
Resource Identification Initiative To cite this cell line use: IMGTi001-B (RRID:CVCL_VQ14)
Comments From: Research Institute of Medical Genetics; Tomsk; Russia.
Population: Caucasian.
Karyotypic information: r(22),del22q13.32-q13.33,dup22q13.32,del3q13.31 (PubMed=30144655).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Phelan-McDermid syndrome (NCIt: C157124)
Ring chromosome 22 syndrome (NCIt: C179702)
Monosomy 22q13.3 (ORDO: Orphanet_48652)
Ring chromosome 22 syndrome (ORDO: Orphanet_1446)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A9Q1 (TAF5)
Sex of cell Female
Age at sampling 3Y
Category Induced pluripotent stem cell

PubMed=30144655; DOI=10.1016/j.scr.2018.08.012
Nikitina T.V., Menzorov A.G., Kashevarova A.A., Gridina M.M., Khabarova A.A., Yakovleva Y.S., Lopatkina M.E., Kizilova E.A., Vasilyev S.A., Serov O.L., Lebedev I.N.
Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22.
Stem Cell Res. 31:244-248(2018)

Nikitina T.V., Kashevarova A.A., Lebedev I.N.
Chromosomal instability and karyotype correction in human induced pluripotent stem cells.
Russ. J. Genet. 55:1183-1195(2019)

PubMed=33619287; DOI=10.1038/s41598-021-83399-3
Nikitina T.V., Kashevarova A.A., Gridina M.M., Lopatkina M.E., Khabarova A.A., Yakovleva Y.S., Menzorov A.G., Minina Y.A., Pristyazhnyuk I.E., Vasilyev S.A., Fedotov D.A., Serov O.L., Lebedev I.N.
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming.
Sci. Rep. 11:4325-4325(2021)

Cell line databases/resources hPSCreg; IMGTi001-B
Biological sample resources BioSamples; SAMEA4862238
Encyclopedic resources Wikidata; Q94316259
Entry history
Entry creation07-Sep-2018
Last entry update29-Jun-2023
Version number10