Congenital Malrotation Of Intestine Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0221210
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Genes

77 genes associated with the disease Congenital Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
ACTG2 actin, gamma 2, smooth muscle, enteric
AMER1 APC membrane recruitment protein 1
ARID1B AT rich interactive domain 1B (SWI1-like)
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
ASXL1 additional sex combs like transcriptional regulator 1
BCOR BCL6 corepressor
CCDC22 coiled-coil domain containing 22
CENPF centromere protein F, 350/400kDa
CFC1 cripto, FRL-1, cryptic family 1
CHRM3 cholinergic receptor, muscarinic 3
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
CLMP CXADR-like membrane protein
COMT catechol-O-methyltransferase
DHCR24 24-dehydrocholesterol reductase
DHCR7 7-dehydrocholesterol reductase
EYA1 EYA transcriptional coactivator and phosphatase 1
FBN2 fibrillin 2
FGFR2 fibroblast growth factor receptor 2
FLI1 Fli-1 proto-oncogene, ETS transcription factor
FLNA filamin A, alpha
FOXF1 forkhead box F1
GATA6 GATA binding protein 6
GP1BB glycoprotein Ib (platelet), beta polypeptide
GPC3 glypican 3
GPC4 glypican 4
HDAC3 histone deacetylase 3
HDAC8 histone deacetylase 8
HIRA histone cell cycle regulator
HMGA2 high mobility group AT-hook 2
HNRNPU heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
ISL1 ISL LIM homeobox 1
JMJD1C jumonji domain containing 1C
KAT6A K(lysine) acetyltransferase 6A
KDM6A lysine (K)-specific demethylase 6A
KIF7 kinesin family member 7
KLHL7 kelch-like family member 7
KMT2A lysine (K)-specific methyltransferase 2A
KMT2D lysine (K)-specific methyltransferase 2D
LBR lamin B receptor
LEMD3 LEM domain containing 3
LMOD1 leiomodin 1 (smooth muscle)
LRP2 low density lipoprotein receptor-related protein 2
MED12 mediator complex subunit 12
MKS1 Meckel syndrome, type 1
MMP21 matrix metallopeptidase 21
MYH11 myosin, heavy chain 11, smooth muscle
MYLK myosin light chain kinase
MYRF myelin regulatory factor
NIPBL Nipped-B homolog (Drosophila)
NOTCH2 notch 2
NPHP3 nephronophthisis 3 (adolescent)
PIGN phosphatidylinositol glycan anchor biosynthesis, class N
PIGQ phosphatidylinositol glycan anchor biosynthesis, class Q
PORCN porcupine homolog (Drosophila)
RAD21 RAD21 homolog (S. pombe)
RARB retinoic acid receptor, beta
RFX6 regulatory factor X, 6
RREB1 ras responsive element binding protein 1
SALL4 spalt-like transcription factor 4
SEC24C SEC24 family member C
SETD5 SET domain containing 5
SIX1 SIX homeobox 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
SMO smoothened, frizzled class receptor
TBX1 T-box 1
TEF thyrotrophic embryonic factor
TGFB1 transforming growth factor, beta 1
TICRR TOPBP1-interacting checkpoint and replication regulator
TP63 tumor protein p63
TTC7A tetratricopeptide repeat domain 7A
UBE3B ubiquitin protein ligase E3B
UFD1 ubiquitin recognition factor in ER associated degradation 1
WASHC5 WASH complex subunit 5
YES1 YES proto-oncogene 1, Src family tyrosine kinase
ZFPM2 zinc finger protein, FOG family member 2