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Cellosaurus HPS1631 (CVCL_YS40)

[Text version]
Cell line name HPS1631
Synonyms BRCi019-E
Accession CVCL_YS40
Resource Identification Initiative To cite this cell line use: HPS1631 (RRID:CVCL_YS40)
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_YS36 ! HPS1627
CVCL_YS37 ! HPS1628
CVCL_YS38 ! HPS1629
CVCL_YS39 ! HPS1630
Sex of cell Female
Age at sampling <10Y
Category Induced pluripotent stem cell
Cell line collections (Providers) RCB; HPS1631
Cell line databases/resources hPSCreg; BRCi019-E
Encyclopedic resources Wikidata; Q94219809
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number5