Cellosaurus ICGi025-F (CVCL_A7MK)
Cell line name | ICGi025-F |
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Synonyms | iPSC-r(8)-6; iTAF11-12 |
Accession | CVCL_A7MK |
Resource Identification Initiative | To cite this cell line use: ICGi025-F (RRID:CVCL_A7MK) |
Comments | From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia. Population: Caucasian. Omics: Array-based CGH. Omics: SNP array analysis. Caution: We assigned the ICGi025-F name for consistency with the ICGi025-A cell line. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Disease | Developmental delay (NCIt: C116942) Ring chromosome 8 syndrome (NCIt: C175705) Ring chromosome 8 syndrome (ORDO: Orphanet_1450) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Hierarchy | Parent: CVCL_A7ML (TAF11) |
Sex of cell | Male |
Age at sampling | 1Y4M |
Category | Induced pluripotent stem cell |
Publications | PubMed=33619287; DOI=10.1038/s41598-021-83399-3 |
Cross-references | |
Encyclopedic resources | Wikidata; Q107115424 |
Entry history | |
Entry creation | 20-May-2021 |
Last entry update | 29-Jun-2023 |
Version number | 5 |