Congenital Omphalocele Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0795690
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Genes

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

Symbol Name
ACTG2 actin, gamma 2, smooth muscle, enteric
ADNP activity-dependent neuroprotector homeobox
AFP alpha-fetoprotein
BHLHA9 basic helix-loop-helix family, member a9
BHMT betaine--homocysteine S-methyltransferase
CCL21 chemokine (C-C motif) ligand 21
CD320 CD320 molecule
CD96 CD96 molecule
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CEP120 centrosomal protein 120kDa
CHD7 chromodomain helicase DNA binding protein 7
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CHUK conserved helix-loop-helix ubiquitous kinase
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
DACT1 dishevelled-binding antagonist of beta-catenin 1
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
EPHB2 EPH receptor B2
EYA1 EYA transcriptional coactivator and phosphatase 1
EYA2 EYA transcriptional coactivator and phosphatase 2
FGFR1 fibroblast growth factor receptor 1
FLNA filamin A, alpha
FLNB filamin B, beta
FRAS1 Fraser extracellular matrix complex subunit 1
FREM1 FRAS1 related extracellular matrix 1
FREM2 FRAS1 related extracellular matrix protein 2
GDF11 growth differentiation factor 11
GJB2 gap junction protein, beta 2, 26kDa
GPC3 glypican 3
GPC4 glypican 4
GRIP1 glutamate receptor interacting protein 1
GYPA glycophorin A (MNS blood group)
GYPB glycophorin B (MNS blood group)
GYPE glycophorin E (MNS blood group)
HIC1 hypermethylated in cancer 1
HOXD13 homeobox D13
HYLS1 hydrolethalus syndrome 1
IFT80 intraflagellar transport 80
IFT81 intraflagellar transport 81
IGF2 insulin-like growth factor 2
ISL1 ISL LIM homeobox 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LBR lamin B receptor
LMOD1 leiomodin 1 (smooth muscle)
LRP1 low density lipoprotein receptor-related protein 1
LRP2 low density lipoprotein receptor-related protein 2
MAPK1 mitogen-activated protein kinase 1
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MBTPS2 membrane-bound transcription factor peptidase, site 2
MKS1 Meckel syndrome, type 1
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MMP2 matrix metallopeptidase 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MYH11 myosin, heavy chain 11, smooth muscle
MYLK myosin light chain kinase
NEK9 NIMA-related kinase 9
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NXN nucleoredoxin
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PCSK5 proprotein convertase subtilisin/kexin type 5
PIGN phosphatidylinositol glycan anchor biosynthesis, class N
PITX2 paired-like homeodomain 2
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
PORCN porcupine homolog (Drosophila)
RAB23 RAB23, member RAS oncogene family
SDS serine dehydratase
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SLC19A1 solute carrier family 19 (folate transporter), member 1
SPECC1L sperm antigen with calponin homology and coiled-coil domains 1-like
TCN2 transcobalamin II
TGM1 transglutaminase 1
THRA thyroid hormone receptor, alpha
TP63 tumor protein p63
TSHB thyroid stimulating hormone, beta
TTC7A tetratricopeptide repeat domain 7A
TWIST2 twist family bHLH transcription factor 2
WDR20 WD repeat domain 20
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60
YWHAE tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon