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Prepair 1000+
Prepair 500+
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Retinitis Pigmentosa Superpanel
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Severe Combined Immunodeficiency (absent T present B cells)
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Stickler Syndrome
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TCGA_PANCAN_2018
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Vascular Malformations SuperPanel
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Version
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0.2
Gene or Genomic Entity Name
PPM1D
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07 Jan 2020
NCGC v0.0
PPM1D
Lavinia Gordon gene: PPM1D was added
gene: PPM1D was added to NCGC. Sources: NCGC
Mode of inheritance for gene: PPM1D was set to Other
Phenotypes for gene: PPM1D were set to NA