inguinal hernia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal. (Human Disease Ontology, DOID_0060320)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000023
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Genes

82 genes associated with the inguinal hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
AMH anti-Mullerian hormone
AMHR2 anti-Mullerian hormone receptor, type II
AR androgen receptor
ARSB arylsulfatase B
ATP6V0A2 ATPase, H+ transporting, lysosomal V0 subunit a2
B3GAT3 beta-1,3-glucuronyltransferase 3
BMPER BMP binding endothelial regulator
CBS cystathionine-beta-synthase
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
COL3A1 collagen, type III, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
DSE dermatan sulfate epimerase
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
ELN elastin
ELOVL4 ELOVL fatty acid elongase 4
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
FBLN5 fibulin 5
FGD1 FYVE, RhoGEF and PH domain containing 1
FGFR1 fibroblast growth factor receptor 1
FKBP14 FK506 binding protein 14, 22 kDa
GALNS galactosamine (N-acetyl)-6-sulfatase
GATA6 GATA binding protein 6
GLB1 galactosidase, beta 1
GLI3 GLI family zinc finger 3
GLRA1 glycine receptor, alpha 1
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GPC3 glypican 3
GUSB glucuronidase, beta
HSPG2 heparan sulfate proteoglycan 2
IDS iduronate 2-sulfatase
IDUA iduronidase, alpha-L-
IRX5 iroquois homeobox 5
KIF7 kinesin family member 7
LTBP4 latent transforming growth factor beta binding protein 4
MAN2B1 mannosidase, alpha, class 2B, member 1
MBTPS2 membrane-bound transcription factor peptidase, site 2
MED12 mediator complex subunit 12
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NEU1 sialidase 1 (lysosomal sialidase)
NIPBL Nipped-B homolog (Drosophila)
NOTCH1 notch 1
NOTCH2 notch 2
OFD1 oral-facial-digital syndrome 1
P3H1 prolyl 3-hydroxylase 1
PIEZO2 piezo-type mechanosensitive ion channel component 2
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
PLOD2 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2
PORCN porcupine homolog (Drosophila)
PRDM5 PR domain containing 5
PTDSS1 phosphatidylserine synthase 1
PYCR1 pyrroline-5-carboxylate reductase 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SATB2 SATB homeobox 2
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SKI SKI proto-oncogene
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
SMAD3 SMAD family member 3
SRCAP Snf2-related CREBBP activator protein
STRA6 stimulated by retinoic acid 6
TBX1 T-box 1
TBX3 T-box 3
TGFB2 transforming growth factor, beta 2
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)
TMCO1 transmembrane and coiled-coil domains 1
TMEM70 transmembrane protein 70
UBA1 ubiquitin-like modifier activating enzyme 1
WDR19 WD repeat domain 19
WDR35 WD repeat domain 35
WNT5A wingless-type MMTV integration site family, member 5A
ZEB1 zinc finger E-box binding homeobox 1