Hypotonia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0860006
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Genes

13 genes associated with the disease Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CAMKMT calmodulin-lysine N-methyltransferase
CCDC174 coiled-coil domain containing 174
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CTBP1 C-terminal binding protein 1
CYCS cytochrome c, somatic
EBF3 early B-cell factor 3
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
NALCN sodium leak channel, non selective
PPM1B protein phosphatase, Mg2+/Mn2+ dependent, 1B
PREPL prolyl endopeptidase-like
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
TBCK TBC1 domain containing kinase
UNC80 unc-80 homolog (C. elegans)