PADI6

peptidyl arginine deiminase 6
OMIM: 610363
PanelMode of inheritanceDetails
1 panel
R-numbers: R417.2
Signed-off version 2.0
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
Preimplantation embryonic lethality 2 OMIM:617234, preimplantation embryonic lethality 2 MONDO:0014978, Beckwith-Wiedemann syndrome, Multi Locus Imprinting Disturbance