Cellosaurus IMGTi001-A (CVCL_VQ13)
Cell line name | IMGTi001-A |
---|---|
Synonyms | iPSC-r(22)-1; iTAF5-29 |
Accession | CVCL_VQ13 |
Resource Identification Initiative | To cite this cell line use: IMGTi001-A (RRID:CVCL_VQ13) |
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 |
Publications | PubMed=30144655; DOI=10.1016/j.scr.2018.08.012 DOI=10.1134/S1022795419100090 PubMed=33619287; DOI=10.1038/s41598-021-83399-3; PMCID=PMC7900208 |
Cross-references | |
Cell line databases/resources | hPSCreg; IMGTi001-A |
Biological sample resources | BioSamples; SAMEA4862236 |
Encyclopedic resources | Wikidata; Q94316254 |
Entry history | |
Entry creation | 07-Sep-2018 |
Last entry update | 29-Jun-2023 |
Version number | 10 |