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Cellosaurus CIPi001-A (CVCL_B3S5)

[Text version]
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
Ji X.-N., Gao Y.-Y., Zhang P.-P., Jin Z.-Q., Zhang Y., Yang M.-N., Zhang X., Chen Q.
Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion.
Stem Cell Res. 59:102634-102634(2022)

Cross-references
Cell line databases/resources hPSCreg; CIPi001-A
Biological sample resources BioSamples; SAMEA10271033
Encyclopedic resources Wikidata; Q110432723
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4