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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.

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2019-10-15

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Lamolda, Mar
Montes, Rosa
Simón, Iris
Perales, Sonia
Martínez-Navajas, Gonzalo
Lopez-Onieva, Lourdes
Ríos-Pelegrina, Rosa
Del Moral, Raimundo García
Griñan-Lison, Carmen
Marchal, Juan A

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Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) is a rare platelet disorder caused by mutations in RUNX1. We generated an iPSC line (GENYOi005-A) from a FPDMM patient with a non-previously reported variant p.Thr196Ala. Non-integrative Sendai viruses expressing the Yamanaka reprogramming factors were used to reprogram peripheral blood mononuclear cells from this FPDMM patient. Characterization of GENYOi005-A included genetic analysis of RUNX1 locus, Short Tandem Repeats profiling, alkaline phosphatase enzymatic activity, expression of pluripotency-associated factors and differentiation studies in vitro and in vivo. This iPSC line will provide a powerful tool to study developmental alterations of FPDMM patients.

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Blood Coagulation Disorders, Inherited
Blood Platelet Disorders
Cell Differentiation
Cells, Cultured
Cellular Reprogramming
Core Binding Factor Alpha 2 Subunit
Female
Humans
Induced Pluripotent Stem Cells
Leukemia, Myeloid, Acute
Leukocytes, Mononuclear
Middle Aged
Mutation

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