2P21 Microdeletion Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4304537
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Genes

4 genes associated with the disease 2P21 Microdeletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CAMKMT calmodulin-lysine N-methyltransferase
PPM1B protein phosphatase, Mg2+/Mn2+ dependent, 1B
PREPL prolyl endopeptidase-like
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1