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Cellosaurus HPS1628 (CVCL_YS37)

[Text version]
Cell line name HPS1628
Synonyms BRCi019-B
Accession CVCL_YS37
Resource Identification Initiative To cite this cell line use: HPS1628 (RRID:CVCL_YS37)
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_YS38 ! HPS1629
CVCL_YS39 ! HPS1630
CVCL_YS40 ! HPS1631
Sex of cell Female
Age at sampling <10Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1628
Cell line databases/resources hPSCreg; BRCi019-B
Encyclopedic resources Wikidata; Q94219801
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number5