Cellosaurus cell line HPS1627 (CVCL

Cross-references
Cell line name	HPS1627
Synonyms	BRCi019-A
Accession	CVCL_YS36
Secondary accession	CVCL_C0HH
Resource Identification Initiative	To cite this cell line use: HPS1627 (RRID:CVCL_YS36)
Comments	Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease	22q11.2 deletion syndrome (NCIt: C2989) 22q11.2 deletion syndrome (ORDO: Orphanet_567)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_YS37 ! HPS1628 CVCL_YS38 ! HPS1629 CVCL_YS39 ! HPS1630 CVCL_YS40 ! HPS1631
Sex of cell	Female
Age at sampling	<10Y
Category	Induced pluripotent stem cell
Publications	PubMed=35292424; DOI=10.1016/j.scr.2022.102744 Shimizu T., Matsuo-Takasaki M., Luijkx D., Takami M., Arai Y., Noguchi M., Nakamura Y., Hayata T., Saito M.K., Hayashi Y. Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion. Stem Cell Res. 61:102744-102744(2022)
Cell line collections (Providers)	RCB; HPS1627
Cell line databases/resources	hPSCreg; BRCi019-A
Encyclopedic resources	Wikidata; Q94219799
Entry history
Entry creation	12-Mar-2020
Last entry update	29-Jun-2023
Version number	6