Symphysis Pubis Dysfunction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C2609259
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Genes

21 genes associated with the disease Symphysis Pubis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARSD arylsulfatase D
COL2A1 collagen, type II, alpha 1
DSC1 desmocollin 1
EVX2 even-skipped homeobox 2
FBLN1 fibulin 1
GALC galactosylceramidase
HOXA13 homeobox A13
HOXD13 homeobox D13
KRT7 keratin 7, type II
LAMP2 lysosomal-associated membrane protein 2
LRRK2 leucine-rich repeat kinase 2
MGAM maltase-glucoamylase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PYCARD PYD and CARD domain containing
RIMS2 regulating synaptic membrane exocytosis 2
SCLY selenocysteine lyase
SI sucrase-isomaltase (alpha-glucosidase)
SNCA synuclein, alpha (non A4 component of amyloid precursor)
STS steroid sulfatase (microsomal), isozyme S
TAL1 T-cell acute lymphocytic leukemia 1