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Cellosaurus HPS1627 (CVCL_YS36)

[Text version]
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

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 creation12-Mar-2020
Last entry update29-Jun-2023
Version number6