Conn 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/C1384514
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Genes

79 genes associated with the disease Conn Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADD1 adducin 1 (alpha)
ADIPOQ adiponectin, C1Q and collagen domain containing
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
AGTR2 angiotensin II receptor, type 2
APBB3 amyloid beta (A4) precursor protein-binding, family B, member 3
APOA1 apolipoprotein A-I
ARMC5 armadillo repeat containing 5
ATF3 activating transcription factor 3
ATM ATM serine/threonine kinase
ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3
ATP6AP2 ATPase, H+ transporting, lysosomal accessory protein 2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit
CASP1 caspase 1, apoptosis-related cysteine peptidase
CD44 CD44 molecule (Indian blood group)
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
CLCN2 chloride channel, voltage-sensitive 2
CLCNKB chloride channel, voltage-sensitive Kb
CPA1 carboxypeptidase A1 (pancreatic)
CRY1 cryptochrome circadian clock 1
CRY2 cryptochrome circadian clock 2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP21A2 cytochrome P450, family 21, subfamily A, polypeptide 2
CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3
EDN1 endothelin 1
ENPEP glutamyl aminopeptidase (aminopeptidase A)
FAM131A family with sequence similarity 131, member A
FLNB filamin B, beta
GCG glucagon
GNAS GNAS complex locus
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
HSD3B1 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KCNK3 potassium channel, two pore domain subfamily K, member 3
KCNK5 potassium channel, two pore domain subfamily K, member 5
KCNK9 potassium channel, two pore domain subfamily K, member 9
KNG1 kininogen 1
KRAS Kirsten rat sarcoma viral oncogene homolog
LGALS14 lectin, galactoside-binding, soluble, 14
LGALS3 lectin, galactoside-binding, soluble, 3
LHCGR luteinizing hormone/choriogonadotropin receptor
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MSR1 macrophage scavenger receptor 1
MT3 metallothionein 3
MTDH metadherin
NGB neuroglobin
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
NLRP3 NLR family, pyrin domain containing 3
NPPA natriuretic peptide A
NR0B1 nuclear receptor subfamily 0, group B, member 1
NR3C2 nuclear receptor subfamily 3, group C, member 2
NR5A1 nuclear receptor subfamily 5, group A, member 1
PCP4 Purkinje cell protein 4
PMPCA peptidase (mitochondrial processing) alpha
POMC proopiomelanocortin
PPP1R2P9 protein phosphatase 1, regulatory (inhibitor) subunit 2 pseudogene 9
PRKACA protein kinase, cAMP-dependent, catalytic, alpha
PTH parathyroid hormone
PTX3 pentraxin 3, long
REN renin
RET ret proto-oncogene
SCARB1 scavenger receptor class B, member 1
SCNN1B sodium channel, non voltage gated 1 beta subunit
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SIAH1 siah E3 ubiquitin protein ligase 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
SRA1 steroid receptor RNA activator 1
UTS2 urotensin 2
VPREB3 pre-B lymphocyte 3