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Cellosaurus GENYOi005-A (CVCL_WZ24)

[Text version]

Cell line name GENYOi005-A
Synonyms FPD/AML-PBMC-iPSC4F73
Accession CVCL_WZ24
Resource Identification Initiative To cite this cell line use: GENYOi005-A (RRID:CVCL_WZ24)
Comments From: Centre for Genomics and Oncological Research (GENYO); Granada; Spain.
Derived from sampling site: Peripheral blood.
Sequence variations Heterozygous for RUNX1 p.Thr196Ala (c.586A>G) (PubMed=31698193).
Disease Familial platelet disorder with associated myeloid malignancy (NCIt: C162696)
Familial platelet disorder with associated myeloid malignancy (ORDO: Orphanet_71290)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 54Y
Category Induced pluripotent stem cell

PubMed=31698193; DOI=10.1016/j.scr.2019.101603
Lamolda M., Montes R., Simon I., Perales S., Martinez-Navajas G., Lopez-Onieva L., Rios-Pelegrina R., Del Moral R.G., Grinan-Lison C., Marchal J.A., Lozano M.L., Ramos-Mejia V., Rivera J., Bastida J.M., Real P.J.
GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with familial platelet disorder with associated myeloid malignancy (FPDMM) carrying a p.Thr196Ala variant.
Stem Cell Res. 41:101603-101603(2019)

Cell line databases/resources hPSCreg; GENYOi005-A
Biological sample resources BioSamples; SAMEA5959283
Other Wikidata; Q93560855
Entry history
Entry creation06-Sep-2019
Last entry update02-Jul-2020
Version number3