ID   ICGi025-D
AC   CVCL_A7MI
SY   iPSC-r(8)-4; iTAF11-9
DR   Wikidata; Q107115422
RX   PubMed=33619287;
CC   From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
CC   Population: Caucasian.
CC   Omics: Array-based CGH.
CC   Omics: SNP array analysis.
CC   Caution: We assigned the ICGi025-D name for consistency with the ICGi025-A cell line.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C116942; Developmental delay
DI   NCIt; C175705; Ring chromosome 8 syndrome
DI   ORDO; Orphanet_1450; Ring chromosome 8 syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_A7ML ! TAF11
SX   Male
AG   1Y4M
CA   Induced pluripotent stem cell
DT   Created: 20-05-21; Last updated: 29-06-23; Version: 5
//
RX   PubMed=33619287; DOI=10.1038/s41598-021-83399-3; PMCID=PMC7900208;
RA   Nikitina T.V., Kashevarova A.A., Gridina M.M., Lopatkina M.E.,
RA   Khabarova A.A., Yakovleva Y.S., Menzorov A.G., Minina J.M.,
RA   Pristyazhnyuk I.E., Vasilyev S.A., Fedotov D.A., Serov O.L.,
RA   Lebedev I.N.;
RT   "Complex biology of constitutional ring chromosomes structure and
RT   (in)stability revealed by somatic cell reprogramming.";
RL   Sci. Rep. 11:4325-4325(2021).
//