Cellosaurus ICGi024-B (CVCL_A7MQ)
| Cell line name | ICGi024-B |
|---|---|
| Synonyms | iPSC-r(18)-1; iTAF12-3 |
| Accession | CVCL_A7MQ |
| Resource Identification Initiative | To cite this cell line use: ICGi024-B (RRID:CVCL_A7MQ) |
| 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 ICGi024-B name for consistency with the ICGi024-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 18 syndrome (NCIt: C175706) Ring chromosome 18 syndrome (ORDO: Orphanet_1442) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_A7MS (TAF12) |
| Sex of cell | Male |
| Age at sampling | 3Y |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=33619287; DOI=10.1038/s41598-021-83399-3; PMCID=PMC7900208 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q107115417 |
| Entry history | |
| Entry creation | 20-May-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 5 |