Cellosaurus CIPi001-A (CVCL_B3S5)
| Cell line name | CIPi001-A |
|---|---|
| Synonyms | iPSC-16p11.2 deletion |
| Accession | CVCL_B3S5 |
| Resource Identification Initiative | To cite this cell line use: CIPi001-A (RRID:CVCL_B3S5) |
| Comments | From: Children's Hospital of Capital Institute of Pediatrics; Beijing; China. Population: Chinese. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Benign familial infantile seizures (NCIt: C183308) Chromosome 16p11.2 deletion syndrome (NCIt: C120408) Benign familial infantile epilepsy (ORDO: Orphanet_306) Proximal 16p11.2 microdeletion syndrome (ORDO: Orphanet_261197) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 4Y3M |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=34995844; DOI=10.1016/j.scr.2021.102634 |
| Cross-references | |
| Cell line databases/resources | hPSCreg; CIPi001-A |
| Biological sample resources | BioSamples; SAMEA10271033 |
| Encyclopedic resources | Wikidata; Q110432723 |
| Entry history | |
| Entry creation | 16-Dec-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |