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 Tomoya Shimizu, Mami Matsuo-Takasaki, Dorian Luijkx, Miho Takami, Yutaka Arai, Michiya Noguchi, Yukio Nakamura, Tadayoshi Hayata, Megumu K. Saito, Yohei Hayashi; 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