aorta Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group cardiovascular (Genetic Association Database)
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33 genes associated with the disease aorta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
C9ORF84 chromosome 9 open reading frame 84
CNTN1 contactin 1
CRCP CGRP receptor component
FHIT fragile histidine triad
GLRA3 glycine receptor, alpha 3
GNA12 guanine nucleotide binding protein (G protein) alpha 12
GOT2 glutamic-oxaloacetic transaminase 2, mitochondrial
GRID1 glutamate receptor, ionotropic, delta 1
HMCN1 hemicentin 1
KCTD7 potassium channel tetramerization domain containing 7
LOXL1 lysyl oxidase-like 1
MACROD2 MACRO domain containing 2
MAGI2 membrane associated guanylate kinase, WW and PDZ domain containing 2
MAGOHB mago-nashi homolog B (Drosophila)
MAOB monoamine oxidase B
MARCH1 membrane-associated ring finger (C3HC4) 1, E3 ubiquitin protein ligase
MPRIP myosin phosphatase Rho interacting protein
MTHFD1L methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like
NAB1 NGFI-A binding protein 1 (EGR1 binding protein 1)
NRG3 neuregulin 3
PCDH9 protocadherin 9
PLCH1 phospholipase C, eta 1
PPFIA2 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2
QKI QKI, KH domain containing, RNA binding
RALYL RALY RNA binding protein-like
SLC10A1 solute carrier family 10 (sodium/bile acid cotransporter), member 1
SLC35F1 solute carrier family 35, member F1
SMG6 SMG6 nonsense mediated mRNA decay factor
THSD7A thrombospondin, type I, domain containing 7A
TMEM232 transmembrane protein 232
WDFY4 WDFY family member 4
WWOX WW domain containing oxidoreductase
ZFPM2 zinc finger protein, FOG family member 2