Conotruncal Anomaly Face Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0795907
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Genes

17 genes associated with the disease Conotruncal Anomaly Face Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
AWAT1 acyl-CoA wax alcohol acyltransferase 1
COMT catechol-O-methyltransferase
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
CXCL8 chemokine (C-X-C motif) ligand 8
DGCR2 DiGeorge syndrome critical region gene 2
DGCR6 DiGeorge syndrome critical region gene 6
DGCR8 DGCR8 microprocessor complex subunit
ESS2 ess-2 splicing factor homolog
FGF8 fibroblast growth factor 8 (androgen-induced)
GP1BB glycoprotein Ib (platelet), beta polypeptide
HIRA histone cell cycle regulator
JMJD1C jumonji domain containing 1C
RREB1 ras responsive element binding protein 1
SEC24C SEC24 family member C
TBX1 T-box 1
UFD1 ubiquitin recognition factor in ER associated degradation 1