Heart Failure, Congestive Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

28 genes associated with the Heart Failure, Congestive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADRA2C adrenoceptor alpha 2C
ADRB1 adrenoceptor beta 1
ADRB2 adrenoceptor beta 2, surface
ADRB3 adrenoceptor beta 3
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
AMPD1 adenosine monophosphate deaminase 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
EDN1 endothelin 1
EDNRA endothelin receptor type A
HFE hemochromatosis
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL10 interleukin 10
LMNA lamin A/C
MMP3 matrix metallopeptidase 3
MMP9 matrix metallopeptidase 9
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NOS3 nitric oxide synthase 3 (endothelial cell)
SCNN1B sodium channel, non voltage gated 1 beta subunit
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TGFB1 transforming growth factor, beta 1
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UGT2B7 UDP glucuronosyltransferase 2 family, polypeptide B7
VEGFA vascular endothelial growth factor A